Detailed description page of humcfs

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Humcfs_4136 details
Primary information
Humcfs IdHumcfs_4136
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000161681
gene_nameSHANK1
havana_transcript_idOTTHUMT00000465240
gene_location50661965-50716919
gene_orientation-
exon_idENSE00003226011, ENSE00001124209, ENSE00001116535, ENSE00001116534, ENSE00001116531, ENSE00001124231, ENSE00001116524, ENSE00001124248, ENSE00001124254, ENSE00001124264, ENSE00001124269, ENSE000011165
exon_number22
gene_descriptionSH3 and multiple ankyrin repeat domains 1
disease_descriptionAnxiety Disorders,Fragile X Syndrome,Motor Skills Disorders,Autism Spectrum Disorders,Nonorganic psychosis,Intellectual Disability,Mild Mental Retardation,Renal Cell Carcinoma,Schizophrenia,Psychotic Disorders,High-functioning autism,Profound intellectual disabilities,Memory impairment,Autistic Disorder,Atrial Septal Defects
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank