The PAX8 gene homepage

General information
Gene symbol PAX8
Gene name paired box 8
Chromosome 2
Chromosomal band q13
Imprinted Unknown
Genomic reference NG_012384.1
Transcript reference NM_003466.3
Associated with diseases CHNG2
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 63
Unique public DNA variants reported 52
Individuals with public variants 16
Hidden variants 1
Date created September 13, 2012
Date last updated February 26, 2024
Version PAX8:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 8622
Entrez Gene 7849
PubMed articles PAX8
OMIM - Gene 167415
OMIM - Diseases CHNG2 (hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia, type 2 (CHNG2))
HGMD PAX8
GeneCards PAX8
GeneTests PAX8
Orphanet PAX8


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001601 2 transcript variant PAX8A NM_003466.3 NP_003457.1 63


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