H2AC12 (H2A clustered histone 12) - Rat Genome Database

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Gene: H2AC12 (H2A clustered histone 12) Homo sapiens
Analyze
Symbol: H2AC12
Name: H2A clustered histone 12
RGD ID: 1349795
HGNC Page HGNC:13671
Description: Predicted to enable nucleosomal DNA binding activity. Predicted to be involved in heterochromatin organization. Located in extracellular exosome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: dJ86C11.1; H2A histone family member; H2A/S; H2AFALii; H2AH; HIST1H2AH; histone 1, h2ah; histone cluster 1 H2A family member h; histone cluster 1, H2ah; histone H2A type 1-H; histone H2A/s; MGC171151
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38627,147,106 - 27,147,562 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl627,147,106 - 27,147,562 (+)EnsemblGRCh38hg38GRCh38
GRCh37627,114,885 - 27,115,341 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36627,222,887 - 27,223,373 (+)NCBINCBI36Build 36hg18NCBI36
Build 34627,222,886 - 27,223,325NCBI
Celera628,720,909 - 28,721,395 (+)NCBICelera
Cytogenetic Map6p22.1NCBI
HuRef626,922,924 - 26,923,404 (+)NCBIHuRef
CHM1_1627,117,174 - 27,117,654 (+)NCBICHM1_1
T2T-CHM13v2.0627,015,922 - 27,016,378 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
chromosome  (IEA)
extracellular exosome  (HDA)
nucleosome  (IBA,IEA)
nucleus  (IBA,IEA)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9566873   PMID:10064132   PMID:10384058   PMID:11080476   PMID:11689053   PMID:12408966   PMID:12477932   PMID:14574404   PMID:14657027   PMID:15010469   PMID:15078818   PMID:15386022  
PMID:15489334   PMID:15823041   PMID:16319397   PMID:16359901   PMID:16702407   PMID:17074886   PMID:20458337   PMID:21319273   PMID:21873635   PMID:21951318   PMID:22810585   PMID:22865885  
PMID:23376485   PMID:23533145   PMID:25798074   PMID:25963833   PMID:26237645   PMID:26318153   PMID:27545878   PMID:27591049   PMID:28225217   PMID:28330616   PMID:28947420   PMID:28973437  
PMID:28977666   PMID:29162697   PMID:29507755   PMID:29676528   PMID:29777862   PMID:29845934   PMID:29859926   PMID:29987050   PMID:30021884   PMID:30575818   PMID:30725116   PMID:30890647  
PMID:31300519   PMID:31409639   PMID:31980649   PMID:32041737   PMID:32416067   PMID:32529326   PMID:32538781   PMID:32780723   PMID:32812023   PMID:33536335   PMID:33567341   PMID:33838681  
PMID:34244565   PMID:34349018   PMID:34709727   PMID:35007762   PMID:35575683   PMID:35906200   PMID:35944360   PMID:36057605   PMID:36180920   PMID:36215168   PMID:36282215   PMID:36470425  
PMID:36517590   PMID:36574265   PMID:37689310   PMID:37866880  


