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Center for Computational Systems Medicine
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Gene summary

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Gene structure and Gene expression level

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Sex-biased somatic mutation

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DNA methylation with beta values in gene

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Exon skipping events with PSI in TCGA

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RNA A-to-I editing events in TCGA

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Sex-biased TF-Gene network of gene

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Sex-biased RBP-ES network of gene

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Sex-biased CeRNA regulation of gene

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Sex-biased eQTL regulation of gene

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Sex-biased eQTM regulation of gene

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Sex-biased sQTL regulation of gene

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Sex-biased sQTM regulation of gene

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Related disease information of gene

Gene: ENSG00000168056

Summary for LTBP3

check button Gene summary

Gene informationEnsembl ID

ENSG00000168056

Gene symbol

LTBP3

Gene namelatent transforming growth factor beta binding protein 3
HGNC

6716

Entrez ID

4054

Gene typeprotein_coding
SynonymsLTBP3|
UniProtAcc

Q9NS15


check buttonDrugs associated with this gene(DrugBank).
Gene IDGene SymbolDrug IDDrug NameDrug Type

check buttonCancer therapeutic drugs associated with this gene(NCI).
Gene IDGene NameDrug IDDrug NameDrug TypeCancer

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Structure and expression level for LTBP3

check buttonAS events and RNA A-to-I editing events of the gene in TCGA based on Genvode V22 structure.
∗For more information on exon skipping events please check the ExonskipDB database.
∗For more information on exon skipping events please check the CAeditome database.
UCSC result

check buttonLandscape of gene expressions across multiple cancer types.
gene expression analysis

check buttonDifferentially expressed gene analysis between tumor male and tumor female samples.
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type

check buttonDifferentially expressed gene analysis between tumor male and normal male samples.
DEG result
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type
LTBP34.71e+03-1.14e+002.82e-01-4.03e+005.54e-052.66e-04BLCA

check buttonDifferentially expressed gene analysis between tumor female and normal female samples.
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type

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Sex-biased somatic mutation for LTBP3

∗For more information on exon skipping events please check the ExonskipDB database.
Gene IDCancer TypeHugo SymbolMaleFemalepvalorci.upci.lowadjPval

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DNA methylation with beta values for LTBP3

check buttonLandscape of DNA methylation across multiple cancer types.
methylation heatmap

check buttonDifferentially expressed CpG sites between male tumor and female tumor patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta

check buttonDifferentially expressed CpG sites between male tumor and male normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta
KIRCcg17451760chr11:65559685CGI:chr11:65557931-65558738promoter4.33e-015.57e-01-4.71e+002.46e-067.96e-06-1.23e-01
COADcg14749448chr11:65558401CGI:chr11:65557931-65558738promoter,gene body3.59e-012.46e-014.17e+003.11e-051.40e-041.13e-01
BLCAcg17969560chr11:65557297CGI:chr11:65557931-65558738promoter,gene body6.14e-014.39e-013.71e+002.05e-046.76e-041.75e-01
BLCAcg08965235chr11:65557687CGI:chr11:65557931-65558738promoter,gene body,CDS,UTR,exon4.01e-012.55e-012.04e+004.14e-024.32e-021.46e-01
BLCAcg11171811chr11:65559254CGI:chr11:65557931-65558738promoter7.97e-016.89e-012.89e+003.86e-036.63e-031.08e-01
CHOLcg16477774chr11:65557778CGI:chr11:65557931-65558738promoter,gene body,CDS,UTR,exon1.33e-012.35e-01-2.14e+003.25e-023.87e-02-1.02e-01

check buttonDifferentially expressed CpG sites between female tumor and female normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta
BRCAcg17969560chr11:65557297CGI:chr11:65557931-65558738promoter,gene body4.90e-013.64e-018.58e+009.72e-184.38e-171.26e-01
BRCAcg11171811chr11:65559254CGI:chr11:65557931-65558738promoter8.41e-016.63e-011.34e+015.42e-415.45e-391.78e-01
BRCAcg17451760chr11:65559685CGI:chr11:65557931-65558738promoter5.45e-013.82e-011.22e+014.34e-341.10e-321.63e-01

