ATM
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Homo sapiens |
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ATM is differentially expressed in 353 experiments: 126 organism parts: bone marrow, ovary, ... (124 more);, 241 disease states: normal, prostate carcinoma, ... (239 more);, 115 cell types 373 cell lines 54 compound treatments and 87 other conditions. |
| Synonyms |
ATDC, TELO1, ATA, ATD, ATC, TEL1 |
| Orthologs |
TEL1
(Saccharomyces cerevisiae)
Atm
(Rattus norvegicus)
ENSCING00000000816
(Ciona intestinalis)
Atm
(Mus musculus)
ATM
(Gallus gallus)
atm
(Danio rerio)
ATM
(Bos taurus)
atm
(Danio rerio)
tefu
(Drosophila melanogaster)
atm
(Xenopus laevis)
B3VMJ2_CANFA
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology ID |
GO:0008219, GO:0003677, GO:0016023, GO:0008630, GO:0007050, GO:0010212, GO:0016572, GO:0007094, GO:0007131, GO:0007165, GO:0007292, GO:0016303, GO:0007420, GO:0051402, GO:0007507, GO:0016773, GO:0000077, GO:0000075, GO:0005488, GO:0005524, GO:0005515, GO:0047485, GO:0006915, GO:0005737, GO:0005634, GO:0005654, GO:0005819, GO:0006974, GO:0004672, GO:0004674, GO:0000724, GO:0043065, GO:0043066, GO:0000781, GO:0006468, GO:0000166, GO:0006302, GO:0018105, GO:0051726, GO:0001756, GO:0046777, GO:0046983, GO:0006281, GO:0001666, GO:0031572, GO:0035174, GO:0071044, GO:0002331, GO:0006977, GO:0006975, GO:0004677, GO:0030889, GO:0032403, GO:0042159, GO:0043517, GO:0043525, GO:0071480, GO:0090399, GO:0035404 |
| Gene Ontology Term |
chromosome, telomeric region, reciprocal meiotic recombination, histone phosphorylation, DNA damage checkpoint, DNA binding, double-strand break repair via homologous recombination, protein binding, apoptosis, phosphotransferase activity, alcohol group as acceptor, DNA repair, cytoplasm, DNA damage response, signal transduction resulting in induction of apoptosis, peptidyl-serine phosphorylation, negative regulation of apoptosis, protein N-terminus binding, cell cycle arrest, 1-phosphatidylinositol-3-kinase activity, response to hypoxia, somitogenesis, positive regulation of apoptosis, double-strand break repair, response to ionizing radiation, ATP binding, protein dimerization activity, histone serine kinase activity, spindle, regulation of cell cycle, female gamete generation, nucleus, heart development, cell death, cytoplasmic membrane-bounded vesicle, nucleotide binding, protein serine/threonine kinase activity, binding, nucleoplasm, cell cycle checkpoint, response to DNA damage stimulus, brain development, signal transduction, neuron apoptosis, G2/M transition DNA damage checkpoint, mitotic cell cycle spindle assembly checkpoint, protein kinase activity, cellular response to gamma radiation, DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest, DNA damage induced protein phosphorylation, pre-B cell allelic exclusion, negative regulation of B cell proliferation, positive regulation of neuron apoptosis, protein complex binding, positive regulation of DNA damage response, signal transduction by p53 class mediator, DNA-dependent protein kinase activity, histone mRNA catabolic process, lipoprotein catabolic process, protein autophosphorylation, protein phosphorylation, replicative senescence, histone-serine phosphorylation |
| InterPro ID |
IPR000403, IPR014009, IPR003152, IPR003151, IPR021668 |
| InterPro Term |
PIK_FAT, PIK-rel_kinase_FAT, FATC, PI3/4_kinase_cat, TAN |
| Ensembl Family |
ENSFM00360000109902 |
| Ensembl Family Description |
SERINE/THREONINE KINASE TEL1 EC_2.7.11.1 ATM HOMOLOG DNA DAMAGE CHECKPOINT KINASE TEL1 TELOMERE LENGTH REGULATION 1 |
| EMBL-Bank ID |
AP001925, U33841, U55757, U55756, U55743, U55742, U55741, U55740, U55734, U55735, U55732, U55733, U55738, U55739, U55736, U55737, U55751, U55750, U55753, U55752, U55755, U55754, U55744, U55745, U55746, U55747, U55748, U55749, U55714, U55715, U55712, U55713, U55710, U55711, U55718, U55719, U55716, U55717, U55731, U55730, U55724, U55725, U55726, U55727, U55720, U55721, U55722, U55723, U55728, U55729, U55705, U55704, U55707, U55709, U55708, AY220758, U26455, U67092, BC137169, U82828, CH471065, X91196, AP005718 |
| Ensembl Protein ID |
ENSP00000388058, ENSP00000278616, ENSP00000374162, ENSP00000433955, ENSP00000431839, ENSP00000435524, ENSP00000435747, ENSP00000432560, ENSP00000432318, ENSP00000434327 |
| UniProt Accession |
Q13315, E9PRG7, E7EV38, E9PFP9, E9PIN0, E9PIQ5 |
| Description |
ataxia telangiectasia mutated [Source:HGNC Symbol;Acc:795] |
| UniGene ID |
Hs.367437, Hs.658151 |
| Ensembl Gene ID |
ENSG00000149311 |
| Gene-Disease Assocation |
BREAST CANCER, ATAXIA-TELANGIECTASIA; AT |
| HGNC Symbol |
ATM |
| RefSeq ID |
NP_000042, NM_000051 |
| Entrez Gene ID |
472 |
| Ensembl Transcript ID |
ENST00000532931, ENST00000452508, ENST00000530958, ENST00000532637, ENST00000532765, ENST00000526567, ENST00000278616, ENST00000419286, ENST00000534625, ENST00000531957, ENST00000525056, ENST00000525012, ENST00000533979, ENST00000525178, ENST00000527891, ENST00000525537, ENST00000527805, ENST00000389511, ENST00000527181, ENST00000531525, ENST00000527389, ENST00000524792, ENST00000529588, ENST00000533733, ENST00000533690, ENST00000533526, ENST00000533470 |
| Design Element |
ENST00000525537, ENST00000532931, ENST00000525012, ENST00000531957, Hs2.194382.3.S1_3p_x_at, gnf1h11246_at, Hs.194382.2.S1_3p_at, ENST00000533690, ENST00000525056, 210858_x_at, ENST00000526567, U67092_s_at, 1862_at, U33841_at, ENST00000533979, 2001_g_at, Hs2.382828.1.S1_3p_at, ENST00000419286, ENST00000529588, U67092_at, 91853_at, ENST00000533733, 1553387_at, Hs2.194382.4.S1_3p_x_at, 1553387_3p_at, ENST00000531525, ENST00000525178, 1570352_at, g4502266_3p_a_at, 208442_s_at, ENST00000527181, ENST00000389511, 1863_s_at, ENST00000533470, ENST00000534625, ENST00000527805, ENST00000533526, ENST00000532765, X91196_s_at, 1554631_at, 2000_at, ENST00000527389, ENST00000532637, ENST00000524792, ENST00000452508, ENST00000530958, ENST00000278616, ENST00000527891, 212672_at |
| Search EB-eye |
ENSG00000149311
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