Human (GRCh38.p14)
Description

sorting nexin 7 [Source:HGNC Symbol;Acc:HGNC:14971]

Location

Chromosome 1: 98,661,701-98,760,500 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 5 transcripts (splice variants), 207 orthologues and 15 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000306121.8SNX7-2011736451aaENSP00000304429.3
 
Protein coding
CCDS755Q9UNH6-3 NM_015976.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000529992.5SNX7-2051589396aaENSP00000434731.1
 
Protein coding
CCDS756E9PNL2 -GENCODE basicTSL:2
ENST00000454199.1SNX7-202497108aaENSP00000388266.1
 
Protein coding
B7ZC83 -TSL:4CDS 3' incomplete
ENST00000528824.1SNX7-204156236aaENSP00000435172.1
 
Nonsense mediated decay
E9PLE1 -TSL:1
ENST00000473868.5SNX7-203253No protein-
 
Protein coding CDS not defined
--TSL:3