Primary information |
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Humcfs Id | Humcfs_4656 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000099797 |
gene_name | TECR |
havana_transcript_id | OTTHUMT00000466002 |
gene_location | 14529592-14565977 |
gene_orientation | + |
exon_id | ENSE00003143901, ENSE00003661096, ENSE00003620887, ENSE00003606297, ENSE00003528071, ENSE00003544807, ENSE00003507247, ENSE00003476036, ENSE00003786664, ENSE00003587283, ENSE00003691202, ENSE000034724 |
exon_number | 13 |
gene_description | trans-2,3-enoyl-CoA reductase |
disease_description | Congenital Abnormality,MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14,Mental Retardation,Dyskeratosis Congenita,Aortic Aneurysm, Thoracic,Heart Diseases |
miRNA_location | 804941-804963 |
miRNA_strand | . |
miRNA_id | MIMAT0019878 |
miRNA_name | hsa-miR-4745-5p |
miRNA_derived | MI0017384 |
Technique | FISH |
PMID | 3568428 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |