The KLF1 gene homepage

General information
Gene symbol KLF1
Gene name Kruppel like factor 1
Chromosome 19
Chromosomal band p13.13
Imprinted Unknown
Genomic reference NG_013087.1
Transcript reference NM_006563.3, NM_006563.4
Associated with diseases Hypochromic anemia, WD
Citation reference(s) -
Refseq URL Coding DNA reference sequence
Curators (0) -
Total number of public variants reported 23
Unique public DNA variants reported 19
Individuals with public variants 39
Hidden variants -
Notes This gene encodes a hematopoietic-specific transcription factor that induces high-level expression of adult beta-globin and other erythroid genes. The zinc-finger protein binds to the DNA sequence CCACACCCT found in the beta hemoglobin promoter. Heterozygous loss-of-function mutations in this gene result in the dominant In(Lu) blood phenotype. [provided by RefSeq, Oct 2009]
Date created February 02, 2018
Date last updated April 25, 2019
Version KLF1:190425

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
Homepage URL http://www.genomed.org/lovd3/genes/KLF1
HGNC 6345
Entrez Gene 10661
PubMed articles KLF1
OMIM - Gene 600599
OMIM - Diseases WD (wilson disease)
HGMD KLF1
GeneCards KLF1
GeneTests KLF1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000070 19 Kruppel like factor 1 (expired, new version available) NM_006563.3 NP_006554.1 23
00000133 19 Kruppel-like factor 1 (erythroid) NM_006563.4 - -


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