CCDC34 - coiled-coil domain containing 34 Gene

Also Known as L15; RAMA3; SPGF76; NY-REN-41

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 91057

About CCDC34

Cytogenetic location: 11p14.1 Genomic coordinates (GRCh38): 11:27,338,512-27,363,215 (from NCBI)

This gene has 3 transcripts (splice variants) and 175 orthologues. Broad expression in testis (RPKM 12.6), colon (RPKM 2.4) and 21 other tissues.

CCDC34 Products (2)

mRNA Protein Name
NM_030771.2 NP_110398.1 coiled-coil domain-containing protein 34 isoform 1
NM_080654.3 NP_542385.1 coiled-coil domain-containing protein 34 isoform 2

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Biological Process GO Annotation Evidence References Source
involved in spermatogenesis IMP
IMP: Inferred from mutant phenotype
34348960 GOA
Cellular Component GO Annotation Evidence References Source
located in sperm midpiece IDA
IDA: Inferred from direct assay
34348960 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

CCDC34 Protein Structure

DUF4207

DUF4207: Domain of unknown function (DUF4207) (58 - 321)

  • 0
  • 100
  • 200
  • 300
  • 373 a.a.
Protein Preferred Names Protein Names

coiled-coil domain-containing protein 34

  • NY-REN-41 antigen

Related Diseases

Diseases Alias
Spermatogenic Failure 76

  • SPGF76
Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome

  • Wagr Syndrome

  • 11p Partial Monosomy Syndrome

  • Chromosome 11p13 Deletion Syndrome

  • Wilms Tumor, Aniridia, Genitourinary Anomalies And Mental Retardation Syndrome

  • 11p Deletion Syndrome

  • Chromosome 11p Deletion Syndrome

  • Wagr Complex

  • Wilms Tumor-Aniridia-Genitourinary Anomalies-Intellectual Disability Syndrome

  • Deletion 11p13

  • WAGR

  • Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome

  • Chromosome 11p Deletion

  • 11p Deletion

  • 11p Monosomy

  • Deletion 11p

  • Monosomy 11p

  • Partial Monosomy 11p

  • Agr Triad

  • Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome

  • Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome

  • Wagr Contiguous Gene Syndrome

  • Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome

  • Wilms Tumor-Aniridia-Genitourinary Anomalies-Mr Syndrome

  • Del(11)(P13)

  • Monosomy 11p13

  • Chromosome 11, Deletion 11p
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-RS02044 CCDC34 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus CCDC34 VGNC VGNC:81913
Macaca mulatta CCDC34 VGNC VGNC:70855
Mus musculus CCDC34 MGD MGI:1915451
Rattus norvegicus CCDC34 RGD RGD:1560583
Bos taurus CCDC34 VGNC VGNC:54860
Others CCDC34 NCBI