Detailed description page of humcfs

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MNX1 details
Primary information
gene_nameMNX1
Humcfs IdHumcfs_2184
chromosome_numberchromosome7
nameFRA7I
chrlocation147900001-159138663
cytoband7q36
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000130675
havana_transcript_idOTTHUMT00000347856
gene_location156994051-157009697
gene_orientation-
exon_idENSE00001875685, ENSE00001928865
exon_number2
gene_descriptionmotor neuron and pancreas homeobox 1
disease_descriptionCongenital meningocele,Congenital Abnormality,Acute Megakaryocytic Leukemias,Situs ambiguus,Chronic Lymphocytic Leukemia,Meningocele,Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse,Neuroblastoma,Amyotrophic Lateral Sclerosis,Gestational Diabetes,Radial polydactyly,Hodgkin Disease,Situs Inversus,Congenital defects,Diabetes,Liver carcinoma,Central neuroblastoma,Hematologic Neoplasms,Holoprosencephaly,Neonatal diabetes mellitus,leukemia,Leukemogenesis,Caudal Regression Syndrome,Leukemia, Myelocytic, Acute,Leukemia, Lymphocytic, Acute, L1,Diabetes Mellitus,Spinal meningocele,Sacral agenesis,Poorly Differentiated Hepatocellular Carcinoma,Currarino triad,DIABETES MELLITUS, PERMANENT NEONATAL,Anorectal Anomalies,Myeloid Leukemia,Childhood Leukemia,insulinoma
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID12393800
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