UMAD1 (UBAP1-MVB12-associated (UMA) domain containing 1) - Rat Genome Database

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Gene: UMAD1 (UBAP1-MVB12-associated (UMA) domain containing 1) Homo sapiens
Analyze
Symbol: UMAD1
Name: UBAP1-MVB12-associated (UMA) domain containing 1
RGD ID: 7248298
HGNC Page HGNC:48955
Description: INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; aflatoxin B1; aristolochic acid A
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: RPA3 antisense RNA 1; RPA3 opposite strand; RPA3-AS1; RPA3OS; UBAP1-MVB12-associated (UMA)-domain containing protein 1; uncharacterized protein LOC729852
RGD Orthologs
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
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
GRCh3877,640,752 - 7,879,223 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl77,640,711 - 7,968,020 (+)EnsemblGRCh38hg38GRCh38
GRCh3777,680,383 - 7,918,854 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3677,646,946 - 7,885,379 (+)NCBINCBI36Build 36hg18NCBI36
Celera77,648,774 - 7,886,583 (+)NCBICelera
Cytogenetic Map7p21.3NCBI
HuRef77,528,962 - 7,768,166 (+)NCBIHuRef
CHM1_177,680,059 - 7,918,614 (+)NCBICHM1_1
T2T-CHM13v2.077,758,575 - 7,997,716 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v277,727,574 - 7,965,020 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12690205   PMID:16344560   PMID:20448139   PMID:21216879   PMID:21221126   PMID:23251661   PMID:24556642   PMID:26496610   PMID:27609421   PMID:30561431   PMID:32296183   PMID:32393512  
PMID:32737115   PMID:35271311  


Genomics

Comparative Map Data
UMAD1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3877,640,752 - 7,879,223 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl77,640,711 - 7,968,020 (+)EnsemblGRCh38hg38GRCh38
GRCh3777,680,383 - 7,918,854 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3677,646,946 - 7,885,379 (+)NCBINCBI36Build 36hg18NCBI36
Celera77,648,774 - 7,886,583 (+)NCBICelera
Cytogenetic Map7p21.3NCBI
HuRef77,528,962 - 7,768,166 (+)NCBIHuRef
CHM1_177,680,059 - 7,918,614 (+)NCBICHM1_1
T2T-CHM13v2.077,758,575 - 7,997,716 (+)NCBIT2T-CHM13v2.0
CRA_TCAGchr7v277,727,574 - 7,965,020 (+)NCBI
Umad1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3968,259,288 - 8,428,767 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl68,259,288 - 8,459,470 (+)EnsemblGRCm39 Ensembl
GRCm3868,259,288 - 8,428,767 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl68,259,288 - 8,459,470 (+)EnsemblGRCm38mm10GRCm38
MGSCv3768,209,288 - 8,378,767 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3668,209,140 - 8,378,767 (+)NCBIMGSCv36mm8
Celera68,400,980 - 8,571,396 (+)NCBICelera
Cytogenetic Map6A1NCBI
cM Map63.53NCBI
Umad1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543214,753,435 - 14,985,781 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495543214,727,561 - 14,937,479 (+)NCBIChiLan1.0ChiLan1.0
UMAD1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2612,540,164 - 12,779,028 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1760,864,837 - 61,103,744 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v078,365,232 - 8,603,837 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.177,750,269 - 7,954,543 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl77,750,296 - 8,042,663 (+)Ensemblpanpan1.1panPan2
MIOS
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11423,234,618 - 23,464,148 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1423,171,050 - 23,555,257 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1422,809,607 - 23,039,139 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01423,049,136 - 23,279,030 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1423,048,899 - 23,369,693 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11423,201,259 - 23,431,216 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01422,934,228 - 23,170,130 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01423,191,855 - 23,421,537 (+)NCBIUU_Cfam_GSD_1.0
Umad1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511836,596,223 - 36,827,357 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365852,035,591 - 2,216,616 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365852,035,630 - 2,267,059 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
UMAD1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl977,914,963 - 78,216,736 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1977,914,945 - 78,136,269 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
UMAD1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Vero_WHO_p1.0NW_02366604253,816,159 - 54,056,555 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Umad1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248135,285,151 - 5,564,280 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248135,252,295 - 5,509,657 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in UMAD1
11 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NR_034084.1(RPA3OS):n.257-35788C>T single nucleotide variant Lung cancer [RCV000106482] Chr7:7765882 [GRCh38]
Chr7:7805513 [GRCh37]
Chr7:7p21.3		 uncertain significance
NR_034084.1(RPA3OS):n.257-24550G>C single nucleotide variant Lung cancer [RCV000106484] Chr7:7777120 [GRCh38]
Chr7:7816751 [GRCh37]
Chr7:7p21.3		 uncertain significance
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7p22.3-15.2(chr7:54185-26827634)x3 copy number gain See cases [RCV000136557] Chr7:54185..26827634 [GRCh38]
Chr7:54185..26867253 [GRCh37]
Chr7:149268..26833778 [NCBI36]
Chr7:7p22.3-15.2		 pathogenic
GRCh38/hg38 7p22.1-15.2(chr7:5682209-27230311)x3 copy number gain See cases [RCV000136649] Chr7:5682209..27230311 [GRCh38]
Chr7:5721840..27269930 [GRCh37]
Chr7:5688366..27236455 [NCBI36]
Chr7:7p22.1-15.2		 pathogenic
GRCh38/hg38 7p22.1-21.3(chr7:6887830-8054546)x3 copy number gain See cases [RCV000137744] Chr7:6887830..8054546 [GRCh38]
Chr7:6927461..8094176 [GRCh37]
Chr7:6893986..8060701 [NCBI36]
Chr7:7p22.1-21.3		 uncertain significance
GRCh38/hg38 7p22.3-15.3(chr7:45130-25221165)x3 copy number gain See cases [RCV000137824] Chr7:45130..25221165 [GRCh38]
Chr7:45130..25260784 [GRCh37]
Chr7:140213..25227309 [NCBI36]
Chr7:7p22.3-15.3		 pathogenic
GRCh38/hg38 7p22.1-21.3(chr7:6831253-8010127)x3 copy number gain See cases [RCV000138318] Chr7:6831253..8010127 [GRCh38]
Chr7:6870884..8049757 [GRCh37]
Chr7:6837409..8016282 [NCBI36]
Chr7:7p22.1-21.3		 likely benign
GRCh38/hg38 7p21.3(chr7:7815001-8767755)x3 copy number gain See cases [RCV000139667] Chr7:7815001..8767755 [GRCh38]
Chr7:7854632..8807385 [GRCh37]
Chr7:7821157..8773910 [NCBI36]
Chr7:7p21.3		 likely benign
GRCh38/hg38 7p21.3(chr7:7249455-10718595)x3 copy number gain See cases [RCV000139695] Chr7:7249455..10718595 [GRCh38]
Chr7:7289086..10758222 [GRCh37]
Chr7:7255611..10724747 [NCBI36]
Chr7:7p21.3		 likely benign
GRCh38/hg38 7p22.3-15.2(chr7:1698124-27207295)x3 copy number gain See cases [RCV000143060] Chr7:1698124..27207295 [GRCh38]
Chr7:1737760..27246914 [GRCh37]
Chr7:1704286..27213439 [NCBI36]
Chr7:7p22.3-15.2		 pathogenic
GRCh38/hg38 7p22.3-15.2(chr7:43360-27196404)x3 copy number gain See cases [RCV000143586] Chr7:43360..27196404 [GRCh38]
Chr7:43360..27236023 [GRCh37]
Chr7:138443..27202548 [NCBI36]
Chr7:7p22.3-15.2		 pathogenic
GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3 copy number gain See cases [RCV000051159] Chr7:54185..41875885 [GRCh38]
Chr7:54185..41915483 [GRCh37]
Chr7:149268..41882008 [NCBI36]
Chr7:7p22.3-14.1		 pathogenic
GRCh38/hg38 7p22.1-21.3(chr7:6106402-11012657)x1 copy number loss See cases [RCV000050923] Chr7:6106402..11012657 [GRCh38]
Chr7:6146033..11052284 [GRCh37]
Chr7:6112559..11018809 [NCBI36]
Chr7:7p22.1-21.3		 pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3		 pathogenic
GRCh38/hg38 7p22.3-15.3(chr7:53985-24361531)x3 copy number gain See cases [RCV000053528] Chr7:53985..24361531 [GRCh38]
Chr7:53985..24401150 [GRCh37]
Chr7:149068..24367675 [NCBI36]
Chr7:7p22.3-15.3		 pathogenic
GRCh38/hg38 7p22.3-21.3(chr7:54185-8274834)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053529]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053529]|See cases [RCV000053529] Chr7:54185..8274834 [GRCh38]
Chr7:54185..8314464 [GRCh37]
Chr7:149268..8280989 [NCBI36]
Chr7:7p22.3-21.3		 pathogenic
GRCh38/hg38 7p22.3-14.2(chr7:54185-37089712)x3 copy number gain See cases [RCV000053530] Chr7:54185..37089712 [GRCh38]
Chr7:54185..37129317 [GRCh37]
Chr7:149268..37095842 [NCBI36]
Chr7:7p22.3-14.2		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1360
Count of miRNA genes:789
Interacting mature miRNAs:907
Transcripts:ENST00000406829, ENST00000463725, ENST00000468567, ENST00000469183, ENST00000471760, ENST00000482067, ENST00000493246
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.


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
Medium 573 1020 1158 171 647 109 1356 145 1321 279 685 1073 77 1 109 1030 5 2
Low 1866 1937 568 453 1285 356 3001 2037 2411 139 775 540 98 1095 1758 1
Below cutoff 34 19 15 2 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001302348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001302349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001302350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC004948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC007161 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC009473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI565121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236948 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA576342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA678734 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC313244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC340488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC354992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC368552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000406829
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,772,361 - 7,879,223 (+)Ensembl
RefSeq Acc Id: ENST00000463725   ⟹   ENSP00000490879
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,752 - 7,877,443 (+)Ensembl
RefSeq Acc Id: ENST00000471760
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,784 - 7,692,508 (+)Ensembl
RefSeq Acc Id: ENST00000482067   ⟹   ENSP00000490046
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,794 - 7,968,020 (+)Ensembl
RefSeq Acc Id: ENST00000493246
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,711 - 7,738,822 (+)Ensembl
RefSeq Acc Id: ENST00000636849   ⟹   ENSP00000489648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,776 - 7,879,185 (+)Ensembl
RefSeq Acc Id: ENST00000638342   ⟹   ENSP00000491286
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,757 - 7,877,661 (+)Ensembl
RefSeq Acc Id: ENST00000639110   ⟹   ENSP00000491319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,784 - 7,879,205 (+)Ensembl
