FAM89A - family with sequence similarity 89 member A Gene

Homo sapiens

Also known as C1orf153

Gene ID: 375061 | Gene type: protein coding

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04727	FAM89A Human Pre-designed siRNA Set A		/	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

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