Expression Atlas results for ENSMUSG00000031229

    Atrx Mus musculus alpha thalassemia/mental retardation syndrome X-linked homolog (human)
Synonyms DXHXS6677E, HP1-BP38, Hp1bp2, Rad54, XH2, Xnp
Orthologs ATRX (Bos taurus), ATRX (Canis familiaris), ENSCING00000003076 (Ciona intestinalis), ENSCSAVG00000000356 (Ciona savignyi), ENSCSAVG00000002116 (Ciona savignyi), atrx (Danio rerio), ATRX (Equus caballus), ATRX (Homo sapiens), ATRX (Gallus gallus), ATRX (Macaca mulatta), Atrx (Rattus norvegicus), ATRX (Sus scrofa), atrx (Xenopus tropicalis), XNP (Drosophila melanogaster), xnp-1 (Caenorhabditis elegans), RAD54 (Saccharomyces cerevisiae)
Gene Ontology nuclear chromosome, heterochromatin, nucleic acid binding, DNA binding, chromatin binding, helicase activity, protein binding, ATP binding, nucleus, nucleolus, cytoplasm, mitochondrion, ATP catabolic process, DNA repair, nucleosome assembly, DNA replication-independent nucleosome assembly, chromatin remodeling, transcription, DNA-templated, spermatogenesis, zinc ion binding, positive regulation of nuclear cell cycle DNA replication, DNA translocase activity, PML body, DNA damage response, signal transduction by p53 class mediator, forebrain development, replication fork processing, telomeric heterochromatin, positive regulation of telomere maintenance, methylated histone binding, histone binding, positive regulation of transcription from RNA polymerase II promoter, Sertoli cell development, chromo shadow domain binding, SWI/SNF superfamily-type complex, seminiferous tubule development, cellular response to hydroxyurea, negative regulation of telomeric RNA transcription from RNA pol II promoter
InterPro SNF2-related (domain), Helicase, C-terminal (domain), Zinc finger, FYVE/PHD-type (domain), Helicase, superfamily 1/2, ATP-binding domain (domain), P-loop containing nucleoside triphosphate hydrolase (domain)
Ensembl Family TRANSCRIPTIONAL REGULATOR ATRX EC_3.6.4.12 ATP DEPENDENT HELICASE X LINKED NUCLEAR, UNKNOWN
Ensembl Gene ENSMUSG00000031229
Entrez 22589
UniProt A6PWK7, A6PWK8, A6PWK9, A6PWL2, Q3TA30, Q3TP53, Q3TSV4, Q3UU22, Q3UY26, Q61687, Q8C2S3, Q8C4Z6
EMAGE MGI:103067
MGI alpha thalassemia/mental retardation syndrome X-linked homolog (human)
Gene Biotype protein_coding
Design Element 102030_at, 10606263, 133207_f_at, 1420945_at, 1420946_at, 1420947_at, 1420948_s_at, 1433537_at, 1450051_at, 1453734_at, 162859_at, 4329726, 4361712, 4365616, 4421894, 4424983, 4443433, 4452980, 4461410, 4474265, 4479696, 4494318, 4528792, 4533609, 4580618, 4581696, 4616502, 4635691, 4643048, 4651340, 4692703, 4712662, 4721993, 4734371, 4740204, 4764440, 4773444, 4776713, 4815554, 4816296, 4822062, 4879990, 4918896, 4932194, 4935333, 4967293, 4999620, 5002345, 5005577, 5013580, 5050729, 5072086, 5104552, 5112160, 5125854, 5154179, 5162388, 5187074, 5189747, 5214394, 5230506, 5243408, 5301194, 5318387, 5352417, 5382328, 5409750, 5443547, 5454416, 5477019, 5489699, 5524901, 5542053, 5555104, 5587943, 5596882, 5598679, 5603877, 5605394, A_51_P118664, A_51_P413366, A_66_P118592, A_66_P119643
    Baseline Expression Results in tissues
c Expression Level cut-off: 0.5
    Differential Expression 21 results
Showing 21 results cutoffs: adjusted p-value 0.05    log2-fold change 1.0