NOC3L - NOC3 like DNA replication regulator Gene

Also Known as AD24; FAD24; C10orf117

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 64318

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

NOC3p: Nucleolar complex-associated protein (211 - 308)

CBF

CBF: CBF/Mak21 family (557 - 708)

  • 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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS09401 NOC3L Human Pre-designed siRNA Set A Pre-designed Set / 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
Others NOC3L NCBI