The KITLG gene homepage

General information
Gene symbol KITLG
Gene name KIT ligand
Chromosome 12
Chromosomal band q22
Imprinted Unknown
Genomic reference NG_012098.1
Transcript reference NM_000899.4, NM_003994.5
Associated with diseases FPH, SHEP-7
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 18
Unique public DNA variants reported 8
Individuals with public variants 16
Hidden variants 39
Date created November 30, -0001
Date last updated September 28, 2016
Version KITLG:160928

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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:6343
Entrez Gene 4254
PubMed articles KITLG
OMIM - Gene 184745
OMIM - Diseases FPH (hyperpigmentation, progressive, familial (FPH))
SHEP-7 (pigmentation, hair, blond/brown, type 7 (SHEP-7, skin/hair/eye pigmentation))


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00012393 12 transcript variant a NM_003994.5 NP_003985.2 18
00012394 12 transcript variant b NM_000899.4 NP_000890.1 18