Details for Gene TG

GENE NAME TG
CHROMOSOME 8
ENSEMBL ID None
ENTREZ ID ENSG00000042832
UNIPROT ACCESSION NUMBER P01266
GO MOLECULAR FUNCTION ['hormone activity', 'identical protein binding', 'protein binding']
ESSENTIAL IN MOUSE Non-essential
PATHWAYS hsa04918; hsa05320
51 combinations linked to TG OLI467; OLI567; OLI1073; OLI1809; OLI466; OLI520; OLI1023; OLI1507; OLI1085; OLI565; OLI1024; OLI1609; OLI1503; OLI1807; OLI596; OLI1608; OLI1502; OLI1092; OLI1025; OLI993; OLI1093; OLI584; OLI1500; OLI1083; OLI1090; OLI1493; OLI1808; OLI468; OLI1082; OLI1022; OLI990; OLI470; OLI469; OLI1026; OLI580; OLI587; OLI031; OLI1094; OLI1087; OLI994; OLI1084; OLI564; OLI995; OLI1506; OLI474; OLI519; OLI989; OLI1501; OLI563; OLI566; OLI1021
50 variants linked to TG TG:c.5042-2A>G, ; TG:p.Asn212Ser; TG:p.Arg2585Trp; TG:p.Ile1931Val; TG:c.2864delA, Glu955GlyfsTer11; TG:c.6844_6847del, p.Leu2282IlefsTer61; TG:p.Val1738Ile; TG:p.Ser1912Asn; TG:p.Arg896Gln; TG:c.5372delT, p.Leu1791CysfsTer12; TG:c.886C>T, p.Arg296Ter; TG:c.2060delG, p.Cys687LeufsTer34; TG:c.1514G>A, p.Gly505Asp; TG:c.3416C>T, p.Ser1139Leu; TG:c.2762-1G>A, ; TG:p.Gly1456Arg; TG:p.Asp1767Gly; TG:p.Arg1136Gln; TG:p.Arg1250Leu; TG:p.Gln870His; TG:p.Val1105Ile; TG:c.6759_6765del, p.Ser2254MetfsTer88; TG:c.2307G>A, p.Trp769Ter; TG:c.3040G>A, p.Asp1014Asn; TG:c.3808C>T, p.Arg1270Cys; TG:c.5791A>G, p.Ile1931Val; TG:c.1958G>A, p.Gly653Asp; TG:c.199G>A, p.Gly67Ser; TG:c.2381G>T, p.Gly794Val; TG:c.5299_5301del, p.Asp1767del; TG:c.2610G>T, p.Glu870His; TG:p.Gly174Val; TG:c.4859C>T, p.Thr1620Met; TG:c.6791G>T, p.Cys2264Phe; TG:p.Ser1222Leu; TG:p.Gln1644fs; TG:c.2269G>A, p.Asp757Asn; TG:c.2183C>A, p.Thr728Lys; TG:c.3067C>T, p.Arg1023Trp; TG:c.7753C>T, p.Arg2585Trp; TG:c.521G>T, p.Gly174Val; TG:c.3665C>T, p.Ser1222Leu; TG:c.4932dupG, p.Gln1644fs; TG:c.3067C>T, p.Pro1023Trp; TG:c.993G>C, p.Gln331His; TG:c.5984A>G, p.Glu1995Gly; TG:c.848G>T, p.Arg283Leu; TG:c.3908G>A, p.Gly1303Asp; TG:c.6130C>T, p.Arg2044Cys; TG:c.2360G>A, p.Arg787Gln
1 disease linked to TG Congenital hypothyroidism
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