Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
G |
3: 124,201,334 (GRCm39) |
I443T |
probably damaging |
Het |
2310002L09Rik |
A |
G |
4: 73,861,091 (GRCm39) |
C170R |
possibly damaging |
Het |
4933415A04Rik |
GTGTGTGTGTATGTGTGTGT |
GTGTGTGTGT |
11: 43,478,237 (GRCm39) |
|
probably null |
Het |
A2m |
A |
C |
6: 121,637,063 (GRCm39) |
T809P |
possibly damaging |
Het |
Abca12 |
T |
C |
1: 71,374,887 (GRCm39) |
D340G |
probably benign |
Het |
Abcg8 |
A |
T |
17: 84,999,919 (GRCm39) |
D191V |
probably damaging |
Het |
Acan |
G |
T |
7: 78,739,356 (GRCm39) |
V255F |
probably damaging |
Het |
Ace |
G |
A |
11: 105,879,663 (GRCm39) |
V1248I |
probably benign |
Het |
Adgre1 |
A |
T |
17: 57,709,519 (GRCm39) |
Q87L |
unknown |
Het |
Adgrl1 |
G |
A |
8: 84,665,617 (GRCm39) |
V1435M |
probably benign |
Het |
Ano8 |
T |
C |
8: 71,934,933 (GRCm39) |
D423G |
probably damaging |
Het |
Aox3 |
T |
C |
1: 58,219,810 (GRCm39) |
Y1137H |
probably damaging |
Het |
Arl5a |
T |
C |
2: 52,295,068 (GRCm39) |
D114G |
probably benign |
Het |
B3galt9 |
T |
G |
2: 34,728,437 (GRCm39) |
C79G |
probably damaging |
Het |
Baiap2l2 |
G |
T |
15: 79,143,911 (GRCm39) |
N394K |
probably benign |
Het |
Cap1 |
A |
T |
4: 122,756,467 (GRCm39) |
C355S |
probably damaging |
Het |
Ccdc25 |
A |
T |
14: 66,077,933 (GRCm39) |
D22V |
probably damaging |
Het |
Ceacam2 |
T |
C |
7: 25,238,076 (GRCm39) |
D116G |
probably damaging |
Het |
Clec4b2 |
A |
G |
6: 123,149,974 (GRCm39) |
|
probably benign |
Het |
Coq8b |
T |
C |
7: 26,949,962 (GRCm39) |
I347T |
probably damaging |
Het |
Ctbp2 |
C |
A |
7: 132,591,789 (GRCm39) |
V338L |
probably benign |
Het |
Cyp2d22 |
A |
G |
15: 82,258,612 (GRCm39) |
V83A |
possibly damaging |
Het |
Daam1 |
G |
A |
12: 72,024,423 (GRCm39) |
R797H |
probably benign |
Het |
Dab1 |
C |
A |
4: 104,577,756 (GRCm39) |
S275* |
probably null |
Het |
Dgkz |
T |
C |
2: 91,767,404 (GRCm39) |
E863G |
probably benign |
Het |
Dhx34 |
G |
A |
7: 15,946,789 (GRCm39) |
A515V |
possibly damaging |
Het |
Dnah14 |
T |
C |
1: 181,530,049 (GRCm39) |
|
probably null |
Het |
Dnmt3b |
C |
A |
2: 153,514,140 (GRCm39) |
N384K |
probably benign |
Het |
Dock5 |
A |
G |
14: 68,033,454 (GRCm39) |
Y972H |
probably benign |
Het |
Etv5 |
A |
T |
16: 22,231,597 (GRCm39) |
Y138* |
probably null |
Het |
Fdps |
A |
G |
3: 89,008,397 (GRCm39) |
S4P |
probably damaging |
Het |
Gart |
A |
G |
16: 91,419,853 (GRCm39) |
F885L |
possibly damaging |
Het |
Gm32687 |
A |
T |
10: 81,715,328 (GRCm39) |
H240L |
probably damaging |
Het |
Gm4553 |
C |
T |
7: 141,719,384 (GRCm39) |
G15R |
unknown |
Het |
Gm572 |
C |
T |
4: 148,753,408 (GRCm39) |
T351M |
probably damaging |
Het |
Gpr3 |
A |
T |
4: 132,937,748 (GRCm39) |
L308Q |
probably damaging |
Het |
Gpsm2 |
A |
G |
3: 108,609,097 (GRCm39) |
V174A |
probably benign |
Het |
Gucy1a1 |
T |
C |
3: 82,002,096 (GRCm39) |
H661R |
unknown |
Het |
Heatr4 |
A |
T |
12: 84,004,499 (GRCm39) |
M774K |
probably damaging |
Het |
Hmgcr |
A |
G |
13: 96,799,605 (GRCm39) |
I163T |
possibly damaging |
Het |
Ift81 |
C |
T |
5: 122,747,394 (GRCm39) |
V91M |
probably damaging |
Het |
Igsf10 |
G |
T |
3: 59,238,964 (GRCm39) |
Q406K |
probably damaging |
Het |
Il10ra |
A |
G |
9: 45,171,697 (GRCm39) |
V257A |
probably benign |
Het |
Ina |
A |
T |
19: 47,012,082 (GRCm39) |
K500I |
|
Het |
Lce1i |
A |
T |
3: 92,685,066 (GRCm39) |
C37S |
unknown |
Het |
Lrrc59 |
A |
T |
11: 94,525,811 (GRCm39) |
D133V |
probably damaging |
Het |
Magi3 |
A |
G |
3: 103,941,354 (GRCm39) |
I867T |
probably damaging |
Het |
Mmaa |
T |
A |
8: 79,995,830 (GRCm39) |
R298W |
probably damaging |
Het |
Mon1a |
G |
T |
9: 107,777,327 (GRCm39) |
V77F |
probably benign |
Het |
Mrc2 |
A |
G |
11: 105,237,285 (GRCm39) |
T1030A |
probably benign |
Het |
Mrps27 |
T |
A |
13: 99,541,504 (GRCm39) |
S162T |
probably benign |
Het |
Mtmr12 |
T |
A |
15: 12,245,097 (GRCm39) |
M204K |
probably damaging |
Het |
Mtus1 |
A |
G |
8: 41,507,687 (GRCm39) |
I21T |
possibly damaging |
Het |
Myh2 |
T |
C |
11: 67,085,690 (GRCm39) |
V1844A |
probably benign |
Het |
Myh7 |
C |
G |
14: 55,226,258 (GRCm39) |
D461H |
probably damaging |
Het |
Nbr1 |
T |
G |
11: 101,447,067 (GRCm39) |
F18V |
probably damaging |
Het |
Npy2r |
T |
C |
3: 82,447,689 (GRCm39) |
N362S |
probably benign |
Het |
Ocln |
T |
A |
13: 100,676,106 (GRCm39) |
Y129F |
probably damaging |
Het |
Or2t1 |
T |
C |
14: 14,328,384 (GRCm38) |
I91T |
probably damaging |
Het |
Or4c10 |
T |
C |
2: 89,760,225 (GRCm39) |
I24T |
probably benign |
Het |
Or8c20 |
A |
G |
9: 38,260,573 (GRCm39) |
M59V |
probably benign |
Het |
Pik3c2b |
T |
G |
1: 133,007,579 (GRCm39) |
|
probably null |
Het |
Prss39 |
A |
G |
1: 34,541,709 (GRCm39) |
D262G |
probably damaging |
Het |
Ptk7 |
T |
A |
17: 46,882,569 (GRCm39) |
D886V |
possibly damaging |
Het |
Ptprg |
T |
A |
14: 12,226,452 (GRCm38) |
D1348E |
probably damaging |
Het |
Rabgap1 |
T |
C |
2: 37,427,339 (GRCm39) |
I640T |
possibly damaging |
Het |
Rogdi |
A |
G |
16: 4,827,098 (GRCm39) |
Y303H |
probably damaging |
Het |
Rps6kb1 |
A |
T |
11: 86,404,148 (GRCm39) |
M283K |
probably damaging |
Het |
Sardh |
T |
A |
2: 27,131,529 (GRCm39) |
T188S |
possibly damaging |
Het |
Sebox |
A |
G |
11: 78,394,919 (GRCm39) |
E87G |
probably damaging |
Het |
Smchd1 |
A |
T |
17: 71,665,193 (GRCm39) |
M1830K |
probably damaging |
Het |
Spata31h1 |
A |
C |
10: 82,126,366 (GRCm39) |
S2215A |
possibly damaging |
Het |
Spink8 |
G |
A |
9: 109,645,848 (GRCm39) |
V7I |
probably benign |
Het |
Src |
G |
A |
2: 157,299,164 (GRCm39) |
V54M |
probably benign |
Het |
Taar2 |
A |
G |
10: 23,816,621 (GRCm39) |
I54V |
probably benign |
Het |
Tpo |
A |
T |
12: 30,181,859 (GRCm39) |
V12E |
possibly damaging |
Het |
Txk |
T |
C |
5: 72,864,918 (GRCm39) |
D373G |
probably damaging |
Het |
Ubr5 |
G |
A |
15: 37,980,076 (GRCm39) |
A2434V |
probably null |
Het |
Vil1 |
C |
T |
1: 74,465,754 (GRCm39) |
T515M |
probably benign |
Het |
Wdr47 |
G |
T |
3: 108,525,837 (GRCm39) |
C120F |
probably damaging |
Het |
Ylpm1 |
C |
T |
12: 85,059,799 (GRCm39) |
P335L |
unknown |
Het |
Zfp148 |
T |
A |
16: 33,288,545 (GRCm39) |
I220N |
probably damaging |
Het |
Zfp992 |
A |
T |
4: 146,551,622 (GRCm39) |
K448* |
probably null |
Het |
Zfp994 |
T |
C |
17: 22,419,406 (GRCm39) |
I514M |
probably benign |
Het |
Zp2 |
A |
T |
7: 119,734,998 (GRCm39) |
I429N |
probably damaging |
Het |
|
