Detailed description page of humcfs

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Humcfs_1711 details
Primary information
Humcfs IdHumcfs_1711
chromosome_numberchromosome6
nameFRA6F
chrlocation105500001-114600000
cytoband6q21
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000112367
gene_nameFIG4
havana_transcript_idOTTHUMT00000041770
gene_location109786006-109791571
gene_orientation+
exon_idENSE00001634482, ENSE00000975485, ENSE00003787581
exon_number3
gene_descriptionFIG4 phosphoinositide 5-phosphatase
disease_descriptionSeizures,CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J,AMYOTROPHIC LATERAL SCLEROSIS 11,Congenital Abnormality,POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL,Charcot-Marie-Tooth Disease,Lateral Sclerosis,Papillon-Lefevre Disease,Motor Neuron Disease,Peripheral demyelinating neuropathy,Segmental demyelination,Amyotrophic Lateral Sclerosis,Inherited neuropathies,Tremor,Yunis Varon syndrome,Neuropathy,Hereditary Motor and Sensory Neuropathies,Polymicrogyria, Bilateral Occipital,Peripheral Neuropathy,Primary Lateral Sclerosis, Adult, 1,Polymicrogyria,Malignant Glioma,Glioma,Demyelinating Diseases,Epilepsy,Lysosomal Storage Diseases
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID12370818
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