Incidental Mutation 'R1965:Kmt2a'
ID 218293
Institutional Source Beutler Lab
Gene Symbol Kmt2a
Ensembl Gene ENSMUSG00000002028
Gene Name lysine (K)-specific methyltransferase 2A
Synonyms Mll, ALL-1, Mll1, Cxxc7, All1, HTRX1, trithorax Drosophila
MMRRC Submission 039978-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1965 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 44714652-44792594 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 44732757 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000002095] [ENSMUST00000114689]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000002095
AA Change: V2517A
SMART Domains Protein: ENSMUSP00000002095
Gene: ENSMUSG00000002028
AA Change: V2517A

DomainStartEndE-ValueType
low complexity region 14 29 N/A INTRINSIC
low complexity region 41 102 N/A INTRINSIC
PDB:3U88|N 103 151 6e-15 PDB
AT_hook 171 183 2.12e2 SMART
AT_hook 217 229 4.68e1 SMART
AT_hook 298 310 2.8e0 SMART
coiled coil region 366 394 N/A INTRINSIC
low complexity region 450 489 N/A INTRINSIC
low complexity region 524 535 N/A INTRINSIC
low complexity region 544 574 N/A INTRINSIC
low complexity region 589 601 N/A INTRINSIC
low complexity region 660 674 N/A INTRINSIC
low complexity region 717 732 N/A INTRINSIC
low complexity region 760 790 N/A INTRINSIC
low complexity region 866 892 N/A INTRINSIC
low complexity region 989 1005 N/A INTRINSIC
Pfam:zf-CXXC 1144 1191 1.1e-15 PFAM
low complexity region 1204 1233 N/A INTRINSIC
low complexity region 1236 1283 N/A INTRINSIC
low complexity region 1295 1316 N/A INTRINSIC
low complexity region 1323 1345 N/A INTRINSIC
low complexity region 1353 1366 N/A INTRINSIC
PHD 1432 1479 5.57e-3 SMART
PHD 1480 1530 1.17e-10 SMART
PHD 1567 1624 7.94e-8 SMART
BROMO 1632 1766 2.24e-10 SMART
low complexity region 1816 1850 N/A INTRINSIC
PHD 1931 1977 1.74e-4 SMART
low complexity region 1990 2001 N/A INTRINSIC
FYRN 2029 2072 2.33e-20 SMART
low complexity region 2180 2194 N/A INTRINSIC
low complexity region 2215 2227 N/A INTRINSIC
low complexity region 2607 2618 N/A INTRINSIC
low complexity region 2789 2800 N/A INTRINSIC
low complexity region 2824 2833 N/A INTRINSIC
low complexity region 2856 2878 N/A INTRINSIC
low complexity region 2902 2909 N/A INTRINSIC
low complexity region 3115 3141 N/A INTRINSIC
low complexity region 3164 3175 N/A INTRINSIC
low complexity region 3228 3239 N/A INTRINSIC
low complexity region 3299 3312 N/A INTRINSIC
low complexity region 3342 3351 N/A INTRINSIC
low complexity region 3405 3419 N/A INTRINSIC
low complexity region 3498 3526 N/A INTRINSIC
low complexity region 3620 3633 N/A INTRINSIC
FYRC 3662 3747 8.54e-37 SMART
SET 3823 3945 6.09e-45 SMART
PostSET 3947 3963 1.65e-4 SMART
Predicted Effect unknown
Transcript: ENSMUST00000114689
AA Change: V2520A
SMART Domains Protein: ENSMUSP00000110337
Gene: ENSMUSG00000002028
AA Change: V2520A

DomainStartEndE-ValueType
low complexity region 14 29 N/A INTRINSIC
low complexity region 41 102 N/A INTRINSIC
PDB:3U88|N 103 151 6e-15 PDB
AT_hook 171 183 2.12e2 SMART
AT_hook 217 229 4.68e1 SMART
AT_hook 298 310 2.8e0 SMART
coiled coil region 366 394 N/A INTRINSIC
low complexity region 450 489 N/A INTRINSIC
low complexity region 524 535 N/A INTRINSIC
low complexity region 544 574 N/A INTRINSIC
low complexity region 589 601 N/A INTRINSIC
low complexity region 660 674 N/A INTRINSIC
low complexity region 717 732 N/A INTRINSIC
low complexity region 760 790 N/A INTRINSIC
low complexity region 866 892 N/A INTRINSIC
low complexity region 989 1005 N/A INTRINSIC
Pfam:zf-CXXC 1144 1191 1.1e-15 PFAM
low complexity region 1204 1233 N/A INTRINSIC
low complexity region 1236 1283 N/A INTRINSIC
low complexity region 1295 1316 N/A INTRINSIC
low complexity region 1323 1345 N/A INTRINSIC
low complexity region 1353 1366 N/A INTRINSIC
PHD 1432 1479 5.57e-3 SMART
PHD 1480 1530 1.17e-10 SMART
PHD 1567 1627 9.12e-8 SMART
BROMO 1635 1769 2.24e-10 SMART
low complexity region 1819 1853 N/A INTRINSIC
PHD 1934 1980 1.74e-4 SMART
low complexity region 1993 2004 N/A INTRINSIC
FYRN 2032 2075 2.33e-20 SMART
low complexity region 2183 2197 N/A INTRINSIC
low complexity region 2218 2230 N/A INTRINSIC
low complexity region 2610 2621 N/A INTRINSIC
low complexity region 2792 2803 N/A INTRINSIC
low complexity region 2827 2836 N/A INTRINSIC
low complexity region 2859 2881 N/A INTRINSIC
low complexity region 2905 2912 N/A INTRINSIC
low complexity region 3118 3144 N/A INTRINSIC
low complexity region 3167 3178 N/A INTRINSIC
low complexity region 3231 3242 N/A INTRINSIC
low complexity region 3302 3315 N/A INTRINSIC
low complexity region 3345 3354 N/A INTRINSIC
low complexity region 3408 3422 N/A INTRINSIC
low complexity region 3501 3529 N/A INTRINSIC
low complexity region 3623 3636 N/A INTRINSIC
FYRC 3665 3750 8.54e-37 SMART
SET 3826 3948 6.09e-45 SMART
PostSET 3950 3966 1.65e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000138119
Predicted Effect probably benign
Transcript: ENSMUST00000152241
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.6%
  • 20x: 93.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a transcriptional coactivator that plays an essential role in regulating gene expression during early development and hematopoiesis. The encoded protein contains multiple conserved functional domains. One of these domains, the SET domain, is responsible for its histone H3 lysine 4 (H3K4) methyltransferase activity which mediates chromatin modifications associated with epigenetic transcriptional activation. This protein is processed by the enzyme Taspase 1 into two fragments, MLL-C and MLL-N. These fragments reassociate and further assemble into different multiprotein complexes that regulate the transcription of specific target genes, including many of the HOX genes. Multiple chromosomal translocations involving this gene are the cause of certain acute lymphoid leukemias and acute myeloid leukemias. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010]
PHENOTYPE: Homozygotes for targeted null mutations die at embryonic day 11.5-14.5 with edematous bodies, petechiae, and hematopoietic insufficiency. Heterozygotes show reduced growth, hematopoietic abnormalities, and homeotic transformations of the axial skeleton. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 88 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aco1 T G 4: 40,175,730 (GRCm39) L157R probably damaging Het
Acot11 A T 4: 106,606,550 (GRCm39) L513Q probably damaging Het
Amd1 A G 10: 40,170,755 (GRCm39) I52T probably benign Het
Ap2b1 T C 11: 83,237,721 (GRCm39) I557T probably benign Het
Arel1 T A 12: 84,987,173 (GRCm39) probably null Het
Arg1 T A 10: 24,792,762 (GRCm39) probably null Het
Atf1 A T 15: 100,152,052 (GRCm39) M135L probably benign Het
Atf2 T C 2: 73,681,242 (GRCm39) E77G possibly damaging Het
Axin1 G T 17: 26,403,199 (GRCm39) A394S probably damaging Het
Axin1 A T 17: 26,409,202 (GRCm39) Q734L probably damaging Het
Brd8 G C 18: 34,735,819 (GRCm39) A886G probably damaging Het
Ccdc39 T C 3: 33,880,629 (GRCm39) K446R probably damaging Het
Celf3 T C 3: 94,392,634 (GRCm39) V35A probably damaging Het
Cfap299 T A 5: 98,494,093 (GRCm39) D32E probably damaging Het
Ckap2 T C 8: 22,665,803 (GRCm39) T415A possibly damaging Het
Crybg3 T C 16: 59,323,600 (GRCm39) Y1066C probably damaging Het
Csmd3 T C 15: 47,713,144 (GRCm39) H1506R probably benign Het
Dnah10 A G 5: 124,852,267 (GRCm39) D1808G probably damaging Het
Dsc3 C T 18: 20,113,729 (GRCm39) G398R probably damaging Het
Emc2 A G 15: 43,390,863 (GRCm39) Q293R probably damaging Het
Evc2 A G 5: 37,520,876 (GRCm39) N251D possibly damaging Het
Fam151a A T 4: 106,591,112 (GRCm39) probably benign Het
Fbxw16 T A 9: 109,270,289 (GRCm39) I151F probably damaging Het
Fmnl2 A G 2: 53,004,880 (GRCm39) D658G probably damaging Het
Fnip2 G A 3: 79,400,779 (GRCm39) T314I probably benign Het
Foxc2 T A 8: 121,843,413 (GRCm39) S20R probably damaging Het
Fpr-rs6 C T 17: 20,402,918 (GRCm39) G148R probably damaging Het
Fsip2 T C 2: 82,823,124 (GRCm39) S6286P possibly damaging Het
Fyb2 A T 4: 104,770,846 (GRCm39) I54F probably benign Het
Gbf1 T C 19: 46,260,003 (GRCm39) F999L probably damaging Het
Gldc G A 19: 30,114,513 (GRCm39) R466* probably null Het
Gm12695 T A 4: 96,651,082 (GRCm39) S124C probably benign Het
Gm4846 A T 1: 166,314,533 (GRCm39) I370N possibly damaging Het
Gsdmc3 T C 15: 63,730,296 (GRCm39) T423A probably damaging Het
Hjurp GT GTT 1: 88,194,246 (GRCm39) probably null Het
Jarid2 T A 13: 45,059,752 (GRCm39) N661K probably damaging Het
Kcnmb3 T C 3: 32,526,492 (GRCm39) Y233C probably damaging Het
Kidins220 A G 12: 25,044,905 (GRCm39) D191G probably damaging Het
Krt1 T C 15: 101,757,427 (GRCm39) D261G probably benign Het
Lrba A G 3: 86,513,175 (GRCm39) probably null Het
Myo1f C T 17: 33,817,146 (GRCm39) R730* probably null Het
Ncoa7 C A 10: 30,530,426 (GRCm39) E30* probably null Het
Neurod4 T A 10: 130,106,918 (GRCm39) K119* probably null Het
Npy5r T C 8: 67,133,929 (GRCm39) D288G probably benign Het
Nr3c2 A T 8: 77,636,092 (GRCm39) I398L probably damaging Het
Or10a5 T C 7: 106,635,565 (GRCm39) S68P probably damaging Het
Or12j4 C A 7: 140,046,574 (GRCm39) F153L probably benign Het
Or4b1 T C 2: 89,979,748 (GRCm39) S201G probably damaging Het
Or4k35 T C 2: 111,099,938 (GRCm39) Y258C probably damaging Het
Or51v8 A T 7: 103,320,103 (GRCm39) I45N probably damaging Het
Or5g25 T C 2: 85,478,090 (GRCm39) T192A possibly damaging Het
Or5w8 A G 2: 87,687,759 (GRCm39) K80R probably benign Het
Or9m1b A G 2: 87,836,648 (GRCm39) F149S probably damaging Het
P3r3urf G A 4: 116,031,376 (GRCm39) C82Y probably damaging Het
Pcf11 A T 7: 92,310,809 (GRCm39) M393K probably benign Het
Pck2 T C 14: 55,779,964 (GRCm39) V71A probably benign Het
Pdzd8 G T 19: 59,288,554 (GRCm39) L949I probably benign Het
Pdzrn4 G A 15: 92,644,190 (GRCm39) probably null Het
Phospho1 A G 11: 95,721,705 (GRCm39) N125S probably damaging Het
Pirb A T 7: 3,720,637 (GRCm39) L287Q probably benign Het
Ppid A T 3: 79,509,606 (GRCm39) K308* probably null Het
Ppp1r1b A G 11: 98,246,189 (GRCm39) E57G probably damaging Het
Prtg T G 9: 72,755,604 (GRCm39) S269A probably benign Het
Rbbp5 T A 1: 132,422,035 (GRCm39) S312T probably damaging Het
Rbm11 T A 16: 75,395,656 (GRCm39) probably null Het
Retreg1 A G 15: 25,970,250 (GRCm39) T139A probably damaging Het
Riok3 T A 18: 12,270,019 (GRCm39) H120Q probably damaging Het
Rln1 A T 19: 29,311,995 (GRCm39) M1K probably null Het
Rpp30 C T 19: 36,066,549 (GRCm39) S94L probably damaging Het
Sccpdh C T 1: 179,511,879 (GRCm39) P117L probably damaging Het
Serac1 T C 17: 6,099,274 (GRCm39) K506E possibly damaging Het
Serping1 G T 2: 84,596,072 (GRCm39) T454K probably damaging Het
Slc1a2 T A 2: 102,570,245 (GRCm39) N174K probably damaging Het
Slc2a2 A G 3: 28,773,634 (GRCm39) Q313R probably damaging Het
Slc46a2 T A 4: 59,914,249 (GRCm39) S225C probably damaging Het
Smarcc2 G A 10: 128,310,627 (GRCm39) E419K probably damaging Het
Stkld1 T A 2: 26,836,744 (GRCm39) probably null Het
Szt2 A G 4: 118,241,162 (GRCm39) M1704T probably benign Het
Tasor T G 14: 27,164,511 (GRCm39) C272W probably damaging Het
Tfcp2l1 C T 1: 118,580,653 (GRCm39) Q116* probably null Het
Timm44 A G 8: 4,310,603 (GRCm39) M383T possibly damaging Het
Tnpo2 G A 8: 85,771,946 (GRCm39) probably null Het
Tnrc6b A G 15: 80,764,640 (GRCm39) K714R probably damaging Het
