Detailed description page of humcfs

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TMEM67 details
Primary information
gene_nameTMEM67
Humcfs IdHumcfs_2342
chromosome_numberchromosome8
nameFRA8B
chrlocation93300001-99000000
cytoband8q22.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000164953
havana_transcript_idOTTHUMT00000378408
gene_location93785269-93795504
gene_orientation+
exon_idENSE00002126168, ENSE00003469218, ENSE00003553174, ENSE00003482226, ENSE00002120338, ENSE00003630971, ENSE00002093939
exon_number7
gene_descriptiontransmembrane protein 67
disease_descriptionCongenital Abnormality,Hepatic Fibrosis, Congenital,Liver diseases,Fibrosis, Liver,Cystic Kidney Diseases,Polydactyly,Autosomal Recessive Polycystic Kidney Disease,Congenital cerebral hernia,Meckel-Gruber syndrome,COACH syndrome,Nephronophthisis,Hydrocephalus,Oculomotor apraxia,Oculovestibuloauditory syndrome,Familial aplasia of the vermis,Pneumocystis jiroveci pneumonia,Liver Cirrhosis,Polycystic Kidney Diseases,POLYCYSTIC KIDNEY DISEASE 1,Bardet-Biedl Syndrome,Meckel syndrome type 3,Meckel syndrome type 1,NEPHRONOPHTHISIS 11,Congestive heart failure,JOUBERT SYNDROME 6
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID14562053
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