The TMCO1 gene homepage

General information
Gene symbol TMCO1
Gene name transmembrane and coiled-coil domains 1
Chromosome 1
Chromosomal band q22-q25
Imprinted Unknown
Genomic reference NG_032004.1
Transcript reference NM_019026.4
Exon/intron information NM_019026.4 exon/intron table
Associated with diseases CFSMR, CFSMR, ID
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 17
Unique public DNA variants reported 15
Individuals with public variants 1
Hidden variants 6
Date created May 03, 2013
Date last updated May 09, 2022
Version TMCO1:220509

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_019026.4.
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
HGNC 18188
Entrez Gene 54499
PubMed articles TMCO1
OMIM - Gene 614123
OMIM - Diseases CFSMR (Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome)
CFSMR (dysmorphism, craniofacial, skeletal anomalies, and mental retardation syndrome (CFSMR))
GeneCards TMCO1
GeneTests TMCO1
Orphanet TMCO1

Active transcripts




NCBI ID     

NCBI Protein ID     

00021230 1 transcript variant 1 NM_019026.4 NP_061899.2 17

Copyright & disclaimer
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