TMEM184B - transmembrane protein 184B Gene

Also Known as FM08; HS5O6A; C22orf5; HSPC256

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 25829

About TMEM184B

This gene has 13 transcripts (splice variants), 268 orthologues and 3 paralogues. Ubiquitous expression in placenta (RPKM 20.3), fat (RPKM 18.2) and 25 other tissues.

Summary

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

TMEM184B Products (3)

mRNA Protein Name
NM_001195071.1 NP_001182000.1 transmembrane protein 184B isoform a
NM_001195072.2 NP_001182001.1 transmembrane protein 184B isoform b
NM_012264.5 NP_036396.2 transmembrane protein 184B isoform a

TMEM184B Protein Structure

Solute_trans_a

Solute_trans_a: Organic solute transporter Ostalpha (45 - 319)

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

transmembrane protein 184B

  • putative MAPK-activating protein FM08

TMEM184B Antibodies

Cat. No. Product Name Application Reactivity
HY-P89897 TMEM184B Antibody (YA9241) WB, ICC/IF, IF-Tissue, IP, ELISA human, mouse, rat

Related Diseases

Diseases Alias
Amyloidosis, Finnish Type

  • Finnish Type Amyloidosis

  • Meretoja Syndrome

  • Amyloidosis V

  • Amyloidosis, Meretoja Type

  • Amyloid Cranial Neuropathy With Lattice Corneal Dystrophy

  • Lattice Corneal Dystrophy Type Ii

  • Familial Amyloidosis, Finnish Type

  • Familial Amyloid Polyneuropathy Type Iv

  • Amyloidosis Due To Mutant Gelsolin

  • Agel Amyloidosis

  • Gelsolin Amyloidosis

  • Hereditary Gelsolin Amyloidosis

  • Lattice Corneal Dystrophy Type Ii Finnish

  • Gelsolin-Related Amyloidosis

  • Kymenlaakso Syndrome

  • Lattice Corneal Dystrophy, Gelsolin Type

  • Hereditary Amyloidosis, Finnish Type

  • Lattice Corneal Dystrophy Type 2

  • Amyloidosis 5

  • AMYL5

  • Agel

  • Familial Amyloidosis Finnish Type

  • Meretoja Type Amyloidosis

  • Type Iv Familial Amyloid Polyneuropathy

  • Familial Amyloid Polyneuropathy, Type V

  • Familial Amyloid Polyneuropathy, Type Iv
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS14690 TMEM184B Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris TMEM184B VGNC VGNC:47509
Mus musculus TMEM184B MGD MGI:2445179
Felis catus TMEM184B VGNC VGNC:66299
Rattus norvegicus TMEM184B RGD RGD:1306591
Bos taurus TMEM184B VGNC VGNC:36010
Macaca mulatta TMEM184B VGNC VGNC:78898
Others TMEM184B NCBI