1. Gene
  2. CCDC14 - coiled-coil domain containing 14 Gene

CCDC14 - coiled-coil domain containing 14 Gene

Homo sapiens
Gene ID: 64770 | Gene type: protein coding

About CCDC14

Cytogenetic location: 3q21.1 Genomic coordinates (GRCh38): 3:123,885,176-123,961,229 (from NCBI)

This gene has 22 transcripts (splice variants) and 159 orthologues. Ubiquitous expression in testis (RPKM 10.7), bone marrow (RPKM 8.7) and 25 other tissues.

Summary

Involved in protein localization to centrosome. Located in centriolar satellite. [provided by Alliance of Genome Resources, Apr 2022]

CCDC14 Products(7)

mRNA Protein Name
NM_001308317.2 NP_001295246.1 coiled-coil domain-containing protein 14 isoform 2
NM_001366335.1 NP_001353264.1 coiled-coil domain-containing protein 14 isoform 3
NM_001366336.1 NP_001353265.1 coiled-coil domain-containing protein 14 isoform 2
NM_001366337.1 NP_001353266.1 coiled-coil domain-containing protein 14 isoform 2
NM_001366338.1 NP_001353267.1 coiled-coil domain-containing protein 14 isoform 4
NM_001366339.1 NP_001353268.1 coiled-coil domain-containing protein 14 isoform 5
NM_022757.5 NP_073594.5 coiled-coil domain-containing protein 14 isoform 1

CCDC14 Protein Structure

CCDC14

CCDC14: Coiled-coil domain-containing protein 14 (97 - 125)

CCDC14

CCDC14: Coiled-coil domain-containing protein 14 (126 - 912)

  • 0
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  • 400
  • 600
  • 800
  • 912 a.a.
Protein Preferred Names Protein Names

coiled-coil domain-containing protein 14

Related Diseases

Diseases Alias
Noonan Syndrome 1

Noonan Syndrome

NS1

Male Turner Syndrome

Female Pseudo-Turner Syndrome

Turner Phenotype With Normal Karyotype

Noonan Syndrome With Pigmented Villonodular Synovitis

Turner'S Phenotype, Karyotype Normal

Familial Turner Syndrome

Noonan'S Syndrome

Noonan-Ehmke Syndrome

Ns

Pseudo-Ullrich-Turner Syndrome

Turner Syndrome In Female With X Chromosome

Turner-Like Syndrome

Ullrich-Noonan Syndrome

Noonan-Like/Multiple Giant Cell Lesion Syndrome

Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

Pterygium Colli Syndrome

Noonan Syndrome, Type 1

Turner Syndrome, Male

Theileriasis

Theileriosis

Infection By Theileria

Primary Autosomal Recessive Microcephaly

Autosomal Recessive Primary Microcephaly

Mcph

True Microcephaly

Microcephalia Vera

Microcephaly Vera

Microcephaly Primary Hereditary

Microcephaly, Primary, Autosomal Recessive

Primary Microcephaly

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
Bos taurus CCDC14 VGNC VGNC:26851
Felis catus CCDC14 VGNC VGNC:60462
Canis familiaris CCDC14 VGNC VGNC:38795
Mus musculus CCDC14 MGD MGI:2443448
Rattus norvegicus CCDC14 RGD RGD:1562189
Macaca mulatta CCDC14 VGNC VGNC:70863