Other mutations in CN725425 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01541:CN725425
|
APN |
15 |
91,129,955 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02176:CN725425
|
APN |
15 |
91,130,024 (GRCm39) |
missense |
probably benign |
|
3-1:CN725425
|
UTSW |
15 |
91,144,724 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0449:CN725425
|
UTSW |
15 |
91,123,147 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0554:CN725425
|
UTSW |
15 |
91,144,966 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1442:CN725425
|
UTSW |
15 |
91,123,158 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1670:CN725425
|
UTSW |
15 |
91,130,018 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1674:CN725425
|
UTSW |
15 |
91,131,124 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2425:CN725425
|
UTSW |
15 |
91,130,058 (GRCm39) |
missense |
probably damaging |
0.97 |
R3966:CN725425
|
UTSW |
15 |
91,126,890 (GRCm39) |
critical splice donor site |
probably null |
|
R4959:CN725425
|
UTSW |
15 |
91,129,904 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4973:CN725425
|
UTSW |
15 |
91,129,904 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5506:CN725425
|
UTSW |
15 |
91,120,029 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5512:CN725425
|
UTSW |
15 |
91,124,959 (GRCm39) |
missense |
probably benign |
|
R5726:CN725425
|
UTSW |
15 |
91,144,706 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5808:CN725425
|
UTSW |
15 |
91,129,847 (GRCm39) |
missense |
probably benign |
0.32 |
R5820:CN725425
|
UTSW |
15 |
91,144,900 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5945:CN725425
|
UTSW |
15 |
91,129,980 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6366:CN725425
|
UTSW |
15 |
91,131,124 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6441:CN725425
|
UTSW |
15 |
91,120,005 (GRCm39) |
missense |
probably benign |
0.33 |
R6484:CN725425
|
UTSW |
15 |
91,144,775 (GRCm39) |
missense |
probably benign |
0.32 |
R6523:CN725425
|
UTSW |
15 |
91,115,784 (GRCm39) |
missense |
probably benign |
0.01 |
R6721:CN725425
|
UTSW |
15 |
91,115,821 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6901:CN725425
|
UTSW |
15 |
91,124,966 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7341:CN725425
|
UTSW |
15 |
91,126,873 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7654:CN725425
|
UTSW |
15 |
91,123,638 (GRCm39) |
missense |
probably benign |
0.04 |
R7704:CN725425
|
UTSW |
15 |
91,119,993 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7880:CN725425
|
UTSW |
15 |
91,130,308 (GRCm39) |
nonsense |
probably null |
|
R8371:CN725425
|
UTSW |
15 |
91,124,973 (GRCm39) |
missense |
probably benign |
0.33 |
R8964:CN725425
|
UTSW |
15 |
91,119,972 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8968:CN725425
|
UTSW |
15 |
91,130,090 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9505:CN725425
|
UTSW |
15 |
91,124,867 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9632:CN725425
|
UTSW |
15 |
91,126,851 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9689:CN725425
|
UTSW |
15 |
91,120,030 (GRCm39) |
missense |
possibly damaging |
0.70 |
Z1088:CN725425
|
UTSW |
15 |
91,129,965 (GRCm39) |
missense |
possibly damaging |
0.95 |
|