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Protein-coding gene in the species Homo sapiens

SNTG1

SNTG1
All data from the card 17
Aliases
SNTG1, G1SYN, SYN4, syntrophin gamma 1
External IDs
OMIM: 608714; MGI: 1918346; GeneCards: SNTG1
Chr.
Chromosome 8 (human)
Band
8q11.21
End
50,796,692 bp
Chr.
Chromosome 1 (mouse)
Band
1|1 A1-A2
End
9,299,878 bp
BioGPS
More reference expression data
Databases
NCBI: entry; OMA: entry
Species
Human
Entrez
54212
Ensembl
ENSG00000147481
UniProt
Q9NSN8
RefSeq (mRNA)
NM_001287813NM_001287814NM_018967NM_001321773NM_001321775NM_001321776NM_001321777NM_001321778
RefSeq (protein)
NP_001274742NP_001274743NP_001308702NP_001308704NP_001308705NP_001308706NP_001308707NP_061840NP_001274742.1NP_061840.1NP_001308702.1
Location (UCSC)
Chr 8: 49.91 – 50.8 Mb

Gamma-1-syntrophin is a protein that in humans is encoded by the SNTG1 gene.

The protein encoded by this gene is a member of the syntrophin family. Syntrophins are cytoplasmic peripheral membrane proteins that typically contain 2 pleckstrin homology (PH) domains, a PDZ domain that bisects the first PH domain, and a C-terminal domain that mediates dystrophin binding. This gene is specifically expressed in the brain. Transcript variants for this gene have been described, but their full-length nature has not been determined.

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Text from Wikipedia, CC BY-SA 4.0 · Source article