Gene Gene information from NCBI Gene database.
Entrez ID 5097
Gene name Protocadherin 1
Gene symbol PCDH1
Synonyms (NCBI Gene)
PC42PCDH42
Chromosome 5
Chromosome location 5q31.3
Summary This gene belongs to the protocadherin subfamily within the cadherin superfamily. The encoded protein is a membrane protein found at cell-cell boundaries. It is involved in neural cell adhesion, suggesting a possible role in neuronal development. The prot
miRNA miRNA information provided by mirtarbase database.
60
miRTarBase ID miRNA Experiments Reference
MIRT535463 hsa-miR-495-3p PAR-CLIP 22012620
MIRT535462 hsa-miR-5688 PAR-CLIP 22012620
MIRT738875 hsa-miR-3199 HITS-CLIP 33718276
MIRT738877 hsa-miR-4697-5p HITS-CLIP 33718276
MIRT535463 hsa-miR-495-3p PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding IEA
GO:0005654 Component Nucleoplasm IDA
GO:0005730 Component Nucleolus IDA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603626 8655 ENSG00000156453
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q08174
Protein name Protocadherin-1 (Cadherin-like protein 1) (Protocadherin-42) (PC42)
Protein function May be involved in cell-cell interaction processes and in cell adhesion.
PDB 6BX7 , 6MGA , 6PIM , 6VFP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08266 Cadherin_2 59 142 Cadherin-like Domain
PF00028 Cadherin 173 271 Cadherin domain Domain
PF00028 Cadherin 285 378 Cadherin domain Domain
PF00028 Cadherin 401 497 Cadherin domain Domain
PF00028 Cadherin 511 603 Cadherin domain Domain
PF00028 Cadherin 617 706 Cadherin domain Domain
PF00028 Cadherin 727 813 Cadherin domain Domain
PF08374 Protocadherin 815 1029 Protocadherin Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in the brain and neuro-glial cells.
Sequence
MDSGAGGRRCPEAALLILGPPRMEHLRHSPGPGGQRLLLPSMLLALLLLLAPSPGHATRV
VYKVPEEQPPNTLIGSLAADYGFPDVGHLYKLEVGAPYLRVDGKTGDIFTTETSIDREGL
RECQNQLPGDPCILEFEVSITD
LVQNGSPRLLEGQIEVQDINDNTPNFASPVITLAIPEN
TNIGSLFPIPLASDRDAGPNGVASYELQAGPEAQELFGLQVAEDQEEKQPQLIVMGNLDR
ERWDSYDLTIKVQDGGSPPRASSALLRVTVL
DTNDNAPKFERPSYEAELSENSPIGHSVI
QVKANDSDQGANAEIEYTFHQAPEVVRRLLRLDRNTGLITVQGPVDREDLSTLRFSVLAK
DRGTNPKSARAQVVVTVK
DMNDNAPTIEIRGIGLVTHQDGMANISEDVAEETAVALVQVS
DRDEGENAAVTCVVAGDVPFQLRQASETGSDSKKKYFLQTTTPLDYEKVKDYTIEIVAVD
SGNPPLSSTNSLKVQVV
DVNDNAPVFTQSVTEVAFPENNKPGEVIAEITASDADSGSNAE
LVYSLEPEPAAKGLFTISPETGEIQVKTSLDREQRESYELKVVAADRGSPSLQGTATVLV
NVL
DCNDNDPKFMLSGYNFSVMENMPALSPVGMVTVIDGDKGENAQVQLSVEQDNGDFVI
QNGTGTILSSLSFDREQQSTYTFQLKAVDGGVPPRSAYVGVTINVL
DENDNAPYITAPSN
TSHKLLTPQTRLGETVSQVAAEDFDSGVNAELIYSIAGGNPYGLFQIGSHSGAITLEKEI
ERRHHGLHRLVVKVSDRGKPPRYGTALVHLYVN
ETLANRTLLETLLGHSLDTPLDIDIAG
DPEYERSKQRGNILFGVVAGVVAVALLIALAVLVRYCRQREAKSGYQAGKKETKDLYAPK
PSGKASKGNKSKGKKSKSPKPVKPVEDEDEAGLQKSLKFNLMSDAPGDSPRIHLPLNYPP
GSPDLGRHYRSNSPLPSIQLQPQSPSASKKHQVVQDLPPANTFVGTGDTTSTGSEQYSDY
SYRTNPPKY
PSKQVGQPFQLSTPQPLPHPYHGAIWTEVWE
Sequence length 1060
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Virion - Lassa virus and SFTS virus  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
14
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Esophageal atresia/tracheoesophageal fistula Likely pathogenic rs1753000062 RCV001172297
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Gastric cancer Conflicting classifications of pathogenicity ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Asthma Associate 23988763, 26209277, 27701444
★☆☆☆☆
Found in Text Mining only
Carcinoma Pancreatic Ductal Associate 35864095
★☆☆☆☆
Found in Text Mining only
Dermatitis Atopic Associate 23988763
★☆☆☆☆
Found in Text Mining only
Dyslexia Associate 29409727
★☆☆☆☆
Found in Text Mining only
Esophageal atresia with or without tracheoesophageal fistula Associate 32641753
★☆☆☆☆
Found in Text Mining only
Inflammation Associate 26227965
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Stimulate 35864095
★☆☆☆☆
Found in Text Mining only
Melanoma Associate 9182820
★☆☆☆☆
Found in Text Mining only
Neoplasm Metastasis Associate 37957639
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Associate 37957639
★☆☆☆☆
Found in Text Mining only