CLDN1 - claudin 1 Gene
Also Known as CLD1; SEMP1; ILVASC
Species: Homo sapiens
About CLDN1
This gene has 2 transcripts (splice variants), 245 orthologues, 22 paralogues and is associated with 3 phenotypes. Biased expression in skin (RPKM 138.8), liver (RPKM 107.2) and 6 other tissues.
Summary
Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space. These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet. The protein encoded by this gene, a member of the Claudin family, is an integral membrane protein and a component of tight junction strands. Loss of function mutations result in neonatal ichthyosis-sclerosing cholangitis syndrome. [provided by RefSeq, Jul 2008]
CLDN1 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_021101.5 | NP_066924.1 | claudin-1 |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables identical protein binding |
IPI
IPI: Inferred from physical interaction
|
25849148 | GOA |
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
20375010 | GOA |
| enables virus receptor activity |
IMP
IMP: Inferred from mutant phenotype
|
20375010 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in bicellular tight junction assembly |
IMP
IMP: Inferred from mutant phenotype
|
25849148 | GOA |
| acts upstream of or within cell-cell junction organization |
IMP
IMP: Inferred from mutant phenotype
|
20164257 | GOA |
| involved in establishment of skin barrier |
IMP
IMP: Inferred from mutant phenotype
|
23407391 | GOA |
| involved in positive regulation of cell migration |
IMP
IMP: Inferred from mutant phenotype
|
28412298 | GOA |
| involved in positive regulation of epithelial cell proliferation involved in wound healing |
IMP
IMP: Inferred from mutant phenotype
|
28412298 | GOA |
| involved in positive regulation of wound healing |
IMP
IMP: Inferred from mutant phenotype
|
28412298 | GOA |
| involved in protein complex oligomerization |
IDA
IDA: Inferred from direct assay
|
23704991 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in basolateral plasma membrane |
IDA
IDA: Inferred from direct assay
|
20375010 | GOA |
| located in bicellular tight junction |
IDA
IDA: Inferred from direct assay
|
20375010 | GOA |
| located in plasma membrane |
IDA
IDA: Inferred from direct assay
|
11090614 | GOA |
| located in plasma membrane |
IMP
IMP: Inferred from mutant phenotype
|
23407391 | GOA |
| part of protein-containing complex |
IDA
IDA: Inferred from direct assay
|
25849148 | GOA |
| located in tight junction |
IDA
IDA: Inferred from direct assay
|
30734065 | GOA |
CLDN1 Protein Structure
PMP22_Claudin: PMP-22/EMP/MP20/Claudin family (5 - 182)
- 0
- 100
- 200
- 211 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
claudin-1 |
|
CLDN1 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
CLDN1 | O95832 | TMEM179B | Homo sapiens | Q7Z7N9 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | TMEM179B | Homo sapiens | Q7Z7N9 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | TMEM179B | Homo sapiens | Q7Z7N9 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | FNDC9 | Homo sapiens | Q8TBE3 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | FNDC9 | Homo sapiens | Q8TBE3 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | FNDC9 | Homo sapiens | Q8TBE3 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | MS4A3 | Homo sapiens | Q96HJ5 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | MS4A3 | Homo sapiens | Q96HJ5 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | MS4A3 | Homo sapiens | Q96HJ5 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | CD69 | Homo sapiens | Q07108 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | CD69 | Homo sapiens | Q07108 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | CD69 | Homo sapiens | Q07108 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | TMEM9 | Homo sapiens | Q9P0T7 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | TMEM9 | Homo sapiens | Q9P0T7 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | TMEM9 | Homo sapiens | Q9P0T7 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | CD79A | Homo sapiens | P11912 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | CD79A | Homo sapiens | P11912 | 32296183 | |
|
Intra
|
CLDN1 | O95832 | CD79A | Homo sapiens | P11912 | 32296183 |
CLDN1 Antibodies
| Cat. No. | 상품명 | 신청 | Reactivity |
|---|---|---|---|
| HY-P81222A | Claudin 1 Antibody (YA3551) | WB, IHC-P | Human, Mouse, Rat |
| HY-P85953 | Claudin 1 Antibody (YA5645) | IHC-P, WB, ICC/IF, ELISA | Human, Mouse, Rat |
| HY-P86518 | Claudin 1 Antibody (YA6210) | WB, IHC-P, ICC/IF, IP, ELISA | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis |
|
|
| Sclerosing Cholangitis |
|
|
| Cholangitis |
|
|
| Ichthyosis |
|
|
| Alopecia |
|
|
| Adenocarcinoma In Situ |
|
|
| Sclerosing Cholangitis, Neonatal |
|
|
| Perineurioma |
|
|
| Hepatitis C Virus |
|
|
| Dengue Virus |
|
|
| Meckel Diverticulum |
|
|
| Prostate Transitional Cell Carcinoma |
|
|
| Hypotrichosis |
|
|
| Colorectal Cancer |
|
|
| Focal Segmental Glomerulosclerosis |
|
|
| Barth Syndrome |
|
|
| Inflammatory Bowel Disease |
|
|
| Breast Cancer |
|
|
Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Bos taurus | CLDN1 | VGNC | VGNC:27402 |
| Canis familiaris | CLDN1 | VGNC | VGNC:39308 |
| Macaca mulatta | CLDN1 | VGNC | VGNC:71242 |
| Felis catus | CLDN1 | VGNC | VGNC:102670 |
| Rattus norvegicus | CLDN1 | RGD | RGD:68422 |
| Mus musculus | CLDN1 | MGD | MGI:1276109 |
| Others | CLDN1 | NCBI |