The MED17 gene homepage

General information
Gene symbol MED17
Gene name mediator complex subunit 17
Chromosome 11
Chromosomal band q21
Imprinted Unknown
Genomic reference NG_028028.1
Transcript reference NM_004268.4
Associated with diseases ID, microcephaly, postnatal progressive, with seizures and brain atrophy
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 34
Unique public DNA variants reported 27
Individuals with public variants 1
Hidden variants 2
Date created May 03, 2013
Date last updated September 15, 2022
Version MED17:220915

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 2375
Entrez Gene 9440
PubMed articles MED17
OMIM - Gene 603810
OMIM - Diseases microcephaly, postnatal progressive, with seizures and brain atrophy
Orphanet MED17

Active transcripts




NCBI ID     

NCBI Protein ID     

00011966 11 mediator complex subunit 17 NM_004268.4 NP_004259.3 34

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