Incidental Mutation 'R7250:Kmt2c'
ID 563816
Institutional Source Beutler Lab
Gene Symbol Kmt2c
Ensembl Gene ENSMUSG00000038056
Gene Name lysine (K)-specific methyltransferase 2C
Synonyms Mll3, HALR, E330008K23Rik
MMRRC Submission 045350-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R7250 (G1)
Quality Score 225.009
Status Not validated
Chromosome 5
Chromosomal Location 25476796-25703781 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 25514805 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 3013 (T3013A)
Ref Sequence ENSEMBL: ENSMUSP00000043874 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045291]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000045291
AA Change: T3013A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000043874
Gene: ENSMUSG00000038056
AA Change: T3013A

DomainStartEndE-ValueType
low complexity region 9 32 N/A INTRINSIC
AT_hook 34 46 9.68e-1 SMART
low complexity region 73 87 N/A INTRINSIC
PHD 283 330 2.56e-2 SMART
C1 329 384 5.45e-1 SMART
PHD 342 388 4.19e-7 SMART
RING 343 387 1.45e-1 SMART
PHD 389 435 4.77e-11 SMART
RING 390 434 1.46e0 SMART
PHD 465 517 8.25e-6 SMART
low complexity region 776 789 N/A INTRINSIC
AT_hook 898 910 1.41e2 SMART
PHD 953 1002 2.89e-10 SMART
RING 954 1001 4.74e0 SMART
C1 994 1045 8.38e-2 SMART
PHD 1003 1049 1.05e-12 SMART
PHD 1080 1131 2.08e-2 SMART
low complexity region 1189 1201 N/A INTRINSIC
low complexity region 1337 1348 N/A INTRINSIC
low complexity region 1394 1406 N/A INTRINSIC
low complexity region 1431 1442 N/A INTRINSIC
low complexity region 1520 1539 N/A INTRINSIC
low complexity region 1557 1570 N/A INTRINSIC
HMG 1639 1703 2.64e-3 SMART
low complexity region 1708 1724 N/A INTRINSIC
coiled coil region 1745 1789 N/A INTRINSIC
low complexity region 1847 1860 N/A INTRINSIC
low complexity region 1864 1891 N/A INTRINSIC
internal_repeat_3 1893 2084 1.27e-14 PROSPERO
internal_repeat_3 2123 2306 1.27e-14 PROSPERO
low complexity region 2336 2348 N/A INTRINSIC
low complexity region 2375 2394 N/A INTRINSIC
low complexity region 2427 2440 N/A INTRINSIC
low complexity region 2516 2527 N/A INTRINSIC
low complexity region 2696 2720 N/A INTRINSIC
low complexity region 2723 2742 N/A INTRINSIC
low complexity region 2930 2943 N/A INTRINSIC
coiled coil region 3048 3075 N/A INTRINSIC
low complexity region 3156 3165 N/A INTRINSIC
low complexity region 3173 3195 N/A INTRINSIC
coiled coil region 3226 3270 N/A INTRINSIC
low complexity region 3277 3290 N/A INTRINSIC
coiled coil region 3389 3427 N/A INTRINSIC
low complexity region 3460 3486 N/A INTRINSIC
low complexity region 3597 3611 N/A INTRINSIC
low complexity region 3649 3667 N/A INTRINSIC
low complexity region 3769 3783 N/A INTRINSIC
low complexity region 3822 3827 N/A INTRINSIC
low complexity region 3860 3869 N/A INTRINSIC
low complexity region 3887 3904 N/A INTRINSIC
low complexity region 3994 4009 N/A INTRINSIC
low complexity region 4015 4038 N/A INTRINSIC
low complexity region 4293 4309 N/A INTRINSIC
low complexity region 4412 4419 N/A INTRINSIC
PHD 4454 4500 2.94e-2 SMART
RING 4455 4499 8.1e0 SMART
FYRN 4554 4597 1.18e-21 SMART
FYRC 4603 4690 4.54e-32 SMART
SET 4764 4886 3.17e-34 SMART
PostSET 4888 4904 1.82e-6 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000172556
SMART Domains Protein: ENSMUSP00000133941
Gene: ENSMUSG00000038056

DomainStartEndE-ValueType
SCOP:d2spca_ 84 177 1e-3 SMART
low complexity region 196 209 N/A INTRINSIC
coiled coil region 307 345 N/A INTRINSIC
low complexity region 379 405 N/A INTRINSIC
low complexity region 516 530 N/A INTRINSIC
low complexity region 568 586 N/A INTRINSIC
low complexity region 688 702 N/A INTRINSIC
low complexity region 735 752 N/A INTRINSIC
low complexity region 842 857 N/A INTRINSIC
low complexity region 863 886 N/A INTRINSIC
low complexity region 1141 1157 N/A INTRINSIC
low complexity region 1260 1267 N/A INTRINSIC
PHD 1302 1348 2.94e-2 SMART
FYRN 1402 1445 1.18e-21 SMART
FYRC 1451 1538 4.54e-32 SMART
SET 1608 1730 3.17e-34 SMART
PostSET 1732 1748 1.82e-6 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the myeloid/lymphoid or mixed-lineage leukemia (MLL) family and encodes a nuclear protein with an AT hook DNA-binding domain, a DHHC-type zinc finger, six PHD-type zinc fingers, a SET domain, a post-SET domain and a RING-type zinc finger. This protein is a member of the ASC-2/NCOA6 complex (ASCOM), which possesses histone methylation activity and is involved in transcriptional coactivation. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele display partial embryonic lethality, delayed eyelid opening, postnatal growth retardation, impaired fertility in both sexes, and decreased proliferation of cultured mouse embryonic fibroblasts. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 101 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930480E11Rik G T X: 77,414,311 (GRCm39) M345I probably benign Het
Actl7b T A 4: 56,741,035 (GRCm39) M108L probably benign Het
Adgrf3 T A 5: 30,400,680 (GRCm39) I934L probably damaging Het
Adprm A G 11: 66,932,450 (GRCm39) V153A probably benign Het
Aif1l G A 2: 31,859,764 (GRCm39) V109M probably damaging Het
Asphd1 T A 7: 126,545,942 (GRCm39) E307V probably damaging Het
Ate1 T A 7: 130,121,701 (GRCm39) probably benign Het
Borcs7 A G 19: 46,688,047 (GRCm39) H64R probably damaging Het
C1qtnf1 A G 11: 118,339,176 (GRCm39) *282W probably null Het
Cacna1c A G 6: 118,574,966 (GRCm39) C1985R Het
Cacna1c A T 6: 118,673,412 (GRCm39) V647E Het
Cacna1d A G 14: 29,797,108 (GRCm39) S1497P probably damaging Het
Cacna1e T A 1: 154,576,235 (GRCm39) I133F possibly damaging Het
Ccdc63 A T 5: 122,260,906 (GRCm39) L206H probably damaging Het
Cenatac A G 9: 44,323,748 (GRCm39) probably null Het
Cspg4b T G 13: 113,455,349 (GRCm39) I465R Het
D430041D05Rik T C 2: 104,086,961 (GRCm39) T672A possibly damaging Het
D630045J12Rik G T 6: 38,119,546 (GRCm39) T1732K possibly damaging Het
D930020B18Rik T C 10: 121,507,736 (GRCm39) I158T probably damaging Het
Ddx52 G A 11: 83,835,392 (GRCm39) G106D probably benign Het
Dock2 A G 11: 34,586,032 (GRCm39) V550A probably benign Het
Dock2 C T 11: 34,586,120 (GRCm39) D521N probably damaging Het
F13b T C 1: 139,444,227 (GRCm39) probably null Het
Fchsd2 A G 7: 100,908,892 (GRCm39) K431R possibly damaging Het
Fez1 C T 9: 36,779,090 (GRCm39) R256C probably damaging Het
Gjd4 T A 18: 9,280,391 (GRCm39) Q229L probably benign Het
Gpr45 T A 1: 43,071,531 (GRCm39) I58N probably damaging Het
Gstm1 T A 3: 107,923,709 (GRCm39) I99F probably damaging Het
Gtpbp8 T A 16: 44,564,225 (GRCm39) T149S probably damaging Het
H2-Ab1 A G 17: 34,486,481 (GRCm39) D180G probably damaging Het
Hdhd5 A G 6: 120,494,016 (GRCm39) I188T possibly damaging Het
Hfm1 T C 5: 107,052,197 (GRCm39) I300V probably benign Het
Hnrnpr T G 4: 136,059,746 (GRCm39) D283E probably benign Het
Hsp90b1 T C 10: 86,527,572 (GRCm39) E768G unknown Het
Kcna4 C A 2: 107,126,663 (GRCm39) Q466K possibly damaging Het
Kcnk6 A G 7: 28,931,619 (GRCm39) L97P probably benign Het
Kics2 T C 10: 121,581,376 (GRCm39) S126P possibly damaging Het
Klf5 A G 14: 99,536,455 (GRCm39) S9G probably benign Het
Lancl1 A G 1: 67,048,458 (GRCm39) Y207H possibly damaging Het
Lipe G C 7: 25,088,085 (GRCm39) probably benign Het
Lrrc66 T A 5: 73,768,224 (GRCm39) H239L probably benign Het
Ltbp2 C T 12: 84,834,166 (GRCm39) W1441* probably null Het
Man2a1 T C 17: 64,943,583 (GRCm39) S213P probably benign Het
Mapre2 C T 18: 23,991,119 (GRCm39) A171V possibly damaging Het
Mdn1 T A 4: 32,695,427 (GRCm39) D1155E probably damaging Het
Mki67 T C 7: 135,301,053 (GRCm39) D1327G possibly damaging Het
Mx2 T C 16: 97,348,664 (GRCm39) I279T probably damaging Het
Myo5c A G 9: 75,169,497 (GRCm39) T441A probably damaging Het
Nlrp9a T G 7: 26,258,143 (GRCm39) V587G possibly damaging Het
Npas2 A T 1: 39,377,188 (GRCm39) T517S probably damaging Het
Npy1r T C 8: 67,157,712 (GRCm39) S341P probably benign Het
Ntm A G 9: 29,322,988 (GRCm39) W11R probably benign Het
Nxpe2 A T 9: 48,238,096 (GRCm39) I53N possibly damaging Het
Onecut2 T C 18: 64,519,511 (GRCm39) F443L probably benign Het
Or10g6 T A 9: 39,934,050 (GRCm39) Y120* probably null Het
Or2r2 A G 6: 42,463,689 (GRCm39) V146A probably benign Het
Or52ac1 A T 7: 104,245,738 (GRCm39) Y217N probably damaging Het
Parp2 T A 14: 51,054,801 (GRCm39) V248E probably benign Het
Pcdh12 C A 18: 38,415,029 (GRCm39) V699L probably benign Het
Pja2 G A 17: 64,616,451 (GRCm39) P148L probably benign Het
Poglut3 C T 9: 53,301,821 (GRCm39) Q158* probably null Het
Ppip5k2 T G 1: 97,673,187 (GRCm39) D415A probably benign Het
Prss47 A G 13: 65,200,355 (GRCm39) S74P probably benign Het
Ptprg G T 14: 12,166,767 (GRCm38) M723I probably benign Het
Qsox2 A T 2: 26,118,444 (GRCm39) I109N probably damaging Het
Ranbp3l A G 15: 9,041,853 (GRCm39) E217G probably benign Het
Rgl2 C T 17: 34,152,403 (GRCm39) R367W probably damaging Het
Rgs12 T A 5: 35,122,841 (GRCm39) F208Y probably damaging Het
Rin3 C T 12: 102,334,893 (GRCm39) T268I unknown Het
Rttn T A 18: 89,007,647 (GRCm39) D427E probably benign Het
Samd13 G A 3: 146,352,079 (GRCm39) P91S probably benign Het
Samd9l T C 6: 3,374,201 (GRCm39) D1020G possibly damaging Het
Sec62 T G 3: 30,866,496 (GRCm39) L201V possibly damaging Het
Setdb1 C T 3: 95,261,852 (GRCm39) probably null Het
Sf3a3 A T 4: 124,616,708 (GRCm39) T197S probably benign Het
Slc20a1 A T 2: 129,051,844 (GRCm39) I618F possibly damaging Het
Slc38a3 A T 9: 107,533,865 (GRCm39) M186K probably benign Het
Slc39a13 T C 2: 90,893,503 (GRCm39) T319A probably benign Het
Slc44a4 T C 17: 35,137,520 (GRCm39) probably null Het
St3gal1 A C 15: 66,978,578 (GRCm39) D314E possibly damaging Het
Suclg1 A G 6: 73,248,074 (GRCm39) N265S probably benign Het
Sult2b1 A T 7: 45,433,361 (GRCm39) V2D unknown Het
Supv3l1 T A 10: 62,280,846 (GRCm39) I182F probably damaging Het
Tcp11l2 T C 10: 84,423,105 (GRCm39) probably null Het
Tenm2 C A 11: 35,963,625 (GRCm39) L935F probably damaging Het
Tnks T A 8: 35,318,912 (GRCm39) I790F probably damaging Het
Top2b C T 14: 16,420,411 (GRCm38) T1274I probably benign Het
Tpi1 A T 6: 124,789,441 (GRCm39) I178N probably damaging Het
Trav9d-1 A T 14: 53,030,153 (GRCm39) S86C probably damaging Het
Treml2 A G 17: 48,616,155 (GRCm39) E265G probably benign Het
Trpm7 A T 2: 126,668,685 (GRCm39) S744T possibly damaging Het
Usp33 T A 3: 152,097,999 (GRCm39) L909* probably null Het
Vcan A G 13: 89,869,805 (GRCm39) I210T probably damaging Het
Vcan A T 13: 89,879,576 (GRCm39) probably null Het
Vsig10l A T 7: 43,113,099 (GRCm39) D17V probably benign Het
Zbtb7b T A 3: 89,286,976 (GRCm39) T498S probably benign Het
Zfp366 T A 13: 99,366,076 (GRCm39) H412Q probably damaging Het
Zfp53 C A 17: 21,729,840 (GRCm39) D624E probably damaging Het
Zfp827 A T 8: 79,916,721 (GRCm39) D432V Het
Zic1 T C 9: 91,247,028 (GRCm39) T15A probably damaging Het
Zswim8 T C 14: 20,770,036 (GRCm39) C1368R probably damaging Het
Other mutations in Kmt2c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00436:Kmt2c APN 5 25,486,259 (GRCm39) missense probably damaging 0.99
IGL00694:Kmt2c APN 5 25,498,159 (GRCm39) missense probably damaging 0.99
IGL00780:Kmt2c APN 5 25,516,049 (GRCm39) missense probably benign 0.00
IGL00811:Kmt2c APN 5 25,579,531 (GRCm39) missense possibly damaging 0.75
IGL00885:Kmt2c APN 5 25,614,169 (GRCm39) missense possibly damaging 0.80
IGL00948:Kmt2c APN 5 25,582,159 (GRCm39) missense probably benign 0.08
IGL00959:Kmt2c APN 5 25,481,227 (GRCm39) missense probably damaging 1.00
IGL01022:Kmt2c APN 5 25,507,699 (GRCm39) unclassified probably benign
IGL01146:Kmt2c APN 5 25,513,510 (GRCm39) missense probably damaging 0.96
IGL01154:Kmt2c APN 5 25,489,397 (GRCm39) missense probably damaging 1.00
IGL01434:Kmt2c APN 5 25,614,306 (GRCm39) missense probably damaging 1.00
IGL01464:Kmt2c APN 5 25,557,242 (GRCm39) missense possibly damaging 0.90
IGL01525:Kmt2c APN 5 25,534,439 (GRCm39) splice site probably benign
IGL01530:Kmt2c APN 5 25,518,498 (GRCm39) missense probably benign 0.08
IGL01550:Kmt2c APN 5 25,486,274 (GRCm39) missense probably damaging 1.00
IGL01598:Kmt2c APN 5 25,478,664 (GRCm39) makesense probably null
IGL01598:Kmt2c APN 5 25,559,769 (GRCm39) missense probably damaging 1.00
IGL01608:Kmt2c APN 5 25,559,809 (GRCm39) missense probably damaging 0.97
IGL01663:Kmt2c APN 5 25,515,668 (GRCm39) missense probably damaging 1.00
IGL01707:Kmt2c APN 5 25,505,096 (GRCm39) missense probably damaging 1.00
IGL01714:Kmt2c APN 5 25,518,398 (GRCm39) missense probably benign
IGL01784:Kmt2c APN 5 25,518,524 (GRCm39) missense probably damaging 1.00
IGL01813:Kmt2c APN 5 25,495,802 (GRCm39) missense possibly damaging 0.82
IGL01825:Kmt2c APN 5 25,515,594 (GRCm39) missense probably damaging 1.00
IGL01834:Kmt2c APN 5 25,600,453 (GRCm39) missense probably benign 0.05
IGL02072:Kmt2c APN 5 25,610,430 (GRCm39) missense possibly damaging 0.96
IGL02159:Kmt2c APN 5 25,516,341 (GRCm39) missense probably benign 0.18
IGL02303:Kmt2c APN 5 25,515,155 (GRCm39) missense probably damaging 0.96
IGL02417:Kmt2c APN 5 25,578,018 (GRCm39) missense probably benign
IGL02578:Kmt2c APN 5 25,571,198 (GRCm39) intron probably benign
IGL02811:Kmt2c APN 5 25,520,026 (GRCm39) nonsense probably null
IGL02943:Kmt2c APN 5 25,495,821 (GRCm39) missense probably damaging 1.00
IGL03000:Kmt2c APN 5 25,489,170 (GRCm39) missense probably damaging 1.00
IGL03040:Kmt2c APN 5 25,515,350 (GRCm39) missense probably benign
IGL03076:Kmt2c APN 5 25,504,149 (GRCm39) nonsense probably null
IGL03088:Kmt2c APN 5 25,504,802 (GRCm39) missense probably damaging 0.99
IGL03131:Kmt2c APN 5 25,520,359 (GRCm39) missense probably benign 0.00
FR4304:Kmt2c UTSW 5 25,520,764 (GRCm39) small insertion probably benign
FR4976:Kmt2c UTSW 5 25,520,761 (GRCm39) small insertion probably benign
PIT4520001:Kmt2c UTSW 5 25,520,664 (GRCm39) missense probably benign 0.12
PIT4585001:Kmt2c UTSW 5 25,520,104 (GRCm39) missense probably benign 0.21
R0313:Kmt2c UTSW 5 25,549,928 (GRCm39) missense probably damaging 1.00
R0374:Kmt2c UTSW 5 25,514,706 (GRCm39) missense probably damaging 1.00
R0411:Kmt2c UTSW 5 25,580,955 (GRCm39) missense probably damaging 1.00
R0422:Kmt2c UTSW 5 25,520,662 (GRCm39) missense probably benign
R0453:Kmt2c UTSW 5 25,559,745 (GRCm39) missense probably damaging 1.00
R0616:Kmt2c UTSW 5 25,504,250 (GRCm39) missense probably benign
R0619:Kmt2c UTSW 5 25,503,914 (GRCm39) missense probably benign 0.21
R0671:Kmt2c UTSW 5 25,609,363 (GRCm39) missense probably damaging 1.00
R0736:Kmt2c UTSW 5 25,500,432 (GRCm39) missense probably benign
R0745:Kmt2c UTSW 5 25,564,696 (GRCm39) splice site probably null
R0760:Kmt2c UTSW 5 25,558,315 (GRCm39) missense possibly damaging 0.68
R0784:Kmt2c UTSW 5 25,515,893 (GRCm39) missense probably benign 0.00
R0882:Kmt2c UTSW 5 25,500,605 (GRCm39) missense possibly damaging 0.90
R0893:Kmt2c UTSW 5 25,556,268 (GRCm39) splice site probably benign
R0942:Kmt2c UTSW 5 25,520,301 (GRCm39) missense probably benign 0.10
R1110:Kmt2c UTSW 5 25,519,360 (GRCm39) missense probably benign 0.01
R1137:Kmt2c UTSW 5 25,515,981 (GRCm39) missense possibly damaging 0.80
R1255:Kmt2c UTSW 5 25,556,151 (GRCm39) missense probably damaging 1.00
R1300:Kmt2c UTSW 5 25,610,452 (GRCm39) missense probably damaging 0.99
R1497:Kmt2c UTSW 5 25,519,513 (GRCm39) missense possibly damaging 0.80
R1594:Kmt2c UTSW 5 25,519,876 (GRCm39) missense probably benign 0.01
R1611:Kmt2c UTSW 5 25,564,309 (GRCm39) critical splice donor site probably null
R1617:Kmt2c UTSW 5 25,580,925 (GRCm39) missense probably benign 0.01
R1720:Kmt2c UTSW 5 25,504,182 (GRCm39) missense probably benign 0.05
R1723:Kmt2c UTSW 5 25,520,003 (GRCm39) missense probably damaging 1.00
R1724:Kmt2c UTSW 5 25,520,003 (GRCm39) missense probably damaging 1.00
R1726:Kmt2c UTSW 5 25,520,003 (GRCm39) missense probably damaging 1.00
R1736:Kmt2c UTSW 5 25,495,525 (GRCm39) missense probably damaging 1.00
R1778:Kmt2c UTSW 5 25,577,972 (GRCm39) missense probably benign 0.02
R1809:Kmt2c UTSW 5 25,489,190 (GRCm39) missense probably damaging 1.00
R1845:Kmt2c UTSW 5 25,578,434 (GRCm39) missense probably benign 0.45
R1895:Kmt2c UTSW 5 25,520,152 (GRCm39) missense probably benign 0.34
R1946:Kmt2c UTSW 5 25,520,152 (GRCm39) missense probably benign 0.34
R1989:Kmt2c UTSW 5 25,703,542 (GRCm39) missense possibly damaging 0.93
R2039:Kmt2c UTSW 5 25,534,038 (GRCm39) missense possibly damaging 0.53
R2049:Kmt2c UTSW 5 25,490,077 (GRCm39) missense probably damaging 1.00
R2079:Kmt2c UTSW 5 25,557,278 (GRCm39) missense possibly damaging 0.82
R2080:Kmt2c UTSW 5 25,559,715 (GRCm39) missense probably damaging 1.00
R2107:Kmt2c UTSW 5 25,514,822 (GRCm39) missense probably benign 0.01
R2186:Kmt2c UTSW 5 25,492,110 (GRCm39) missense probably damaging 1.00
R2395:Kmt2c UTSW 5 25,520,150 (GRCm39) missense probably benign
R2983:Kmt2c UTSW 5 25,520,755 (GRCm39) small deletion probably benign
R3109:Kmt2c UTSW 5 25,480,733 (GRCm39) missense probably damaging 1.00
R3500:Kmt2c UTSW 5 25,504,477 (GRCm39) missense probably benign 0.02
R3738:Kmt2c UTSW 5 25,610,381 (GRCm39) missense probably benign 0.41
R3809:Kmt2c UTSW 5 25,614,136 (GRCm39) missense possibly damaging 0.87
R4088:Kmt2c UTSW 5 25,492,711 (GRCm39) missense probably benign
R4107:Kmt2c UTSW 5 25,503,918 (GRCm39) missense possibly damaging 0.51
R4212:Kmt2c UTSW 5 25,552,357 (GRCm39) critical splice donor site probably null
R4376:Kmt2c UTSW 5 25,520,324 (GRCm39) missense probably benign 0.00
R4377:Kmt2c UTSW 5 25,520,324 (GRCm39) missense probably benign 0.00
R4383:Kmt2c UTSW 5 25,556,060 (GRCm39) missense possibly damaging 0.77
R4435:Kmt2c UTSW 5 25,519,875 (GRCm39) missense possibly damaging 0.63
R4456:Kmt2c UTSW 5 25,515,210 (GRCm39) missense probably benign
R4461:Kmt2c UTSW 5 25,504,874 (GRCm39) missense probably benign 0.00
R4519:Kmt2c UTSW 5 25,568,475 (GRCm39) missense probably damaging 1.00
R4550:Kmt2c UTSW 5 25,505,172 (GRCm39) missense probably damaging 1.00
R4557:Kmt2c UTSW 5 25,505,313 (GRCm39) missense probably damaging 1.00
R4610:Kmt2c UTSW 5 25,559,382 (GRCm39) missense probably damaging 1.00
R4671:Kmt2c UTSW 5 25,571,175 (GRCm39) missense probably damaging 1.00
R4704:Kmt2c UTSW 5 25,519,025 (GRCm39) nonsense probably null
R4781:Kmt2c UTSW 5 25,648,823 (GRCm39) missense probably damaging 1.00
R4844:Kmt2c UTSW 5 25,520,111 (GRCm39) missense probably benign
R4855:Kmt2c UTSW 5 25,519,555 (GRCm39) missense probably benign 0.00
R4919:Kmt2c UTSW 5 25,519,393 (GRCm39) missense possibly damaging 0.80
R4971:Kmt2c UTSW 5 25,515,870 (GRCm39) missense probably benign 0.00
R4983:Kmt2c UTSW 5 25,500,509 (GRCm39) missense possibly damaging 0.51
R5012:Kmt2c UTSW 5 25,504,710 (GRCm39) nonsense probably null
R5033:Kmt2c UTSW 5 25,519,706 (GRCm39) missense probably benign 0.03
R5093:Kmt2c UTSW 5 25,614,205 (GRCm39) missense probably benign 0.17
R5125:Kmt2c UTSW 5 25,489,379 (GRCm39) missense probably damaging 0.99
R5231:Kmt2c UTSW 5 25,520,471 (GRCm39) missense possibly damaging 0.89
R5254:Kmt2c UTSW 5 25,519,592 (GRCm39) missense probably benign 0.01
R5396:Kmt2c UTSW 5 25,499,732 (GRCm39) splice site probably null
R5415:Kmt2c UTSW 5 25,519,699 (GRCm39) missense probably benign 0.21
R5523:Kmt2c UTSW 5 25,504,337 (GRCm39) missense probably benign 0.00
R5554:Kmt2c UTSW 5 25,499,608 (GRCm39) missense probably damaging 1.00
R5701:Kmt2c UTSW 5 25,519,015 (GRCm39) missense probably benign 0.16
R5762:Kmt2c UTSW 5 25,515,455 (GRCm39) missense probably benign 0.01
R5819:Kmt2c UTSW 5 25,614,130 (GRCm39) critical splice donor site probably null
