Homo sapiens (human): 3014 Help Entry 3014              CDS       T01001                                  Symbol H2AX, H2A.X, H2A/X, H2AFX Name (RefSeq) H2A.X variant histone   KO K11251   histone H2A Organism hsa  Homo sapiens (human) Pathway hsa03082   ATP-dependent chromatin remodeling hsa04217   Necroptosis hsa04613   Neutrophil extracellular trap formation hsa05034   Alcoholism hsa05322   Systemic lupus erythematosus Network nt06506  Double-strand break repair   Element N01439   Double-strand break signaling Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09126 Chromosome    03082 ATP-dependent chromatin remodeling     3014 (H2AX)  09140 Cellular Processes   09143 Cell growth and death    04217 Necroptosis     3014 (H2AX)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     3014 (H2AX)  09160 Human Diseases   09163 Immune disease    05322 Systemic lupus erythematosus     3014 (H2AX)   09165 Substance dependence    05034 Alcoholism     3014 (H2AX)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03036 Chromosome and associated proteins [BR:hsa03036]     3014 (H2AX)   09183 Protein families: signaling and cellular processes    04147 Exosome [BR:hsa04147]     3014 (H2AX) Chromosome and associated proteins [BR:hsa03036]  Eukaryotic type   Nucleosome assembly factors    Histones     3014 (H2AX) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)    3014 (H2AX) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Histone_H2A_C Histone CBFD_NFYB_HMF Motif Other DBs NCBI-GeneID:  3014 NCBI-ProteinID:  NP_002096 OMIM:  601772 HGNC:  4739 Ensembl:  ENSG00000188486 UniProt:  P16104 Structure PDBPDBj LinkDB All DBs Position 11:complement(119093874..119095465) Genome browser AA seq 143 aa AA seqDB search MSGRGKTGGKARAKAKSRSSRAGLQFPVGRVHRLLRKGHYAERVGAGAPVYLAAVLEYLT AEILELAGNAARDNKKTRIIPRHLQLAIRNDEELNKLLGGVTIAQGGVLPNIQAVLLPKK TSATVGPKAPSGGKKATQASQEY NT seq 432 nt NT seq  +upstreamnt  +downstreamnt atgtcgggccgcggcaagactggcggcaaggcccgcgccaaggccaagtcgcgctcgtcg cgcgccggcctccagttcccagtgggccgtgtacaccggctgctgcggaagggccactac gccgagcgcgttggcgccggcgcgccagtgtacctggcggcagtgctggagtacctcacc gctgagatcctggagctggcgggcaatgcggcccgcgacaacaagaagacgcgaatcatc ccccgccacctgcagctggccatccgcaacgacgaggagctcaacaagctgctgggcggc gtgacgatcgcccagggaggcgtcctgcccaacatccaggccgtgctgctgcccaagaag accagcgccaccgtggggccgaaggcgccctcgggcggcaagaaggccacccaggcctcc caggagtactaa

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