KLHDC7B - kelch domain containing 7B Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 113730

About KLHDC7B

This gene has 3 transcripts (splice variants), 53 orthologues and 54 paralogues.

KLHDC7B Products (1)

mRNA Protein Name
NM_138433.5 NP_612442.3 kelch domain-containing protein 7B

Gene Ontology

  • Molecular Function
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 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

KLHDC7B Protein Structure

Kelch_1

Kelch_1: Kelch motif (343 - 391)

Kelch_1

Kelch_1: Kelch motif (395 - 435)

  • 0
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  • 500
  • 594 a.a.
Protein Preferred Names Protein Names

kelch domain-containing protein 7B

KLHDC7B Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
KLHDC7B Q96G42 HNRNPUL1 Homo sapiens Q9BUJ2
Validated Y2H
32296183
Intra
KLHDC7B Q96G42 PATZ1 Homo sapiens Q9HBE1-4
Validated Y2H
32296183
Intra
KLHDC7B Q96G42 WWOX Homo sapiens Q9NZC7-5
Validated Y2H
32296183
Intra
KLHDC7B Q96G42 A1CF Homo sapiens Q9NQ94
Validated Y2H
32296183
Intra
KLHDC7B Q96G42 RHOXF2 Homo sapiens Q9BQY4
Validated Y2H
32296183
Intra
KLHDC7B Q96G42 MAPRE3 Homo sapiens Q9UPY8
Validated Y2H
32296183
Intra
KLHDC7B Q96G42 RBPMS Homo sapiens Q93062-3
Y2H Array
32296183
Intra
KLHDC7B Q96G42 ZC3H10 Homo sapiens Q96K80
Validated Y2H
32296183
Intra
KLHDC7B Q96G42 SPMIP9 Homo sapiens Q96LM6
Validated Y2H
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Deafness, Autosomal Recessive 28

  • DFNB28

  • Autosomal Recessive Nonsyndromic Deafness 28

  • Autosomal Recessive Deafness 28

  • Deafness, Autosomal Recessive, 28

  • Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 28

  • Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 28

  • Deafness, Autosomal Recessive, Type 28
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS07351 KLHDC7B Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus KLHDC7B VGNC VGNC:30638
Mus musculus KLHDC7B MGD MGI:3648212
Felis catus KLHDC7B VGNC VGNC:82380
Rattus norvegicus KLHDC7B RGD RGD:1562257
Others KLHDC7B NCBI