FAM83H

Summary: The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3). [provided by RefSeq, Mar 2010].

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Name
OMIM ID
Ensembl ID
HGNC ID
PHARMGKB ID
Map Location
Namefamily with sequence similarity 83 member H
OMIM IDMIM:611927
Ensembl IDEnsembl:ENSG00000180921
HGNC IDHGNC:HGNC:24797
PHARMGKB IDPA144596434
Map Location8q24.3

GO terms in FAM83H


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Term Type
Evidence Type
GO Term ID
GO Des.
MF IPI GO:0019901 protein kinase binding
MF IDA GO:1990254 keratin filament binding
CC IEA GO:0005737 cytoplasm
CC IDA GO:0045095 keratin filament
BP IMP GO:0030335 positive regulation of cell migration
BP IEA GO:0031214 biomineral tissue development
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Gene expression in normal tissue: FAM83H

Gene-model tissue-cancer distribution: Bubble Plot

undefinetissue: undefine cancer: undefined model num: 0undefinedtissue: undefined cancer: PANCAN model num: 3

Gene-drug pathway distribution

ERK MAPK signaling1RTK signaling1

Pathways in FAM83H


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Database
Pathway ID
Pathway Des.
No matching records found

Gene-Drug: Aster Plot


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Drug ID
Drug Name
Model Num.
iGMDRD409 Saracatinib 1
iGMDRD353 PD0325901 2
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution

Gene Structure: PDB

Models in FAM83H

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Model
Level
Reference ID
Tissue
Cancer
Drug
Clinical Response
Source
No matching records found

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