Primary information |
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gene_name | AP3D1 |
Humcfs Id | Humcfs_4917 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000065000 |
havana_transcript_id | OTTHUMT00000450916 |
gene_location | 2101829-2110882 |
gene_orientation | - |
exon_id | ENSE00003712282, ENSE00003672079, ENSE00002951990, ENSE00003599653, ENSE00003528793, ENSE00002956920 |
exon_number | 6 |
gene_description | adaptor-related protein complex 3, delta 1 subunit |
disease_description | Cerebrovascular 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_location | NA |
miRNA_strand | NA |
miRNA_id | NA |
miRNA_name | NA |
miRNA_derived | NA |
Technique | FISH |
PMID | 3568428 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |