MSH6
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Homo sapiens |
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MSH6 is differentially expressed in 347 experiments: 146 organism parts: testis, lung, ... (144 more);, 260 disease states: normal, cervical carcinoma, ... (258 more);, 113 cell types 407 cell lines 49 compound treatments and 88 other conditions. |
| Synonyms |
GTBP |
| Orthologs |
LOC100360342
(Rattus norvegicus)
E1BWV7_CHICK
(Gallus gallus)
msh6
(Danio rerio)
E1B9Q4_BOVIN
(Bos taurus)
MSH6
(Saccharomyces cerevisiae)
F6SHJ0_CIOIN
(Ciona intestinalis)
Msh6
(Mus musculus)
Msh6
(Drosophila melanogaster)
msh6
(Xenopus laevis)
MSH6
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
response to UV, reciprocal meiotic recombination, DNA binding, protein binding, DNA repair, nuclear chromatin, double-stranded DNA binding, damaged DNA binding, DNA damage response, signal transduction resulting in induction of apoptosis, ATPase activity, nuclear chromosome, MutSalpha complex, determination of adult lifespan, mismatched DNA binding, meiotic mismatch repair, ATP binding, magnesium ion binding, DNA-dependent ATPase activity, nucleus, mismatch repair, nucleotide binding, chromatin binding, four-way junction DNA binding, guanine/thymine mispair binding, MutLalpha complex binding, somatic recombination of immunoglobulin gene segments, ATP catabolic process, ADP binding, positive regulation of helicase activity, induction of apoptosis by intracellular signals, oxidized purine DNA binding, somatic hypermutation of immunoglobulin genes, negative regulation of DNA recombination, isotype switching, single guanine insertion binding, single thymine insertion binding |
| Gene Ontology ID |
GO:0003684, GO:0003682, GO:0003677, GO:0003690, GO:0008340, GO:0008094, GO:0009411, GO:0008630, GO:0007131, GO:0016887, GO:0005524, GO:0005515, GO:0005634, GO:0030983, GO:0000710, GO:0000790, GO:0000166, GO:0000287, GO:0000228, GO:0006298, GO:0006281, GO:0000400, GO:0032301, GO:0008629, GO:0016446, GO:0016447, GO:0051096, GO:0032405, GO:0006200, GO:0043531, GO:0045910, GO:0045190, GO:0032142, GO:0032143, GO:0032137, GO:0032357 |
| InterPro Term |
DNA_mismatch_repair_MutS_core, DNA_mismatch_repair_MutS_clamp, DNA_mismatch_repair_MutS-lik_N, DNA_mismatch_repair_MutS_connt, DNA_mismatch_repair_MutS_C, PWWP, DNA_mismatch_repair_Msh6 |
| InterPro ID |
IPR007861, IPR007860, IPR017261, IPR007695, IPR007696, IPR000313, IPR000432 |
| Entrez Gene ID |
2956 |
| EMBL-Bank ID |
AK293921, D89645, D89646, AY082894, U28946, BC004246, AC006509, U54777, U73733, U73732, U73734, U73737, U73736 |
| HGNC Symbol |
MSH6 |
| Ensembl Gene ID |
ENSG00000116062 |
| Ensembl Protein ID |
ENSP00000405294, ENSP00000413366, ENSP00000397484, ENSP00000390382, ENSP00000410570, ENSP00000406248, ENSP00000234420, ENSP00000446475, ENSP00000445199, ENSP00000438580, ENSP00000442745 |
| Description |
mutS homolog 6 (E. coli) [Source:HGNC Symbol;Acc:7329] |
| UniProt Accession |
C9J7Y7, P52701, C9J8Y8, Q1L838, C9JH55, B4DF41, E7ER38, F5H2F9, F5H769, F5H3S1, F8WAX8, F8W7G9 |
| UniGene ID |
Hs.445052 |
| Gene-Disease Assocation |
ENDOMETRIAL CANCER, MISMATCH REPAIR CANCER SYNDROME, BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1, MutS, E. COLI, HOMOLOG OF, 6; MSH6 |
| RefSeq ID |
NP_000170, NM_000179 |
| Ensembl Transcript ID |
ENST00000543270, ENST00000493177, ENST00000540021, ENST00000234420, ENST00000411819, ENST00000445503, ENST00000544857, ENST00000420813, ENST00000456246, ENST00000455383, ENST00000538136, ENST00000446255 |
| Ensembl Family Description |
DNA MISMATCH REPAIR MSH6 G/T MISMATCH BINDING GTBP GTMBP MUTS ALPHA 160 KDA SUBUNIT P160 |
| Ensembl Family |
ENSFM00650001140016 |
| Design Element |
gnf1h10057_at, U73737_at, 211449_at, ENST00000540021, 1017_at, ENST00000446255, 2003_s_at, ENST00000543270, g4504190_3p_at, ENST00000544857, 202911_at, g2687868_3p_a_at, ENST00000456246, ENST00000445503, g2687868_3p_at, 211450_s_at, ENST00000420813, ENST00000455383, ENST00000234420, ENST00000493177, ENST00000538136, ENST00000411819 |
| Search EB-eye |
ENSG00000116062
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