1. Gene
  2. FAM83A - family with sequence similarity 83 member A Gene

FAM83A - family with sequence similarity 83 member A Gene

Homo sapiens

Also known as BJ-TSA-9

Gene ID: 84985 | Gene type: protein coding

About FAM83A

This gene has 9 transcripts (splice variants), 161 orthologues and 7 paralogues. Biased expression in esophagus (RPKM 21.0), skin (RPKM 1.8) and 1 other tissue.

Summary

Enables identical protein binding activity; phosphatidylinositol 3-kinase regulatory subunit binding activity; and protein kinase binding activity. Involved in cell population proliferation and epidermal growth factor receptor signaling pathway. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

FAM83A Products(5)

mRNA Protein Name
NM_001288587.3 NP_001275516.1 protein FAM83A isoform c
NM_001321630.2 NP_001308559.1 protein FAM83A isoform d
NM_001394396.1 NP_001381325.1 protein FAM83A isoform a
NM_032899.6 NP_116288.2 protein FAM83A isoform a
NM_207006.3 NP_996889.1 protein FAM83A isoform b
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables phosphatidylinositol 3-kinase regulatory subunit binding IDA
IDA: Inferred from direct assay
22886303 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
enables protein kinase binding IDA
IDA: Inferred from direct assay
22886303 GOA
enables protein kinase binding IPI
IPI: Inferred from physical interaction
22886303 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cell population proliferation IMP
IMP: Inferred from mutant phenotype
22886303 GOA
involved in epidermal growth factor receptor signaling pathway IDA
IDA: Inferred from direct assay
22886303 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

FAM83A Protein Structure

DUF1669

DUF1669: Protein of unknown function (DUF1669) (15 - 296)

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  • 434 a.a.
Protein Preferred Names Protein Names

