NOC3L - NOC3 like DNA replication regulator Gene

Homo sapiens

Also known as AD24; FAD24; C10orf117

Gene ID: 64318 | Gene type: protein coding

About NOC3L

Cytogenetic location: 10q23.33 Genomic coordinates (GRCh38): 10:94,314,907-94,362,939 (from NCBI)

This gene has 3 transcripts (splice variants) and 199 orthologues. Ubiquitous expression in thyroid (RPKM 7.2), testis (RPKM 6.7) and 25 other tissues.

Summary

Enables RNA binding activity. Predicted to be involved in DNA replication initiation. Predicted to act upstream of or within fat cell differentiation. Located in mitochondrion; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

NOC3L Products(1)

mRNA	Protein	Name
NM_022451.11	NP_071896.8	nucleolar complex protein 3 homolog

NOC3L Protein Structure

NOC3p

CBF

0
200
400
600
800 a.a.

Protein Preferred Names

Protein Names

nucleolar complex protein 3 homolog

NOC3 protein homolog

Related Diseases

Diseases

Alias

Nephrotic Syndrome, Type 3

NPHS3	Nephrotic Syndrome Type 3
Nephrotic Syndrome, Early-Onset, Type 3	Early Onset Nephrotic Syndrome Type 3
Nephrotic Syndrome 3	Early-Onset Nephrotic Syndrome Type 3

Shipyard Eye

Epidemic Keratoconjunctivitis

Ekc

Brachydactyly, Type A4

Brachymesophalangy Ii And V	Temtamy Type Brachydactyly
Brachydactyly Type A4	BDA4
Brachymesophalangy 2 And 5	Brachydactyly Temtamy Type
Brachydactyly, Temtamy Type

Myasthenic Syndrome, Congenital, 5

Endplate Acetylcholinesterase Deficiency	Congenital Myasthenic Syndrome 5
CMS5	Ead
Engel Congenital Myasthenic Syndrome	Myasthenic Syndrome, Congenital, Engel Type
Cms Ic	Congenital Myasthenic Syndrome Type Ic
Congenital Myasthenic Syndrome Type Ic, Formerly	Cms1c, Formerly
Cms Ic, Formerly	Congenital Myasthenic Syndrome Engel Type
End Plate Acetylcholinesterase Deficiency	Synaptic Congenital Myasthenic Syndromes
Cms1c	Cmse
Congenital Myasthenic Syndrome Type 1c	End-Plate Acetylcholinesterase Deficiency
Myasthenic Syndrome, Congenital, Type 5

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-RS09401	NOC3L Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	NOC3L	VGNC	VGNC:63846
Bos taurus	NOC3L	VGNC	VGNC:32147
Canis familiaris	NOC3L	VGNC	VGNC:43874
Mus musculus	NOC3L	MGD	MGI:1932610
Rattus norvegicus	NOC3L	RGD	RGD:1560656
Macaca mulatta	NOC3L	VGNC	VGNC:75240

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