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SFR1P2 SFR1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 730792, updated on 17-Jun-2024

Summary

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Official Symbol
SFR1P2provided by HGNC
Official Full Name
SFR1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:51532
See related
AllianceGenome:HGNC:51532
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See SFR1P2 in Genome Data Viewer
Location:
Xq21.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (85849243..85850160, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (84280360..84281277, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (85104248..85105165, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene POF1B actin binding protein Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:84682018-84682570 Neighboring gene microRNA 1321 Neighboring gene CHM Rab escort protein Neighboring gene MPRA-validated peak7401 silencer Neighboring gene microRNA 361 Neighboring gene MPRA-validated peak7402 silencer Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:85257530-85258040 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:85270410-85271332 Neighboring gene NADH:ubiquinone oxidoreductase subunit A5 pseudogene 7

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • MEI5 meiotic recombination protein homolog pseudogene
  • SWI5-dependent recombination repair 1 pseudogene

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_022614.2 

    Range
    101..1018
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    85849243..85850160 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    84280360..84281277 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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