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CEP162 - centrosomal protein 162 Gene

Also Known as QN1; C6orf84; KIAA1009

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 22832

About CEP162

Cytogenetic location: 6q14.2-q14.3 Genomic coordinates (GRCh38): 6:84,124,250-84,227,643 (from NCBI)

This gene has 7 transcripts (splice variants) and 172 orthologues. Broad expression in testis (RPKM 6.2), thyroid (RPKM 2.2) and 24 other tissues.

Summary

Involved in cilium assembly. Located in axonemal microtubule; centriole; and centrosome. [provided by Alliance of Genome Resources, Apr 2022]

CEP162 Products (2)

mRNA	Protein	Name
NM_001286206.2	NP_001273135.1	centrosomal protein of 162 kDa isoform b
NM_014895.4	NP_055710.2	centrosomal protein of 162 kDa isoform a

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	23644468	GOA

Biological Process GO Annotation	Evidence	References	Source
involved in cilium assembly	IMP IMP: Inferred from mutant phenotype	23644468	GOA

Cellular Component GO Annotation	Evidence	References	Source
located in axonemal microtubule	IDA IDA: Inferred from direct assay	23644468	GOA
located in centriole	IDA IDA: Inferred from direct assay	23644468	GOA
located in centrosome	IDA IDA: Inferred from direct assay	21399614	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
centrosomal protein of 162 kDa	centrosomal protein 162kDa

CEP162 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	CEP162	Q5TB80	CEP135	Homo sapiens	Q66GS9	Anti Tag CoIP	26638075
Intra	CEP162	Q5TB80	CEP290	Homo sapiens	O15078	Anti Bait CoIP	23644468
Intra	CEP162	Q5TB80	CEP290	Homo sapiens	O15078	BioID	26638075
Intra	CEP162	Q5TB80	CEP290	Homo sapiens	O15078	Anti Tag CoIP	26638075
Intra	CEP162	Q5TB80	CEP120	Homo sapiens	Q8N960	BioID	26638075
Intra	CEP162	Q5TB80	CEP120	Homo sapiens	Q8N960	Anti Tag CoIP	26638075

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Seckel Syndrome 7	SCKL7 Microcephalic Primordial Dwarfism, Dauber Type Seckel Syndrome, Type 7
Orofaciodigital Syndrome Ix	OFD9 Orofaciodigital Syndrome With Retinal Abnormalities Oral-Facial-Digital Syndrome With Retinal Abnormalities Orofaciodigital Syndrome 9 Oral-Facial-Digital Syndrome Type 9 Ofds Ix Oral-Facial-Digital Syndrome, Type Ix Ofd Syndrome 9 Ofds 9 Oral Facial Digital Syndrome 9 Oral Facial Digital Syndrome Type 9 Orofaciodigital Syndrome Type 9 Orofaciodigital Syndrome, Type Ix
Retinitis Pigmentosa 83	RP83 Retinitis Pigmentosa, Type 83
Cone-Rod Dystrophy 20	CORD20 Dystrophy, Cone-Rod, Type 20
Joubert Syndrome 1	Joubert Syndrome Jbts Cerebellooculorenal Syndrome 1 JBTS1 Joubert-Boltshauser Syndrome Cerebelloparenchymal Disorder Iv Cpd4 Cors1 Joubert Syndrome And Related Disorders Jsrd Familial Aplasia Of The Vermis Joubert Syndrome Related Disorders Js Cerebellar Vermis Agenesis Cerebelloparenchymal Disorder 4 Agenesis Of Cerebellar Vermis Cerebello-Oculo-Renal Syndrome Cors Joubert-Bolthauser Syndrome Cpd Iv Classic Joubert Syndrome Joubert Syndrome Type A Pure Joubert Syndrome Cerebello-Oculo-Renal Syndrome 1 Joubert Syndrome-1 Joubert Syndrome, Type 1 Joubert'S 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

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS02503	CEP162 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	CEP162	VGNC	VGNC:71067
Mus musculus	CEP162	MGD	MGI:1925343
Canis familiaris	CEP162	VGNC	VGNC:39120
Bos taurus	CEP162	VGNC	VGNC:27195
Rattus norvegicus	CEP162	RGD	RGD:1307365
Felis catus	CEP162	VGNC	VGNC:60769
Others	CEP162	NCBI