Incidental Mutation 'FR4737:Sry'
ID 511776
Institutional Source Beutler Lab
Gene Symbol Sry
Ensembl Gene ENSMUSG00000069036
Gene Name sex determining region of Chr Y
Synonyms Tdy, Tdf
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.318) question?
Stock # FR4737 ()
Quality Score 214.458
Status Not validated
Chromosome Y
Chromosomal Location 2662471-2663658 bp(-) (GRCm38)
Type of Mutation small insertion (1 aa in frame mutation)
DNA Base Change (assembly) GTG to GTGTTG at 2662837 bp (GRCm38)
Zygosity Homozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000088717 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091178]
AlphaFold Q05738
Predicted Effect probably benign
Transcript: ENSMUST00000091178
SMART Domains Protein: ENSMUSP00000088717
Gene: ENSMUSG00000069036

HMG 4 74 2.76e-24 SMART
low complexity region 144 366 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.6%
  • 10x: 98.8%
  • 20x: 97.0%
Validation Efficiency
MGI Phenotype PHENOTYPE: Variations in expression of alleles on specific backgrounds result in partial and/or complete male to female sex reversal. Deletion of alleles results in XY females. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 209 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001K19Rik TCT TCTCCT 12: 110,668,448 (GRCm38) probably benign Het
2010300C02Rik C A 1: 37,625,036 (GRCm38) E594* probably null Homo
2010300C02Rik T A 1: 37,625,035 (GRCm38) E594V probably benign Homo
4930402H24Rik CC CCTGC 2: 130,770,752 (GRCm38) probably benign Het
4932415D10Rik TTCA T 10: 82,285,469 (GRCm38) probably benign Homo
4932438A13Rik TTATTAT TTATTATTATTATTACTATTAT 3: 37,050,754 (GRCm38) probably benign Het
A630001G21Rik CTGTT CT 1: 85,723,135 (GRCm38) probably benign Homo
Abcb11 C A 2: 69,243,518 (GRCm38) R1221L probably damaging Homo
Abcb4 GAAA G 5: 8,896,597 (GRCm38) probably benign Homo
Ahdc1 CT CTCGT 4: 133,062,759 (GRCm38) probably benign Homo
Alpk3 TCT TCTACT 7: 81,077,762 (GRCm38) probably benign Het
Amfr C G 8: 94,005,159 (GRCm38) G30R probably damaging Homo
Ankrd35 GC GCTAC 3: 96,683,849 (GRCm38) probably benign Homo
Anxa7 C T 14: 20,469,411 (GRCm38) G113E probably damaging Homo
Apc CAATAAAGC CAATAAAGCTAATAAAGC 18: 34,281,999 (GRCm38) probably benign Homo
Apol6 GTTT GTTTCTTT 15: 77,051,442 (GRCm38) probably null Homo
Arpc1b GGTGGC GGTGGCGTGGC 5: 145,126,787 (GRCm38) probably null Het
AY358078 C T 14: 51,805,698 (GRCm38) S281L unknown Homo
BC051142 CAG CAGAAG 17: 34,460,051 (GRCm38) probably benign Het
BC051142 GCA GCATCA 17: 34,460,068 (GRCm38) probably benign Het
Blm ACCTGC ACCTGCCTGC 7: 80,463,771 (GRCm38) probably null Het
Blm T TACCA 7: 80,463,774 (GRCm38) probably null Het
Blzf1 TTGT TT 1: 164,303,917 (GRCm38) probably null Homo
Btnl10 A AAGG 11: 58,923,931 (GRCm38) probably benign Homo
Cacna1a ACC ACCCCC 8: 84,638,726 (GRCm38) probably benign Homo
Cacna1a ACC ACCGCC 8: 84,638,720 (GRCm38) probably benign Het
Catsper2 TTC TTCTTTTACTTTGTC 2: 121,397,540 (GRCm38) probably benign Homo
