Detailed description page of humcfs

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Humcfs_3892 details
Primary information
Humcfs IdHumcfs_3892
chromosome_numberchromosome16
nameFRA16D
chrlocation79200001-81700000
cytoband16q23.2
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000153815
gene_nameCMIP
havana_transcript_idOTTHUMT00000432402
gene_location81610307-81709957
gene_orientation+
exon_idENSE00002256933, ENSE00003615745, ENSE00003594353, ENSE00003735458, ENSE00003740621, ENSE00003741062, ENSE00003746150, ENSE00003729547, ENSE00003721317, ENSE00003718146, ENSE00003528175, ENSE000034922
exon_number20
gene_descriptionc-Maf inducing protein
disease_descriptionSpecific language impairment,Dyslexia,Autism Spectrum Disorders,Nephrotic Syndrome,Nephrotic Syndrome, Minimal Change,Developmental delay (disorder),melanoma,Language Disorders,Diabetes Mellitus, Non-Insulin-Dependent
miRNA_location81385021-81385042
miRNA_strand+
miRNA_idMIMAT0019833
miRNA_namehsa-miR-4720-5p
miRNA_derived MI0017355
TechniqueFISH
PMID11013073
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank