Detailed description page of humcfs

This page displays user query in tabular form.

Humcfs_3987 details
Primary information
Humcfs IdHumcfs_3987
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000170892
gene_nameTSEN34
havana_transcript_idOTTHUMT00000157368
gene_location54189938-54192355
gene_orientation+
exon_idENSE00001601199, ENSE00003566288, ENSE00001276594, ENSE00001661155
exon_number4
gene_descriptionTSEN34 tRNA splicing endonuclease subunit
disease_descriptionCongenital pontocerebellar hypoplasia,Intellectual Disability,Deglutition Disorders,Pontocerebellar Hypoplasia Type 2C,Movement Disorders,Vision Disorders,Microcephaly,Obesity,Pontoneocerebellar hypoplasia,Pontocerebellar Hypoplasia Type 2
miRNA_location53752411-53752432
miRNA_strand+
miRNA_idMIMAT0005452
miRNA_namehsa-miR-519a-5p
miRNA_derived MI0003178
TechniqueKaryotyping
PMID2579891
Get Gene Informations in: Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank