Property Summary

NCBI Gene PubMed Count 7
PubMed Score 0.00

Knowledge Summary

Patent

No data available

TINX Plot

  Disease Sources (2)

Disease Target Count
Parkinson Disease 105
Disease Target Count P-value
lung carcinoma 2844 1.27733617835299E-20
atypical teratoid / rhabdoid tumor 4369 4.64427012640037E-6
medulloblastoma, large-cell 6234 1.08979091948932E-5
glioblastoma 5572 1.97738412545448E-5
ovarian cancer 8492 4.77102363671845E-5
adult high grade glioma 2148 7.12933711395501E-5
group 3 medulloblastoma 2254 8.33848887268544E-4
subependymal giant cell astrocytoma 2287 0.0049767093960499
non primary Sjogren syndrome sicca 840 0.0143812696272534

Synonym

Accession Q96LR1 C9JG53
Symbols C17orf69
MGC57346

Gene

 GO Component (1)

 Compartment GO Term (0)

AA Sequence

MHPWLGSALGFPKCRGIHLCACGNGWTPGETLSQNKTEITKNKVTCWRPHGCEPNTGLGYQGSHTSKYTL      1 - 70
LPWNLLKTKPLPPSHGKEGGKEAKVPSGDNSGRGEVPRAQEGQAACGRAASGDSQEGMRRGYEERATAQR     71 - 140
PAVRSAETTAHGTWIYP                                                         141 - 157
//

Text Mined References (8)

PMID Year Title
21292315 2011 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
19915575 2009 Genome-wide association study reveals genetic risk underlying Parkinson's disease.
19416867 2009 The transcriptome of human CD34+ hematopoietic stem-progenitor cells.
16625196 2006 DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.
14702039 2004 Complete sequencing and characterization of 21,243 full-length human cDNAs.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
11181995 2001 The sequence of the human genome.
8889548 1996 Normalization and subtraction: two approaches to facilitate gene discovery.