| FOXI3 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | FOXI3 , forkhead box I3 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 612351 MGI: 3511278 HomoloGene: 52949 GeneCards: FOXI3 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Forkead box I3 (FOXI3) is a protein that in humans is encoded by the FOXI3 gene. FOXI3 is a forkhead box transcription factor that is expressed in the development of hair and teeth. One of its mutations is a dominant allele responsible for the heterozygous Hh hairless trait in dogs. It was identified in 2008. [5]
T-box transcription factor TBX19 is a protein that in humans is encoded by the TBX19 gene.
HR is a gene encoding Protein hairless.
R-spondin 2 also known as roof plate-specific spondin-2 is a secreted protein that in humans that is encoded by the RSPO2 gene.
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.
HFM1 is a gene that in humans encodes a protein necessary for homologous recombination of chromosomes. Biallelic mutations in HFM1 cause recessive primary ovarian insufficiency.
Forkhead box I1 is a protein that in humans is encoded by the FOXI1 gene.
Tectonic family member 3 is a protein in humans that is encoded by the TCTN3 gene.
Storkhead box 1 is a protein in humans that is encoded by the STOX1 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.
SLC41A1 is a protein that in humans is encoded by the gene SLC41A1. It is homologous to the prokaryotic Mg++ transfer protein MgtE
The KSR2 gene is Kinase suppressor of ras 2 it is a protein that in humans is encoded by the KSR2 gene. KSR2 mutation effects in humans by obesity and because KSR2 gene reduces the ERK signaling and it reduces glucose and fatty acid oxidation. KSR2 mutation reduces the glucose and fatty acid oxidation process but it makes growth factor "Epidermal growth factor (EGF)" reaction more faster to simulate cell growth and KSR2 cause insulin resistance, KSA2 gene also regulates how the body uses the energy, and it usually causes type 2 diabetes.
Forkhead box B1 is a protein that in humans is encoded by the FOXB1 gene.
Biliverdin reductase A is a protein that in humans is encoded by the BLVRA gene.
Forkhead box Q1 is a protein that in humans is encoded by the FOXQ1 gene.
Left-right determination factor 2 is a protein that in humans is encoded by the LEFTY2 gene.
Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene.
Ribonuclease H2 subunit C is a protein that in humans is encoded by the RNASEH2C gene. RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits, and degrades the RNA of RNA:DNA hybrids.
Forkhead box S1 is a protein that in humans is encoded by the FOXS1 gene.
SLC45A1 is a member of the SLC45 family of solute carriers. Analysis of the protein function in a recombinant yeast expression assay show that it can: (i) transport a disaccharide, such as glucose and sucrose (ii) perform secondary active transport in a proton-dependent manner.
