CEP128 - centrosomal protein 128 Gene

Homo sapiens

Also known as C14orf61; LEDP/132; C14orf145

Gene ID: 145508 | Gene type: protein coding

About CEP128

This gene has 16 transcripts (splice variants) and 186 orthologues. Low expression observed in reference dataset.

Summary

Involved in protein localization. Located in centriole and spindle pole. Part of centriolar subdistal appendage. [provided by Alliance of Genome Resources, Apr 2022]

CEP128 Products(1)

mRNA	Protein	Name
NM_152446.5	NP_689659.2	centrosomal protein of 128 kDa

Protein Preferred Names

Protein Names

centrosomal protein of 128 kDa

centrosomal protein 128kDa

Related Diseases

Diseases

Alias

Familial Hyperthyroidism Due To Mutations In Tsh Receptor

Familial Non-Immune Hyperthyroidism	Resistance To Thyroid Stimulating Hormone
Nonautoimmune Hyperthyroidism	Hyperthyroidism, Nonautoimmune

Hypothyroidism, Congenital, Nongoitrous, 1

Tsh Resistance	CHNG1
Hypothyroidism Due To Tsh Receptor Mutations	Thyrotropin Resistance
Thyroid-Stimulating Hormone	Rtsh
Hypothyroidism Due To Unresponsiveness To Thyrotropin	Congenital Nongoitrous Hypothyroidism 1
Thyroid-Stimulating Hormone, Resistance To	Hypothyroidism, Nonautoimmune
Hypothyroidism, Congenital, Due To Tsh Resistance	Hypothyroidism, Congenital, Non-Goitrous, 1
Congenital Hypothyroidism Due To Tsh Resistance	Non-Autoimmune Hypothyroidism
Thyroid-Stimulating Hormone Resistance	Hypothyroidism, Congenital, Nongoitrous, Type 1
Hypothyroidism, Congenital, Nongoitrous, 3	Thyroid Hormone Resistance Syndrome

Hyperthyroidism, Nonautoimmune

Hyperthyroidism, Congenital Nonautoimmune	Hyperthyroidism, Nonautoimmune, Autosomal Dominant
Toxic Thyroid Hyperplasia, Autosomal Dominant	Nonautoimmune Hyperthyroidism
Congenital Nonautoimmune Hyperthyroidism	Hyperthyroidism, Non-Autoimmune
HTNA	Familial Hyperthyroidism Due To Mutations In Tsh Receptor
Familial Non-Immune Hyperthyroidism	Hyperthyroidism Congenital Non-Autoimmune
Hyperthyroidism Non-Autoimmune Autosomal Dominant	Resistance To Thyroid Stimulating Hormone
Toxic Thyroid Hyperplasia Autosomal Dominant

Epilepsy

Epilepsy Syndrome	Epileptic Syndrome
Epilepsies	Symptomatic Epilepsies
Post Traumatic Epilepsy	Traumatic Epilepsy
Traumatic Epileptic	Epilepsy Due To Hippocampal Sclerosis
Epilepsy With Ammon'S Horn Sclerosis	Epilepsy Due To Cortical Dysplasia
Epilepsy Due To Neuronal Migration Disorders

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

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-RS02499	CEP128 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	CEP128	VGNC	VGNC:60766
Canis familiaris	CEP128	VGNC	VGNC:39117
Rattus norvegicus	CEP128	RGD	RGD:1595693
Mus musculus	CEP128	MGD	MGI:1922466
Macaca mulatta	CEP128	VGNC	VGNC:71062
Bos taurus	CEP128	VGNC	VGNC:53080

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