R5838:Kmt2c UTSW 5 25,489,469 (GRCm39) missense probably damaging 1.00
R5912:Kmt2c UTSW 5 25,552,467 (GRCm39) missense possibly damaging 0.80
R5951:Kmt2c UTSW 5 25,535,801 (GRCm39) missense probably benign 0.15
R5988:Kmt2c UTSW 5 25,516,118 (GRCm39) missense probably benign 0.02
R5999:Kmt2c UTSW 5 25,489,203 (GRCm39) missense probably damaging 1.00
R6104:Kmt2c UTSW 5 25,504,127 (GRCm39) missense probably benign
R6254:Kmt2c UTSW 5 25,554,872 (GRCm39) missense possibly damaging 0.94
R6311:Kmt2c UTSW 5 25,648,816 (GRCm39) critical splice donor site probably null
R6329:Kmt2c UTSW 5 25,520,600 (GRCm39) missense probably benign 0.01
R6347:Kmt2c UTSW 5 25,515,833 (GRCm39) missense possibly damaging 0.54
R6364:Kmt2c UTSW 5 25,514,634 (GRCm39) missense probably null 0.99
R6379:Kmt2c UTSW 5 25,564,339 (GRCm39) missense probably damaging 1.00
R6588:Kmt2c UTSW 5 25,528,787 (GRCm39) missense probably damaging 0.99
R6628:Kmt2c UTSW 5 25,503,926 (GRCm39) missense probably benign
R6733:Kmt2c UTSW 5 25,614,291 (GRCm39) missense probably damaging 1.00
R6787:Kmt2c UTSW 5 25,480,737 (GRCm39) splice site probably null
R6816:Kmt2c UTSW 5 25,610,530 (GRCm39) splice site probably null
R6862:Kmt2c UTSW 5 25,515,515 (GRCm39) missense probably damaging 1.00
R7150:Kmt2c UTSW 5 25,505,360 (GRCm39) missense possibly damaging 0.89
R7220:Kmt2c UTSW 5 25,549,923 (GRCm39) missense probably damaging 1.00
R7250:Kmt2c UTSW 5 25,504,489 (GRCm39) missense probably damaging 1.00
R7402:Kmt2c UTSW 5 25,600,418 (GRCm39) missense probably damaging 1.00
R7465:Kmt2c UTSW 5 25,507,847 (GRCm39) missense probably damaging 1.00
R7467:Kmt2c UTSW 5 25,513,530 (GRCm39) missense probably damaging 1.00
R7491:Kmt2c UTSW 5 25,489,562 (GRCm39) missense probably damaging 0.99
R7549:Kmt2c UTSW 5 25,619,968 (GRCm39) missense possibly damaging 0.95
R7637:Kmt2c UTSW 5 25,520,093 (GRCm39) missense probably damaging 1.00
R7652:Kmt2c UTSW 5 25,520,717 (GRCm39) missense probably benign 0.01
R7714:Kmt2c UTSW 5 25,580,364 (GRCm39) missense probably benign
R7838:Kmt2c UTSW 5 25,499,697 (GRCm39) missense possibly damaging 0.57
R7891:Kmt2c UTSW 5 25,505,109 (GRCm39) missense probably damaging 1.00
R7892:Kmt2c UTSW 5 25,504,814 (GRCm39) missense probably benign 0.18
R7895:Kmt2c UTSW 5 25,578,174 (GRCm39) missense possibly damaging 0.65
R7960:Kmt2c UTSW 5 25,520,194 (GRCm39) missense probably benign 0.01
R7974:Kmt2c UTSW 5 25,505,561 (GRCm39) missense probably damaging 1.00
R7978:Kmt2c UTSW 5 25,564,676 (GRCm39) missense probably benign 0.00
R8011:Kmt2c UTSW 5 25,556,232 (GRCm39) missense probably damaging 0.99
R8021:Kmt2c UTSW 5 25,492,117 (GRCm39) missense possibly damaging 0.88
R8022:Kmt2c UTSW 5 25,486,678 (GRCm39) missense possibly damaging 0.83
R8079:Kmt2c UTSW 5 25,507,730 (GRCm39) missense probably damaging 0.98
R8087:Kmt2c UTSW 5 25,534,250 (GRCm39) missense probably damaging 1.00
R8109:Kmt2c UTSW 5 25,486,382 (GRCm39) missense probably damaging 1.00
R8161:Kmt2c UTSW 5 25,579,562 (GRCm39) missense probably benign 0.00
R8169:Kmt2c UTSW 5 25,559,685 (GRCm39) missense probably damaging 1.00
R8206:Kmt2c UTSW 5 25,519,537 (GRCm39) missense probably damaging 0.98
R8218:Kmt2c UTSW 5 25,488,104 (GRCm39) missense probably damaging 1.00
R8223:Kmt2c UTSW 5 25,529,216 (GRCm39) missense possibly damaging 0.89
R8260:Kmt2c UTSW 5 25,610,514 (GRCm39) missense possibly damaging 0.87
R8330:Kmt2c UTSW 5 25,509,692 (GRCm39) missense probably null 1.00
R8355:Kmt2c UTSW 5 25,559,499 (GRCm39) critical splice acceptor site probably null
R8455:Kmt2c UTSW 5 25,559,499 (GRCm39) critical splice acceptor site probably null
R8508:Kmt2c UTSW 5 25,519,120 (GRCm39) missense probably benign 0.34
R8885:Kmt2c UTSW 5 25,520,077 (GRCm39) missense probably benign 0.34
R8907:Kmt2c UTSW 5 25,514,609 (GRCm39) missense probably damaging 1.00
R8924:Kmt2c UTSW 5 25,503,885 (GRCm39) missense probably benign
R8969:Kmt2c UTSW 5 25,519,387 (GRCm39) missense possibly damaging 0.82
R9019:Kmt2c UTSW 5 25,488,208 (GRCm39) missense probably damaging 1.00
R9035:Kmt2c UTSW 5 25,524,010 (GRCm39) missense probably damaging 1.00
R9074:Kmt2c UTSW 5 25,489,343 (GRCm39) missense probably damaging 1.00
R9125:Kmt2c UTSW 5 25,489,194 (GRCm39) missense possibly damaging 0.86
R9130:Kmt2c UTSW 5 25,516,102 (GRCm39) missense probably benign 0.01
R9171:Kmt2c UTSW 5 25,486,309 (GRCm39) missense probably damaging 1.00
R9235:Kmt2c UTSW 5 25,504,997 (GRCm39) missense probably damaging 1.00
R9288:Kmt2c UTSW 5 25,554,860 (GRCm39) missense probably benign 0.34
R9288:Kmt2c UTSW 5 25,497,907 (GRCm39) missense probably damaging 1.00
R9336:Kmt2c UTSW 5 25,614,165 (GRCm39) missense probably benign 0.06
R9443:Kmt2c UTSW 5 25,515,045 (GRCm39) missense probably damaging 1.00
R9481:Kmt2c UTSW 5 25,554,860 (GRCm39) missense probably benign 0.34
R9481:Kmt2c UTSW 5 25,497,907 (GRCm39) missense probably damaging 1.00
R9526:Kmt2c UTSW 5 25,486,355 (GRCm39) missense probably damaging 1.00
R9653:Kmt2c UTSW 5 25,507,819 (GRCm39) missense probably damaging 1.00
R9729:Kmt2c UTSW 5 25,489,758 (GRCm39) missense probably damaging 1.00
R9731:Kmt2c UTSW 5 25,577,956 (GRCm39) missense probably benign 0.18
R9784:Kmt2c UTSW 5 25,549,959 (GRCm39) missense probably damaging 1.00
RF001:Kmt2c UTSW 5 25,520,773 (GRCm39) small insertion probably benign
RF006:Kmt2c UTSW 5 25,520,770 (GRCm39) small insertion probably benign
RF011:Kmt2c UTSW 5 25,543,457 (GRCm39) missense probably damaging 1.00
RF041:Kmt2c UTSW 5 25,520,773 (GRCm39) small insertion probably benign
RF047:Kmt2c UTSW 5 25,520,758 (GRCm39) small insertion probably benign
RF051:Kmt2c UTSW 5 25,518,477 (GRCm39) unclassified probably benign
RF055:Kmt2c UTSW 5 25,520,770 (GRCm39) small insertion probably benign
RF059:Kmt2c UTSW 5 25,518,477 (GRCm39) unclassified probably benign
RF063:Kmt2c UTSW 5 25,520,762 (GRCm39) small insertion probably benign
X0024:Kmt2c UTSW 5 25,610,483 (GRCm39) missense probably benign 0.26
X0027:Kmt2c UTSW 5 25,535,885 (GRCm39) missense possibly damaging 0.90
Z1176:Kmt2c UTSW 5 25,559,411 (GRCm39) missense probably damaging 1.00
Z1177:Kmt2c UTSW 5 25,571,195 (GRCm39) critical splice acceptor site probably null
Z1177:Kmt2c UTSW 5 25,505,001 (GRCm39) missense probably benign 0.00
Z1177:Kmt2c UTSW 5 25,500,395 (GRCm39) critical splice donor site probably null
Predicted Primers PCR Primer
(F):5'- TGACCGCTGACGAATCATGG -3'
(R):5'- CACCATCCACTCATGGGTCAAG -3'

Sequencing Primer
(F):5'- CTGACGAATCATGGCTTGC -3'
(R):5'- ACTCATGGGTCAAGTTTGCC -3'
Posted On 2019-06-26