H2AC6 (H2A clustered histone 6) - Rat Genome Database

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Gene: H2AC6 (H2A clustered histone 6) Homo sapiens
Analyze
Symbol: H2AC6
Name: H2A clustered histone 6
RGD ID: 1345959
HGNC Page HGNC
Description: Predicted to have DNA binding activity. Involved in negative regulation of cell population proliferation. Localizes to nucleus.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: dJ221C16.4; H2A histone family, member L; H2A/l; H2AFL; HIST1H2AC; histone 1, H2ac; histone cluster 1 H2A family member c; histone cluster 1, H2ac; histone H2A type 1-C; histone H2A/l; histone H2AC; MGC99519
RGD Orthologs
Rat
Bonobo
Dog
Squirrel
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl626,124,145 - 26,139,116 (+)EnsemblGRCh38hg38GRCh38
GRCh38626,124,172 - 26,124,690 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37626,124,400 - 26,124,918 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36626,232,352 - 26,232,897 (+)NCBINCBI36hg18NCBI36
Build 34626,232,351 - 26,232,897NCBI
Celera627,353,637 - 27,354,182 (+)NCBI
Cytogenetic Map6p22.2NCBI
HuRef626,067,412 - 26,067,957 (+)NCBIHuRef
CHM1_1626,126,610 - 26,127,155 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-catechin  (EXP)
(-)-demecolcine  (EXP)
(-)-epigallocatechin 3-gallate  (EXP)
14-Deoxy-11,12-didehydroandrographolide  (EXP)
17beta-estradiol  (EXP)
2-methylcholine  (EXP)
3,4-dichloroaniline  (EXP)
acrolein  (EXP)
aflatoxin B1  (EXP)
aflatoxin M1  (EXP)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
AM-251  (EXP)
antirheumatic drug  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenous acid  (EXP)
Azaspiracid  (EXP)
belinostat  (EXP)
benzo[a]pyrene  (EXP)
benzo[a]pyrene diol epoxide I  (EXP)
berberine  (EXP)
bisphenol A  (EXP)
cadmium dichloride  (EXP)
cisplatin  (EXP)
cobalt dichloride  (EXP)
copper atom  (EXP)
copper(0)  (EXP)
copper(II) sulfate  (EXP)
coumestrol  (EXP)
crocidolite asbestos  (EXP)
decabromodiphenyl ether  (EXP)
diarsenic trioxide  (EXP)
dichromium trioxide  (EXP)
dicrotophos  (EXP)
dimethyl sulfoxide  (EXP)
dinophysistoxin 1  (EXP)
diuron  (EXP)
dorsomorphin  (EXP)
doxorubicin  (EXP)
Enterolactone  (EXP)
entinostat  (EXP)
formaldehyde  (EXP)
gamma-linolenic acid  (EXP)
genistein  (EXP)
hydroquinone O-beta-D-glucopyranoside  (EXP)
irinotecan  (EXP)
kojic acid  (EXP)
lead diacetate  (EXP)
leflunomide  (EXP)
mercury dibromide  (EXP)
methyl methanesulfonate  (EXP)
methylisothiazolinone  (EXP)
N-methyl-4-phenylpyridinium  (EXP)
okadaic acid  (EXP)
ozone  (EXP)
paracetamol  (EXP)
pentanal  (EXP)
phenylmercury acetate  (EXP)
potassium chromate  (EXP)
propanal  (EXP)
quercetin  (EXP)
resveratrol  (EXP)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium arsenate  (EXP)
sodium arsenite  (EXP)
sodium dichromate  (EXP)
sunitinib  (EXP)
thapsigargin  (EXP)
trichostatin A  (EXP)
tunicamycin  (EXP)
urethane  (EXP)
valproic acid  (EXP)
vincristine  (EXP)
vorinostat  (EXP)
zinc atom  (EXP)
zinc(0)  (EXP)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:9119399   PMID:9149941   PMID:9439656   PMID:9566873   PMID:11080476   PMID:11689053   PMID:12408966   PMID:12477932   PMID:14657027   PMID:15010469   PMID:15078818   PMID:15386022  
PMID:15489334   PMID:15635413   PMID:15823041   PMID:16169070   PMID:16319397   PMID:16359901   PMID:16457589   PMID:16702407   PMID:20085707   PMID:21630459   PMID:21873635   PMID:22623428  
PMID:22810585   PMID:23533145   PMID:23956221   PMID:24740910   PMID:25544563   PMID:25798074   PMID:25963833   PMID:26318153   PMID:26514267   PMID:27976729   PMID:28927264   PMID:29507755  
PMID:29845934   PMID:30349055   PMID:30532072   PMID:31091453   PMID:31180492   PMID:31300519   PMID:31586073   PMID:31980649   PMID:32780723   PMID:32814053   PMID:32877691  


Genomics

Comparative Map Data
H2AC6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl626,124,145 - 26,139,116 (+)EnsemblGRCh38hg38GRCh38
GRCh38626,124,172 - 26,124,690 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37626,124,400 - 26,124,918 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36626,232,352 - 26,232,897 (+)NCBINCBI36hg18NCBI36
Build 34626,232,351 - 26,232,897NCBI
Celera627,353,637 - 27,354,182 (+)NCBI
Cytogenetic Map6p22.2NCBI
HuRef626,067,412 - 26,067,957 (+)NCBIHuRef
CHM1_1626,126,610 - 26,127,155 (+)NCBICHM1_1
LOC103690190
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21742,707,863 - 42,708,420 (-)NCBI
Rnor_6.0 Ensembl1743,632,397 - 43,632,789 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl1744,747,796 - 44,748,188 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01744,747,686 - 44,748,229 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Celera1753,752,922 - 53,753,393 (+)NCBICelera
Cytogenetic Map17p11NCBI
LOC100990167
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1626,617,061 - 26,635,088 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl626,617,143 - 26,617,535 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0625,959,401 - 25,974,202 (+)NCBIMhudiblu_PPA_v0panPan3
H2AC6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13524,066,960 - 24,075,002 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3524,067,113 - 24,067,505 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3523,945,139 - 23,953,452 (+)NCBI
ROS_Cfam_1.03524,181,771 - 24,190,087 (+)NCBI
UMICH_Zoey_3.13523,997,959 - 24,006,273 (+)NCBI
UNSW_CanFamBas_1.03524,049,029 - 24,057,345 (+)NCBI
UU_Cfam_GSD_1.03525,481,660 - 25,489,975 (+)NCBI
LOC101975635
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244049461,655,330 - 1,655,993 (-)NCBI
SpeTri2.0NW_0049366711,965,690 - 1,967,463 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0

