1. Gene
  2. NUP35 - nucleoporin 35 Gene

NUP35 - nucleoporin 35 Gene

Homo sapiens

Also known as MP44; NP44; MP-44; NUP53

Gene ID: 129401 | Gene type: protein coding

About NUP35

Cytogenetic location: 2q32.1 Genomic coordinates (GRCh38): 2:183,117,514-183,161,680 (from NCBI)

This gene has 10 transcripts (splice variants) and 215 orthologues. Ubiquitous expression in testis (RPKM 6.9), adrenal (RPKM 3.5) and 25 other tissues.

Summary

This gene encodes a member of the nucleoporin family. The encoded protein contains two membrane binding regions, is localized to the nuclear rim, and is part of the nuclear pore complex. All molecules entering or leaving the nucleus either diffuse through or are actively transported by the nuclear pore complex. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 7 and 10. [provided by RefSeq, Dec 2013]

NUP35 Products(3)

mRNA Protein Name
NM_001287584.2 NP_001274513.1 nucleoporin NUP35 isoform b
NM_001287585.2 NP_001274514.1 nucleoporin NUP35 isoform c
NM_138285.5 NP_612142.2 nucleoporin NUP35 isoform a
Gene Ontology
  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Cellular Component GO Annotation Evidence Reference Source
located in nuclear envelope IDA
IDA: Inferred from direct assay
24315095 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

NUP35 Protein Structure

Nup35_RRM

Nup35_RRM: Nup53/35/40-type RNA recognition motif (169 - 250)

  • 0
  • 100
  • 200
  • 300
  • 326 a.a.
Protein Preferred Names Protein Names

nucleoporin NUP35

mitotic phosphoprotein 44

NUP35 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
NUP35 Q8NFH5 KCTD9 Homo sapiens Q7L273 25416956
Intra
NUP35 Q8NFH5 KCTD9 Homo sapiens Q7L273 28514442
Intra
NUP35 Q8NFH5 KCTD9 Homo sapiens Q7L273 25416956
Intra
NUP35 Q8NFH5 KCTD9 Homo sapiens Q7L273 33961781
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Seminal Vesicle Tumor

Tumor Of Seminal Vesicle

Seminal Vesicle Neoplasm

Seminal Vesicle Tumour

Tumour Of Seminal Vesicle

Achalasia-Addisonianism-Alacrima Syndrome

Allgrove Syndrome

Triple-A Syndrome

Achalasia-Addisonianism-Alacrimia Syndrome

Alacrima-Achalasia-Adrenal Insufficiency Neurologic Disorder

Triple A Syndrome

Aaa Syndrome

AAAS

Glucocorticoid Deficiency With Achalasia

Glucocorticoid Deficiency And Achalasia

Addisonian-Achalasia Syndrome

Hypoadrenalism With Achalasia

Alacrima-Achalasia-Addisonianism

Aaa

Acth-Resistant Adrenal Insufficiency, Achalasia And Alacrima

Achalasia Addisonianism Alacrimia Syndrome

Achalasia Alacrima Syndrome

Addisonian Achalasia Syndrome

Achalasia-Addisonian Syndrome

Achalasia-Alacrima Syndrome

2a Syndrome

3a Syndrome

4a Syndrome

Adrenal Insufficiency-Achalasia-Alacrima Syndrome

Double A Syndrome

Quaternary A Syndrome

Acth-Resistant Adrenal Insufficiency With Achalasia And Alacrima

Allgrove'S Syndrome

Adrenal Gland Hypofunction

Adrenal Cortical Hypofunction

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 NUP35 MGD MGI:1916732
Bos taurus NUP35 VGNC VGNC:32359
Macaca mulatta NUP35 VGNC VGNC:75486
Canis familiaris NUP35 VGNC VGNC:44053
Felis catus NUP35 VGNC VGNC:63924
Rattus norvegicus NUP35 RGD RGD:1303069