Property Summary

NCBI Gene PubMed Count 8
PubMed Score 32.53
PubTator Score 0.33

Knowledge Summary

Patent

No data available

TINX Plot

  Disease Sources (2)

Disease Target Count P-value
Breast cancer 3099 4.42289370125033E-7
group 4 medulloblastoma 1875 2.33797953609433E-6
osteosarcoma 7933 1.52806592033421E-5
pediatric high grade glioma 2712 2.21108882526904E-5
Disease Target Count Z-score Confidence
Enamel erosion 15 3.2 1.6

Expression

  Differential Expression (4)

Disease log2 FC p
osteosarcoma 1.731 0.000
group 4 medulloblastoma 1.300 0.000
pediatric high grade glioma 1.300 0.000
Breast cancer -1.100 0.000

Synonym

Accession Q96CX3 B4DLY7 Q96NU9
Symbols ZNF
ZNF52

Gene

  Ortholog (1)

Species Source
Chimp OMA EggNOG

AA Sequence

MNSSQISLRMKHGRVNMQKKPSKCSECGKFFTQRSSLTQHQRIHRGEKPYVCSECGSCFRKQSNLTQHLR      1 - 70
IHTGEKPYKCNECEKAFQTKAILVQHLRIHTGEKPYKCNECGKAFCQSPSLIKHQRIHTGEKPYKCTECG     71 - 140
KAFSQSICLTRHQRSHSGDKPFKCNECGKAFNQSACLMQHQRIHSGEKPYTCTECGKAFTQNSSLVEHER    141 - 210
THTGEKLYKCSECEKTFRKQAHLSEHYRIHTGEKPYECVGCGKSFRHSSALLRHQRLHAGE             211 - 271
//

Text Mined References (8)

PMID Year Title
25556234 2015 New host factors important for respiratory syncytial virus (RSV) replication revealed by a novel microfluidics screen for interactors of matrix (M) protein.
16344560 2006 Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.
15489334 2004 The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
15342556 2004 Sequence comparison of human and mouse genes reveals a homologous block structure in the promoter regions.
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.
1946370 1991 Characterization and mapping of human genes encoding zinc finger proteins.
1505991 1992 Clustering of C2-H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomes.