Detailed description page of humcfs
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Humcfs_4893 details |
Primary information | |
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Humcfs Id | Humcfs_4893 |
chromosome_number | chromosome19 |
name | FRA19B |
chrlocation | 1-20000000 |
cytoband | 19p13 |
type | Folic acid |
frequency | Rare |
gene_ensembl_id | ENSG00000008441 |
gene_name | NFIX |
havana_transcript_id | OTTHUMT00000452773 |
gene_location | 13024939-13094770 |
gene_orientation | + |
exon_id | ENSE00002838696, ENSE00003634013, ENSE00003567637, ENSE00003525435, ENSE00003585342, ENSE00003480560, ENSE00003591998, ENSE00003673903, ENSE00002770106 |
exon_number | 9 |
gene_description | nuclear factor I/X (CCAAT-binding transcription factor) |
disease_description | Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension,Colorado Tick Fever,Malignant neoplasm of stomach,Partial agenesis of corpus callosum,Manic,Weaver syndrome,Neuroblastoma,Scheuermann's Disease,Bipolar Disorder,Hydrocephalus,SOTOS SYNDROME 2,Stomach Carcinoma,Intervertebral Disc Degeneration,Impaired cognition,Marshall-Smith syndrome,Central neuroblastoma,Dementia,Down Syndrome,Alzheimer's Disease |
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 |