Primary information |
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Humcfs Id | Humcfs_5031 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000196684 |
gene_name | HSH2D |
havana_transcript_id | OTTHUMT00000460274 |
gene_location | 16143736-16157329 |
gene_orientation | + |
exon_id | ENSE00002939774, ENSE00002748362, ENSE00003575154, ENSE00003473849, ENSE00003475979, ENSE00002889449 |
exon_number | 6 |
gene_description | hematopoietic SH2 domain containing |
disease_description | Atherosclerosis,Septicemia,Sepsis,Intestinal Diseases,Midline facial cleft - Tessier cleft 0,Arteriosclerosis,Frontonasal dysplasia,Lymphoma,Endometriosis |
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 |