Detailed description page of humcfs

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Humcfs_3822 details
Primary information
Humcfs IdHumcfs_3822
chromosome_numberchromosome16
nameFRA16B
chrlocation66700001-70800000
cytoband16q22.1
typeDistamycinA
frequencyRare
gene_ensembl_idENSG00000102977
gene_nameACD
havana_transcript_idOTTHUMT00000268881
gene_location67657512-67660810
gene_orientation-
exon_idENSE00003355614, ENSE00003624232, ENSE00003673908, ENSE00003629179, ENSE00003507372, ENSE00003502012, ENSE00003562308, ENSE00003676212, ENSE00003527690, ENSE00003611675, ENSE00000844202, ENSE000019434
exon_number12
gene_descriptionadrenocortical dysplasia homolog (mouse)
disease_descriptionCongenital Abnormality,Spinocerebellar Ataxia Type 7,Cardiovascular Diseases,GLUCOCORTICOID DEFICIENCY 1,Chronic Lymphocytic Leukemia,Ischemic Cerebrovascular Accident,Late-Infantile Neuronal Ceroid Lipfuscinosis,Aplastic Anemia,HIV Infections,Malignant neoplasm of breast,Cohen syndrome,melanoma,Renal Cell Carcinoma,Congenital chromosomal disease,Pancytopenia,Anisometropia,Dyskeratosis Congenita,Bone Marrow Diseases,Diabetes Mellitus, Non-Insulin-Dependent,Liver carcinoma,Ischemic stroke,Hereditary Melanoma,Lung diseases,Angle Closure Glaucoma,Precursor B-cell lymphoblastic leukemia,Neuronal Ceroid-Lipofuscinoses,Brachydactyly,Cerebrovascular Disorders,cystic disease,HOYERAAL-HREIDARSSON SYNDROME
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID3338799
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