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Exon skipping events with PSI in TCGA for LTBP3

∗Please access ExonSkipDB for exon skipping annotation.
check buttonLandscape of exon skipping events across multiple cancer types.
AS event heatmap

check buttonDifferentially expressed exon skipping events between male tumor and female tumor patients.
Cancer TypeExon Skippingave.female_Tave.female_Nwilcoxon.wwilcoxon.ppadjdPSI

check buttonDifferentially expressed exon skipping events between male tumor and male normal patients.
Cancer TypeExon Skippingave.female_Tave.female_Nwilcoxon.wwilcoxon.ppadjdPSI
LUADexon_skip_742431.05e-012.27e-01-4.01e+006.11e-053.26e-04-1.22e-01
ESCAexon_skip_742434.39e-016.53e-01-4.38e+001.18e-056.20e-03-2.13e-01
CHOLexon_skip_742431.61e-013.67e-01-2.96e+003.09e-031.32e-02-2.06e-01

check buttonDifferentially expressed exon skipping events between female tumor and female normal patients.
Cancer TypeExon Skippingave.female_Tave.female_Nwilcoxon.wwilcoxon.ppadjdPSI

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RNA A-to-I editing events in TCGA for LTBP3

∗Please access CAeditome for RNA editing annotation.
check buttonLandscape of RNA editing events across multiple cancer types.
ED heatmap

check buttonDifferentially expressed RNA editing events between male tumor and female tumor patients.
Cancer TypeTranscriptEditingave.male_Tave.female_Twilcoxon.wwilcoxon.pp_adjdFre
KIRCLTBP3-201chr11_65550798_-2.17e-013.38e-01-2.34e+001.92e-024.45e-02-1.21e-01
LUADLTBP3-201chr11_65550166_-1.54e-012.54e-01-2.46e+001.37e-023.27e-02-9.97e-02
LGGLTBP3-201chr11_65549699_-4.26e-013.59e-012.33e+001.99e-024.55e-026.70e-02
LGGLTBP3-201chr11_65550798_-1.91e-011.28e-013.14e+001.71e-034.01e-026.35e-02
THCALTBP3-201chr11_65549469_-2.22e-013.17e-01-2.20e+002.78e-024.91e-02-9.48e-02
THCALTBP3-201chr11_65549537_-2.09e-012.64e-01-2.29e+002.22e-024.91e-02-5.50e-02
SARCLTBP3-201chr11_65550777_-4.09e-012.65e-012.03e+004.24e-024.97e-021.44e-01
GBMLTBP3-201chr11_65549469_-2.02e-012.77e-01-3.04e+002.34e-034.96e-02-7.47e-02
GBMLTBP3-201chr11_65550290_-2.82e-011.76e-012.15e+003.12e-024.96e-021.06e-01
GBMLTBP3-201chr11_65550641_-5.87e-014.82e-012.17e+003.01e-024.96e-021.05e-01
GBMLTBP3-201chr11_65550762_-8.29e-017.59e-012.24e+002.51e-024.96e-027.05e-02
THYMLTBP3-201chr11_65550165_-2.45e-013.88e-01-2.20e+002.77e-024.73e-02-1.43e-01

check buttonDifferentially expressed RNA editing events between male tumor and male normal patients.
Cancer TypeTranscriptEditingave.male_Tave.female_Twilcoxon.wwilcoxon.pp_adjdFre

check buttonDifferentially expressed RNA editing events between female tumor and female normal patients.
Cancer TypeTranscriptEditingave.male_Tave.female_Twilcoxon.wwilcoxon.pp_adjdFre
BRCALTBP3-201chr11_65549514_-4.27e-012.92e-013.16e+001.58e-032.90e-031.35e-01
BRCALTBP3-201chr11_65549811_-3.80e-012.85e-012.87e+004.06e-036.52e-039.52e-02
BRCALTBP3-201chr11_65550777_-4.20e-012.86e-012.36e+001.84e-022.29e-021.34e-01

check buttonProtein coding RNA editing(s).
Editing PositionVariant TypeGene SymbolTranscript IDNTchangeAAchange

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Sex-biased TF-Gene network for LTBP3

check buttonTFs related to LTBP3.
∗The female-biased TF-gene edges were identified if Female_Edge_threshold>0.98 and Male_Edge_threshold<=0.98.
∗The male-biased TF-gene edges were identified if Male_Edge_threshold>0.98 and Female_Edge_threshold<=0.98.
Cancer TypeTFTarget GeneMale Edge ScoreMale Edge ThresholdFemale Edge ScoreFemale Edge ThresholdType

check buttonLTBP3 related gene.
∗Only the gene encode TF might with this result.
∗For more information please check Sex-biased TF-Coding gene network.

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Sex-biased RBP-ES network for LTBP3

check buttonRBPs related to ES in LTBP3.
∗The female-biased RBP-ES edges were identified if Female_Edge_threshold>0.98 and Male_Edge_threshold<=0.98.
∗The male-biased RBP-ES edges were identified if Male_Edge_threshold>0.98 and Female_Edge_threshold<=0.98.
RBP ES
Cancer TypeRBPTarget ESMale Edge ScoreMale Edge ThresholdFemale Edge ScoreFemale Edge ThresholdType
STADHNRNPH2exon_skip_743048.43e+009.85e-018.05e+008.09e-03Male-biased
STADRBM4exon_skip_742899.22e+009.85e-018.89e+001.22e-02Male-biased
STADZC3H10exon_skip_742456.69e+009.82e-016.11e+001.62e-03Male-biased
ACCRBM4exon_skip_742369.54e+009.94e-018.97e+003.55e-03Male-biased
UVMHNRNPH2exon_skip_742937.85e+002.14e-038.28e+009.90e-01Female-biased
UVMRBM4exon_skip_742369.18e+009.85e-018.90e+001.16e-02Male-biased
THYMHNRNPH2exon_skip_742938.33e+009.92e-017.76e+008.14e-04Male-biased
LUSCHNRNPH2exon_skip_743048.64e+009.87e-018.23e+007.31e-03Male-biased
LUSCRBM4exon_skip_742369.73e+009.87e-019.37e+001.02e-02Male-biased
COADHNRNPH2exon_skip_742937.79e+001.00e-028.13e+009.82e-01Female-biased
COADHNRNPH2exon_skip_743048.03e+006.40e-038.41e+009.87e-01Female-biased
CHOLHNRNPH2exon_skip_743107.10e+009.80e-016.64e+006.35e-03Male-biased
KIRPRBM4exon_skip_742369.03e+001.64e-029.32e+009.80e-01Female-biased
BRCAFXR2exon_skip_742439.25e+007.10e-039.98e+009.91e-01Female-biased
ESCAHNRNPH2exon_skip_742937.78e+002.72e-038.39e+009.91e-01Female-biased
READHNRNPH2exon_skip_742938.37e+009.91e-017.89e+002.01e-03Male-biased
PCPGHNRNPH2exon_skip_742366.22e+002.34e-036.66e+009.81e-01Female-biased
PCPGPCBP2exon_skip_743106.96e+009.85e-016.41e+007.64e-04Male-biased
MESOHNRNPH2exon_skip_742366.56e+009.80e-016.05e+002.20e-03Male-biased
MESOHNRNPH2exon_skip_742937.93e+003.91e-038.36e+009.89e-01Female-biased
MESOHNRNPH2exon_skip_743048.12e+008.97e-038.48e+009.84e-01Female-biased
MESOHNRNPH2exon_skip_743106.49e+002.73e-036.96e+009.83e-01Female-biased
GBMHNRNPH2exon_skip_742937.92e+008.53e-038.27e+009.84e-01Female-biased
PAADHNRNPH2exon_skip_742937.98e+003.64e-038.36e+009.89e-01Female-biased
KIRCRBM4exon_skip_742369.56e+001.57e-029.84e+009.82e-01Female-biased
KICHHNRNPH2exon_skip_742938.39e+009.84e-018.06e+008.81e-03Male-biased

check buttonLTBP3 related ES.
∗Only the gene encode RBP might with this result.
∗For more information please check Sex-biased RBP-ES network in cancer.

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Sex-biased CeRNA regulation of gene

check buttonSex-biased CeRNA regulation of gene.
Gene IDceRNA(lncRNA-miRNA-mRNA)GroupCancer Type

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Sex-biased eQTL regulation of gene

check buttonSex-biased eQTL regulation of gene (The figures only show the pairs with FDR <1e-5. For more information please check the below table).
eQTLDescription

check buttonMale-specific eQTL regulation.
SNP IDSNP InfoPosition to GeneEffect ScoreFDRCancer TypeBiased Type
rs11229385chr11:58371421:C:T-0.06817472313453140.0410421162628785THCAFemale-baised eQTL
rs146435517chr11:74573033:C:A-0.3795291519858760.00434100319755633KIRPFemale-baised eQTL
rs35500564chr11:74588234:G:A-0.3795291519858760.00434100319755633KIRPFemale-baised eQTL
rs34601749chr11:74601743:C:T-0.3795291519858760.00434100319755633KIRPFemale-baised eQTL
rs12807883chr11:74616947:A:G-0.3795291519858760.00434100319755633KIRPFemale-baised eQTL
rs34450669chr11:74617983:C:T-0.3795291519858760.00434100319755633KIRPFemale-baised eQTL
rs71465929chr11:74630667:G:C-0.3795291519858760.00434100319755633KIRPFemale-baised eQTL
rs11228519chr11:69140391:G:A-0.08947995623744380.0187906645581806KIRCFemale-baised eQTL
rs11228526chr11:69148379:G:T-0.08630266708044630.0268340063250901KIRCFemale-baised eQTL
rs7946900chr11:69149266:G:A-0.08630266708044630.0268340063250901KIRCFemale-baised eQTL
rs9736830chr11:60013005:A:G-0.06881215120190290.0347445033933133KIRCFemale-baised eQTL
rs2924689chr11:68816203:T:C-0.08922152580234150.042912286239847KIRCFemale-baised eQTL
rs10792034chr11:69253750:T:C-0.07429768914726850.0493816548072933KIRCFemale-baised eQTL
rs190721473chr11:62021355:C:T--0.1043481243013230.00323058802761256LUADFemale-baised eQTL
rs77133046chr11:62018039:C:T--0.1030053135522030.0039861982807941LUADFemale-baised eQTL
rs75235696chr11:62001796:G:C--0.09931860838923390.00708032224536249LUADFemale-baised eQTL
rs79123263chr11:62004714:G:A--0.09843282973328310.00807795116914165LUADFemale-baised eQTL
rs147468083chr11:62006207:C:T--0.09843282973328310.00807795116914165LUADFemale-baised eQTL
rs147478419chr11:62008102:G:C--0.09843282973328310.00807795116914165LUADFemale-baised eQTL
rs3862736chr11:61523605:A:G-0.08843779211560190.0491249747859358LUADFemale-baised eQTL

check buttonFemale-specific eQTL regulation.
SNP IDSNP InfoPosition to GeneEffect ScoreFDRCancer TypeBiased Type
rs3794186chr11:68053569:G:A-0.1098619803085490.00292542697615054COADMale-baised eQTL
rs112754197chr11:68048708:G:A-0.1028043478725960.00819283546412262COADMale-baised eQTL
rs1384060chr11:56319845:A:G-0.04743258452058730.0435266202514138COADMale-baised eQTL

check buttonOpposite sex-biased eQTL regulation.
SNP IDSNP InfoPosition to GeneMale EffectMale FDRFemale EffectFemale FDRSex-biased Gene in CancerCancer Type

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Sex-biased eQTM regulation of gene

check buttonSex-biased eQTM regulation of gene (The figures only show the pairs with FDR<1e-5. For more information please check the below table).
eQTMDescription
eQTM boxplot analysisGene ID: ENSG00000168056
CpG Site: cg17969560
Position to Gene: gene,promoter
Male Effect: -0.386525575986042
Female Effect: -

check buttonMale-specific eQTM regulation.
CpG SiteCpG PostionPosition to GeneEffect ScoreFDRCor.rCor.PvalueCancer Type
cg17969560chr11:65557297gene,promoter-0.3865255759860421.30354381981898e-05-0.364128331663770572.1374791501484256e-08LUAD

check buttonFemale-specific eQTM regulation.
CpG SiteCpG PostionPosition to GeneEffect ScoreFDRCor.rCor.PvalueCancer Type

check buttonOpposite sex-biased eQTM regulation.
CpG SiteCpG PostionCpG IslandPosition to GeneMale EffectMale FDRFemale EffectFemale FDRMale CorMale P-valueFemale CorFemale P-valueSex-biased Coding GeneCancer Type

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Sex-biased sQTL regulation of gene

check buttonSex-biased sQTL regulation of gene (The figures only show the pairs with FDR <1e-5. For more information please check the below table).
sQTLDescription

check buttonMale-specific sQTL regulation.
ES IDSkipped ExonORF AnnoSNP IDSNP InfoSNP Position to ESEffect ScoreFDRCancer TypeBiased Type
exon_skip_74243chr11:65540012:65540153In-framers7950197chr11:65678655:T:CDistant upstream-0.0634556511894710.00602468782658909THCAFemale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers555465chr11:65701337:C:TDistant upstream0.0570711223710790.0228161529743571THCAFemale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers507859chr11:65704511:G:ADistant upstream0.056856030618290.0276331543348705THCAFemale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers11227249chr11:65670001:C:TDistant upstream0.05879128244995660.0371152333540771THCAFemale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers573589chr11:65716510:C:TDistant upstream0.0535980987415940.0489116696859355THCAFemale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers591966chr11:64978032:T:CDistant downstream-0.03751575792304910.0460592788764375COADFemale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers77600363chr11:66421290:G:TDistant upstream0.0731427950030650.0423367950974899PAADFemale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers79994868chr11:66421943:G:ADistant upstream0.0731427950030650.0423367950974899PAADFemale-baised sQTL

check buttonFemale-specific sQTL regulation.
ES IDSkipped ExonORF AnnoSNP IDSNP InfoSNP Position to ESEffect ScoreFDRCancer TypeBiased Type
exon_skip_74243chr11:65540012:65540153In-framers7952306chr11:64861141:G:TDistant downstream-0.02391892664480020.025655233062796HNSCMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers7943238chr11:64861899:T:ADistant downstream-0.02391892664480020.025655233062796HNSCMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers2444846chr11:66499235:T:CDistant upstream0.02670720359763010.00880806720166431COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers8432chr11:66532044:A:GDistant upstream0.02791419056147310.0130027137438535COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers2279863chr11:66480225:G:TDistant upstream-0.02612121056110330.0144840511845285COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers3107024chr11:66434744:C:TDistant upstream-0.02614969888889680.0169774962916352COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers1700184chr11:66449344:C:TDistant upstream0.02596779250736120.0180874609485947COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers1791686chr11:66532992:G:ADistant upstream-0.02688583436979890.0213949542501542COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers75546553chr11:66491445:G:ADistant upstream-0.0261265134470220.02177435391203COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers1671063chr11:66504671:A:GDistant upstream0.02588702412952010.023718730361003COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers1671062chr11:66514067:A:GDistant upstream0.02588702412952010.023718730361003COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers10736656chr11:66517797:G:ADistant upstream0.02588702412952010.023718730361003COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers1671065chr11:66518906:T:CDistant upstream0.02588702412952010.023718730361003COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers1791687chr11:66459713:G:CDistant upstream0.02439939601752790.035064720094003COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers7925093chr11:66466473:C:GDistant upstream0.02496124377452480.0358864529528498COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers7925108chr11:66466552:A:GDistant upstream0.02496124377452480.0358864529528498COADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers12800339chr11:65179769:T:CDistant downstream0.07700781510030380.0263567874664983PAADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers12422027chr11:65181084:A:GDistant downstream0.07700781510030380.0263567874664983PAADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers6591178chr11:65177494:G:ADistant downstream0.07692211665885820.0359043794774063PAADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers34281454chr11:65179808:A:CDistant downstream0.07574972774221660.0471645505659558PAADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers2277307chr11:65183372:A:TDistant downstream0.07574972774221660.0471645505659558PAADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers17583chr11:65183499:C:TDistant downstream0.07574972774221660.0471645505659558PAADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers17886894chr11:65184368:C:TDistant downstream0.07574972774221660.0471645505659558PAADMale-baised sQTL
exon_skip_74243chr11:65540012:65540153In-framers3825072chr11:65186582:C:TDistant downstream0.07574972774221660.0471645505659558PAADMale-baised sQTL

check buttonOpposite sex-biased sQTL regulation.
ES IDSkipped ExonORF AnnoSNP IDSNP InfoSNP Position to ESMale EffectMale FDRFemale EffectFemale FDRCancer Type

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Sex-biased sQTM regulation of gene

check buttonSex-biased sQTM regulation of gene (The figures only show the pairs with FDR <1e-5. For more information please check the below table).
sQTMDescription

check buttonMale-specific sQTM regulation.
EX IDSkipped ExonCPG SiteCPG PositionPosition to EX EventsEffect ScoreFDRCor.rCor.PvalueORF_annoCancer Type

check buttonFemale-specific sQTM regulation.
EX IDSkipped ExonCPG SiteCPG PositionPosition to EX EventsEffect ScoreFDRCor.rCor.PvalueORF_annoCancer Type

check buttonOpposite sex-biased sQTM regulation.
EX IDEX InfoSkipped ExonCPG SiteCPG PositionCPG IslandPosition to EX EventsMale EffectMale FDRFemale EffectFemale FDRMale CorrelationMale P-valueFemale CorrelationFemale P-valueORF_annoCancer Type

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Related disease information of LTBP3

check buttonDiseases associated with this gene (DisGeNET).
Gene IDGene SymbolDisease IDDisease NameNumber of PMIDSource
ENSG00000168056LTBP3C0002452Amelogenesis Imperfecta1CTD_human
ENSG00000168056LTBP3C0005940Bone Diseases1CTD_human
ENSG00000168056LTBP3C0018273Growth Disorders2CTD_human
ENSG00000168056LTBP3C0020608Hypodontia2CTD_human
ENSG00000168056LTBP3C0022821Kyphosis deformity of spine1CTD_human
ENSG00000168056LTBP3C0026267Mitral Valve Prolapse Syndrome1CTD_human
ENSG00000168056LTBP3C0029408Degenerative polyarthritis2CTD_human
ENSG00000168056LTBP3C0029410Osteoarthritis of hip1CTD_human
ENSG00000168056LTBP3C0029464Osteosclerosis2CTD_human
ENSG00000168056LTBP3C0086743Osteoarthrosis Deformans2CTD_human
ENSG00000168056LTBP3C0376634Craniofacial Abnormalities2CTD_human
ENSG00000168056LTBP3C0399352Developmental absence of tooth2CTD_human
ENSG00000168056LTBP3C0432228Brachyolmia1CTD_human
ENSG00000168056LTBP3C2751297Tooth Agenesis, Selective, 61CTD_human
ENSG00000168056LTBP3C3489529Tooth Agenesis, Familial2CTD_human