ATG13 (autophagy related 13) - Rat Genome Database

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Gene: ATG13 (autophagy related 13) Homo sapiens
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Symbol: ATG13
Name: autophagy related 13
RGD ID: 1602498
HGNC Page HGNC:29091
Description: Enables protein kinase binding activity and protein serine/threonine kinase activator activity. Involved in autophagosome assembly; negative regulation of cell population proliferation; and positive regulation of autophagy. Located in mitochondrion and phagophore assembly site. Part of Atg1/ULK1 kinase complex. Is active in phagophore assembly site membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ATG13 autophagy related 13 homolog; autophagy-related protein 13; FLJ20698; KIAA0652; PARATARG8
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
GRCh381146,617,553 - 46,674,518 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1146,617,527 - 46,674,818 (+)EnsemblGRCh38hg38GRCh38
GRCh371146,639,103 - 46,696,068 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361146,595,703 - 46,652,644 (+)NCBINCBI36Build 36hg18NCBI36
Celera1146,786,959 - 46,844,582 (+)NCBICelera
Cytogenetic Map11p11.2NCBI
HuRef1146,345,178 - 46,403,609 (+)NCBIHuRef
CHM1_11146,637,238 - 46,695,980 (+)NCBICHM1_1
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
Object Symbol
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Original Reference(s)
ATG13HumanLiver Reperfusion Injury amelioratesISOAtg13 (Mus musculus)329902072 RGD 
Object Symbol
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Original Reference(s)
ATG13Humancongenital disorder of glycosylation type IIc  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Rambam Hasharon syndromeClinVarPMID:28492532
ATG13Humancongenital disorder of glycosylation type IIc  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Rambam Hasharon syndromeClinVarPMID:16455955 more ...
ATG13Humanintellectual disability  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Intellectual disabilityClinVar 
ATG13Humanprostate cancer  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Malignant tumor of prostateClinVarPMID:23265383

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Original Reference(s)
ATG13Human(-)-anisomycin decreases expressionEXP 6480464Anisomycin results in decreased expression of ATG13 proteinCTDPMID:27629431
ATG13Human17beta-estradiol increases expressionISOAtg13 (Mus musculus)6480464Estradiol results in increased expression of ATG13 mRNACTDPMID:39298647
ATG13Human3-chloropropane-1,2-diol increases expressionISOAtg13 (Rattus norvegicus)6480464alpha-Chlorohydrin results in increased expression of ATG13 proteinCTDPMID:34915118
ATG13Humanantimycin A multiple interactionsEXP 6480464Antimycin A promotes the reaction [ATG13 protein results in increased expression of ULK1 protein] and ATG13 protein promotes the reaction [Antimycin A results in increased expression of ULK1 protein]CTDPMID:27629431
ATG13Humanarsenite(3-) increases expressionISOAtg13 (Mus musculus)6480464arsenite results in increased expression of ATG13 mRNACTDPMID:33053406
ATG13Humanarsenite(3-) increases expressionEXP 6480464arsenite results in increased expression of ATG13 proteinCTDPMID:34929507
ATG13Humanarsenous acid increases expressionISOAtg13 (Mus musculus)6480464Arsenic Trioxide results in increased expression of ATG13 mRNACTDPMID:32112876
ATG13Humanatrazine multiple interactionsISOAtg13 (Mus musculus)6480464Lycopene inhibits the reaction [Atrazine results in increased expression of ATG13 mRNA]CTDPMID:30360616
ATG13Humanatrazine increases expressionISOAtg13 (Mus musculus)6480464Atrazine results in increased expression of ATG13 mRNACTDPMID:30360616
ATG13Humanbenzo[a]pyrene increases expressionEXP 6480464Benzo(a)pyrene results in increased expression of ATG13 proteinCTDPMID:32717239
ATG13Humanbis(2-ethylhexyl) phthalate increases expressionISOAtg13 (Mus musculus)6480464Diethylhexyl Phthalate results in increased expression of ATG13 mRNACTDPMID:34319233
ATG13Humanbisphenol A affects expressionISOAtg13 (Rattus norvegicus)6480464bisphenol A affects the expression of ATG13 mRNACTDPMID:25181051
ATG13Humanbisphenol A decreases methylationEXP 6480464bisphenol A results in decreased methylation of ATG13 geneCTDPMID:31601247
ATG13Humanbisphenol A decreases expressionISOAtg13 (Rattus norvegicus)6480464bisphenol A results in decreased expression of ATG13 mRNACTDPMID:34947998
ATG13Humanbisphenol F increases expressionISOAtg13 (Mus musculus)6480464bisphenol F results in increased expression of ATG13 mRNACTDPMID:38685157
ATG13Humancadmium atom decreases expressionISOAtg13 (Mus musculus)6480464Cadmium results in decreased expression of ATG13 mRNACTDPMID:24067728
ATG13Humancadmium sulfide increases expressionEXP 6480464cadmium sulfide results in increased expression of ATG13 mRNACTDPMID:27866839
ATG13Humancarbon nanotube decreases expressionISOAtg13 (Mus musculus)6480464Nanotubes more ...CTDPMID:25554681
ATG13Humancisplatin multiple interactionsEXP 6480464[Cisplatin co-treated with jinfukang] results in increased expression of ATG13 mRNACTDPMID:27392435
ATG13Humancisplatin increases expressionEXP 6480464Cisplatin results in increased expression of ATG13 mRNACTDPMID:27392435

