URB1 (URB1 ribosome biogenesis homolog) - Rat Genome Database

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Gene: URB1 (URB1 ribosome biogenesis homolog) Homo sapiens
Analyze
Symbol: URB1
Name: URB1 ribosome biogenesis homolog
RGD ID: 1353651
HGNC Page HGNC:17344
Description: Enables RNA binding activity. Predicted to be involved in maturation of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) and maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA). Located in fibrillar center.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C21orf108; KIAA0539; NPA1; nucleolar pre-ribosomal-associated protein 1; nucleolar preribosomal-associated protein 1; nucleolar protein 254 kDa; URB1 ribosome biogenesis 1 homolog; URB1 ribosome biogenesis 1 homolog (S. cerevisiae)
RGD Orthologs
Mouse
Rat
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
GRCh382132,311,018 - 32,393,012 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2132,311,018 - 32,393,012 (-)EnsemblGRCh38hg38GRCh38
GRCh372133,683,329 - 33,765,321 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,683,330 - 33,765,312 (-)NCBINCBI36Build 36hg18NCBI36
Celera2118,866,931 - 18,948,939 (-)NCBICelera
Cytogenetic Map21q22.11NCBI
HuRef2119,092,100 - 19,174,182 (-)NCBIHuRef
CHM1_12133,245,146 - 33,327,161 (-)NCBICHM1_1
T2T-CHM13v2.02130,680,775 - 30,762,860 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


1 to 10 of 10 rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
URB1Humanamyotrophic lateral sclerosis type 1  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 1ClinVarPMID:17237124 more ...
URB1Humanautosomal dominant intellectual developmental disorder 7  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: DYRK1A-related intellectual disability syndromeClinVarPMID:17237124 more ...
URB1HumanFamilial Platelet Disorder with Associated Myeloid Malignancy  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1ClinVarPMID:17237124 more ...
URB1Humangenetic disease  IAGP (Homo sapiens) more ...8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVar 
URB1HumanGlucocorticoid Deficiency 2  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Glucocorticoid deficiency 2ClinVarPMID:25741868
URB1HumanGlucocorticoid Deficiency 2  IAGP (Homo sapiens) and (Homo sapiens)8554872ClinVar Annotator: match by term: Glucocorticoid deficiency 2ClinVarPMID:25741868 and PMID:28492532
URB1HumanGlucocorticoid Deficiency 2  IAGP (Homo sapiens) more ...8554872ClinVar more ...ClinVar 
URB1Humanimmunodeficiency 28  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Immunodeficiency 28ClinVarPMID:17237124 more ...
URB1HumanParkinson's disease 20  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Early-onset Parkinson disease 20ClinVarPMID:28492532
URB1HumanZTTK syndrome  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: ZTTK syndromeClinVarPMID:25741868
1 to 10 of 10 rows

1 to 20 of 55 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
URB1Human(+)-schisandrin B multiple interactionsISOUrb1 (Rattus norvegicus)6480464schizandrin B inhibits the reaction [Carbon Tetrachloride results in increased expression of URB1 mRNA]CTDPMID:31150632
URB1Human1,2,4-trichloro-5-(2,5-dichlorophenyl)benzene multiple interactionsISOUrb1 (Mus musculus)6480464[2 more ...CTDPMID:25510870
URB1Human1,2-dichloroethane decreases expressionISOUrb1 (Mus musculus)6480464ethylene dichloride results in decreased expression of URB1 mRNACTDPMID:28960355
URB1Human1-chloro-2,4-dinitrobenzene affects bindingEXP 6480464Dinitrochlorobenzene binds to URB1 proteinCTDPMID:32991956
URB1Human17beta-estradiol increases expressionEXP 6480464Estradiol results in increased expression of URB1 mRNACTDPMID:23019147 and PMID:31614463
URB1Human2,2',4,4',5,5'-hexachlorobiphenyl multiple interactionsISOUrb1 (Mus musculus)6480464[2 more ...CTDPMID:25510870
URB1Human2,2',5,5'-tetrachlorobiphenyl multiple interactionsISOUrb1 (Mus musculus)6480464[2 more ...CTDPMID:25510870
URB1Human2,4,4'-trichlorobiphenyl multiple interactionsISOUrb1 (Mus musculus)6480464[2 more ...CTDPMID:25510870
URB1Human3-isobutyl-1-methyl-7H-xanthine multiple interactionsEXP 6480464[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol A] results in decreased expression of URB1 mRNA more ...CTDPMID:28628672
URB1Human4,4'-sulfonyldiphenol multiple interactionsEXP 6480464[INS protein co-treated with Dexamethasone co-treated with 1-Methyl-3-isobutylxanthine co-treated with Indomethacin co-treated with bisphenol S] results in decreased expression of URB1 mRNACTDPMID:28628672
URB1Human4,4'-sulfonyldiphenol increases methylationEXP 6480464bisphenol S results in increased methylation of URB1 geneCTDPMID:31601247
URB1Humanaflatoxin B1 increases methylationEXP 6480464Aflatoxin B1 results in increased methylation of URB1 geneCTDPMID:27153756
URB1Humanaflatoxin B1 decreases methylationEXP 6480464Aflatoxin B1 results in decreased methylation of URB1 exonCTDPMID:30157460
URB1Humanall-trans-retinoic acid decreases expressionEXP 6480464Tretinoin results in decreased expression of URB1 mRNACTDPMID:33167477
URB1Humanamphetamine decreases expressionISOUrb1 (Rattus norvegicus)6480464Amphetamine results in decreased expression of URB1 mRNACTDPMID:30779732
URB1Humanaristolochic acid A increases expressionEXP 6480464aristolochic acid I results in increased expression of URB1 mRNACTDPMID:33212167
URB1Humanarsenite(3-) decreases expressionISOUrb1 (Mus musculus)6480464arsenite results in decreased expression of URB1 proteinCTDPMID:37955338
URB1Humanbenzo[a]pyrene increases methylationEXP 6480464Benzo(a)pyrene results in increased methylation of URB1 3' UTRCTDPMID:27901495
URB1Humanbenzo[e]pyrene decreases methylationEXP 6480464benzo(e)pyrene results in decreased methylation of URB1 exonCTDPMID:30157460
URB1Humanbis(2-ethylhexyl) phthalate increases expressionISOUrb1 (Mus musculus)6480464Diethylhexyl Phthalate results in increased expression of URB1 mRNACTDPMID:34319233

1 to 20 of 55 rows

Biological Process

  

Cellular Component

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
URB1Humanfibrillar center located_inIDA 150520179 HPAGO_REF:0000052
URB1Humannucleolus located_inIEAUniProtKB-SubCell:SL-0188150520179 UniProtGO_REF:0000044
URB1Humannucleolus located_inIDA 150520179 PMID:16963496UniProtPMID:16963496
URB1Humannucleolus located_inNAS 150520179 PMID:12429849UniProtPMID:12429849
URB1Humannucleolus is_active_inIBAPANTHER:PTN000337405 more ...150520179 GO_CentralGO_REF:0000033
URB1Humannucleus located_inIEAUniProtKB-KW:KW-0539150520179 UniProtGO_REF:0000043

Molecular Function

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
URB1HumanRNA binding enablesHDA 150520179 PMID:22658674 and PMID:22681889UniProtPMID:22658674 and PMID:22681889


#
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
PMID:9628581   PMID:10773462   PMID:12168954   PMID:12429849   PMID:12477932   PMID:14637006   PMID:15226434   PMID:16963496   PMID:17081983   PMID:17474147   PMID:18029348   PMID:20360068  
PMID:21873635   PMID:21900206   PMID:22586326   PMID:22658674   PMID:22681889   PMID:24639526   PMID:24711643   PMID:25665578   PMID:25693804   PMID:26186194   PMID:26496610   PMID:27609421  
PMID:28514442   PMID:29246861   PMID:29467282   PMID:29478914   PMID:29507755   PMID:29509190   PMID:29568061   PMID:29676528   PMID:29991511   PMID:30804502   PMID:30833792   PMID:30948266  
PMID:31073040   PMID:31527615   PMID:31586073   PMID:31886628   PMID:31995728   PMID:32707033   PMID:32838362   PMID:32888357   PMID:33060197   PMID:33766124   PMID:33957083   PMID:33961781  
PMID:34079125   PMID:34091597   PMID:34186245   PMID:34349018   PMID:34373451   PMID:35384245   PMID:35748872   PMID:35850772   PMID:35915203   PMID:36215168   PMID:36232890   PMID:36424410  
PMID:36912080   PMID:37054706   PMID:37167062   PMID:37317656   PMID:37689310   PMID:37723588   PMID:37827155   PMID:39501047  



URB1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382132,311,018 - 32,393,012 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2132,311,018 - 32,393,012 (-)EnsemblGRCh38hg38GRCh38
GRCh372133,683,329 - 33,765,321 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362133,683,330 - 33,765,312 (-)NCBINCBI36Build 36hg18NCBI36
Celera2118,866,931 - 18,948,939 (-)NCBICelera
Cytogenetic Map21q22.11NCBI
HuRef2119,092,100 - 19,174,182 (-)NCBIHuRef
CHM1_12133,245,146 - 33,327,161 (-)NCBICHM1_1
T2T-CHM13v2.02130,680,775 - 30,762,860 (-)NCBIT2T-CHM13v2.0
Urb1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391690,548,415 - 90,607,312 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1690,548,415 - 90,607,301 (-)EnsemblGRCm39 Ensembl
GRCm381690,751,527 - 90,810,467 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1690,751,527 - 90,810,413 (-)EnsemblGRCm38mm10GRCm38
MGSCv371690,751,772 - 90,810,658 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361690,640,386 - 90,699,251 (-)NCBIMGSCv36mm8
Celera1691,832,957 - 91,891,665 (-)NCBICelera
Cytogenetic Map16C3.3NCBI
cM Map1651.92NCBI
Urb1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81143,490,633 - 43,551,398 (-)NCBIGRCr8
mRatBN7.21130,004,539 - 30,065,315 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1130,004,539 - 30,065,363 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1138,690,104 - 38,750,824 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01131,361,515 - 31,422,227 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01130,536,196 - 30,596,923 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01130,916,740 - 30,977,423 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1130,916,730 - 30,977,483 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01134,528,215 - 34,588,898 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41130,732,790 - 30,793,473 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11130,738,941 - 30,818,441 (-)NCBI
Celera1129,672,337 - 29,733,034 (-)NCBICelera
Cytogenetic Map11q11NCBI
Urb1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495540731,848,012 - 31,915,362 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495540731,849,103 - 31,915,457 (-)NCBIChiLan1.0ChiLan1.0
URB1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22228,388,428 - 28,513,989 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12123,248,051 - 23,375,791 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02118,637,996 - 18,761,045 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12132,028,801 - 32,141,275 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2132,061,966 - 32,141,275 (-)Ensemblpanpan1.1panPan2
URB1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13127,087,196 - 27,158,144 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3127,087,570 - 27,158,164 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3127,080,534 - 27,151,483 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.03127,207,657 - 27,278,618 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl3127,207,735 - 27,278,625 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.13127,152,622 - 27,223,569 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.03127,164,342 - 27,235,271 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.03127,672,375 - 27,742,811 (-)NCBIUU_Cfam_GSD_1.0
Urb1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440497127,679,168 - 27,748,856 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365009,718,925 - 9,788,666 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365009,718,981 - 9,790,094 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
URB1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13195,974,790 - 196,047,863 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113195,974,790 - 196,047,882 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
URB1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1259,733,260 - 59,811,990 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl259,733,902 - 59,814,018 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660712,275,305 - 2,354,903 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Urb1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474520,648,230 - 20,715,549 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474520,647,661 - 20,716,262 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in URB1
270 total Variants

1 to 10 of 349 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000050445] Chr21:7749532..46670405 [GRCh38]
Chr21:15499847..48090317 [GRCh37]
Chr21:14421718..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic|conflicting interpretations of pathogenicity|conflicting data from submitters
GRCh38/hg38 21q22.11(chr21:31339386-32311519)x1 copy number loss See cases [RCV000052805] Chr21:31339386..32311519 [GRCh38]
Chr21:32711701..33683830 [GRCh37]
Chr21:31633572..32605701 [NCBI36]
Chr21:21q22.11
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053042] Chr21:7749532..46623792 [GRCh38]
Chr21:14595524..48043704 [GRCh37]
Chr21:13517395..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46653090)x3 copy number gain See cases [RCV000053040] Chr21:7749532..46653090 [GRCh38]
Chr21:14539679..48073002 [GRCh37]
Chr21:13461550..46897430 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053043] Chr21:7749532..46623792 [GRCh38]
Chr21:14629063..48043704 [GRCh37]
Chr21:13550934..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670546)x3 copy number gain See cases [RCV000053045] Chr21:7749532..46670546 [GRCh38]
Chr21:15499647..48090458 [GRCh37]
Chr21:14421518..46914886 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053065] Chr21:7749532..46661140 [GRCh38]
Chr21:15499647..48081052 [GRCh37]
Chr21:14421518..46905480 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46661140)x3 copy number gain See cases [RCV000053067] Chr21:7749532..46661140 [GRCh38]
Chr21:15499847..48081052 [GRCh37]
Chr21:14421718..46905480 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46670405)x3 copy number gain See cases [RCV000053068] Chr21:7749532..46670405 [GRCh38]
Chr21:20655360..48090317 [GRCh37]
Chr21:19577231..46914745 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
GRCh38/hg38 21p11.2-q22.3(chr21:7749532-46623792)x3 copy number gain See cases [RCV000053039] Chr21:7749532..46623792 [GRCh38]
Chr21:14524963..48043704 [GRCh37]
Chr21:13446834..46868132 [NCBI36]
Chr21:21p11.2-q22.3
pathogenic
1 to 10 of 349 rows

Predicted Target Of
Summary Value
Count of predictions:2178
Count of miRNA genes:1091
Interacting mature miRNAs:1331
Transcripts:ENST00000382751, ENST00000480196, ENST00000492603
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.


The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
597189800GWAS1285874_Hfree androgen index QTL GWAS1285874 (human)4e-14free androgen index213237832332378324Human
597607405GWAS1664265_Hsquamous cell carcinoma QTL GWAS1664265 (human)6e-12squamous cell carcinoma213235330632353307Human
597107283GWAS1203357_Htestosterone measurement QTL GWAS1203357 (human)2e-13testosterone measurementserum testosterone level (CMO:0000568)213237832332378324Human
597190350GWAS1286424_Htestosterone measurement QTL GWAS1286424 (human)1e-16testosterone measurementserum testosterone level (CMO:0000568)213237832332378324Human
597095614GWAS1191688_Htestosterone measurement QTL GWAS1191688 (human)3e-20testosterone measurementserum testosterone level (CMO:0000568)213237832332378324Human
2303081MAMTS49_HMammary tumor susceptibility QTL 49 (human)1.72Mammary tumor susceptibility211795044843950448Human
597152699GWAS1248773_Hlifestyle measurement, anxiety disorder measurement QTL GWAS1248773 (human)2e-10anxiety-related behavior trait (VT:0010716)213231719732317198Human
597096633GWAS1192707_Htestosterone measurement QTL GWAS1192707 (human)4e-31testosterone measurementserum testosterone level (CMO:0000568)213237832332378324Human

SHGC-87585  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,685,879 - 33,686,005UniSTSGRCh37
Build 362132,607,750 - 32,607,876RGDNCBI36
Celera2118,869,480 - 18,869,606RGD
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map21q22.1UniSTS
HuRef2119,094,649 - 19,094,775UniSTS
TNG Radiation Hybrid Map2110773.0UniSTS
GeneMap99-GB4 RH Map21164.65UniSTS
NCBI RH Map21227.0UniSTS
D21S314  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,698,602 - 33,698,777UniSTSGRCh37
GRCh372133,698,605 - 33,698,912UniSTSGRCh37
Build 362132,620,476 - 32,620,783RGDNCBI36
Celera2118,882,206 - 18,882,513RGD
Celera2118,882,203 - 18,882,378UniSTS
Cytogenetic Map21q22.11UniSTS
HuRef2119,107,373 - 19,107,548UniSTS
HuRef2119,107,376 - 19,107,683UniSTS
TNG Radiation Hybrid Map2110764.0UniSTS
Stanford-G3 RH Map21742.0UniSTS
ECD00639  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,764,399 - 33,765,295UniSTSGRCh37
Build 362132,686,270 - 32,687,166RGDNCBI36
Celera2118,948,026 - 18,948,922RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,173,269 - 19,174,165UniSTS
ECD04303  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,750,289 - 33,751,057UniSTSGRCh37
Build 362132,672,160 - 32,672,928RGDNCBI36
Celera2118,933,915 - 18,934,683RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,159,158 - 19,159,926UniSTS
ECD05309  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,749,509 - 33,750,248UniSTSGRCh37
Build 362132,671,380 - 32,672,119RGDNCBI36
Celera2118,933,135 - 18,933,874RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,158,378 - 19,159,117UniSTS
ECD05563  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,747,223 - 33,747,955UniSTSGRCh37
Build 362132,669,094 - 32,669,826RGDNCBI36
Celera2118,930,849 - 18,931,581RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,156,093 - 19,156,825UniSTS
ECD05936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,751,152 - 33,751,874UniSTSGRCh37
Build 362132,673,023 - 32,673,745RGDNCBI36
Celera2118,934,778 - 18,935,500RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,160,021 - 19,160,743UniSTS
ECD06160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,757,396 - 33,758,112UniSTSGRCh37
Build 362132,679,267 - 32,679,983RGDNCBI36
Celera2118,941,022 - 18,941,738RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,166,265 - 19,166,981UniSTS
ECD06936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,755,556 - 33,756,251UniSTSGRCh37
Build 362132,677,427 - 32,678,122RGDNCBI36
Celera2118,939,182 - 18,939,877RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,164,425 - 19,165,120UniSTS
ECD07444  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,753,084 - 33,753,765UniSTSGRCh37
Build 362132,674,955 - 32,675,636RGDNCBI36
Celera2118,936,710 - 18,937,391RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,161,953 - 19,162,634UniSTS
ECD07600  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,850 - 33,755,527UniSTSGRCh37
Build 362132,676,721 - 32,677,398RGDNCBI36
Celera2118,938,476 - 18,939,153RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,163,719 - 19,164,396UniSTS
ECD08047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,158 - 33,754,823UniSTSGRCh37
Build 362132,676,029 - 32,676,694RGDNCBI36
Celera2118,937,784 - 18,938,449RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,163,027 - 19,163,692UniSTS
ECD08266  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,752,408 - 33,753,067UniSTSGRCh37
Build 362132,674,279 - 32,674,938RGDNCBI36
Celera2118,936,034 - 18,936,693RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,161,277 - 19,161,936UniSTS
ECD10199  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,765,499 - 33,766,107UniSTSGRCh37
Build 362132,687,370 - 32,687,978RGDNCBI36
Celera2118,949,126 - 18,949,734RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,174,369 - 19,174,977UniSTS
ECD10568  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,766,165 - 33,766,763UniSTSGRCh37
Build 362132,688,036 - 32,688,634RGDNCBI36
Celera2118,949,792 - 18,950,390RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,175,035 - 19,175,633UniSTS
ECD10886  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,756,393 - 33,756,981UniSTSGRCh37
Build 362132,678,264 - 32,678,852RGDNCBI36
Celera2118,940,019 - 18,940,607RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,165,262 - 19,165,850UniSTS
ECD18015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,217 - 33,759,593UniSTSGRCh37
Build 362132,681,088 - 32,681,464RGDNCBI36
Celera2118,942,843 - 18,943,219RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,168,086 - 19,168,462UniSTS
ECD18144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,748,318 - 33,748,689UniSTSGRCh37
Build 362132,670,189 - 32,670,560RGDNCBI36
Celera2118,931,944 - 18,932,315RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,157,188 - 19,157,559UniSTS
ECD19328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,754 - 33,760,079UniSTSGRCh37
Build 362132,681,625 - 32,681,950RGDNCBI36
Celera2118,943,380 - 18,943,706RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,168,623 - 19,168,949UniSTS
ECD19944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,762,351 - 33,762,654UniSTSGRCh37
Build 362132,684,222 - 32,684,525RGDNCBI36
Celera2118,945,978 - 18,946,281RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,171,221 - 19,171,524UniSTS
ECD20271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,760,858 - 33,761,148UniSTSGRCh37
Build 362132,682,729 - 32,683,019RGDNCBI36
Celera2118,944,485 - 18,944,775RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,169,728 - 19,170,018UniSTS
ECD21182  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,766,974 - 33,767,232UniSTSGRCh37
Build 362132,688,845 - 32,689,103RGDNCBI36
Celera2118,950,601 - 18,950,859RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,175,844 - 19,176,102UniSTS
SHGC-57897  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,765,948 - 33,766,071UniSTSGRCh37
Build 362132,687,819 - 32,687,942RGDNCBI36
Celera2118,949,575 - 18,949,698RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,174,818 - 19,174,941UniSTS
TNG Radiation Hybrid Map2110807.0UniSTS
REN80729  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,746,183 - 33,746,410UniSTSGRCh37
Build 362132,668,054 - 32,668,281RGDNCBI36
Celera2118,929,809 - 18,930,036RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,155,053 - 19,155,280UniSTS
REN80730  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,746,401 - 33,746,663UniSTSGRCh37
Build 362132,668,272 - 32,668,534RGDNCBI36
Celera2118,930,027 - 18,930,289RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,155,271 - 19,155,533UniSTS
REN80731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,746,640 - 33,746,866UniSTSGRCh37
Build 362132,668,511 - 32,668,737RGDNCBI36
Celera2118,930,266 - 18,930,492RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,155,510 - 19,155,736UniSTS
REN80732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,746,855 - 33,747,103UniSTSGRCh37
Build 362132,668,726 - 32,668,974RGDNCBI36
Celera2118,930,481 - 18,930,729RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,155,725 - 19,155,973UniSTS
REN80733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,747,099 - 33,747,354UniSTSGRCh37
Build 362132,668,970 - 32,669,225RGDNCBI36
Celera2118,930,725 - 18,930,980RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,155,969 - 19,156,224UniSTS
REN80734  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,747,343 - 33,747,585UniSTSGRCh37
Build 362132,669,214 - 32,669,456RGDNCBI36
Celera2118,930,969 - 18,931,211RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,156,213 - 19,156,455UniSTS
REN80735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,747,576 - 33,747,800UniSTSGRCh37
Build 362132,669,447 - 32,669,671RGDNCBI36
Celera2118,931,202 - 18,931,426RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,156,446 - 19,156,670UniSTS
REN80736  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,747,774 - 33,748,017UniSTSGRCh37
Build 362132,669,645 - 32,669,888RGDNCBI36
Celera2118,931,400 - 18,931,643RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,156,644 - 19,156,887UniSTS
REN80737  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,747,959 - 33,748,201UniSTSGRCh37
Build 362132,669,830 - 32,670,072RGDNCBI36
Celera2118,931,585 - 18,931,827RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,156,829 - 19,157,071UniSTS
REN80738  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,748,177 - 33,748,447UniSTSGRCh37
Build 362132,670,048 - 32,670,318RGDNCBI36
Celera2118,931,803 - 18,932,073RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,157,047 - 19,157,317UniSTS
REN80739  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,748,419 - 33,748,665UniSTSGRCh37
Build 362132,670,290 - 32,670,536RGDNCBI36
Celera2118,932,045 - 18,932,291RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,157,289 - 19,157,535UniSTS
REN80740  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,748,642 - 33,748,866UniSTSGRCh37
Build 362132,670,513 - 32,670,737RGDNCBI36
Celera2118,932,268 - 18,932,492RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,157,512 - 19,157,736UniSTS
REN80741  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,748,836 - 33,749,101UniSTSGRCh37
Build 362132,670,707 - 32,670,972RGDNCBI36
Celera2118,932,462 - 18,932,727RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,157,706 - 19,157,966UniSTS
REN80742  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,749,100 - 33,749,351UniSTSGRCh37
Build 362132,670,971 - 32,671,222RGDNCBI36
Celera2118,932,726 - 18,932,977RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,157,965 - 19,158,220UniSTS
REN80743  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,749,343 - 33,749,596UniSTSGRCh37
Build 362132,671,214 - 32,671,467RGDNCBI36
Celera2118,932,969 - 18,933,222RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,158,212 - 19,158,465UniSTS
REN80744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,749,575 - 33,749,836UniSTSGRCh37
Build 362132,671,446 - 32,671,707RGDNCBI36
Celera2118,933,201 - 18,933,462RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,158,444 - 19,158,705UniSTS
REN80745  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,749,813 - 33,750,074UniSTSGRCh37
Build 362132,671,684 - 32,671,945RGDNCBI36
Celera2118,933,439 - 18,933,700RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,158,682 - 19,158,943UniSTS
REN80746  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,750,051 - 33,750,276UniSTSGRCh37
Build 362132,671,922 - 32,672,147RGDNCBI36
Celera2118,933,677 - 18,933,902RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,158,920 - 19,159,145UniSTS
REN80747  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,750,254 - 33,750,511UniSTSGRCh37
Build 362132,672,125 - 32,672,382RGDNCBI36
Celera2118,933,880 - 18,934,137RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,159,123 - 19,159,380UniSTS
REN80748  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,750,488 - 33,750,733UniSTSGRCh37
Build 362132,672,359 - 32,672,604RGDNCBI36
Celera2118,934,114 - 18,934,359RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,159,357 - 19,159,602UniSTS
REN80749  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,750,710 - 33,750,959UniSTSGRCh37
Build 362132,672,581 - 32,672,830RGDNCBI36
Celera2118,934,336 - 18,934,585RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,159,579 - 19,159,828UniSTS
REN80750  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,750,935 - 33,751,197UniSTSGRCh37
Build 362132,672,806 - 32,673,068RGDNCBI36
Celera2118,934,561 - 18,934,823RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,159,804 - 19,160,066UniSTS
REN80751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,751,182 - 33,751,426UniSTSGRCh37
Build 362132,673,053 - 32,673,297RGDNCBI36
Celera2118,934,808 - 18,935,052RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,160,051 - 19,160,295UniSTS
REN80752  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,751,416 - 33,751,675UniSTSGRCh37
Build 362132,673,287 - 32,673,546RGDNCBI36
Celera2118,935,042 - 18,935,301RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,160,285 - 19,160,544UniSTS
REN80753  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,751,652 - 33,751,884UniSTSGRCh37
Build 362132,673,523 - 32,673,755RGDNCBI36
Celera2118,935,278 - 18,935,510RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,160,521 - 19,160,753UniSTS
REN80754  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,751,754 - 33,751,995UniSTSGRCh37
Build 362132,673,625 - 32,673,866RGDNCBI36
Celera2118,935,380 - 18,935,621RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,160,623 - 19,160,864UniSTS
REN80755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,752,185 - 33,752,420UniSTSGRCh37
Build 362132,674,056 - 32,674,291RGDNCBI36
Celera2118,935,811 - 18,936,046RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,161,054 - 19,161,289UniSTS
REN80756  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,752,409 - 33,752,659UniSTSGRCh37
Build 362132,674,280 - 32,674,530RGDNCBI36
Celera2118,936,035 - 18,936,285RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,161,278 - 19,161,528UniSTS
REN80757  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,752,608 - 33,752,868UniSTSGRCh37
Build 362132,674,479 - 32,674,739RGDNCBI36
Celera2118,936,234 - 18,936,494RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,161,477 - 19,161,737UniSTS
REN80758  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,752,845 - 33,753,104UniSTSGRCh37
Build 362132,674,716 - 32,674,975RGDNCBI36
Celera2118,936,471 - 18,936,730RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,161,714 - 19,161,973UniSTS
REN80759  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,753,081 - 33,753,332UniSTSGRCh37
Build 362132,674,952 - 32,675,203RGDNCBI36
Celera2118,936,707 - 18,936,958RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,161,950 - 19,162,201UniSTS
REN80760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,753,315 - 33,753,564UniSTSGRCh37
Build 362132,675,186 - 32,675,435RGDNCBI36
Celera2118,936,941 - 18,937,190RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,162,184 - 19,162,433UniSTS
REN80761  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,753,539 - 33,753,784UniSTSGRCh37
Build 362132,675,410 - 32,675,655RGDNCBI36
Celera2118,937,165 - 18,937,410RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,162,408 - 19,162,653UniSTS
REN80762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,753,754 - 33,754,006UniSTSGRCh37
Build 362132,675,625 - 32,675,877RGDNCBI36
Celera2118,937,380 - 18,937,632RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,162,623 - 19,162,875UniSTS
REN80763  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,000 - 33,754,247UniSTSGRCh37
Build 362132,675,871 - 32,676,118RGDNCBI36
Celera2118,937,626 - 18,937,873RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,162,869 - 19,163,116UniSTS
REN80764  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,221 - 33,754,458UniSTSGRCh37
Build 362132,676,092 - 32,676,329RGDNCBI36
Celera2118,937,847 - 18,938,084RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,163,090 - 19,163,327UniSTS
REN80765  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,435 - 33,754,665UniSTSGRCh37
Build 362132,676,306 - 32,676,536RGDNCBI36
Celera2118,938,061 - 18,938,291RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,163,304 - 19,163,534UniSTS
REN80766  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,645 - 33,754,910UniSTSGRCh37
Build 362132,676,516 - 32,676,781RGDNCBI36
Celera2118,938,271 - 18,938,536RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,163,514 - 19,163,779UniSTS
REN80767  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,854 - 33,755,105UniSTSGRCh37
Build 362132,676,725 - 32,676,976RGDNCBI36
Celera2118,938,480 - 18,938,731RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,163,723 - 19,163,974UniSTS
REN80768  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,755,091 - 33,755,335UniSTSGRCh37
Build 362132,676,962 - 32,677,206RGDNCBI36
Celera2118,938,717 - 18,938,961RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,163,960 - 19,164,204UniSTS
REN80769  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,755,321 - 33,755,584UniSTSGRCh37
Build 362132,677,192 - 32,677,455RGDNCBI36
Celera2118,938,947 - 18,939,210RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,164,190 - 19,164,453UniSTS
REN80770  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,755,576 - 33,755,800UniSTSGRCh37
Build 362132,677,447 - 32,677,671RGDNCBI36
Celera2118,939,202 - 18,939,426RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,164,445 - 19,164,669UniSTS
REN80771  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,755,792 - 33,756,051UniSTSGRCh37
Build 362132,677,663 - 32,677,922RGDNCBI36
Celera2118,939,418 - 18,939,677RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,164,661 - 19,164,920UniSTS
REN80772  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,756,029 - 33,756,266UniSTSGRCh37
Build 362132,677,900 - 32,678,137RGDNCBI36
Celera2118,939,655 - 18,939,892RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,164,898 - 19,165,135UniSTS
REN80773  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,756,248 - 33,756,512UniSTSGRCh37
Build 362132,678,119 - 32,678,383RGDNCBI36
Celera2118,939,874 - 18,940,138RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,165,117 - 19,165,381UniSTS
REN80774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,756,511 - 33,756,762UniSTSGRCh37
Build 362132,678,382 - 32,678,633RGDNCBI36
Celera2118,940,137 - 18,940,388RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,165,380 - 19,165,631UniSTS
REN80775  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,756,734 - 33,756,993UniSTSGRCh37
Build 362132,678,605 - 32,678,864RGDNCBI36
Celera2118,940,360 - 18,940,619RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,165,603 - 19,165,862UniSTS
REN80776  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,756,790 - 33,757,014UniSTSGRCh37
Build 362132,678,661 - 32,678,885RGDNCBI36
Celera2118,940,416 - 18,940,640RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,165,659 - 19,165,883UniSTS
REN80777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,757,328 - 33,757,556UniSTSGRCh37
Build 362132,679,199 - 32,679,427RGDNCBI36
Celera2118,940,954 - 18,941,182RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,166,197 - 19,166,425UniSTS
REN80778  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,757,547 - 33,757,808UniSTSGRCh37
Build 362132,679,418 - 32,679,679RGDNCBI36
Celera2118,941,173 - 18,941,434RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,166,416 - 19,166,677UniSTS
REN80779  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,757,787 - 33,758,049UniSTSGRCh37
Build 362132,679,658 - 32,679,920RGDNCBI36
Celera2118,941,413 - 18,941,675RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,166,656 - 19,166,918UniSTS
REN80780  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,757,946 - 33,758,179UniSTSGRCh37
Build 362132,679,817 - 32,680,050RGDNCBI36
Celera2118,941,572 - 18,941,805RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,166,815 - 19,167,048UniSTS
REN80781  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,758,360 - 33,758,608UniSTSGRCh37
Build 362132,680,231 - 32,680,479RGDNCBI36
Celera2118,941,986 - 18,942,234RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,167,229 - 19,167,477UniSTS
REN80782  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,758,597 - 33,758,850UniSTSGRCh37
Build 362132,680,468 - 32,680,721RGDNCBI36
Celera2118,942,223 - 18,942,476RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,167,466 - 19,167,719UniSTS
REN80783  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,758,828 - 33,759,071UniSTSGRCh37
Build 362132,680,699 - 32,680,942RGDNCBI36
Celera2118,942,454 - 18,942,697RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,167,697 - 19,167,940UniSTS
REN80784  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,066 - 33,759,336UniSTSGRCh37
Build 362132,680,937 - 32,681,207RGDNCBI36
Celera2118,942,692 - 18,942,962RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,167,935 - 19,168,205UniSTS
REN80785  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,332 - 33,759,595UniSTSGRCh37
Build 362132,681,203 - 32,681,466RGDNCBI36
Celera2118,942,958 - 18,943,221RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,168,201 - 19,168,464UniSTS
REN80786  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,567 - 33,759,808UniSTSGRCh37
Build 362132,681,438 - 32,681,679RGDNCBI36
Celera2118,943,193 - 18,943,434RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,168,436 - 19,168,677UniSTS
REN80787  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,774 - 33,760,015UniSTSGRCh37
Build 362132,681,645 - 32,681,886RGDNCBI36
Celera2118,943,400 - 18,943,642RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,168,643 - 19,168,885UniSTS
REN80788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,990 - 33,760,234UniSTSGRCh37
Build 362132,681,861 - 32,682,105RGDNCBI36
Celera2118,943,617 - 18,943,861RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,168,860 - 19,169,104UniSTS
REN80789  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,760,211 - 33,760,459UniSTSGRCh37
Build 362132,682,082 - 32,682,330RGDNCBI36
Celera2118,943,838 - 18,944,086RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,169,081 - 19,169,329UniSTS
REN80790  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,760,441 - 33,760,665UniSTSGRCh37
Build 362132,682,312 - 32,682,536RGDNCBI36
Celera2118,944,068 - 18,944,292RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,169,311 - 19,169,535UniSTS
REN80791  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,760,642 - 33,760,903UniSTSGRCh37
Build 362132,682,513 - 32,682,774RGDNCBI36
Celera2118,944,269 - 18,944,530RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,169,512 - 19,169,773UniSTS
REN80792  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,760,881 - 33,761,131UniSTSGRCh37
Build 362132,682,752 - 32,683,002RGDNCBI36
Celera2118,944,508 - 18,944,758RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,169,751 - 19,170,001UniSTS
REN80793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,761,108 - 33,761,334UniSTSGRCh37
Build 362132,682,979 - 32,683,205RGDNCBI36
Celera2118,944,735 - 18,944,961RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,169,978 - 19,170,204UniSTS
REN80794  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,761,310 - 33,761,560UniSTSGRCh37
Build 362132,683,181 - 32,683,431RGDNCBI36
Celera2118,944,937 - 18,945,187RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,170,180 - 19,170,430UniSTS
REN80795  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,761,540 - 33,761,794UniSTSGRCh37
Build 362132,683,411 - 32,683,665RGDNCBI36
Celera2118,945,167 - 18,945,421RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,170,410 - 19,170,664UniSTS
REN80796  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,761,771 - 33,762,025UniSTSGRCh37
Build 362132,683,642 - 32,683,896RGDNCBI36
Celera2118,945,398 - 18,945,652RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,170,641 - 19,170,895UniSTS
REN80797  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,762,006 - 33,762,230UniSTSGRCh37
Build 362132,683,877 - 32,684,101RGDNCBI36
Celera2118,945,633 - 18,945,857RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,170,876 - 19,171,100UniSTS
REN80798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,762,220 - 33,762,472UniSTSGRCh37
Build 362132,684,091 - 32,684,343RGDNCBI36
Celera2118,945,847 - 18,946,099RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,171,090 - 19,171,342UniSTS
REN80799  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,762,429 - 33,762,679UniSTSGRCh37
Build 362132,684,300 - 32,684,550RGDNCBI36
Celera2118,946,056 - 18,946,306RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,171,299 - 19,171,549UniSTS
REN80800  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,763,687 - 33,763,920UniSTSGRCh37
Build 362132,685,558 - 32,685,791RGDNCBI36
Celera2118,947,314 - 18,947,547RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,172,557 - 19,172,790UniSTS
REN80801  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,763,858 - 33,764,101UniSTSGRCh37
Build 362132,685,729 - 32,685,972RGDNCBI36
Celera2118,947,485 - 18,947,728RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,172,728 - 19,172,971UniSTS
REN80802  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,763,999 - 33,764,223UniSTSGRCh37
Build 362132,685,870 - 32,686,094RGDNCBI36
Celera2118,947,626 - 18,947,850RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,172,869 - 19,173,093UniSTS
REN80803  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,764,194 - 33,764,453UniSTSGRCh37
Build 362132,686,065 - 32,686,324RGDNCBI36
Celera2118,947,821 - 18,948,080RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,173,064 - 19,173,323UniSTS
REN80804  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,764,415 - 33,764,664UniSTSGRCh37
Build 362132,686,286 - 32,686,535RGDNCBI36
Celera2118,948,042 - 18,948,291RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,173,285 - 19,173,534UniSTS
REN80805  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,764,636 - 33,764,870UniSTSGRCh37
Build 362132,686,507 - 32,686,741RGDNCBI36
Celera2118,948,263 - 18,948,497RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,173,506 - 19,173,740UniSTS
REN80806  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,764,847 - 33,765,118UniSTSGRCh37
Build 362132,686,718 - 32,686,989RGDNCBI36
Celera2118,948,474 - 18,948,745RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,173,717 - 19,173,988UniSTS
REN80807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,764,901 - 33,765,145UniSTSGRCh37
Build 362132,686,772 - 32,687,016RGDNCBI36
Celera2118,948,528 - 18,948,772RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,173,771 - 19,174,015UniSTS
REN80808  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,765,240 - 33,765,473UniSTSGRCh37
Build 362132,687,111 - 32,687,344RGDNCBI36
Celera2118,948,867 - 18,949,100RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,174,110 - 19,174,343UniSTS
REN80809  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,765,465 - 33,765,723UniSTSGRCh37
Build 362132,687,336 - 32,687,594RGDNCBI36
Celera2118,949,092 - 18,949,350RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,174,335 - 19,174,593UniSTS
REN80810  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,765,702 - 33,765,951UniSTSGRCh37
Build 362132,687,573 - 32,687,822RGDNCBI36
Celera2118,949,329 - 18,949,578RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,174,572 - 19,174,821UniSTS
REN80811  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,765,936 - 33,766,161UniSTSGRCh37
Build 362132,687,807 - 32,688,032RGDNCBI36
Celera2118,949,563 - 18,949,788RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,174,806 - 19,175,031UniSTS
REN80812  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,766,130 - 33,766,392UniSTSGRCh37
Build 362132,688,001 - 32,688,263RGDNCBI36
Celera2118,949,757 - 18,950,019RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,175,000 - 19,175,262UniSTS
REN80813  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,766,377 - 33,766,631UniSTSGRCh37
Build 362132,688,248 - 32,688,502RGDNCBI36
Celera2118,950,004 - 18,950,258RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,175,247 - 19,175,501UniSTS
REN80814  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,766,619 - 33,766,885UniSTSGRCh37
Build 362132,688,490 - 32,688,756RGDNCBI36
Celera2118,950,246 - 18,950,512RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,175,489 - 19,175,755UniSTS
REN80815  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,766,857 - 33,767,092UniSTSGRCh37
Build 362132,688,728 - 32,688,963RGDNCBI36
Celera2118,950,484 - 18,950,719RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,175,727 - 19,175,962UniSTS
REN80816  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,767,041 - 33,767,300UniSTSGRCh37
Build 362132,688,912 - 32,689,171RGDNCBI36
Celera2118,950,668 - 18,950,927RGD
Cytogenetic Map21q22.11UniSTS
HuRef2119,175,911 - 19,176,170UniSTS
stSG606350  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,750,790 - 33,751,865UniSTSGRCh37
Build 362132,672,661 - 32,673,736RGDNCBI36
Celera2118,934,416 - 18,935,491RGD
HuRef2119,159,659 - 19,160,734UniSTS
stSG606351  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,751,849 - 33,752,870UniSTSGRCh37
Build 362132,673,720 - 32,674,741RGDNCBI36
Celera2118,935,475 - 18,936,496RGD
HuRef2119,160,718 - 19,161,739UniSTS
stSG606352  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,752,862 - 33,754,177UniSTSGRCh37
Build 362132,674,733 - 32,676,048RGDNCBI36
Celera2118,936,488 - 18,937,803RGD
HuRef2119,161,731 - 19,163,046UniSTS
stSG606353  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,158 - 33,754,373UniSTSGRCh37
Build 362132,676,029 - 32,676,244RGDNCBI36
Celera2118,937,784 - 18,937,999RGD
HuRef2119,163,027 - 19,163,242UniSTS
stSG606354  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,754,375 - 33,755,575UniSTSGRCh37
Build 362132,676,246 - 32,677,446RGDNCBI36
Celera2118,938,001 - 18,939,201RGD
HuRef2119,163,244 - 19,164,444UniSTS
stSG606355  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,755,556 - 33,756,586UniSTSGRCh37
Build 362132,677,427 - 32,678,457RGDNCBI36
Celera2118,939,182 - 18,940,212RGD
HuRef2119,164,425 - 19,165,455UniSTS
stSG606356  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,756,567 - 33,757,978UniSTSGRCh37
Build 362132,678,438 - 32,679,849RGDNCBI36
Celera2118,940,193 - 18,941,604RGD
HuRef2119,165,436 - 19,166,847UniSTS
stSG606357  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,757,964 - 33,759,423UniSTSGRCh37
Build 362132,679,835 - 32,681,294RGDNCBI36
Celera2118,941,590 - 18,943,049RGD
HuRef2119,166,833 - 19,168,292UniSTS
stSG606358  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,759,471 - 33,760,721UniSTSGRCh37
Build 362132,681,342 - 32,682,592RGDNCBI36
Celera2118,943,097 - 18,944,348RGD
HuRef2119,168,340 - 19,169,591UniSTS
stSG606359  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,760,702 - 33,761,939UniSTSGRCh37
Build 362132,682,573 - 32,683,810RGDNCBI36
Celera2118,944,329 - 18,945,566RGD
HuRef2119,169,572 - 19,170,809UniSTS
stSG606360  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,761,920 - 33,762,651UniSTSGRCh37
Build 362132,683,791 - 32,684,522RGDNCBI36
Celera2118,945,547 - 18,946,278RGD
HuRef2119,170,790 - 19,171,521UniSTS
stSG606361  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,764,402 - 33,765,482UniSTSGRCh37
Build 362132,686,273 - 32,687,353RGDNCBI36
Celera2118,948,029 - 18,949,109RGD
HuRef2119,173,272 - 19,174,352UniSTS
stSG606362  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372133,765,499 - 33,766,550UniSTSGRCh37
Build 362132,687,370 - 32,688,421RGDNCBI36
Celera2118,949,126 - 18,950,177RGD
HuRef2119,174,369 - 19,175,420UniSTS
D21S314  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.11UniSTS




adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1950 465 2270 7305 6471 53 3734 1 852 1744 1617 175 1


1 to 16 of 16 rows
RefSeq Transcripts NM_014825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB011111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF231919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF432264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC041033 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC062356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471079 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068257 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF457216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF511388 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 16 of 16 rows

Ensembl Acc Id: ENST00000382751   ⟹   ENSP00000372199
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2132,311,018 - 32,393,012 (-)Ensembl
Ensembl Acc Id: ENST00000480196
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2132,333,113 - 32,334,334 (-)Ensembl
Ensembl Acc Id: ENST00000492603
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2132,334,209 - 32,335,630 (-)Ensembl
RefSeq Acc Id: NM_014825   ⟹   NP_055640
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382132,311,018 - 32,393,012 (-)NCBI
GRCh372133,683,330 - 33,765,312 (-)RGD
Celera2118,866,931 - 18,948,939 (-)RGD
HuRef2119,092,100 - 19,174,182 (-)RGD
CHM1_12133,245,146 - 33,327,161 (-)NCBI
T2T-CHM13v2.02130,680,775 - 30,762,860 (-)NCBI
Sequence:
1 to 9 of 9 rows
Protein RefSeqs NP_055640 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAF72943 (Get FASTA)   NCBI Sequence Viewer  
  AAL28110 (Get FASTA)   NCBI Sequence Viewer  
  BAA25465 (Get FASTA)   NCBI Sequence Viewer  
  EAX09876 (Get FASTA)   NCBI Sequence Viewer  
  EAX09877 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000372199
  ENSP00000372199.3
GenBank Protein O60287 (Get FASTA)   NCBI Sequence Viewer  
1 to 9 of 9 rows
RefSeq Acc Id: NP_055640   ⟸   NM_014825
- UniProtKB: Q96NX1 (UniProtKB/Swiss-Prot),   D3DSE5 (UniProtKB/Swiss-Prot),   Q9NYQ1 (UniProtKB/Swiss-Prot),   O60287 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000372199   ⟸   ENST00000382751

