FAM167A - family with sequence similarity 167 member A Gene

Also Known as D8S265; C8orf13; DIORA-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 83648

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 References 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

FAM167: FAM167 (130 - 214)

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

protein FAM167A

  • disordered autoimmunity 1

FAM167A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
FAM167A Q96KS9 FLJ13057 Homo sapiens Q53SE7
Y2H Array
25416956
Intra
FAM167A Q96KS9 PPP3CA Homo sapiens Q08209-2
Y2H Array
32296183
Intra
FAM167A Q96KS9 PPP3CA Homo sapiens Q08209-2
Y2H Prey Pooling
32296183
Intra
FAM167A Q96KS9 GMCL1 Homo sapiens Q96IK5
Anti Tag CoIP
33961781
Intra
FAM167A Q96KS9 GMCL1 Homo sapiens Q96IK5
Anti Tag CoIP
28514442
Intra
FAM167A Q96KS9 GMCL1 Homo sapiens Q96IK5
Y2H Array
31515488
Intra
FAM167A Q96KS9 GMCL1 Homo sapiens Q96IK5
Y2H Prey Pooling
32296183
Intra
FAM167A Q96KS9 GMCL1 Homo sapiens Q96IK5
Y2H Array
32296183
Intra
FAM167A Q96KS9 HIP1 Homo sapiens O00291
Validated Y2H
32814053
Intra
FAM167A Q96KS9 HIP1 Homo sapiens O00291
Y2H Pooling
32814053
Intra
FAM167A Q96KS9 HIP1 Homo sapiens O00291
Y2H Array
32814053
Intra
FAM167A Q96KS9 COQ8A Homo sapiens Q8NI60
Y2H Array
32814053
Intra
FAM167A Q96KS9 COQ8A Homo sapiens Q8NI60
Y2H Pooling
32814053
Intra
FAM167A Q96KS9 COQ8A Homo sapiens Q8NI60
Validated Y2H
32814053
Intra
FAM167A Q96KS9 PRPH Homo sapiens P41219
Anti Tag CoIP
33961781
Intra
FAM167A Q96KS9 PRPH Homo sapiens P41219
Validated Y2H
32814053
Intra
FAM167A Q96KS9 PRPH Homo sapiens P41219
Y2H Pooling
32814053
Intra
FAM167A Q96KS9 PRPH Homo sapiens P41219
Y2H Array
32814053
Intra
FAM167A Q96KS9 PRKCG Homo sapiens P05129
Y2H Pooling
32814053
Intra
FAM167A Q96KS9 PRKCG Homo sapiens P05129
Validated Y2H
32814053
Intra
FAM167A Q96KS9 PRKCG Homo sapiens P05129
Y2H Array
32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant FAM167A Proteins

Cat. No. Product Name Accession Purity
HY-P71678 FAM167A Protein, Human (HEK293, Myc, His) Q96KS9 (M1-C214) ≥ 90%, as determined by reducing SDS-PAGE.

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

Pre-clinical Phase

Bioactive Molecules (3)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS04690 FAM167A Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS19837 Fam167a Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS26334 Fam167a Rat Pre-designed siRNA Set A Pre-designed Set / 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