Detailed description page of humcfs

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ROR2 details
Primary information
gene_nameROR2
Humcfs IdHumcfs_2511
chromosome_numberchromosome9
nameFRA9D
chrlocation90400001-91800000
cytoband9q22.1
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000169071
havana_transcript_idOTTHUMT00000053041
gene_location91563091-91948880
gene_orientation-
exon_idENSE00001468104, ENSE00001468105, ENSE00001468106, ENSE00001468107, ENSE00001468109, ENSE00003663788, ENSE00003675079, ENSE00003678701, ENSE00003540333, ENSE00003475771, ENSE00003667654, ENSE000035783
exon_number13
gene_descriptionreceptor tyrosine kinase-like orphan receptor 2
disease_descriptionRobinow Syndrome,Basal Cell Nevus Syndrome,Prostate carcinoma,Fibromatosis, Aggressive,Osteoarthritis of distal interphalangeal joint,Rhabdoid Tumor of the Kidney,BRACHYDACTYLY, TYPE B1,Osteosarcoma of bone,LATERAL MENINGOCELE SYNDROME,Neoplasm Metastasis,Congenital Abnormality,Ventricular Septal Defects,Dwarfism,leiomyosarcoma,melanoma,Malignant neoplasm of prostate,Renal Cell Carcinoma,Degenerative polyarthritis,ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,Cerebral Hemorrhage,Kidney Diseases,Cerebrovascular accident,Osteoarthritis of the hand,Carcinogenesis,Bone Diseases,Gastrointestinal Stromal Tumors,Multiple Myeloma,ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OF PHALANGES AND METACARPALS/METATARSALS,Medulloblastoma,Brachydactyly syndrome type B,Glioma,Brachydactyly,Osteosarcoma,Skeletal dysplasia,Glioblastoma,Syndactyly,Metastatic melanoma,Xenograft Model,Conventional (Clear Cell) Renal Cell Carcinoma,Sarcoma,Subarachnoid Hemorrhage,Osteopo
miRNA_location91636277-91636296
miRNA_strand-
miRNA_idMIMAT00181841
miRNA_namehsa-miR-3910
miRNA_derived MI0016431
TechniqueFISH
PMID14562053
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