THADA | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | THADA , GITA, ARMC13, armadillo repeat containing, THADA armadillo repeat containing, Trm732 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 611800 MGI: 3039623 HomoloGene: 75175 GeneCards: THADA | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Thyroid adenoma associated is a protein in humans that is encoded by the THADA gene. [5]
Zinc finger protein 3 is a protein that in humans is encoded by the ZNF3 gene.
IgGFc-binding protein is a protein that in humans is encoded by the FCGBP gene.
EH-domain containing 4, also known as EHD4, is a human gene belonging to the EHD protein family.
Potassium voltage-gated channel subfamily H member 6 is a protein that in humans is encoded by the KCNH6 gene. The protein encoded by this gene is a voltage-gated potassium channel subunit.
Neurofilament, heavy polypeptide (NEFH) is a protein that in humans is encoded by the NEFH gene.
Mitochondrial glycine transporter is a protein that in humans is encoded by the SLC25A38 gene. SLC25A38 is involved in mitochondrial handling of glycine and is needed for the first step in heme synthesis. Mutations in this gene can lead to an autosomal recessive form of sideroblastic anemia.
Zinc finger and BTB domain containing 11 is a protein that in humans is encoded by the ZBTB11 gene.
BarH-like homeobox 2 is a protein in humans that is encoded by the BARHL2 gene.
Dynein, axonemal, heavy chain 7 is a protein in humans that is encoded by the DNAH7 gene.
Inositol monophosphatase 3 also known as inositol monophosphatase domain-containing protein 1 (IMPAD1) is an enzyme that in humans is encoded by the IMPAD1 gene.
Solute carrier family 15, member 4 is a protein in humans that is encoded by the SLC15A4 gene.
Forkhead box B1 is a protein that in humans is encoded by the FOXB1 gene.
Solute carrier organic anion transporter family member 4C1 is a protein that in humans is encoded by the SLCO4C1 gene, which is located on chromosome 5q21. The OATP4C1 protein is expressed in the basolateral membrane of the nephron of the human kidney, where it is involved in the uptake of organic anions for elimination in the urine. The drug digoxin is an important substrate of this transporter.
Forkhead box Q1 is a protein that in humans is encoded by the FOXQ1 gene.
Jumonji domain containing 1C is a protein that in humans is encoded by the JMJD1C gene.
HIG1 hypoxia inducible domain family member 1B is a protein that in humans is encoded by the HIGD1B gene.
Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene.
Forkhead box S1 is a protein that in humans is encoded by the FOXS1 gene.
NOTCH regulated ankyrin repeat protein is a protein that in humans is encoded by the NRARP gene.
Tetraspanin 14 is a protein that in humans is encoded by the TSPAN14 gene.