Detailed description page of humcfs

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Humcfs_2965 details
Primary information
Humcfs IdHumcfs_2965
chromosome_numberchromosome11
nameFRA11B
chrlocation114500001-121200000
cytoband11q23.3
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000149573
gene_nameMPZL2
havana_transcript_idOTTHUMT00000392116
gene_location118256911-118264536
gene_orientation-
exon_idENSE00001800629, ENSE00003529254, ENSE00003467285, ENSE00003653516, ENSE00002200582
exon_number5
gene_descriptionmyelin protein zero-like 2
disease_descriptionPheochromocytoma,Dementia,Goiter,Coronary Arteriosclerosis,Sensorineural Hearing Loss (disorder),Presenile dementia,Impaired cognition,Enlarged Vestibular Aqueduct,Brain Infarction,Pendred's syndrome,Hypothyroidism,Hearing Loss, Mixed Conductive-Sensorineural,Congenital ear anomaly NOS (disorder),Malignant neoplasm of breast,Breast Carcinoma,Coronary heart disease
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID17063465
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