Variant ID: 9-27173062-G-A

NM_000459.3(TEK):c.761-158G>A

This variant was identified in 3 publications




Publications:


Investigation of the Possible Role of Tie2 Pathway and TEK Gene in Asthma and Allergic Conjunctivitis.

Frontiers In Genetics
Z Gál, A Gézsi, V Molnár, A Nagy, A Kiss, M Sultész, Z Csoma, L Tamási, G Gálffy, BL Bálint, S Póliska, C Szalai
Publication Date: 2020

Variant appearance in text: rs3824410
PubMed Link: 32180797
PubMed Central Link
Variant Present in the following documents:
  • Main text
View BVdb publication page



Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

Human Genetics
M Kabra, W Zhang, S Rathi, AK Mandal, S Senthil, G Pyatla, M Ramappa, S Banerjee, K Shekhar, S Marmamula, AL Mettla, I Kaur, RC Khanna, H Khanna, S Chakrabarti
Publication Date: 2017-08

Variant appearance in text: rs3824410
PubMed Link: 28620713
PubMed Central Link
Variant Present in the following documents:
  • Main text
View BVdb publication page



Germline Genetic Variants in TEK, ANGPT1, ANGPT2, MMP9, FGF2 and VEGFA Are Associated with Pathologic Complete Response to Bevacizumab in Breast Cancer Patients.

Plos One
I Makhoul, VK Todorova, ER Siegel, SW Erickson, I Dhakal, VR Raj, JY Lee, MS Orloff, RJ Griffin, RS Henry-Tillman, S Klimberg, LF Hutchins, SA Kadlubar
Publication Date: 2017

Variant appearance in text: rs3824410
PubMed Link: 28045923
PubMed Central Link
Variant Present in the following documents:
  • pone.0168550.s011.xlsx
  • pone.0168550.s006.xlsx
  • pone.0168550.s007.xlsx
  • pone.0168550.s004.xlsx
  • pone.0168550.s009.xlsx
  • pone.0168550.s005.xlsx
  • pone.0168550.s003.xlsx
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000380036.4 c.761-158G>A - intron_variant - 5/22
ENST00000406359.4 c.761-158G>A - intron_variant - 5/21
ENST00000519080.1 c.320-158G>A - intron_variant - 3/9
ENST00000519097.1 c.449-158G>A - intron_variant - 4/20
NM_000459.4 c.761-158G>A - intron_variant - 5/22
NM_001290077.1 c.761-158G>A - intron_variant - 5/21
NM_001290078.1 c.449-158G>A - intron_variant - 4/20