Primary information |
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Humcfs Id | Humcfs_3892 |
chromosome_number | chromosome16 |
name | FRA16D |
chrlocation | 79200001-81700000 |
cytoband | 16q23.2 |
type | Aphidicolin |
frequency | Common |
gene_ensembl_id | ENSG00000153815 |
gene_name | CMIP |
havana_transcript_id | OTTHUMT00000432402 |
gene_location | 81610307-81709957 |
gene_orientation | + |
exon_id | ENSE00002256933, ENSE00003615745, ENSE00003594353, ENSE00003735458, ENSE00003740621, ENSE00003741062, ENSE00003746150, ENSE00003729547, ENSE00003721317, ENSE00003718146, ENSE00003528175, ENSE000034922 |
exon_number | 20 |
gene_description | c-Maf inducing protein |
disease_description | Specific language impairment,Dyslexia,Autism Spectrum Disorders,Nephrotic Syndrome,Nephrotic Syndrome, Minimal Change,Developmental delay (disorder),melanoma,Language Disorders,Diabetes Mellitus, Non-Insulin-Dependent |
miRNA_location | 81385021-81385042 |
miRNA_strand | + |
miRNA_id | MIMAT0019833 |
miRNA_name | hsa-miR-4720-5p |
miRNA_derived | MI0017355 |
Technique | FISH |
PMID | 11013073 |
Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |