Human (GRCh37.p13)
Description

paired box 8 [Source:HGNC Symbol;Acc:8622]

Location

Chromosome 2: 113,973,574-114,036,527 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 13 transcripts (splice variants), 8 paralogues and is associated with 62 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000429538.3PAX8-0014084450aaENSP00000395498.3
 
Protein coding
CCDS46398Q06710 R9W7C9 NM_003466.3GENCODE basic
ENST00000348715.5PAX8-0043966398aaENSP00000314750.5
 
Protein coding
CCDS46399Q06710 NM_013952.3GENCODE basic
ENST00000263335.7PAX8-0023735321aaENSP00000263335.7
 
Protein coding
CCDS42736Q06710 NM_013953.3GENCODE basic
ENST00000397647.3PAX8-0033633287aaENSP00000380768.3
 
Protein coding
CCDS42735Q06710 NM_013992.3GENCODE basic
ENST00000263334.5PAX8-2011197398aaENSP00000263334.5
 
Protein coding
CCDS46399Q06710 -GENCODE basic
ENST00000465084.1PAX8-00965698aaENSP00000452547.1
 
Protein coding
--CDS 5' incomplete
ENST00000468980.2PAX8-006525173aaENSP00000451240.1
 
Protein coding
--CDS 5' incomplete
ENST00000497038.2PAX8-0088162aaENSP00000451618.2
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000554830.1PAX8-01255631aaENSP00000451213.1
 
Nonsense mediated decay
G3V3F3 --
ENST00000485840.1PAX8-0052757No protein-
 
Retained intron
---
ENST00000467778.1PAX8-0071414No protein-
 
Retained intron
---
ENST00000554352.1PAX8-013567No protein-
 
Retained intron
---
ENST00000480684.1PAX8-010527No protein-
 
Retained intron
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