RefSeq Acc Id: ENST00000639343   ⟹   ENSP00000491077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,784 - 7,879,210 (+)Ensembl
RefSeq Acc Id: ENST00000682710   ⟹   ENSP00000507605
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl77,640,752 - 7,879,223 (+)Ensembl
RefSeq Acc Id: NM_001302348   ⟹   NP_001289277
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3877,640,752 - 7,879,223 (+)NCBI
CHM1_177,679,984 - 7,918,614 (+)NCBI
T2T-CHM13v2.077,758,575 - 7,997,716 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001302349   ⟹   NP_001289278
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3877,640,752 - 7,879,223 (+)NCBI
CHM1_177,679,984 - 7,918,614 (+)NCBI
T2T-CHM13v2.077,758,575 - 7,997,716 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001302350   ⟹   NP_001289279
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3877,640,752 - 7,879,223 (+)NCBI
CHM1_177,679,984 - 7,918,614 (+)NCBI
T2T-CHM13v2.077,758,575 - 7,997,716 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_001289279   ⟸   NM_001302350
- Peptide Label: isoform b
- UniProtKB: C9J7I0 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001289277   ⟸   NM_001302348
- Peptide Label: isoform a
- UniProtKB: C9J7I0 (UniProtKB/Swiss-Prot),   A4D104 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001289278   ⟸   NM_001302349
- Peptide Label: isoform a
- UniProtKB: C9J7I0 (UniProtKB/Swiss-Prot),   A4D104 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000490879   ⟸   ENST00000463725
RefSeq Acc Id: ENSP00000489648   ⟸   ENST00000636849
RefSeq Acc Id: ENSP00000491286   ⟸   ENST00000638342
RefSeq Acc Id: ENSP00000491319   ⟸   ENST00000639110
RefSeq Acc Id: ENSP00000491077   ⟸   ENST00000639343
RefSeq Acc Id: ENSP00000490046   ⟸   ENST00000482067
RefSeq Acc Id: ENSP00000507605   ⟸   ENST00000682710
Protein Domains
UMA

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-C9J7I0-F1-model_v2 AlphaFold C9J7I0 1-137 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:48955 AgrOrtholog
COSMIC UMAD1 COSMIC
Ensembl Genes ENSG00000219545 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000463725.5 UniProtKB/TrEMBL
  ENST00000482067.3 UniProtKB/TrEMBL
  ENST00000636849 ENTREZGENE
  ENST00000636849.1 UniProtKB/Swiss-Prot
  ENST00000638342.1 UniProtKB/TrEMBL
  ENST00000639110.1 UniProtKB/TrEMBL
  ENST00000639343.1 UniProtKB/TrEMBL
  ENST00000682710 ENTREZGENE
  ENST00000682710.1 UniProtKB/Swiss-Prot
GTEx ENSG00000219545 GTEx
HGNC ID HGNC:48955 ENTREZGENE
Human Proteome Map UMAD1 Human Proteome Map
InterPro UMA UniProtKB/Swiss-Prot
KEGG Report hsa:729852 UniProtKB/Swiss-Prot
NCBI Gene RPA3-AS1 ENTREZGENE
PANTHER UBAP1-MVB12-ASSOCIATED (UMA)-DOMAIN CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot
  UBAP1-MVB12-ASSOCIATED (UMA)-DOMAIN CONTAINING PROTEIN 1 UniProtKB/Swiss-Prot
  UBAP1-MVB12-ASSOCIATED (UMA)-DOMAIN CONTAINING PROTEIN 1 UniProtKB/TrEMBL
  UBAP1-MVB12-ASSOCIATED (UMA)-DOMAIN CONTAINING PROTEIN 1 UniProtKB/TrEMBL
PharmGKB PA166123751 PharmGKB
PROSITE UMA UniProtKB/Swiss-Prot
UniProt A0A1B0GUC2_HUMAN UniProtKB/TrEMBL
  A0A1B0GWD2_HUMAN UniProtKB/TrEMBL
  A0A1W2PNU7_HUMAN UniProtKB/TrEMBL
  A0A1W2PP33_HUMAN UniProtKB/TrEMBL
  A4D104 ENTREZGENE
  C9J7I0 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A4D104 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2014-10-15 UMAD1  UBAP1-MVB12-associated (UMA) domain containing 1  RPA3OS  RPA3 opposite strand  Symbol and/or name change 5135510 APPROVED
2014-04-15 RPA3OS  RPA3 opposite strand  RPA3-AS1  RPA3 antisense RNA 1  Symbol and/or name change 5135510 APPROVED