Gene Gene information from NCBI Gene database.
Entrez ID 80157
Gene name Cell wall biogenesis 43 C-terminal homolog
Gene symbol CWH43
Synonyms (NCBI Gene)
CWH43-CPGAP2IP
Chromosome 4
Chromosome location 4p11
miRNA miRNA information provided by mirtarbase database.
5
miRTarBase ID miRNA Experiments Reference
MIRT2207765 hsa-miR-1260 CLIP-seq
MIRT2207766 hsa-miR-1260b CLIP-seq
MIRT2207767 hsa-miR-188-3p CLIP-seq
MIRT2207768 hsa-miR-3156-3p CLIP-seq
MIRT2207769 hsa-miR-4301 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
28
GO ID Ontology Definition Evidence Reference
GO:0002790 Process Peptide secretion IEA
GO:0005576 Component Extracellular region IEA
GO:0005783 Component Endoplasmic reticulum IBA
GO:0006486 Process Protein glycosylation IEA
GO:0006487 Process Protein N-linked glycosylation IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618561 26133 ENSG00000109182
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H720
Protein name PGAP2-interacting protein (Cell wall biogenesis protein 43 C-terminal homolog)
Protein function Involved in lipid remodeling during GPI-anchor maturation.
Family and domains
Sequence
MPSLWREILLESLLGCVSWSLYHDLGPMIYYFPLQTLELTGLEGFSIAFLSPIFLTITPF
WKLVNKKWMLTLLRIITIGSIASFQAPNAKLRLMVLALGVSSSLIVQAVTWWSGSHLQRY
LRIWGFILGQIVLVVLRIWYTSLNPIWSYQMSNKVILTLSAIATLDRIGTDGDCSKPEEK
KTGEVATGMASRPNWLLAGAAFGSLVFLTHWVFGEVSLVSRWAVSGHPHPGPDPNPFGGA
VLLCLASGLMLPSCLWFRGTGLIWWVTGTASAAGLLYLHTWAAAVSGCVFAIFTASMWPQ
TLGHLINSGTNPGKTMTIAMIFYLLEIFFCAWCTAFKFVPGGVYARERSDVLLGTMMLII
GLNMLFGPKKNLDLLLQTKNSSKVLFRKSEKYMKLFLWLLVGVGLLGLGLRHKAYERKLG
KVAPTKEVSAAIWPFRFGYDNEGWSSLERSAHLLNETGADFITILESDASKPYMGNNDLT
MWLGEKLGFYTDFGPSTRYHTWGIMALSRYPIVKSEHHLLPSPEGEIAPAITLTVNISGK
LVDFVVTHFGNHEDDLDRKLQAIAVSKLLKSSSNQVIFLGYITSAPGSRDYLQLTEHGNV
KDIDSTDHDRWCEYIMYRGLIRLGYARISHAELSDSEIQMAKFRIPDDPTNYRDNQKVVI
DHREVSEKIHFNPRFGSYKEGHNYENNHHFHMNTPKYFL
Sequence length 699
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial cancer of breast Benign rs142768963 RCV005910729
Thyroid cancer, nonmedullary, 1 Benign rs142768963 RCV005910730
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Colorectal Neoplasms Inhibit 37894942
Mucocutaneous Lymph Node Syndrome Associate 38259468
Neoplasms Inhibit 37894942