Incidental Mutation 'R1753:Kmt2d'
ID 193784
Institutional Source Beutler Lab
Gene Symbol Kmt2d
Ensembl Gene ENSMUSG00000048154
Gene Name lysine (K)-specific methyltransferase 2D
Synonyms Mll4, Mll2, C430014K11Rik
MMRRC Submission 039785-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1753 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 98729550-98769085 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to T at 98741363 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000023741] [ENSMUST00000178486]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000023741
AA Change: T4565K
SMART Domains Protein: ENSMUSP00000023741
Gene: ENSMUSG00000048154
AA Change: T4565K

DomainStartEndE-ValueType
low complexity region 135 145 N/A INTRINSIC
PHD 171 218 1.65e-5 SMART
RING 172 217 2.01e0 SMART
PHD 228 274 2.13e-8 SMART
RING 229 273 2.11e-3 SMART
PHD 275 321 1.57e-11 SMART
RING 276 320 2.36e0 SMART
low complexity region 430 489 N/A INTRINSIC
low complexity region 500 562 N/A INTRINSIC
low complexity region 564 613 N/A INTRINSIC
low complexity region 619 717 N/A INTRINSIC
internal_repeat_3 719 768 2.82e-8 PROSPERO
internal_repeat_3 773 822 2.82e-8 PROSPERO
low complexity region 826 842 N/A INTRINSIC
low complexity region 844 919 N/A INTRINSIC
low complexity region 958 981 N/A INTRINSIC
low complexity region 985 1023 N/A INTRINSIC
low complexity region 1069 1076 N/A INTRINSIC
low complexity region 1139 1153 N/A INTRINSIC
low complexity region 1259 1285 N/A INTRINSIC
low complexity region 1307 1314 N/A INTRINSIC
PHD 1335 1384 7.01e-9 SMART
RING 1336 1383 1.46e1 SMART
PHD 1385 1431 8.56e-13 SMART
PHD 1462 1513 1.11e-6 SMART
RING 1463 1512 1.46e1 SMART
low complexity region 1514 1538 N/A INTRINSIC
low complexity region 1567 1576 N/A INTRINSIC
low complexity region 1589 1612 N/A INTRINSIC
low complexity region 1634 1646 N/A INTRINSIC
low complexity region 1707 1719 N/A INTRINSIC
low complexity region 1883 1896 N/A INTRINSIC
low complexity region 1931 1950 N/A INTRINSIC
HMG 1969 2037 6.35e-6 SMART
low complexity region 2064 2079 N/A INTRINSIC
low complexity region 2147 2167 N/A INTRINSIC
low complexity region 2170 2181 N/A INTRINSIC
low complexity region 2306 2323 N/A INTRINSIC
low complexity region 2334 2359 N/A INTRINSIC
low complexity region 2366 2388 N/A INTRINSIC
low complexity region 2402 2419 N/A INTRINSIC
low complexity region 2546 2559 N/A INTRINSIC
low complexity region 2610 2622 N/A INTRINSIC
coiled coil region 2632 2665 N/A INTRINSIC
coiled coil region 2768 2813 N/A INTRINSIC
low complexity region 2855 2868 N/A INTRINSIC
low complexity region 2887 2899 N/A INTRINSIC
low complexity region 3151 3165 N/A INTRINSIC
low complexity region 3189 3204 N/A INTRINSIC
low complexity region 3241 3263 N/A INTRINSIC
low complexity region 3390 3400 N/A INTRINSIC
low complexity region 3629 3659 N/A INTRINSIC
coiled coil region 3712 3749 N/A INTRINSIC
low complexity region 3781 3801 N/A INTRINSIC
coiled coil region 3910 4003 N/A INTRINSIC
low complexity region 4128 4159 N/A INTRINSIC
low complexity region 4167 4183 N/A INTRINSIC
low complexity region 4226 4246 N/A INTRINSIC
low complexity region 4266 4293 N/A INTRINSIC
low complexity region 4306 4322 N/A INTRINSIC
low complexity region 4361 4378 N/A INTRINSIC
