KLF13 - KLF transcription factor 13 Gene

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

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 51621

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
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
17053787 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

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

KLF13 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
KLF13 Q9Y2Y9 PRP4K Homo sapiens Q13523 17513757
Intra
KLF13 Q9Y2Y9 PRP4K Homo sapiens Q13523 17513757
Intra
KLF13 Q9Y2Y9 GATA4 Homo sapiens P43694 17053787
Cross: Cross-species interaction Intra: Intraspecies interaction

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
Others KLF13 NCBI