Detailed description page of humcfs

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Humcfs_3936 details
Primary information
Humcfs IdHumcfs_3936
chromosome_numberchromosome17
nameFRA17B
chrlocation57600001-58300000
cytoband17q23.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000011143
gene_nameMKS1
havana_transcript_idOTTHUMT00000443953
gene_location58207562-58214379
gene_orientation-
exon_idENSE00002731953, ENSE00002693747, ENSE00003694300, ENSE00003599918, ENSE00003687863, ENSE00003681629, ENSE00003639447, ENSE00003616896, ENSE00002717263
exon_number9
gene_descriptionMeckel syndrome, type 1
disease_descriptionSquamous cell carcinoma,Congenital Abnormality,Dandy-Walker Syndrome,Bardet-Biedl Syndrome,Non-Small Cell Lung Carcinoma,Malignant neoplasm of breast,Polydactyly,Breast Carcinoma,Heartburn acidity,Carcinoma of lung,Uterine Corpus Sarcoma,Malignant neoplasm of lung,Cerebral Palsy,Cystic kidney,Congenital cerebral hernia,Meckel-Gruber syndrome,Nephronophthisis,MRSA - Methicillin resistant Staphylococcus aureus infection,Familial aplasia of the vermis,BARDET-BIEDL SYNDROME 13,Glioma,Meckel syndrome type 1,Squamous cell carcinoma of lung,Glioblastoma,Sarcoma
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID11085503
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