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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, 51 paralogues and is associated with 4 phenotypes.

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