1. Gene
  2. NOLC1 - nucleolar and coiled-body phosphoprotein 1 Gene

NOLC1 - nucleolar and coiled-body phosphoprotein 1 Gene

Homo sapiens

Also known as P130; Srp40; NOPP130; NOPP140; NS5ATP13

Gene ID: 9221 | Gene type: protein coding

About NOLC1

Cytogenetic location: 10q24.32 Genomic coordinates (GRCh38): 10:102,152,389-102,163,870 (from NCBI)

This gene has 9 transcripts (splice variants) and 171 orthologues. Ubiquitous expression in brain (RPKM 23.0), thyroid (RPKM 22.8) and 25 other tissues.

Summary

Enables protein heterodimerization activity and protein-macromolecule adaptor activity. Involved in neural crest cell development; neural crest formation; and regulation of translation. Located in fibrillar center. [provided by Alliance of Genome Resources, Apr 2022]

NOLC1 Products(3)

mRNA Protein Name
NM_001284388.2 NP_001271317.1 nucleolar and coiled-body phosphoprotein 1 isoform 1
NM_001284389.2 NP_001271318.1 nucleolar and coiled-body phosphoprotein 1 isoform 3
NM_004741.5 NP_004732.2 nucleolar and coiled-body phosphoprotein 1 isoform 2

NOLC1 Protein Structure

SRP40_C

SRP40_C: SRP40, C-terminal domain (624 - 696)

  • 0
  • 200
  • 400
  • 600
  • 699 a.a.
Protein Preferred Names Protein Names

nucleolar and coiled-body phosphoprotein 1

140 kDa nucleolar phosphoprotein

Related Diseases

Diseases Alias
Hepatitis C Virus

Hepatitis C Virus, Susceptibility To

Hepatitis C Virus Infection, Response To Therapy Of

Hcv

Hcv, Susceptibility To

Hepatitis C Virus, Resistance To

Hepatitis C Virus, Response To Therapy Of

Resistance To Hepatitis C Virus

Lissencephaly

Pachygyria

Broad Gyri Of Cerebrum

Large Gyri Of Cerebrum

Macrogyria

Treacher Collins Syndrome 1

Treacher Collins Syndrome

Mandibulofacial Dysostosis

Treacher Collins-Franceschetti Syndrome

Tcof

Tcs

Mfd1

Franceschetti-Klein Syndrome

TCS1

Franceschetti Syndrome

Franceschetti-Zwahlen-Klein Syndrome

Zygoauromandibular Dysplasia

Treacher-Collins Syndrome

Mandibulofacial Dysostosis Without Limb Anomalies

Bilateral And Symmetric Oto-Mandibular Dysplasia

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

Orthologs Information

Species Symbol Source ID
Canis familiaris NOLC1 VGNC VGNC:43885
Macaca mulatta NOLC1 VGNC VGNC:75178
Bos taurus NOLC1 VGNC VGNC:32161
Mus musculus NOLC1 MGD MGI:1918019
Rattus norvegicus NOLC1 RGD RGD:621578
Felis catus NOLC1 VGNC VGNC:63854