Property Summary

NCBI Gene PubMed Count 20
PubMed Score 7.28
PubTator Score 130.10

Knowledge Summary


No data available


  Differential Expression (10)

Disease log2 FC p
posterior fossa group A ependymoma 1.300 4.4e-08
glioblastoma 2.000 4.1e-05
medulloblastoma 1.900 3.8e-08
atypical teratoid / rhabdoid tumor 2.000 6.3e-08
medulloblastoma, large-cell 1.900 1.4e-04
primitive neuroectodermal tumor 1.600 5.9e-04
non-small cell lung cancer 1.420 1.3e-18
pediatric high grade glioma 1.700 5.8e-06
Breast cancer 1.100 2.9e-06
ovarian cancer 1.100 1.1e-05

Gene RIF (6)

23860123 Data shows increased apoptosis and susceptibility to endoplasmic reticulum (ER) stress after Tcf19 knockdown.
23860123 Knockdown of Tcf19 reduces proliferation and increases apoptosis. Tcf19 is found in pancreatic islets in mouse and human.
23760081 Genome association studies identified TCF19 as a new risk-associated loci for chronic hepatitis B on the HLA region of chromosome 6.
21076979 A linkage disequilibrium analysis established TCF19, POU5F1, CCHCR1 and PSORS1C1 as potential causal genes for the type 1 diabetes.
20587610 Observational study of gene-disease association. (HuGE Navigator)
19851445 Observational study of gene-disease association. (HuGE Navigator)

AA Sequence


Text Mined References (21)

PMID Year Title
24509480 2014 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
23955597 2013 Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
23860123 2013 Tcf19 is a novel islet factor necessary for proliferation and survival in the INS-1 ?-cell line.
23760081 2013 A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
21912425 2013 A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients.
21801394 2011 Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
21323541 2011 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.
21076979 2011 Conditional meta-analysis stratifying on detailed HLA genotypes identifies a novel type 1 diabetes locus around TCF19 in the MHC.
20587610 2010 Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.
19851445 2009 High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regions.
17525332 2007 ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage.
16702430 2006 Rapid evolution of major histocompatibility complex class I genes in primates generates new disease alleles in humans via hitchhiking diversity.
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.
14574404 2003 The DNA sequence and analysis of human chromosome 6.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
10777095 2000 Genetic polymorphisms in the cell growth regulated gene, SC1 telomeric of the HLA-C gene and lack of association of psoriasis vulgaris.
8595903 1995 Feature mapping of the HLA class I region: localization of the POU5F1 and TCF19 genes.
1868030 1991 A new growth-regulated complementary DNA with the sequence of a putative trans-activating factor.