KEGG   Homo sapiens (human): 474381
Entry
474381            CDS       T01001                                 
Symbol
H2AB2, H2A.B.1, H2A.Bbd, H2AB3, H2AFB2
Name
(RefSeq) H2A.B variant histone 2
  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
    474381 (H2AB2)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    474381 (H2AB2)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    474381 (H2AB2)
 09160 Human Diseases
  09163 Immune disease
   05322 Systemic lupus erythematosus
    474381 (H2AB2)
  09165 Substance dependence
   05034 Alcoholism
    474381 (H2AB2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    474381 (H2AB2)
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    474381 (H2AB2)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Nucleosome assembly factors
   Histones
    474381 (H2AB2)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   474381 (H2AB2)
SSDB
Motif
Pfam: Histone CBFD_NFYB_HMF
Other DBs
NCBI-GeneID: 474381
NCBI-ProteinID: NP_001017991
OMIM: 301038
HGNC: 18298
Ensembl: ENSG00000277858
UniProt: P0C5Z0
Structure
LinkDB
Position
X:155380709..155381299
AA seq 115 aa
MPRRRRRRGSSGAGGRGRTCSRTVRAELSFSVSQVERSLREGHYAQRLSRTAPVYLAAVI
EYLTAKVLELAGNEAQNSGERNITPLLLDMVVHNDRLLSTLFNTTTISQVAPGED
NT seq 348 nt   +upstreamnt  +downstreamnt
atgccgaggaggaggagacgccgagggtcctccggtgctggcggccgggggcggacctgc
tctcgcaccgtccgagcggagctttcgttttcagtgagccaggtggagcgcagtctacgg
gagggccactacgctcagcgcctgagtcgcacggcgccggtctacctcgctgcggttatt
gagtacctgacggccaaggtcctggagctggcgggcaacgaggcccagaacagcggagag
cggaacatcactcccctgctgctggacatggtggttcacaacgacaggctactgagcacc
cttttcaacacgaccaccatctctcaagtggcccctggcgaggactag

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