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Biological Process
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Original Reference(s)
ATG13Humanautophagosome assembly involved_inIDA 150520179 PMID:19225151ComplexPortalPMID:19225151
ATG13Humanautophagosome assembly involved_inIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
ATG13Humanautophagosome assembly acts_upstream_of_or_withinIMP 150520179 PMID:19211835MGIPMID:19211835
ATG13Humanautophagosome assembly involved_inIMP 150520179 PMID:19211835UniProtPMID:19211835
ATG13Humanautophagosome assembly involved_inIEAInterPro:IPR040182150520179 InterProGO_REF:0000002
ATG13Humanautophagy involved_inIEAInterPro:IPR018731150520179 InterProGO_REF:0000002
ATG13Humanautophagy involved_inIEAUniProtKB-KW:KW-0072150520179 UniProtGO_REF:0000043
ATG13Humanmitophagy involved_inIBAMGI:1196429 more ...150520179 GO_CentralGO_REF:0000033
ATG13Humanmitophagy involved_inIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
ATG13Humannegative regulation of cell population proliferation involved_inIDA 150520179 PMID:21795849ComplexPortalPMID:21795849
ATG13Humannegative regulation of cell population proliferation involved_inIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
ATG13Humanpiecemeal microautophagy of the nucleus involved_inIBAPANTHER:PTN001268151 and SGD:S000006389150520179 GO_CentralGO_REF:0000033
ATG13Humanpositive regulation of autophagy involved_inIDA 150520179 PMID:29487085UniProtPMID:29487085
ATG13Humanpositive regulation of autophagy involved_inIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
ATG13Humanpositive regulation of autophagy involved_inISOComplexPortal:CPX-380150520179 ComplexPortalGO_REF:0000114
ATG13Humanpositive regulation of protein targeting to mitochondrion involved_inHMP 150520179 PMID:24270810ParkinsonsUK-UCLPMID:24270810
ATG13Humanprotein localization to phagophore assembly site involved_inIBAPANTHER:PTN001268151 and SGD:S000006389150520179 GO_CentralGO_REF:0000033
ATG13Humanresponse to mitochondrial depolarisation involved_inIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
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Cellular Component
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Original Reference(s)
ATG13HumanAtg1/ULK1 kinase complex part_ofIPI 150520179 PMID:19597335ComplexPortalPMID:19597335
ATG13HumanAtg1/ULK1 kinase complex part_ofIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
ATG13HumanAtg1/ULK1 kinase complex part_ofIBAFB:FBgn0261108 more ...150520179 GO_CentralGO_REF:0000033
ATG13HumanAtg1/ULK1 kinase complex part_ofIEAInterPro:IPR018731150520179 InterProGO_REF:0000002
ATG13HumanAtg1/ULK1 kinase complex part_ofIPIUniProtKB:O75385 and UniProtKB:Q8TDY2150520179 PMID:19211835UniProtPMID:19211835
ATG13Humanautophagosome is_active_inIBACGD:CAL0000176796 more ...150520179 GO_CentralGO_REF:0000033
ATG13Humancytoplasm located_inIEAUniProtKB-KW:KW-0963150520179 UniProtGO_REF:0000043
ATG13Humancytoplasm is_active_inIC 150520179 PMID:29487085UniProtPMID:29487085
ATG13Humancytosol located_inIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
ATG13Humancytosol is_active_inIBAMGI:1196429 and PANTHER:PTN001268151150520179 GO_CentralGO_REF:0000033
ATG13Humancytosol located_inIEAUniProtKB-SubCell:SL-0091150520179 UniProtGO_REF:0000044
ATG13Humancytosol located_inTAS 150520179 ReactomeReactome:R-HSA-5665868 more ...
ATG13Humanendoplasmic reticulum membrane located_inTAS 150520179 ReactomeReactome:R-HSA-1632857 more ...
ATG13Humanmitochondrion located_inIDA 150520179 PMID:21855797ParkinsonsUK-UCLPMID:21855797
ATG13Humanphagophore assembly site located_inISSUniProtKB:Q91YI1150520179 UniProtGO_REF:0000024
ATG13Humanphagophore assembly site is_active_inIBAMGI:1196429 more ...150520179 GO_CentralGO_REF:0000033
ATG13Humanphagophore assembly site located_inIDA 150520179 PMID:19597335ComplexPortalPMID:19597335
ATG13Humanphagophore assembly site located_inIEAUniProtKB:Q91YI1 and ensembl:ENSMUSP00000076081150520179 EnsemblGO_REF:0000107
ATG13Humanphagophore assembly site located_inIEAUniProtKB-SubCell:SL-0220150520179 UniProtGO_REF:0000044
ATG13Humanphagophore assembly site membrane is_active_inIDA 150520179 PMID:19597335UniProtPMID:19597335
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Molecular Function
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Original Reference(s)
ATG13Humanprotein binding enablesIPIUniProtKB:Q9BSB4150520179 PMID:19597335 more ...IntActPMID:19597335 more ...
ATG13Humanprotein binding enablesIPIUniProtKB:O75385150520179 PMID:23524951 more ...IntActPMID:23524951 more ...
ATG13Humanprotein binding enablesIPIUniProtKB:O75385 more ...150520179 PMID:19597335 and PMID:23392225IntActPMID:19597335 and PMID:23392225
ATG13Humanprotein binding enablesIPIUniProtKB:Q96LT7-1150520179 PMID:29950492IntActPMID:29950492
ATG13Humanprotein binding enablesIPIUniProtKB:P60520150520179 PMID:21900206IntActPMID:21900206
ATG13Humanprotein binding enablesIPIUniProtKB:O60238 and UniProtKB:Q9Z2F7150520179 PMID:20200478ParkinsonsUK-UCLPMID:20200478
ATG13Humanprotein binding enablesIPIUniProtKB:O95166 more ...150520179 PMID:24290141IntActPMID:24290141
ATG13Humanprotein binding enablesIPIUniProtKB:O75385 more ...150520179 PMID:20562859IntActPMID:20562859
ATG13Humanprotein binding enablesIPIUniProtKB:Q96LT7-1 and UniProtKB:Q96LT7-2150520179 PMID:27334615IntActPMID:27334615
ATG13Humanprotein binding enablesIPIUniProtKB:P37173 and UniProtKB:P45973150520179 PMID:32814053IntActPMID:32814053
ATG13Humanprotein binding enablesIPIUniProtKB:Q8TEV9150520179 PMID:28195531HGNCPMID:28195531
ATG13Humanprotein binding enablesIPIUniProtKB:O75385 and UniProtKB:Q8TDY2150520179 PMID:19211835 and PMID:31806350UniProtPMID:19211835 and PMID:31806350
ATG13Humanprotein binding enablesIPIUniProtKB:O75665 and UniProtKB:Q8TDY2150520179 PMID:33368531IntActPMID:33368531
ATG13Humanprotein binding enablesIPIUniProtKB:O75385 more ...150520179 PMID:35271311IntActPMID:35271311
ATG13Humanprotein binding enablesIPIUniProtKB:O75385 and UniProtKB:Q9BSB4150520179 PMID:34524948IntActPMID:34524948
ATG13Humanprotein kinase binding enablesIPIUniProtKB:O75385 and UniProtKB:Q8IYT8150520179 PMID:18936157UniProtPMID:18936157
ATG13Humanprotein kinase binding enablesIDA 150520179 PMID:29487085UniProtPMID:29487085
ATG13Humanprotein kinase regulator activity enablesIBAPANTHER:PTN001268151 more ...150520179 GO_CentralGO_REF:0000033
ATG13Humanprotein serine/threonine kinase activator activity enablesIDA 150520179 PMID:19225151UniProtPMID:19225151
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RGD Manual Annotations


  
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Original Reference(s)
ATG13Humanautophagy pathway   TAS 4889529 RGD 

Imported Annotations - PID (archival)

Object Symbol
Species
Term
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Evidence
With
Reference
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Original Reference(s)
ATG13HumanmTOR signaling pathway   EXP 6484113 PIDPID:200096
Object Symbol
Species
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Qualifier
Evidence
With
Reference
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Original Reference(s)
ATG13HumanIntellectual disability  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Intellectual disabilityClinVar 
ATG13HumanProstate cancer  IAGP (Homo sapiens)8554872ClinVar Annotator: match by term: Prostatic cancerClinVarPMID:23265383

#
Reference Title
Reference Citation
1. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
4. Hepatic interferon regulatory factor 8 expression mediates liver ischemia/reperfusion injury in mice. Shi G, etal., Biochem Pharmacol. 2021 Oct;192:114728. doi: 10.1016/j.bcp.2021.114728. Epub 2021 Aug 13.
5. Mammalian autophagy: core molecular machinery and signaling regulation. Yang Z and Klionsky DJ, Curr Opin Cell Biol. 2010 Apr;22(2):124-31. Epub 2009 Dec 23.
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PMID:8125298   PMID:8619474   PMID:9110174   PMID:9734811   PMID:12107413   PMID:12477932   PMID:14702039   PMID:15489334   PMID:16196087   PMID:16344560   PMID:17204848   PMID:17207965  
PMID:18936157   PMID:19211835   PMID:19225151   PMID:19258318   PMID:19287211   PMID:19597335   PMID:19690328   PMID:20200478   PMID:20562859   PMID:20694011   PMID:21460630   PMID:21460634  
PMID:21475306   PMID:21795849   PMID:21832049   PMID:21855797   PMID:21873635   PMID:21900206   PMID:21976705   PMID:22020285   PMID:23043107   PMID:23262492   PMID:23392225   PMID:23524951  
PMID:24100292   PMID:24270810   PMID:24290141   PMID:25040165   PMID:25126726   PMID:25686248   PMID:25909887   PMID:26018823   PMID:26299944   PMID:26687479   PMID:26687681   PMID:27046250  
PMID:27203176   PMID:27334615   PMID:27387056   PMID:27617292   PMID:28059666   PMID:28195531   PMID:28253953   PMID:28514442   PMID:28611215   PMID:28639909   PMID:28718761   PMID:29196462  
PMID:29313410   PMID:29453315   PMID:29487085   PMID:29634390   PMID:29950492   PMID:30081750   PMID:30404831   PMID:30669939   PMID:30853401   PMID:30853402   PMID:31270922   PMID:31732843  
PMID:31806350   PMID:32035621   PMID:32111227   PMID:32296183   PMID:32320309   PMID:32453962   PMID:32516310   PMID:32529326   PMID:32543267   PMID:32556086   PMID:32668203   PMID:32707033  
PMID:32814053   PMID:33226137   PMID:33368531   PMID:33422265   PMID:33450483   PMID:33499712   PMID:33682133   PMID:33961781   PMID:34226595   PMID:34369648   PMID:34502089   PMID:34524948  
PMID:34917906   PMID:35220397   PMID:35271311   PMID:35487443   PMID:35545034   PMID:35670107   PMID:36169801   PMID:36736316   PMID:36897256   PMID:36898370   PMID:36931259   PMID:36949045  
PMID:37394799   PMID:37567770   PMID:37689310  
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ATG13
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381146,617,553 - 46,674,518 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1146,617,527 - 46,674,818 (+)EnsemblGRCh38hg38GRCh38
GRCh371146,639,103 - 46,696,068 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361146,595,703 - 46,652,644 (+)NCBINCBI36Build 36hg18NCBI36
Celera1146,786,959 - 46,844,582 (+)NCBICelera
Cytogenetic Map11p11.2NCBI
HuRef1146,345,178 - 46,403,609 (+)NCBIHuRef
CHM1_11146,637,238 - 46,695,980 (+)NCBICHM1_1
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBIT2T-CHM13v2.0
Atg13
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39291,504,957 - 91,540,947 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl291,504,963 - 91,540,921 (-)EnsemblGRCm39 Ensembl
GRCm38291,674,612 - 91,710,597 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl291,674,618 - 91,710,576 (-)EnsemblGRCm38mm10GRCm38
MGSCv37291,514,782 - 91,550,733 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36291,475,464 - 91,511,415 (-)NCBIMGSCv36mm8
Celera293,064,097 - 93,099,336 (-)NCBICelera
Cytogenetic Map2E1NCBI
cM Map250.63NCBI
Atg13
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8398,102,831 - 98,136,741 (-)NCBIGRCr8
mRatBN7.2377,647,069 - 77,681,028 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl377,645,790 - 77,681,043 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx381,122,107 - 81,156,207 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0389,721,130 - 89,755,231 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0387,572,391 - 87,606,504 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0380,580,549 - 80,614,554 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl380,581,247 - 80,601,410 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0387,279,649 - 87,313,654 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4376,056,642 - 76,090,287 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1375,953,473 - 75,986,537 (-)NCBI
Celera376,851,283 - 76,885,195 (-)NCBICelera
Cytogenetic Map3q24NCBI
Atg13
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554221,398,593 - 1,432,438 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554221,398,646 - 1,432,440 (-)NCBIChiLan1.0ChiLan1.0
ATG13
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2948,833,991 - 48,878,284 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11148,840,876 - 48,898,053 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01146,567,728 - 46,623,609 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11147,126,380 - 47,182,848 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1147,126,380 - 47,182,850 (+)Ensemblpanpan1.1panPan2
ATG13
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11842,834,538 - 42,886,873 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1842,836,755 - 42,886,855 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1841,563,260 - 41,615,540 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01843,490,641 - 43,542,934 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1843,482,301 - 43,542,937 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11842,975,663 - 43,027,961 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01842,531,296 - 42,583,663 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01843,260,591 - 43,313,187 (-)NCBIUU_Cfam_GSD_1.0
Atg13
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494720,311,338 - 20,361,623 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365622,423,001 - 2,473,232 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365622,424,398 - 2,473,103 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ATG13
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl215,856,860 - 15,916,109 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1215,856,859 - 15,916,122 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2217,207,885 - 17,266,756 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ATG13
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1118,651,872 - 18,712,395 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl118,652,998 - 18,712,482 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666038115,936,173 - 115,995,623 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Atg13
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247671,924,672 - 1,953,868 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

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Variants in ATG13
52 total Variants

1 to 10 of 77 rows
Name
Type
Condition(s)
Position(s)
Clinical significance
GRCh38/hg38 11p13-11.2(chr11:35663578-46959820)x1 copy number loss See cases [RCV000052679] Chr11:35663578..46959820 [GRCh38]
Chr11:35685126..46981371 [GRCh37]
Chr11:35641702..46937947 [NCBI36]
Chr11:11p13-11.2
pathogenic
GRCh38/hg38 11p12-11.2(chr11:36508280-48643003)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052680]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052680]|See cases [RCV000052680] Chr11:36508280..48643003 [GRCh38]
Chr11:36529830..48664555 [GRCh37]
Chr11:36486406..48621131 [NCBI36]
Chr11:11p12-11.2
pathogenic
ATG13:c.790-759C>T single nucleotide variant Malignant melanoma [RCV000069371] Chr11:46664090 [GRCh38]
Chr11:46685640 [GRCh37]
Chr11:46642216 [NCBI36]
Chr11:11p11.2
not provided
ATG13:c.1200G>A single nucleotide variant Malignant melanoma [RCV000069372] Chr11:46668546 [GRCh38]
Chr11:46690096 [GRCh37]
Chr11:46646672 [NCBI36]
Chr11:11p11.2
not provided
NM_001142673.2(ATG13):c.1477-946A>G single nucleotide variant Lung cancer [RCV000110091] Chr11:46671309 [GRCh38]
Chr11:46692859 [GRCh37]
Chr11:11p11.2
uncertain significance
NM_001346311.2(ATG13):c.1576-1G>C single nucleotide variant Malignant tumor of prostate [RCV000149106] Chr11:46672254 [GRCh38]
Chr11:46693804 [GRCh37]
Chr11:11p11.2
uncertain significance
GRCh38/hg38 11p12-11.2(chr11:41118322-48643003)x1 copy number loss See cases [RCV000135405] Chr11:41118322..48643003 [GRCh38]
Chr11:41139872..48664555 [GRCh37]
Chr11:41096448..48621131 [NCBI36]
Chr11:11p12-11.2
pathogenic
GRCh38/hg38 11p12-11.12(chr11:39179252-49135735)x1 copy number loss See cases [RCV000137391] Chr11:39179252..49135735 [GRCh38]
Chr11:39200802..49157287 [GRCh37]
Chr11:39157378..49113863 [NCBI36]
Chr11:11p12-11.12
pathogenic
GRCh38/hg38 11p12-11.12(chr11:42727555-49135735)x3 copy number gain See cases [RCV000139422] Chr11:42727555..49135735 [GRCh38]
Chr11:42749105..49157287 [GRCh37]
Chr11:42705681..49113863 [NCBI36]
Chr11:11p12-11.12
likely pathogenic
GRCh38/hg38 11p11.2(chr11:46420955-46728372)x3 copy number gain See cases [RCV000141333] Chr11:46420955..46728372 [GRCh38]
Chr11:46442505..46749922 [GRCh37]
Chr11:46399081..46706498 [NCBI36]
Chr11:11p11.2
uncertain significance
1 to 10 of 77 rows

Predicted Target Of
Summary Value
Count of predictions:14628
Count of miRNA genes:1305
Interacting mature miRNAs:1700
Transcripts:ENST00000312040, ENST00000359513, ENST00000395549, ENST00000434074, ENST00000451945, ENST00000524625, ENST00000525009, ENST00000525850, ENST00000526485, ENST00000526508, ENST00000526715, ENST00000527907, ENST00000528145, ENST00000528494, ENST00000528704, ENST00000528984, ENST00000529395, ENST00000529655, ENST00000530500, ENST00000530942, ENST00000531933, ENST00000532067, ENST00000533316, ENST00000533325, ENST00000534610, ENST00000577256, ENST00000578626, ENST00000579280, ENST00000580238, ENST00000581416, ENST00000581438, ENST00000582547, ENST00000583249
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.


1 to 9 of 9 rows
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
597059733GWAS1155807_Hreaction time measurement QTL GWAS1155807 (human)7e-09cognitive behavior trait (VT:0010450)114667018746670188Human
597021741GWAS1117815_Hinterleukin 17 measurement QTL GWAS1117815 (human)0.000008blood interleukin-17 amount (VT:0008613)114667005546670056Human
597072190GWAS1168264_HHeadache QTL GWAS1168264 (human)4e-08Headache114667393346673934Human
597234787GWAS1330861_Happendicular lean mass QTL GWAS1330861 (human)2e-11appendicular lean mass114662816946628170Human
597271650GWAS1367724_Hsystolic blood pressure QTL GWAS1367724 (human)4e-09systolic blood pressuresystolic blood pressure (CMO:0000004)114662710946627110Human
597319921GWAS1415995_HAlzheimer disease, polygenic risk score QTL GWAS1415995 (human)3e-08Alzheimer disease, polygenic risk score114667018746670188Human
597077352GWAS1173426_Hage at first sexual intercourse measurement QTL GWAS1173426 (human)5e-09age at first sexual intercourse measurement114665480746654808Human
597264630GWAS1360704_Hdiastolic blood pressure QTL GWAS1360704 (human)1e-09diastolic blood pressurediastolic blood pressure (CMO:0000005)114662710946627110Human
597253398GWAS1349472_Hnon-melanoma skin carcinoma QTL GWAS1349472 (human)0.000003non-melanoma skin carcinoma114663285446632855Human

1 to 9 of 9 rows
D11S3306  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371146,694,896 - 46,695,219UniSTSGRCh37
Build 361146,651,472 - 46,651,795RGDNCBI36
Celera1146,843,110 - 46,843,433RGD
Cytogenetic Map11p11.2UniSTS
HuRef1146,400,936 - 46,401,259UniSTS
T16117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371146,695,873 - 46,696,029UniSTSGRCh37
Build 361146,652,449 - 46,652,605RGDNCBI36
Celera1146,844,087 - 46,844,243RGD
Cytogenetic Map11p11.2UniSTS
HuRef1146,401,913 - 46,402,069UniSTS
Whitehead-YAC Contig Map11 UniSTS
D11S2311E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371146,694,340 - 46,694,500UniSTSGRCh37
Build 361146,650,916 - 46,651,076RGDNCBI36
Celera1146,842,554 - 46,842,714RGD
Cytogenetic Map11p11.2UniSTS
HuRef1146,400,380 - 46,400,540UniSTS
GeneMap99-GB4 RH Map11167.08UniSTS
NCBI RH Map11285.0UniSTS
RH15977  
Human AssemblyChrPosition (strand)SourceJBrowse
Celera1146,842,518 - 46,842,704RGD
Cytogenetic Map11p11.2UniSTS
HuRef1146,400,344 - 46,400,530UniSTS
GeneMap99-GB4 RH Map11163.64UniSTS




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 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1


1 to 30 of 89 rows
RefSeq Transcripts NG_051811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001142673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001205119 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001205120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001205121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001205122 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346313 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346314 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346315 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346316 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346318 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346319 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346320 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346322 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346323 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346325 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346327 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346329 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001346334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 30 of 89 rows

Ensembl Acc Id: ENST00000359513   ⟹   ENSP00000352500
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,596 - 46,674,818 (+)Ensembl
Ensembl Acc Id: ENST00000395549   ⟹   ENSP00000378919
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,791 - 46,657,191 (+)Ensembl
Ensembl Acc Id: ENST00000524625   ⟹   ENSP00000433543
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,577 - 46,674,520 (+)Ensembl
Ensembl Acc Id: ENST00000525009   ⟹   ENSP00000436174
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,664,000 - 46,669,441 (+)Ensembl
Ensembl Acc Id: ENST00000525850
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,648,727 - 46,657,618 (+)Ensembl
Ensembl Acc Id: ENST00000526485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,672,795 - 46,674,513 (+)Ensembl
Ensembl Acc Id: ENST00000526508   ⟹   ENSP00000431974
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,563 - 46,674,520 (+)Ensembl
Ensembl Acc Id: ENST00000526715
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,545 - 46,630,022 (+)Ensembl
Ensembl Acc Id: ENST00000527907
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,656,953 - 46,667,865 (+)Ensembl
Ensembl Acc Id: ENST00000528145
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,644,337 - 46,656,398 (+)Ensembl
Ensembl Acc Id: ENST00000528494   ⟹   ENSP00000432412
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,600 - 46,672,726 (+)Ensembl
Ensembl Acc Id: ENST00000528704
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,657,060 - 46,659,402 (+)Ensembl
Ensembl Acc Id: ENST00000528984
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,656,951 - 46,664,149 (+)Ensembl
Ensembl Acc Id: ENST00000529395   ⟹   ENSP00000431877
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,665,509 - 46,669,532 (+)Ensembl
Ensembl Acc Id: ENST00000529655   ⟹   ENSP00000433756
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,541 - 46,673,041 (+)Ensembl
Ensembl Acc Id: ENST00000530500   ⟹   ENSP00000434390
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,563 - 46,672,660 (+)Ensembl
Ensembl Acc Id: ENST00000530942
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,578 - 46,630,028 (+)Ensembl
Ensembl Acc Id: ENST00000531933   ⟹   ENSP00000434125
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,659,422 - 46,672,773 (+)Ensembl
Ensembl Acc Id: ENST00000532067   ⟹   ENSP00000437191
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,667,872 - 46,668,882 (+)Ensembl
Ensembl Acc Id: ENST00000533316
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,659,335 - 46,668,890 (+)Ensembl
Ensembl Acc Id: ENST00000533325   ⟹   ENSP00000436931
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,549 - 46,650,216 (+)Ensembl
Ensembl Acc Id: ENST00000534610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,582 - 46,660,029 (+)Ensembl
Ensembl Acc Id: ENST00000577256   ⟹   ENSP00000462167
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,568 - 46,645,889 (+)Ensembl
Ensembl Acc Id: ENST00000578626   ⟹   ENSP00000462644
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,568 - 46,645,369 (+)Ensembl
Ensembl Acc Id: ENST00000579280
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,535 - 46,625,364 (+)Ensembl
Ensembl Acc Id: ENST00000580238   ⟹   ENSP00000463808
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,527 - 46,645,367 (+)Ensembl
Ensembl Acc Id: ENST00000581416   ⟹   ENSP00000464274
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,536 - 46,645,419 (+)Ensembl
Ensembl Acc Id: ENST00000581438   ⟹   ENSP00000463550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,557 - 46,644,331 (+)Ensembl
Ensembl Acc Id: ENST00000582547   ⟹   ENSP00000464091
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,585 - 46,645,383 (+)Ensembl
Ensembl Acc Id: ENST00000583249   ⟹   ENSP00000463998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,557 - 46,645,350 (+)Ensembl
Ensembl Acc Id: ENST00000683050   ⟹   ENSP00000507809
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1146,617,553 - 46,674,518 (+)Ensembl
RefSeq Acc Id: NM_001142673   ⟹   NP_001136145
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
GRCh371146,638,826 - 46,697,569 (+)ENTREZGENE
GRCh371146,638,826 - 46,697,569 (+)NCBI
Celera1146,786,959 - 46,844,582 (+)RGD
HuRef1146,345,178 - 46,403,609 (+)ENTREZGENE
CHM1_11146,637,238 - 46,695,980 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001205119   ⟹   NP_001192048
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
GRCh371146,638,826 - 46,697,569 (+)NCBI
HuRef1146,345,178 - 46,403,609 (+)ENTREZGENE
CHM1_11146,637,238 - 46,695,980 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001205120   ⟹   NP_001192049
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
GRCh371146,638,826 - 46,697,569 (+)NCBI
HuRef1146,345,178 - 46,403,609 (+)ENTREZGENE
CHM1_11146,637,238 - 46,695,980 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001205121   ⟹   NP_001192050
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
GRCh371146,638,826 - 46,697,569 (+)NCBI
HuRef1146,345,178 - 46,403,609 (+)ENTREZGENE
CHM1_11146,637,238 - 46,695,980 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001205122   ⟹   NP_001192051
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
GRCh371146,638,826 - 46,697,569 (+)NCBI
HuRef1146,345,178 - 46,403,609 (+)ENTREZGENE
CHM1_11146,637,238 - 46,695,980 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346311   ⟹   NP_001333240
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346312   ⟹   NP_001333241
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346313   ⟹   NP_001333242
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346314   ⟹   NP_001333243
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346315   ⟹   NP_001333244
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346316   ⟹   NP_001333245
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346317   ⟹   NP_001333246
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346318   ⟹   NP_001333247
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346319   ⟹   NP_001333248
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346320   ⟹   NP_001333249
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346321   ⟹   NP_001333250
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346322   ⟹   NP_001333251
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346323   ⟹   NP_001333252
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346324   ⟹   NP_001333253
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346325   ⟹   NP_001333254
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346326   ⟹   NP_001333255
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346327   ⟹   NP_001333256
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346328   ⟹   NP_001333257
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346329   ⟹   NP_001333258
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346330   ⟹   NP_001333259
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346331   ⟹   NP_001333260
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346332   ⟹   NP_001333261
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346333   ⟹   NP_001333262
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346334   ⟹   NP_001333263
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346335   ⟹   NP_001333264
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346336   ⟹   NP_001333265
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346337   ⟹   NP_001333266
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346338   ⟹   NP_001333267
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346340   ⟹   NP_001333269
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346342   ⟹   NP_001333271
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346344   ⟹   NP_001333273
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346346   ⟹   NP_001333275
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346348   ⟹   NP_001333277
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346349   ⟹   NP_001333278
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346350   ⟹   NP_001333279
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346351   ⟹   NP_001333280
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346352   ⟹   NP_001333281
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346353   ⟹   NP_001333282
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346354   ⟹   NP_001333283
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346355   ⟹   NP_001333284
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346356   ⟹   NP_001333285
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346357   ⟹   NP_001333286
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346358   ⟹   NP_001333287
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346359   ⟹   NP_001333288
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001346360   ⟹   NP_001333289
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NM_014741   ⟹   NP_055556
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
GRCh371146,638,826 - 46,697,569 (+)ENTREZGENE
GRCh371146,638,826 - 46,697,569 (+)NCBI
Build 361146,595,703 - 46,652,644 (+)NCBI Archive
Celera1146,786,959 - 46,844,582 (+)RGD
HuRef1146,345,178 - 46,403,609 (+)ENTREZGENE
CHM1_11146,637,238 - 46,695,980 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NR_144422
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NR_144423
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
RefSeq Acc Id: NR_144424
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,553 - 46,674,518 (+)NCBI
T2T-CHM13v2.01146,773,592 - 46,830,534 (+)NCBI
Sequence:
1 to 30 of 85 rows
Protein RefSeqs NP_001136145 (Get FASTA)   NCBI Sequence Viewer  
  NP_001192048 (Get FASTA)   NCBI Sequence Viewer  
  NP_001192049 (Get FASTA)   NCBI Sequence Viewer  
  NP_001192050 (Get FASTA)   NCBI Sequence Viewer  
  NP_001192051 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333240 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333241 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333242 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333243 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333244 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333245 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333246 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333247 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333248 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333249 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333250 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333251 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333252 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333253 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333254 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333255 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333256 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333257 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333258 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333259 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333260 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333261 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333262 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333263 (Get FASTA)   NCBI Sequence Viewer  
  NP_001333264 (Get FASTA)   NCBI Sequence Viewer  
1 to 30 of 85 rows
1 to 5 of 71 rows
1 to 5 of 71 rows
RefSeq Acc Id: NP_055556   ⟸   NM_014741
- Peptide Label: isoform f
- UniProtKB: A8KAP4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001136145   ⟸   NM_001142673
- Peptide Label: isoform c
- UniProtKB: Q9BRL3 (UniProtKB/Swiss-Prot),   Q53EN6 (UniProtKB/Swiss-Prot),   E9PQZ8 (UniProtKB/Swiss-Prot),   D3DQQ2 (UniProtKB/Swiss-Prot),   D3DQQ1 (UniProtKB/Swiss-Prot),   B4DFI4 (UniProtKB/Swiss-Prot),   Q9H8B0 (UniProtKB/Swiss-Prot),   O75143 (UniProtKB/Swiss-Prot),   A8K0S6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001192050   ⟸   NM_001205121
- Peptide Label: isoform f
- UniProtKB: A8KAP4 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001192048   ⟸   NM_001205119
- Peptide Label: isoform a
- UniProtKB: A8K0S6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001192049   ⟸   NM_001205120
- Peptide Label: isoform c
- UniProtKB: Q9BRL3 (UniProtKB/Swiss-Prot),   Q53EN6 (UniProtKB/Swiss-Prot),   E9PQZ8 (UniProtKB/Swiss-Prot),   D3DQQ2 (UniProtKB/Swiss-Prot),   D3DQQ1 (UniProtKB/Swiss-Prot),   B4DFI4 (UniProtKB/Swiss-Prot),   Q9H8B0 (UniProtKB/Swiss-Prot),   O75143 (UniProtKB/Swiss-Prot),   A8K0S6 (UniProtKB/TrEMBL)
- Sequence:
Name Modeler Protein Id AA Range Protein Structure
AF-O75143-F1-model_v2 AlphaFold O75143 1-517 view protein structure

RGD ID:6788829
Promoter ID:HG_KWN:12766
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000359513,   ENST00000395549,   NM_001142673,   NM_014741,   NR_024587,   NR_024588,   NR_024589,   UC001NCY.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361146,595,206 - 46,595,937 (+)MPROMDB
RGD ID:7220191
Promoter ID:EPDNEW_H15841
Type:initiation region
Name:ATG13_2
Description:autophagy related 13
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15842  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,305 - 46,617,365EPDNEW
RGD ID:7220193
Promoter ID:EPDNEW_H15842
Type:initiation region
Name:ATG13_1
Description:autophagy related 13
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H15841  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381146,617,563 - 46,617,623EPDNEW


1 to 40 of 60 rows
Database
Acc Id
Source(s)
COSMIC ATG13 COSMIC
Ensembl Genes ENSG00000175224 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000359513 ENTREZGENE
  ENST00000359513.8 UniProtKB/Swiss-Prot
  ENST00000524625 ENTREZGENE
  ENST00000524625.5 UniProtKB/Swiss-Prot
  ENST00000526508 ENTREZGENE
  ENST00000526508.5 UniProtKB/Swiss-Prot
  ENST00000528494 ENTREZGENE
  ENST00000528494.5 UniProtKB/Swiss-Prot
  ENST00000529655 ENTREZGENE
  ENST00000529655.5 UniProtKB/Swiss-Prot
  ENST00000530500 ENTREZGENE
  ENST00000530500.5 UniProtKB/Swiss-Prot
  ENST00000683050 ENTREZGENE
  ENST00000683050.1 UniProtKB/Swiss-Prot
Gene3D-CATH 3.30.900.10 UniProtKB/Swiss-Prot
GTEx ENSG00000175224 GTEx
HGNC ID HGNC:29091 ENTREZGENE
Human Proteome Map ATG13 Human Proteome Map
InterPro ATG13 UniProtKB/Swiss-Prot
  HORMA_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:9776 UniProtKB/Swiss-Prot
NCBI Gene 9776 ENTREZGENE
OMIM 615088 OMIM
PANTHER AUTOPHAGY-RELATED PROTEIN 13 UniProtKB/Swiss-Prot
  PTHR13430 UniProtKB/Swiss-Prot
PharmGKB PA165543187 PharmGKB
UniProt A0A1B0GXJ3_HUMAN UniProtKB/TrEMBL
  A8K0S6 ENTREZGENE, UniProtKB/TrEMBL
  A8KAP4 ENTREZGENE, UniProtKB/TrEMBL
  ATG13_HUMAN UniProtKB/Swiss-Prot
  B4DFI4 ENTREZGENE
  B4DKE5 ENTREZGENE, UniProtKB/TrEMBL
  D3DQQ1 ENTREZGENE
  D3DQQ2 ENTREZGENE
  E9PPR2_HUMAN UniProtKB/TrEMBL
  E9PQZ8 ENTREZGENE
  H0YCL5_HUMAN UniProtKB/TrEMBL
  H0YDR0_HUMAN UniProtKB/TrEMBL
1 to 40 of 60 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2012-06-12 ATG13  autophagy related 13  ATG13  ATG13 autophagy related 13 homolog (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED
2011-07-27 ATG13  ATG13 autophagy related 13 homolog (S. cerevisiae)  KIAA0652  KIAA0652  Symbol and/or name change 5135510 APPROVED