Detailed description page of humcfs

This page displays user query in tabular form.

Humcfs_3515 details
Primary information
Humcfs IdHumcfs_3515
chromosome_numberchromosome12
nameFRA12E
chrlocation109000001-133851895
cytoband12q24
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000139428
gene_nameMMAB
havana_transcript_idOTTHUMT00000403129
gene_location109556697-109573497
gene_orientation-
exon_idENSE00002243355, ENSE00003671438, ENSE00003672319, ENSE00003481491, ENSE00003546036, ENSE00003688708, ENSE00003505825
exon_number7
gene_descriptionmethylmalonic aciduria (cobalamin deficiency) cblB type
disease_descriptionSquamous cell carcinoma,Nijmegen Breakage Syndrome,Arteriosclerosis,Fanconi Anemia,Osteosarcoma of bone,Alpha thalassemia-mental retardation syndrome,Cervix carcinoma,ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED,Tooth Crowding,Stomach Carcinoma,Chronic Lymphocytic Leukemia,IGA Glomerulonephritis,Hypertriglyceridemia,Triple Negative Breast Neoplasms,Severe mental retardation (I.Q. 20-34),Neoplasm Metastasis,HIV Infections,Malignant neoplasm of breast,Experimental Autoimmune Encephalomyelitis,Urothelial Carcinoma,Turcot syndrome (disorder),Age-related cataract,Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse,melanoma,FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder),Hypertriglyceridemia result,Atherosclerosis,Diabetes Mellitus, Insulin-Dependent,Malignant neoplasm of lung,Congenital chromosomal disease,Mitral Valve Stenosis,Acute lymphocytic leukemia,Breast Carcinoma,Mental Retardation,Dyskeratosis Congenita,alpha-Thalassemia,Myocardial
miRNA_location121444279-121444305
miRNA_strand-
miRNA_idMIMAT0028112
miRNA_namehsa-miR-7107-3p
miRNA_derived MI0022958
TechniqueKaryotyping
PMID14526166
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank