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Gene id 10
Gene Summary     SNPs    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed references    

Gene Summary
Gene Symbol NAT2   Gene   UCSC   Ensembl
Aliases AAC2, NAT-2, PNAT
Gene name N-acetyltransferase 2
Alternate names arylamine N-acetyltransferase 2, N-acetyltransferase 2 (arylamine N-acetyltransferase), N-acetyltransferase type 2, arylamide acetylase 2,
Gene location 8p22 (18386584: 18401218)     Exons: 3     NC_000008.11
Gene summary(Entrez) This gene encodes an enzyme that functions to both activate and deactivate arylamine and hydrazine drugs and carcinogens. Polymorphisms in this gene are responsible for the N-acetylation polymorphism in which human populations segregate into rapid, intermediate, and slow acetylator phenotypes. Polymorphisms in this gene are also associated with higher incidences of cancer and drug toxicity. A second arylamine N-acetyltransferase gene (NAT1) is located near this gene (NAT2). [provided by RefSeq, Jul 2008]
OMIM 612182

SNPs

 rs4244593

Strand:    Allele origin:   Allele change: A/C/T   Mutation type: snp

CM000679.2   g.17516904T>A
CM000679.2   g.17516904T>G
NC_000017.10   g.17420218T>G
NC_000017.11   g.17516904T>A
NC_000017.11   g.17516904T>G
NM_001267551.1   c.255-4250A>C
NM_001267551.1   c.255-4250A>T
NM_001267552.1   c.321-4250A>C
NM_001267552.1   c.321-4250A>T
NM_007169.2   c.210-4250A>C
NM_007169.2   c.210-4250A>T
NM_148172.2   c.321-4250A>C
NM_148172.2   c.321-4250A>T
NM_148173.1   c.210-4250A>C
NM_148173.1   c.210-4250A>T
rs10757269

Strand:    Allele origin:   Allele change: A/C/G   Mutation type: snp

CM000671.2   g.22072265A>C
CM000671.2   g.22072265A>G
NC_000009.11   g.22072264A>G
NC_000009.12   g.22072265A>C
NC_000009.12   g.22072265A>G
NR_003529.3   n.2448+5912A>C
NR_003529.3   n.2448+5912A>G
NR_047532.1   n.1075+15878A>C
NR_047532.1   n.1075+15878A>G
NR_047533.1   n.645-5414A>C
NR_047533.1   n.645-5414A>G
NR_047534.1   n.644+23037A>C
NR_047534.1   n.644+23037A>G
NR_047535.1   n.780+15878A>C
NR_047535.1   n.780+15878A>G
NR_047536.1   n.644+23037A>C
NR_047536.1   n.644+23037A>G
NR_047537.1   n.780+15878A>C
NR_047537.1   n.780+15878A>G
NR_047538.1   n.644+23037A>C
NR_047538.1   n.644+23037A>G
NR_047539.1   n.2449-5414A>C
NR_047539.1   n.2449-5414A>G
NR_047540.1   n.1049-5414A>C
NR_047540.1   n.1049-5414A>G
NR_047541.1   n.856-5414A>C
NR_047541.1   n.856-5414A>G
NR_047542.1   n.781-5414A>C
NR_047542.1   n.781-5414A>G
NR_047543.1   n.780+15878A>C
NR_047543.1   n.780+15878A>G
NR_120536.1   n.644+23037A>C
NR_120536.1   n.644+23037A>G
rs10757272

Strand:    Allele origin:   Allele change: C/T   Mutation type: snp

CM000671.2   g.22088261C>T
NC_000009.11   g.22088260C>T
NC_000009.12   g.22088261C>T
NR_003529.3   n.2449-8111C>T
NR_047532.1   n.1076-4047C>T
NR_047534.1   n.645-8997C>T
NR_047535.1   n.781-24059C>T
NR_047536.1   n.645-24059C>T
NR_047537.1   n.780+31874C>T
NR_047538.1   n.645-31939C>T
NR_047543.1   n.781-24059C>T
NR_120536.1   n.645-32243C>T
rs10965215

Strand:    Allele origin:   Allele change: A/G   Mutation type: snp

CM000671.2   g.22029446G>A
NC_000009.11   g.22029445G>A
NC_000009.12   g.22029446G>A
NR_003529.3   n.385G>A
NR_047532.1   n.385G>A
NR_047533.1   n.372-17305G>A
NR_047534.1   n.372-17305G>A
NR_047535.1   n.372-17305G>A
NR_047536.1   n.372-17305G>A
NR_047537.1   n.372-17305G>A
NR_047538.1   n.372-17305G>A
NR_047539.1   n.385G>A
NR_047540.1   n.372-17305G>A
NR_047541.1   n.372-17305G>A
NR_047542.1   n.372-17305G>A
NR_047543.1   n.372-17305G>A
NR_120536.1   n.372-17305G>A
rs10965235

Strand:    Allele origin:   Allele change: A/C   Mutation type: snp

CM000671.2   g.22115106C>A
NC_000009.11   g.22115105C>A
NC_000009.12   g.22115106C>A
NR_003529.3   n.2908+1307C>A
NR_047532.1   n.1697+1307C>A
NR_047534.1   n.961+1307C>A
NR_047535.1   n.856+2711C>A
NR_047536.1   n.720+2711C>A
NR_047537.1   n.781-5094C>A
NR_047538.1   n.645-5094C>A
NR_047543.1   n.990+1307C>A
NR_120536.1   n.645-5398C>A
rs1255998

Strand:    Allele origin:   Allele change: A/C/G   Mutation type: snp

CM000676.2   g.64227153G>C
CM000676.2   g.64227153G>T
NC_000014.8   g.64693871G>C
NC_000014.9   g.64227153G>C
NC_000014.9   g.64227153G>T
NG_011535.1   g.116398C>A
NG_011535.1   g.116398C>G
NG_011756.1   g.379189G>C
NG_011756.1   g.379189G>T
NM_001040275.1   c.*380C>A
NM_001040275.1   c.*380C>G
NM_001214902.1   c.*737C>A
NM_001214902.1   c.*737C>G
NM_001291712.1   c.*380C>A
NM_001291712.1   c.*380C>G
NM_001291723.1   c.*380C>A
NM_001291723.1   c.*380C>G
NR_073496.1   n.2472C>A
NR_073496.1   n.2472C>G
NR_073505.1   n.2611C>G
XR_001750187.1   n.2304C>A
XR_001750187.1   n.2304C>G
rs1333042

Strand:    Allele origin:   Allele change: A/G   Mutation type: snp

CM000671.2   g.22103814A>G
NC_000009.11   g.22103813A>G
NC_000009.12   g.22103814A>G
NR_003529.3   n.2698+6450A>G
NR_047532.1   n.1487+6450A>G
NR_047534.1   n.751+6450A>G
NR_047535.1   n.781-8506A>G
NR_047536.1   n.645-8506A>G
NR_047537.1   n.781-16386A>G
NR_047538.1   n.645-16386A>G
NR_047543.1   n.781-8506A>G
NR_120536.1   n.645-16690A>G
rs1537370

Strand:    Allele origin:   Allele change: C/T   Mutation type: snp

CM000671.2   g.22084311C>T
NC_000009.11   g.22084310C>T
NC_000009.12   g.22084311C>T
NR_003529.3   n.2449-12061C>T
NR_047532.1   n.1076-7997C>T
NR_047534.1   n.645-12947C>T
NR_047535.1   n.780+27924C>T
NR_047536.1   n.645-28009C>T
NR_047537.1   n.780+27924C>T
NR_047538.1   n.644+35083C>T
NR_047543.1   n.780+27924C>T
NR_120536.1   n.644+35083C>T
rs17761446

Strand:    Allele origin:   Allele change: G/T   Mutation type: snp

CM000671.2   g.22118103T>G
NC_000009.11   g.22118102T>G
NC_000009.12   g.22118103T>G
NR_003529.3   n.2909-541T>G
NR_047532.1   n.1698-541T>G
NR_047534.1   n.962-541T>G
NR_047535.1   n.857-541T>G
NR_047536.1   n.721-541T>G
NR_047537.1   n.781-2097T>G
NR_047538.1   n.645-2097T>G
NR_047543.1   n.991-541T>G
NR_120536.1   n.645-2401T>G
rs17834457

Strand:    Allele origin:   Allele change: C/G/T   Mutation type: snp

CM000671.2   g.22118027C>G
CM000671.2   g.22118027C>T
NC_000009.11   g.22118026C>T
NC_000009.12   g.22118027C>G
NC_000009.12   g.22118027C>T
NR_003529.3   n.2909-617C>G
NR_003529.3   n.2909-617C>T
NR_047532.1   n.1698-617C>G
NR_047532.1   n.1698-617C>T
NR_047534.1   n.962-617C>G
NR_047534.1   n.962-617C>T
NR_047535.1   n.857-617C>G
NR_047535.1   n.857-617C>T
NR_047536.1   n.721-617C>G
NR_047536.1   n.721-617C>T
NR_047537.1   n.781-2173C>G
NR_047537.1   n.781-2173C>T
NR_047538.1   n.645-2173C>G
NR_047538.1   n.645-2173C>T
NR_047543.1   n.991-617C>G
NR_047543.1   n.991-617C>T
NR_120536.1   n.645-2477C>G
NR_120536.1   n.645-2477C>T
rs1799930

Strand:    Allele origin: G(germline)/A(germline)  Allele change: A/G   Mutation type: snp

CM000670.2   g.18400593G>A
NC_000008.10   g.18258103G>A
NC_000008.11   g.18400593G>A
NG_012246.1   g.14349G>A
NM_000015.2   c.590G>A
NP_000006.2   p.Arg197Gln
XP_016868427.1   p.Arg197Gln
Clinical Significance: drug-response

rs1256049

Strand: -   Allele origin: unknown  Allele change: A/G   Mutation type: snp

  
NC_000014.9   g.64257333C>T
NC_000014.8   g.64724051C>T
NG_011535.1   g.86218G>A
NM_001040275.1   c.984G>A
NM_001214903.1   c.984G>A
NM_001214902.1   c.984G>A
NM_001271876.1   c.984G>A
NM_001271877.1   c.952+3116G>A
NM_001291712.1   c.984G>A
NM_001291723.1   c.984G>A
NM_001  
rs1801270

Strand:    Allele origin: A(unknown)/C(germline,unknown)  Allele change: A/C/T   Mutation type: snp

CM000668.2   g.36684194C>A
CM000668.2   g.36684194C>T
NC_000006.11   g.36651971C>A
NC_000006.12   g.36684194C>A
NC_000006.12   g.36684194C>T
NG_009364.1   g.10513C>A
NG_009364.1   g.10513C>T
NM_000389.4   c.93C>A
NM_000389.4   c.93C>T
NM_001220777.1   c.93C>A
NM_001220777.1   c.93C>T
NM_001220778.1   c.93C>A
NM_001220778.1   c.93C>T
NM_001291549.1   c.195C>A
NM_001291549.1   c.195C>T
NM_078467.2   c.93C>A
NM_078467.2   c.93C>T
NP_000380.1   p.Ser31=
NP_000380.1   p.Ser31Arg
NP_001207706.1   p.Ser31=
NP_001207706.1   p.Ser31Arg
NP_001207707.1   p.Ser31=
NP_001207707.1   p.Ser31Arg
NP_001278478.1   p.Ser65=
NP_001278478.1   p.Ser65Arg
NP_510867.1   p.Ser31=
NP_510867.1   p.Ser31Arg
XP_005248844.1   p.Ser65Arg
Clinical Significance: Benign

rs213950

Strand:    Allele origin: G(germline)/A(germline)  Allele change: A/G   Mutation type: snp

CM000669.2   g.117559479G>A
NC_000007.13   g.117199533G=
NC_000007.13   g.117199533G>A
NC_000007.14   g.117559479G=
NC_000007.14   g.117559479G>A
NG_016465.4   g.98696G=
NG_016465.4   g.98696G>A
NM_000492.3   c.1408G=
NM_000492.3   c.1408G>A
NP_000483.3   p.Val470=
NP_000483.3   p.Val470Met
NR_149084.1   n.221+1254C=
NR_149084.1   n.221+1254C>T
XP_011514053.1   p.Val500=
XP_011514053.1   p.Val500Met
XP_011514055.1   p.Val389=
XP_011514055.1   p.Val389Met
XP_011514056.1   p.Val389=
XP_011514056.1   p.Val389Met
XP_016867188.1   p.Val389=
XP_016867188.1   p.Val389Met
Clinical Significance: other

rs2157719

Strand:    Allele origin:   Allele change: A/G   Mutation type: snp

CM000671.2   g.22033367C>T
NC_000009.11   g.22033366C>T
NC_000009.12   g.22033367C>T
NR_003529.3   n.846+381C>T
NR_047532.1   n.533+3773C>T
NR_047533.1   n.372-13384C>T
NR_047534.1   n.372-13384C>T
NR_047535.1   n.372-13384C>T
NR_047536.1   n.372-13384C>T
NR_047537.1   n.372-13384C>T
NR_047538.1   n.372-13384C>T
NR_047539.1   n.846+381C>T
NR_047540.1   n.372-13384C>T
NR_047541.1   n.372-13384C>T
NR_047542.1   n.372-13384C>T
NR_047543.1   n.372-13384C>T
NR_120536.1   n.372-13384C>T
rs2383206

Strand:    Allele origin:   Allele change: A/G   Mutation type: snp

CM000671.2   g.22115027A>G
NC_000009.11   g.22115026A>G
NC_000009.12   g.22115027A>G
NR_003529.3   n.2908+1228A>G
NR_047532.1   n.1697+1228A>G
NR_047534.1   n.961+1228A>G
NR_047535.1   n.856+2632A>G
NR_047536.1   n.720+2632A>G
NR_047537.1   n.781-5173A>G
NR_047538.1   n.645-5173A>G
NR_047543.1   n.990+1228A>G
NR_120536.1   n.645-5477A>G
rs3731197

Strand:    Allele origin:   Allele change: A/G   Mutation type: snp

CM000671.2   g.21991372C>T
NC_000009.11   g.21991371C>T
NC_000009.12   g.21991372C>T
NG_007485.1   g.8120G>A
NM_058195.3   c.193+2767G>A
XR_242496.1   n.347+2767G>A
rs4957014

Strand:    Allele origin:   Allele change: G/T   Mutation type: snp

CM000667.2   g.287899T>G
NC_000005.10   g.287899T>G
NC_000005.9   g.288014T>G
NM_001267556.1   c.163+15127T>G
NM_001267557.1   c.163+15127T>G
NM_001267558.1   c.-48+15127T>G
NM_001267559.1   c.163+15127T>G
NM_013232.3   c.163+15127T>G
rs4986938

Strand: -   Allele origin: unknown  Allele change: A/G   Mutation type: snp

NG_011535.1   g.110453G>A
NC_000014.9   g.64233098C>T
NC_000014.8   g.64699816C>T
NM_001040275.1   c.1406+1872G>A
NM_001214902.1   c.1406+1872G>A
NM_001271876.1   c.1406+1872G>A
NM_001271877.1   c.*39G>A
NM_001291723.1   c.1406+1872G>A
NM_001291712.1   c.1406+1872G>A
NM_00  
rs4977756

Strand:    Allele origin:   Allele change: A/G   Mutation type: snp

CM000671.2   g.22068653G>A
NC_000009.11   g.22068652G>A
NC_000009.12   g.22068653G>A
NR_003529.3   n.2448+2300G>A
NR_047532.1   n.1075+12266G>A
NR_047533.1   n.645-9026G>A
NR_047534.1   n.644+19425G>A
NR_047535.1   n.780+12266G>A
NR_047536.1   n.644+19425G>A
NR_047537.1   n.780+12266G>A
NR_047538.1   n.644+19425G>A
NR_047539.1   n.2448+2300G>A
NR_047540.1   n.1048+2300G>A
NR_047541.1   n.855+4635G>A
NR_047542.1   n.781-9026G>A
NR_047543.1   n.780+12266G>A
NR_120536.1   n.644+19425G>A
rs6475606

Strand:    Allele origin:   Allele change: C/T   Mutation type: snp

CM000671.2   g.22081851C>T
NC_000009.11   g.22081850C>T
NC_000009.12   g.22081851C>T
NR_003529.3   n.2449-14521C>T
NR_047532.1   n.1076-10457C>T
NR_047534.1   n.645-15407C>T
NR_047535.1   n.780+25464C>T
NR_047536.1   n.645-30469C>T
NR_047537.1   n.780+25464C>T
NR_047538.1   n.644+32623C>T
NR_047543.1   n.780+25464C>T
NR_120536.1   n.644+32623C>T
rs708272

Strand:    Allele origin:   Allele change: C/T   Mutation type: snp

CM000678.2   g.56962376G>A
NC_000016.10   g.56962376G>A
NC_000016.9   g.56996288G>A
NG_008952.1   g.5454G>A
NM_000078.2   c.118+279G>A
NM_001286085.1   c.118+279G>A
rs7865618

Strand:    Allele origin:   Allele change: A/G/T   Mutation type: snp

CM000671.2   g.22031006G>A
CM000671.2   g.22031006G>T
NC_000009.11   g.22031005G>A
NC_000009.12   g.22031006G>A
NC_000009.12   g.22031006G>T
NR_003529.3   n.533+1412G>A
NR_003529.3   n.533+1412G>T
NR_047532.1   n.533+1412G>A
NR_047532.1   n.533+1412G>T
NR_047533.1   n.372-15745G>A
NR_047533.1   n.372-15745G>T
NR_047534.1   n.372-15745G>A
NR_047534.1   n.372-15745G>T
NR_047535.1   n.372-15745G>A
NR_047535.1   n.372-15745G>T
NR_047536.1   n.372-15745G>A
NR_047536.1   n.372-15745G>T
NR_047537.1   n.372-15745G>A
NR_047537.1   n.372-15745G>T
NR_047538.1   n.372-15745G>A
NR_047538.1   n.372-15745G>T
NR_047539.1   n.533+1412G>A
NR_047539.1   n.533+1412G>T
NR_047540.1   n.372-15745G>A
NR_047540.1   n.372-15745G>T
NR_047541.1   n.372-15745G>A
NR_047541.1   n.372-15745G>T
NR_047542.1   n.372-15745G>A
NR_047542.1   n.372-15745G>T
NR_047543.1   n.372-15745G>A
NR_047543.1   n.372-15745G>T
NR_120536.1   n.372-15745G>A
NR_120536.1   n.372-15745G>T
rs944052

Strand:    Allele origin:   Allele change: C/T   Mutation type: snp

CM000676.2   g.64339114G>A
NC_000014.8   g.64805832G>A
NC_000014.9   g.64339114G>A
NG_011535.1   g.4437C>T
NM_001291712.1   c.-2292C>T
NM_001291723.1   c.-1307C>T
NR_073496.1   n.-564C>T
NR_073505.1   n.-564C>T
rs944797

Strand:    Allele origin:   Allele change: C/T   Mutation type: snp

CM000671.2   g.22115287T>C
NC_000009.11   g.22115286T>C
NC_000009.11   g.22115286T>G
NC_000009.12   g.22115287T>C
NR_003529.3   n.2908+1488T>C
NR_003529.3   n.2908+1488T>G
NR_047532.1   n.1697+1488T>C
NR_047532.1   n.1697+1488T>G
NR_047534.1   n.961+1488T>C
NR_047534.1   n.961+1488T>G
NR_047535.1   n.856+2892T>C
NR_047535.1   n.856+2892T>G
NR_047536.1   n.720+2892T>C
NR_047536.1   n.720+2892T>G
NR_047537.1   n.781-4913T>C
NR_047537.1   n.781-4913T>G
NR_047538.1   n.645-4913T>C
NR_047538.1   n.645-4913T>G
NR_047543.1   n.990+1488T>C
NR_047543.1   n.990+1488T>G
NR_120536.1   n.645-5217T>C
NR_120536.1   n.645-5217T>G

Protein Summary
Protein general information P11245  

Name: Arylamine N acetyltransferase 2 (EC 2.3.1.5) (Arylamide acetylase 2) (N acetyltransferase type 2) (NAT 2) (Polymorphic arylamine N acetyltransferase) (PNAT)

Length: 290  Mass: 33,542

Sequence MDIEAYFERIGYKNSRNKLDLETLTDILEHQIRAVPFENLNMHCGQAMELGLEAIFDHIVRRNRGGWCLQVNQLL
YWALTTIGFQTTMLGGYFYIPPVNKYSTGMVHLLLQVTIDGRNYIVDAGSGSSSQMWQPLELISGKDQPQVPCIF
CLTEERGIWYLDQIRREQYITNKEFLNSHLLPKKKHQKIYLFTLEPRTIEDFESMNTYLQTSPTSSFITTSFCSL
QTPEGVYCLVGFILTYRKFNYKDNTDLVEFKTLTEEEVEEVLKNIFKISLGRNLVPKPGDGSLTI
Structural information
Interpro:  IPR001447

Pfam:  		 PF00797

PDB:  		 2PFR
PDBsum:   2PFR
STRING:   ENSP00000286479;
Other Databases GeneCards:  NAT2;  Malacards:  NAT2

Gene ontology


GO accessionTerm nameEvidence codeGo category
GO:0004060 arylamine N-acetyltransfe
rase activity
 TAS molecular_function
GO:0005515 protein binding
 IPI molecular_function
GO:0005829 cytosol
 TAS cellular_component
GO:0005829 cytosol
 TAS cellular_component
GO:0006805 xenobiotic metabolic proc
ess
 TAS biological_process
GO:0004060 arylamine N-acetyltransfe
rase activity
 IEA molecular_function
GO:0004060 arylamine N-acetyltransfe
rase activity
 TAS molecular_function
GO:0004060 arylamine N-acetyltransfe
rase activity
 TAS molecular_function
GO:0005515 protein binding
 IPI molecular_function
GO:0005737 cytoplasm
 IEA cellular_component
GO:0005737 cytoplasm
 IEA cellular_component
GO:0005829 cytosol
 TAS cellular_component
GO:0005829 cytosol
 TAS cellular_component
GO:0006805 xenobiotic metabolic proc
ess
 TAS biological_process
GO:0008152 metabolic process
 IEA biological_process
GO:0016407 acetyltransferase activit
y
 IEA molecular_function
GO:0016740 transferase activity
 IEA molecular_function
GO:0016746 transferase activity, tra
nsferring acyl groups
 IEA molecular_function
GO:0004060 arylamine N-acetyltransfe
rase activity
 TAS molecular_function
GO:0004060 arylamine N-acetyltransfe
rase activity
 TAS molecular_function
GO:0005515 protein binding
 IPI molecular_function
GO:0005829 cytosol
 TAS cellular_component
GO:0005829 cytosol
 TAS cellular_component
GO:0006805 xenobiotic metabolic proc
ess
 TAS biological_process

KEGG pathways

hsa01100  Metabolic pathways
hsa05204  Chemical carcinogenesis
hsa00983  Drug metabolism - other enzymes
hsa00232  Caffeine metabolism

Diseases

Associated diseases References
Alzheimer's disease PMID: 14582397
Asthma PMID: 11927838
Atopy PMID: 10340922
Cancer PMID: 16006997
Chronic obstructive pulmonary disease (COPD) PMID: 12884528
Cleft lip PMID: 18449058
Connective tissue diseases PMID: 19527514
Crohn's disease PMID: 16097053
Dermatitis PMID: 19834256
Diabetes PMID: 7995004
Endometriosis PMID: 22547312
Fetal loss PMID: 16782969
Idiopathic male infertility PMID: 24928356
Inflammatory bowel disease PMID: 17068223
Limb deficiency defects PMID: 16906563
Macular degeneration PMID: 15774926
Male infertility PMID: 24488272
Endometriosis PMID: 11675475
Endometriosis INFBASE10381818
Parkinson's disease PMID: 10634239
Periodontitis PMID: 11846845
Preeclampsia PMID: 11751440
Premature ovarian failure ( POF) PMID: 18630123
Preterm delivery PMID: 11520401
Psoriasis PMID: 19334527
Rheumatoid arthritis PMID: 12465141
Schizophrenia PMID: 11393533
Spinal dysraphism PMID: 19161160
Systemic lupus erythematosus PMID: 10599336

PubMed references


PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
11675475 Endometrio
sis
 NAT 2 *5, *6 and *7 UK
NAT 2
 Show abstract
12760253 Endometrio
sis
74 patients wit
h extragenital
endometriosis
 CYP1A1
mEPHX1
CYP2E1
NAT2
and GSTM1
 Show abstract
15588473 Endometrio
sis
 NAT2 *4 allele result in allelic variants *5, *6 and *7 South I
ndian
 516 (252 unrela
ted women with
endometriosis,
264 controls)
 Endometriosis
 Show abstract
10381818 Endometrio
sis
 NAT2*5 allele French
 137 (36 minimal
/mild endometri
osis, 29 modera
te/severe endom
etriosis, 72 co
ntrols)
 GSTT1
NAT2
GSTM1
 Show abstract