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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
-
NG_052797.1 RefSeqGene
- Range
-
5330..188454
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_001347990.2 → NP_001334919.1 MAM domain-containing protein 2 isoform 2 precursor
Status: VALIDATED
- Description
- Transcript Variant: This variant (3) differs in the 3' structure, resulting in a novel 3' coding region and 3' UTR, compared to variant 1. The encoded isoform (2) has a distinct C-terminus and is shorter than isoform 1.
- Source sequence(s)
-
AI003621, AL392044
- UniProtKB/TrEMBL
-
A0A0G2JQ91
-
NM_153267.5 → NP_694999.3 MAM domain-containing protein 2 isoform 1 precursor
See identical proteins and their annotated locations for NP_694999.3
Status: VALIDATED
- Description
- Transcript Variant: This variant (1) represents the longest transcript and encodes the longer isoform (1).
- Source sequence(s)
-
AL158153, AL392044, BC063634
- Consensus CDS
-
CCDS6631.1
- UniProtKB/Swiss-Prot
- Q5VW47, Q7Z304, Q8WX43, Q96BM4
- UniProtKB/TrEMBL
-
B4E320
- Related
- ENSP00000366387.4, ENST00000377182.5
- Conserved Domains (2) summary
-
- cd06263
Location:509 → 664
- MAM; Meprin, A5 protein, and protein tyrosine phosphatase Mu (MAM) domain. MAM is an extracellular domain which mediates protein-protein interactions and is found in a diverse set of proteins, many of which are known to function in cell adhesion. Members ...
- pfam00629
Location:509 → 666
- MAM; MAM domain, meprin/A5/mu
RNA
-
NR_125850.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (2) uses an alternate splice site in an internal exon compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
AL158153, AL392044, BC040299
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000009.12 Reference GRCh38.p14 Primary Assembly
- Range
-
70043581..70226972
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Reference GRCh38.p14 ALT_REF_LOCI_1
Genomic
-
NW_003315930.1 Reference GRCh38.p14 ALT_REF_LOCI_1
- Range
-
19469..158535
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060933.1 Alternate T2T-CHM13v2.0
- Range
-
82210377..82393821
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)