ZRANB3 - zinc finger RANBP2-type containing 3 Gene

Also Known as AH2; 4933425L19Rik

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84083

About ZRANB3

Cytogenetic location: 2q21.3 Genomic coordinates (GRCh38): 2:135,196,969-135,531,218 (from NCBI)

This gene has 11 transcripts (splice variants), 197 orthologues and 30 paralogues. Broad expression in testis (RPKM 1.8), thyroid (RPKM 0.8) and 24 other tissues.

Summary

Enables ATP-dependent DNA/DNA annealing activity; K63-linked polyubiquitin modification-dependent protein binding activity; and endodeoxyribonuclease activity. Involved in several processes, including DNA metabolic process; DNA rewinding; and negative regulation of DNA recombination. Located in nuclear replication fork and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ZRANB3 Products (3)

mRNA Protein Name
NM_001286568.2 NP_001273497.1 DNA annealing helicase and endonuclease ZRANB3 isoform 2
NM_001286569.1 NP_001273498.1 DNA annealing helicase and endonuclease ZRANB3 isoform 3
NM_032143.4 NP_115519.2 DNA annealing helicase and endonuclease ZRANB3 isoform 1
Molecular Function GO Annotation Evidence References Source
enables ATP-dependent DNA/DNA annealing activity IDA
IDA: Inferred from direct assay
21078962 GOA
enables DNA endonuclease activity IDA
IDA: Inferred from direct assay
22759634 GOA
NOT enables DNA helicase activity IDA
IDA: Inferred from direct assay
21078962 GOA
enables K63-linked polyubiquitin modification-dependent protein binding IDA
IDA: Inferred from direct assay
22704558 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
22704558 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA damage response IDA
IDA: Inferred from direct assay
22704558 GOA
involved in DNA repair IDA
IDA: Inferred from direct assay
22759634 GOA
involved in DNA rewinding IDA
IDA: Inferred from direct assay
21078962 GOA
involved in negative regulation of DNA recombination IDA
IDA: Inferred from direct assay
22704558 GOA
involved in replication fork processing IDA
IDA: Inferred from direct assay
22704558 GOA
involved in replication fork reversal IDA
IDA: Inferred from direct assay
22704558 GOA
involved in response to UV IDA
IDA: Inferred from direct assay
22704558 GOA
Cellular Component GO Annotation Evidence References Source
located in nuclear replication fork IDA
IDA: Inferred from direct assay
22704558 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

ZRANB3 Protein Structure

SNF2_N

SNF2_N: SNF2 family N-terminal domain (51 - 286)

Helicase_C

Helicase_C: Helicase conserved C-terminal domain (361 - 435)

zf-RanBP

zf-RanBP: Zn-finger in Ran binding protein and others (625 - 647)

HNH

HNH: HNH endonuclease (1011 - 1051)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1079 a.a.
Protein Preferred Names Protein Names

DNA annealing helicase and endonuclease ZRANB3

  • annealing helicase 2

ZRANB3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ZRANB3 Q5FWF4 PCNA Homo sapiens P12004 22759634
Intra
ZRANB3 Q5FWF4 PCNA Homo sapiens P12004 22759634
Intra
ZRANB3 Q5FWF4 PCNA Homo sapiens P12004 22759634
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Schimke Immunoosseous Dysplasia
  • Schimke Immuno-Osseous Dysplasia

  • SIOD

  • Immunoosseous Dysplasia, Schimke Type

  • Schimke Syndrome

  • Immunoosseous Dysplasia Schimke Type

  • Spondyloepiphyseal Dysplasia - Nephrotic Syndrome

  • Spondyloepiphyseal Dysplasia Nephrotic Syndrome

  • Spondyloepiphyseal Dysplasia-Nephrotic Syndrome

Amelogenesis Imperfecta, Type If
  • Amelogenesis Imperfecta Type 1f

  • AI1F

  • Amelogenesis Imperfecta, Hypoplastic Type If

  • Amelogenesis Imperfecta Type If

  • Amelogenesis Imperfecta Hypoplastic Type If

  • Amelogenesis Imperfecta 1f

Chronic Inducible Urticaria
Hypotrichosis 7
  • Woolly Hair, Autosomal Recessive 2, With Or Without Hypotrichosis

  • HYPT7

  • Hypotrichosis, Localized, Autosomal Recessive 2

  • Lah2

  • Ah

  • Total Hypotrichosis, Mari Type

  • Wh/Ht

  • Hypotrichosis, Autosomal Recessive

  • Hypotrichosis, Total, Mari Type

  • Woolly Hair, Autosomal Recessive 2 With Or Without Hypotrichosis

  • Total Mari Type Hypotrichosis

  • Alopecia Universalis Congenita, Mari Type

  • Mari Type Alopecia Universalis Congenita

  • Autosomal Recessive Hypotrichosis

  • Autosomal Recessive Localized Hypotrichosis

  • Autosomal Recessive Woolly Hair With Or Without Hypotrichosis

  • Htl

  • Hypotrichoses

  • Hypotrichosis

  • Lah

  • Alopecia Universalis Congenita Mari Type

  • Hypotrichosis Autosomal Recessive

  • Hypotrichosis Localized Autosomal Recessive 2

  • Total Hypotrichosis Mari Type

  • Woolly Hair Autosomal Recessive 2

  • ARWH2

  • Woolly Hair Autosomal Recessive 2 With Or Without Hypotrichosis

Chronic Intestinal Vascular Insufficiency
  • Chronic Mesenteric Ischemia

  • Cmi - Chronic Mesenteric Ischaemia

Cerebellar Ataxia Type 9
  • Sca9

Fanconi Anemia, Complementation Group A
  • Fanconi Anemia

  • Fanconi Pancytopenia

  • Fanconi Anemia Complementation Group A

  • FANCA

  • Fa

  • Fanconi Panmyelopathy

  • Fanconi'S Anemia

  • Fanconi Anaemia

  • Fanconi'S Anaemia

  • Fanconi Hypoplastic Anemia

  • Estren-Dameshek Variant Of Fanconi Anemia

  • Estren-Dameshek Variant Of Fanconi Pancytopenia

  • Fanconi Anemia Estren-Dameshek Variant

  • Fanconis Anemia

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
Mus musculus ZRANB3 MGD MGI:1918362
Macaca mulatta ZRANB3 VGNC VGNC:79486
Felis catus ZRANB3 VGNC VGNC:80416
Canis familiaris ZRANB3 VGNC VGNC:48849
Rattus norvegicus ZRANB3 RGD RGD:1564952
Bos taurus ZRANB3 VGNC VGNC:37373
Others ZRANB3 NCBI