TTC19 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB

General information
Gene symbol	TTC19
Gene name	tetratricopeptide repeat domain 19
Chromosome	17
Chromosomal band	p11.2
Imprinted	Unknown
Genomic reference	NC_000017.10
Transcript reference	NM_017775.3, NR_037985.1
Associated with diseases	MC3DN2
Citation reference(s)	-
Curators (0)	-
Total number of public variants reported	71
Unique public DNA variants reported	70
Individuals with public variants	0
Hidden variants	0
Download all this gene's data	Download all data
Notes	MSeqDR-LSDB
Date created	November 07, 2013

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	26006
Entrez Gene	54902
PubMed articles	TTC19
OMIM - Gene	613814
OMIM - Diseases	MC3DN2 (Mitochondrial complex III deficiency, nuclear type 2, 615157 (3))
HGMD	TTC19
GeneCards	TTC19
GeneTests	TTC19

Active transcripts

Legend

Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

ID	Chr	Name	NCBI ID	NCBI Protein ID	Variants
00000351	17	transcript variant 2	NR_037985.1	-	71
00000352	17	transcript variant 1	NM_017775.3	NP_060245.2	71

Copyright & disclaimer
Sources: GeneDX http://www.genedx.com ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium