Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
A |
G |
7: 119,174,864 (GRCm39) |
T210A |
probably damaging |
Het |
Adgb |
T |
A |
10: 10,276,316 (GRCm39) |
T351S |
probably benign |
Het |
Akap9 |
A |
G |
5: 4,018,755 (GRCm39) |
H1112R |
probably damaging |
Het |
Angptl6 |
A |
T |
9: 20,786,939 (GRCm39) |
Y261* |
probably null |
Het |
Arhgef10l |
A |
C |
4: 140,306,590 (GRCm39) |
F395V |
probably damaging |
Het |
Bub1 |
T |
C |
2: 127,659,373 (GRCm39) |
N328S |
probably benign |
Het |
Cacna1s |
A |
G |
1: 136,039,731 (GRCm39) |
N1186D |
probably damaging |
Het |
Cacna2d2 |
C |
A |
9: 107,386,474 (GRCm39) |
F200L |
probably damaging |
Het |
Calca |
G |
A |
7: 114,232,919 (GRCm39) |
S110L |
probably benign |
Het |
Ccdc120 |
G |
A |
X: 7,601,601 (GRCm39) |
P263S |
probably benign |
Het |
Dcaf8l |
A |
G |
X: 88,448,857 (GRCm39) |
V424A |
possibly damaging |
Het |
Dgki |
C |
A |
6: 37,126,599 (GRCm39) |
|
probably benign |
Het |
Ear1 |
G |
T |
14: 44,056,502 (GRCm39) |
S122* |
probably null |
Het |
F5 |
A |
T |
1: 164,023,163 (GRCm39) |
T1574S |
probably benign |
Het |
Fam227b |
T |
C |
2: 125,968,762 (GRCm39) |
|
probably null |
Het |
Gm20521 |
T |
A |
14: 55,134,680 (GRCm39) |
S301T |
possibly damaging |
Het |
Hsd17b7 |
A |
T |
1: 169,787,287 (GRCm39) |
I239N |
probably benign |
Het |
Itih1 |
C |
A |
14: 30,663,514 (GRCm39) |
E163D |
probably benign |
Het |
Lama1 |
A |
T |
17: 68,086,099 (GRCm39) |
Y1446F |
probably benign |
Het |
Lama3 |
C |
T |
18: 12,572,406 (GRCm39) |
T537M |
possibly damaging |
Het |
Lars1 |
G |
T |
18: 42,354,636 (GRCm39) |
Y770* |
probably null |
Het |
Lrp2 |
A |
T |
2: 69,313,477 (GRCm39) |
V2418E |
probably damaging |
Het |
Maip1 |
A |
G |
1: 57,446,359 (GRCm39) |
E143G |
probably damaging |
Het |
Mast4 |
G |
T |
13: 102,897,472 (GRCm39) |
S739* |
probably null |
Het |
Mctp1 |
C |
T |
13: 76,949,632 (GRCm39) |
Q555* |
probably null |
Het |
Med14 |
A |
T |
X: 12,613,742 (GRCm39) |
D291E |
probably benign |
Het |
Mgat2 |
T |
A |
12: 69,231,777 (GRCm39) |
V117D |
probably damaging |
Het |
Myt1 |
A |
C |
2: 181,439,594 (GRCm39) |
Y372S |
probably benign |
Het |
Naa16 |
T |
A |
14: 79,577,068 (GRCm39) |
Q735H |
probably damaging |
Het |
Ncf4 |
A |
G |
15: 78,135,102 (GRCm39) |
Y53C |
probably damaging |
Het |
Nlrp4a |
A |
T |
7: 26,148,934 (GRCm39) |
K180N |
probably benign |
Het |
Nova1 |
A |
G |
12: 46,746,861 (GRCm39) |
V472A |
probably damaging |
Het |
Nup153 |
T |
C |
13: 46,847,315 (GRCm39) |
T705A |
probably benign |
Het |
Odf2 |
T |
A |
2: 29,791,091 (GRCm39) |
N79K |
probably benign |
Het |
Or4f7 |
A |
G |
2: 111,644,768 (GRCm39) |
I101T |
possibly damaging |
Het |
Pard3b |
G |
A |
1: 62,237,930 (GRCm39) |
|
probably benign |
Het |
Pde8b |
G |
A |
13: 95,182,906 (GRCm39) |
T388I |
probably damaging |
Het |
Phactr2 |
A |
G |
10: 13,264,457 (GRCm39) |
|
probably benign |
Het |
Phf12 |
T |
C |
11: 77,874,186 (GRCm39) |
S17P |
probably damaging |
Het |
Psmg2 |
T |
A |
18: 67,779,102 (GRCm39) |
L90* |
probably null |
Het |
Ryr2 |
T |
C |
13: 11,658,788 (GRCm39) |
|
probably null |
Het |
Sec23b |
T |
C |
2: 144,423,952 (GRCm39) |
F534L |
probably benign |
Het |
Sin3b |
A |
G |
8: 73,483,686 (GRCm39) |
|
probably benign |
Het |
Slc30a5 |
A |
T |
13: 100,947,818 (GRCm39) |
L463Q |
probably damaging |
Het |
Slc35g3 |
T |
C |
11: 69,651,895 (GRCm39) |
H52R |
possibly damaging |
Het |
Slc6a3 |
G |
T |
13: 73,719,585 (GRCm39) |
S538I |
probably damaging |
Het |
Socs2 |
G |
T |
10: 95,248,713 (GRCm39) |
C133* |
probably null |
Het |
Srebf2 |
G |
A |
15: 82,076,423 (GRCm39) |
R691H |
probably benign |
Het |
Tlr11 |
C |
A |
14: 50,598,557 (GRCm39) |
P181Q |
probably damaging |
Het |
Tlr7 |
T |
A |
X: 166,089,203 (GRCm39) |
Q761L |
possibly damaging |
Het |
Tmem120b |
T |
A |
5: 123,240,336 (GRCm39) |
Y90N |
possibly damaging |
Het |
Tpcn1 |
T |
C |
5: 120,675,631 (GRCm39) |
I778V |
possibly damaging |
Het |
Ttll8 |
T |
C |
15: 88,803,797 (GRCm39) |
T385A |
probably benign |
Het |
Vmn1r223 |
G |
A |
13: 23,434,153 (GRCm39) |
R249H |
probably damaging |
Het |
Vmn2r53 |
A |
T |
7: 12,334,937 (GRCm39) |
I241N |
possibly damaging |
Het |
Wdfy3 |
T |
C |
5: 102,083,863 (GRCm39) |
R808G |
probably damaging |
Het |
Zfyve26 |
T |
A |
12: 79,308,565 (GRCm39) |
S231C |
probably damaging |
Het |
|
Other mutations in Mllt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00941:Mllt1
|
APN |
17 |
57,202,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02554:Mllt1
|
APN |
17 |
57,206,806 (GRCm39) |
missense |
probably benign |
|
Weissblut
|
UTSW |
17 |
57,212,819 (GRCm39) |
missense |
probably damaging |
0.99 |
R2176:Mllt1
|
UTSW |
17 |
57,204,398 (GRCm39) |
missense |
probably benign |
0.00 |
R4455:Mllt1
|
UTSW |
17 |
57,226,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R4760:Mllt1
|
UTSW |
17 |
57,209,630 (GRCm39) |
missense |
probably benign |
0.05 |
R4864:Mllt1
|
UTSW |
17 |
57,212,819 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Mllt1
|
UTSW |
17 |
57,206,813 (GRCm39) |
missense |
probably benign |
|
R4916:Mllt1
|
UTSW |
17 |
57,206,813 (GRCm39) |
missense |
probably benign |
|
R4917:Mllt1
|
UTSW |
17 |
57,206,813 (GRCm39) |
missense |
probably benign |
|
R4918:Mllt1
|
UTSW |
17 |
57,206,813 (GRCm39) |
missense |
probably benign |
|
R6169:Mllt1
|
UTSW |
17 |
57,206,822 (GRCm39) |
missense |
probably benign |
|
R6508:Mllt1
|
UTSW |
17 |
57,234,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R7216:Mllt1
|
UTSW |
17 |
57,234,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R8865:Mllt1
|
UTSW |
17 |
57,207,295 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9094:Mllt1
|
UTSW |
17 |
57,212,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R9485:Mllt1
|
UTSW |
17 |
57,207,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Mllt1
|
UTSW |
17 |
57,209,572 (GRCm39) |
missense |
probably benign |
0.05 |
RF002:Mllt1
|
UTSW |
17 |
57,203,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
RF002:Mllt1
|
UTSW |
17 |
57,203,300 (GRCm39) |
missense |
probably benign |
0.09 |
|