Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1366
Gene name Gene Name - the full gene name approved by the HGNC.
Claudin 7
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CLDN7
Synonyms (NCBI Gene) Gene synonyms aliases
CEPTRL2, CLDN-7, CPETRL2, Hs.84359, claudin-1
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellula
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017878 hsa-miR-335-5p Microarray 18185580
MIRT042085 hsa-miR-484 CLASH 23622248
MIRT736372 hsa-miR-1193 Luciferase reporter assay, Western blotting, qRT-PCR 32547067
MIRT895523 hsa-miR-1183 CLIP-seq
MIRT895524 hsa-miR-1289 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
CTBP1 Repression 19277896
ELF3 Unknown 17060315
HDAC1 Activation 19277896
RUNX3 Activation 19706291
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005198 Function Structural molecule activity IEA
GO:0005515 Function Protein binding IPI 16054130, 20651236, 25416956, 32296183
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005886 Component Plasma membrane IDA 20375010
GO:0005923 Component Bicellular tight junction IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
609131 2049 ENSG00000181885
Protein
UniProt ID O95471
Protein name Claudin-7 (CLDN-7)
Protein function Plays a major role in tight junction-specific obliteration of the intercellular space.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00822 PMP22_Claudin 4 182 PMP-22/EMP/MP20/Claudin family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in kidney, lung and prostate. Isoform 1 seems to be predominant, except in some normal prostate samples, where isoform 2 is the major form. Down-regulated in breast cancers, including ductal carcinoma in situ (DCIS), lobular
Sequence
Sequence length 211
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Virion - Hepatitis viruses
Cell adhesion molecules
Tight junction
Leukocyte transendothelial migration
Pathogenic Escherichia coli infection
Hepatitis C
 
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 17013881
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Inhibit 17585317
Adenocarcinoma Associate 27687058
Adenoma Associate 21310043
Adenoma Chromophobe Associate 17449941
Adenoma Oxyphilic Associate 15858144, 17449941
Adenomyosis Associate 37019419
Ameloblastoma Associate 31473941
Biliary Tract Neoplasms Associate 18854598
Breast Neoplasms Associate 19277896, 20103682, 21883696, 26919310, 36412442, 36691073, 39175074
Breast Neoplasms Stimulate 33714203