Genomics

Comparative Map Data
H2AC12
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38627,147,106 - 27,147,562 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl627,147,106 - 27,147,562 (+)EnsemblGRCh38hg38GRCh38
GRCh37627,114,885 - 27,115,341 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36627,222,887 - 27,223,373 (+)NCBINCBI36Build 36hg18NCBI36
Build 34627,222,886 - 27,223,325NCBI
Celera628,720,909 - 28,721,395 (+)NCBICelera
Cytogenetic Map6p22.1NCBI
HuRef626,922,924 - 26,923,404 (+)NCBIHuRef
CHM1_1627,117,174 - 27,117,654 (+)NCBICHM1_1
T2T-CHM13v2.0627,015,922 - 27,016,378 (+)NCBIT2T-CHM13v2.0
H2ac12
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391322,219,292 - 22,219,813 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1322,219,334 - 22,219,738 (-)EnsemblGRCm39 Ensembl
GRCm381322,035,122 - 22,035,643 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1322,035,164 - 22,035,568 (-)EnsemblGRCm38mm10GRCm38
MGSCv371322,127,035 - 22,127,421 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361322,042,631 - 22,043,017 (-)NCBIMGSCv36mm8
Celera1322,307,610 - 22,307,996 (-)NCBICelera
Cytogenetic Map13A3.1NCBI
cM Map138.14NCBI
H2ac12
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81747,182,193 - 47,182,658 (+)NCBIGRCr8
mRatBN7.21742,486,415 - 42,486,880 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1742,486,415 - 42,486,941 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.01744,527,990 - 44,528,557 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1744,528,125 - 44,528,511 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01758,940,554 - 58,942,457 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41750,119,480 - 50,119,866 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1753,974,759 - 53,975,326 (-)NCBICelera
Cytogenetic Map17p11NCBI
LOC100982497
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2541,779,821 - 41,795,629 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1637,781,292 - 37,797,102 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0626,980,174 - 26,981,215 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1627,642,074 - 27,642,553 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl627,642,115 - 27,642,501 (+)Ensemblpanpan1.1panPan2
H2AC12
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13524,558,456 - 24,559,356 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3524,558,493 - 24,558,879 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3524,414,716 - 24,415,520 (+)NCBIDog10K_Boxer_Tasha
H2AC17
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl721,632,862 - 21,936,037 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1721,632,867 - 21,633,939 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2723,188,135 - 23,188,608 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103221968
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11745,362,328 - 45,362,820 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604426,842,068 - 26,842,554 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in H2AC12
6 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6p22.3-21.33(chr6:18120520-30767516)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052180]|See cases [RCV000052180] Chr6:18120520..30767516 [GRCh38]
Chr6:18120751..30735293 [GRCh37]
Chr6:18228730..30843272 [NCBI36]
Chr6:6p22.3-21.33		 pathogenic
GRCh38/hg38 6p22.2-22.1(chr6:26280579-28727313)x3 copy number gain See cases [RCV000133692] Chr6:26280579..28727313 [GRCh38]
Chr6:26280807..28695090 [GRCh37]
Chr6:26388786..28803069 [NCBI36]
Chr6:6p22.2-22.1		 uncertain significance
GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3 copy number gain See cases [RCV000138956] Chr6:3224310..30657190 [GRCh38]
Chr6:3224544..30624967 [GRCh37]
Chr6:3169543..30732946 [NCBI36]
Chr6:6p25.2-21.33		 pathogenic
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3 copy number gain See cases [RCV000143497] Chr6:156974..46789291 [GRCh38]
Chr6:156974..46757028 [GRCh37]
Chr6:101974..46864987 [NCBI36]
Chr6:6p25.3-12.3		 pathogenic
GRCh37/hg19 6p22.2-22.1(chr6:26545571-27115102)x3 copy number gain Breast ductal adenocarcinoma [RCV000207103] Chr6:26545571..27115102 [GRCh37]
Chr6:6p22.2-22.1		 uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
NM_080596.3(H2AC12):c.134G>C (p.Gly45Ala) single nucleotide variant not specified [RCV004325242] Chr6:27147262 [GRCh38]
Chr6:27115041 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.103C>T (p.Leu35Phe) single nucleotide variant not specified [RCV004287544] Chr6:27147231 [GRCh38]
Chr6:27115010 [GRCh37]
Chr6:6p22.1		 uncertain significance
GRCh37/hg19 6p22.2-22.1(chr6:26928203-27344831)x3 copy number gain not provided [RCV000682658] Chr6:26928203..27344831 [GRCh37]
Chr6:6p22.2-22.1		 uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p22.1(chr6:27093821-27158033)x3 copy number gain not provided [RCV000745567] Chr6:27093821..27158033 [GRCh37]
Chr6:6p22.1		 benign
NM_080596.3(H2AC12):c.62G>T (p.Arg21Leu) single nucleotide variant not specified [RCV004250332] Chr6:27147190 [GRCh38]
Chr6:27114969 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.106C>T (p.Arg36Cys) single nucleotide variant not specified [RCV004250350] Chr6:27147234 [GRCh38]
Chr6:27115013 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.4T>G (p.Ser2Ala) single nucleotide variant not specified [RCV004316316] Chr6:27147132 [GRCh38]
Chr6:27114911 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.65C>T (p.Ala22Val) single nucleotide variant not specified [RCV004339452] Chr6:27147193 [GRCh38]
Chr6:27114972 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.112G>A (p.Gly38Ser) single nucleotide variant not specified [RCV004396487] Chr6:27147240 [GRCh38]
Chr6:27115019 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.199G>A (p.Ala67Thr) single nucleotide variant not specified [RCV004396488] Chr6:27147327 [GRCh38]
Chr6:27115106 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.224A>G (p.Lys75Arg) single nucleotide variant not specified [RCV004396492] Chr6:27147352 [GRCh38]
Chr6:27115131 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.22G>A (p.Gly8Ser) single nucleotide variant not specified [RCV004396494] Chr6:27147150 [GRCh38]
Chr6:27114929 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.10C>T (p.Arg4Cys) single nucleotide variant not specified [RCV004396486] Chr6:27147138 [GRCh38]
Chr6:27114917 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.200C>T (p.Ala67Val) single nucleotide variant not specified [RCV004396490] Chr6:27147328 [GRCh38]
Chr6:27115107 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.20A>G (p.Gln7Arg) single nucleotide variant not specified [RCV004396491] Chr6:27147148 [GRCh38]
Chr6:27114927 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.91G>A (p.Val31Met) single nucleotide variant not specified [RCV004396496] Chr6:27147219 [GRCh38]
Chr6:27114998 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.19C>G (p.Gln7Glu) single nucleotide variant not specified [RCV004396489] Chr6:27147147 [GRCh38]
Chr6:27114926 [GRCh37]
Chr6:6p22.1		 uncertain significance
NM_080596.3(H2AC12):c.5C>T (p.Ser2Phe) single nucleotide variant not specified [RCV004396495] Chr6:27147133 [GRCh38]
Chr6:27114912 [GRCh37]
Chr6:6p22.1		 uncertain significance

QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1358854MULTSCL4_HMultiple sclerosis susceptibility QTL 4 (human)Multiple sclerosis susceptibility6691196032911960Human
1358839MULTSCL5_HMultiple sclerosis susceptibility QTL 5 (human)Multiple sclerosis susceptibility61958431145584311Human
1643377BW325_HBody weight QTL 325 (human)2.320.0005Body fat amount6691196032911960Human
1643569GLUCO21_HGlucose level QTL 21 (human)0.021Glucose levelnon-insulin-dependent6691196032911960Human
1298458BW9_HBody weight QTL 9 (human)2.70.0002Body fat amount6691196032911960Human
1298431RA11_HRheumatoid arthritis QTL 11 (human)0.0000024Joint/bone inflammationrheumatoid arthritis61991188340191709Human
1358857MULTSCL19_HMultiple sclerosis susceptibility QTL 19 (human)Multiple sclerosis susceptibility61958431145584311Human
1643399BMD5_HBone mineral density QTL 5 (human)2.320.0005Bone mineral density6691196032911960Human

Markers in Region
HIST1H2AH__7487  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37627,115,017 - 27,115,546UniSTSGRCh37
Build 36627,222,996 - 27,223,525RGDNCBI36
Celera628,721,018 - 28,721,547RGD
HuRef626,923,080 - 26,923,609UniSTS
D6S2252  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37627,113,003 - 27,113,153UniSTSGRCh37
Build 36627,220,982 - 27,221,132RGDNCBI36
Celera628,719,002 - 28,719,154RGD
Cytogenetic Map6p21.33UniSTS
HuRef626,921,058 - 26,921,216UniSTS
UniSTS:480645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37627,114,908 - 27,115,344UniSTSGRCh37
Build 36627,222,887 - 27,223,323RGDNCBI36
Celera628,720,909 - 28,721,345RGD
HuRef626,922,971 - 26,923,407UniSTS
UniSTS:482788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372144,985,120 - 44,985,500UniSTSGRCh37
GRCh37627,114,197 - 27,114,577UniSTSGRCh37
Build 36627,222,176 - 27,222,556RGDNCBI36
Celera2130,091,648 - 30,092,028UniSTS
Celera628,720,198 - 28,720,578RGD
HuRef2130,353,673 - 30,354,053UniSTS
HuRef626,922,260 - 26,922,640UniSTS
UniSTS:483466  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37627,114,861 - 27,115,317UniSTSGRCh37
Build 36627,222,840 - 27,223,296RGDNCBI36
Celera628,720,862 - 28,721,318RGD
HuRef626,922,924 - 26,923,380UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High 2 3
Medium 14 9 2 45 2 5 2 1 1 1
Low 509 409 168 49 916 35 795 109 328 35 596 430 22 237 339 3
Below cutoff 962 1128 502 146 471 73 1399 645 879 72 350 549 77 466 893

Sequence


Ensembl Acc Id: ENST00000377459   ⟹   ENSP00000366679
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl627,147,106 - 27,147,562 (+)Ensembl
RefSeq Acc Id: NM_080596   ⟹   NP_542163
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38627,147,106 - 27,147,562 (+)NCBI
GRCh37627,114,908 - 27,115,346 (+)ENTREZGENE
Build 36627,222,887 - 27,223,325 (+)NCBI Archive
Celera628,720,909 - 28,721,395 (+)RGD
HuRef626,922,924 - 26,923,404 (+)NCBI
CHM1_1627,117,174 - 27,117,654 (+)NCBI
T2T-CHM13v2.0627,015,922 - 27,016,378 (+)NCBI
Sequence:
RefSeq Acc Id: NP_542163   ⟸   NM_080596
- UniProtKB: Q96KK5 (UniProtKB/Swiss-Prot),   A3KPC7 (UniProtKB/TrEMBL),   B2R5B3 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000366679   ⟸   ENST00000377459
Protein Domains
Histone H2A C-terminal   Histone H2A/H2B/H3

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96KK5-F1-model_v2 AlphaFold Q96KK5 1-128 view protein structure

Promoters
RGD ID:6804304
Promoter ID:HG_KWN:52630
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000377459,   NM_080593
Position:
Human AssemblyChrPosition (strand)Source
Build 36627,221,786 - 27,223,437 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13671 AgrOrtholog
COSMIC H2AC12 COSMIC
Ensembl Genes ENSG00000274997 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000377459 ENTREZGENE
  ENST00000377459.3 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.20.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000274997 GTEx
HGNC ID HGNC:13671 ENTREZGENE
Human Proteome Map H2AC12 Human Proteome Map
InterPro Histone-fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Histone_H2A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Histone_H2A/H2B/H3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Histone_H2A_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Histone_H2A_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:85235 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 85235 ENTREZGENE
OMIM 615013 OMIM
PANTHER HISTONE H2A.J UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR23430 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Histone UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Histone_H2A_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS HISTONEH2A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE HISTONE_H2A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART H2A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF47113 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A3KPC7 ENTREZGENE, UniProtKB/TrEMBL
  B2R5B3 ENTREZGENE
  H2A1H_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-07-30 H2AC12  H2A clustered histone 12  HIST1H2AH  histone cluster 1 H2A family member h  Symbol and/or name change 5135510 APPROVED
2016-08-23 HIST1H2AH  histone cluster 1 H2A family member h  HIST1H2AH  histone cluster 1, H2ah  Symbol and/or name change 5135510 APPROVED