Property Summary

NCBI Gene PubMed Count 12
PubMed Score 11.48

Knowledge Summary

Patent

No data available

TINX Plot

  Disease Sources (2)

Disease Target Count P-value
glioblastoma 5572 7.40104583394109E-6
group 4 medulloblastoma 1875 9.32763411816525E-6
pediatric high grade glioma 2712 6.20417032042845E-4
breast carcinoma 1614 0.00104979111545673
chronic lymphosyte leukemia 232 0.00108775667004291
primary Sjogren syndrome 789 0.0088230705973817
adrenocortical carcinoma 1427 0.0110418968660283
active Crohn's disease 918 0.0171127518988939
sarcoidosis 368 0.0178406679736215
spina bifida 1064 0.0430324916823974
Disease Target Count Z-score Confidence
Myocardial stunning 8 3.465 1.7

Expression

  Differential Expression (10)

Disease log2 FC p
chronic lymphosyte leukemia 1.200 0.001
glioblastoma 1.100 0.000
group 4 medulloblastoma 1.800 0.000
adrenocortical carcinoma 1.107 0.011
active Crohn's disease 1.176 0.017
sarcoidosis 1.200 0.018
breast carcinoma 1.100 0.001
pediatric high grade glioma 1.100 0.001
primary Sjogren syndrome 1.200 0.009
spina bifida -1.760 0.043

Synonym

Accession Q03936 A6NNF9 Q8N492 Q8NB35
Symbols TF12
HPF12
HTF12
HEL-203

Gene

  Ortholog (2)

Species Source
Chimp OMA EggNOG
Macaque OMA EggNOG Inparanoid

Gene RIF (3)

PMID Text
20628086 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
20379614 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
19913121 Observational study of gene-disease association. (HuGE Navigator)

AA Sequence

MGPLTFRDVKIEFSLEEWQCLDTAQRNLYRDVMLENYRNLVFLGIAVSKPDLITWLEQGKEPWNLKRHEM      1 - 70
VDKTPVMCSHFAQDVWPEHSIKDSFQKVILRTYGKYGHENLQLRKDHKSVDACKVYKGGYNGLNQCLTTT     71 - 140
DSKIFQCDKYVKVFHKFPNVNRNKIRHTGKKPFKCKNRGKSFCMLSQLTQHKKIHTREYSYKCEECGKAF    141 - 210
NWSSTLTKHKIIHTGEKPYKCEECGKAFNRSSNLTKHKIIHTGEKPYKCEECGKAFNRSSTLTKHKRIHT    211 - 280
EEKPYKCEECGKAFNQFSILNKHKRIHMEDKPYKCEECGKAFRVFSILKKHKIIHTGEKPYKCEECGKAF    281 - 350
NQFSNLTKHKIIHTGEKPYKCDECGKAFNQSSTLTKHKRIHTGEKPYKCEECGKAFKQSSTLTEHKIIHT    351 - 420
GEKPYKCEKCGKAFSWSSAFTKHKRNHMEDKPYKCEECGKAFSVFSTLTKHKIIHTREKPYKCEECGKAF    421 - 490
NQSSIFTKHKIIHTEGKSYKCEKCGNAFNQSSNLTARKIIYTGEKPYKYEECDKAFNKFSTLITHQIIYT    491 - 560
GEKPCKHECGRAFNKSSNYTKEKLQT                                                561 - 586
//

Text Mined References (13)

PMID Year Title
20628086 2010 Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
20379614 Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
19913121 2009 Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
18029348 2008 Toward a confocal subcellular atlas of the human proteome.
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.
12853948 2003 The DNA sequence of human chromosome 7.
12477932 2002 Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.
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