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Center for Computational Systems Medicine
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Gene summary

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Gene structures and expression levels

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Exon skipping events with PSIs in TCGA

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Exon skipping events with PSIs in GTEx

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Open reading frame (ORF) annotation in the exon skipping event

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Exon skipping events in the canonical protein sequence

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SNVs in the skipped exons with depth of coverage

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Splicing Quantitative Trait Loci (sQTLs) in the skipped exons

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon

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Related drugs with this gene

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Related diseases with this gene

Gene summary for ADAM28

check button Gene summary
Gene informationGene symbol

ADAM28

Gene ID

10863

Gene nameADAM metallopeptidase domain 28
SynonymsADAM 28|MDC-L|MDCL|eMDC II|eMDCII
Cytomap

8p21.2

Type of geneprotein-coding
Descriptiondisintegrin and metalloproteinase domain-containing protein 28epididymal metalloproteinase-like, disintegrin-like, and cysteine-rich protein IIepididymial metalloproteinase-like, disintegrin-like, and cysteine-rich protein IImetalloproteinase-like, dis
Modification date20180519
UniProtAcc

Q9UKQ2

ContextPubMed: ADAM28 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract]
- Title (PMID)

check button Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez
GeneGO IDGO termPubMed ID

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Exon skipping events across known transcript of Ensembl for ADAM28 from UCSC genome browser

check buttonSkipped exons in TCGA and GTEx based on Ensembl gene isoform structure.
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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Gene isoform structures and expression levels for ADAM28

check button Expression levels of gene isoforms across TCGA.
gencode gene structure

check button Expression levels of gene isoforms across GTEx.
gencode gene structure


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Exon skipping events with PSIs in TCGA for ADAM28

check button Information of exkip skipping event in TCGA.
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_482265824151623:24151708:24157486:24157590:24166153:2416628124157486:24157590ENSG00000042980.8ENST00000523379.1
exon_skip_482266824151623:24151708:24157486:24157590:24167406:2416748324157486:24157590ENSG00000042980.8ENST00000397649.3,ENST00000437154.2,ENST00000540823.1,ENST00000520448.1
exon_skip_482270824157490:24157590:24166153:24166281:24167406:2416748324166153:24166281ENSG00000042980.8ENST00000523379.1
exon_skip_482271824157486:24157590:24167406:24167483:24167675:2416775424167406:24167483ENSG00000042980.8ENST00000523440.1,ENST00000397649.3,ENST00000437154.2,ENST00000540823.1,ENST00000520448.1,ENST00000265769.4
exon_skip_482272824167675:24167754:24168873:24168950:24170900:2417109324168873:24168950ENSG00000042980.8ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4
exon_skip_482273824167675:24167754:24168873:24168950:24177748:2417782024168873:24168950ENSG00000042980.8ENST00000540823.1
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENSG00000042980.8ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4
exon_skip_482277824170900:24171093:24177748:24177820:24178730:2417880224177748:24177820ENSG00000042980.8ENST00000437154.2,ENST00000265769.4
exon_skip_482285824201018:24201097:24207376:24207485:24208744:2420879924207376:24207485ENSG00000042980.8ENST00000518326.1,ENST00000521629.1,ENST00000265769.4
exon_skip_482286824201018:24201101:24207376:24207485:24208744:2420879924207376:24207485ENSG00000042980.8ENST00000397649.3,ENST00000520448.1
exon_skip_482289824208744:24208823:24209499:24209565:24211282:2421134524209499:24209565ENSG00000042980.8ENST00000397649.3,ENST00000520448.1,ENST00000265769.4
exon_skip_482290824208744:24208823:24209499:24209565:24211896:2421198524209499:24209565ENSG00000042980.8ENST00000521629.1
exon_skip_482295824209499:24209565:24211282:24211345:24211896:2421198524211282:24211345ENSG00000042980.8ENST00000397649.3,ENST00000520448.1,ENST00000265769.4

check button PSI values of skipped exons in TCGA.
psi tcga

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Exon skipping events with PSIs in GTEx for ADAM28

check button Information of exkip skipping event in GTEx
Exon skip IDchrExons involved in exon skippingSkipped exonENSGENSTs
exon_skip_482270824157490:24157590:24166153:24166281:24167406:2416748324166153:24166281ENSG00000042980.8ENST00000523379.1
exon_skip_482271824157486:24157590:24167406:24167483:24167675:2416775424167406:24167483ENSG00000042980.8ENST00000265769.4,ENST00000520448.1,ENST00000540823.1,ENST00000397649.3,ENST00000437154.2,ENST00000523440.1
exon_skip_482272824167675:24167754:24168873:24168950:24170900:2417109324168873:24168950ENSG00000042980.8ENST00000265769.4,ENST00000520448.1,ENST00000397649.3,ENST00000437154.2
exon_skip_482273824167675:24167754:24168873:24168950:24177748:2417782024168873:24168950ENSG00000042980.8ENST00000540823.1
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENSG00000042980.8ENST00000265769.4,ENST00000520448.1,ENST00000397649.3,ENST00000437154.2
exon_skip_482285824201018:24201097:24207376:24207485:24208744:2420879924207376:24207485ENSG00000042980.8ENST00000265769.4,ENST00000521629.1,ENST00000518326.1
exon_skip_482289824208744:24208823:24209499:24209565:24211282:2421134524209499:24209565ENSG00000042980.8ENST00000265769.4,ENST00000520448.1,ENST00000397649.3
exon_skip_482290824208744:24208823:24209499:24209565:24211896:2421198524209499:24209565ENSG00000042980.8ENST00000521629.1
exon_skip_482295824209499:24209565:24211282:24211345:24211896:2421198524211282:24211345ENSG00000042980.8ENST00000265769.4,ENST00000520448.1,ENST00000397649.3

check button PSI values of skipped exons in GTEx.
psi gtex

* Skipped exon sequences.

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Open reading frame (ORF) annotation in the exon skipping event for ADAM28

check button Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000002657692416740624167483Frame-shift
ENST000002657692416887324168950Frame-shift
ENST000002657692417090024171093Frame-shift
ENST000002657692420737624207485Frame-shift
ENST000002657692417774824177820In-frame
ENST000002657692420949924209565In-frame
ENST000002657692421128224211345In-frame

check button Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.
ENSTStart of skipped exonEnd of skipped exonORF
ENST000002657692416740624167483Frame-shift
ENST000002657692416887324168950Frame-shift
ENST000002657692417090024171093Frame-shift
ENST000002657692420737624207485Frame-shift
ENST000002657692420949924209565In-frame
ENST000002657692421128224211345In-frame

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Infer the effects of exon skipping event on protein functional features for ADAM28

check button Exon skipping at the protein sequence level and followed lost functional features.
* Click on the image to enlarge it in a new window.
prot feature distribution

check button Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST0000026576970697752417774824177820687758192216
ENST000002657697069775242094992420956522892354726748
ENST000002657697069775242112822421134523552417748769

check button Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.
ENSTLength of mRNALength of AA seq.Genomic startGenomic endmRNA startmRNA endAA startAA end
ENST000002657697069775242094992420956522892354726748
ENST000002657697069775242112822421134523552417748769

check button Lost protein functional features of individual exon skipping events in TCGA.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature
Q9UKQ2192216199775ChainID=PRO_0000029129;Note=Disintegrin and metalloproteinase domain-containing protein 28
Q9UKQ2192216204399DomainNote=Peptidase M12B;Ontology_term=ECO:0000255;evidence=ECO:0000255|PROSITE-ProRule:PRU00276
Q9UKQ219221619198PropeptideID=PRO_0000029128;Ontology_term=ECO:0000250;evidence=ECO:0000250
Q9UKQ2192216199665Topological domainNote=Extracellular;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q9UKQ2726748541775Alternative sequenceID=VSP_005487;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:10506182;Dbxref=PMID:10506182
Q9UKQ2726748199775ChainID=PRO_0000029129;Note=Disintegrin and metalloproteinase domain-containing protein 28
Q9UKQ2726748687775Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q9UKQ2748769541775Alternative sequenceID=VSP_005487;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:10506182;Dbxref=PMID:10506182
Q9UKQ2748769199775ChainID=PRO_0000029129;Note=Disintegrin and metalloproteinase domain-containing protein 28
Q9UKQ2748769765765Natural variantID=VAR_024596;Note=V->M;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:10506182,ECO:0000269|PubMed:10587367,ECO:0000269|PubMed:15489334,ECO:0000269|Ref.4;Dbxref=dbSNP:rs7814768,PMID:10506182,PMID:10587367,PMID:15
Q9UKQ2748769687775Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255


check button Lost protein functional features of individual exon skipping events in GTEx.
UniProt acc.Start of exon skipping (AA)End of exon skipping (AA)Protein feature start (AA)Protein feature end (AA)Category of protein featureDescription of feature
Q9UKQ2726748541775Alternative sequenceID=VSP_005487;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:10506182;Dbxref=PMID:10506182
Q9UKQ2726748199775ChainID=PRO_0000029129;Note=Disintegrin and metalloproteinase domain-containing protein 28
Q9UKQ2726748687775Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255
Q9UKQ2748769541775Alternative sequenceID=VSP_005487;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:10506182;Dbxref=PMID:10506182
Q9UKQ2748769199775ChainID=PRO_0000029129;Note=Disintegrin and metalloproteinase domain-containing protein 28
Q9UKQ2748769765765Natural variantID=VAR_024596;Note=V->M;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:10506182,ECO:0000269|PubMed:10587367,ECO:0000269|PubMed:15489334,ECO:0000269|Ref.4;Dbxref=dbSNP:rs7814768,PMID:10506182,PMID:10587367,PMID:15
Q9UKQ2748769687775Topological domainNote=Cytoplasmic;Ontology_term=ECO:0000255;evidence=ECO:0000255


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SNVs in the skipped exons for ADAM28

check button - Lollipop plot for presenting exon skipping associated SNVs.
* Click on the image to enlarge it in a new window.
lollipop

check button - Differential PSIs between mutated versus non-mutated samples.

check button - Non-synonymous mutations located in the skipped exons in TCGA.
Cancer typeSampleESIDSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
COADTCGA-G4-6588-01exon_skip_482271
24167407241674832416747324167473Frame_Shift_DelA-p.L72fs
GBMTCGA-19-5951-01exon_skip_482271
24167407241674832416747324167473Frame_Shift_DelA-p.K73fs
PRADTCGA-KK-A59V-01exon_skip_482271
24167407241674832416747324167473Frame_Shift_DelA-p.K74fs
STADTCGA-BR-4280-01exon_skip_482271
24167407241674832416747324167473Frame_Shift_DelA-p.L72fs
STADTCGA-D7-A6EY-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_DelAA-p.K74fs
STADTCGA-HU-A4GQ-01exon_skip_482271
24167407241674832416747324167473Frame_Shift_DelA-p.L72fs
LIHCTCGA-DD-A39Y-01exon_skip_482275
24170901241710932417099424170994Frame_Shift_DelC-p.N159fs
LIHCTCGA-DD-A3A0-01exon_skip_482275
24170901241710932417099424170994Frame_Shift_DelC-p.N159fs
LIHCTCGA-G3-A3CJ-01exon_skip_482275
24170901241710932417100224171002Frame_Shift_DelA-p.E162fs
STADTCGA-VQ-A8DL-01exon_skip_482277
24177749241778202417779224177799Frame_Shift_DelAATATTAT-p.207_209del
STADTCGA-VQ-A8DL-01exon_skip_482277
24177749241778202417779224177799Frame_Shift_DelAATATTAT-p.EYY207fs
LIHCTCGA-DD-A1EG-01exon_skip_482295
24211283242113452421130424211304Frame_Shift_DelC-p.P757fs
ACCTCGA-OR-A5LJ-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.L72fs
ACCTCGA-OR-A5LJ-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.LK72fs
COADTCGA-AA-3555-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.L72fs
COADTCGA-CM-6171-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.L72fs
HNSCTCGA-T3-A92N-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.LK72fs
PAADTCGA-IB-7651-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.LK72fs
STADTCGA-R5-A7ZI-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.LK72fs
STADTCGA-VQ-A8P2-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.LK72fs
UCECTCGA-BS-A0TJ-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.L72fs
UCECTCGA-D1-A17H-01exon_skip_482271
24167407241674832416747224167473Frame_Shift_Ins-Ap.L72fs
STADTCGA-BR-4368-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_Ins-Ap.L72fs
STADTCGA-BR-6452-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_Ins-Ap.L72fs
STADTCGA-BR-6566-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_Ins-Ap.L72fs
STADTCGA-BR-8372-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_Ins-Ap.L72fs
STADTCGA-BR-8487-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_Ins-Ap.L72fs
STADTCGA-CG-4306-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_Ins-Ap.L72fs
STADTCGA-HU-A4G8-01exon_skip_482271
24167407241674832416747324167474Frame_Shift_Ins-Ap.L72fs
THCATCGA-DO-A1JZ-01exon_skip_482285
exon_skip_482286
24207377242074852420741324207414Frame_Shift_Ins-Gp.G676fs
HNSCTCGA-CN-6021-01exon_skip_482272
exon_skip_482273
24168874241689502416889224168892Nonsense_MutationGTp.G109*
UCECTCGA-AP-A051-01exon_skip_482272
exon_skip_482273
24168874241689502416889224168892Nonsense_MutationGTp.G109*
SKCMTCGA-EE-A29S-06exon_skip_482277
24177749241778202417777024177770Nonsense_MutationCTp.Q200*
SKCMTCGA-EE-A29S-06exon_skip_482277
24177749241778202417777024177770Nonsense_MutationCTp.Q200X
LGGTCGA-TQ-A7RV-01exon_skip_482271
24167407241674832416748224167485Splice_SiteAAGT-p.76_splice

check button - Depth of coverage in the three exons composing exon skipping event
Depth of coverage in three exonsMutation description

check button - Non-synonymous mutations located in the skipped exons in CCLE.
SampleSkipped exon startSkipped exon endMutation startMutation endMutation typeReference seqMutation seqAAchange
MFE319_ENDOMETRIUM24167407241674832416747224167473Frame_Shift_Ins-AAp.K73fs
SNGM_ENDOMETRIUM24157487241575902415750824157508Missense_MutationCAp.P23H
SNUC5_LARGE_INTESTINE24167407241674832416746124167461Missense_MutationGAp.V69M
A704_KIDNEY24168874241689502416890524168905Missense_MutationAGp.N113S
MIAPACA2_PANCREAS24168874241689502416891924168919Missense_MutationGAp.D118N
TT_OESOPHAGUS24168874241689502416892524168925Missense_MutationAGp.S120G
KURAMOCHI_OVARY24168874241689502416893824168938Missense_MutationGTp.C124F
IGR1_SKIN24170901241710932417096224170962Missense_MutationGAp.D149N
NUGC3_STOMACH24170901241710932417104924171049Missense_MutationCGp.H178D
HCC2998_LARGE_INTESTINE24170901241710932417105224171052Missense_MutationGAp.D179N
HCC1569_BREAST24177749241778202417775324177753Missense_MutationTCp.L194S
CHSA0011_BONE24207377242074852420741624207416Missense_MutationTCp.V677A
SW1088_CENTRAL_NERVOUS_SYSTEM24211283242113452421130124211301Missense_MutationCTp.L755F
LN464_CENTRAL_NERVOUS_SYSTEM24157487241575902415751924157519Nonsense_MutationATp.K27*
ACN_AUTONOMIC_GANGLIA24157487241575902415751924157519Nonsense_MutationATp.K27*

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for ADAM28

check button sQTL information located at the skipped exons.
Exon skip IDChromosomeThree exonsSkippped exonENSTCancer typeSNP idLocationDNA change (ref/var)P-value
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4ESCArs6996616chr8:24171051C/T5.17e-05
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4ESCArs6996616chr8:24171051C/T5.17e-05
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4ESCArs6996616chr8:24171051C/T1.11e-04
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4BRCArs6996616chr8:24171051C/T4.34e-06
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4BRCArs6996616chr8:24171051C/T9.03e-06
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LAMLrs6996616chr8:24171051C/T9.68e-07
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LGGrs6996616chr8:24171051C/T2.08e-04
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LGGrs6996616chr8:24171051C/T2.08e-04
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4KIRCrs6996616chr8:24171051C/T1.40e-05
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LUADrs6996616chr8:24171051C/T1.44e-04
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LUADrs6996616chr8:24171051C/T2.93e-04
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LUADrs6996616chr8:24171051C/T6.33e-04
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LUSCrs6996616chr8:24171051C/T7.07e-05
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LUSCrs6996616chr8:24171051C/T7.07e-05
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4LUSCrs6996616chr8:24171051C/T2.27e-03
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4PAADrs6996616chr8:24171051C/T3.46e-04
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4STADrs6996616chr8:24171051C/T4.81e-07
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4STADrs6996616chr8:24171051C/T1.29e-03
exon_skip_482275824168873:24168950:24170900:24171093:24177748:2417781524170900:24171093ENST00000397649.3,ENST00000437154.2,ENST00000520448.1,ENST00000265769.4STADrs6996616chr8:24171051C/T1.29e-03

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ADAM28


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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for ADAM28


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RelatedDrugs for ADAM28

check button Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)
GeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
Q9UKQ2DB03088Pidolic AcidDisintegrin and metalloproteinase domain-containing protein 28small moleculeapproved|investigational

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RelatedDiseases for ADAM28

check button Diseases associated with this gene.
(DisGeNet 4.0)
GeneDisease IDDisease name# pubmedsSource
ADAM28C0024121Lung Neoplasms1CTD_human