CCDC102B - coiled-coil domain containing 102B Gene

Homo sapiens

Also known as AN; ACY1L; HsT1731; C18orf14

Gene ID: 79839 | Gene type: protein coding

About CCDC102B

This gene has 11 transcripts (splice variants), 51 orthologues and 43 paralogues. Broad expression in placenta (RPKM 1.5), lung (RPKM 1.1) and 20 other tissues.

CCDC102B Products(2)

mRNA	Protein	Name
NM_001093729.2	NP_001087198.2	coiled-coil domain-containing protein 102B
NM_024781.3	NP_079057.3	coiled-coil domain-containing protein 102B

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	25416956	GOA
enables protein serine/threonine kinase binding	IPI IPI: Inferred from physical interaction	30404835	GOA

Biological Process GO Annotation	Evidence	Reference	Source
involved in centriole-centriole cohesion	IMP IMP: Inferred from mutant phenotype	30404835	GOA

Cellular Component GO Annotation	Evidence	Reference	Source
located in centriole	IDA IDA: Inferred from direct assay	30404835	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 102B

Related Diseases

Diseases

Alias

Scleral Staphyloma

Scleral Ectasia

Staphyloma Of Sclera

Degenerative Myopia

Pathological Myopia	Myopia, Degenerative
Degenerative Progressive High Myopia	Progressive High Myopia
Progressive High Myopia

Myopia

Near-Sightedness	Short-Sightedness
Nearsightedness	Nearsighted
Near Vision	Close Sighted
Myopic	Short-Sighted
Near Sighted

Diaphragmatic Hernia, Congenital

Congenital Diaphragmatic Hernia	Diaphragmatic Hernia
Cdh	Congenital Diaphragmatic Defect
Hernia, Diaphragmatic	Dih
Hernia, Congenital Diaphragmatic	Hcd
Diaphragmatic Defect, Congenital	Diaphragm, Unilateral Agenesis Of
Hemidiaphragm, Agenesis Of	Diaphragmatic Hernia 1
Agenesis Of Hemidiaphragm	Unilateral Agenesis Of Diaphragm
Hernia Diaphragmatic	Hernia Diaphragmatic Congenital
Hernia, Diaphragmatic, Type 1	Hiatus Hernia
Oesophageal Hiatus Hernia	Paraoesophageal Hernia
Sliding Hiatus Hernia	Congenital Diaphragm Hernia
Congenital Diaphragm Defect With Hernia	Gross Congenital Diaphragm Defect

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS02023	CCDC102B Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

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