Wdfy3 A G 5: 102,099,178 (GRCm39) L290P probably damaging Het
Wdr59 A G 8: 112,177,709 (GRCm39) F898L probably damaging Het
Zfp120 A T 2: 149,959,318 (GRCm39) C335S probably damaging Het
Zfp518a T C 19: 40,901,954 (GRCm39) S628P probably benign Het
Zfp879 A T 11: 50,724,355 (GRCm39) C234S probably damaging Het
Other mutations in Kmt2a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00492:Kmt2a APN 9 44,719,231 (GRCm39) unclassified probably benign
IGL00667:Kmt2a APN 9 44,735,683 (GRCm39) utr 3 prime probably benign
IGL00828:Kmt2a APN 9 44,732,073 (GRCm39) unclassified probably benign
IGL01080:Kmt2a APN 9 44,720,389 (GRCm39) missense unknown
IGL01131:Kmt2a APN 9 44,732,467 (GRCm39) unclassified probably benign
IGL01294:Kmt2a APN 9 44,731,594 (GRCm39) unclassified probably benign
IGL01432:Kmt2a APN 9 44,720,393 (GRCm39) missense unknown
IGL01646:Kmt2a APN 9 44,736,781 (GRCm39) utr 3 prime probably benign
IGL01777:Kmt2a APN 9 44,760,302 (GRCm39) missense probably damaging 0.99
IGL01944:Kmt2a APN 9 44,761,064 (GRCm39) missense probably damaging 1.00
IGL02125:Kmt2a APN 9 44,759,983 (GRCm39) missense probably damaging 1.00
IGL02207:Kmt2a APN 9 44,758,979 (GRCm39) missense probably damaging 0.98
IGL02424:Kmt2a APN 9 44,735,932 (GRCm39) utr 3 prime probably benign
IGL02499:Kmt2a APN 9 44,741,806 (GRCm39) splice site probably benign
IGL02574:Kmt2a APN 9 44,741,810 (GRCm39) splice site probably benign
IGL02711:Kmt2a APN 9 44,735,820 (GRCm39) splice site probably benign
IGL02828:Kmt2a APN 9 44,733,244 (GRCm39) unclassified probably benign
IGL03012:Kmt2a APN 9 44,722,263 (GRCm39) unclassified probably benign
IGL03242:Kmt2a APN 9 44,759,689 (GRCm39) missense probably damaging 0.99
IGL03294:Kmt2a APN 9 44,731,862 (GRCm39) unclassified probably benign
IGL03326:Kmt2a APN 9 44,730,044 (GRCm39) nonsense probably null
Chromas UTSW 9 44,731,639 (GRCm39) unclassified probably benign
Heteros UTSW 9 44,740,108 (GRCm39) nonsense probably null
Polonium UTSW 9 44,725,938 (GRCm39) nonsense probably null
Pyknos UTSW 9 44,738,125 (GRCm39) utr 3 prime probably benign
Skies UTSW 9 44,740,558 (GRCm39) utr 3 prime probably benign
spacious UTSW 9 44,758,942 (GRCm39) missense probably benign 0.03
ukrainium UTSW 9 44,753,997 (GRCm39) unclassified probably benign
Uranium UTSW 9 44,761,154 (GRCm39) nonsense probably null
PIT4402001:Kmt2a UTSW 9 44,752,359 (GRCm39) missense unknown
R0076:Kmt2a UTSW 9 44,741,356 (GRCm39) utr 3 prime probably benign
R0076:Kmt2a UTSW 9 44,741,356 (GRCm39) utr 3 prime probably benign
R0180:Kmt2a UTSW 9 44,738,148 (GRCm39) utr 3 prime probably benign
R0363:Kmt2a UTSW 9 44,721,010 (GRCm39) critical splice donor site probably null
R0411:Kmt2a UTSW 9 44,731,261 (GRCm39) unclassified probably benign
R0555:Kmt2a UTSW 9 44,758,868 (GRCm39) missense probably damaging 1.00
R0587:Kmt2a UTSW 9 44,758,831 (GRCm39) missense probably damaging 0.99
R0865:Kmt2a UTSW 9 44,730,067 (GRCm39) unclassified probably benign
R0988:Kmt2a UTSW 9 44,759,846 (GRCm39) missense probably benign 0.03
R1006:Kmt2a UTSW 9 44,758,993 (GRCm39) missense probably damaging 0.99
R1108:Kmt2a UTSW 9 44,760,359 (GRCm39) missense probably damaging 1.00
R1292:Kmt2a UTSW 9 44,725,991 (GRCm39) utr 3 prime probably benign
R1322:Kmt2a UTSW 9 44,732,418 (GRCm39) unclassified probably benign
R1476:Kmt2a UTSW 9 44,735,932 (GRCm39) utr 3 prime probably benign
R1485:Kmt2a UTSW 9 44,738,225 (GRCm39) utr 3 prime probably benign
R1487:Kmt2a UTSW 9 44,745,287 (GRCm39) utr 3 prime probably benign
R1493:Kmt2a UTSW 9 44,758,202 (GRCm39) missense probably damaging 1.00
R1499:Kmt2a UTSW 9 44,759,563 (GRCm39) missense probably benign 0.36
R1507:Kmt2a UTSW 9 44,729,700 (GRCm39) unclassified probably benign
R1603:Kmt2a UTSW 9 44,752,858 (GRCm39) splice site probably null
R1635:Kmt2a UTSW 9 44,735,666 (GRCm39) utr 3 prime probably benign
R1662:Kmt2a UTSW 9 44,747,967 (GRCm39) utr 3 prime probably benign
R1711:Kmt2a UTSW 9 44,752,918 (GRCm39) missense unknown
R1785:Kmt2a UTSW 9 44,730,972 (GRCm39) unclassified probably benign
R1786:Kmt2a UTSW 9 44,730,972 (GRCm39) unclassified probably benign
R1919:Kmt2a UTSW 9 44,731,642 (GRCm39) unclassified probably benign
R1964:Kmt2a UTSW 9 44,731,941 (GRCm39) missense probably benign 0.23
R2029:Kmt2a UTSW 9 44,729,747 (GRCm39) missense probably benign 0.23
R2054:Kmt2a UTSW 9 44,734,671 (GRCm39) utr 3 prime probably benign
R2259:Kmt2a UTSW 9 44,792,440 (GRCm39) unclassified probably benign
R2382:Kmt2a UTSW 9 44,732,207 (GRCm39) unclassified probably benign
R2483:Kmt2a UTSW 9 44,760,263 (GRCm39) missense probably damaging 0.99
R3033:Kmt2a UTSW 9 44,733,160 (GRCm39) unclassified probably benign
R3423:Kmt2a UTSW 9 44,731,394 (GRCm39) unclassified probably benign
R3428:Kmt2a UTSW 9 44,759,416 (GRCm39) missense probably benign 0.06
R3605:Kmt2a UTSW 9 44,760,493 (GRCm39) missense probably damaging 1.00
R3607:Kmt2a UTSW 9 44,760,493 (GRCm39) missense probably damaging 1.00
R3611:Kmt2a UTSW 9 44,733,763 (GRCm39) unclassified probably benign
R3623:Kmt2a UTSW 9 44,760,263 (GRCm39) missense probably damaging 0.99
R3745:Kmt2a UTSW 9 44,742,637 (GRCm39) utr 3 prime probably benign
R3806:Kmt2a UTSW 9 44,731,653 (GRCm39) unclassified probably benign
R3841:Kmt2a UTSW 9 44,742,588 (GRCm39) utr 3 prime probably benign
R3855:Kmt2a UTSW 9 44,741,796 (GRCm39) utr 3 prime probably benign
R4027:Kmt2a UTSW 9 44,747,990 (GRCm39) utr 3 prime probably benign
R4124:Kmt2a UTSW 9 44,731,093 (GRCm39) unclassified probably benign
R4177:Kmt2a UTSW 9 44,732,280 (GRCm39) unclassified probably benign
R4296:Kmt2a UTSW 9 44,732,472 (GRCm39) unclassified probably benign
R4414:Kmt2a UTSW 9 44,721,077 (GRCm39) unclassified probably benign
R4461:Kmt2a UTSW 9 44,760,263 (GRCm39) missense probably damaging 0.99
R4668:Kmt2a UTSW 9 44,735,869 (GRCm39) utr 3 prime probably benign
R4761:Kmt2a UTSW 9 44,760,421 (GRCm39) missense probably damaging 1.00
R4812:Kmt2a UTSW 9 44,742,651 (GRCm39) utr 3 prime probably benign
R4815:Kmt2a UTSW 9 44,732,553 (GRCm39) unclassified probably benign
R4817:Kmt2a UTSW 9 44,732,763 (GRCm39) unclassified probably benign
R4888:Kmt2a UTSW 9 44,732,977 (GRCm39) unclassified probably benign
R4958:Kmt2a UTSW 9 44,759,764 (GRCm39) missense probably damaging 1.00
R5055:Kmt2a UTSW 9 44,729,649 (GRCm39) unclassified probably benign
R5065:Kmt2a UTSW 9 44,753,997 (GRCm39) unclassified probably benign
R5185:Kmt2a UTSW 9 44,731,543 (GRCm39) unclassified probably benign
R5358:Kmt2a UTSW 9 44,730,571 (GRCm39) unclassified probably benign
R5411:Kmt2a UTSW 9 44,759,782 (GRCm39) missense probably damaging 1.00
R5420:Kmt2a UTSW 9 44,759,633 (GRCm39) missense probably damaging 1.00
R5483:Kmt2a UTSW 9 44,735,921 (GRCm39) utr 3 prime probably benign
R5487:Kmt2a UTSW 9 44,733,272 (GRCm39) unclassified probably benign
R5488:Kmt2a UTSW 9 44,752,335 (GRCm39) utr 3 prime probably benign
R5489:Kmt2a UTSW 9 44,752,335 (GRCm39) utr 3 prime probably benign
R5538:Kmt2a UTSW 9 44,731,639 (GRCm39) unclassified probably benign
R5576:Kmt2a UTSW 9 44,753,931 (GRCm39) missense possibly damaging 0.94
R5631:Kmt2a UTSW 9 44,731,985 (GRCm39) unclassified probably benign
R5781:Kmt2a UTSW 9 44,759,139 (GRCm39) nonsense probably null
R5789:Kmt2a UTSW 9 44,731,201 (GRCm39) unclassified probably benign
R5932:Kmt2a UTSW 9 44,731,944 (GRCm39) unclassified probably benign
R6027:Kmt2a UTSW 9 44,730,587 (GRCm39) unclassified probably benign
R6191:Kmt2a UTSW 9 44,738,125 (GRCm39) utr 3 prime probably benign
R6239:Kmt2a UTSW 9 44,731,093 (GRCm39) unclassified probably benign
R6291:Kmt2a UTSW 9 44,744,171 (GRCm39) utr 3 prime probably benign
R6344:Kmt2a UTSW 9 44,733,156 (GRCm39) unclassified probably benign
R6611:Kmt2a UTSW 9 44,760,569 (GRCm39) missense probably damaging 0.98
R6641:Kmt2a UTSW 9 44,731,132 (GRCm39) unclassified probably benign
R6651:Kmt2a UTSW 9 44,740,108 (GRCm39) nonsense probably null
R6825:Kmt2a UTSW 9 44,729,704 (GRCm39) unclassified probably benign
R6853:Kmt2a UTSW 9 44,729,704 (GRCm39) unclassified probably benign
R6897:Kmt2a UTSW 9 44,758,942 (GRCm39) missense probably benign 0.03
R6930:Kmt2a UTSW 9 44,753,962 (GRCm39) unclassified probably benign
R6932:Kmt2a UTSW 9 44,740,558 (GRCm39) utr 3 prime probably benign
R6957:Kmt2a UTSW 9 44,731,319 (GRCm39) unclassified probably benign
R7170:Kmt2a UTSW 9 44,722,018 (GRCm39) missense unknown
R7202:Kmt2a UTSW 9 44,759,012 (GRCm39) missense probably benign 0.03
R7481:Kmt2a UTSW 9 44,720,368 (GRCm39) missense unknown
R7538:Kmt2a UTSW 9 44,759,041 (GRCm39) missense probably damaging 0.99
R7597:Kmt2a UTSW 9 44,742,650 (GRCm39) missense unknown
R7741:Kmt2a UTSW 9 44,719,359 (GRCm39) missense unknown
R7767:Kmt2a UTSW 9 44,730,295 (GRCm39) missense unknown
R7768:Kmt2a UTSW 9 44,731,900 (GRCm39) missense unknown
R7861:Kmt2a UTSW 9 44,730,031 (GRCm39) missense unknown
R7894:Kmt2a UTSW 9 44,761,154 (GRCm39) nonsense probably null
R7922:Kmt2a UTSW 9 44,754,157 (GRCm39) missense unknown
R7943:Kmt2a UTSW 9 44,760,437 (GRCm39) missense probably damaging 0.97
R7997:Kmt2a UTSW 9 44,745,220 (GRCm39) missense unknown
R8033:Kmt2a UTSW 9 44,756,767 (GRCm39) missense probably damaging 1.00
R8055:Kmt2a UTSW 9 44,732,378 (GRCm39) missense unknown
R8139:Kmt2a UTSW 9 44,730,587 (GRCm39) unclassified probably benign
R8156:Kmt2a UTSW 9 44,733,686 (GRCm39) missense unknown
R8224:Kmt2a UTSW 9 44,719,326 (GRCm39) missense unknown
R8427:Kmt2a UTSW 9 44,756,720 (GRCm39) missense probably damaging 1.00
R8535:Kmt2a UTSW 9 44,730,812 (GRCm39) missense possibly damaging 0.91
R8693:Kmt2a UTSW 9 44,721,981 (GRCm39) missense unknown
R8757:Kmt2a UTSW 9 44,754,210 (GRCm39) missense unknown
R8840:Kmt2a UTSW 9 44,721,016 (GRCm39) missense unknown
R8933:Kmt2a UTSW 9 44,733,802 (GRCm39) unclassified probably benign
R8998:Kmt2a UTSW 9 44,733,174 (GRCm39) missense unknown
R9013:Kmt2a UTSW 9 44,761,208 (GRCm39) missense probably damaging 0.97
R9053:Kmt2a UTSW 9 44,732,716 (GRCm39) missense unknown
R9084:Kmt2a UTSW 9 44,740,130 (GRCm39) missense unknown
R9146:Kmt2a UTSW 9 44,725,938 (GRCm39) nonsense probably null
R9162:Kmt2a UTSW 9 44,759,363 (GRCm39) missense probably benign 0.32
R9231:Kmt2a UTSW 9 44,759,912 (GRCm39) missense probably damaging 0.99
R9250:Kmt2a UTSW 9 44,759,683 (GRCm39) missense possibly damaging 0.82
R9262:Kmt2a UTSW 9 44,731,222 (GRCm39) missense probably benign 0.23
R9323:Kmt2a UTSW 9 44,731,261 (GRCm39) unclassified probably benign
R9472:Kmt2a UTSW 9 44,733,453 (GRCm39) missense unknown
R9510:Kmt2a UTSW 9 44,734,531 (GRCm39) missense unknown
R9524:Kmt2a UTSW 9 44,730,294 (GRCm39) missense unknown
R9662:Kmt2a UTSW 9 44,731,428 (GRCm39) missense unknown
R9664:Kmt2a UTSW 9 44,760,102 (GRCm39) nonsense probably null
R9691:Kmt2a UTSW 9 44,731,557 (GRCm39) missense unknown
R9750:Kmt2a UTSW 9 44,747,499 (GRCm39) missense unknown
X0021:Kmt2a UTSW 9 44,742,532 (GRCm39) utr 3 prime probably benign
X0025:Kmt2a UTSW 9 44,736,689 (GRCm39) nonsense probably null
X0026:Kmt2a UTSW 9 44,732,203 (GRCm39) unclassified probably benign
X0027:Kmt2a UTSW 9 44,792,194 (GRCm39) missense possibly damaging 0.85
Z1176:Kmt2a UTSW 9 44,759,276 (GRCm39) missense probably damaging 1.00
Z1177:Kmt2a UTSW 9 44,730,418 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TCTGTCCTGTTCTGGAAGATTC -3'
(R):5'- AGCCAGAGTTTGCTGATGAG -3'

Sequencing Primer
(F):5'- CCTGTTCTGGAAGATTCTGGTAG -3'
(R):5'- GCTGATGAGGTGTTGACTCC -3'
Posted On 2014-08-01