UBALD2 (UBA like domain containing 2) - Rat Genome Database

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Gene: UBALD2 (UBA like domain containing 2) Homo sapiens
Analyze
Symbol: UBALD2
Name: UBA like domain containing 2
RGD ID: 1605547
HGNC Page HGNC:28438
Description: ASSOCIATED WITH genetic disease; INTERACTS WITH (-)-demecolcine; (-)-epigallocatechin 3-gallate; 17beta-estradiol
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FAM100B; family with sequence similarity 100, member B; hypothetical protein LOC283991; MGC29814; MGC71792; UBA-like domain containing 2; UBA-like domain-containing protein 2
RGD Orthologs
Mouse
Rat
Chinchilla
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
GRCh381776,265,348 - 76,271,298 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1776,265,348 - 76,271,298 (+)EnsemblGRCh38hg38GRCh38
GRCh371774,261,429 - 74,267,379 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361771,773,043 - 71,778,970 (+)NCBINCBI36Build 36hg18NCBI36
Celera1770,855,214 - 70,861,308 (+)NCBICelera
Cytogenetic Map17q25.1NCBI
HuRef1769,689,808 - 69,695,885 (+)NCBIHuRef
CHM1_11774,326,185 - 74,332,279 (+)NCBICHM1_1
T2T-CHM13v2.01777,161,904 - 77,167,854 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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:12477932   PMID:15489334   PMID:18976975   PMID:32393512   PMID:32513696   PMID:33961781  


Genomics

Comparative Map Data
UBALD2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381776,265,348 - 76,271,298 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1776,265,348 - 76,271,298 (+)EnsemblGRCh38hg38GRCh38
GRCh371774,261,429 - 74,267,379 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361771,773,043 - 71,778,970 (+)NCBINCBI36Build 36hg18NCBI36
Celera1770,855,214 - 70,861,308 (+)NCBICelera
Cytogenetic Map17q25.1NCBI
HuRef1769,689,808 - 69,695,885 (+)NCBIHuRef
CHM1_11774,326,185 - 74,332,279 (+)NCBICHM1_1
T2T-CHM13v2.01777,161,904 - 77,167,854 (+)NCBIT2T-CHM13v2.0
Ubald2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3911116,324,920 - 116,329,903 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl11116,324,920 - 116,329,903 (+)EnsemblGRCm39 Ensembl
GRCm3811116,434,094 - 116,439,077 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl11116,434,094 - 116,439,077 (+)EnsemblGRCm38mm10GRCm38
MGSCv3711116,295,408 - 116,300,391 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3611116,250,303 - 116,254,633 (+)NCBIMGSCv36mm8
Celera11128,202,339 - 128,207,311 (+)NCBICelera
Cytogenetic Map11E2NCBI
cM Map1181.29NCBI
Ubald2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr810102,161,370 - 102,165,952 (+)NCBIGRCr8
mRatBN7.210101,662,507 - 101,667,089 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl10101,658,127 - 101,667,061 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx10106,718,905 - 106,723,499 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.010106,181,985 - 106,186,579 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.010101,583,402 - 101,587,984 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.010105,392,999 - 105,397,642 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl10105,393,072 - 105,396,863 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.010105,053,919 - 105,059,080 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.410106,543,188 - 106,547,768 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.110106,557,693 - 106,562,272 (+)NCBI
Celera10100,235,164 - 100,240,182 (+)NCBICelera
Cytogenetic Map10q32.1NCBI
Ubald2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555066,015,245 - 6,024,283 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049555066,018,472 - 6,027,133 (-)NCBIChiLan1.0ChiLan1.0
UBALD2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21992,307,977 - 92,314,136 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11797,133,475 - 97,139,345 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01770,213,144 - 70,219,285 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11775,765,980 - 75,771,718 (+)NCBIpanpan1.1PanPan1.1panPan2
UBALD2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.194,411,036 - 4,415,507 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl94,411,882 - 4,412,199 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha95,091,650 - 5,096,974 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.095,081,308 - 5,086,643 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl95,081,160 - 5,087,026 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.195,121,424 - 5,126,757 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.095,230,882 - 5,236,199 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.095,291,042 - 5,296,375 (-)NCBIUU_Cfam_GSD_1.0
Ubald2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244056025,028,954 - 5,047,325 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365941,381,758 - 1,382,133 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365941,378,576 - 1,383,010 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
UBALD2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl125,203,195 - 5,208,679 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1125,203,188 - 5,208,673 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2125,106,927 - 5,112,387 (-)NCBISscrofa10.2Sscrofa10.2susScr3
UBALD2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11645,407,295 - 45,413,700 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1645,408,068 - 45,413,398 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607716,155,027 - 16,161,428 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ubald2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248016,144,982 - 6,150,639 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248016,145,097 - 6,150,066 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in UBALD2
5 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3 copy number gain See cases [RCV000052486] Chr17:69209079..83086677 [GRCh38]
Chr17:67205220..81044553 [GRCh37]
Chr17:64716815..78637842 [NCBI36]
Chr17:17q24.3-25.3		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3 copy number gain See cases [RCV000143342] Chr17:69916435..83102552 [GRCh38]
Chr17:67912576..81048189 [GRCh37]
Chr17:65424171..78653717 [NCBI36]
Chr17:17q24.3-25.3		 pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3 copy number gain See cases [RCV000447539] Chr17:73951701..81041938 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:64241326-81041938)x3 copy number gain See cases [RCV000447577] Chr17:64241326..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3		 pathogenic
GRCh37/hg19 17q25.1-25.2(chr17:73992637-75099218)x4 copy number gain See cases [RCV000510197] Chr17:73992637..75099218 [GRCh37]
Chr17:17q25.1-25.2		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3 copy number gain See cases [RCV000510919] Chr17:73951701..81041938 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3 copy number gain See cases [RCV000512573] Chr17:67002415..81041938 [GRCh37]
Chr17:17q24.2-25.3		 pathogenic
GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3 copy number gain not provided [RCV000683952] Chr17:63689671..81041938 [GRCh37]
Chr17:17q24.1-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3 copy number gain not provided [RCV000762750] Chr17:64159738..74891024 [GRCh37]
Chr17:17q24.1-25.2		 likely pathogenic
GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3 copy number gain not provided [RCV000849900] Chr17:62778720..81041938 [GRCh37]
Chr17:17q24.1-25.3		 pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73261871-78608763)x3 copy number gain not provided [RCV001006919] Chr17:73261871..78608763 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3 copy number gain not provided [RCV002276051] Chr17:73481509..81043199 [GRCh37]
Chr17:17q25.1-25.3		 pathogenic
NM_182565.4(UBALD2):c.202A>T (p.Thr68Ser) single nucleotide variant Inborn genetic diseases [RCV002840442] Chr17:76270212 [GRCh38]
Chr17:74266293 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_182565.4(UBALD2):c.365C>T (p.Ala122Val) single nucleotide variant Inborn genetic diseases [RCV002926435] Chr17:76270375 [GRCh38]
Chr17:74266456 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_182565.4(UBALD2):c.412C>T (p.Arg138Cys) single nucleotide variant Inborn genetic diseases [RCV002955397] Chr17:76270422 [GRCh38]
Chr17:74266503 [GRCh37]
Chr17:17q25.1		 likely benign
NM_182565.4(UBALD2):c.469A>G (p.Met157Val) single nucleotide variant Inborn genetic diseases [RCV003215540] Chr17:76270479 [GRCh38]
Chr17:74266560 [GRCh37]
Chr17:17q25.1		 uncertain significance
NM_182565.4(UBALD2):c.257G>A (p.Arg86His) single nucleotide variant Inborn genetic diseases [RCV003361239] Chr17:76270267 [GRCh38]
Chr17:74266348 [GRCh37]
Chr17:17q25.1		 uncertain significance
GRCh37/hg19 17q25.1(chr17:74056941-74313663)x3 copy number gain not provided [RCV003485165] Chr17:74056941..74313663 [GRCh37]
Chr17:17q25.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1316
Count of miRNA genes:710
Interacting mature miRNAs:851
Transcripts:ENST00000327490, ENST00000587913, ENST00000589240
Prediction methods: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
RH79079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371774,266,970 - 74,267,152UniSTSGRCh37
Build 361771,778,565 - 71,778,747RGDNCBI36
Celera1770,860,899 - 70,861,081RGD
Cytogenetic Map17q25.1UniSTS
HuRef1769,695,490 - 69,695,672UniSTS
GeneMap99-GB4 RH Map17489.29UniSTS
NCBI RH Map17793.9UniSTS
SHGC-64300  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371774,267,172 - 74,267,326UniSTSGRCh37
Build 361771,778,767 - 71,778,921RGDNCBI36
Celera1770,861,101 - 70,861,255RGD
Cytogenetic Map17q25.1UniSTS
HuRef1769,695,692 - 69,695,832UniSTS
TNG Radiation Hybrid Map1733994.0UniSTS


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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 4
Medium 2433 2857 1569 487 1947 329 4344 2087 3576 414 1441 1608 171 1204 2777 4
Low 6 134 157 137 4 136 13 110 158 5 15 5 4 1 11 2 2
Below cutoff

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000327490   ⟹   ENSP00000331298
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1776,265,348 - 76,271,298 (+)Ensembl
RefSeq Acc Id: ENST00000587913   ⟹   ENSP00000468297
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1776,265,371 - 76,270,383 (+)Ensembl
RefSeq Acc Id: ENST00000589240   ⟹   ENSP00000466518
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1776,265,703 - 76,270,586 (+)Ensembl
RefSeq Acc Id: NM_182565   ⟹   NP_872371
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381776,265,348 - 76,271,298 (+)NCBI
GRCh371774,261,286 - 74,267,379 (+)RGD
Build 361771,773,043 - 71,778,970 (+)NCBI Archive
Celera1770,855,214 - 70,861,308 (+)RGD
HuRef1769,689,808 - 69,695,885 (+)ENTREZGENE
CHM1_11774,326,185 - 74,332,279 (+)NCBI
T2T-CHM13v2.01777,161,904 - 77,167,854 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_872371 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH35511 (Get FASTA)   NCBI Sequence Viewer  
  AAH60859 (Get FASTA)   NCBI Sequence Viewer  
  EAW89383 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000331298
  ENSP00000331298.6
  ENSP00000466518.1
  ENSP00000468297.1
GenBank Protein Q8IYN6 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_872371   ⟸   NM_182565
- UniProtKB: Q8IYN6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000468297   ⟸   ENST00000587913
RefSeq Acc Id: ENSP00000466518   ⟸   ENST00000589240
RefSeq Acc Id: ENSP00000331298   ⟸   ENST00000327490

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8IYN6-F1-model_v2 AlphaFold Q8IYN6 1-164 view protein structure

Promoters
RGD ID:6794127
Promoter ID:HG_KWN:27160
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:OTTHUMT00000255920,   UC002JRC.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361771,772,386 - 71,773,097 (+)MPROMDB
RGD ID:7236395
Promoter ID:EPDNEW_H23943
Type:initiation region
Name:UBALD2_2
Description:UBA like domain containing 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23944  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381776,265,202 - 76,265,262EPDNEW
RGD ID:7236397
Promoter ID:EPDNEW_H23944
Type:initiation region
Name:UBALD2_1
Description:UBA like domain containing 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23943  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381776,265,353 - 76,265,413EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28438 AgrOrtholog
COSMIC UBALD2 COSMIC
Ensembl Genes ENSG00000185262 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000327490 ENTREZGENE
  ENST00000327490.8 UniProtKB/Swiss-Prot
  ENST00000587913.1 UniProtKB/TrEMBL
  ENST00000589240.1 UniProtKB/TrEMBL
Gene3D-CATH DNA helicase RuvA subunit, C-terminal domain UniProtKB/Swiss-Prot
GTEx ENSG00000185262 GTEx
HGNC ID HGNC:28438 ENTREZGENE
Human Proteome Map UBALD2 Human Proteome Map
InterPro UBA-like_sf UniProtKB/Swiss-Prot
  UBALD1/2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:283991 UniProtKB/Swiss-Prot
NCBI Gene 283991 ENTREZGENE
PANTHER PTHR31993 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  UBA-LIKE DOMAIN-CONTAINING PROTEIN 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam UBA_4 UniProtKB/Swiss-Prot
PharmGKB PA142671783 PharmGKB
Superfamily-SCOP SSF46934 UniProtKB/Swiss-Prot
UniProt K7EMI7_HUMAN UniProtKB/TrEMBL
  K7ERK7_HUMAN UniProtKB/TrEMBL
  Q8IYN6 ENTREZGENE, UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-02 UBALD2  UBA like domain containing 2    UBA-like domain containing 2  Symbol and/or name change 5135510 APPROVED
2012-12-04 UBALD2  UBA-like domain containing 2  FAM100B  family with sequence similarity 100, member B  Symbol and/or name change 5135510 APPROVED