Ccdc170 ACC ACCTCC 10: 4,561,023 (GRCm38) probably benign Het
Ccdc170 AC ACCCC 10: 4,561,029 (GRCm38) probably benign Het
Ccdc73 TAAG T 2: 104,991,840 (GRCm38) probably benign Homo
Ccnk TTCCCAC T 12: 108,202,507 (GRCm38) probably benign Het
Cdan1 A C 2: 120,724,971 (GRCm38) V763G probably damaging Het
Cdk6 A G 5: 3,344,211 (GRCm38) probably benign Het
Cdx1 GCTGCT GCTGCTTCTGCT 18: 61,019,878 (GRCm38) probably benign Het
Cdx1 TGCTGC TGCTGCCGCTGC 18: 61,019,874 (GRCm38) probably benign Het
Cfap46 CCTTCT CCTTCTTCT 7: 139,638,930 (GRCm38) probably benign Homo
Chd4 GC GCTCCCCC 6: 125,122,131 (GRCm38) probably benign Homo
Cluh CC CCTGAGGC 11: 74,669,533 (GRCm38) probably benign Het
Cluh GAGCCT GAGCCTAAGCCT 11: 74,669,524 (GRCm38) probably benign Het
Cluh CCCCGAGCC CCCCGAGCCCGAGCC 11: 74,669,514 (GRCm38) probably benign Het
Cluh AGCCTG AGCCTGCGCCTG 11: 74,669,519 (GRCm38) probably benign Het
Cntnap1 AGCCCC AGCCCCCGCCCC 11: 101,189,569 (GRCm38) probably benign Het
Cntnap1 CCCAGC CCCAGCGCCAGC 11: 101,189,590 (GRCm38) probably benign Het
Cntnap1 GCCCCA GCCCCACCCCCA 11: 101,189,582 (GRCm38) probably benign Het
Cntnap1 GCCCCA GCCCCAACCCCA 11: 101,189,576 (GRCm38) probably benign Het
Cul9 CTC CTCTTC 17: 46,500,858 (GRCm38) probably benign Het
Cul9 CTCTTC CTCTTCTTC 17: 46,500,846 (GRCm38) probably benign Het
Cyth2 C A 7: 45,813,042 (GRCm38) S102I possibly damaging Het
Dbr1 AGGAGG AGGAGGCGGAGG 9: 99,583,686 (GRCm38) probably benign Het
Dbr1 GGAGG GGAGGACGAGG 9: 99,583,699 (GRCm38) probably benign Het
Dhx8 CGAGAC CGAGACGGAGAC 11: 101,738,182 (GRCm38) probably benign Homo
Dhx8 GACCGA GACCGATACCGA 11: 101,738,179 (GRCm38) probably benign Homo
Dhx8 GAGACC GAGACCCAGACC 11: 101,738,189 (GRCm38) probably benign Homo
Dnah8 ACTGCCCCT ACT 17: 30,635,465 (GRCm38) probably benign Het
Dnah8 CCTCCCG C 17: 30,635,477 (GRCm38) probably benign Homo
Dnajb5 AGGTG A 4: 42,957,126 (GRCm38) probably null Het
Dusp10 G T 1: 184,037,056 (GRCm38) C73F probably damaging Homo
E4f1 CCG CCGACG 17: 24,455,192 (GRCm38) probably benign Homo
Eif3a TTA TTATTATA 19: 60,775,289 (GRCm38) probably benign Het
Fam81b TTC TTCGTC 13: 76,271,319 (GRCm38) probably benign Het
Fbxo22 G A 9: 55,209,382 (GRCm38) R56H probably damaging Het
Fcgr1 CTTCT C 3: 96,284,504 (GRCm38) probably null Het
Fcgr1 T C 3: 96,287,094 (GRCm38) D159G probably benign Homo
Fmn1 CCTCCT CCTCCTACTCCT 2: 113,525,778 (GRCm38) probably benign Het
Fmn1 CC CCCCCTGC 2: 113,525,781 (GRCm38) probably benign Het
Fmn1 CC CCTCCTTC 2: 113,525,784 (GRCm38) probably benign Het
G530012D18Rik GA GACAGAGATA 1: 85,577,178 (GRCm38) probably null Het
Gli3 G A 13: 15,644,357 (GRCm38) R248H probably damaging Het
Gm16503 G A 4: 147,541,253 (GRCm38) G68E unknown Het
Gm19345 GGATGGCAGGTG GG 7: 19,857,602 (GRCm38) probably null Het
Gm4340 GCA GCAACA 10: 104,196,077 (GRCm38) probably benign Het
Gm4340 AG AGCGG 10: 104,196,100 (GRCm38) probably benign Het
Gm4340 AGC AGCTGC 10: 104,196,097 (GRCm38) probably benign Het
