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PCBD1 (pterin-4 alpha-carbinolamine dehydratase 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5092
Gene nameGene Name - the full gene name approved by the HGNC.
Pterin-4 alpha-carbinolamine dehydratase 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
PCBD1
SynonymsGene synonyms aliases
DCOH, PCBD, PCD, PHS
ChromosomeChromosome number
10
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q22.1
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the pterin-4-alpha-carbinolamine dehydratase family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The encoded protein functions as both
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs104894172 C>A Likely-pathogenic Stop gained, intron variant, coding sequence variant
rs104894177 A>G Pathogenic Intron variant, missense variant, coding sequence variant
rs115117837 C>G,T Pathogenic, likely-benign Intron variant, missense variant, coding sequence variant
rs121913014 G>A Pathogenic Intron variant, missense variant, coding sequence variant
rs121913015 G>A Pathogenic Intron variant, stop gained, coding sequence variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT043343 hsa-miR-331-3p CLASH 23622248
MIRT1216231 hsa-miR-10a CLIP-seq
MIRT1216232 hsa-miR-10b CLIP-seq
MIRT1216233 hsa-miR-1182 CLIP-seq
MIRT1216234 hsa-miR-1207-5p CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003713 Function Transcription coactivator activity IEA
GO:0004505 Function Phenylalanine 4-monooxygenase activity IEA
GO:0005515 Function Protein binding IPI 16189514, 20195357, 25416956, 26871637, 29892012, 31515488, 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005829 Component Cytosol IDA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P61457
Protein name Pterin-4-alpha-carbinolamine dehydratase (PHS) (EC 4.2.1.96) (4-alpha-hydroxy-tetrahydropterin dehydratase) (Dimerization cofactor of hepatocyte nuclear factor 1-alpha) (DCoH) (Dimerization cofactor of HNF1) (Phenylalanine hydroxylase-stimulating protein)
Protein function Involved in tetrahydrobiopterin biosynthesis (By similarity). Seems to both prevent the formation of 7-pterins and accelerate the formation of quinonoid-BH2. Coactivator for HNF1A-dependent transcription (By similarity). Regulates the dimerizati
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01329 Pterin_4a
6 99
Pterin 4 alpha carbinolamine dehydratase
Domain
Sequence
Sequence length 104
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Folate biosynthesis
Metabolic pathways
  Phenylalanine metabolism
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Hyperphenylalaninemia Hyperphenylalaninaemia, Hyperphenylalaninemia with primapterinuria, Pterin-4 alpha-carbinolamine dehydratase deficiency rs104894274, rs794726656, rs104894278, rs62514958, rs5030856, rs62517167, rs1035794099, rs775029664, rs1589052989, rs770562664, rs1273776043, rs569240271, rs761235755, rs1277990552, rs370032864, rs1841794635, rs755829473, rs1841794857 24204001, 9760199, 8352282, 24848070, 27604308, 8618906, 9585615, 27246466, 25333069
Lung adenocarcinoma Adenocarcinoma of lung (disorder) rs28934576, rs121913530, rs397516975, rs587776805, rs121913469, rs121913364, rs121913351, rs121913366, rs397516896, rs397516977, rs397516981, rs397517127, rs121913344, rs727504233, rs121913370, rs760043106, rs1057519788, rs1131692238, rs1131692237, rs1554350382 27602772
Unknown
Disease name Disease term dbSNP ID References
Motor delay Clumsiness - motor delay
Transient hyperphenylalaninemia Transient hyperphenylalaninemia

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