1. Gene
  2. NOMO3 - NODAL modulator 3 Gene

NOMO3 - NODAL modulator 3 Gene

Homo sapiens

Also known as Nomo

Gene ID: 408050 | Gene type: protein coding

About NOMO3

Cytogenetic location: 16p13.11 Genomic coordinates (GRCh38): 16:16,232,528-16,294,811 (from NCBI)

This gene has 30 transcripts (splice variants), 1 gene allele, 201 orthologues and 2 paralogues. Ubiquitous expression in brain (RPKM 58.4), heart (RPKM 50.4) and 25 other tissues.

Summary

This gene encodes a protein originally thought to be related to the collagenase gene family. This gene is one of three highly similar genes in a duplicated region on the short arm of chromosome 16. These three genes encode closely related proteins that may have the same function. The protein encoded by one of these genes has been identified as part of a protein complex that participates in the Nodal signaling pathway during vertebrate development. Mutations in ABCC6, which is located nearby, rather than mutations in this gene are associated with pseudoxanthoma elasticum. [provided by RefSeq, Jul 2008]

NOMO3 Products(1)

mRNA Protein Name
NM_001004067.4 NP_001004067.1 nodal modulator 3 precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
22046132 GOA
enables ribosome binding IDA
IDA: Inferred from direct assay
32820719 GOA
Biological Process GO Annotation Evidence Reference Source
involved in multi-pass transmembrane protein insertion into ER membrane IDA
IDA: Inferred from direct assay
36261522 GOA
Cellular Component GO Annotation Evidence Reference Source
part of multi-pass translocon complex IDA
IDA: Inferred from direct assay
36261522 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

NOMO3 Protein Structure

CarboxypepD_reg

CarboxypepD_reg: Carboxypeptidase regulatory-like domain (130 - 203)

CarboxypepD_reg

CarboxypepD_reg: Carboxypeptidase regulatory-like domain (330 - 403)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1222 a.a.
Protein Preferred Names Protein Names

nodal modulator 3

pM5 protein 3

NOMO3 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Cross
NOMO3 P69849 P0C6X7-PRO_0000037315 Human SARS coronavirus P0C6X7-PRO_0000037315 22046132
Cross
NOMO3 P69849 P0C6X7-PRO_0000037315 Human SARS coronavirus P0C6X7-PRO_0000037315 22046132
Intra
NOMO3 P69849 GET4 Homo sapiens Q7L5D6 33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Pseudoxanthoma Elasticum

PXE

Gronblad-Strandberg Syndrome

Pseudoxanthoma Elasticum, Modifier Of Severity Of

Gronblad-Strandberg-Touraine Syndrome

Gronblad Strandberg Syndrome

Groenblad-Strandberg Syndrome

Nevus Elasticus

Pxe - [Pseudoxanthoma Elasticum]

Superficial Urinary Bladder Cancer

Superficial Urinary Bladder Carcinoma

Carcinoma Of Urinary Bladder, Superficial

Supraglottis Cancer

Malignant Tumor Of Supraglottis

Supraglottis

Ca Larynx - Supraglottis

Malignant Neoplasm Of Extrinsic Larynx

Malignant Neoplasm Of Supraglottis

Malignant Supraglottic Tumor

Neoplasm Of Supraglottis

Microphthalmia, Isolated 4

Isolated Microphthalmia 4

MCOP4

Microphthalmia, Isolated, 4

Isolated Clinical Anophthalmia

Microphthalmia, Isolated, Type 4

Ulcerative Stomatitis

Stomatitis Ulcerative

Aphthous Stomatitis

Minor Oral Aphthous Ulceration

Leber Congenital Amaurosis 17

LCA17

Leber Congenital Amaurosis, Type 17

Noma

Cancrum Oris

Gangrenous Stomatitis

Oro-Facial Gangrene

Noma Neonatorum

Oral Gangrene

Oro-Facial Noma

Stomatitis Gangrenosa

Stomatonecrosis

Gangrene Stomatitis

Bladder Squamous Cell Carcinoma

Squamous Cell Carcinoma Of Bladder

Epidermoid Carcinoma Of The Urinary Bladder

Carcinoma Squamous Cell Bladder

Afferent Loop Syndrome

Afferent Limb Syndrome

Multiple Synostoses Syndrome

Symphalangism-Brachydactyly Syndrome

Deafness-Hermann Type Symphalangism Syndrome

Facio-Audio-Symphalangism

Hearing Loss-Hermann Type Symphalangism Syndrome

Wl Syndrome

Multiple Synostosis Syndrome

Shipyard Eye

Epidemic Keratoconjunctivitis

Ekc

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
Mus musculus NOMO3 MGD MGI:2385850