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PCBD1

PCBD1

Protein-coding gene in the species Homo sapiens

Pterin-4-alpha-carbinolamine dehydratase is an enzyme that in humans is encoded by the PCBD1 gene. This gene encodes pterin-4 alpha-carbinolamine dehydratase, an enzyme

PCBD1

Magnesium deficiency

Condition of low level of magnesium in the body

by genetic mutations in SLC12A3, CLNCKB, BSND, KCNJ10, FXYD2, HNF1B or PCBD1. In these diseases, the hypomagnesemia is accompanied by other defects in

Magnesium deficiency

Magnesium_deficiency

Pterin-4 alpha-carbinolamine dehydratase deficiency

Medical condition

tetrahydrobiopterin deficiency. This condition is associated with mutations of the PCBD1 gene. As of 2020, PCDD was the rarest form of BH4 deficiency in terms of

Pterin-4 alpha-carbinolamine dehydratase deficiency

Pterin-4_alpha-carbinolamine_dehydratase_deficiency

List of genetic disorders

Tay–Sachs disease HEXA (15) recessive Tetrahydrobiopterin deficiency GCH1, PCBD1, PTS, QDPR, MTHFR, DHFR recessive Thanatophoric dysplasia FGFR3 dominant

List of genetic disorders

List_of_genetic_disorders

DYRK1B

Protein-coding gene in the species Homo sapiens

exons within the catalytic domain. DYRK1B has been shown to interact with: PCBD1 and RANBP9. One lone missense mutation in Dyrk1B gene (R102C) was found

DYRK1B

Tetrahydrobiopterin deficiency

Medical condition

signs and symptoms of the disorder.[citation needed] Mutations in the GCH1, PCBD1, PTS and QDPR genes directly cause BH4 deficiency. Additionally, mutations

Tetrahydrobiopterin deficiency

Tetrahydrobiopterin_deficiency

List of human protein-coding genes 6

Q96AQ6 11769 PC HGNC:8636; P11498 11770 PCARE HGNC:34383; A6NGG8 11771 PCBD1 HGNC:8646; P61457 11772 PCBD2 HGNC:24474; Q9H0N5 11773 PCBP1 HGNC:8647;

List of human protein-coding genes 6

List_of_human_protein-coding_genes_6

Chromosome 10

Human chromosome

encoding enzyme bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2 PCBD1: 6-pyruvoyl-tetrahydropterin synthase/dimerization cofactor of hepatocyte

Chromosome 10

Chromosome_10

HNF1A

Protein-coding gene in humans

has been shown to interact with: CREB-binding protein and EP300, PCAF, PCBD1, RAC3, Src, DCoH Hepatocyte nuclear factors Maturity onset diabetes of the

HNF1A