PCDH19
protein-coding gene in the species Homo sapiens
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PCDH19
Summary
PCDH19 is a gene[1].
Key Facts
- PCDH19's instance of is recorded as gene[2].
- PCDH19 is a type of protein-coding gene[3].
- PCDH19's HomoloGene ID is recorded as 18916[4].
- PCDH19's genomic start is recorded as 100291644[5].
- PCDH19's genomic start is recorded as 99546642[6].
- PCDH19's genomic end is recorded as 100410273[7].
- PCDH19's genomic end is recorded as 99665271[8].
- PCDH19's ortholog is recorded as Pcdh19[9].
- PCDH19's ortholog is recorded as Pcdh19[10].
- PCDH19's ortholog is recorded as pcdh19[11].
- PCDH19's encodes is recorded as Protocadherin 19[12].
- PCDH19's found in taxon is recorded as Homo sapiens[13].
- PCDH19's chromosome is recorded as human X chromosome[14].
- PCDH19's genetic association is recorded as epilepsy[15].
- PCDH19's genetic association is recorded as X-linked intellectual disability-epilepsy syndrome[16].
- PCDH19's strand orientation is recorded as reverse strand[17].
- PCDH19's exact match is recorded as http://identifiers.org/ncbigene/57526[18].
- PCDH19's cytogenetic location is recorded as Xq22.1[19].
- PCDH19's expressed in is recorded as entorhinal cortex[20].
- PCDH19's expressed in is recorded as middle temporal gyrus[21].
- PCDH19's expressed in is recorded as superior frontal gyrus[22].
- PCDH19's expressed in is recorded as Brodmann area 46[23].
- PCDH19's expressed in is recorded as hippocampus proper[24].
- PCDH19's expressed in is recorded as Brodmann area 23[25].
- PCDH19's expressed in is recorded as postcentral gyrus[26].