Detailed description page of humcfs

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Humcfs_4917 details
Primary information
Humcfs IdHumcfs_4917
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000065000
gene_nameAP3D1
havana_transcript_idOTTHUMT00000450916
gene_location2101829-2110882
gene_orientation-
exon_idENSE00003712282, ENSE00003672079, ENSE00002951990, ENSE00003599653, ENSE00003528793, ENSE00002956920
exon_number6
gene_descriptionadaptor-related protein complex 3, delta 1 subunit
disease_descriptionCerebrovascular accident,Platelet Storage Pool Deficiency,Cerebral Hemorrhage,Albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells,Infection,Tobacco Use Disorder,Schizophrenia,Hermanski-Pudlak Syndrome,Myocardial Infarction,Subarachnoid Hemorrhage,HERMANSKY-PUDLAK SYNDROME 2,Intracranial Hemorrhages
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank