1. Gene
  2. KPNA3 - karyopherin subunit alpha 3 Gene

KPNA3 - karyopherin subunit alpha 3 Gene

Homo sapiens

Also known as SRP1; SRP4; IPOA4; SPG88; hSRP1; SRP1gamma

Gene ID: 3839 | Gene type: protein coding

About KPNA3

Cytogenetic location: 13q14.2 Genomic coordinates (GRCh38): 13:49,699,320-49,792,682 (from NCBI)

This gene has 2 transcripts (splice variants), 232 orthologues, 6 paralogues and is associated with 1 phenotype. Ubiquitous expression in testis (RPKM 17.5), brain (RPKM 15.2) and 25 other tissues.

Summary

The transport of molecules between the nucleus and the cytoplasm in eukaryotic cells is mediated by the nuclear pore complex (NPC), which consists of 60-100 proteins. Small molecules (up to 70 kD) can pass through the nuclear pore by nonselective diffusion while larger molecules are transported by an active process. The protein encoded by this gene belongs to the importin alpha family, and is involved in nuclear protein import. [provided by RefSeq, Jan 2009]

KPNA3 Products(1)

mRNA Protein Name
NM_002267.4 NP_002258.2 importin subunit alpha-4

KPNA3 Protein Structure

IBB

IBB: Importin beta binding domain (4 - 93)

Arm

Arm: Armadillo/beta-catenin-like repeat (104 - 144)

Arm

Arm: Armadillo/beta-catenin-like repeat (147 - 184)

Arm

Arm: Armadillo/beta-catenin-like repeat (189 - 229)

Arm

Arm: Armadillo/beta-catenin-like repeat (233 - 271)

Arm

Arm: Armadillo/beta-catenin-like repeat (274 - 312)

Arm

Arm: Armadillo/beta-catenin-like repeat (315 - 355)

Arm

Arm: Armadillo/beta-catenin-like repeat (357 - 396)

Arm

Arm: Armadillo/beta-catenin-like repeat (402 - 438)

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  • 100
  • 200
  • 300
  • 400
  • 521 a.a.
Protein Preferred Names Protein Names

importin subunit alpha-4

SRP1-gamma

Related Diseases

Diseases Alias
Spastic Paraplegia 37, Autosomal Dominant

SPG37

Autosomal Dominant Spastic Paraplegia Type 37

Hereditary Spastic Paraplegia 37

Autosomal Dominant Spastic Paraplegia 37

Influenza

Flu

Influenza With Non-Respiratory Manifestation

Influenza With Other Manifestations

Influenza, Human

Influenza, Susceptibility To

Seasonal Influenza, Virus Identified

Charcot-Marie-Tooth Disease, Axonal, Type 2dd

CMT2DD

Charcot-Marie-Tooth Neuropathy, Type 2dd

Charcot-Marie-Tooth Disease Type 2dd

Atp1a1-Related Autosomal Dominant Charcot-Marie-Tooth Disease Type 2

Atp1a1-Related Cmt2

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2dd

Charcot-Marie-Tooth Disease 2dd

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
Felis catus KPNA3 VGNC VGNC:67975
Rattus norvegicus KPNA3 RGD RGD:1311339
Canis familiaris KPNA3 VGNC VGNC:42501
Macaca mulatta KPNA3 VGNC VGNC:74200
Mus musculus KPNA3 MGD MGI:1100863
Bos taurus KPNA3 VGNC VGNC:30702