BEND7 - BEN domain containing 7 Gene

Also Known as C10orf30

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 222389

About BEND7

This gene has 13 transcripts (splice variants) and 116 orthologues. Broad expression in thyroid (RPKM 4.1), small intestine (RPKM 3.0) and 22 other tissues.

Summary

Predicted to enable DNA binding activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

BEND7 Products (8)

mRNA Protein Name
NM_001100912.2 NP_001094382.1 BEN domain-containing protein 7 isoform 2
NM_001369863.1 NP_001356792.1 BEN domain-containing protein 7 isoform 3
NM_001370075.2 NP_001357004.2 BEN domain-containing protein 7 isoform 4
NM_001378149.1 NP_001365078.1 BEN domain-containing protein 7 isoform 5
NM_001378150.1 NP_001365079.1 BEN domain-containing protein 7 isoform 6
NM_001378151.1 NP_001365080.1 BEN domain-containing protein 7 isoform 7
NM_001387359.1 NP_001374288.1 BEN domain-containing protein 7 isoform 8
NM_152751.3 NP_689964.2 BEN domain-containing protein 7 isoform 1

Gene Ontology

  • Molecular Function
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 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

BEND7 Protein Structure

BEN

BEN: BEN domain (258 - 339)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 468 a.a.
Protein Preferred Names Protein Names

BEN domain-containing protein 7

BEND7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
BEND7 Q8N7W2 NIF3L1 Homo sapiens Q9GZT8
Y2H Pooling
19060904
Intra
BEND7 Q8N7W2 NIF3L1 Homo sapiens Q9GZT8
Y2H Array
19060904
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome

  • Icf Syndrome

  • Immunodeficiency Syndrome, Variable

  • Ciid

  • Centromeric Instability, Immunodeficiency Syndrome

  • Immune Deficiency, Variable, With Centromeric Instability Of Chromosomes 1, 9, And 16

  • Icf
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-RS01473 BEND7 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus BEND7 VGNC VGNC:83507
Mus musculus BEND7 MGD MGI:2443100
Bos taurus BEND7 VGNC VGNC:26470
Rattus norvegicus BEND7 RGD RGD:1305898
Macaca mulatta BEND7 VGNC VGNC:100300
Canis familiaris BEND7 VGNC VGNC:38433
Others BEND7 NCBI