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NEDD1 - NEDD1 gamma-tubulin ring complex targeting factor Gene

Also Known as GCP-WD; TUBGCP7

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 121441

About NEDD1

Cytogenetic location: 12q23.1 Genomic coordinates (GRCh38): 12:96,907,257-96,953,780 (from NCBI)

This gene has 13 transcripts (splice variants), 109 orthologues and 26 paralogues. Ubiquitous expression in testis (RPKM 11.1), lymph node (RPKM 7.2) and 25 other tissues.

Summary

Predicted to be involved in protein localization to centrosome. Located in centrosome; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

NEDD1 Products (4)

mRNA	Protein	Name
NM_001135175.2	NP_001128647.1	protein NEDD1 isoform a
NM_001135176.2	NP_001128648.1	protein NEDD1 isoform b
NM_001135177.2	NP_001128649.1	protein NEDD1 isoform c
NM_152905.4	NP_690869.1	protein NEDD1 isoform b

Gene Ontology

Molecular Function
Cellular Component

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	19369198	GOA

Cellular Component GO Annotation	Evidence	References	Source
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

NEDD1 Protein Structure

WD40

0
200
400
600
660 a.a.

Protein Preferred Names	Protein Names
protein NEDD1	NEDD-1

Related Diseases

Diseases	Alias
Primary Autosomal Recessive Microcephaly	Autosomal Recessive Primary Microcephaly Mcph True Microcephaly Microcephalia Vera Microcephaly Vera Microcephaly Primary Hereditary Microcephaly, Primary, Autosomal Recessive Primary Microcephaly
Cone-Rod Dystrophy 2	Cone-Rod Dystrophy CORD2 Cone-Rod Retinal Dystrophy Rcrd2 Cone-Rod Retinal Dystrophy 2 Crd2 Cord Crd Retinal Cone-Rod Dystrophy Cone-Rod Retinal Dystrophy-2 Retinal Cone-Rod Dystrophy 2 Tapetoretinal Degeneration Cone-Rod Degeneration Cone Rod Dystrophy Dystrophy, Cone-Rod Dystrophy, Cone-Rod, Type 2 Retinitis Pigmentosa Retinitis Pigmentosa 2 Progressive Cone-Rod Dystrophy
Congenital Nervous System Abnormality	Congenital Neurologic Anomaly Congenital Nervous System Disorder

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.	상품명	효과	Purity	Rare Diseases
HY-RS09178	NEDD1 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	NEDD1	MGD	MGI:97293
Felis catus	NEDD1	VGNC	VGNC:68449
Macaca mulatta	NEDD1	VGNC	VGNC:75301
Bos taurus	NEDD1	VGNC	VGNC:31982
Canis familiaris	NEDD1	VGNC	VGNC:43720
Rattus norvegicus	NEDD1	RGD	RGD:1307750
Others	NEDD1	NCBI