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    DCLRE1C DNA cross-link repair 1C [ Homo sapiens (human) ]

    Gene ID: 64421, updated on 30-Oct-2024

    Summary

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    Official Symbol
    DCLRE1Cprovided by HGNC
    Official Full Name
    DNA cross-link repair 1Cprovided by HGNC
    Primary source
    HGNC:HGNC:17642
    See related
    Ensembl:ENSG00000152457 MIM:605988; AllianceGenome:HGNC:17642
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    SCIDA; SNM1C; A-SCID; RS-SCID; DCLREC1C
    Summary
    This gene encodes a nuclear protein that is involved in V(D)J recombination and DNA repair. The encoded protein has single-strand-specific 5'-3' exonuclease activity; it also exhibits endonuclease activity on 5' and 3' overhangs and hairpins. The protein also functions in the regulation of the cell cycle in response to DNA damage. Mutations in this gene can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]
    Expression
    Ubiquitous expression in lymph node (RPKM 3.7), spleen (RPKM 2.8) and 24 other tissues See more
    Orthologs
    mouse all
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    Genomic context

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    See DCLRE1C in Genome Data Viewer
    Location:
    10p13
    Exon count:
    20
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (14897359..14954432, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (14911323..14968389, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (14939358..14996431, complement)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3085 Neighboring gene Myb/SANT DNA binding domain containing 7 Neighboring gene heat shock protein family A (Hsp70) member 14 Neighboring gene SUV39H2 divergent transcript Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2164 Neighboring gene SUV39H2 histone lysine methyltransferase Neighboring gene NANOG hESC enhancer GRCh37_chr10:14946352-14947052 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3086 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3087 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr10:14994732-14995460 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr10:14995461-14996188 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2165 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2166 Neighboring gene meiosis/spermiogenesis associated 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr10:15033655-15034186 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr10:15034187-15034717 Neighboring gene olfactory receptor family 7 subfamily E member 110 pseudogene Neighboring gene olfactory receptor family 7 subfamily E member 26 pseudogene

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Expression

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    • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
    • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
    • BioProject: PRJEB4337
    • Publication: PMID 24309898
    • Analysis date: Wed Apr 4 07:08:55 2018

    Bibliography

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    Related articles in PubMed

    1. The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events. Pannicke U, et al. Hum Mutat, 2010 Feb. PMID 19953608
    2. The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlation. Lee PP, et al. Clin Immunol, 2013 Dec. PMID 24230999
    3. Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families. Kobayashi N, et al. Hum Genet, 2003 Apr. PMID 12592555
    4. Expansion of clonotype-restricted HLA-identical maternal CD4+ T cells in a patient with severe combined immunodeficiency and a homozygous mutation in the Artemis gene. Kobayashi N, et al. Clin Immunol, 2003 Aug. PMID 12921762
    5. Increased Artemis levels confer radioresistance to both high and low LET radiation exposures. Sridharan DM, et al. Radiat Oncol, 2012 Jun 19. PMID 22713703, Free PMC Article

    See all (101) citations in PubMed

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?
    1. Lentiviral Gene Therapy for Artemis-Deficient SCID.
      Title: Lentiviral Gene Therapy for Artemis-Deficient SCID.
    2. Dynamics of the Artemis and DNA-PKcs Complex in the Repair of Double-Strand Breaks.
      Title: Dynamics of the Artemis and DNA-PKcs Complex in the Repair of Double-Strand Breaks.
    3. Structural analysis of the basal state of the Artemis:DNA-PKcs complex.
      Title: Structural analysis of the basal state of the Artemis:DNA-PKcs complex.
    4. Staring at the Naked Goddess: Unraveling the Structure and Reactivity of Artemis Endonuclease Interacting with a DNA Double Strand.
      Title: Staring at the Naked Goddess: Unraveling the Structure and Reactivity of Artemis Endonuclease Interacting with a DNA Double Strand.
    5. Structural analysis of the catalytic domain of Artemis endonuclease/SNM1C reveals distinct structural features.
      Title: Structural analysis of the catalytic domain of Artemis endonuclease/SNM1C reveals distinct structural features.
    6. Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency.
      Title: Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency.
    7. study presents one of three affected siblings who was diagnosed with DCLRE1C-deficient combined immunodeficiencies
      Title: Intrauterine detection of DCLRE1C (Artemis) mutation by restriction fragment length polymorphism.
    8. The results suggest that TDP1 and Artemis perform different functions in the repair of terminally blocked double-stranded breaks (DSBs) by the classical nonhomologous end joining pathway, and that whereas an Artemis deficiency prevents end joining of some DSBs, a TDP1 deficiency tends to promote DSB misjoining.
      Title: TDP1 suppresses mis-joining of radiomimetic DNA double-strand breaks and cooperates with Artemis to promote optimal nonhomologous end joining.
    9. Study provides evidence that Replication forks can break quickly in S-phase upon DNA replication stress induction by an endonucleolytic mechanism independent of MUS81. Two nucleases ARTEMIS and XPF-ERCC1 are responsible for this Rapid-Replication Fork Breakage (RRFB) which takes place during S and G2 phases of the cell cycle.
      Title: DNA replication stress triggers rapid DNA replication fork breakage by Artemis and XPF.
    10. Data suggest that stimulation of Artemis nuclease/DCLRE1C activity by XRCC4-DNA ligase IV hetero-complex and efficiency of blunt-end ligation are determined by structural configurations at the DNA ends. (XRCC4 = X-ray repair cross complementing 4)
      Title: Effects of DNA end configuration on XRCC4-DNA ligase IV and its stimulation of Artemis activity.
    Submit: New GeneRIF Correction See all GeneRIFs (69)

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    Review eQTL and phenotype association data in this region using PheGenI

    Associated conditions

    Description Tests
    Histiocytic medullary reticulosis
    MedGen: C2700553 OMIM: 603554 GeneReviews: Not available
    		Compare labs
    Severe combined immunodeficiency due to DCLRE1C deficiency
    MedGen: C1865370 OMIM: 602450 GeneReviews: Not available
    		Compare labs

    Variation

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    See variants in ClinVar

    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    See Variation Viewer (GRCh38)

    Genotypes

    Pathways from PubChem

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    Interactions

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    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

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    Markers

    Homology

    Clone Names

    • FLJ11360, FLJ36438

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables 5'-3' DNA exonuclease activity IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables 5'-3' exonuclease activity IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    enables damaged DNA binding IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    enables endonuclease activity TAS
    Traceable Author Statement
    more info
    		  
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    		 PubMed 
    enables single-stranded DNA endodeoxyribonuclease activity IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    Process Evidence Code Pubs
    involved_in B cell differentiation IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in V(D)J recombination IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in adaptive immune response IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in double-strand break repair via nonhomologous end joining IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in double-strand break repair via nonhomologous end joining TAS
    Traceable Author Statement
    more info
    		  
    involved_in interstrand cross-link repair IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    involved_in response to ionizing radiation IEA
    Inferred from Electronic Annotation
    more info
    		  
    involved_in telomere maintenance IBA
    Inferred from Biological aspect of Ancestor
    more info
    		  
    Component Evidence Code Pubs
    located_in Golgi apparatus IDA
    Inferred from Direct Assay
    more info
    		  
    part_of nonhomologous end joining complex IDA
    Inferred from Direct Assay
    more info
    		 PubMed 
    located_in nucleoplasm IDA
    Inferred from Direct Assay
    more info
    		  
    located_in nucleoplasm TAS
    Traceable Author Statement
    more info
    		  

    General protein information

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    Preferred Names
    protein artemis
    Names
    DNA cross-link repair 1C (PSO2 homolog, S. cerevisiae)
    SNM1 homolog C
    SNM1-like protein
    severe combined immunodeficiency, type a (Athabascan)

    NCBI Reference Sequences (RefSeq)

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    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_007276.1 RefSeqGene

      Range
      4664..54225
      Download
      GenBank, FASTA, Sequence Viewer (Graphics), LRG_54

    mRNA and Protein(s)

    1. NM_001033855.3 → NP_001029027.1  protein artemis isoform a

      See identical proteins and their annotated locations for NP_001029027.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (a) encodes the longest isoform (a).
      Source sequence(s)
      AJ296101, AL360083, AW954867, BQ932042
      Consensus CDS
      CCDS31149.1
      UniProtKB/Swiss-Prot
      D3DRT6, Q1HCL2, Q5JSR4, Q5JSR5, Q5JSR7, Q5JSR8, Q5JSR9, Q5JSS0, Q5JSS7, Q6PK14, Q8N101, Q8N132, Q8TBW9, Q96SD1, Q9BVW9, Q9HAM4
      UniProtKB/TrEMBL
      A0A8V8TM57
      Related
      ENSP00000367527.2, ENST00000378278.7
      Conserved Domains (2) summary
      pfam07522
      Location:239 → 343
      DRMBL; DNA repair metallo-beta-lactamase
      cd16297
      Location:1 → 171
      artemis-SNM1C-like_MBL-fold; artemis-SNM1C and related proteins; MBL-fold metallo-hydrolase domain

    2. NM_001033857.3 → NP_001029029.1  protein artemis isoform c

      See identical proteins and their annotated locations for NP_001029029.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (d, also called V1) contains an alternate exon in the 5' UTR and initiates translation at a downstream in-frame start codon, compared to variant a. It encodes isoform c, which has a shorter N-terminus than isoform a. Variants c, d, f, and h encode the same isoform (c).
      Source sequence(s)
      AF395747, AK021422, AL360083, BQ932042
      Consensus CDS
      CCDS31150.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:119 → 223
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:1 → 51
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    3. NM_001033858.3 → NP_001029030.1  protein artemis isoform c

      See identical proteins and their annotated locations for NP_001029030.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (c, also called V5) contains two alternate exons in the 5' region and initiates translation at a downstream in-frame start codon, compared to variant a. It encodes isoform c, which has a shorter N-terminus than isoform a. Variants c, d, f, and h encode the same isoform (c).
      Source sequence(s)
      AF395751, AK022922, AL360083, BQ932042
      Consensus CDS
      CCDS31150.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:119 → 223
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:1 → 51
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    4. NM_001289076.2 → NP_001276005.1  protein artemis isoform b

      See identical proteins and their annotated locations for NP_001276005.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (e) lacks two exons in the 5' coding region and intiates translation at an alternate downstream start codon, compared to variant a. It encodes isoform b, which has a shorter and distinct N-terminus compared to variant a. Variants b, e, and g encode the same isoform (b).
      Source sequence(s)
      AL360083, BC009185, BQ932042
      Consensus CDS
      CCDS7105.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:124 → 228
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:7 → 56
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    5. NM_001289077.2 → NP_001276006.1  protein artemis isoform c

      See identical proteins and their annotated locations for NP_001276006.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (f, also called V2) contains an alternate exon in the 5' UTR and initiates translation at a downstream in-frame start codon, compared to variant a. It encodes isoform c, which has a shorter N-terminus than isoform a. Variants c, d, f, and h encode the same isoform (c).
      Source sequence(s)
      AF395748, AL360083, BQ932042
      Consensus CDS
      CCDS31150.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:119 → 223
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:1 → 51
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    6. NM_001289078.2 → NP_001276007.1  protein artemis isoform b

      See identical proteins and their annotated locations for NP_001276007.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (g, also called V4) lacks two exons in the 5' coding region and intiates translation at an alternate downstream start codon, compared to variant a. It encodes isoform b, which has a shorter and distinct N-terminus compared to variant a. Variants b, e, and g encode the same isoform (b).
      Source sequence(s)
      AF395750, AL360083, BQ932042
      Consensus CDS
      CCDS7105.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:124 → 228
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:7 → 56
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    7. NM_001289079.2 → NP_001276008.1  protein artemis isoform c

      See identical proteins and their annotated locations for NP_001276008.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (h, also called V6) contains two alternate exons in the 5' region and initiates translation at a downstream in-frame start codon, compared to variant a. It encodes isoform c, which has a shorter N-terminus than isoform a. Variants c, d, f, and h encode the same isoform (c).
      Source sequence(s)
      AF395752, AL360083, BQ932042
      Consensus CDS
      CCDS31150.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:119 → 223
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:1 → 51
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    8. NM_001350965.2 → NP_001337894.1  protein artemis isoform d

      Status: REVIEWED

      Source sequence(s)
      AC069544, AJ296101, AL360083, AW954867, BC022254, BM987109, BQ932042
      Consensus CDS
      CCDS91218.1
      UniProtKB/TrEMBL
      A0A8V8TKN9, A0A8V8TM57
      Related
      ENSP00000513066.1, ENST00000697047.1
      Conserved Domains (1) summary
      cd16297
      Location:1 → 171
      artemis-SNM1C-like_MBL-fold; artemis-SNM1C and related proteins; MBL-fold metallo-hydrolase domain

    9. NM_001350966.2 → NP_001337895.1  protein artemis isoform e

      Status: REVIEWED

      Source sequence(s)
      AC069544, AJ296101, AL360083, BC022254, BM987109, BQ932042, EL735962
      Consensus CDS
      CCDS91216.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:124 → 228
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:7 → 56
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    10. NM_001350967.2 → NP_001337896.1  protein artemis isoform f

      Status: REVIEWED

      Source sequence(s)
      AC069544, AJ296101, AL360083, AW954867, BC022254, BM987109, DA291339
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:119 → 223
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:1 → 51
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    11. NM_022487.4 → NP_071932.2  protein artemis isoform b

      See identical proteins and their annotated locations for NP_071932.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (b, also called V3) lacks an exon in the 5' coding region and initiates translation at an alternate downstream start codon, compared to variant a. It encodes isoform b, which has a shorter and distinct N-terminus compared to variant a. Variants b, e, and g encode the same isoform (b).
      Source sequence(s)
      AK021422, AL360083, BE799340, BQ932042
      Consensus CDS
      CCDS7105.1
      UniProtKB/TrEMBL
      A8K3I3
      Conserved Domains (2) summary
      pfam07522
      Location:124 → 228
      DRMBL; DNA repair metallo-beta-lactamase
      cl23716
      Location:7 → 56
      metallo-hydrolase-like_MBL-fold; mainly hydrolytic enzymes and related proteins which carry out various biological functions; MBL-fold metallohydrolase domain

    RNA

    1. NR_110297.2 RNA Sequence

      Status: REVIEWED

      Description
      Transcript Variant: This variant (i) contains three alternate internal exons, compared to variant 1. This variant is represented as non-coding because the predicted protein does not meet RefSeq quality criteria.
      Source sequence(s)
      AL360083, BC108276, BQ932042
      Related
      ENST00000378241.6

    2. NR_146960.1 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AC069544, AJ296101, AL360083, BC022254, BF356378, BM987109, BQ932042, DB110328, EL735962

    3. NR_146961.2 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AF395747, AK021422, AL360083, BI494665, BQ708910, BQ932042, DA764814

    4. NR_146962.1 RNA Sequence

      Status: REVIEWED

      Source sequence(s)
      AJ296101, AL360083, AW954867, BC067233, BI494665, BQ708910, BQ932042

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      14897359..14954432 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_047425650.1 → XP_047281606.1  protein artemis isoform X1

    2. XM_047425648.1 → XP_047281604.1  protein artemis isoform X1

    3. XM_047425651.1 → XP_047281607.1  protein artemis isoform X1

    4. XM_047425652.1 → XP_047281608.1  protein artemis isoform X2

    5. XM_047425649.1 → XP_047281605.1  protein artemis isoform X1

    6. XM_011519620.4 → XP_011517922.1  protein artemis isoform X3

      UniProtKB/TrEMBL
      A0A8V8TKH3
      Related
      ENSP00000512999.1, ENST00000492201.6
      Conserved Domains (2) summary
      pfam07522
      Location:239 → 343
      DRMBL; DNA repair metallo-beta-lactamase
      cd16297
      Location:1 → 171
      artemis-SNM1C-like_MBL-fold; artemis-SNM1C and related proteins; MBL-fold metallo-hydrolase domain

    7. XM_011519621.3 → XP_011517923.1  protein artemis isoform X4

      UniProtKB/TrEMBL
      A0A8V8TKH3, A0A8V8TLX1
      Related
      ENSP00000513091.1, ENST00000697076.1
      Conserved Domains (2) summary
      pfam07522
      Location:239 → 308
      DRMBL; DNA repair metallo-beta-lactamase
      cd16297
      Location:1 → 171
      artemis-SNM1C-like_MBL-fold; artemis-SNM1C and related proteins; MBL-fold metallo-hydrolase domain

    RNA

    1. XR_930515.3 RNA Sequence

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      14911323..14968389 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. XM_054366596.1 → XP_054222571.1  protein artemis isoform X3

    2. XM_054366593.1 → XP_054222568.1  protein artemis isoform X1

    3. XM_054366591.1 → XP_054222566.1  protein artemis isoform X1

    4. XM_054366594.1 → XP_054222569.1  protein artemis isoform X1

    5. XM_054366595.1 → XP_054222570.1  protein artemis isoform X2

    6. XM_054366592.1 → XP_054222567.1  protein artemis isoform X1

    7. XM_054366597.1 → XP_054222572.1  protein artemis isoform X4

      UniProtKB/TrEMBL
      A0A8V8TLX1

    RNA

    1. XR_008488251.1 RNA Sequence

    Nucleotide Protein
    Heading Accession and Version
    Protein Accession Links
    GenPept Link UniProtKB Link
    Q96SD1.2 GenPept UniProtKB/Swiss-Prot:Q96SD1

    Gene LinkOut

    The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

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