SexAnnoDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Gene summary

leaf

Gene structure and Gene expression level

leaf

Sex-biased somatic mutation

leaf

DNA methylation with beta values in gene

leaf

Exon skipping events with PSI in TCGA

leaf

RNA A-to-I editing events in TCGA

leaf

Sex-biased TF-Gene network of gene

leaf

Sex-biased RBP-ES network of gene

leaf

Sex-biased CeRNA regulation of gene

leaf

Sex-biased eQTL regulation of gene

leaf

Sex-biased eQTM regulation of gene

leaf

Sex-biased sQTL regulation of gene

leaf

Sex-biased sQTM regulation of gene

leaf

Related disease information of gene

Gene: ENSG00000187498

Summary for COL4A1

check button Gene summary

Gene informationEnsembl ID

ENSG00000187498

Gene symbol

COL4A1

Gene namecollagen type IV alpha 1 chain
HGNC

2202

Entrez ID

1282

Gene typeprotein_coding
SynonymsCOL4A1|
UniProtAcc

P02462


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

Top

Structure and expression level for COL4A1

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
COL4A11.41e+041.92e+004.74e-014.05e+005.13e-052.43e-04CHOL

check buttonDifferentially expressed gene analysis between tumor female and normal female samples.
DEG result
Coding NameBase Meanlog2FoldChangelfcSEStatP valueP.adjust ValueCancer Type
COL4A11.22e+041.58e+002.08e-017.63e+002.34e-142.14e-13COAD

Top

Sex-biased somatic mutation for COL4A1

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

Top

DNA methylation with beta values for COL4A1

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
BRCAcg06659727chr13:110307081CGI:chr13:110306544-110308243UTR,promoter,exon,gene body2.32e-013.87e-01-1.97e+004.94e-024.97e-02-1.55e-01
BRCAcg20327444chr13:110307300CGI:chr13:110306544-110308243promoter1.21e-013.65e-01-2.22e+002.67e-023.91e-02-2.45e-01
BRCAcg24089600chr13:110307830CGI:chr13:110306544-110308243promoter2.77e-014.92e-01-2.60e+009.30e-032.60e-02-2.15e-01
BRCAcg17541528chr13:110307303CGI:chr13:110306544-110308243promoter2.11e-013.96e-01-2.01e+004.50e-024.80e-02-1.85e-01
BRCAcg22757824chr13:110307839CGI:chr13:110306544-110308243promoter2.25e-014.53e-01-2.76e+005.83e-032.17e-02-2.29e-01
BRCAcg25530246chr13:110308216CGI:chr13:110306544-110308243promoter5.34e-022.09e-01-2.03e+004.22e-024.69e-02-1.55e-01
BRCAcg15871127chr13:110307851CGI:chr13:110306544-110308243promoter2.80e-014.33e-01-2.50e+001.25e-022.90e-02-1.53e-01
BRCAcg27546237chr13:110308105CGI:chr13:110306544-110308243promoter1.99e-013.97e-01-2.81e+004.98e-032.03e-02-1.99e-01
PAADcg21938148chr13:110306630CGI:chr13:110306544-110308243promoter,gene body2.15e-013.28e-01-3.46e+005.36e-042.67e-03-1.13e-01

check buttonDifferentially expressed CpG sites between male tumor and male normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta
HNSCcg06659727chr13:110307081CGI:chr13:110306544-110308243UTR,promoter,exon,gene body2.11e-019.51e-022.94e+003.27e-034.96e-031.16e-01
HNSCcg01956420chr13:110307321CGI:chr13:110306544-110308243promoter1.74e-013.92e-022.92e+003.51e-035.26e-031.35e-01
HNSCcg24089600chr13:110307830CGI:chr13:110306544-110308243promoter2.11e-017.57e-022.71e+006.63e-039.04e-031.36e-01
HNSCcg21938148chr13:110306630CGI:chr13:110306544-110308243promoter,gene body1.21e-011.70e-022.95e+003.15e-034.80e-031.04e-01
HNSCcg17541528chr13:110307303CGI:chr13:110306544-110308243promoter1.79e-015.29e-022.51e+001.21e-021.50e-021.27e-01
HNSCcg22757824chr13:110307839CGI:chr13:110306544-110308243promoter1.78e-014.96e-022.98e+002.87e-034.44e-031.29e-01
LUSCcg01956420chr13:110307321CGI:chr13:110306544-110308243promoter1.35e-013.11e-022.98e+002.91e-035.47e-031.04e-01
LUSCcg17541528chr13:110307303CGI:chr13:110306544-110308243promoter1.50e-012.75e-023.12e+001.79e-033.87e-031.22e-01
BLCAcg06659727chr13:110307081CGI:chr13:110306544-110308243UTR,promoter,exon,gene body3.79e-011.60e-012.84e+004.50e-037.49e-032.18e-01
BLCAcg20327444chr13:110307300CGI:chr13:110306544-110308243promoter2.81e-016.75e-022.80e+005.12e-038.29e-032.14e-01
BLCAcg01956420chr13:110307321CGI:chr13:110306544-110308243promoter3.52e-011.15e-012.46e+001.39e-021.83e-022.38e-01
BLCAcg24089600chr13:110307830CGI:chr13:110306544-110308243promoter4.08e-011.04e-013.47e+005.13e-041.35e-033.04e-01
BLCAcg21938148chr13:110306630CGI:chr13:110306544-110308243promoter,gene body2.17e-011.81e-022.24e+002.48e-022.90e-021.99e-01
BLCAcg17541528chr13:110307303CGI:chr13:110306544-110308243promoter3.82e-011.17e-012.81e+004.89e-037.99e-032.65e-01
BLCAcg22757824chr13:110307839CGI:chr13:110306544-110308243promoter3.65e-016.43e-023.41e+006.40e-041.61e-033.00e-01
BLCAcg13596497chr13:110306757CGI:chr13:110306544-110308243promoter,gene body3.72e-011.31e-013.56e+003.66e-041.04e-032.41e-01
BLCAcg15871127chr13:110307851CGI:chr13:110306544-110308243promoter3.74e-011.78e-013.12e+001.79e-033.59e-031.96e-01
BLCAcg27546237chr13:110308105CGI:chr13:110306544-110308243promoter2.90e-011.06e-012.54e+001.12e-021.55e-021.84e-01

check buttonDifferentially expressed CpG sites between female tumor and female normal patients.
Cancer TypeCpG SitePositionCpG IslandPosition to Geneave1ave2wilcoxon.wwilcoxon.ppadjdBeta
BRCAcg06659727chr13:110307081CGI:chr13:110306544-110308243UTR,promoter,exon,gene body2.32e-018.26e-027.33e+002.23e-137.18e-131.49e-01
BRCAcg01956420chr13:110307321CGI:chr13:110306544-110308243promoter1.69e-014.12e-025.41e+006.20e-081.29e-071.28e-01
BRCAcg24089600chr13:110307830CGI:chr13:110306544-110308243promoter2.77e-015.59e-021.07e+011.23e-261.23e-252.21e-01
BRCAcg17541528chr13:110307303CGI:chr13:110306544-110308243promoter2.11e-014.89e-026.45e+001.09e-102.86e-101.62e-01
BRCAcg22757824chr13:110307839CGI:chr13:110306544-110308243promoter2.25e-014.36e-021.02e+012.49e-241.98e-231.81e-01
BRCAcg13596497chr13:110306757CGI:chr13:110306544-110308243promoter,gene body2.51e-018.61e-021.07e+017.90e-278.04e-261.65e-01
BRCAcg15871127chr13:110307851CGI:chr13:110306544-110308243promoter2.80e-011.36e-019.28e+001.75e-209.83e-201.44e-01
BRCAcg27546237chr13:110308105CGI:chr13:110306544-110308243promoter1.99e-016.53e-029.92e+003.45e-232.47e-221.33e-01
LUADcg15262516chr13:110306071CGI:chr13:110306544-110308243promoter,gene body1.81e-017.92e-022.62e+008.75e-031.43e-021.02e-01

Top

Exon skipping events with PSI in TCGA for COL4A1

∗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

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

Top

RNA A-to-I editing events in TCGA for COL4A1

∗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
LUADCOL4A1-006chr13_110289551_-2.91e-011.80e-012.60e+009.37e-032.78e-021.10e-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

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

Top

Sex-biased TF-Gene network for COL4A1

check buttonTFs related to COL4A1.
∗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 buttonCOL4A1 related gene.
∗Only the gene encode TF might with this result.
∗For more information please check Sex-biased TF-Coding gene network.

Top

Sex-biased RBP-ES network for COL4A1

check buttonRBPs related to ES in COL4A1.
∗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
THYMBRUNOL4exon_skip_1045977.88e+008.43e-038.22e+009.84e-01Female-biased
THYMBRUNOL5exon_skip_1045977.90e+008.49e-038.23e+009.84e-01Female-biased
THYMhnRNPLLexon_skip_1045977.79e+008.35e-038.12e+009.84e-01Female-biased
COADSAMD4Aexon_skip_1046076.65e+009.82e-016.06e+009.58e-04Male-biased
DLBCBRUNOL4exon_skip_1045978.23e+009.86e-017.85e+006.31e-03Male-biased
DLBCBRUNOL5exon_skip_1045978.25e+009.86e-017.87e+006.29e-03Male-biased
DLBChnRNPLLexon_skip_1045978.14e+009.85e-017.76e+006.35e-03Male-biased
LUADSAMD4Aexon_skip_1045988.54e+009.91e-018.09e+002.91e-03Male-biased
CHOLIGF2BP1exon_skip_1046081.03e+019.87e-019.94e+001.18e-02Male-biased
KIRPSAMD4Aexon_skip_1045988.48e+009.90e-018.06e+003.68e-03Male-biased
MESOBRUNOL4exon_skip_1045977.89e+006.27e-038.28e+009.86e-01Female-biased
MESOBRUNOL5exon_skip_1045977.91e+006.25e-038.30e+009.86e-01Female-biased
MESOHNRNPH2exon_skip_1046177.98e+006.90e-038.36e+009.86e-01Female-biased
MESOhnRNPLLexon_skip_1045977.80e+006.34e-038.19e+009.86e-01Female-biased
MESOSAMD4Aexon_skip_1046077.12e+009.85e-016.61e+002.22e-03Male-biased
LGGSAMD4Aexon_skip_1045988.84e+009.88e-018.48e+007.17e-03Male-biased
GBMIGF2BP1exon_skip_1046089.96e+009.98e-031.03e+019.89e-01Female-biased
PAADHNRNPH2exon_skip_1046177.98e+007.78e-038.30e+009.85e-01Female-biased
KICHSAMD4Aexon_skip_1045988.18e+005.63e-038.55e+009.88e-01Female-biased
BLCASAMD4Aexon_skip_1045988.00e+004.86e-038.42e+009.88e-01Female-biased
HNSCSAMD4Aexon_skip_1045987.94e+002.92e-048.63e+009.94e-01Female-biased

check buttonCOL4A1 related ES.
∗Only the gene encode RBP might with this result.
∗For more information please check Sex-biased RBP-ES network in cancer.

Top

Sex-biased CeRNA regulation of gene

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

Top

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
rs79193277chr13:110091218:G:A-0.115589327350680.0402449620703177LUSCFemale-baised eQTL
rs56119221chr13:113234407:C:G-0.04764390421125920.0215108806156504LUADFemale-baised eQTL
rs72658216chr13:109187956:C:T-0.05083410690528530.0471153904655932LUADFemale-baised eQTL
rs76277274chr13:100303686:A:C-0.05263234034737760.0473923295660315LUADFemale-baised eQTL

check buttonFemale-specific eQTL regulation.
SNP IDSNP InfoPosition to GeneEffect ScoreFDRCancer TypeBiased Type
rs1298629chr13:105950373:A:G--0.1134865038261970.000335748158642006STADMale-baised eQTL
rs2249748chr13:105954547:G:T--0.08951176340108460.0185286148896685STADMale-baised eQTL
rs9586621chr13:104746350:G:A-0.09112306023999910.0062675083838947BLCAMale-baised eQTL
rs9300965chr13:104747444:C:T-0.07602474494836020.0344369127528052BLCAMale-baised eQTL
rs9300967chr13:104749797:A:G-0.07645493954645860.0426434259860103BLCAMale-baised eQTL
rs61239565chr13:110002113:G:A-0.1402843350660140.00115273286002479COADMale-baised eQTL
rs183711260chr13:109992109:A:T-0.1441821774835950.00137768939515976COADMale-baised eQTL
rs144036587chr13:109993294:A:C-0.1441821774835950.00137768939515976COADMale-baised eQTL
rs79751079chr13:109995555:T:A-0.142085354124060.00142964157408026COADMale-baised eQTL
rs3742209chr13:109986013:G:A-0.14326266586940.00155079972827515COADMale-baised eQTL
rs7998434chr13:110007018:T:C-0.1376969429958410.00248982869732914COADMale-baised eQTL
rs373605189chr13:103069767:G:A-0.1457629113345360.00270506347222877COADMale-baised eQTL
rs77118982chr13:103075484:A:G-0.1457629113345360.00270506347222877COADMale-baised eQTL
rs77324237chr13:103076098:G:C-0.1457629113345360.00270506347222877COADMale-baised eQTL
rs75595545chr13:103079360:T:G-0.1451358732686970.00291804630218765COADMale-baised eQTL
rs1540461chr13:101696166:A:G-0.07488524445886110.00307337298429486COADMale-baised eQTL
rs73618805chr13:110012079:C:G-0.1432005422453750.00323361904957098COADMale-baised eQTL
rs1540460chr13:101696355:A:T-0.07281090075710050.00370197054387937COADMale-baised eQTL
rs7994568chr13:106145017:A:G-0.08501545865683220.00832285103289039COADMale-baised eQTL
rs9514512chr13:106237418:T:A-0.123319567971490.009512410320104COADMale-baised eQTL
rs16968630chr13:106445562:G:C-0.0956801945442110.0117046177052615COADMale-baised eQTL
rs35174640chr13:106607761:G:A-0.05463038733771860.0205540864185893COADMale-baised eQTL
rs4771752chr13:111433525:A:C-0.0564649797220410.0212921705569297COADMale-baised eQTL
rs9555796chr13:111433099:C:A-0.05610165795062750.0220645436745865COADMale-baised eQTL
rs4771751chr13:111433513:A:G-0.05609482158053290.0220695782863303COADMale-baised eQTL
rs9587782chr13:109144444:A:G-0.07942589699452680.0253360966711384COADMale-baised eQTL
rs35763512chr13:109397244:G:A-0.07407437450158280.0259602833445229COADMale-baised eQTL
rs61972637chr13:106027430:A:G-0.08462213759480410.0298855113626536COADMale-baised eQTL
rs2893073chr13:101690493:A:G-0.05879230225827930.0302769876492819COADMale-baised eQTL
rs12430541chr13:109984580:C:A-0.08960743497721110.0371503124409479COADMale-baised eQTL
rs9518498chr13:101705147:A:G-0.05669851296837350.0389591591971647COADMale-baised eQTL
rs1436264chr13:101689258:G:C-0.05822364215172470.0396159673494251COADMale-baised eQTL
rs61972635chr13:106021775:C:T-0.08156630931856530.0399175402145721COADMale-baised eQTL
rs61972636chr13:106025618:A:G-0.08156630931856530.0399175402145721COADMale-baised eQTL
rs16961281chr13:103066474:G:A-0.1070888997507830.0458672065967834COADMale-baised eQTL
rs12429986chr13:109982695:G:A-0.08621623126794760.0468046158098982COADMale-baised eQTL
rs9301351chr13:109084425:C:T-0.08338925710758680.0480920574272739COADMale-baised eQTL
rs9521350chr13:109403777:C:T-0.06558526758288340.0487662095953665COADMale-baised eQTL
rs9518915chr13:103061969:T:G-0.0969870285233440.0491034199861454COADMale-baised eQTL

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

Top

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: ENSG00000187498
CpG Site: cg02658690
Position to Gene: gene
Male Effect: -
Female Effect: -0.450467640589683
eQTM boxplot analysisGene ID: ENSG00000187498
CpG Site: cg20818806
Position to Gene: gene
Male Effect: -
Female Effect: -0.450467640589683

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

check buttonFemale-specific eQTM regulation.
CpG SiteCpG PostionPosition to GeneEffect ScoreFDRCor.rCor.PvalueCancer Type
cg02658690chr13:110233499gene-0.4504676405896831.36223663353247e-22-0.60833627397209633.335536774605328e-27LUAD
cg20818806chr13:110233579gene-0.4504676405896831.36223663353247e-22-0.60833627397209633.335536774605328e-27LUAD

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

Top

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

check buttonFemale-specific sQTL regulation.
ES IDSkipped ExonORF AnnoSNP IDSNP InfoSNP Position to ESEffect ScoreFDRCancer TypeBiased Type

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

Top

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

Top

Related disease information of COL4A1

check buttonDiseases associated with this gene (DisGeNET).
Gene IDGene SymbolDisease IDDisease NameNumber of PMIDSource
ENSG00000187498COL4A1C0002878Anemia, Hemolytic1CTD_human
ENSG00000187498COL4A1C0002879Anemia, Hemolytic, Acquired1CTD_human
ENSG00000187498COL4A1C0002889Anemia, Microangiopathic1CTD_human
ENSG00000187498COL4A1C0011881Diabetic Nephropathy2CTD_human
ENSG00000187498COL4A1C0015393Eye Abnormalities1CTD_human
ENSG00000187498COL4A1C0017667Nodular glomerulosclerosis2CTD_human
ENSG00000187498COL4A1C0017668Focal glomerulosclerosis2CTD_human
ENSG00000187498COL4A1C0023893Liver Cirrhosis, Experimental1CTD_human
ENSG00000187498COL4A1C0027726Nephrotic Syndrome1CTD_human
ENSG00000187498COL4A1C0086432Hyalinosis, Segmental Glomerular2CTD_human
ENSG00000187498COL4A1C0221021Microangiopathic hemolytic anemia1CTD_human
ENSG00000187498COL4A1C0265341Rieger syndrome2CTD_human
ENSG00000187498COL4A1C0266484Schizencephaly1CTD_human
ENSG00000187498COL4A1C0266548Axenfeld anomaly (disorder)2CTD_human
ENSG00000187498COL4A1C0270612Leukoencephalopathy1CTD_human
ENSG00000187498COL4A1C0302892Congenital porencephaly2CTD_human
ENSG00000187498COL4A1C1135196Heart Failure, Diastolic1CTD_human
ENSG00000187498COL4A1C1280768Axenfeld syndrome2CTD_human
ENSG00000187498COL4A1C1843512BRAIN SMALL VESSEL DISEASE WITH HEMORRHAGE2CTD_human
ENSG00000187498COL4A1C1858991Childhood Ataxia with Central Nervous System Hypomyelinization1CTD_human
ENSG00000187498COL4A1C1867327RETINAL ARTERIES, TORTUOSITY OF1CTD_human
ENSG00000187498COL4A1C1867983PORENCEPHALY, FAMILIAL2CTD_human
ENSG00000187498COL4A1C2673195Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps1CTD_human
ENSG00000187498COL4A1C2675650Brain Small Vessel Disease With Axenfeld-Rieger Anomaly2CTD_human
ENSG00000187498COL4A1C2678503AXENFELD-RIEGER SYNDROME, TYPE 32CTD_human
ENSG00000187498COL4A1C2937358Cerebral Hemorrhage1CTD_human
ENSG00000187498COL4A1C3495488Axenfeld-Rieger syndrome2CTD_human
ENSG00000187498COL4A1C3698507Post-traumatic Porencephaly2CTD_human
ENSG00000187498COL4A1C3714873Axenfeld-Rieger Syndrome, Type 12CTD_human
ENSG00000187498COL4A1C4082173Porencephaly2CTD_human
ENSG00000187498COL4A1C4082301Developmental Porencephaly2CTD_human
ENSG00000187498COL4A1C4551998Porencephaly, Type 1, Autosomal Dominant2CTD_human