Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot3 |
C |
A |
12: 84,105,561 (GRCm39) |
C251* |
probably null |
Het |
Acsbg1 |
A |
G |
9: 54,529,789 (GRCm39) |
C273R |
probably damaging |
Het |
Adh6a |
A |
G |
3: 138,031,884 (GRCm39) |
T259A |
probably damaging |
Het |
Aknad1 |
A |
G |
3: 108,689,255 (GRCm39) |
H639R |
possibly damaging |
Het |
Alkal2 |
G |
T |
12: 30,934,850 (GRCm39) |
G23V |
probably damaging |
Het |
Ampd3 |
A |
G |
7: 110,399,937 (GRCm39) |
R342G |
probably damaging |
Het |
Arid5b |
G |
T |
10: 67,933,217 (GRCm39) |
A895E |
probably damaging |
Het |
BB014433 |
GCACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTACACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTGCACACAGCTTTGG |
GCACACAGCTTTGGAGGTGTACACACCCGGGTTGGGGCCTCTGCACACAGCTTTGG |
8: 15,092,160 (GRCm39) |
|
probably benign |
Het |
Bmp8a |
G |
T |
4: 123,236,482 (GRCm39) |
P7Q |
unknown |
Het |
Boll |
A |
C |
1: 55,362,837 (GRCm39) |
V187G |
possibly damaging |
Het |
Ccdc162 |
A |
T |
10: 41,457,306 (GRCm39) |
C1544S |
probably benign |
Het |
Cmss1 |
A |
C |
16: 57,127,757 (GRCm39) |
M182R |
possibly damaging |
Het |
Cntn3 |
T |
C |
6: 102,186,254 (GRCm39) |
M578V |
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,286,032 (GRCm39) |
W2718R |
probably damaging |
Het |
Dsg1a |
T |
A |
18: 20,466,831 (GRCm39) |
I567N |
probably damaging |
Het |
Epc2 |
T |
A |
2: 49,412,527 (GRCm39) |
D168E |
probably damaging |
Het |
Ern2 |
G |
A |
7: 121,780,515 (GRCm39) |
Q162* |
probably null |
Het |
F11r |
G |
T |
1: 171,265,111 (GRCm39) |
|
probably benign |
Het |
Fcgrt |
T |
C |
7: 44,751,987 (GRCm39) |
Y59C |
probably damaging |
Het |
Fmn2 |
G |
T |
1: 174,436,011 (GRCm39) |
E661* |
probably null |
Het |
Gbp4 |
T |
A |
5: 105,266,328 (GRCm39) |
Q571L |
probably benign |
Het |
Gm29106 |
A |
T |
1: 118,126,593 (GRCm39) |
H95L |
probably damaging |
Het |
Gphn |
G |
A |
12: 78,711,280 (GRCm39) |
V621M |
probably damaging |
Het |
Grwd1 |
T |
C |
7: 45,480,036 (GRCm39) |
Y57C |
probably damaging |
Het |
Insyn2b |
C |
A |
11: 34,351,964 (GRCm39) |
A2D |
probably damaging |
Het |
Irs2 |
G |
A |
8: 11,054,848 (GRCm39) |
Q1195* |
probably null |
Het |
Itpr1 |
G |
C |
6: 108,487,699 (GRCm39) |
C2375S |
probably benign |
Het |
Kcnmb4 |
A |
T |
10: 116,282,290 (GRCm39) |
Y136N |
probably benign |
Het |
Matn2 |
C |
T |
15: 34,345,511 (GRCm39) |
P173S |
probably damaging |
Het |
Med17 |
A |
C |
9: 15,173,655 (GRCm39) |
D606E |
probably damaging |
Het |
Mpl |
A |
G |
4: 118,301,254 (GRCm39) |
V537A |
|
Het |
Mrpl1 |
C |
G |
5: 96,374,226 (GRCm39) |
A167G |
probably benign |
Het |
Mrpl21 |
T |
C |
19: 3,342,487 (GRCm39) |
F206S |
unknown |
Het |
Msh6 |
T |
A |
17: 88,292,598 (GRCm39) |
M451K |
probably damaging |
Het |
Myo10 |
T |
C |
15: 25,804,481 (GRCm39) |
I1592T |
possibly damaging |
Het |
Naip1 |
A |
T |
13: 100,562,374 (GRCm39) |
D930E |
possibly damaging |
Het |
Necap2 |
T |
C |
4: 140,795,534 (GRCm39) |
I242V |
probably benign |
Het |
Nfya |
A |
G |
17: 48,699,073 (GRCm39) |
V240A |
possibly damaging |
Het |
Olfml2b |
A |
G |
1: 170,496,353 (GRCm39) |
D328G |
probably damaging |
Het |
Or10ak13 |
A |
T |
4: 118,639,203 (GRCm39) |
M193K |
probably benign |
Het |
Or4k35 |
T |
A |
2: 111,099,983 (GRCm39) |
H243L |
probably damaging |
Het |
Or5b24 |
T |
G |
19: 12,912,399 (GRCm39) |
V99G |
probably benign |
Het |
Or5p53 |
T |
G |
7: 107,532,892 (GRCm39) |
L55R |
probably damaging |
Het |
Phf8-ps |
C |
A |
17: 33,286,038 (GRCm39) |
A255S |
probably benign |
Het |
Pkd1l3 |
T |
C |
8: 110,361,982 (GRCm39) |
V1018A |
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,596,842 (GRCm39) |
L761P |
probably damaging |
Het |
Ppp1r36 |
T |
C |
12: 76,485,215 (GRCm39) |
S313P |
possibly damaging |
Het |
Ptpru |
C |
A |
4: 131,535,646 (GRCm39) |
G444C |
probably damaging |
Het |
Rfxank |
A |
T |
8: 70,587,960 (GRCm39) |
V149D |
probably damaging |
Het |
Rimbp2 |
G |
A |
5: 128,857,395 (GRCm39) |
H819Y |
probably damaging |
Het |
Sgms1 |
T |
C |
19: 32,101,821 (GRCm39) |
Y395C |
probably damaging |
Het |
Siae |
G |
A |
9: 37,542,901 (GRCm39) |
|
probably null |
Het |
Slc46a2 |
T |
A |
4: 59,914,713 (GRCm39) |
D70V |
probably damaging |
Het |
Smpdl3a |
A |
C |
10: 57,677,032 (GRCm39) |
L43F |
possibly damaging |
Het |
Spcs1 |
T |
A |
14: 30,722,103 (GRCm39) |
D146V |
possibly damaging |
Het |
Srcin1 |
T |
C |
11: 97,442,804 (GRCm39) |
D8G |
probably damaging |
Het |
Stra6 |
G |
T |
9: 58,056,488 (GRCm39) |
L373F |
probably damaging |
Het |
Tacc1 |
A |
T |
8: 25,672,299 (GRCm39) |
S310T |
possibly damaging |
Het |
Tnfaip3 |
A |
G |
10: 18,887,258 (GRCm39) |
V89A |
probably damaging |
Het |
Top1 |
C |
T |
2: 160,488,009 (GRCm39) |
|
probably benign |
Het |
Trappc13 |
T |
G |
13: 104,297,509 (GRCm39) |
I132L |
probably benign |
Het |
Trpt1 |
C |
T |
19: 6,976,349 (GRCm39) |
Q249* |
probably null |
Het |
Tsnaxip1 |
A |
C |
8: 106,569,179 (GRCm39) |
K510Q |
probably damaging |
Het |
Usp39 |
A |
T |
6: 72,305,657 (GRCm39) |
N375K |
probably benign |
Het |
Vldlr |
T |
A |
19: 27,212,258 (GRCm39) |
C91S |
probably damaging |
Het |
Vmn1r232 |
T |
A |
17: 21,134,239 (GRCm39) |
L120F |
probably benign |
Het |
Vmn2r71 |
T |
C |
7: 85,264,707 (GRCm39) |
V13A |
probably benign |
Het |
Wdr11 |
T |
A |
7: 129,208,412 (GRCm39) |
V389E |
possibly damaging |
Het |
Wsb2 |
A |
T |
5: 117,514,766 (GRCm39) |
I321F |
possibly damaging |
Het |
Zan |
A |
T |
5: 137,389,949 (GRCm39) |
V4841E |
unknown |
Het |
Zfy1 |
A |
T |
Y: 725,723 (GRCm39) |
F681I |
possibly damaging |
Het |
Zpld1 |
C |
A |
16: 55,067,017 (GRCm39) |
E179D |
probably benign |
Het |
|
Other mutations in Tlr12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00568:Tlr12
|
APN |
4 |
128,511,215 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00654:Tlr12
|
APN |
4 |
128,511,233 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01290:Tlr12
|
APN |
4 |
128,511,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01406:Tlr12
|
APN |
4 |
128,510,132 (GRCm39) |
nonsense |
probably null |
|
IGL01550:Tlr12
|
APN |
4 |
128,509,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02590:Tlr12
|
APN |
4 |
128,511,182 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02592:Tlr12
|
APN |
4 |
128,511,479 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02635:Tlr12
|
APN |
4 |
128,510,609 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02714:Tlr12
|
APN |
4 |
128,511,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03104:Tlr12
|
APN |
4 |
128,509,685 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03131:Tlr12
|
APN |
4 |
128,509,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03329:Tlr12
|
APN |
4 |
128,510,645 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03354:Tlr12
|
APN |
4 |
128,509,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R0848:Tlr12
|
UTSW |
4 |
128,510,084 (GRCm39) |
missense |
probably benign |
0.05 |
R1536:Tlr12
|
UTSW |
4 |
128,511,545 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1807:Tlr12
|
UTSW |
4 |
128,511,229 (GRCm39) |
missense |
probably benign |
0.21 |
R1989:Tlr12
|
UTSW |
4 |
128,510,862 (GRCm39) |
missense |
probably benign |
0.04 |
R2905:Tlr12
|
UTSW |
4 |
128,509,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R3870:Tlr12
|
UTSW |
4 |
128,510,361 (GRCm39) |
missense |
probably benign |
0.00 |
R4026:Tlr12
|
UTSW |
4 |
128,510,301 (GRCm39) |
missense |
probably benign |
0.00 |
R4296:Tlr12
|
UTSW |
4 |
128,511,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4398:Tlr12
|
UTSW |
4 |
128,509,988 (GRCm39) |
missense |
probably benign |
0.09 |
R4528:Tlr12
|
UTSW |
4 |
128,511,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4559:Tlr12
|
UTSW |
4 |
128,509,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R4599:Tlr12
|
UTSW |
4 |
128,511,125 (GRCm39) |
missense |
probably benign |
0.06 |
R4999:Tlr12
|
UTSW |
4 |
128,511,473 (GRCm39) |
missense |
probably benign |
0.38 |
R5054:Tlr12
|
UTSW |
4 |
128,511,063 (GRCm39) |
nonsense |
probably null |
|
R5177:Tlr12
|
UTSW |
4 |
128,512,169 (GRCm39) |
missense |
probably damaging |
0.96 |
R5207:Tlr12
|
UTSW |
4 |
128,510,502 (GRCm39) |
nonsense |
probably null |
|
R5533:Tlr12
|
UTSW |
4 |
128,509,656 (GRCm39) |
missense |
probably damaging |
0.99 |
R6484:Tlr12
|
UTSW |
4 |
128,509,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6568:Tlr12
|
UTSW |
4 |
128,511,785 (GRCm39) |
missense |
probably benign |
0.10 |
R6821:Tlr12
|
UTSW |
4 |
128,510,685 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7465:Tlr12
|
UTSW |
4 |
128,509,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7594:Tlr12
|
UTSW |
4 |
128,511,473 (GRCm39) |
missense |
probably benign |
0.38 |
R7810:Tlr12
|
UTSW |
4 |
128,510,501 (GRCm39) |
missense |
probably benign |
0.00 |
R7957:Tlr12
|
UTSW |
4 |
128,510,483 (GRCm39) |
missense |
probably benign |
0.33 |
R8258:Tlr12
|
UTSW |
4 |
128,511,492 (GRCm39) |
missense |
probably benign |
0.38 |
R8259:Tlr12
|
UTSW |
4 |
128,511,492 (GRCm39) |
missense |
probably benign |
0.38 |
R8422:Tlr12
|
UTSW |
4 |
128,510,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R9098:Tlr12
|
UTSW |
4 |
128,510,870 (GRCm39) |
missense |
probably benign |
0.00 |
|