Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
C |
T |
6: 23,077,152 (GRCm39) |
G736R |
possibly damaging |
Het |
Acta2 |
G |
A |
19: 34,229,931 (GRCm39) |
T8I |
probably benign |
Het |
Ankar |
A |
T |
1: 72,738,053 (GRCm39) |
V43E |
possibly damaging |
Het |
Apof |
A |
G |
10: 128,105,505 (GRCm39) |
I220V |
probably benign |
Het |
Asxl1 |
G |
T |
2: 153,239,705 (GRCm39) |
A499S |
probably benign |
Het |
Baz2a |
T |
A |
10: 127,957,942 (GRCm39) |
D1069E |
possibly damaging |
Het |
Baz2b |
T |
C |
2: 59,807,792 (GRCm39) |
T156A |
possibly damaging |
Het |
Bbc3 |
A |
T |
7: 16,051,082 (GRCm39) |
R169W |
unknown |
Het |
C5ar1 |
T |
A |
7: 15,982,691 (GRCm39) |
I110L |
probably benign |
Het |
Cd19 |
C |
A |
7: 126,010,975 (GRCm39) |
R323L |
probably damaging |
Het |
Cdc14b |
A |
T |
13: 64,344,489 (GRCm39) |
C113* |
probably null |
Het |
Cngb1 |
C |
A |
8: 95,980,811 (GRCm39) |
W914L |
possibly damaging |
Het |
Colgalt2 |
A |
G |
1: 152,379,895 (GRCm39) |
K445E |
probably damaging |
Het |
Crebrf |
A |
G |
17: 26,982,461 (GRCm39) |
M608V |
unknown |
Het |
Csf1 |
T |
A |
3: 107,656,191 (GRCm39) |
H280L |
probably benign |
Het |
Cyp2j11 |
C |
A |
4: 96,233,357 (GRCm39) |
R113L |
probably damaging |
Het |
D5Ertd579e |
G |
A |
5: 36,771,129 (GRCm39) |
H1089Y |
probably damaging |
Het |
Ddx60 |
C |
T |
8: 62,393,708 (GRCm39) |
T48M |
possibly damaging |
Het |
Defa40 |
T |
A |
8: 21,739,910 (GRCm39) |
S45T |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,518,032 (GRCm39) |
D1315G |
probably damaging |
Het |
Dock2 |
T |
G |
11: 34,586,105 (GRCm39) |
N526H |
probably damaging |
Het |
Dram2 |
T |
C |
3: 106,480,999 (GRCm39) |
*268Q |
probably null |
Het |
Emc8 |
A |
G |
8: 121,394,657 (GRCm39) |
Y21H |
possibly damaging |
Het |
Fam162a |
A |
G |
16: 35,891,863 (GRCm39) |
L4P |
probably damaging |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fbxw10 |
T |
A |
11: 62,744,124 (GRCm39) |
I307N |
probably benign |
Het |
Fbxw16 |
A |
G |
9: 109,268,619 (GRCm39) |
V257A |
possibly damaging |
Het |
Fer1l6 |
T |
A |
15: 58,445,096 (GRCm39) |
|
probably null |
Het |
Galnt7 |
A |
G |
8: 58,037,054 (GRCm39) |
Y112H |
possibly damaging |
Het |
Gigyf2 |
T |
C |
1: 87,356,326 (GRCm39) |
I803T |
unknown |
Het |
Gm28729 |
A |
G |
9: 96,403,288 (GRCm39) |
I44T |
possibly damaging |
Het |
Gm5447 |
A |
G |
13: 31,158,377 (GRCm39) |
I34V |
not run |
Het |
H2-M9 |
A |
T |
17: 36,953,303 (GRCm39) |
|
probably null |
Het |
Helz |
G |
A |
11: 107,527,104 (GRCm39) |
C864Y |
probably damaging |
Het |
Il25 |
A |
G |
14: 55,170,679 (GRCm39) |
Y84C |
probably null |
Het |
Itga10 |
T |
A |
3: 96,555,471 (GRCm39) |
C142S |
probably damaging |
Het |
Kcna10 |
A |
T |
3: 107,101,395 (GRCm39) |
M9L |
probably damaging |
Het |
Klhl6 |
G |
T |
16: 19,775,863 (GRCm39) |
Q232K |
possibly damaging |
Het |
Mb21d2 |
T |
G |
16: 28,748,298 (GRCm39) |
I40L |
possibly damaging |
Het |
Mdm1 |
T |
C |
10: 117,988,171 (GRCm39) |
S334P |
probably benign |
Het |
Mllt10 |
T |
A |
2: 18,175,090 (GRCm39) |
D549E |
probably benign |
Het |
Nars2 |
A |
G |
7: 96,689,137 (GRCm39) |
K353R |
probably benign |
Het |
Nav1 |
T |
A |
1: 135,512,647 (GRCm39) |
M138L |
probably benign |
Het |
Neb |
T |
C |
2: 52,083,902 (GRCm39) |
T5635A |
probably benign |
Het |
Nktr |
A |
C |
9: 121,579,393 (GRCm39) |
I1154L |
unknown |
Het |
Or14j8 |
A |
T |
17: 38,263,171 (GRCm39) |
V248D |
probably damaging |
Het |
Or2a57 |
T |
G |
6: 43,213,228 (GRCm39) |
S229A |
probably damaging |
Het |
Or4g17 |
T |
A |
2: 111,209,543 (GRCm39) |
L66Q |
probably damaging |
Het |
Oxld1 |
T |
C |
11: 120,347,963 (GRCm39) |
D78G |
probably benign |
Het |
Pde1b |
T |
C |
15: 103,433,256 (GRCm39) |
I255T |
probably benign |
Het |
Pkp4 |
T |
A |
2: 59,138,481 (GRCm39) |
F244I |
probably benign |
Het |
Polg2 |
C |
A |
11: 106,664,540 (GRCm39) |
V305L |
probably benign |
Het |
Pramel34 |
C |
T |
5: 93,784,099 (GRCm39) |
C455Y |
probably damaging |
Het |
Ptpn18 |
G |
A |
1: 34,512,445 (GRCm39) |
D417N |
possibly damaging |
Het |
Sash1 |
T |
C |
10: 8,632,509 (GRCm39) |
D242G |
possibly damaging |
Het |
Six4 |
T |
C |
12: 73,159,304 (GRCm39) |
T219A |
possibly damaging |
Het |
Slc28a3 |
A |
C |
13: 58,710,835 (GRCm39) |
Y562* |
probably null |
Het |
Soat1 |
A |
T |
1: 156,266,887 (GRCm39) |
W310R |
probably damaging |
Het |
Son |
CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC |
CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC |
16: 91,453,579 (GRCm39) |
|
probably benign |
Het |
Spef2 |
T |
C |
15: 9,740,671 (GRCm39) |
N30D |
probably benign |
Het |
Spopfm2 |
A |
T |
3: 94,083,411 (GRCm39) |
N133K |
probably benign |
Het |
Srebf2 |
T |
A |
15: 82,057,075 (GRCm39) |
I270N |
probably damaging |
Het |
St8sia3 |
T |
C |
18: 64,404,589 (GRCm39) |
W289R |
probably damaging |
Het |
Stx5a |
T |
A |
19: 8,720,868 (GRCm39) |
|
probably benign |
Het |
Tacc1 |
T |
C |
8: 25,654,480 (GRCm39) |
D689G |
probably damaging |
Het |
Tacc3 |
A |
G |
5: 33,818,628 (GRCm39) |
D21G |
probably benign |
Het |
Tapt1 |
G |
A |
5: 44,346,030 (GRCm39) |
R307* |
probably null |
Het |
Tbc1d9b |
T |
A |
11: 50,022,312 (GRCm39) |
V16E |
probably damaging |
Het |
Tchhl1 |
G |
A |
3: 93,377,971 (GRCm39) |
R225K |
probably benign |
Het |
Thumpd3 |
G |
A |
6: 113,032,730 (GRCm39) |
G156D |
probably benign |
Het |
Tmem178 |
C |
T |
17: 81,252,331 (GRCm39) |
P72S |
probably benign |
Het |
Tmem52 |
C |
T |
4: 155,553,926 (GRCm39) |
P46S |
probably benign |
Het |
Tmem94 |
G |
T |
11: 115,677,082 (GRCm39) |
R118L |
possibly damaging |
Het |
Tulp3 |
A |
T |
6: 128,303,792 (GRCm39) |
V269D |
probably benign |
Het |
Ubr1 |
A |
G |
2: 120,720,255 (GRCm39) |
|
probably null |
Het |
Upf1 |
G |
A |
8: 70,786,073 (GRCm39) |
S962L |
probably benign |
Het |
Vcpip1 |
C |
T |
1: 9,816,745 (GRCm39) |
R546Q |
probably damaging |
Het |
Vmn2r49 |
A |
C |
7: 9,722,820 (GRCm39) |
S151R |
probably benign |
Het |
Wac |
T |
C |
18: 7,871,746 (GRCm39) |
|
probably null |
Het |
Wrn |
C |
T |
8: 33,826,024 (GRCm39) |
|
probably null |
Het |
Zfp286 |
C |
A |
11: 62,671,627 (GRCm39) |
D149Y |
probably benign |
Het |
Zfp748 |
A |
G |
13: 67,690,091 (GRCm39) |
C390R |
probably damaging |
Het |
Zfp873 |
A |
G |
10: 81,896,210 (GRCm39) |
T314A |
possibly damaging |
Het |
Zfyve1 |
C |
T |
12: 83,598,261 (GRCm39) |
D656N |
probably benign |
Het |
Zmym1 |
T |
A |
4: 126,952,728 (GRCm39) |
K18* |
probably null |
Het |
|
Other mutations in Mlxipl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00771:Mlxipl
|
APN |
5 |
135,161,632 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01872:Mlxipl
|
APN |
5 |
135,142,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02694:Mlxipl
|
APN |
5 |
135,152,872 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03070:Mlxipl
|
APN |
5 |
135,161,307 (GRCm39) |
missense |
possibly damaging |
0.93 |
Scarlet
|
UTSW |
5 |
135,162,884 (GRCm39) |
missense |
possibly damaging |
0.93 |
H8441:Mlxipl
|
UTSW |
5 |
135,152,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03054:Mlxipl
|
UTSW |
5 |
135,162,110 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0003:Mlxipl
|
UTSW |
5 |
135,162,043 (GRCm39) |
unclassified |
probably benign |
|
R0126:Mlxipl
|
UTSW |
5 |
135,161,177 (GRCm39) |
missense |
probably damaging |
0.96 |
R0458:Mlxipl
|
UTSW |
5 |
135,162,224 (GRCm39) |
missense |
probably benign |
0.33 |
R0513:Mlxipl
|
UTSW |
5 |
135,166,117 (GRCm39) |
missense |
probably benign |
0.33 |
R0580:Mlxipl
|
UTSW |
5 |
135,152,829 (GRCm39) |
missense |
probably benign |
0.01 |
R0744:Mlxipl
|
UTSW |
5 |
135,161,329 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0827:Mlxipl
|
UTSW |
5 |
135,161,592 (GRCm39) |
missense |
probably benign |
0.00 |
R1052:Mlxipl
|
UTSW |
5 |
135,142,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R1241:Mlxipl
|
UTSW |
5 |
135,161,572 (GRCm39) |
missense |
probably benign |
0.01 |
R1795:Mlxipl
|
UTSW |
5 |
135,136,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Mlxipl
|
UTSW |
5 |
135,162,422 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2038:Mlxipl
|
UTSW |
5 |
135,135,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R2064:Mlxipl
|
UTSW |
5 |
135,161,631 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2069:Mlxipl
|
UTSW |
5 |
135,135,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R2081:Mlxipl
|
UTSW |
5 |
135,142,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R2095:Mlxipl
|
UTSW |
5 |
135,150,974 (GRCm39) |
splice site |
probably benign |
|
R3114:Mlxipl
|
UTSW |
5 |
135,162,516 (GRCm39) |
splice site |
probably benign |
|
R4018:Mlxipl
|
UTSW |
5 |
135,161,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R4090:Mlxipl
|
UTSW |
5 |
135,161,381 (GRCm39) |
missense |
probably benign |
0.33 |
R4321:Mlxipl
|
UTSW |
5 |
135,164,304 (GRCm39) |
nonsense |
probably null |
|
R4414:Mlxipl
|
UTSW |
5 |
135,166,253 (GRCm39) |
unclassified |
probably benign |
|
R5706:Mlxipl
|
UTSW |
5 |
135,162,458 (GRCm39) |
missense |
probably benign |
0.33 |
R6088:Mlxipl
|
UTSW |
5 |
135,162,884 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6508:Mlxipl
|
UTSW |
5 |
135,157,474 (GRCm39) |
missense |
probably benign |
0.03 |
R6704:Mlxipl
|
UTSW |
5 |
135,166,094 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7060:Mlxipl
|
UTSW |
5 |
135,161,169 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7095:Mlxipl
|
UTSW |
5 |
135,162,884 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7128:Mlxipl
|
UTSW |
5 |
135,162,705 (GRCm39) |
missense |
probably damaging |
0.98 |
R7510:Mlxipl
|
UTSW |
5 |
135,161,972 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7669:Mlxipl
|
UTSW |
5 |
135,161,224 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7737:Mlxipl
|
UTSW |
5 |
135,164,235 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7806:Mlxipl
|
UTSW |
5 |
135,163,397 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7910:Mlxipl
|
UTSW |
5 |
135,161,263 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8118:Mlxipl
|
UTSW |
5 |
135,166,102 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8363:Mlxipl
|
UTSW |
5 |
135,135,930 (GRCm39) |
missense |
probably benign |
0.18 |
R8701:Mlxipl
|
UTSW |
5 |
135,136,045 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8725:Mlxipl
|
UTSW |
5 |
135,157,483 (GRCm39) |
missense |
probably benign |
0.01 |
R9235:Mlxipl
|
UTSW |
5 |
135,157,541 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9566:Mlxipl
|
UTSW |
5 |
135,152,616 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9727:Mlxipl
|
UTSW |
5 |
135,150,388 (GRCm39) |
nonsense |
probably null |
|
|