CEP162 - centrosomal protein 162 Gene

Homo sapiens

Also known as QN1; C6orf84; KIAA1009

Gene ID: 22832 | Gene type: protein coding

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.

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

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

Protein Preferred Names

Protein Names

centrosomal protein of 162 kDa

centrosomal protein 162kDa

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

Pre-clinical Phase

Bioactive Molecules (1)

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

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

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