Incidental Mutation 'R7023:Kmt2e'
ID |
545752 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Kmt2e
|
Ensembl Gene |
ENSMUSG00000029004 |
Gene Name |
lysine (K)-specific methyltransferase 2E |
Synonyms |
9530077A04Rik, 1810033J14Rik, D230038D11Rik, Mll5 |
MMRRC Submission |
045124-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7023 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
23639439-23709233 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 23705485 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Arginine
at position 1303
(H1303R)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000110781
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088392]
[ENSMUST00000094962]
[ENSMUST00000115128]
[ENSMUST00000126586]
[ENSMUST00000146375]
[ENSMUST00000196260]
[ENSMUST00000196929]
|
AlphaFold |
Q3UG20 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000088392
|
SMART Domains |
Protein: ENSMUSP00000085734 Gene: ENSMUSG00000062604
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
46 |
N/A |
INTRINSIC |
Pfam:Pkinase
|
79 |
228 |
1.3e-22 |
PFAM |
Pfam:Pkinase_Tyr
|
79 |
228 |
1e-9 |
PFAM |
coiled coil region
|
263 |
314 |
N/A |
INTRINSIC |
coiled coil region
|
339 |
373 |
N/A |
INTRINSIC |
low complexity region
|
393 |
406 |
N/A |
INTRINSIC |
Pfam:Pkinase
|
506 |
680 |
1.9e-18 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000094962
AA Change: H1303R
PolyPhen 2
Score 0.463 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000092569 Gene: ENSMUSG00000029004 AA Change: H1303R
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
38 |
N/A |
INTRINSIC |
low complexity region
|
48 |
55 |
N/A |
INTRINSIC |
low complexity region
|
70 |
81 |
N/A |
INTRINSIC |
low complexity region
|
100 |
109 |
N/A |
INTRINSIC |
PHD
|
120 |
164 |
4.25e-8 |
SMART |
SET
|
328 |
453 |
2.13e-26 |
SMART |
low complexity region
|
487 |
503 |
N/A |
INTRINSIC |
low complexity region
|
569 |
582 |
N/A |
INTRINSIC |
low complexity region
|
854 |
867 |
N/A |
INTRINSIC |
low complexity region
|
882 |
908 |
N/A |
INTRINSIC |
low complexity region
|
933 |
945 |
N/A |
INTRINSIC |
low complexity region
|
951 |
960 |
N/A |
INTRINSIC |
low complexity region
|
1184 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1214 |
1237 |
N/A |
INTRINSIC |
low complexity region
|
1294 |
1312 |
N/A |
INTRINSIC |
low complexity region
|
1348 |
1367 |
N/A |
INTRINSIC |
internal_repeat_1
|
1434 |
1496 |
6.13e-7 |
PROSPERO |
low complexity region
|
1506 |
1518 |
N/A |
INTRINSIC |
low complexity region
|
1625 |
1641 |
N/A |
INTRINSIC |
low complexity region
|
1677 |
1705 |
N/A |
INTRINSIC |
low complexity region
|
1720 |
1731 |
N/A |
INTRINSIC |
internal_repeat_1
|
1783 |
1842 |
6.13e-7 |
PROSPERO |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000115128
AA Change: H1303R
PolyPhen 2
Score 0.463 (Sensitivity: 0.89; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000110781 Gene: ENSMUSG00000029004 AA Change: H1303R
Domain | Start | End | E-Value | Type |
low complexity region
|
23 |
38 |
N/A |
INTRINSIC |
low complexity region
|
48 |
55 |
N/A |
INTRINSIC |
low complexity region
|
70 |
81 |
N/A |
INTRINSIC |
low complexity region
|
100 |
109 |
N/A |
INTRINSIC |
PHD
|
120 |
164 |
4.25e-8 |
SMART |
SET
|
328 |
453 |
2.13e-26 |
SMART |
low complexity region
|
487 |
503 |
N/A |
INTRINSIC |
low complexity region
|
569 |
582 |
N/A |
INTRINSIC |
low complexity region
|
854 |
867 |
N/A |
INTRINSIC |
low complexity region
|
882 |
908 |
N/A |
INTRINSIC |
low complexity region
|
933 |
945 |
N/A |
INTRINSIC |
low complexity region
|
951 |
960 |
N/A |
INTRINSIC |
low complexity region
|
1184 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1214 |
1237 |
N/A |
INTRINSIC |
low complexity region
|
1294 |
1312 |
N/A |
INTRINSIC |
low complexity region
|
1348 |
1367 |
N/A |
INTRINSIC |
internal_repeat_1
|
1434 |
1496 |
6.13e-7 |
PROSPERO |
low complexity region
|
1506 |
1518 |
N/A |
INTRINSIC |
low complexity region
|
1625 |
1641 |
N/A |
INTRINSIC |
low complexity region
|
1677 |
1705 |
N/A |
INTRINSIC |
low complexity region
|
1720 |
1731 |
N/A |
INTRINSIC |
internal_repeat_1
|
1783 |
1842 |
6.13e-7 |
PROSPERO |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000126586
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000146375
|
SMART Domains |
Protein: ENSMUSP00000142547 Gene: ENSMUSG00000029004
Domain | Start | End | E-Value | Type |
low complexity region
|
104 |
117 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194010
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000196260
|
SMART Domains |
Protein: ENSMUSP00000143791 Gene: ENSMUSG00000029004
Domain | Start | End | E-Value | Type |
low complexity region
|
49 |
62 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000196929
|
SMART Domains |
Protein: ENSMUSP00000143216 Gene: ENSMUSG00000062604
Domain | Start | End | E-Value | Type |
Pfam:Pkinase_Tyr
|
1 |
131 |
2.6e-8 |
PFAM |
Pfam:Pkinase
|
2 |
130 |
2.3e-18 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 98.9%
|
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 protein with an N-terminal PHD zinc finger and a central SET domain. Overexpression of the protein inhibits cell cycle progression. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a null allele exhibit neonatal and postnatal lethality, reduced fertility and growth, and abnormal lymphopoiesis. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
A |
G |
13: 119,610,443 (GRCm39) |
H372R |
probably benign |
Het |
4933405O20Rik |
T |
C |
7: 50,250,001 (GRCm39) |
I345T |
probably damaging |
Het |
4933427D14Rik |
A |
G |
11: 72,069,229 (GRCm39) |
|
probably null |
Het |
6430548M08Rik |
T |
C |
8: 120,872,096 (GRCm39) |
V8A |
probably damaging |
Het |
Adam2 |
A |
T |
14: 66,280,505 (GRCm39) |
D501E |
probably benign |
Het |
Agbl3 |
T |
C |
6: 34,791,704 (GRCm39) |
V602A |
probably benign |
Het |
Akap12 |
T |
C |
10: 4,306,895 (GRCm39) |
M1235T |
probably benign |
Het |
Arid5a |
G |
A |
1: 36,356,631 (GRCm39) |
|
probably benign |
Het |
Asxl1 |
T |
A |
2: 153,242,469 (GRCm39) |
D1006E |
probably benign |
Het |
AY074887 |
T |
C |
9: 54,858,149 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
T |
A |
17: 30,746,546 (GRCm39) |
R93S |
probably benign |
Het |
Cabp2 |
A |
T |
19: 4,132,658 (GRCm39) |
|
probably null |
Het |
Cacna1e |
T |
C |
1: 154,601,439 (GRCm39) |
D76G |
probably null |
Het |
Cd177 |
A |
G |
7: 24,459,187 (GRCm39) |
I74T |
probably benign |
Het |
Chchd1 |
G |
A |
14: 20,753,310 (GRCm39) |
|
probably benign |
Het |
Col28a1 |
T |
C |
6: 8,083,763 (GRCm39) |
R565G |
possibly damaging |
Het |
Cpvl |
T |
A |
6: 53,944,797 (GRCm39) |
I80F |
probably benign |
Het |
Csgalnact1 |
T |
C |
8: 68,811,081 (GRCm39) |
T530A |
probably benign |
Het |
Cybrd1 |
A |
G |
2: 70,968,922 (GRCm39) |
D265G |
probably benign |
Het |
Cyp2c69 |
A |
T |
19: 39,865,986 (GRCm39) |
N202K |
probably benign |
Het |
D1Pas1 |
A |
G |
1: 186,700,205 (GRCm39) |
N45D |
probably damaging |
Het |
Dclre1a |
A |
G |
19: 56,528,638 (GRCm39) |
V839A |
probably damaging |
Het |
Degs1 |
A |
T |
1: 182,106,630 (GRCm39) |
Y210N |
probably damaging |
Het |
Doc2g |
A |
G |
19: 4,054,778 (GRCm39) |
S220G |
probably benign |
Het |
Epb41l2 |
T |
A |
10: 25,388,875 (GRCm39) |
L885Q |
probably damaging |
Het |
Fabp1 |
A |
T |
6: 71,180,069 (GRCm39) |
|
probably null |
Het |
Fat2 |
G |
A |
11: 55,201,328 (GRCm39) |
S582L |
probably benign |
Het |
Fcgbpl1 |
T |
A |
7: 27,839,463 (GRCm39) |
C425* |
probably null |
Het |
Fras1 |
A |
G |
5: 96,857,943 (GRCm39) |
N2079S |
probably benign |
Het |
Gdf6 |
T |
C |
4: 9,860,210 (GRCm39) |
Y431H |
probably damaging |
Het |
Gfra1 |
A |
T |
19: 58,442,764 (GRCm39) |
L6Q |
probably damaging |
Het |
Gm45861 |
T |
G |
8: 28,071,034 (GRCm39) |
S1305A |
unknown |
Het |
Gse1 |
T |
C |
8: 120,957,387 (GRCm39) |
|
probably benign |
Het |
Lck |
T |
C |
4: 129,442,658 (GRCm39) |
D499G |
possibly damaging |
Het |
Lepr |
A |
T |
4: 101,646,484 (GRCm39) |
Y805F |
probably damaging |
Het |
Lin7a |
A |
T |
10: 107,218,489 (GRCm39) |
Y11F |
possibly damaging |
Het |
Lrrc43 |
A |
G |
5: 123,641,826 (GRCm39) |
K559E |
probably damaging |
Het |
Megf6 |
T |
C |
4: 154,338,602 (GRCm39) |
L467P |
possibly damaging |
Het |
Mprip |
G |
A |
11: 59,628,215 (GRCm39) |
G221R |
probably damaging |
Het |
Myo5c |
T |
C |
9: 75,208,738 (GRCm39) |
V1683A |
probably damaging |
Het |
Nbeal2 |
G |
A |
9: 110,467,686 (GRCm39) |
R501W |
probably damaging |
Het |
Ncf1 |
G |
T |
5: 134,254,116 (GRCm39) |
A219E |
possibly damaging |
Het |
Nckap1l |
T |
C |
15: 103,384,493 (GRCm39) |
I616T |
probably benign |
Het |
Nlrp2 |
A |
T |
7: 5,331,228 (GRCm39) |
C389* |
probably null |
Het |
Nrg3 |
T |
C |
14: 38,098,333 (GRCm39) |
E507G |
probably damaging |
Het |
Or4p19 |
A |
G |
2: 88,242,759 (GRCm39) |
L81P |
probably damaging |
Het |
P4ha2 |
A |
T |
11: 54,022,072 (GRCm39) |
T532S |
probably benign |
Het |
Pappa |
A |
T |
4: 65,269,955 (GRCm39) |
H1623L |
probably benign |
Het |
Paqr6 |
A |
G |
3: 88,273,353 (GRCm39) |
Y115C |
probably damaging |
Het |
Pcolce2 |
A |
T |
9: 95,560,521 (GRCm39) |
Q190L |
probably benign |
Het |
Poll |
A |
G |
19: 45,547,277 (GRCm39) |
I65T |
probably benign |
Het |
Prmt9 |
T |
C |
8: 78,276,086 (GRCm39) |
|
probably benign |
Het |
Prpf39 |
T |
C |
12: 65,100,074 (GRCm39) |
V130A |
possibly damaging |
Het |
Prpf6 |
A |
G |
2: 181,262,433 (GRCm39) |
D144G |
probably damaging |
Het |
Rgs6 |
T |
A |
12: 83,138,878 (GRCm39) |
|
probably benign |
Het |
Rimbp2 |
A |
G |
5: 128,879,847 (GRCm39) |
|
probably null |
Het |
Ripor2 |
A |
G |
13: 24,855,829 (GRCm39) |
T90A |
probably benign |
Het |
Rnf150 |
T |
C |
8: 83,590,706 (GRCm39) |
F23S |
probably damaging |
Het |
Rpp40 |
G |
A |
13: 36,082,889 (GRCm39) |
R200W |
possibly damaging |
Het |
Rtp3 |
G |
A |
9: 110,815,714 (GRCm39) |
S217L |
probably benign |
Het |
Sacs |
A |
C |
14: 61,446,264 (GRCm39) |
K2770T |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,442,610 (GRCm39) |
I1545N |
probably damaging |
Het |
Scn2b |
G |
T |
9: 45,037,438 (GRCm39) |
V162L |
probably damaging |
Het |
Sema6d |
A |
G |
2: 124,506,831 (GRCm39) |
T880A |
probably damaging |
Het |
Slc36a4 |
A |
G |
9: 15,630,929 (GRCm39) |
D16G |
probably benign |
Het |
Slc4a8 |
T |
A |
15: 100,689,524 (GRCm39) |
I378K |
probably benign |
Het |
Smco2 |
T |
A |
6: 146,760,354 (GRCm39) |
L70* |
probably null |
Het |
Sptb |
C |
T |
12: 76,671,862 (GRCm39) |
V364I |
probably damaging |
Het |
Susd4 |
A |
G |
1: 182,592,613 (GRCm39) |
H3R |
probably damaging |
Het |
Tbc1d16 |
T |
C |
11: 119,049,617 (GRCm39) |
Q293R |
probably damaging |
Het |
Tnfsf9 |
T |
A |
17: 57,414,317 (GRCm39) |
M248K |
possibly damaging |
Het |
Toporsl |
A |
G |
4: 52,611,211 (GRCm39) |
N368S |
possibly damaging |
Het |
Trip11 |
T |
C |
12: 101,852,126 (GRCm39) |
E361G |
probably benign |
Het |
Trrap |
T |
A |
5: 144,728,964 (GRCm39) |
M626K |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,773,218 (GRCm39) |
S2395T |
probably damaging |
Het |
Ubqln3 |
T |
C |
7: 103,790,630 (GRCm39) |
R487G |
probably damaging |
Het |
Vdac1 |
A |
G |
11: 52,265,193 (GRCm39) |
Y22C |
probably damaging |
Het |
Vmn1r59 |
C |
T |
7: 5,457,477 (GRCm39) |
M94I |
probably benign |
Het |
Vmn2r10 |
G |
T |
5: 109,149,894 (GRCm39) |
D383E |
probably damaging |
Het |
Vmn2r115 |
T |
C |
17: 23,578,785 (GRCm39) |
Y753H |
probably damaging |
Het |
Vmn2r97 |
G |
T |
17: 19,134,663 (GRCm39) |
C27F |
probably damaging |
Het |
Wasf1 |
T |
A |
10: 40,812,471 (GRCm39) |
V420E |
unknown |
Het |
Zfp94 |
A |
T |
7: 24,002,821 (GRCm39) |
L201Q |
probably damaging |
Het |
Zgpat |
TGGAGGAGGAGGAGGAGGA |
TGGAGGAGGAGGAGGA |
2: 181,007,811 (GRCm39) |
|
probably benign |
Het |
Zmym4 |
C |
A |
4: 126,762,593 (GRCm39) |
R1410L |
probably damaging |
Het |
|
Other mutations in Kmt2e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00783:Kmt2e
|
APN |
5 |
23,697,356 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01330:Kmt2e
|
APN |
5 |
23,702,946 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01457:Kmt2e
|
APN |
5 |
23,707,017 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01691:Kmt2e
|
APN |
5 |
23,702,089 (GRCm39) |
missense |
probably benign |
|
IGL02274:Kmt2e
|
APN |
5 |
23,705,758 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02934:Kmt2e
|
APN |
5 |
23,702,882 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02964:Kmt2e
|
APN |
5 |
23,672,098 (GRCm39) |
splice site |
probably benign |
|
IGL03011:Kmt2e
|
APN |
5 |
23,702,540 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03291:Kmt2e
|
APN |
5 |
23,704,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R0035:Kmt2e
|
UTSW |
5 |
23,690,619 (GRCm39) |
splice site |
probably benign |
|
R0446:Kmt2e
|
UTSW |
5 |
23,702,532 (GRCm39) |
splice site |
probably null |
|
R0498:Kmt2e
|
UTSW |
5 |
23,683,970 (GRCm39) |
nonsense |
probably null |
|
R0699:Kmt2e
|
UTSW |
5 |
23,678,581 (GRCm39) |
missense |
probably benign |
0.01 |
R0701:Kmt2e
|
UTSW |
5 |
23,678,581 (GRCm39) |
missense |
probably benign |
0.01 |
R0761:Kmt2e
|
UTSW |
5 |
23,708,032 (GRCm39) |
nonsense |
probably null |
|
R1110:Kmt2e
|
UTSW |
5 |
23,707,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Kmt2e
|
UTSW |
5 |
23,707,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R1432:Kmt2e
|
UTSW |
5 |
23,655,319 (GRCm39) |
missense |
probably benign |
0.39 |
R1495:Kmt2e
|
UTSW |
5 |
23,704,325 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1505:Kmt2e
|
UTSW |
5 |
23,705,533 (GRCm39) |
missense |
probably null |
0.01 |
R1623:Kmt2e
|
UTSW |
5 |
23,687,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R1675:Kmt2e
|
UTSW |
5 |
23,687,451 (GRCm39) |
nonsense |
probably null |
|
R1691:Kmt2e
|
UTSW |
5 |
23,669,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Kmt2e
|
UTSW |
5 |
23,697,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R1820:Kmt2e
|
UTSW |
5 |
23,678,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1846:Kmt2e
|
UTSW |
5 |
23,704,484 (GRCm39) |
intron |
probably benign |
|
R1912:Kmt2e
|
UTSW |
5 |
23,697,393 (GRCm39) |
missense |
probably benign |
0.07 |
R2070:Kmt2e
|
UTSW |
5 |
23,706,993 (GRCm39) |
missense |
probably benign |
|
R2195:Kmt2e
|
UTSW |
5 |
23,707,194 (GRCm39) |
splice site |
probably null |
|
R2571:Kmt2e
|
UTSW |
5 |
23,706,885 (GRCm39) |
missense |
probably benign |
0.08 |
R3901:Kmt2e
|
UTSW |
5 |
23,706,640 (GRCm39) |
missense |
probably benign |
0.02 |
R3902:Kmt2e
|
UTSW |
5 |
23,706,640 (GRCm39) |
missense |
probably benign |
0.02 |
R3905:Kmt2e
|
UTSW |
5 |
23,706,624 (GRCm39) |
missense |
probably benign |
0.01 |
R3906:Kmt2e
|
UTSW |
5 |
23,706,624 (GRCm39) |
missense |
probably benign |
0.01 |
R3909:Kmt2e
|
UTSW |
5 |
23,706,624 (GRCm39) |
missense |
probably benign |
0.01 |
R3956:Kmt2e
|
UTSW |
5 |
23,701,023 (GRCm39) |
missense |
probably benign |
0.00 |
R4242:Kmt2e
|
UTSW |
5 |
23,707,820 (GRCm39) |
unclassified |
probably benign |
|
R4299:Kmt2e
|
UTSW |
5 |
23,669,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4448:Kmt2e
|
UTSW |
5 |
23,669,788 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4528:Kmt2e
|
UTSW |
5 |
23,678,556 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4574:Kmt2e
|
UTSW |
5 |
23,697,405 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4719:Kmt2e
|
UTSW |
5 |
23,697,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R4754:Kmt2e
|
UTSW |
5 |
23,687,439 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4787:Kmt2e
|
UTSW |
5 |
23,668,081 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4812:Kmt2e
|
UTSW |
5 |
23,707,585 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4853:Kmt2e
|
UTSW |
5 |
23,707,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R5138:Kmt2e
|
UTSW |
5 |
23,707,693 (GRCm39) |
missense |
probably damaging |
0.99 |
R5306:Kmt2e
|
UTSW |
5 |
23,704,331 (GRCm39) |
missense |
probably damaging |
0.98 |
R5659:Kmt2e
|
UTSW |
5 |
23,702,805 (GRCm39) |
missense |
probably damaging |
0.99 |
R5907:Kmt2e
|
UTSW |
5 |
23,669,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Kmt2e
|
UTSW |
5 |
23,704,440 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6280:Kmt2e
|
UTSW |
5 |
23,704,514 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6353:Kmt2e
|
UTSW |
5 |
23,698,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R6375:Kmt2e
|
UTSW |
5 |
23,704,517 (GRCm39) |
missense |
probably benign |
|
R6553:Kmt2e
|
UTSW |
5 |
23,668,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R6572:Kmt2e
|
UTSW |
5 |
23,702,579 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6678:Kmt2e
|
UTSW |
5 |
23,704,293 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6791:Kmt2e
|
UTSW |
5 |
23,704,474 (GRCm39) |
intron |
probably benign |
|
R6792:Kmt2e
|
UTSW |
5 |
23,704,474 (GRCm39) |
intron |
probably benign |
|
R6794:Kmt2e
|
UTSW |
5 |
23,704,474 (GRCm39) |
intron |
probably benign |
|
R6797:Kmt2e
|
UTSW |
5 |
23,687,505 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6947:Kmt2e
|
UTSW |
5 |
23,702,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R7036:Kmt2e
|
UTSW |
5 |
23,683,741 (GRCm39) |
missense |
probably null |
1.00 |
R7173:Kmt2e
|
UTSW |
5 |
23,669,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R7202:Kmt2e
|
UTSW |
5 |
23,697,292 (GRCm39) |
unclassified |
probably benign |
|
R7563:Kmt2e
|
UTSW |
5 |
23,705,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R7571:Kmt2e
|
UTSW |
5 |
23,683,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R7604:Kmt2e
|
UTSW |
5 |
23,706,763 (GRCm39) |
missense |
not run |
|
R7722:Kmt2e
|
UTSW |
5 |
23,702,016 (GRCm39) |
missense |
probably benign |
0.00 |
R7758:Kmt2e
|
UTSW |
5 |
23,701,068 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7794:Kmt2e
|
UTSW |
5 |
23,669,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Kmt2e
|
UTSW |
5 |
23,706,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8341:Kmt2e
|
UTSW |
5 |
23,704,451 (GRCm39) |
missense |
probably damaging |
0.98 |
R8383:Kmt2e
|
UTSW |
5 |
23,690,539 (GRCm39) |
missense |
probably benign |
0.08 |
R8400:Kmt2e
|
UTSW |
5 |
23,702,090 (GRCm39) |
missense |
probably benign |
0.17 |
R8546:Kmt2e
|
UTSW |
5 |
23,686,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R8750:Kmt2e
|
UTSW |
5 |
23,698,215 (GRCm39) |
missense |
probably benign |
|
R8786:Kmt2e
|
UTSW |
5 |
23,669,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Kmt2e
|
UTSW |
5 |
23,669,770 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9660:Kmt2e
|
UTSW |
5 |
23,683,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R9786:Kmt2e
|
UTSW |
5 |
23,702,982 (GRCm39) |
missense |
probably benign |
0.16 |
RF026:Kmt2e
|
UTSW |
5 |
23,683,507 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF028:Kmt2e
|
UTSW |
5 |
23,683,507 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF040:Kmt2e
|
UTSW |
5 |
23,683,507 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF042:Kmt2e
|
UTSW |
5 |
23,683,507 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1177:Kmt2e
|
UTSW |
5 |
23,686,206 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- ACTTCAGTGGAGCAAGTGAG -3'
(R):5'- CACAGAGTGCTCACTGTACAC -3'
Sequencing Primer
(F):5'- GTTACCAGAGAGCCTTACTGC -3'
(R):5'- ACCTGCCATGAGTTCACT -3'
|
Posted On |
2019-05-13 |