Human (GRCh38.p14)
Description

paired box 1 [Source:HGNC Symbol;Acc:HGNC:8615]

Location

Chromosome 20: 21,705,659-21,718,481 forward strand.

GRCh38:CM000682.2

About this gene

This gene has 4 transcripts (splice variants), 220 orthologues, 50 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000613128.5PAX1-2045342457aaENSP00000481334.1
 
Protein coding
CCDS74709A0A087WXV5 NM_001257096.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000398485.6PAX1-2012838534aaENSP00000381499.2
 
Protein coding
CCDS13146P15863-1 -GENCODE basicTSL:5
ENST00000444366.2PAX1-2021850433aaENSP00000410355.2
 
Protein coding
P15863-2 -GENCODE basicTSL:2
ENST00000485038.1PAX1-203487No protein-
 
Retained intron
--TSL:3