Position Markers
RH46761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37626,124,438 - 26,124,576UniSTSGRCh37
Build 36626,232,417 - 26,232,555RGDNCBI36
Celera627,353,702 - 27,353,840RGD
Cytogenetic Map6p22.1UniSTS
HuRef626,067,477 - 26,067,615UniSTS
GeneMap99-GB4 RH Map6105.5UniSTS
RH46705  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37626,138,892 - 26,139,012UniSTSGRCh37
Build 36626,246,871 - 26,246,991RGDNCBI36
Celera627,368,188 - 27,368,308RGD
Cytogenetic Map6p22.1UniSTS
HuRef626,081,868 - 26,081,988UniSTS
GeneMap99-GB4 RH Map6105.5UniSTS
NCBI RH Map6317.2UniSTS
STS-H58932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37626,138,367 - 26,138,558UniSTSGRCh37
Build 36626,246,346 - 26,246,537RGDNCBI36
Celera627,367,663 - 27,367,854RGD
Cytogenetic Map6p22.1UniSTS
HuRef626,081,343 - 26,081,534UniSTS
GeneMap99-GB4 RH Map6105.76UniSTS
NCBI RH Map6335.4UniSTS
D6S2133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37626,138,982 - 26,139,130UniSTSGRCh37
Build 36626,246,961 - 26,247,109RGDNCBI36
Celera627,368,278 - 27,368,426RGD
Cytogenetic Map6p22.1UniSTS
HuRef626,081,958 - 26,082,106UniSTS
A006T34  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37626,139,082 - 26,139,329UniSTSGRCh37
Build 36626,247,061 - 26,247,308RGDNCBI36
Celera627,368,378 - 27,368,625RGD
Cytogenetic Map6p22.1UniSTS
HuRef626,082,058 - 26,082,305UniSTS
GeneMap99-GB4 RH Map6105.5UniSTS
NCBI RH Map6317.2UniSTS
A008J29  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37626,124,435 - 26,124,699UniSTSGRCh37
Build 36626,232,414 - 26,232,678RGDNCBI36
Celera627,353,699 - 27,353,963RGD
Cytogenetic Map6p22.1UniSTS
HuRef626,067,474 - 26,067,738UniSTS
GeneMap99-GB4 RH Map6105.5UniSTS
UniSTS:486876  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37626,123,702 - 26,124,132UniSTSGRCh37
Build 36626,231,681 - 26,232,111RGDNCBI36
Celera627,352,966 - 27,353,396RGD
HuRef626,066,741 - 26,067,171UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR629hsa-miR-629-5pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248

Predicted Target Of
Summary Value
Count of predictions:843
Count of miRNA genes:449
Interacting mature miRNAs:471
Transcripts:ENST00000314088, ENST00000377791, ENST00000602637
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 5 5 11
Medium 2106 2450 1644 571 1824 448 3722 1784 2751 358 1244 1545 137 1 909 2480 6 2
Low 333 536 82 53 122 17 635 413 983 61 205 68 37 295 308
Below cutoff

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000314088   ⟹   ENSP00000321389
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl626,124,145 - 26,139,116 (+)Ensembl
RefSeq Acc Id: ENST00000377791   ⟹   ENSP00000367022
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl626,124,145 - 26,139,102 (+)Ensembl
RefSeq Acc Id: ENST00000602637   ⟹   ENSP00000473534
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl626,124,203 - 26,139,084 (+)Ensembl
RefSeq Acc Id: NM_003512   ⟹   NP_003503
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38626,124,172 - 26,124,690 (+)NCBI
GRCh37626,124,370 - 26,139,337 (+)NCBI
Build 36626,232,352 - 26,232,897 (+)NCBI Archive
Celera627,353,637 - 27,354,182 (+)RGD
HuRef626,067,412 - 26,067,957 (+)RGD
CHM1_1626,126,610 - 26,127,155 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_003503   ⟸   NM_003512
- UniProtKB: Q93077 (UniProtKB/Swiss-Prot),   A0A024R017 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000367022   ⟸   ENST00000377791
RefSeq Acc Id: ENSP00000473534   ⟸   ENST00000602637
RefSeq Acc Id: ENSP00000321389   ⟸   ENST00000314088
Protein Domains
Histone   Histone_H2A_C

Promoters
RGD ID:6872250
Promoter ID:EPDNEW_H9290
Type:initiation region
Name:HIST1H2AC_1
Description:histone cluster 1 H2A family member c
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38626,124,172 - 26,124,232EPDNEW
RGD ID:6804325
Promoter ID:HG_KWN:52581
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:ENST00000396980,   UC003NGK.2,   UC003NGN.1,   UC003NGO.1,   UC003NGP.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36626,231,281 - 26,233,277 (-)MPROMDB
RGD ID:6812981
Promoter ID:HG_ACW:67744
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Jurkat,   Lymphoblastoid
Transcripts:HIST1H2AC.GAPR07-UNSPLICED
Position:
Human AssemblyChrPosition (strand)Source
Build 36626,234,711 - 26,235,211 (+)MPROMDB

