Detailed description page of humcfs

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Humcfs_4893 details
Primary information
Humcfs IdHumcfs_4893
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000008441
gene_nameNFIX
havana_transcript_idOTTHUMT00000452773
gene_location13024939-13094770
gene_orientation+
exon_idENSE00002838696, ENSE00003634013, ENSE00003567637, ENSE00003525435, ENSE00003585342, ENSE00003480560, ENSE00003591998, ENSE00003673903, ENSE00002770106
exon_number9
gene_descriptionnuclear factor I/X (CCAAT-binding transcription factor)
disease_descriptionOsteochondrodysplasia, 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_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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