Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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5092 |
Gene nameGene Name - the full gene name approved by the HGNC.
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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.
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PCBD1 |
SynonymsGene synonyms aliases
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DCOH, PCBD, PCD, PHS |
ChromosomeChromosome number
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10 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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10q22.1 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
rs727505360 |
C>A |
Pathogenic |
Coding sequence variant, stop gained, 5 prime UTR variant |
rs770334825 |
A>G |
Pathogenic |
Terminator codon variant, stop lost, intron variant |
rs1589483932 |
T>- |
Pathogenic |
Frameshift variant, coding sequence variant, intron variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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GO ID |
Ontology |
Definition |
Evidence |
Reference |
GO:0003713 |
Function |
Transcription coactivator activity |
IEA |
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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 |
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GO:0005829 |
Component |
Cytosol |
IDA |
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GO:0005829 |
Component |
Cytosol |
TAS |
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GO:0006559 |
Process |
L-phenylalanine catabolic process |
TAS |
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GO:0006729 |
Process |
Tetrahydrobiopterin biosynthetic process |
IEA |
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GO:0008124 |
Function |
4-alpha-hydroxytetrahydrobiopterin dehydratase activity |
IBA |
21873635 |
GO:0042802 |
Function |
Identical protein binding |
IPI |
16189514, 21516116, 25416956, 32296183 |
GO:0043393 |
Process |
Regulation of protein binding |
IEA |
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GO:0045893 |
Process |
Positive regulation of transcription, DNA-templated |
IEA |
|
GO:0070062 |
Component |
Extracellular exosome |
HDA |
19056867, 23533145 |
|
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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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 |
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Sequence |
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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.
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Associated diseases
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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 |
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Transient hyperphenylalaninemia |
Transient hyperphenylalaninemia |
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