1. Gene
  2. CDCA5 - cell division cycle associated 5 Gene

CDCA5 - cell division cycle associated 5 Gene

Homo sapiens

Also known as SORORIN

Gene ID: 113130 | Gene type: protein coding

About CDCA5

Cytogenetic location: 11q13.1 Genomic coordinates (GRCh38): 11:65,061,093-65,084,040 (from NCBI)

This gene has 10 transcripts (splice variants) and 170 orthologues. Biased expression in bone marrow (RPKM 12.1), testis (RPKM 11.0) and 13 other tissues.

Summary

Predicted to enable chromatin binding activity. Involved in double-strand break repair; mitotic sister chromatid segregation; and regulation of cell cycle process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

CDCA5 Products(1)

mRNA Protein Name
NM_080668.4 NP_542399.1 sororin
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
21111234 GOA
enables protein-containing complex binding IDA
IDA: Inferred from direct assay
15837422 GOA
Biological Process GO Annotation Evidence Reference Source
involved in double-strand break repair IMP
IMP: Inferred from mutant phenotype
17349791 GOA
involved in mitotic cell cycle IDA
IDA: Inferred from direct assay
15837422 GOA
involved in mitotic chromosome condensation IMP
IMP: Inferred from mutant phenotype
15837422 GOA
involved in mitotic metaphase chromosome alignment IMP
IMP: Inferred from mutant phenotype
15837422 GOA
involved in mitotic sister chromatid cohesion IMP
IMP: Inferred from mutant phenotype
17349791 GOA
involved in mitotic sister chromatid cohesion IPI
IPI: Inferred from physical interaction
21111234 GOA
involved in positive regulation of exit from mitosis IMP
IMP: Inferred from mutant phenotype
23548868 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

CDCA5 Protein Structure

Sororin

Sororin: Sororin protein (89 - 215)

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

sororin

cell division cycle-associated protein 5

CDCA5 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CDCA5 Q96FF9 PDS5A Homo sapiens Q29RF7
Anti Bait CoIP
21111234
Intra
CDCA5 Q96FF9 PDS5A Homo sapiens Q29RF7
Anti Tag CoIP
26496610
Intra
CDCA5 Q96FF9 NAA11 Homo sapiens Q9BSU3
Validated Y2H
32296183
Intra
CDCA5 Q96FF9 NAA10 Homo sapiens P41227
Anti Tag CoIP
33961781
Intra
CDCA5 Q96FF9 SMC1A Homo sapiens Q14683
Anti Tag CoIP
33961781
Intra
CDCA5 Q96FF9 SMC1A Homo sapiens Q14683
Anti Tag CoIP
26496610
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Cornelia De Lange Syndrome

De Lange Syndrome

Brachmann De Lange Syndrome

Brachmann-De Lange Syndrome

Cdls

Bdls

Typus Degenerativus Amstelodamensis

Roberts-Sc Phocomelia Syndrome

Roberts Syndrome

Sc Phocomelia Syndrome

RBS

Long Bone Deficiencies Associated With Cleft Lip-Palate

Sc Pseudothalidomide Syndrome

Appelt-Gerken-Lenz Syndrome

Pseudothalidomide Syndrome

Tetraphocomelia-Cleft Palate Syndrome

Hypomelia Hypotrichosis Facial Hemangioma Syndrome

Roberts Syndrome/Sc Phocomelia

Roberts Tetraphocomelia Syndrome

Sc Syndrome

Sc Phocomelia

Sc Disease

Sc

Hemoglobin Sc Disease

Filippi Syndrome

Scott Craniodigital Syndrome With Mental Retardation

Type 1 Syndactyly-Microcephaly-Intellectual Disability Syndrome

FLPIS

Scott Bryant Graham Syndrome

Craniodigital-Intellectual Disability Syndrome

Scott Craniodigital Syndrome

Scott-Bryant-Graham Syndrome

Syndactyly, Type I, With Microcephaly And Mental Retardation

Syndactyly Type I With Microcephaly And Intellectual Disability

Unusual Facial Appearance, Microcephaly, Growth And Intellectual Disability And Syndactyly

Craniodigital Syndrome With Intellectual Disability

Craniodigital Syndrome-Intellectual Disability Syndrome

Craniodigital Syndrome-Intellectual Disability, Scott Type

Intellectual Disability-Craniodigital Syndrome

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
Canis familiaris CDCA5 VGNC VGNC:39015
Felis catus CDCA5 VGNC VGNC:60667
Bos taurus CDCA5 VGNC VGNC:56261
Mus musculus CDCA5 MGD MGI:1915099
Rattus norvegicus CDCA5 RGD RGD:1560863
Macaca mulatta CDCA5 VGNC VGNC:100907