Description

synapsin I [Source:HGNC Symbol;Acc:HGNC:11494]

Location
INSDC coordinates

chromosome:GRCh38:CM000685.2:47571898:47619853:1

About this gene

This gene has 2 transcripts (splice variants), 56 orthologues, 2 paralogues, is a member of 1 Ensembl protein family and is associated with 3 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
SYN1-001ENST000002959873209705aaENSP00000295987
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS14280P17600 NM_006950
NP_008881
TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

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 PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
SYN1-002ENST000003406663165669aaENSP00000343206
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS35233P17600 NM_133499
NP_598006
TSL:1

TSL1: All splice junctions of the transcript 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 ALT2APPRIS candidate principal isoform that appears to be conserved in fewer than three tested non-primate species
Glossary entry for APPRIS
APPRIS website

Gene-based displays