CCDC86 - coiled-coil domain containing 86 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79080

About CCDC86

Cytogenetic location: 11q12.2 Genomic coordinates (GRCh38): 11:60,842,113-60,851,081 (from NCBI)

This gene has 4 transcripts (splice variants) and 188 orthologues. Broad expression in testis (RPKM 26.3), adrenal (RPKM 10.0) and 25 other tissues.

Summary

Enables RNA binding activity. Located in chromosome; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

CCDC86 Products (1)

mRNA Protein Name
NM_024098.4 NP_077003.1 coiled-coil domain-containing protein 86

Gene Ontology

  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Verweise Source
enables protein binding IPI
IPI: Inferred from physical interaction
15607035 GOA
Cellular Component GO Annotation Evidence Verweise Source
located in nucleus IDA
IDA: Inferred from direct assay
17300783 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
Protein Preferred Names Protein Names

coiled-coil domain-containing protein 86

  • cyclon

CCDC86 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Cross
CCDC86 Q9H6F5 P27958-PRO_0000037576 Hepatitis C virus P27958-PRO_0000037576
Pull Down
15607035
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Glycogen Storage Disease Ixb

  • GSD9B

  • Gsd Ixb

  • Phosphorylase Kinase Deficiency Of Liver And Muscle, Autosomal Recessive

  • Glycogen Storage Disease Type 9b

  • Glycogen Storage Disease Type Ixb

  • Glycogenosis Due To Liver And Muscle Phosphorylase Kinase Deficiency

  • Glycogenosis Type 9b

  • Glycogenosis Type Ixb

  • Gsd Due To Liver And Muscle Phosphorylase Kinase Deficiency

  • Gsd Type 9b

  • Gsd Type Ixb

  • Glycogenosis Of Liver And Muscle, Autosomal Recessive

  • Glycogen Storage Disease Due To Liver And Muscle Phosphorylase Kinase Deficiency

  • Glycogen Storage Disease 9b

  • Gsd-Ixb

  • Phosphorylase Kinase Deficiency Of Liver And Muscle

  • Storage Disease, Glycogen, Type Ixb
Glycogen Storage Disease Ix
Extratemporal Epilepsy
Granulomatosis With Polyangiitis

  • GPA

  • Wegener Granulomatosis

  • Wegener Granulomatosis, Formerly

  • Midline Granulomatosis

  • Wg, Formerly

  • Necrotizing Respiratory Granulomatosis

  • Wg

  • Wegeners Granulomatosis

  • Pauci-Immune Glomerulonephritis Associated With Granulomatosis With Polyangiitis
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)
Art. -Nr. Produktname
Wirkung
Reinheit
Rare Diseases
HY-RS02060 CCDC86 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus CCDC86 VGNC VGNC:60522
Rattus norvegicus CCDC86 RGD RGD:1359280
Mus musculus CCDC86 MGD MGI:1277220
Canis familiaris CCDC86 VGNC VGNC:38865
Macaca mulatta CCDC86 VGNC VGNC:70893
Bos taurus CCDC86 VGNC VGNC:97248
Others CCDC86 NCBI