Detailed description page of humcfs

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Humcfs_4902 details
Primary information
Humcfs IdHumcfs_4902
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000132024
gene_nameCC2D1A
havana_transcript_idOTTHUMT00000457956
gene_location13906442-13930659
gene_orientation+
exon_idENSE00002931436, ENSE00003540473, ENSE00001780634, ENSE00001783446, ENSE00003527532, ENSE00003663129, ENSE00003591962, ENSE00003515041, ENSE00003486219, ENSE00003520778, ENSE00003625332, ENSE000036300
exon_number29
gene_descriptioncoiled-coil and C2 domain containing 1A
disease_descriptionXenograft Model,Impaired cognition,MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3,Carcinoma of lung,Major Depressive Disorder,Intellectual Disability,Unipolar Depression,Malignant neoplasm of lung,Pancreatic carcinoma,Mental Retardation,Malignant neoplasm of pancreas,HIV Infections,Age related macular degeneration
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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