1. Gene
  2. JKAMP - JNK1/MAPK8 associated membrane protein Gene

JKAMP - JNK1/MAPK8 associated membrane protein Gene

Homo sapiens

Also known as JAMP; CDA06; HSPC213; HSPC327; C14orf100; C24orf100

Gene ID: 51528 | Gene type: protein coding

About JKAMP

Cytogenetic location: 14q23.1 Genomic coordinates (GRCh38): 14:59,484,517-59,505,410 (from NCBI)

This gene has 14 transcripts (splice variants) and 219 orthologues. Ubiquitous expression in testis (RPKM 16.2), adrenal (RPKM 14.0) and 25 other tissues.

Summary

Enables ubiquitin protein ligase binding activity. Involved in ubiquitin-dependent ERAD pathway. Predicted to be located in endoplasmic reticulum membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

JKAMP Products(6)

mRNA Protein Name
NM_001098625.3 NP_001092095.1 JNK1/MAPK8-associated membrane protein isoform 2
NM_001284201.2 NP_001271130.1 JNK1/MAPK8-associated membrane protein isoform 3
NM_001284202.2 NP_001271131.1 JNK1/MAPK8-associated membrane protein isoform 4
NM_001284203.2 NP_001271132.1 JNK1/MAPK8-associated membrane protein isoform 5
NM_001284204.2 NP_001271133.1 JNK1/MAPK8-associated membrane protein isoform 6
NM_016475.5 NP_057559.2 JNK1/MAPK8-associated membrane protein isoform 1

JKAMP Protein Structure

DUF766

DUF766: Protein of unknown function (DUF766) (9 - 301)

  • 0
  • 100
  • 200
  • 311 a.a.
Protein Preferred Names Protein Names

JNK1/MAPK8-associated membrane protein

JNK-associated membrane protein

Related Diseases

Diseases Alias
Large Cell Medulloblastoma
Medulloblastoma

MDB

Cpnet

Localized Primitive Neuroectodermal Tumor

Classic Medulloblastoma

Medulloblastoma Predisposition Syndrome

Medulloblastoma, Somatic

Brain Medulloblastoma

Cns Pnet

Infratentorial Primitive Neuroectodermal Tumor

Neuroectodermal Tumors, Primitive

Medulloblastomas

Desmoplastic Medulloblastoma

Medulloblastoma, With Extensive Nodularity

Medulloblastoma Of Unspecified Site

Medullomyoblastoma Of Unspecified Site

Nemaline Myopathy 5

Amish Nemaline Myopathy

NEM5

Anm

Nemaline Myopathy, Amish Type

Nemaline Myopathy 5, Amish Type

Nemaline Myopathy, Caused By Mutation In The Troponin T1 Gene

Nemaline Myopathy, Type 5

Nemaline Myopathy Amish Type

Tnnt1-Related Nemaline Myopathy

Myopathy, Nemaline, 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

Orthologs Information

Species Symbol Source ID
Canis familiaris JKAMP VGNC VGNC:42186
Rattus norvegicus JKAMP RGD RGD:1308917
Felis catus JKAMP VGNC VGNC:63006
Macaca mulatta JKAMP VGNC VGNC:73867
Bos taurus JKAMP VGNC VGNC:30375
Mus musculus JKAMP MGD MGI:1915057