coiled coil region 4591 4613 N/A INTRINSIC
low complexity region 4661 4684 N/A INTRINSIC
low complexity region 4745 4755 N/A INTRINSIC
low complexity region 4877 4896 N/A INTRINSIC
low complexity region 4957 4983 N/A INTRINSIC
low complexity region 4989 5029 N/A INTRINSIC
low complexity region 5100 5107 N/A INTRINSIC
PHD 5142 5188 4.67e-5 SMART
RING 5143 5187 4.87e0 SMART
FYRN 5242 5285 5.07e-21 SMART
FYRC 5291 5378 2.51e-43 SMART
SET 5448 5570 5.69e-36 SMART
PostSET 5572 5588 3.58e-5 SMART
Predicted Effect unknown
Transcript: ENSMUST00000178486
AA Change: T4565K
SMART Domains Protein: ENSMUSP00000135941
Gene: ENSMUSG00000048154
AA Change: T4565K

DomainStartEndE-ValueType
low complexity region 135 145 N/A INTRINSIC
PHD 171 218 1.65e-5 SMART
RING 172 217 2.01e0 SMART
PHD 228 274 2.13e-8 SMART
RING 229 273 2.11e-3 SMART
PHD 275 321 1.57e-11 SMART
RING 276 320 2.36e0 SMART
low complexity region 430 489 N/A INTRINSIC
low complexity region 500 562 N/A INTRINSIC
low complexity region 564 613 N/A INTRINSIC
low complexity region 619 717 N/A INTRINSIC
internal_repeat_3 719 768 2.82e-8 PROSPERO
internal_repeat_3 773 822 2.82e-8 PROSPERO
low complexity region 826 842 N/A INTRINSIC
low complexity region 844 919 N/A INTRINSIC
low complexity region 958 981 N/A INTRINSIC
low complexity region 985 1023 N/A INTRINSIC
low complexity region 1069 1076 N/A INTRINSIC
low complexity region 1139 1153 N/A INTRINSIC
low complexity region 1259 1285 N/A INTRINSIC
low complexity region 1307 1314 N/A INTRINSIC
PHD 1335 1384 7.01e-9 SMART
RING 1336 1383 1.46e1 SMART
PHD 1385 1431 8.56e-13 SMART
PHD 1462 1513 1.11e-6 SMART
RING 1463 1512 1.46e1 SMART
low complexity region 1514 1538 N/A INTRINSIC
low complexity region 1567 1576 N/A INTRINSIC
low complexity region 1589 1612 N/A INTRINSIC
low complexity region 1634 1646 N/A INTRINSIC
low complexity region 1707 1719 N/A INTRINSIC
low complexity region 1883 1896 N/A INTRINSIC
low complexity region 1931 1950 N/A INTRINSIC
HMG 1969 2037 6.35e-6 SMART
low complexity region 2064 2079 N/A INTRINSIC
low complexity region 2147 2167 N/A INTRINSIC
low complexity region 2170 2181 N/A INTRINSIC
low complexity region 2306 2323 N/A INTRINSIC
low complexity region 2334 2359 N/A INTRINSIC
low complexity region 2366 2388 N/A INTRINSIC
low complexity region 2402 2419 N/A INTRINSIC
low complexity region 2546 2559 N/A INTRINSIC
low complexity region 2610 2622 N/A INTRINSIC
coiled coil region 2632 2665 N/A INTRINSIC
coiled coil region 2768 2813 N/A INTRINSIC
low complexity region 2855 2868 N/A INTRINSIC
low complexity region 2887 2899 N/A INTRINSIC
low complexity region 3151 3165 N/A INTRINSIC
low complexity region 3189 3204 N/A INTRINSIC
low complexity region 3241 3263 N/A INTRINSIC
low complexity region 3390 3400 N/A INTRINSIC
low complexity region 3629 3659 N/A INTRINSIC
coiled coil region 3712 3749 N/A INTRINSIC
low complexity region 3781 3801 N/A INTRINSIC
coiled coil region 3910 4003 N/A INTRINSIC
low complexity region 4128 4159 N/A INTRINSIC
low complexity region 4167 4183 N/A INTRINSIC
low complexity region 4226 4246 N/A INTRINSIC
low complexity region 4266 4293 N/A INTRINSIC
low complexity region 4306 4322 N/A INTRINSIC
low complexity region 4361 4378 N/A INTRINSIC
coiled coil region 4591 4613 N/A INTRINSIC
low complexity region 4661 4684 N/A INTRINSIC
low complexity region 4745 4755 N/A INTRINSIC
low complexity region 4877 4896 N/A INTRINSIC
low complexity region 4957 4983 N/A INTRINSIC
low complexity region 4989 5029 N/A INTRINSIC
low complexity region 5100 5107 N/A INTRINSIC
PHD 5142 5188 4.67e-5 SMART
RING 5143 5187 4.87e0 SMART
FYRN 5242 5285 5.07e-21 SMART
FYRC 5291 5378 2.51e-43 SMART
SET 5448 5570 5.69e-36 SMART
PostSET 5572 5588 3.58e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000229651
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 96.9%
  • 10x: 95.3%
  • 20x: 92.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a histone methyltransferase that methylates the Lys-4 position of histone H3. The encoded protein is part of a large protein complex called ASCOM, which has been shown to be a transcriptional regulator of the beta-globin and estrogen receptor genes. Mutations in this gene have been shown to be a cause of Kabuki syndrome. [provided by RefSeq, Oct 2010]
PHENOTYPE: Mice homozygous for a gene trap allele exhibit embryonic lethality around E9.5. Mice homozygous for a conditional allele activated in different cell-types exhibit impaired adipogenesis, impaired myogenesis, perturbed germinal B cell development and promoteion of lymphomagenesis. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 102 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b A T 11: 109,864,542 (GRCm39) F409I probably benign Het
Adamts19 A C 18: 59,140,444 (GRCm39) I848L possibly damaging Het
Adamts5 T C 16: 85,696,240 (GRCm39) S306G probably damaging Het
Adamts8 T G 9: 30,865,910 (GRCm39) I486S probably benign Het
Adgrg5 T C 8: 95,668,680 (GRCm39) F499L possibly damaging Het
Akr1c21 T A 13: 4,627,134 (GRCm39) C145* probably null Het
Anp32b T G 4: 46,460,241 (GRCm39) probably null Het
Arhgap31 A G 16: 38,421,974 (GRCm39) V1364A possibly damaging Het
C2cd6 T C 1: 59,133,992 (GRCm39) R10G possibly damaging Het
Cacna2d1 A G 5: 16,507,352 (GRCm39) E367G possibly damaging Het
Ccdc81 C T 7: 89,515,769 (GRCm39) E637K probably benign Het
Cd2 A T 3: 101,194,815 (GRCm39) M91K possibly damaging Het
Cdc16 C A 8: 13,814,688 (GRCm39) Y157* probably null Het
Celsr3 G T 9: 108,709,056 (GRCm39) V1301F probably damaging Het
Cep164 C T 9: 45,704,235 (GRCm39) G961S probably damaging Het
Cep290 T C 10: 100,349,843 (GRCm39) V630A probably benign Het
Chd5 C T 4: 152,463,272 (GRCm39) S1451F probably damaging Het
Cldn23 A C 8: 36,293,140 (GRCm39) L116R possibly damaging Het
Cngb1 A T 8: 96,024,401 (GRCm39) probably benign Het
Cpb1 G T 3: 20,320,405 (GRCm39) N151K possibly damaging Het
Cpn2 A G 16: 30,078,918 (GRCm39) F261S probably damaging Het
Crlf3 A C 11: 79,948,698 (GRCm39) V249G probably damaging Het
Csmd1 A T 8: 16,207,134 (GRCm39) Y1298* probably null Het
Cstf2t C A 19: 31,061,085 (GRCm39) P207Q possibly damaging Het
Cym A C 3: 107,120,741 (GRCm39) L288R possibly damaging Het
Cyp2j12 C T 4: 96,009,669 (GRCm39) probably null Het
Dlx6 C T 6: 6,863,665 (GRCm39) Q96* probably null Het
Dnah7b T C 1: 46,361,495 (GRCm39) F3465S probably damaging Het
Dnmt3a A T 12: 3,923,342 (GRCm39) M181L possibly damaging Het
Duox1 T A 2: 122,163,910 (GRCm39) M859K probably damaging Het
Eif2b4 A T 5: 31,350,284 (GRCm39) S13T probably benign Het
Ercc6 T C 14: 32,298,956 (GRCm39) V1448A probably benign Het
Esp24 A G 17: 39,350,893 (GRCm39) E31G possibly damaging Het
F2rl2 T A 13: 95,837,969 (GRCm39) M338K probably benign Het
Fbxl9 A T 8: 106,039,824 (GRCm39) V517E probably damaging Het
Fgfbp1 A C 5: 44,137,265 (GRCm39) L9R possibly damaging Het
Gal3st2b A T 1: 93,868,338 (GRCm39) N188Y probably damaging Het
Gpr179 G C 11: 97,237,404 (GRCm39) C372W probably damaging Het
Grn T G 11: 102,324,093 (GRCm39) C61G probably damaging Het
Herc1 T G 9: 66,376,292 (GRCm39) C3371G probably damaging Het
Herc1 T C 9: 66,409,366 (GRCm39) probably null Het
Hmcn1 C T 1: 150,462,219 (GRCm39) G5153D possibly damaging Het
Ifi35 A T 11: 101,347,461 (GRCm39) R31W probably damaging Het
Ifit1bl1 T A 19: 34,571,260 (GRCm39) H399L probably benign Het
Irx3 G A 8: 92,527,362 (GRCm39) P114L probably damaging Het
Kat6a T A 8: 23,425,813 (GRCm39) D1119E probably benign Het
Kng1 A T 16: 22,897,869 (GRCm39) H423L possibly damaging Het
Lrp2 T A 2: 69,326,833 (GRCm39) Q1746L possibly damaging Het
Lrrc63 A T 14: 75,323,784 (GRCm39) probably null Het
Mad2l1 T A 6: 66,516,797 (GRCm39) V163E possibly damaging Het
Map3k19 A G 1: 127,750,417 (GRCm39) M978T probably benign Het
Mon1a A C 9: 107,778,562 (GRCm39) N262T probably damaging Het
Mpo A G 11: 87,686,707 (GRCm39) N85D probably benign Het
Mpp4 T C 1: 59,183,969 (GRCm39) D244G probably null Het
Mstn A G 1: 53,105,717 (GRCm39) Y353C probably damaging Het
Mx1 T A 16: 97,255,358 (GRCm39) N232Y probably damaging Het
Mycs T C X: 5,380,157 (GRCm39) R308G probably benign Het
Myh11 A T 16: 14,095,734 (GRCm39) D9E probably benign Het
Nfe2l3 A T 6: 51,410,392 (GRCm39) Q169L probably null Het
Nr5a1 G T 2: 38,598,431 (GRCm39) T122N possibly damaging Het
Nras A G 3: 102,966,295 (GRCm39) T20A probably damaging Het
Obp2b T A 2: 25,628,652 (GRCm39) probably null Het
Or1l4 A G 2: 37,091,439 (GRCm39) Y62C probably damaging Het
Or51g2 T C 7: 102,622,263 (GRCm39) N312S probably benign Het
Or5aq6 T C 2: 86,923,571 (GRCm39) T57A probably damaging Het
Or5w18 T A 2: 87,633,106 (GRCm39) F124L probably benign Het
Or9s14 G A 1: 92,536,122 (GRCm39) V188M probably benign Het
Pcdh17 A T 14: 84,715,094 (GRCm39) T920S probably benign Het
Pcdh9 T C 14: 94,124,661 (GRCm39) D503G probably benign Het
Pcdhb12 C T 18: 37,569,724 (GRCm39) T290I probably damaging Het
Pde6b C A 5: 108,536,557 (GRCm39) C84* probably null Het
Pex1 A T 5: 3,680,044 (GRCm39) N914I probably damaging Het
Pign A G 1: 105,517,042 (GRCm39) V528A possibly damaging Het
Pkhd1 T G 1: 20,604,129 (GRCm39) D1187A possibly damaging Het
Ppip5k1 T C 2: 121,173,112 (GRCm39) K489E probably damaging Het
Prob1 T C 18: 35,786,305 (GRCm39) T650A possibly damaging Het
Radil T C 5: 142,481,091 (GRCm39) Y572C probably damaging Het
Rapgef2 A G 3: 78,996,098 (GRCm39) I555T possibly damaging Het
Rgs5 G A 1: 169,510,386 (GRCm39) probably null Het
Rnaset2b G A 17: 7,248,506 (GRCm39) probably null Het
S1pr1 A G 3: 115,505,587 (GRCm39) S336P probably benign Het
Slc24a5 A G 2: 124,925,115 (GRCm39) E252G possibly damaging Het
Slc34a2 A T 5: 53,218,733 (GRCm39) I184F probably benign Het
Slc35a3 A G 3: 116,471,597 (GRCm39) V224A possibly damaging Het
Slc39a9 A G 12: 80,723,976 (GRCm39) H211R probably damaging Het
Slu7 A G 11: 43,330,095 (GRCm39) N174S probably benign Het
Smarcd3 A T 5: 24,800,820 (GRCm39) Y131* probably null Het
Syne1 A G 10: 5,317,621 (GRCm39) M491T probably benign Het
Tars1 G A 15: 11,394,329 (GRCm39) Q103* probably null Het
Tmem132d C A 5: 127,866,919 (GRCm39) E660D probably benign Het
Ttn T C 2: 76,575,387 (GRCm39) T16842A probably damaging Het
Ttn T C 2: 76,643,316 (GRCm39) E13201G probably damaging Het
Ttn T A 2: 76,582,605 (GRCm39) M22763L probably benign Het
Ubp1 A T 9: 113,785,037 (GRCm39) I117L possibly damaging Het
Usp24 T A 4: 106,234,756 (GRCm39) H954Q probably benign Het
Vmn1r174 G A 7: 23,453,622 (GRCm39) R96H probably benign Het
Vmn2r63 G A 7: 42,577,669 (GRCm39) Q290* probably null Het
Vnn3 T C 10: 23,741,718 (GRCm39) I341T probably benign Het
Wbp2nl A G 15: 82,189,945 (GRCm39) T46A probably damaging Het
Wdr48 G T 9: 119,753,313 (GRCm39) E625* probably null Het
Wdr6 C T 9: 108,452,363 (GRCm39) V507I probably damaging Het
Zp2 A T 7: 119,737,328 (GRCm39) W287R probably benign Het
Other mutations in Kmt2d
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00229:Kmt2d APN 15 98,760,214 (GRCm39) missense unknown
IGL00927:Kmt2d APN 15 98,742,890 (GRCm39) unclassified probably benign
IGL01123:Kmt2d APN 15 98,735,029 (GRCm39) missense unknown
IGL01288:Kmt2d APN 15 98,762,925 (GRCm39) missense probably damaging 1.00
IGL01538:Kmt2d APN 15 98,758,538 (GRCm39) unclassified probably benign
IGL01575:Kmt2d APN 15 98,744,736 (GRCm39) utr 3 prime probably benign
IGL01584:Kmt2d APN 15 98,754,250 (GRCm39) unclassified probably benign
IGL01750:Kmt2d APN 15 98,751,049 (GRCm39) unclassified probably benign
IGL02163:Kmt2d APN 15 98,733,109 (GRCm39) unclassified probably benign
IGL02209:Kmt2d APN 15 98,752,448 (GRCm39) unclassified probably benign
IGL02253:Kmt2d APN 15 98,756,056 (GRCm39) unclassified probably benign
IGL02271:Kmt2d APN 15 98,764,309 (GRCm39) missense possibly damaging 0.89
IGL02291:Kmt2d APN 15 98,763,373 (GRCm39) splice site probably benign
IGL02448:Kmt2d APN 15 98,741,991 (GRCm39) unclassified probably benign
IGL02472:Kmt2d APN 15 98,747,958 (GRCm39) missense probably benign 0.23
IGL02496:Kmt2d APN 15 98,755,439 (GRCm39) unclassified probably benign
IGL02527:Kmt2d APN 15 98,739,628 (GRCm39) unclassified probably benign
IGL02576:Kmt2d APN 15 98,762,001 (GRCm39) missense unknown
IGL02597:Kmt2d APN 15 98,761,712 (GRCm39) missense unknown
IGL02609:Kmt2d APN 15 98,749,674 (GRCm39) unclassified probably benign
IGL03085:Kmt2d APN 15 98,737,821 (GRCm39) unclassified probably benign
IGL03102:Kmt2d APN 15 98,753,424 (GRCm39) missense probably benign
IGL03123:Kmt2d APN 15 98,759,652 (GRCm39) missense unknown
G1citation:Kmt2d UTSW 15 98,747,340 (GRCm39) unclassified probably benign
R0091:Kmt2d UTSW 15 98,742,360 (GRCm39) unclassified probably benign
R0136:Kmt2d UTSW 15 98,752,159 (GRCm39) unclassified probably benign
R0243:Kmt2d UTSW 15 98,748,018 (GRCm39) unclassified probably benign
R0276:Kmt2d UTSW 15 98,748,192 (GRCm39) unclassified probably benign
R0477:Kmt2d UTSW 15 98,751,462 (GRCm39) unclassified probably benign
R0478:Kmt2d UTSW 15 98,751,462 (GRCm39) unclassified probably benign
R0586:Kmt2d UTSW 15 98,733,088 (GRCm39) unclassified probably benign
R0632:Kmt2d UTSW 15 98,751,462 (GRCm39) unclassified probably benign
R0678:Kmt2d UTSW 15 98,748,294 (GRCm39) unclassified probably benign
R0780:Kmt2d UTSW 15 98,760,738 (GRCm39) missense unknown
R0891:Kmt2d UTSW 15 98,750,572 (GRCm39) unclassified probably benign
R1136:Kmt2d UTSW 15 98,755,646 (GRCm39) unclassified probably benign
R1417:Kmt2d UTSW 15 98,764,311 (GRCm39) missense probably damaging 0.99
R1499:Kmt2d UTSW 15 98,742,819 (GRCm39) unclassified probably benign
R1510:Kmt2d UTSW 15 98,754,258 (GRCm39) unclassified probably benign
R1586:Kmt2d UTSW 15 98,762,934 (GRCm39) splice site probably benign
R1640:Kmt2d UTSW 15 98,742,938 (GRCm39) unclassified probably benign
R1714:Kmt2d UTSW 15 98,760,831 (GRCm39) missense unknown
R1725:Kmt2d UTSW 15 98,743,115 (GRCm39) unclassified probably benign
R1728:Kmt2d UTSW 15 98,763,013 (GRCm39) missense probably damaging 1.00
R1729:Kmt2d UTSW 15 98,763,013 (GRCm39) missense probably damaging 1.00
R1741:Kmt2d UTSW 15 98,743,115 (GRCm39) unclassified probably benign
R1744:Kmt2d UTSW 15 98,762,928 (GRCm39) missense probably damaging 0.99
R1746:Kmt2d UTSW 15 98,762,259 (GRCm39) missense probably damaging 0.97
R1782:Kmt2d UTSW 15 98,755,429 (GRCm39) unclassified probably benign
R1789:Kmt2d UTSW 15 98,749,955 (GRCm39) unclassified probably benign
R1802:Kmt2d UTSW 15 98,760,866 (GRCm39) missense unknown
R1808:Kmt2d UTSW 15 98,764,567 (GRCm39) missense probably damaging 1.00
R1822:Kmt2d UTSW 15 98,759,661 (GRCm39) missense unknown
R1831:Kmt2d UTSW 15 98,753,224 (GRCm39) missense probably damaging 0.97
R1920:Kmt2d UTSW 15 98,753,472 (GRCm39) missense probably damaging 1.00
R1920:Kmt2d UTSW 15 98,753,471 (GRCm39) missense probably damaging 0.96
R1956:Kmt2d UTSW 15 98,757,471 (GRCm39) unclassified probably benign
R2100:Kmt2d UTSW 15 98,744,361 (GRCm39) unclassified probably benign
R2120:Kmt2d UTSW 15 98,737,410 (GRCm39) unclassified probably benign
R2188:Kmt2d UTSW 15 98,737,181 (GRCm39) unclassified probably benign
R2191:Kmt2d UTSW 15 98,758,930 (GRCm39) critical splice donor site probably null
R2234:Kmt2d UTSW 15 98,763,129 (GRCm39) missense probably damaging 0.98
R2422:Kmt2d UTSW 15 98,760,147 (GRCm39) missense unknown
R2762:Kmt2d UTSW 15 98,749,936 (GRCm39) unclassified probably benign
R2895:Kmt2d UTSW 15 98,741,820 (GRCm39) unclassified probably benign
R3624:Kmt2d UTSW 15 98,740,783 (GRCm39) unclassified probably benign
R3791:Kmt2d UTSW 15 98,742,030 (GRCm39) unclassified probably benign
R3794:Kmt2d UTSW 15 98,735,240 (GRCm39) unclassified probably benign
R3871:Kmt2d UTSW 15 98,748,902 (GRCm39) unclassified probably benign
R3958:Kmt2d UTSW 15 98,753,430 (GRCm39) missense possibly damaging 0.69
R3983:Kmt2d UTSW 15 98,743,927 (GRCm39) unclassified probably benign
R4211:Kmt2d UTSW 15 98,738,070 (GRCm39) unclassified probably benign
R4212:Kmt2d UTSW 15 98,742,884 (GRCm39) unclassified probably benign
R4240:Kmt2d UTSW 15 98,742,452 (GRCm39) unclassified probably benign
R4246:Kmt2d UTSW 15 98,737,970 (GRCm39) unclassified probably benign
R4361:Kmt2d UTSW 15 98,761,551 (GRCm39) missense unknown
R4388:Kmt2d UTSW 15 98,751,507 (GRCm39) unclassified probably benign
R4602:Kmt2d UTSW 15 98,748,140 (GRCm39) unclassified probably benign
R4606:Kmt2d UTSW 15 98,737,597 (GRCm39) unclassified probably benign
R4658:Kmt2d UTSW 15 98,750,410 (GRCm39) unclassified probably benign
R4840:Kmt2d UTSW 15 98,759,775 (GRCm39) missense unknown
R4895:Kmt2d UTSW 15 98,742,368 (GRCm39) unclassified probably benign
R4906:Kmt2d UTSW 15 98,747,420 (GRCm39) unclassified probably benign
R4976:Kmt2d UTSW 15 98,745,075 (GRCm39) utr 3 prime probably benign
R5093:Kmt2d UTSW 15 98,754,043 (GRCm39) missense probably damaging 1.00
R5119:Kmt2d UTSW 15 98,745,075 (GRCm39) utr 3 prime probably benign
R5160:Kmt2d UTSW 15 98,738,105 (GRCm39) unclassified probably benign
R5260:Kmt2d UTSW 15 98,740,741 (GRCm39) unclassified probably benign
R5274:Kmt2d UTSW 15 98,752,111 (GRCm39) unclassified probably benign
R5450:Kmt2d UTSW 15 98,752,967 (GRCm39) missense probably damaging 1.00
R5461:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5462:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5463:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5465:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5467:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5481:Kmt2d UTSW 15 98,759,886 (GRCm39) missense unknown
R5509:Kmt2d UTSW 15 98,737,557 (GRCm39) unclassified probably benign
R5534:Kmt2d UTSW 15 98,735,238 (GRCm39) unclassified probably benign
R5536:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5537:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5538:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5546:Kmt2d UTSW 15 98,750,949 (GRCm39) unclassified probably benign
R5595:Kmt2d UTSW 15 98,747,905 (GRCm39) unclassified probably benign
R5645:Kmt2d UTSW 15 98,742,278 (GRCm39) unclassified probably benign
R5679:Kmt2d UTSW 15 98,752,153 (GRCm39) unclassified probably benign
R5710:Kmt2d UTSW 15 98,751,987 (GRCm39) unclassified probably benign
R5755:Kmt2d UTSW 15 98,761,527 (GRCm39) missense unknown
R5817:Kmt2d UTSW 15 98,760,244 (GRCm39) missense unknown
R5841:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5842:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5843:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5844:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R5845:Kmt2d UTSW 15 98,749,990 (GRCm39) unclassified probably benign
R6122:Kmt2d UTSW 15 98,758,573 (GRCm39) unclassified probably benign
R6612:Kmt2d UTSW 15 98,743,739 (GRCm39) unclassified probably benign
R6718:Kmt2d UTSW 15 98,747,467 (GRCm39) unclassified probably benign
R6718:Kmt2d UTSW 15 98,748,420 (GRCm39) unclassified probably benign
R6822:Kmt2d UTSW 15 98,747,340 (GRCm39) unclassified probably benign
R6866:Kmt2d UTSW 15 98,755,274 (GRCm39) unclassified probably benign
R6950:Kmt2d UTSW 15 98,737,901 (GRCm39) unclassified probably benign
R7089:Kmt2d UTSW 15 98,748,153 (GRCm39) missense unknown
R7120:Kmt2d UTSW 15 98,758,946 (GRCm39) missense unknown
R7131:Kmt2d UTSW 15 98,747,497 (GRCm39) unclassified probably benign
R7177:Kmt2d UTSW 15 98,748,267 (GRCm39) missense unknown
R7194:Kmt2d UTSW 15 98,741,714 (GRCm39) missense unknown
R7252:Kmt2d UTSW 15 98,742,147 (GRCm39) missense unknown
R7282:Kmt2d UTSW 15 98,751,985 (GRCm39) missense unknown
R7307:Kmt2d UTSW 15 98,747,299 (GRCm39) missense unknown
R7313:Kmt2d UTSW 15 98,754,504 (GRCm39) missense unknown
R7394:Kmt2d UTSW 15 98,754,265 (GRCm39) missense unknown
R7404:Kmt2d UTSW 15 98,743,376 (GRCm39) missense unknown
R7409:Kmt2d UTSW 15 98,753,235 (GRCm39) missense probably damaging 1.00
R7414:Kmt2d UTSW 15 98,737,737 (GRCm39) missense unknown
R7534:Kmt2d UTSW 15 98,749,899 (GRCm39) missense unknown
R7575:Kmt2d UTSW 15 98,747,492 (GRCm39) unclassified probably benign
R7650:Kmt2d UTSW 15 98,748,751 (GRCm39) missense unknown
R7687:Kmt2d UTSW 15 98,760,001 (GRCm39) missense unknown
R7699:Kmt2d UTSW 15 98,741,600 (GRCm39) missense unknown
R7700:Kmt2d UTSW 15 98,741,600 (GRCm39) missense unknown
R7765:Kmt2d UTSW 15 98,750,215 (GRCm39) missense unknown
R7797:Kmt2d UTSW 15 98,762,287 (GRCm39) missense probably benign 0.24
R7803:Kmt2d UTSW 15 98,760,804 (GRCm39) missense unknown
R7952:Kmt2d UTSW 15 98,748,649 (GRCm39) missense unknown
R8054:Kmt2d UTSW 15 98,741,806 (GRCm39) missense unknown
R8084:Kmt2d UTSW 15 98,739,945 (GRCm39) missense unknown
R8089:Kmt2d UTSW 15 98,740,750 (GRCm39) missense unknown
R8133:Kmt2d UTSW 15 98,762,823 (GRCm39) missense probably damaging 1.00
R8138:Kmt2d UTSW 15 98,741,534 (GRCm39) missense unknown
R8343:Kmt2d UTSW 15 98,750,478 (GRCm39) missense unknown
R8681:Kmt2d UTSW 15 98,743,948 (GRCm39) missense unknown
R8694:Kmt2d UTSW 15 98,742,615 (GRCm39) missense unknown
R8837:Kmt2d UTSW 15 98,762,048 (GRCm39) missense unknown
R8855:Kmt2d UTSW 15 98,754,237 (GRCm39) missense unknown
R8934:Kmt2d UTSW 15 98,759,767 (GRCm39) missense unknown
R9100:Kmt2d UTSW 15 98,747,832 (GRCm39) missense unknown
R9158:Kmt2d UTSW 15 98,741,020 (GRCm39) missense unknown
R9190:Kmt2d UTSW 15 98,749,896 (GRCm39) missense unknown
R9222:Kmt2d UTSW 15 98,747,324 (GRCm39) missense unknown
R9263:Kmt2d UTSW 15 98,747,499 (GRCm39) frame shift probably null
R9336:Kmt2d UTSW 15 98,743,697 (GRCm39) missense unknown
R9397:Kmt2d UTSW 15 98,747,994 (GRCm39) missense unknown
R9415:Kmt2d UTSW 15 98,737,586 (GRCm39) missense unknown
R9482:Kmt2d UTSW 15 98,763,046 (GRCm39) missense probably damaging 1.00
R9529:Kmt2d UTSW 15 98,737,649 (GRCm39) missense unknown
R9610:Kmt2d UTSW 15 98,743,057 (GRCm39) unclassified probably benign
R9611:Kmt2d UTSW 15 98,743,057 (GRCm39) unclassified probably benign
R9611:Kmt2d UTSW 15 98,743,054 (GRCm39) unclassified probably benign
R9612:Kmt2d UTSW 15 98,743,057 (GRCm39) unclassified probably benign
R9613:Kmt2d UTSW 15 98,743,057 (GRCm39) unclassified probably benign
R9644:Kmt2d UTSW 15 98,743,385 (GRCm39) missense unknown
R9716:Kmt2d UTSW 15 98,741,283 (GRCm39) missense unknown
R9763:Kmt2d UTSW 15 98,743,057 (GRCm39) unclassified probably benign
R9782:Kmt2d UTSW 15 98,764,597 (GRCm39) missense probably damaging 1.00
X0018:Kmt2d UTSW 15 98,750,803 (GRCm39) unclassified probably benign
X0024:Kmt2d UTSW 15 98,750,934 (GRCm39) unclassified probably benign
X0062:Kmt2d UTSW 15 98,747,700 (GRCm39) unclassified probably benign
Z1187:Kmt2d UTSW 15 98,749,625 (GRCm39) missense unknown
Z1188:Kmt2d UTSW 15 98,749,625 (GRCm39) missense unknown
Z1189:Kmt2d UTSW 15 98,749,625 (GRCm39) missense unknown
Z1190:Kmt2d UTSW 15 98,749,625 (GRCm39) missense unknown
Z1192:Kmt2d UTSW 15 98,749,625 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- ATCTAGCCAGACCTTGGAGGACAG -3'
(R):5'- CTTCTACGGGCAAAGAATGTGCAAC -3'

Sequencing Primer
(F):5'- CTTGGAGGACAGGCTGC -3'
(R):5'- CTTCGAGCTGAGATCAATGGAC -3'
Posted On 2014-05-23