Homo sapiens (human): 474382 Help Entry 474382            CDS       T01001                                  Symbol H2AB1, H2A.B, H2A.B.2, H2A.Bbd, H2AFB1 Name (RefSeq) H2A.B variant histone 1   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 Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09126 Chromosome    03082 ATP-dependent chromatin remodeling     474382 (H2AB1)  09150 Organismal Systems   09151 Immune system    04613 Neutrophil extracellular trap formation     474382 (H2AB1)  09160 Human Diseases   09163 Immune disease    05322 Systemic lupus erythematosus     474382 (H2AB1)   09165 Substance dependence    05034 Alcoholism     474382 (H2AB1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03036 Chromosome and associated proteins [BR:hsa03036]     474382 (H2AB1)   09183 Protein families: signaling and cellular processes    04147 Exosome [BR:hsa04147]     474382 (H2AB1) Chromosome and associated proteins [BR:hsa03036]  Eukaryotic type   Nucleosome assembly factors    Histones     474382 (H2AB1) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)    474382 (H2AB1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Histone Motif Other DBs NCBI-GeneID:  474382 NCBI-ProteinID:  NP_001017990 OMIM:  301037 HGNC:  22516 Ensembl:  ENSG00000274183 UniProt:  P0C5Y9 LinkDB All DBs Position X:154884972..154885558 Genome browser AA seq 115 aa AA seqDB search MPRRRRRRGSSGAGGRGRTCSRTVRAELSFSVSQVERSLREGHYAQRLSRTAPVYLAAVI EYLTAKVPELAGNEAQNSGERNITPLLLDMVVHNDRLLSTLFNTTTISQVAPGED NT seq 348 nt NT seq  +upstreamnt  +downstreamnt atgccgaggaggaggagacgccgagggtcctccggtgctggcggccgggggcggacctgc tctcgcaccgtccgagcggagctttcgttttcagtgagccaggtggagcgcagtctacgg gagggccactacgctcagcgcctgagtcgcacggcgccggtctacctcgctgcggttatt gagtacctgacggccaaggtcccggagctggcgggcaacgaggcccagaacagcggagag cggaacatcactcccctgctgctggacatggtggttcacaacgacaggctactgagcacc cttttcaacacgaccaccatctctcaagtggcccctggcgaggactag

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