Description

semenogelin I [Source:HGNC Symbol;Acc:HGNC:10742]

Synonyms

CT103, SEMG

Location
INSDC coordinates

chromosome:GRCh38:CM000682.2:45206997:45209772:1

About this gene

This gene has 1 transcript (splice variant), 11 orthologues, 1 paralogue, is a member of 1 Ensembl protein family and is associated with 98 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
SEMG1-001ENST000003727811662462aaENSP00000361867
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS13345P04279 NM_003007
NP_002998
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.

Gene-based displays