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10 Possible Causes for HIST1H2AJ, gene

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  • Saccharomyces Cerevisiae

    We identified most known oxygen-regulated genes and also uncovered new regulated genes.[ncbi.nlm.nih.gov] Xenopus laevis (African clawed frog) / Gene : hist1h2aj, LOC494591 / Production host : Escherichia coli (E. coli) / References : UniProt: Q6AZJ8 , UniProt: P06897 *PLUS #4[pdbj.org] […] may be complimented by introduced homologous genes.[labtimes.org]

  • Systemic Lupus Erythematosus

    Abstract Our purpose was to identify differentially expressed (DE) genes and biological processes associated with gene expression changes in systemic lupus erythematosus ([ncbi.nlm.nih.gov] […] family member k [KO: K11251 ] 8334 HIST1H2AC; histone cluster 1 H2A family member c [KO: K11251 ] 8329 HIST1H2AI; histone cluster 1 H2A family member i [KO: K11251 ] 8331 HIST1H2AJ[genome.jp] The majority of genes demonstrating altered transcript abundance between patients with and without LN were neutrophil-related.[ncbi.nlm.nih.gov]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] A-B: Genetic Testing by Individual Gene Gene Protein Associated Disease(s) AARS2 Alanyl-tRNA Synthetase 2, Mitochondrial Familial Hypertrophic Cardiomyopathy (HCM) ABCA1 ATP-Binding[bcm.edu]

  • Nestor-Guillermo Progeria Syndrome

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] An inherited LMNA gene mutation in atypical Progeria syndrome. Am J Med Genet A 2012;158A(11):2881-7.[scholar.um5.ac.ma]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    The gene symbol is from the HUGO Gene Nomenclature Committee (HGNC) database.[dna.universeofatoms.com] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Combined Oxidative Phosphorylation Deficiency Type 3

    Below are the genes sequenced in this screen and the targeted disease(s) associated with each of these genes.[genepeeks.com] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org]

  • Premature Chromatid Separation Trait

    811 The long hunt for the Huntingtons chorea gene 240 positional cloning of an imprinted gene?[books.google.com] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] An important gene associated with Premature Chromatid Separation Trait is BUB1B (BUB1 Mitotic Checkpoint Serine/Threonine Kinase B).[malacards.org]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    Human Gene Mutation Database (HGMD) RMRP SNPedia medical, phenotypic, and genealogical associations of SNPs for RMRP SNP Genotyping and Copy Number Assay Products No data[genecards.org] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] gene; Usher syndrome type IIIA and retinitis pigmentosa-61 caused by mutations in the CLRN1 gene).[julesberman.blogspot.com]

  • AICA-Ribosiduria

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] The outlier genes identified in the two HPRT deficient patients were different and none of these genes to our knowledge are disease associated.[ojrd.biomedcentral.com]

  • Colobomatous Microphthalmia - Rhizomelic Dysplasia Syndrome

    Note The disease is caused by mutations affecting the gene represented in this entry.[genecards.org] HIST1H2AJ G:602791 . . HIST1H2AK G:602788 . . HIST1H2AL G:602793 . . HIST1H2AM G:602796 . . HIST1H2BA G:609904 . . HIST1H2BB G:602803 . . HIST1H2BC G:602847 . .[usegalaxy.org] Frkp-Related MDDGC5 LGMD2I 607155 Genetic Test Registry Myopathy, Myofibrillar, 2 Alpha-B Crystallinopathy Myopathy, Desmin-Related, Associated With Mutation In The CRYAB Gene[ukgtn.nhs.uk]

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