CDH8
Strwythurau PDB Human UniProt search: PDBe RCSB Rhestr o ddynodwyr PDB 1ZXK, 2A62
Dynodwyr
Cyfenwau	CDH8, Nbla04261, cadherin 8
Dynodwyr allanol	OMIM: 603008 HomoloGene: 55604 GeneCards: CDH8
Patrwm RNA pattern Rhagor o gyfeiriadau
Ontoleg y genyn Gweithrediad moleciwlaidd • calcium ion binding • metal ion binding • identical protein binding • cytoskeletal protein binding • protein homodimerization activity • cadherin binding Cydrannau o'r gell • axon terminus • integral component of membrane • synaptic cleft • bilen • Cellbilen • synaptic membrane • glutamatergic synapse • cell surface • catenin complex Prosesau biolegol • response to cold • cell adhesion • adherens junction organization • synaptic transmission, glutamatergic • homophilic cell adhesion via plasma membrane adhesion molecules • chemical synaptic transmission • GO:1904739 regulation of synapse organization • cell-cell junction assembly • calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules • cell-cell adhesion mediated by cadherin • cell-cell adhesion • GO:0000767 cell morphogenesis Sources:Amigo / QuickGO
Orthologau
Species	Bod dynol	Llygoden
Entrez	1006	n/a
Ensembl	ENSG00000150394	n/a
UniProt	P55286	n/a
RefSeq (mRNA)	NM_001796	n/a
RefSeq (protein)	NP_001787	n/a
Lleoliad (UCSC)	n/a	n/a
PubMed search	[1]	n/a
Wicidata
Gweld/Golygu Bod dynol

Protein sy'n cael ei godio yn y corff dynol gan y genyn CDH8 yw CDH8 a elwir hefyd yn Cadherin 8 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 16, band 16q21.^[2]

Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn CDH8.

• Nbla04261

• "Prenatal ethanol exposure disrupts intraneocortical circuitry, cortical gene expression, and behavior in a mouse model of FASD. ". J Neurosci. 2013. PMID 24285895.
• "Identification of candidate intergenic risk loci in autism spectrum disorder. ". BMC Genomics. 2013. PMID 23879678.
• "Pemphigus vulgaris autoantibody profiling by proteomic technique. ". PLoS One. 2013. PMID 23505434.
• "Ectopic expression of cadherin 8 is sufficient to cause cyst formation in a novel 3D collagen matrix renal tubule culture. ". Am J Physiol Cell Physiol. 2011. PMID 21389276.
• "Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.". J Med Genet. 2011. PMID 20972252.