FAM167A - family with sequence similarity 167 member A Gene

Homo sapiens

Also known as D8S265; C8orf13; DIORA-1

Gene ID: 83648 | Gene type: protein coding

About FAM167A

Cytogenetic location: 8p23.1 Genomic coordinates (GRCh38): 8:11,421,476-11,475,908 (from NCBI)

This gene has 8 transcripts (splice variants), 214 orthologues and 3 paralogues. Biased expression in thyroid (RPKM 28.9), brain (RPKM 11.5) and 4 other tissues.

FAM167A Products(1)

mRNA	Protein	Name
NM_053279.3	NP_444509.2	protein FAM167A

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	25416956	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

FAM167A Protein Structure

FAM167

0
100
200
214 a.a.

Protein Preferred Names

Protein Names

protein FAM167A

disordered autoimmunity 1

Recombinant FAM167A Proteins

Cat. No.	Product Name	Accession	Purity
HY-P71678	FAM167A Protein, Human (HEK293, Myc, His)	Q96KS9 (M1-C214)	≥95%

Related Diseases

Diseases

Alias

Maturity-Onset Diabetes Of The Young, Type 11

Maturity-Onset Diabetes Of The Young Type 11	MODY11
Maturity-Onset Diabetes Of The Young 11	Mody-11
Mody Type 11	Diabetes Of The Young, Maturity-Onset, Type 11

Keratolytic Winter Erythema

KWE	Oudtshoorn Skin Disease
Erythrokeratolysis Hiemalis Ichthyosis	Erythrokeratolysis Hiemalis
Oudtshoorn Skin	Oudtshoorn Disease

Kawasaki Disease

Mucocutaneous Lymph Node Syndrome	Acute Febrile Mucocutaneous Lymph Node Syndrome
Kawasaki Syndrome	Kd
Infantile Polyarteritis	Kawasaki Disease, Susceptibility To
Acute Febrile Mcls	Kawasaki'S Disease
Mlns	KWD

Bacterial Conjunctivitis

Purulent Conjunctivitis

Conjunctivitis, Bacterial

Potocki-Shaffer Syndrome

Proximal 11p Deletion Syndrome	Chromosome 11p11.2 Deletion Syndrome
Pss	11p11.2 Deletion
P11pds	Defect11 Syndrome
Deletion Of Chromosome 11p11.2	POSHS

Systemic Lupus Erythematosus

Lupus Nephritis	SLE
Disseminated Lupus Erythematosus	Systemic Lupus Erythematosus, Susceptibility To
Lupus Erythematosus, Systemic	Lupus Nephritis, Susceptibility To
Libman-Sacks Disease	Systemic Lupus Erythematosus Susceptibility To
Sle - Lupus Erythematosus, Systemic	Le Syndrome
Lupus	Lupus Erythematosus Systemic
Lupus Erythematosus, Systemic, Susceptibility To	Lupus Vulgaris
Lupus Erythematosus, Discoid	Lupus Erythematosus
Systemic Lupus Erythematosus Nos	Sle - [Systemic Lupus Erythematosus]

Limited Scleroderma

Limited Cutaneous Systemic Sclerosis	Limited Systemic Sclerosis
Systemic Sclerosis Sine Scleroderma	Crest Syndrome
Limited Cutaneous Systemic Scleroderma	Scleroderma, Limited
Systemic Sclerosis, Limited	Progressive Systemic Sclerosis Sine Scleroderma
Scleroderma, Sine	Crest - [Calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, And Telangiectasia] Syndrome
Crst - [Calcinosis, Raynaud Phenomenon, Sclerodactyly And Telangiectasia] Syndrome

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-RS04690	FAM167A Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	FAM167A	VGNC	VGNC:28750
Mus musculus	FAM167A	MGD	MGI:3606565
Canis familiaris	FAM167A	VGNC	VGNC:40617
Rattus norvegicus	FAM167A	RGD	RGD:1561302
Macaca mulatta	FAM167A	VGNC	VGNC:83998
Felis catus	FAM167A	VGNC	VGNC:78491
Others	FAM167A	NCBI

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