Name Modeler Protein Id AA Range Protein Structure
AF-O60287-F1-model_v2 AlphaFold O60287 1-2271 view protein structure

RGD ID:13602624
Promoter ID:EPDNEW_H27496
Type:initiation region
Name:URB1_1
Description:URB1 ribosome biogenesis 1 homolog
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
GRCh382132,393,012 - 32,393,072EPDNEW


1 to 27 of 27 rows
Database
Acc Id
Source(s)
COSMIC URB1 COSMIC
Ensembl Genes ENSG00000142207 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000382751 ENTREZGENE
  ENST00000382751.4 UniProtKB/Swiss-Prot
GTEx ENSG00000142207 GTEx
HGNC ID HGNC:17344 ENTREZGENE
Human Proteome Map URB1 Human Proteome Map
InterPro ARM-type_fold UniProtKB/Swiss-Prot
  NopRA1_C UniProtKB/Swiss-Prot
  Npa1_N UniProtKB/Swiss-Prot
  URB1 UniProtKB/Swiss-Prot
KEGG Report hsa:9875 UniProtKB/Swiss-Prot
NCBI Gene 9875 ENTREZGENE
OMIM 608865 OMIM
PANTHER NUCLEOLAR PRE-RIBOSOMAL-ASSOCIATED PROTEIN 1 UniProtKB/Swiss-Prot
  PTHR13500 UniProtKB/Swiss-Prot
Pfam NopRA1 UniProtKB/Swiss-Prot
  Npa1 UniProtKB/Swiss-Prot
PharmGKB PA162408676 PharmGKB
Superfamily-SCOP SSF48371 UniProtKB/Swiss-Prot
UniProt D3DSE5 ENTREZGENE
  NPA1P_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q96NX1 ENTREZGENE
  Q9NYQ1 ENTREZGENE
UniProt Secondary D3DSE5 UniProtKB/Swiss-Prot
  Q96NX1 UniProtKB/Swiss-Prot
  Q9NYQ1 UniProtKB/Swiss-Prot
1 to 27 of 27 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-08-14 URB1  URB1 ribosome biogenesis homolog    URB1 ribosome biogenesis 1 homolog (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED