PTGES3L-AARSD1 (PTGES3L-AARSD1 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: PTGES3L-AARSD1 (PTGES3L-AARSD1 readthrough) Homo sapiens
Analyze
No known orthologs.
Symbol: PTGES3L-AARSD1
Name: PTGES3L-AARSD1 readthrough
RGD ID: 6483691
HGNC Page HGNC:43946
Description: Predicted to enable Ser-tRNA(Ala) hydrolase activity. Predicted to be involved in regulation of translational fidelity. Located in nucleus.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ36765; FLJ56441; MGC2744; MGC4371
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
GRCh381742,950,526 - 42,980,528 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1742,950,526 - 42,980,528 (-)EnsemblGRCh38hg38GRCh38
GRCh371741,102,543 - 41,132,545 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map17q21.31NCBI
HuRef1736,868,387 - 36,898,226 (-)NCBIHuRef
CHM1_11741,338,174 - 41,368,050 (-)NCBICHM1_1
T2T-CHM13v2.01743,807,669 - 43,837,800 (-)NCBIT2T-CHM13v2.0
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

Biological Process

Cellular Component
cytoplasm  (IEA)
nucleus  (HDA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7545954   PMID:11181995   PMID:11230166   PMID:12477932   PMID:14702039   PMID:17974005   PMID:20967262   PMID:24324551   PMID:26344197   PMID:26760575   PMID:31980649   PMID:32296183  
PMID:33545068   PMID:34917906   PMID:36215168   PMID:37827155  


Genomics

Variants

.
Variants in PTGES3L-AARSD1
47 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3 copy number gain See cases [RCV000052479] Chr17:39199873..45629579 [GRCh38]
Chr17:37356126..43706945 [GRCh37]
Chr17:34609652..41062728 [NCBI36]
Chr17:17q12-21.31		 pathogenic
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
NM_001261430.2(PTGES3L):c.433-8_433-7del deletion not specified [RCV000456037] Chr17:42969193..42969194 [GRCh38]
Chr17:41121210..41121211 [GRCh37]
Chr17:17q21.31		 benign
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_001261434.2(AARSD1):c.557G>A (p.Arg186Gln) single nucleotide variant not specified [RCV004324598] Chr17:42956310 [GRCh38]
Chr17:41108327 [GRCh37]
Chr17:17q21.31		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NC_000017.10:g.(?_41052894)_(41154937_?)dup duplication not provided [RCV003105383] Chr17:41052894..41154937 [GRCh37]
Chr17:17q21.31		 uncertain significance
GRCh37/hg19 17q21.31(chr17:41105913-41307101)x3 copy number gain not provided [RCV002475723] Chr17:41105913..41307101 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1220C>T (p.Thr407Met) single nucleotide variant not specified [RCV004080920] Chr17:42950612 [GRCh38]
Chr17:41102629 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.992A>G (p.Asn331Ser) single nucleotide variant not specified [RCV004161805] Chr17:42953740 [GRCh38]
Chr17:41105757 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1024T>G (p.Leu342Val) single nucleotide variant not specified [RCV004088957] Chr17:42951879 [GRCh38]
Chr17:41103896 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1177C>T (p.Arg393Trp) single nucleotide variant not specified [RCV004224175] Chr17:42950655 [GRCh38]
Chr17:41102672 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1196C>T (p.Ala399Val) single nucleotide variant not specified [RCV004150403] Chr17:42950636 [GRCh38]
Chr17:41102653 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.167G>A (p.Gly56Glu) single nucleotide variant not specified [RCV004084138] Chr17:42964110 [GRCh38]
Chr17:41116127 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.287G>A (p.Arg96Gln) single nucleotide variant not specified [RCV004093271] Chr17:42961236 [GRCh38]
Chr17:41113253 [GRCh37]
Chr17:17q21.31		 likely benign
NM_001261434.2(AARSD1):c.1147C>T (p.Arg383Cys) single nucleotide variant not specified [RCV004096863] Chr17:42950685 [GRCh38]
Chr17:41102702 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.635C>G (p.Thr212Ser) single nucleotide variant not specified [RCV004099220] Chr17:42956232 [GRCh38]
Chr17:41108249 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.73G>A (p.Glu25Lys) single nucleotide variant not specified [RCV004174613] Chr17:42964204 [GRCh38]
Chr17:41116221 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.364C>A (p.Leu122Ile) single nucleotide variant not specified [RCV004232299] Chr17:42957163 [GRCh38]
Chr17:41109180 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001136042.2(PTGES3L-AARSD1):c.119C>T (p.Ala40Val) single nucleotide variant not specified [RCV004085509] Chr17:42980064 [GRCh38]
Chr17:41132081 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.320A>G (p.Gln107Arg) single nucleotide variant not specified [RCV004170515] Chr17:42961203 [GRCh38]
Chr17:41113220 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1219A>G (p.Thr407Ala) single nucleotide variant not specified [RCV004225611] Chr17:42950613 [GRCh38]
Chr17:41102630 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.71C>T (p.Ala24Val) single nucleotide variant not specified [RCV004131630] Chr17:42964206 [GRCh38]
Chr17:41116223 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.70G>C (p.Ala24Pro) single nucleotide variant not specified [RCV004131506] Chr17:42964207 [GRCh38]
Chr17:41116224 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.451G>A (p.Val151Ile) single nucleotide variant not specified [RCV004174003] Chr17:42956499 [GRCh38]
Chr17:41108516 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.941T>C (p.Val314Ala) single nucleotide variant not specified [RCV004248106] Chr17:42954888 [GRCh38]
Chr17:41106905 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.190A>G (p.Ile64Val) single nucleotide variant not specified [RCV004257843] Chr17:42961333 [GRCh38]
Chr17:41113350 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.175G>A (p.Asp59Asn) single nucleotide variant not specified [RCV004262907] Chr17:42961348 [GRCh38]
Chr17:41113365 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.929G>T (p.Trp310Leu) single nucleotide variant not specified [RCV004330926] Chr17:42954900 [GRCh38]
Chr17:41106917 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.581G>A (p.Gly194Glu) single nucleotide variant not specified [RCV004275792] Chr17:42956286 [GRCh38]
Chr17:41108303 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1049G>T (p.Gly350Val) single nucleotide variant not specified [RCV004261491] Chr17:42951854 [GRCh38]
Chr17:41103871 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.886C>G (p.Leu296Val) single nucleotide variant not specified [RCV004342499] Chr17:42954943 [GRCh38]
Chr17:41106960 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1104G>C (p.Arg368Ser) single nucleotide variant not specified [RCV004349698] Chr17:42950728 [GRCh38]
Chr17:41102745 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001136042.2(PTGES3L-AARSD1):c.120G>A (p.Ala40=) single nucleotide variant not provided [RCV003413244] Chr17:42980063 [GRCh38]
Chr17:41132080 [GRCh37]
Chr17:17q21.31		 likely benign
NM_001261434.2(AARSD1):c.785C>T (p.Ala262Val) single nucleotide variant not specified [RCV004427490] Chr17:42955851 [GRCh38]
Chr17:41107868 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.934G>A (p.Gly312Ser) single nucleotide variant not specified [RCV004427609] Chr17:42954895 [GRCh38]
Chr17:41106912 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.905A>G (p.His302Arg) single nucleotide variant not specified [RCV004427546] Chr17:42954924 [GRCh38]
Chr17:41106941 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1049G>C (p.Gly350Ala) single nucleotide variant not specified [RCV004427747] Chr17:42951854 [GRCh38]
Chr17:41103871 [GRCh37]
Chr17:17q21.31		 likely benign
NM_001261434.2(AARSD1):c.44C>G (p.Thr15Ser) single nucleotide variant not specified [RCV004430488] Chr17:42964233 [GRCh38]
Chr17:41116250 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1183A>C (p.Met395Leu) single nucleotide variant not specified [RCV004430389] Chr17:42950649 [GRCh38]
Chr17:41102666 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.163G>C (p.Gly55Arg) single nucleotide variant not specified [RCV004430692] Chr17:42964114 [GRCh38]
Chr17:41116131 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.224G>T (p.Arg75Leu) single nucleotide variant not specified [RCV004430815] Chr17:42961299 [GRCh38]
Chr17:41113316 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.535G>A (p.Glu179Lys) single nucleotide variant not specified [RCV004435350] Chr17:42956415 [GRCh38]
Chr17:41108432 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.302G>A (p.Arg101Gln) single nucleotide variant not specified [RCV004432957] Chr17:42961221 [GRCh38]
Chr17:41113238 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1160A>T (p.Lys387Met) single nucleotide variant not specified [RCV004430345] Chr17:42950672 [GRCh38]
Chr17:41102689 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.117C>G (p.Ser39Arg) single nucleotide variant not specified [RCV004430641] Chr17:42964160 [GRCh38]
Chr17:41116177 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1190C>T (p.Ala397Val) single nucleotide variant not specified [RCV004600665] Chr17:42950642 [GRCh38]
Chr17:41102659 [GRCh37]
Chr17:17q21.31		 likely benign
NM_001261434.2(AARSD1):c.493C>T (p.Arg165Trp) single nucleotide variant not specified [RCV004606179] Chr17:42956457 [GRCh38]
Chr17:41108474 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.994G>A (p.Glu332Lys) single nucleotide variant not specified [RCV004606231] Chr17:42953738 [GRCh38]
Chr17:41105755 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.445G>A (p.Glu149Lys) single nucleotide variant not specified [RCV004606293] Chr17:42956505 [GRCh38]
Chr17:41108522 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.526G>T (p.Asp176Tyr) single nucleotide variant not specified [RCV004600753] Chr17:42956424 [GRCh38]
Chr17:41108441 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.812A>T (p.His271Leu) single nucleotide variant not specified [RCV004606030] Chr17:42955207 [GRCh38]
Chr17:41107224 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.962G>T (p.Gly321Val) single nucleotide variant not specified [RCV004607254] Chr17:42953770 [GRCh38]
Chr17:41105787 [GRCh37]
Chr17:17q21.31		 uncertain significance
NM_001261434.2(AARSD1):c.1193A>T (p.Gln398Leu) single nucleotide variant not specified [RCV004606384] Chr17:42950639 [GRCh38]
Chr17:41102656 [GRCh37]
Chr17:17q21.31		 uncertain significance
GRCh37/hg19 17q12-22(chr17:41196270-41277589) copy number loss Breast-ovarian cancer, familial, susceptibility to, 1 [RCV004759419] Chr17:41196270..41277589 [GRCh37]
Chr17:17q12-22		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1326
Count of miRNA genes:627
Interacting mature miRNAs:723
Transcripts:ENST00000360221, ENST00000409103, ENST00000409399, ENST00000421990, ENST00000423601, ENST00000452752, ENST00000454303
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407144992GWAS793968_HPR interval QTL GWAS793968 (human)0.000009PR intervalPR interval (CMO:0000233)174296755242967553Human


Expression

RNA-SEQ Expression


Sequence


Ensembl Acc Id: ENST00000360221   ⟹   ENSP00000353355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1742,950,526 - 42,980,003 (-)Ensembl
Ensembl Acc Id: ENST00000409103   ⟹   ENSP00000386254
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1742,950,546 - 42,979,993 (-)Ensembl
Ensembl Acc Id: ENST00000409399   ⟹   ENSP00000386621
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1742,950,530 - 42,980,490 (-)Ensembl
Ensembl Acc Id: ENST00000421990   ⟹   ENSP00000409924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1742,950,550 - 42,980,528 (-)Ensembl
Ensembl Acc Id: ENST00000423601   ⟹   ENSP00000393780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1742,954,951 - 42,980,138 (-)Ensembl
Ensembl Acc Id: ENST00000452752   ⟹   ENSP00000393019
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1742,961,264 - 42,979,663 (-)Ensembl
Ensembl Acc Id: ENST00000454303   ⟹   ENSP00000407951
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1742,964,219 - 42,980,086 (-)Ensembl
RefSeq Acc Id: NM_001136042   ⟹   NP_001129514
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381742,950,526 - 42,980,528 (-)NCBI
GRCh371741,102,543 - 41,132,545 (-)NCBI
HuRef1736,868,387 - 36,898,226 (-)NCBI
CHM1_11741,338,174 - 41,368,050 (-)NCBI
T2T-CHM13v2.01743,807,669 - 43,837,800 (-)NCBI
Sequence:
RefSeq Acc Id: NM_025267   ⟹   NP_079543
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381742,950,526 - 42,980,012 (-)NCBI
GRCh371741,102,543 - 41,132,545 (-)NCBI
HuRef1736,868,387 - 36,898,226 (-)NCBI
CHM1_11741,338,174 - 41,367,525 (-)NCBI
T2T-CHM13v2.01743,807,669 - 43,837,284 (-)NCBI
Sequence:
RefSeq Acc Id: NP_001129514   ⟸   NM_001136042
- Peptide Label: isoform 1
- UniProtKB: B3KSP9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_079543   ⟸   NM_025267
- Peptide Label: isoform 2
- UniProtKB: B3KSP9 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000393780   ⟸   ENST00000423601
Ensembl Acc Id: ENSP00000393019   ⟸   ENST00000452752
Ensembl Acc Id: ENSP00000353355   ⟸   ENST00000360221
Ensembl Acc Id: ENSP00000407951   ⟸   ENST00000454303
Ensembl Acc Id: ENSP00000386621   ⟸   ENST00000409399
Ensembl Acc Id: ENSP00000386254   ⟸   ENST00000409103
Ensembl Acc Id: ENSP00000409924   ⟸   ENST00000421990
Protein Domains
Alanyl-transfer RNA synthetases family profile   CS

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BTE6-F1-model_v2 AlphaFold Q9BTE6 1-412 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:43946 AgrOrtholog
COSMIC PTGES3L-AARSD1 COSMIC
Ensembl Genes ENSG00000108825 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000266967 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000360221 ENTREZGENE
  ENST00000360221.8 UniProtKB/Swiss-Prot
  ENST00000409103.5 UniProtKB/TrEMBL
  ENST00000409399.6 UniProtKB/TrEMBL
  ENST00000421990 ENTREZGENE
  ENST00000421990.7 UniProtKB/TrEMBL
  ENST00000423601.2 UniProtKB/TrEMBL
  ENST00000427569.7 UniProtKB/Swiss-Prot
  ENST00000452752.5 UniProtKB/TrEMBL
  ENST00000454303.1 UniProtKB/TrEMBL
Gene3D-CATH 2.40.30.130 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  2.60.40.790 UniProtKB/TrEMBL
  Threonyl-trna Synthetase, Chain A, domain 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000108825 GTEx
  ENSG00000266967 GTEx
HGNC ID HGNC:43946 ENTREZGENE
Human Proteome Map PTGES3L-AARSD1 Human Proteome Map
InterPro Ala-tRNA-synth_IIc_core UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Alanyl-tRNA_Editing_Enzymes UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CS-like_domain UniProtKB/TrEMBL
  HSP20-like_chaperone UniProtKB/TrEMBL
  p23-like UniProtKB/TrEMBL
  Thr/Ala-tRNA-synth_IIc_edit UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Transl_B-barrel_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  tRNA_SAD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:100885850 UniProtKB/Swiss-Prot
  hsa:80755 UniProtKB/Swiss-Prot
NCBI Gene PTGES3L-AARSD1 ENTREZGENE
PANTHER ALANYL-TRNA EDITING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ALANYL-TRNA EDITING PROTEIN AARSD1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN PTGES3L-RELATED UniProtKB/TrEMBL
  PTHR22932 UniProtKB/TrEMBL
Pfam tRNA_SAD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE AA_TRNA_LIGASE_II_ALA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PS51203 UniProtKB/TrEMBL
SMART tRNA_SAD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP HSP20_chap UniProtKB/TrEMBL
  SSF50447 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF55186 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt AASD1_HUMAN UniProtKB/Swiss-Prot
  B3KSP9 ENTREZGENE, UniProtKB/TrEMBL
  C9J5N1_HUMAN UniProtKB/TrEMBL
  C9JUA3_HUMAN UniProtKB/TrEMBL
  H7C054_HUMAN UniProtKB/TrEMBL
  L7N2F6_HUMAN UniProtKB/TrEMBL
UniProt Secondary B4DI73 UniProtKB/Swiss-Prot