protein FAM83A

tumor antigen BJ-TSA-9

FAM83A Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
FAM83A Q86UY5 GPSM1 Homo sapiens Q86YR5-3 32296183
Intra
FAM83A Q86UY5 GPSM1 Homo sapiens Q86YR5-3 32296183
Intra
FAM83A Q86UY5 GPSM1 Homo sapiens Q86YR5-3 32296183
Intra
FAM83A Q86UY5 KRTAP8-1 Homo sapiens Q8IUC2 32296183
Intra
FAM83A Q86UY5 KRTAP8-1 Homo sapiens Q8IUC2 32296183
Intra
FAM83A Q86UY5 KRTAP8-1 Homo sapiens Q8IUC2 32296183
Intra
FAM83A Q86UY5 PPP1R16B Homo sapiens Q96T49 32296183
Intra
FAM83A Q86UY5 PPP1R16B Homo sapiens Q96T49 32296183
Intra
FAM83A Q86UY5 PPP1R16B Homo sapiens Q96T49 32296183
Intra
FAM83A Q86UY5 KRT34 Homo sapiens O76011 32296183
Intra
FAM83A Q86UY5 KRT34 Homo sapiens O76011 32296183
Intra
FAM83A Q86UY5 KRTAP6-2 Homo sapiens Q3LI66 32296183
Intra
FAM83A Q86UY5 KRTAP6-2 Homo sapiens Q3LI66 32296183
Intra
FAM83A Q86UY5 FOXI1 Homo sapiens Q12951-2 32296183
Intra
FAM83A Q86UY5 FOXI1 Homo sapiens Q12951-2 32296183
Intra
FAM83A Q86UY5 CSNK1E Homo sapiens P49674 29789297
Intra
FAM83A Q86UY5 ccsb orf id: 14249 Homo sapiens EBI-22320186 32296183
Intra
FAM83A Q86UY5 CSNK1E Homo sapiens P49674 33961781
Intra
FAM83A Q86UY5 ccsb orf id: 14249 Homo sapiens EBI-22320186 32296183
Intra
FAM83A Q86UY5 CSNK1E Homo sapiens P49674 29789297
Intra
FAM83A Q86UY5 146664 Homo sapiens EBI-10182452 25416956
Intra
FAM83A Q86UY5 146664 Homo sapiens EBI-10182452 25416956
Intra
FAM83A Q86UY5 KRTAP6-3 Homo sapiens Q3LI67 32296183
Intra
FAM83A Q86UY5 KRTAP6-3 Homo sapiens Q3LI67 32296183
Intra
FAM83A Q86UY5 q9y649_human Homo sapiens Q9Y649 32814053
Intra
FAM83A Q86UY5 q9y649_human Homo sapiens Q9Y649 32814053
Intra
FAM83A Q86UY5 q9y649_human Homo sapiens Q9Y649 32814053
Intra
FAM83A Q86UY5 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
FAM83A Q86UY5 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
FAM83A Q86UY5 PLAGL2 Homo sapiens Q9UPG8 32296183
Intra
FAM83A Q86UY5 PSMA3 Homo sapiens P25788 32296183
Intra
FAM83A Q86UY5 PSMA3 Homo sapiens P25788 32296183
Intra
FAM83A Q86UY5 FGFR3 Homo sapiens P22607 32814053
Intra
FAM83A Q86UY5 FGFR3 Homo sapiens P22607 32814053
Intra
FAM83A Q86UY5 FGFR3 Homo sapiens P22607 32814053
Intra
FAM83A Q86UY5 GSN Homo sapiens P06396 32814053
Intra
FAM83A Q86UY5 GSN Homo sapiens P06396 32814053
Intra
FAM83A Q86UY5 GSN Homo sapiens P06396 32814053
Intra
FAM83A Q86UY5 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
FAM83A Q86UY5 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
FAM83A Q86UY5 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
FAM83A Q86UY5 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
FAM83A Q86UY5 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
FAM83A Q86UY5 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
FAM83A Q86UY5 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
FAM83A Q86UY5 PMP22 Homo sapiens A0A6Q8PF08 32814053
Intra
FAM83A Q86UY5 BHLHE40 Homo sapiens O14503 32296183
Intra
FAM83A Q86UY5 BHLHE40 Homo sapiens O14503 32296183
Intra
FAM83A Q86UY5 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
FAM83A Q86UY5 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
FAM83A Q86UY5 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
FAM83A Q86UY5 TRIM27 Homo sapiens P14373 25416956
Intra
FAM83A Q86UY5 TRIM27 Homo sapiens P14373 25416956
Intra
FAM83A Q86UY5 DAZAP2 Homo sapiens Q15038 32296183
Intra
FAM83A Q86UY5 DAZAP2 Homo sapiens Q15038 32296183
Intra
FAM83A Q86UY5 TRIM23 Homo sapiens P36406 25416956
Intra
FAM83A Q86UY5 TRIM23 Homo sapiens P36406 25416956
Intra
FAM83A Q86UY5 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
FAM83A Q86UY5 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
FAM83A Q86UY5 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
FAM83A Q86UY5 GCC1 Homo sapiens Q96CN9 32296183
Intra
FAM83A Q86UY5 SMYD1 Homo sapiens Q8NB12 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Amelogenesis Imperfecta, Type Iiia

Ai3

Adhcai

Amelogenesis Imperfecta Type 3

AI3A

Amelogenesis Imperfecta, Type Iii

Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Dominant

Amelogenesis Imperfecta Type 3a

Amelogenesis Imperfecta Hypomineralization Type

Amelogenesis Imperfecta Type Iii

Hypocalcified Amelogenesis Imperfecta

Amelogenesis Imperfecta, Type 3

Amelogenesis Imperfecta, Hypomineralization Type

Autosomal Dominant Amelogenesis Imperfecta Hypocalcification Type

Amelogenesis Imperfecta 3a

Amelogenesis Imperfecta Hypocalcification Type Autosomal Dominant

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

Orthologs Information

Species Symbol Source ID
Macaca mulatta FAM83A VGNC VGNC:72384
Canis familiaris FAM83A VGNC VGNC:40699
Bos taurus FAM83A VGNC VGNC:28832
Rattus norvegicus FAM83A RGD RGD:1565606
Mus musculus FAM83A MGD MGI:2447773
Felis catus FAM83A VGNC VGNC:81657