| Primary information |
|---|
| gene_name | HSH2D |
| Humcfs Id | Humcfs_5031 |
| chromosome_number | chromosome19 |
| name | FRA19B |
| chrlocation | 1-20000000 |
| cytoband | 19p13 |
| type | Folic acid |
| frequency | Rare |
| gene_ensembl_id | ENSG00000196684 |
| 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 |