Description

wingless-type MMTV integration site family, member 1 [Source:HGNC Symbol;Acc:HGNC:12774]

Synonyms

INT1

Location
INSDC coordinates

chromosome:GRCh38:CM000674.2:48978453:48981676:1

About this gene

This gene has 2 transcripts (splice variants), 54 orthologues, 12 paralogues, is a member of 1 Ensembl protein family and is associated with 7 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
WNT1-001ENST000002935491185370aaENSP00000293549
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS8776P04628 NM_005430
NP_005421
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P1

PRINCIPAL1 - APPRIS candidate principal isoform.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

WNT1-201ENST000006131141278359aaENSP00000481240
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A0A087WXR9 -TSL:5

Transcript Support Level 5, for transcripts that are not supported at all by either an mRNA or an EST.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).

Gene-based displays