NEDD8-MDP1 (NEDD8-MDP1 readthrough) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)
Gene: NEDD8-MDP1 (NEDD8-MDP1 readthrough) Homo sapiens
Analyze
No known orthologs.
Symbol: NEDD8-MDP1
Name: NEDD8-MDP1 readthrough
RGD ID: 5013872
HGNC Page HGNC:39551
Description: Predicted to enable phosphatase activity.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: NEDD8-MDP1 read-through transcript
RGD Orthologs
Alliance Orthologs
More Info homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381424,213,943 - 24,232,367 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1424,213,955 - 24,232,352 (-)EnsemblGRCh38hg38GRCh38
GRCh371424,683,149 - 24,701,573 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map14q12NCBI
HuRef144,798,147 - 4,816,345 (-)NCBIHuRef
CHM1_11424,681,793 - 24,700,199 (-)NCBICHM1_1
T2T-CHM13v2.01418,412,319 - 18,430,739 (-)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

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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:20967262   PMID:26186194   PMID:28514442   PMID:30349055   PMID:32552912   PMID:33961781   PMID:35271311   PMID:36089195  


Genomics

Variants

.
Variants in NEDD8-MDP1
19 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q11.2-12(chr14:20151149-27723796)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051484]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051484]|See cases [RCV000051484] Chr14:20151149..27723796 [GRCh38]
Chr14:20619308..28193002 [GRCh37]
Chr14:19689148..27262842 [NCBI36]
Chr14:14q11.2-12		 pathogenic
GRCh38/hg38 14q11.2-21.2(chr14:20196945-45284802)x1 copy number loss See cases [RCV000051485] Chr14:20196945..45284802 [GRCh38]
Chr14:20665104..45754005 [GRCh37]
Chr14:19734944..44823755 [NCBI36]
Chr14:14q11.2-21.2		 pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:23548960-41983402)x1 copy number loss See cases [RCV000051490] Chr14:23548960..41983402 [GRCh38]
Chr14:24018169..42452605 [GRCh37]
Chr14:23088009..41522355 [NCBI36]
Chr14:14q11.2-21.1		 pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20000611-38984415)x3 copy number gain See cases [RCV000053803] Chr14:20000611..38984415 [GRCh38]
Chr14:20468770..39453619 [GRCh37]
Chr14:19538610..38523370 [NCBI36]
Chr14:14q11.2-21.1		 pathogenic
GRCh38/hg38 14q11.2-21.1(chr14:20150949-39746154)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053806]|See cases [RCV000053806] Chr14:20150949..39746154 [GRCh38]
Chr14:20619108..40215358 [GRCh37]
Chr14:19688948..39285109 [NCBI36]
Chr14:14q11.2-21.1		 pathogenic
NM_001199821.1(MDP1):c.263+55G>A single nucleotide variant Malignant melanoma [RCV000070509] Chr14:24214491 [GRCh38]
Chr14:24683697 [GRCh37]
Chr14:23753537 [NCBI36]
Chr14:14q12		 not provided
NM_001199822.1(MDP1):c.317G>T (p.Arg106Met) single nucleotide variant Malignant melanoma [RCV000070510] Chr14:24214492 [GRCh38]
Chr14:24683698 [GRCh37]
Chr14:23753538 [NCBI36]
Chr14:14q12		 not provided
NM_001199823.3(NEDD8-MDP1):c.451C>G (p.Leu151Val) single nucleotide variant Malignant tumor of prostate [RCV000149100] Chr14:24214313 [GRCh38]
Chr14:24683519 [GRCh37]
Chr14:14q12		 uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q11.2-12(chr14:20412587-25018120)x3 copy number gain See cases [RCV000137725] Chr14:20412587..25018120 [GRCh38]
Chr14:20880746..25487326 [GRCh37]
Chr14:19950586..24557166 [NCBI36]
Chr14:14q11.2-12		 likely pathogenic
GRCh38/hg38 14q11.2-21.2(chr14:20022693-44093672)x3 copy number gain See cases [RCV000143186] Chr14:20022693..44093672 [GRCh38]
Chr14:20490852..44562875 [GRCh37]
Chr14:19560692..43632625 [NCBI36]
Chr14:14q11.2-21.2		 pathogenic
GRCh38/hg38 14q11.2-21.3(chr14:20043513-48642042)x3 copy number gain See cases [RCV000143748] Chr14:20043513..48642042 [GRCh38]
