C2orf81 (chromosome 2 open reading frame 81) - Rat Genome Database

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Gene: C2orf81 (chromosome 2 open reading frame 81) Homo sapiens
Analyze
Symbol: C2orf81
Name: chromosome 2 open reading frame 81
RGD ID: 2298834
HGNC Page HGNC:34350
Description: Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: hCG40743; hypothetical protein LOC388963; uncharacterized protein C2orf81; Uncharacterized protein ENSP00000290390
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
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
GRCh38274,414,177 - 74,421,619 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl274,414,176 - 74,421,619 (-)EnsemblGRCh38hg38GRCh38
GRCh37274,641,304 - 74,648,746 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36274,488,432 - 74,498,442 (-)NCBINCBI36Build 36hg18NCBI36
Celera274,472,492 - 74,476,033 (-)NCBICelera
Cytogenetic Map2p13.1NCBI
HuRef274,377,616 - 74,381,157 (-)NCBIHuRef
CHM1_1274,570,728 - 74,574,269 (-)NCBICHM1_1
T2T-CHM13v2.0274,422,733 - 74,430,176 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
nucleus  (IEA)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Dystonia  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:15815621  


Genomics

Comparative Map Data
C2orf81
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38274,414,177 - 74,421,619 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl274,414,176 - 74,421,619 (-)EnsemblGRCh38hg38GRCh38
GRCh37274,641,304 - 74,648,746 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36274,488,432 - 74,498,442 (-)NCBINCBI36Build 36hg18NCBI36
Celera274,472,492 - 74,476,033 (-)NCBICelera
Cytogenetic Map2p13.1NCBI
HuRef274,377,616 - 74,381,157 (-)NCBIHuRef
CHM1_1274,570,728 - 74,574,269 (-)NCBICHM1_1
T2T-CHM13v2.0274,422,733 - 74,430,176 (-)NCBIT2T-CHM13v2.0
1700003E16Rik
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39683,133,386 - 83,139,957 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl683,133,386 - 83,139,927 (+)EnsemblGRCm39 Ensembl
GRCm38683,156,404 - 83,162,975 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl683,156,404 - 83,162,945 (+)EnsemblGRCm38mm10GRCm38
MGSCv37683,106,398 - 83,112,969 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36683,122,062 - 83,128,624 (+)NCBIMGSCv36mm8
Celera685,139,312 - 85,145,879 (+)NCBICelera
Cytogenetic Map6C3NCBI
cM Map635.94NCBI
C4h2orf81
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr84117,219,357 - 117,225,633 (+)NCBIGRCr8
mRatBN7.24115,661,617 - 115,667,929 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl4115,661,638 - 115,703,815 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx4121,138,401 - 121,144,660 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.04116,913,584 - 116,919,841 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.04115,527,857 - 115,534,088 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.04114,854,449 - 114,860,678 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4114,854,458 - 114,860,677 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04179,443,519 - 179,449,748 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44117,367,724 - 117,373,944 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera4104,655,846 - 104,662,066 (+)NCBICelera
Cytogenetic Map4q34NCBI
C12H2orf81
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21251,967,531 - 51,975,074 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12A51,970,282 - 51,977,826 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02A74,480,820 - 74,488,353 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12A75,986,826 - 75,994,278 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A75,985,181 - 75,990,074 (-)Ensemblpanpan1.1panPan2
C17H2orf81
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11748,704,515 - 48,717,648 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1748,346,155 - 48,359,287 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01749,563,883 - 49,577,012 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1749,568,478 - 49,575,973 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11748,580,923 - 48,594,051 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01748,647,365 - 48,660,521 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01749,205,460 - 49,218,589 (+)NCBIUU_Cfam_GSD_1.0
CUNH2orf81
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440629210,091,638 - 10,096,810 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936556640,884 - 647,053 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936556641,090 - 646,268 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
C3H2orf81
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl368,618,504 - 68,623,410 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1368,618,472 - 68,623,425 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2371,799,668 - 71,804,620 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CUNH2orf81
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11432,856,065 - 32,870,044 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604579,303,969 - 79,314,420 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
CUNH2orf81
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474929,079,003 - 29,086,003 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in C2orf81
3 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2p16.1-11.2(chr2:58279519-83586962)x3 copy number gain See cases [RCV000136053] Chr2:58279519..83586962 [GRCh38]
Chr2:58506654..83814086 [GRCh37]
Chr2:58360158..83667597 [NCBI36]
Chr2:2p16.1-11.2		 pathogenic
GRCh38/hg38 2p16.3-11.2(chr2:47620388-86702722)x3 copy number gain See cases [RCV000137586] Chr2:47620388..86702722 [GRCh38]
Chr2:47847527..86929845 [GRCh37]
Chr2:47701031..86783356 [NCBI36]
Chr2:2p16.3-11.2		 uncertain significance
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3 copy number gain See cases [RCV000141494] Chr2:7495123..87705899 [GRCh38]
Chr2:7635254..88005418 [GRCh37]
Chr2:7552705..87786533 [NCBI36]
Chr2:2p25.1-11.2		 benign
GRCh38/hg38 2p13.1-12(chr2:74375779-75517520)x1 copy number loss See cases [RCV000143456] Chr2:74375779..75517520 [GRCh38]
Chr2:74602906..75744646 [GRCh37]
Chr2:74456414..75598154 [NCBI36]
Chr2:2p13.1-12		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p15-11.2(chr2:62245236-86978895)x3 copy number gain See cases [RCV000448688] Chr2:62245236..86978895 [GRCh37]
Chr2:2p15-11.2		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p13.1-11.2(chr2:74365484-89129064)x1 copy number loss See cases [RCV000510763] Chr2:74365484..89129064 [GRCh37]
Chr2:2p13.1-11.2		 pathogenic
Single allele duplication not provided [RCV000677942] Chr2:63671346..85698002 [GRCh37]
Chr2:2p15-11.2		 pathogenic
GRCh37/hg19 2p13.1-11.2(chr2:74527522-89125488)x1 copy number loss not provided [RCV000682167] Chr2:74527522..89125488 [GRCh37]
Chr2:2p13.1-11.2		 pathogenic
Single allele deletion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NC_000002.11:g.(?_71004499)_(74779761_?)del deletion Dystonic disorder [RCV003113211]|Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency [RCV003113210]|not provided [RCV003107716] Chr2:71004499..74779761 [GRCh37]
Chr2:2p13.3-13.1		 pathogenic|no classifications from unflagged records
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NC_000002.11:g.(?_72359356)_(74779761_?)del deletion MOGS-congenital disorder of glycosylation [RCV003109485]|not provided [RCV003116543] Chr2:72359356..74779761 [GRCh37]
Chr2:2p13.2-13.1		 pathogenic|no classifications from unflagged records
NC_000002.11:g.(?_69240632)_(74779761_?)dup duplication not provided [RCV003122858] Chr2:69240632..74779761 [GRCh37]
Chr2:2p13.3-13.1		 uncertain significance
GRCh37/hg19 2p25.1-q13(chr2:11504318-111365996)x1 copy number loss See cases [RCV002287563] Chr2:11504318..111365996 [GRCh37]
Chr2:2p25.1-q13		 pathogenic
NM_001316764.3(C2orf81):c.145G>A (p.Ala49Thr) single nucleotide variant Inborn genetic diseases [RCV002768174] Chr2:74416115 [GRCh38]
Chr2:74643242 [GRCh37]
Chr2:2p13.1		 uncertain significance
NM_001316764.3(C2orf81):c.1231G>A (p.Gly411Ser) single nucleotide variant Inborn genetic diseases [RCV002988008] Chr2:74414946 [GRCh38]
Chr2:74642073 [GRCh37]
Chr2:2p13.1		 uncertain significance
NM_001316764.3(C2orf81):c.968G>A (p.Gly323Glu) single nucleotide variant Inborn genetic diseases [RCV002964627] Chr2:74415209 [GRCh38]
Chr2:74642336 [GRCh37]
Chr2:2p13.1		 uncertain significance
GRCh37/hg19 2p13.1-12(chr2:73716761-75347894)x1 copy number loss not provided [RCV003223078] Chr2:73716761..75347894 [GRCh37]
Chr2:2p13.1-12		 uncertain significance
GRCh37/hg19 2p13.3-12(chr2:71076472-76368354)x1 copy number loss not specified [RCV003986388] Chr2:71076472..76368354 [GRCh37]
Chr2:2p13.3-12		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1731
Count of miRNA genes:674
Interacting mature miRNAs:785
Transcripts:ENST00000290390, ENST00000517883, ENST00000517896, ENST00000518401, ENST00000518863
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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.

Markers in Region
SHGC-57623  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37274,643,059 - 74,643,212UniSTSGRCh37
Build 36274,496,567 - 74,496,720RGDNCBI36
Celera274,474,248 - 74,474,401RGD
Cytogenetic Map2p13.1UniSTS
HuRef274,379,372 - 74,379,525UniSTS
TNG Radiation Hybrid Map247380.0UniSTS


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
High
Medium 2 2 317 5 31 1 376 2 462 120 31
Low 2212 2564 918 210 1271 49 3313 1319 3197 124 681 1109 161 1177 2051
Below cutoff 2 402 205 198 278 197 707 803 2 1 5 1 27 702

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000290390   ⟹   ENSP00000290390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl274,414,178 - 74,417,717 (-)Ensembl
RefSeq Acc Id: ENST00000612891   ⟹   ENSP00000481409
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl274,414,176 - 74,421,560 (-)Ensembl
RefSeq Acc Id: ENST00000638555   ⟹   ENSP00000492454
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl274,416,017 - 74,418,542 (-)Ensembl
RefSeq Acc Id: ENST00000640331   ⟹   ENSP00000491561
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl274,415,408 - 74,421,591 (-)Ensembl
RefSeq Acc Id: ENST00000640371   ⟹   ENSP00000492786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl274,415,597 - 74,417,717 (-)Ensembl
RefSeq Acc Id: ENST00000640868   ⟹   ENSP00000491941
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl274,414,177 - 74,416,583 (-)Ensembl
RefSeq Acc Id: ENST00000684111   ⟹   ENSP00000507340
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl274,414,177 - 74,421,619 (-)Ensembl
RefSeq Acc Id: NM_001145054   ⟹   NP_001138526
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38274,414,177 - 74,417,717 (-)NCBI
GRCh37274,641,303 - 74,644,934 (-)NCBI
Celera274,472,492 - 74,476,033 (-)RGD
HuRef274,377,616 - 74,381,157 (-)RGD
CHM1_1274,570,728 - 74,574,269 (-)NCBI
T2T-CHM13v2.0274,422,733 - 74,426,274 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001316764   ⟹   NP_001303693
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38274,414,177 - 74,421,619 (-)NCBI
CHM1_1274,570,728 - 74,578,175 (-)NCBI
T2T-CHM13v2.0274,422,733 - 74,430,176 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001316765   ⟹   NP_001303694
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38274,414,177 - 74,421,619 (-)NCBI
CHM1_1274,570,728 - 74,578,175 (-)NCBI
T2T-CHM13v2.0274,422,733 - 74,430,176 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001316766   ⟹   NP_001303695
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38274,414,177 - 74,421,619 (-)NCBI
CHM1_1274,570,728 - 74,578,175 (-)NCBI
T2T-CHM13v2.0274,422,733 - 74,430,176 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_001138526   ⟸   NM_001145054
- Peptide Label: isoform 4
- UniProtKB: A6NN90 (UniProtKB/Swiss-Prot),   A0A087WXZ4 (UniProtKB/Swiss-Prot),   G3XAA6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001303694   ⟸   NM_001316765
- Peptide Label: isoform 2
- UniProtKB: A6NN90 (UniProtKB/Swiss-Prot),   A0A087WXZ4 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001303693   ⟸   NM_001316764
- Peptide Label: isoform 1
- UniProtKB: A6NN90 (UniProtKB/Swiss-Prot),   A0A087WXZ4 (UniProtKB/Swiss-Prot),   A0A804HJ35 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001303695   ⟸   NM_001316766
- Peptide Label: isoform 3
- UniProtKB: A0A1W2PQG2 (UniProtKB/TrEMBL),   E5RJQ4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000492454   ⟸   ENST00000638555
RefSeq Acc Id: ENSP00000481409   ⟸   ENST00000612891
RefSeq Acc Id: ENSP00000491941   ⟸   ENST00000640868
RefSeq Acc Id: ENSP00000491561   ⟸   ENST00000640331
RefSeq Acc Id: ENSP00000492786   ⟸   ENST00000640371
RefSeq Acc Id: ENSP00000290390   ⟸   ENST00000290390
RefSeq Acc Id: ENSP00000507340   ⟸   ENST00000684111

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A6NN90-F1-model_v2 AlphaFold A6NN90 1-582 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:34350 AgrOrtholog
COSMIC C2orf81 COSMIC
Ensembl Genes ENSG00000159239 UniProtKB/TrEMBL
  ENSG00000284308 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000290390 ENTREZGENE
  ENST00000290390.9 UniProtKB/TrEMBL
  ENST00000517883.2 UniProtKB/TrEMBL
  ENST00000612891.4 UniProtKB/Swiss-Prot
  ENST00000638555.1 UniProtKB/TrEMBL
  ENST00000640331.1 UniProtKB/TrEMBL
  ENST00000640371.1 UniProtKB/TrEMBL
  ENST00000640868 ENTREZGENE
  ENST00000640868.1 UniProtKB/TrEMBL
  ENST00000684111 ENTREZGENE
  ENST00000684111.1 UniProtKB/TrEMBL
GTEx ENSG00000159239 GTEx
  ENSG00000284308 GTEx
HGNC ID HGNC:34350 ENTREZGENE
Human Proteome Map C2orf81 Human Proteome Map
InterPro DUF4639 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HMGI/Y_DNA-bd_CS UniProtKB/TrEMBL
KEGG Report hsa:388963 UniProtKB/TrEMBL
NCBI Gene 388963 ENTREZGENE
PANTHER CHROMOSOME A3 C2ORF81 HOMOLOG UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR34438 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DUF4639 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA162379643 PharmGKB
PROSITE HMGI_Y UniProtKB/TrEMBL
UniProt A0A087WXZ4 ENTREZGENE
  A0A1W2PPJ4_HUMAN UniProtKB/TrEMBL
  A0A1W2PQG2 ENTREZGENE, UniProtKB/TrEMBL
  A0A1W2PRV2_HUMAN UniProtKB/TrEMBL
  A0A1W2PSA2_HUMAN UniProtKB/TrEMBL
  A0A804HJ35 ENTREZGENE, UniProtKB/TrEMBL
  A6NN90 ENTREZGENE, UniProtKB/Swiss-Prot
  E5RJQ4 ENTREZGENE, UniProtKB/TrEMBL
  G3XAA6 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary A0A087WXZ4 UniProtKB/Swiss-Prot