The POMC gene homepage

General information
Gene symbol POMC
Gene name proopiomelanocortin
Chromosome 2
Chromosomal band p23
Imprinted Unknown
Genomic reference NG_008997.1
Transcript reference NM_000939.2
Exon/intron information NM_000939.2 exon/intron table
Associated with diseases OBAIRH, obesity
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 63
Unique public DNA variants reported 44
Individuals with public variants 63
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated February 26, 2024
Version POMC:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_000939.2.
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
Homepage URL https://www.LOVD.nl/POMC
HGNC 9201
Entrez Gene 5443
PubMed articles POMC
OMIM - Gene 176830
OMIM - Diseases OBAIRH (obesity, adrenal insufficiency, red hair (OBAIRH, proopiomelanocortin deficiency))
obesity (obesity, susceptibility to (incl. leanness))
HGMD POMC
GeneCards POMC
GeneTests POMC
Orphanet POMC


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00025679 2 transcript variant 2 NM_000939.2 NP_000930.1 63


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