FAM89A - family with sequence similarity 89 member A Gene

Also Known as C1orf153

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 375061

About FAM89A

This gene has 3 transcripts (splice variants), 100 orthologues and 2 paralogues. Broad expression in fat (RPKM 41.2), placenta (RPKM 38.9) and 17 other tissues.

FAM89A Products (1)

mRNA Protein Name
NM_198552.3 NP_940954.1 protein FAM89A
Protein Preferred Names Protein Names

protein FAM89A

Related Diseases

Diseases Alias
Immunodeficiency 38 With Basal Ganglia Calcification

  • Mendelian Susceptibility To Mycobacterial Diseases Due To Complete Isg15 Deficiency

  • IMD38

  • Immunodeficiency 38, Mycobacteriosis, Autosomal Recessive

  • Immunodeficiency 38

  • Isg15 Deficiency, Autosomal Recessive

  • Immunodeficiency 38, With Basal Ganglia Calcification

  • Autosomal Recessive Isg15 Deficiency

  • Msmd Due To Complete Isg15 Deficiency

  • Immunodeficiency, Type 38
Robinow Syndrome, Autosomal Dominant 2

  • Autosomal Dominant Robinow Syndrome 2

  • DRS2

  • Robinow, Autosomal Dominant Syndrome, Type 2
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-RS04727 FAM89A Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Rattus norvegicus FAM89A RGD RGD:1309879
Bos taurus FAM89A VGNC VGNC:28842
Canis familiaris FAM89A VGNC VGNC:50879
Mus musculus FAM89A MGD MGI:1916877
Macaca mulatta FAM89A VGNC VGNC:72340
Others FAM89A NCBI