1. Gene
  2. KLF13 - KLF transcription factor 13 Gene

KLF13 - KLF transcription factor 13 Gene

Homo sapiens

Also known as BTEB3; FKLF2; NSLP1; RFLAT1; RFLAT-1

Gene ID: 51621 | Gene type: protein coding

About KLF13

Cytogenetic location: 15q13.3 Genomic coordinates (GRCh38): 15:31,326,835-31,435,665 (from NCBI)

This gene has 7 transcripts (splice variants), 1 gene allele, 118 orthologues, 22 paralogues and is associated with 1 phenotype. Ubiquitous expression in bone marrow (RPKM 34.5), lung (RPKM 27.2) and 24 other tissues.

Summary

KLF13 belongs to a family of transcription factors that contain 3 classical zinc finger DNA-binding domains consisting of a zinc atom tetrahedrally coordinated by 2 cysteines and 2 histidines (C2H2 motif). These transcription factors bind to GC-rich sequences and related GT and CACCC boxes (Scohy et al., 2000 [PubMed 11087666]).[supplied by OMIM, Mar 2008]

KLF13 Products(2)

mRNA Protein Name
NM_001302461.2 NP_001289390.1 Krueppel-like factor 13 isoform 2
NM_015995.4 NP_057079.2 Krueppel-like factor 13 isoform 1

KLF13 Protein Structure

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (183 - 209)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (214 - 236)

  • 0
  • 100
  • 200
  • 288 a.a.
Protein Preferred Names Protein Names

Krueppel-like factor 13

BTE-binding protein 3

Related Diseases

Diseases Alias
Chromosome 15q13.3 Deletion Syndrome

Chromosome 15q13.3 Microdeletion Syndrome

15q13.3 Microdeletion Syndrome

15q13.3 Microdeletion

Microdeletion 15q13.3 Syndrome

Del(15)(Q13.3)

Monosomy 15q13.3

Tricuspid Valve Stenosis

Tricuspid Stenosis

Tricuspid Stricture

Tricuspid Valve Stricture

Tricuspid Insufficiency With Obstruction

Tricuspid Insufficiency With Stenosis

Heart Disease

Heart Failure

Congenital Heart Disease

Heart Diseases

Congenital Heart Defects

Congenital Heart Defect

Heart Malformation

Congenital Anomaly Of Heart

Heart Defect

Heart-Congenital Defect

Congenital Heart Disorder

Heart Defects Congenital

Heart Defects, Congenital

Heart Defects

Heart Disease, Congenital

Disease, Heart, Congenital

Congestive Heart Failure

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus KLF13 RGD RGD:1565099
Bos taurus KLF13 VGNC VGNC:106796
Mus musculus KLF13 MGD MGI:1354948
Macaca mulatta KLF13 VGNC VGNC:84365
Felis catus KLF13 VGNC VGNC:80941