Chr14:20511672..49111245 [GRCh37]
Chr14:19581512..48180995 [NCBI36]
Chr14:14q11.2-21.3		 pathogenic
GRCh37/hg19 14q11.2-12(chr14:19100682-28730087) copy number gain not provided [RCV000767822] Chr14:19100682..28730087 [GRCh37]
Chr14:14q11.2-12		 pathogenic
GRCh37/hg19 14q11.2-12(chr14:19794561-27768254)x3 copy number gain See cases [RCV000240285] Chr14:19794561..27768254 [GRCh37]
Chr14:14q11.2-12		 pathogenic
GRCh37/hg19 14q11.2-22.2(chr14:23164384-54733411)x3 copy number gain See cases [RCV000447658] Chr14:23164384..54733411 [GRCh37]
Chr14:14q11.2-22.2		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-13.1(chr14:19794561-34049214)x3 copy number gain See cases [RCV000448273] Chr14:19794561..34049214 [GRCh37]
Chr14:14q11.2-13.1		 pathogenic
GRCh37/hg19 14q11.2-12(chr14:24233721-31377083)x1 copy number loss See cases [RCV000510673] Chr14:24233721..31377083 [GRCh37]
Chr14:14q11.2-12		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
NC_000014.8:g.(?_23242819)_(25103366_?)dup duplication Lysinuric protein intolerance [RCV003105428]|Specific granule deficiency [RCV003105427] Chr14:23242819..25103366 [GRCh37]
Chr14:14q11.2-12		 uncertain significance
GRCh37/hg19 14q11.2-21.2(chr14:20511672-44829030)x3 copy number gain not provided [RCV001006605] Chr14:20511672..44829030 [GRCh37]
Chr14:14q11.2-21.2		 pathogenic
GRCh37/hg19 14q11.2-21.1(chr14:20511672-42881888)x3 copy number gain not provided [RCV001249358] Chr14:20511672..42881888 [GRCh37]
Chr14:14q11.2-21.1		 not provided
GRCh37/hg19 14q11.2-21.3(chr14:20511672-47481203) copy number gain Seizure [RCV002280625] Chr14:20511672..47481203 [GRCh37]
Chr14:14q11.2-21.3		 pathogenic
NC_000014.8:g.(21162263_36986276)_(36987308_50713602)del deletion Brain-lung-thyroid syndrome [RCV002221171] Chr14:36986276..36987308 [GRCh37]
Chr14:14q11.2-21.3		 pathogenic
NM_138476.4(MDP1):c.32A>G (p.Asp11Gly) single nucleotide variant not specified [RCV004192052] Chr14:24215924 [GRCh38]
Chr14:24685130 [GRCh37]
Chr14:14q12		 uncertain significance
GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3 copy number gain not provided [RCV003485022] Chr14:20511673..61826023 [GRCh37]
Chr14:14q11.2-23.1		 pathogenic
GRCh38/hg38 14q11.2-12(chr14:23984065-25374494)x1 copy number loss See cases [RCV000142873] Chr14:23984065..25374494 [GRCh38]
Chr14:24453274..25843700 [GRCh37]
Chr14:23523114..24913540 [NCBI36]
Chr14:14q11.2-12		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-12(chr14:24163771-24818728)x3 copy number gain not provided [RCV001259179] Chr14:24163771..24818728 [GRCh37]
Chr14:14q11.2-12		 uncertain significance
GRCh37/hg19 14q11.2-12(chr14:24445622-28262222)x1 copy number loss not provided [RCV003483196] Chr14:24445622..28262222 [GRCh37]
Chr14:14q11.2-12		 likely pathogenic
NM_138476.4(MDP1):c.232A>G (p.Asn78Asp) single nucleotide variant not specified [RCV004421592] Chr14:24214577 [GRCh38]
Chr14:24683783 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.376C>T (p.Arg126Trp) single nucleotide variant not specified [RCV004421593] Chr14:24214337 [GRCh38]
Chr14:24683543 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.399A>T (p.Lys133Asn) single nucleotide variant not specified [RCV004421594] Chr14:24214314 [GRCh38]
Chr14:24683520 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.420C>T (p.His140=) single nucleotide variant not specified [RCV004421595] Chr14:24214135 [GRCh38]
Chr14:24683341 [GRCh37]
Chr14:14q12		 likely benign
NM_138476.4(MDP1):c.431G>A (p.Gly144Glu) single nucleotide variant not specified [RCV004421596] Chr14:24214124 [GRCh38]
Chr14:24683330 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.446C>T (p.Thr149Ile) single nucleotide variant not specified [RCV004421597] Chr14:24214109 [GRCh38]
Chr14:24683315 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.479C>T (p.Ala160Val) single nucleotide variant not specified [RCV004421599] Chr14:24214076 [GRCh38]
Chr14:24683282 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.133G>T (p.Val45Phe) single nucleotide variant not specified [RCV004421590] Chr14:24215628 [GRCh38]
Chr14:24684834 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.125G>A (p.Gly42Asp) single nucleotide variant not specified [RCV004421589] Chr14:24215636 [GRCh38]
Chr14:24684842 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.190C>T (p.Pro64Ser) single nucleotide variant not specified [RCV004421591] Chr14:24215571 [GRCh38]
Chr14:24684777 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.456A>G (p.Gln152=) single nucleotide variant not specified [RCV004421598] Chr14:24214099 [GRCh38]
Chr14:24683305 [GRCh37]
Chr14:14q12		 likely benign
NM_138476.4(MDP1):c.450A>C (p.Leu150=) single nucleotide variant not specified [RCV004638037] Chr14:24214105 [GRCh38]
Chr14:24683311 [GRCh37]
Chr14:14q12		 likely benign
NM_138476.4(MDP1):c.5C>G (p.Ala2Gly) single nucleotide variant not specified [RCV004638036] Chr14:24215951 [GRCh38]
Chr14:24685157 [GRCh37]
Chr14:14q12		 uncertain significance
NM_138476.4(MDP1):c.485C>G (p.Thr162Ser) single nucleotide variant not specified [RCV004638035] Chr14:24214070 [GRCh38]
Chr14:24683276 [GRCh37]
Chr14:14q12		 uncertain significance
NM_001199823.3(NEDD8-MDP1):c.428G>A (p.Arg143Gln) single nucleotide variant not specified [RCV004483186] Chr14:24214336 [GRCh38]
Chr14:24683542 [GRCh37]
Chr14:14q12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:656
Count of miRNA genes:417
Interacting mature miRNAs:452
Transcripts:ENST00000530579, ENST00000534348, ENST00000604306, ENST00000605847
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407081031GWAS730007_Hplatelet count QTL GWAS730007 (human)1e-18platelet quantity (VT:0003179)platelet count (CMO:0000029)142422194524221946Human
407078182GWAS727158_Hmean corpuscular volume QTL GWAS727158 (human)3e-13mean corpuscular volumemean corpuscular volume (CMO:0000038)142422194524221946Human
406931399GWAS580375_Htuberculosis QTL GWAS580375 (human)1e-10tuberculosis142421409824214099Human
407134882GWAS783858_Hmean corpuscular volume QTL GWAS783858 (human)4e-11mean corpuscular volumemean corpuscular volume (CMO:0000038)142422194524221946Human
407137614GWAS786590_Hprostate carcinoma QTL GWAS786590 (human)3e-11prostate carcinoma142422194524221946Human
406966348GWAS615324_Hsystolic blood pressure, smoking behaviour measurement QTL GWAS615324 (human)3e-08systolic blood pressure, smoking behaviour measurementsystolic blood pressure (CMO:0000004)142421960824219609Human
407075726GWAS724702_Herythrocyte count QTL GWAS724702 (human)3e-12erythrocyte countred blood cell count (CMO:0000025)142422194524221946Human
406974380GWAS623356_Hmean corpuscular volume QTL GWAS623356 (human)2e-10mean corpuscular volumemean corpuscular volume (CMO:0000038)142422194524221946Human
407131670GWAS780646_Hplatelet count QTL GWAS780646 (human)1e-12platelet quantity (VT:0003179)platelet count (CMO:0000029)142422194524221946Human
406966484GWAS615460_Hlevel of magnesium-dependent phosphatase 1 in blood serum QTL GWAS615460 (human)4e-13level of magnesium-dependent phosphatase 1 in blood serum142421406024214061Human
407214098GWAS863074_Hplatelet count QTL GWAS863074 (human)5e-15platelet quantity (VT:0003179)platelet count (CMO:0000029)142422401824224019Human
407079032GWAS728008_Hmean corpuscular hemoglobin QTL GWAS728008 (human)6e-09mean corpuscular hemoglobinmean corpuscular hemoglobin (CMO:0000290)142422194524221946Human
407139544GWAS788520_Hprostate carcinoma QTL GWAS788520 (human)3e-09prostate carcinoma142422194524221946Human

Markers in Region
WI-15002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371424,683,151 - 24,683,278UniSTSGRCh37
Build 361423,752,991 - 23,753,118RGDNCBI36
Celera144,547,788 - 4,547,915RGD
Cytogenetic Map14qUniSTS
Cytogenetic Map14q12UniSTS
HuRef144,798,155 - 4,798,282UniSTS
GeneMap99-GB4 RH Map1420.64UniSTS
Whitehead-RH Map1427.7UniSTS
NCBI RH Map1438.0UniSTS


Expression

RNA-SEQ Expression

alimentary part of gastrointestinal system
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
170 26 388 189 490 5 130 346 132 249 868 419 51 144 1 265 247 336 12 1

Sequence


Ensembl Acc Id: ENST00000530579   ⟹   ENSP00000432117
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1424,214,372 - 24,232,285 (-)Ensembl
Ensembl Acc Id: ENST00000534348   ⟹   ENSP00000431482
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1424,214,096 - 24,232,352 (-)Ensembl
Ensembl Acc Id: ENST00000604306
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1424,214,378 - 24,232,285 (-)Ensembl
Ensembl Acc Id: ENST00000605847   ⟹   ENSP00000474249
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1424,213,955 - 24,232,336 (-)Ensembl
RefSeq Acc Id: NM_001199823   ⟹   NP_001186752
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381424,213,943 - 24,232,367 (-)NCBI
GRCh371424,683,143 - 24,701,576 (-)ENTREZGENE
HuRef144,798,147 - 4,816,345 (-)ENTREZGENE
CHM1_11424,681,793 - 24,700,199 (-)NCBI
T2T-CHM13v2.01418,412,319 - 18,430,739 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001412116   ⟹   NP_001399045
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01418,412,319 - 18,430,739 (-)NCBI
RefSeq Acc Id: NR_137630
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381424,214,310 - 24,232,367 (-)NCBI
T2T-CHM13v2.01418,412,685 - 18,430,739 (-)NCBI
Sequence:
RefSeq Acc Id: NR_137631
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381424,214,310 - 24,232,367 (-)NCBI
T2T-CHM13v2.01418,412,685 - 18,430,739 (-)NCBI
Sequence:
RefSeq Acc Id: NR_137632
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381424,214,310 - 24,232,367 (-)NCBI
T2T-CHM13v2.01418,412,685 - 18,430,739 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001186752 (Get FASTA)   NCBI Sequence Viewer  
  NP_001399045 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000431482
  ENSP00000431482.1
  ENSP00000432117.2
  ENSP00000474249.1
  ENSP00000494020.1
  ENSP00000494449.1
  ENSP00000496657.1
RefSeq Acc Id: NP_001186752   ⟸   NM_001199823
- Peptide Label: isoform 1
- UniProtKB: E9PL57 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000432117   ⟸   ENST00000530579
Ensembl Acc Id: ENSP00000431482   ⟸   ENST00000534348
Ensembl Acc Id: ENSP00000474249   ⟸   ENST00000605847
RefSeq Acc Id: NP_001399045   ⟸   NM_001412116
- Peptide Label: isoform 2
Protein Domains
Ubiquitin-like


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:39551 AgrOrtholog
COSMIC NEDD8-MDP1 COSMIC
Ensembl Genes ENSG00000255526 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
  ENSG00000285425 UniProtKB/TrEMBL
Ensembl Transcript ENST00000530579.6 UniProtKB/TrEMBL
  ENST00000534348 ENTREZGENE
  ENST00000534348.5 UniProtKB/TrEMBL
  ENST00000604306 ENTREZGENE
  ENST00000605847.5 UniProtKB/TrEMBL
  ENST00000642609.1 UniProtKB/TrEMBL
  ENST00000644380.1 UniProtKB/TrEMBL
  ENST00000644921.1 UniProtKB/TrEMBL
Gene3D-CATH 3.40.50.1000 UniProtKB/TrEMBL
GTEx ENSG00000255526 GTEx
  ENSG00000285425 GTEx
HGNC ID HGNC:39551 ENTREZGENE
Human Proteome Map NEDD8-MDP1 Human Proteome Map
InterPro HAD-like_dom UniProtKB/TrEMBL
  HAD-like_sf UniProtKB/TrEMBL
  MDP-1_euk UniProtKB/TrEMBL
  MDP_1_eu_arc UniProtKB/TrEMBL
  Nedd8-like UniProtKB/TrEMBL
  Ubiquitin UniProtKB/TrEMBL
  Ubiquitin-rel_dom UniProtKB/TrEMBL
  Ubiquitin_CS UniProtKB/TrEMBL
  Ubiquitin_subgr UniProtKB/TrEMBL
  Ubiquitin_ubiquitin-like UniProtKB/TrEMBL
NCBI Gene 100528064 ENTREZGENE
PANTHER MAGNESIUM-DEPENDENT PHOSPHATASE 1 UniProtKB/TrEMBL
  NEDD8 UniProtKB/TrEMBL
  PTHR17901 UniProtKB/TrEMBL
  UBIQUITIN UniProtKB/TrEMBL
Pfam Acid_PPase UniProtKB/TrEMBL
  ubiquitin UniProtKB/TrEMBL
PRINTS UBIQUITIN UniProtKB/TrEMBL
PROSITE UBIQUITIN_1 UniProtKB/TrEMBL
  UBIQUITIN_2 UniProtKB/TrEMBL
SMART UBQ UniProtKB/TrEMBL
Superfamily-SCOP HAD-like_dom UniProtKB/TrEMBL
  SSF54236 UniProtKB/TrEMBL
UniProt E9PL57 ENTREZGENE, UniProtKB/TrEMBL
  E9PS38_HUMAN UniProtKB/TrEMBL
  S4R3E9_HUMAN UniProtKB/TrEMBL