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 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 6p22.2(chr6:25991402-26280693)x3 copy number gain See cases [RCV000139521] Chr6:25991402..26280693 [GRCh38]
Chr6:25991630..26280921 [GRCh37]
Chr6:26099609..26388900 [NCBI36]
Chr6:6p22.2
likely benign
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(chr6:26104332-26365573)x4 copy number gain Ductal breast carcinoma [RCV000207323] Chr6:26104332..26365573 [GRCh37]
Chr6:6p22.2
uncertain significance
GRCh37/hg19 6p22.2(chr6:25839165-26536884)x4 copy number gain See cases [RCV000447433] Chr6:25839165..26536884 [GRCh37]
Chr6:6p22.2
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
GRCh37/hg19 6p22.2(chr6:25851789-26319486)x3 copy number gain not provided [RCV000682656] Chr6:25851789..26319486 [GRCh37]
Chr6:6p22.2
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 6p22.2(chr6:26110314-26338056)x3 copy number gain not provided [RCV000745546] Chr6:26110314..26338056 [GRCh37]
Chr6:6p22.2
benign
GRCh37/hg19 6p22.2(chr6:26110961-26219744)x3 copy number gain not provided [RCV000745547] Chr6:26110961..26219744 [GRCh37]
Chr6:6p22.2
benign
GRCh37/hg19 6p22.2(chr6:26067580-26306202)x3 copy number gain not provided [RCV000849663] Chr6:26067580..26306202 [GRCh37]
Chr6:6p22.2
uncertain significance
GRCh37/hg19 6p22.2(chr6:26067079-26207758)x1 copy number loss not provided [RCV000849592] Chr6:26067079..26207758 [GRCh37]
Chr6:6p22.2
uncertain significance
GRCh37/hg19 6p22.2(chr6:25996066-26303969)x3 copy number gain not provided [RCV000847447] Chr6:25996066..26303969 [GRCh37]
Chr6:6p22.2
uncertain significance
GRCh37/hg19 6p22.2(chr6:25896585-26287389)x4 copy number gain not provided [RCV000845790] Chr6:25896585..26287389 [GRCh37]
Chr6:6p22.2
uncertain significance
GRCh37/hg19 6p22.2(chr6:26046566-26670193)x3 copy number gain not provided [RCV001258882] Chr6:26046566..26670193 [GRCh37]
Chr6:6p22.2
uncertain significance
GRCh37/hg19 6p22.2(chr6:26090243-26265667)x3 copy number gain not provided [RCV001258883] Chr6:26090243..26265667 [GRCh37]
Chr6:6p22.2
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:4733 AgrOrtholog
COSMIC H2AC6 COSMIC
Ensembl Genes ENSG00000180573 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000321389 UniProtKB/Swiss-Prot
  ENSP00000367022 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000473534 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000314088 UniProtKB/Swiss-Prot
  ENST00000377791 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000602637 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.20.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000180573 GTEx
HGNC ID HGNC:4733 ENTREZGENE
Human Proteome Map H2AC6 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:8334 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8334 ENTREZGENE
OMIM 602794 OMIM
Pfam Histone UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Histone_H2A_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA29110 PharmGKB
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 A0A024R017 ENTREZGENE, UniProtKB/TrEMBL
  H2A1C_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary B2R4F7 UniProtKB/Swiss-Prot
  O00775 UniProtKB/Swiss-Prot
  O00776 UniProtKB/Swiss-Prot
  O00777 UniProtKB/Swiss-Prot
  O00778 UniProtKB/Swiss-Prot
  Q540R1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-07-30 H2AC6  H2A clustered histone 6  HIST1H2AC  histone cluster 1 H2A family member c  Symbol and/or name change 5135510 APPROVED
2016-08-23 HIST1H2AC  histone cluster 1 H2A family member c    histone cluster 1, H2ac  Symbol and/or name change 5135510 APPROVED