Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
80157
Gene name Gene Name - the full gene name approved by the HGNC.
Cell wall biogenesis 43 C-terminal homolog
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CWH43
Synonyms (NCBI Gene) Gene synonyms aliases
CWH43-C, PGAP2IP
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p11
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005783 Component Endoplasmic reticulum IBA 21873635
GO:0006506 Process GPI anchor biosynthetic process IBA 21873635
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618561 26133 ENSG00000109182
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Lung cancer Malignant neoplasm of lung rs121913530, rs121913529, rs878855122, rs1057519784, rs770315135 27935865
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Uterine Fibroids Uterine Fibroids GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Colorectal Neoplasms Inhibit 37894942
Mucocutaneous Lymph Node Syndrome Associate 38259468
Neoplasms Inhibit 37894942