Detailed description page of humcfs

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PXMP2 details
Primary information
gene_namePXMP2
Humcfs IdHumcfs_3570
chromosome_numberchromosome12
nameFRA12E
chrlocation109000001-133851895
cytoband12q24
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000176894
havana_transcript_idOTTHUMT00000397556
gene_location132690314-132704898
gene_orientation+
exon_idENSE00002223732, ENSE00003715973, ENSE00003467180, ENSE00002279176, ENSE00002324444
exon_number5
gene_descriptionperoxisomal membrane protein 2, 22kDa
disease_descriptionHereditary Motor and Sensory Neuropathy Type I,Osteosarcoma of bone,Charcot-Marie-Tooth Disease,Paresis,Charcot-Marie-Tooth disease and deafness,Charcot-Marie-Tooth Disease, Demyelinating, Type 1e,Malignant neoplasm of breast,Polyneuropathy,Breast Carcinoma,Segmental glomerulosclerosis,Disorder of hand,Hereditary liability to pressure palsies,Peripheral demyelinating neuropathy,Inherited neuropathies,Sensorineural Hearing Loss (disorder),Carpal Tunnel Syndrome,Nerve compression syndrome,Muscular Atrophy,AMYOTROPHY, HEREDITARY NEURALGIC,Neuropathy,Hereditary Motor and Sensory Neuropathies,Pilocytic Astrocytoma,Charcot-Marie-Tooth Disease, Type Ia (disorder),Peripheral Neuropathy,Entrapment Neuropathies,Polyneuropathy, Motor,Inherited Peripheral Neuropathy,Inflammatory neuropathy,Glioma,Osteosarcoma,myelinopathy,Pelizaeus-Merzbacher Disease,Trisomy,Muscle Weakness,Dejerine-Sottas Disease (disorder),Cranial Neuropathies, Multiple,Dyspnea
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID14526166
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