Gm6309 C T 5: 146,168,183 (GRCm38) V307I probably benign Het
Gpatch11 AGGAA AGGAAGCGGAA 17: 78,842,180 (GRCm38) probably benign Het
Gpatch11 AAGAGG AAGAGGCAGAGG 17: 78,842,171 (GRCm38) probably benign Het
Hoxa10 T A 6: 52,234,186 (GRCm38) Q250L possibly damaging Homo
Hrh1 T C 6: 114,481,123 (GRCm38) I455T possibly damaging Het
Hspa1b GCGCC GC 17: 34,957,129 (GRCm38) probably benign Homo
Iba57 GAAA GAAAAA 11: 59,161,505 (GRCm38) probably null Homo
Igf1r TGGAGC TGGAGCTGGAGAGGGAGC 7: 68,226,181 (GRCm38) probably benign Het
Il17rd CGG CGGAGG 14: 27,082,680 (GRCm38) probably benign Het
Il2 TGG TGGGGCTTGAAGCGG 3: 37,125,828 (GRCm38) probably benign Het
Kcng4 G T 8: 119,633,519 (GRCm38) Y39* probably null Homo
Klra2 G GAAATCCACAT 6: 131,221,852 (GRCm38) probably null Het
Kmt2b CCTCCT CCTCCTTCTCCT 7: 30,586,367 (GRCm38) probably benign Het
Kmt2b TCCTCC TCCTCCCCCTCC 7: 30,586,378 (GRCm38) probably benign Het
Kmt2b CCTCCT CCTCCTGCTCCT 7: 30,586,370 (GRCm38) probably benign Het
Kmt2b TCCTCC TCCTCCCCCTCC 7: 30,586,366 (GRCm38) probably benign Het
Krt10 TCC TCCTCCACC 11: 99,389,279 (GRCm38) probably benign Homo
Krt10 TCCGCC TCCGCCGCC 11: 99,386,197 (GRCm38) probably benign Homo
Krt10 TCCTCC TCCTCCGCCTCC 11: 99,389,273 (GRCm38) probably benign Het
Krtap28-10 TCCCACA TCCCACACCCACA 1: 83,042,123 (GRCm38) probably benign Homo
Krtap4-2 A ACAC 11: 99,635,013 (GRCm38) probably benign Het
Krtap9-3 AC ACAGGTGTCGC 11: 99,598,004 (GRCm38) probably benign Het
Las1l AGG AGGGGG X: 95,940,821 (GRCm38) probably benign Het
Las1l GAG GAGCAG X: 95,940,829 (GRCm38) probably benign Het
Las1l AGG AGGCGG X: 95,940,827 (GRCm38) probably benign Het
Lrit3 GCT GCTTCT 3: 129,788,810 (GRCm38) probably benign Het
Lrit3 TGC TGCAGC 3: 129,788,806 (GRCm38) probably benign Het
Lrit3 AC ACATTC 3: 129,803,913 (GRCm38) probably null Homo
Luzp1 A AGGTGGCCTCTTCAGT 4: 136,543,196 (GRCm38) probably benign Het
Mamld1 AGC AGCCGC X: 71,118,835 (GRCm38) probably benign Het
Mamld1 GCA GCAACA X: 71,118,839 (GRCm38) probably benign Het
Mapk8ip3 G A 17: 24,902,119 (GRCm38) probably null Homo
Nat8f2 T A 6: 85,867,686 (GRCm38) L231F possibly damaging Homo
Nfxl1 CC CCGGGGAC 5: 72,559,121 (GRCm38) probably benign Het
Noc2l CTG CTGTTG 4: 156,240,095 (GRCm38) probably benign Het
Noc2l GGTAG GG 4: 156,241,501 (GRCm38) probably benign Homo
Noc2l GCT GCTTCT 4: 156,240,094 (GRCm38) probably benign Het
Nxpe5 C T 5: 138,229,934 (GRCm38) probably benign Het
Olfr1038-ps CAG CAGAG 2: 86,122,760 (GRCm38) probably null Homo
Olfr418 GGGCTGCTTGTGGCAAT G 1: 173,270,630 (GRCm38) probably null Het
Olfr568 CT CTAATTGCCTT 7: 102,877,233 (GRCm38) probably benign Homo
Olfr644 G C 7: 104,071,292 (GRCm38) probably benign Homo
Olfr890 A G 9: 38,143,188 (GRCm38) I13V probably benign Homo
Osmr C CTCA 15: 6,837,706 (GRCm38) probably null Homo
Patl2 GC GCTAC 2: 122,126,144 (GRCm38) probably null Het
Patl2 CTG CTGTTG 2: 122,126,136 (GRCm38) probably benign Het
Patl2 C CTGA 2: 122,126,145 (GRCm38) probably benign Het
Pdik1l GTTTTTGTTTT GTTTTTGTTTTTTTTTTGTTTT 4: 134,279,367 (GRCm38) probably null Homo
Pdik1l ACCACC ACCACCCCCACC 4: 134,279,506 (GRCm38) probably benign Het
Phc1 GCTG GCTGCTTCTG 6: 122,323,598 (GRCm38) probably benign Het
Piezo1 G A 8: 122,495,569 (GRCm38) R503W probably damaging Homo
Pitrm1 TTTTA T 13: 6,560,596 (GRCm38) probably benign Homo
Pkdrej TG TGGGAGCG 15: 85,819,680 (GRCm38) probably benign Homo
Pla2g4e AGGG A 2: 120,244,724 (GRCm38) probably benign Homo
Plekhs1 AC ACCTCCCCCGAGCC 19: 56,479,863 (GRCm38) probably benign Het
Pnmal2 TGGA T 7: 16,946,006 (GRCm38) probably benign Het
Ppp1r3f C A X: 7,560,336 (GRCm38) G562V probably damaging Homo
Prr13 CTC CTCATC 15: 102,462,173 (GRCm38) probably benign Het
Prss41 CACA C 17: 23,844,097 (GRCm38) probably benign Het
Prtg GTAAC G 9: 72,857,081 (GRCm38) probably benign Het
Ptk2b C T 14: 66,173,849 (GRCm38) R411Q possibly damaging Homo
Ptms C CTTG 6: 124,914,461 (GRCm38) probably benign Homo
Ptms TCT TCTGCT 6: 124,914,457 (GRCm38) probably benign Homo
Ptms TTC TTCGTC 6: 124,914,459 (GRCm38) probably benign Homo
Ptpn23 G T 9: 110,387,633 (GRCm38) P1052T probably benign Homo
Rab3il1 C A 19: 10,033,751 (GRCm38) A264E probably damaging Homo
Rbm6 GCTGT G 9: 107,782,755 (GRCm38) probably null Homo
Rtbdn AGCG AGCGTCCGCG 8: 84,956,168 (GRCm38) probably benign Het
Rtbdn TAG TAGGGGCAG 8: 84,956,161 (GRCm38) probably benign Het
Rtbdn GGC GGCAGCTGC 8: 84,956,177 (GRCm38) probably benign Het
Rtbdn CGGC CGGCAGGGGC 8: 84,956,176 (GRCm38) probably benign Het
Sbp CAAAG CAAAGCTGCTGACAAAAAAG 17: 23,945,382 (GRCm38) probably benign Het
Sbp G GCTGACAACAAAGATC 17: 23,945,389 (GRCm38) probably benign Het
Setd1a GTGGTAGTG GTGGTAGTGTTGGTAGTG 7: 127,785,312 (GRCm38) probably benign Het
Sfswap GCCCACTC GCCCACTCATCCCACTC 5: 129,569,756 (GRCm38) probably benign Het
Six3 GCG GCGCCG 17: 85,621,358 (GRCm38) probably benign Het
Six3 CGG CGGGGG 17: 85,621,365 (GRCm38) probably benign Het
Six3 GGC GGCAGC 17: 85,621,357 (GRCm38) probably benign Het
Six3 GGC GGCAGC 17: 85,621,363 (GRCm38) probably benign Het
Six3 CGG CGGGGG 17: 85,621,362 (GRCm38) probably benign Het
Six3 CGG CGGGGG 17: 85,621,368 (GRCm38) probably benign Het
Slc12a1 ACC ACCTTTGGCCACAACTCC 2: 125,154,214 (GRCm38) probably benign Homo
Spaca1 TCGCTC TCGCTCGCGCTC 4: 34,049,836 (GRCm38) probably benign Het
Spag1 TTC TTCGTC 15: 36,197,733 (GRCm38) probably benign Het
Spag17 AGG AGGCGG 3: 100,056,257 (GRCm38) probably benign Het
Srebf2 G T 15: 82,185,335 (GRCm38) A693S probably damaging Homo
Srpk2 T C 5: 23,545,196 (GRCm38) probably null Homo
Stard9 C CTAAGGGACTAGTAGG 2: 120,696,085 (GRCm38) probably benign Het
Supt20 GCAGCA GCAGCAACAGCA 3: 54,727,657 (GRCm38) probably benign Het
Supt20 CAGCAG CAGCAGGAGCAG 3: 54,727,658 (GRCm38) probably benign Het
Supt20 CAGCAG CAGCAGAAGCAG 3: 54,727,661 (GRCm38) probably benign Het
Tcof1 GGGTA G 18: 60,828,650 (GRCm38) probably benign Homo
Tdpoz3 A C 3: 93,826,674 (GRCm38) N219H probably benign Het
Tesk1 C CCCCG 4: 43,447,004 (GRCm38) probably null Homo
Tob1 CACA CACAACA 11: 94,214,451 (GRCm38) probably benign Het
Tob1 A AGCC 11: 94,214,478 (GRCm38) probably benign Het
Tob1 GCA GCAACA 11: 94,214,464 (GRCm38) probably benign Het
Trav15-2-dv6-2 AG AGAGG 14: 53,649,756 (GRCm38) probably benign Homo
Trav15-2-dv6-2 G GAAA 14: 53,649,757 (GRCm38) probably benign Homo
Trim63 GAGT G 4: 134,327,725 (GRCm38) probably benign Het
Tsen2 G GAGA 6: 115,560,077 (GRCm38) probably benign Het
Ttf2 TC TCCCC 3: 100,963,160 (GRCm38) probably benign Homo
Tusc1 ACCGCC ACCGCCCCCGCC 4: 93,335,313 (GRCm38) probably benign Homo
Ubqlnl TGAG T 7: 104,149,835 (GRCm38) probably benign Homo
Ubtf CCT CCTACT 11: 102,306,948 (GRCm38) probably null Het
Ubtf TCC TCCACC 11: 102,306,950 (GRCm38) probably benign Het
Vps13b G T 15: 35,846,957 (GRCm38) A2629S probably damaging Homo
Wasf3 G T 5: 146,470,250 (GRCm38) R460L probably damaging Het
Zc3h13 TGCGAGATG TGCGAGATGAGCGAGATG 14: 75,323,599 (GRCm38) probably benign Homo
Zc3h13 ATGTGCGAG ATGTGCGAGGTGTGCGAG 14: 75,323,596 (GRCm38) probably benign Homo
Zfhx3 GCAACA GCAACAACAACAACA 8: 108,956,088 (GRCm38) probably benign Het
Zfhx3 GCA GCAACAGCACCA 8: 108,956,103 (GRCm38) probably benign Het
Zfhx3 AGCA AGCAACAGACGCA 8: 108,956,102 (GRCm38) probably benign Het
Zfp111 TCA TCAACA 7: 24,199,805 (GRCm38) probably benign Homo
Zfp112 CATGA CATGATGA 7: 24,125,407 (GRCm38) probably benign Homo
Zfp26 C A 9: 20,438,546 (GRCm38) A241S probably benign Homo
Zfp282 CGG CGGGGG 6: 47,904,799 (GRCm38) probably benign Het
Zfp282 CGG CGGGGG 6: 47,904,790 (GRCm38) probably benign Het
Zfp335 TCC TCCGCC 2: 164,907,475 (GRCm38) probably benign Het
Zfp335 CTC CTCGTC 2: 164,907,474 (GRCm38) probably benign Het
Zfp335 TC TCCCC 2: 164,907,484 (GRCm38) probably benign Het
Zfp462 ACC ACCTCAGCCACAGTCGCC 4: 55,009,760 (GRCm38) probably benign Het
Zfp462 CCACC CCACCTCAGCCACAGTCACC 4: 55,009,758 (GRCm38) probably benign Het
Zfp598 ACCACC ACCACCCCCACC 17: 24,680,776 (GRCm38) probably benign Het
Zfp598 AC ACCACCGC 17: 24,680,791 (GRCm38) probably benign Het
Zfp598 ACCACC ACCACCGCCACC 17: 24,680,782 (GRCm38) probably benign Het
Zfp831 TC TCCGC 2: 174,645,483 (GRCm38) probably benign Het
Zfp831 TCC TCCCCC 2: 174,645,471 (GRCm38) probably benign Het
Zfp831 CTC CTCATC 2: 174,645,476 (GRCm38) probably benign Het
Zfp93 CAGGCATAG CAG 7: 24,275,389 (GRCm38) probably benign Homo
Zscan10 TGACG TG 17: 23,609,445 (GRCm38) probably benign Homo
Other mutations in Sry
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4304:Sry UTSW Y 2,662,837 (GRCm38) small insertion probably benign
FR4340:Sry UTSW Y 2,662,824 (GRCm38) small insertion probably benign
FR4342:Sry UTSW Y 2,663,146 (GRCm38) small deletion probably benign
FR4342:Sry UTSW Y 2,662,835 (GRCm38) small insertion probably benign
FR4342:Sry UTSW Y 2,662,836 (GRCm38) small insertion probably benign
FR4342:Sry UTSW Y 2,662,839 (GRCm38) small insertion probably benign
FR4449:Sry UTSW Y 2,662,832 (GRCm38) small insertion probably benign
FR4449:Sry UTSW Y 2,662,818 (GRCm38) small insertion probably benign
FR4589:Sry UTSW Y 2,662,818 (GRCm38) small insertion probably benign
FR4737:Sry UTSW Y 2,663,195 (GRCm38) small deletion probably benign
FR4737:Sry UTSW Y 2,662,838 (GRCm38) small insertion probably benign
FR4976:Sry UTSW Y 2,662,841 (GRCm38) small insertion probably benign
R0288:Sry UTSW Y 2,662,818 (GRCm38) missense unknown
R0506:Sry UTSW Y 2,662,864 (GRCm38) missense unknown
R0690:Sry UTSW Y 2,662,944 (GRCm38) small deletion probably benign
R0784:Sry UTSW Y 2,662,731 (GRCm38) missense unknown
R1373:Sry UTSW Y 2,662,864 (GRCm38) missense unknown
R1555:Sry UTSW Y 2,662,975 (GRCm38) missense unknown
R1638:Sry UTSW Y 2,663,149 (GRCm38) missense unknown
R2110:Sry UTSW Y 2,662,901 (GRCm38) missense unknown
R2212:Sry UTSW Y 2,663,339 (GRCm38) missense probably damaging 0.99
R3150:Sry UTSW Y 2,662,944 (GRCm38) small deletion probably benign
R3552:Sry UTSW Y 2,663,141 (GRCm38) missense unknown
R4877:Sry UTSW Y 2,662,864 (GRCm38) missense unknown
R4888:Sry UTSW Y 2,663,105 (GRCm38) missense unknown
R5028:Sry UTSW Y 2,663,312 (GRCm38) missense probably damaging 0.97
R5266:Sry UTSW Y 2,662,975 (GRCm38) missense unknown
R5305:Sry UTSW Y 2,662,982 (GRCm38) missense unknown
R5335:Sry UTSW Y 2,663,647 (GRCm38) missense probably benign 0.08
R5587:Sry UTSW Y 2,662,625 (GRCm38) missense unknown
R5915:Sry UTSW Y 2,662,612 (GRCm38) missense unknown
R6183:Sry UTSW Y 2,662,975 (GRCm38) missense unknown
R6184:Sry UTSW Y 2,662,975 (GRCm38) missense unknown
R6187:Sry UTSW Y 2,662,975 (GRCm38) missense unknown
R6976:Sry UTSW Y 2,662,938 (GRCm38) missense unknown
R7358:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R7632:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R7678:Sry UTSW Y 2,663,248 (GRCm38) missense possibly damaging 0.83
R7737:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R7812:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R7829:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R8005:Sry UTSW Y 2,663,303 (GRCm38) missense possibly damaging 0.88
R8028:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R8082:Sry UTSW Y 2,662,589 (GRCm38) missense unknown
R8212:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R8223:Sry UTSW Y 2,663,204 (GRCm38) missense unknown
R8252:Sry UTSW Y 2,663,298 (GRCm38) missense possibly damaging 0.91
R8390:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R9027:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
R9429:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
RF002:Sry UTSW Y 2,662,564 (GRCm38) small deletion probably benign
RF006:Sry UTSW Y 2,662,638 (GRCm38) small deletion probably benign
RF008:Sry UTSW Y 2,662,826 (GRCm38) small insertion probably benign
RF040:Sry UTSW Y 2,662,590 (GRCm38) small insertion probably benign
RF063:Sry UTSW Y 2,662,595 (GRCm38) frame shift probably null
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2018-04-05