Basic Information

TEK

Full name: TEK receptor tyrosine kinase

Gene type: protein coding

HGNC ID: HGNC:11724

Gene location: 9p21.2

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/7010

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:11724

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_000459.5

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/Q02763

AlphaFold: https://alphafold.ebi.ac.uk/entry/Q02763

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/600221

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=7010

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa04010+7010

Variant resources

Gene Disease type Variant type NCBI dbSNP Alleles Variant location
TEK nAMD Intron Variant rs10967760 A>G / A>T chr9:27182827 (GRCh38.p13)
TEK nAMD Intron Variant rs1014049 C>T chr9:27228505 (GRCh38.p13)
TEK nAMD Intron Variant rs615375 G>T chr9:27112313 (GRCh38.p13)
TEK nAMD Intron Variant rs621786 A>C / A>G / A>T chr9:27118809 (GRCh38.p13)
TEK nAMD Intron Variant rs652010 G>A chr9:27123227 (GRCh38.p13)
TEK nAMD Intron Variant rs625767 C>G / C>T chr9:27135715 (GRCh38.p13)
TEK nAMD Intron Variant rs669441 C>G / C>T chr9:27137244 (GRCh38.p13)
TEK nAMD Intron Variant rs7034505 G>A / G>C / G>T chr9:27151396 (GRCh38.p13)
TEK nAMD Intron Variant rs7034591 A>G chr9:27151694 (GRCh38.p13)
TEK nAMD Intron Variant rs664461 T>C / T>G chr9:27152310 (GRCh38.p13)
TEK nAMD Intron Variant rs538679 C>A The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
TEK nAMD Intron Variant rs504947 G>A / G>C / G>T chr9:27156997 (GRCh38.p13)
TEK nAMD Intron Variant rs1413825 A>G chr9:27161813 (GRCh38.p13)
TEK nAMD Intron Variant rs911599 A>G chr9:27165120 (GRCh38.p13)
TEK nAMD Intron Variant rs3818283 A>G / A>T chr9:27169126 (GRCh38.p13)
TEK nAMD Intron Variant rs3739542 C>A / C>G / C>T chr9:27172840 (GRCh38.p13)
TEK nAMD Intron Variant rs666478 C>T chr9:27173182 (GRCh38.p13)
TEK nAMD Intron Variant rs481294 C>A / C>T chr9:27190892 (GRCh38.p13)
TEK nAMD Intron Variant rs3780317 C>T chr9:27190994 (GRCh38.p13)
TEK nAMD Intron Variant rs549099 G>A / G>C / G>T chr9:27194700 (GRCh38.p13)
TEK nAMD Intron Variant rs606342 G>T chr9:27197675 (GRCh38.p13)
TEK nAMD Synonymous Variant rs639225 A>G / A>T chr9:27202872 (GRCh38.p13)
TEK nAMD Intron Variant rs1413828 T>C chr9:27204177 (GRCh38.p13)
TEK nAMD Synonymous Variant rs3737188 T>C chr9:27213582 (GRCh38.p13)
TEK nAMD Intron Variant rs534129 A>G chr9:27214721 (GRCh38.p13)
TEK nAMD Intron Variant rs2756901 T>C chr9:27218055 (GRCh38.p13)
TEK nAMD Intron Variant rs2273717 A>C / A>G / A>T chr9:27228024 (GRCh38.p13)