Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
A |
T |
16: 4,682,200 (GRCm39) |
H1010L |
probably benign |
Het |
A2ml1 |
C |
A |
6: 128,545,706 (GRCm39) |
E474* |
probably null |
Het |
Agtr1b |
T |
C |
3: 20,369,838 (GRCm39) |
H256R |
probably damaging |
Het |
Amacr |
C |
T |
15: 10,982,032 (GRCm39) |
A46V |
possibly damaging |
Het |
Atosb |
A |
T |
4: 43,034,647 (GRCm39) |
|
probably benign |
Het |
Cabp5 |
A |
T |
7: 13,135,260 (GRCm39) |
M67L |
probably damaging |
Het |
Caskin2 |
T |
C |
11: 115,691,842 (GRCm39) |
E981G |
probably damaging |
Het |
Ccdc88a |
A |
G |
11: 29,411,042 (GRCm39) |
|
probably benign |
Het |
Cd180 |
A |
G |
13: 102,839,382 (GRCm39) |
|
probably benign |
Het |
Cd200l1 |
T |
A |
16: 45,264,536 (GRCm39) |
|
probably benign |
Het |
Cemip |
G |
A |
7: 83,613,318 (GRCm39) |
H627Y |
probably damaging |
Het |
Cep131 |
G |
T |
11: 119,964,588 (GRCm39) |
H289Q |
probably damaging |
Het |
Cep350 |
G |
A |
1: 155,836,941 (GRCm39) |
|
probably benign |
Het |
Cfap52 |
A |
T |
11: 67,840,425 (GRCm39) |
C169S |
probably benign |
Het |
Cps1 |
A |
T |
1: 67,205,608 (GRCm39) |
T544S |
possibly damaging |
Het |
Cul7 |
T |
C |
17: 46,962,929 (GRCm39) |
S187P |
probably damaging |
Het |
Dhx40 |
C |
A |
11: 86,661,993 (GRCm39) |
R688L |
probably damaging |
Het |
E330034G19Rik |
C |
A |
14: 24,356,985 (GRCm39) |
Q174K |
probably benign |
Het |
Efna5 |
T |
C |
17: 63,188,031 (GRCm39) |
Y32C |
probably damaging |
Het |
Ethe1 |
A |
G |
7: 24,307,314 (GRCm39) |
H176R |
probably benign |
Het |
Exoc3 |
A |
G |
13: 74,330,394 (GRCm39) |
|
probably null |
Het |
Fam135b |
T |
A |
15: 71,362,686 (GRCm39) |
N232Y |
possibly damaging |
Het |
Fndc9 |
C |
T |
11: 46,128,984 (GRCm39) |
L168F |
probably damaging |
Het |
Fpr-rs3 |
G |
A |
17: 20,844,283 (GRCm39) |
A286V |
probably damaging |
Het |
Immt |
T |
A |
6: 71,823,467 (GRCm39) |
|
probably benign |
Het |
Ipo8 |
A |
T |
6: 148,688,221 (GRCm39) |
L747H |
probably damaging |
Het |
Ireb2 |
A |
T |
9: 54,807,267 (GRCm39) |
N610Y |
probably damaging |
Het |
Irs2 |
A |
G |
8: 11,054,592 (GRCm39) |
V1280A |
probably damaging |
Het |
Kcnj3 |
T |
A |
2: 55,485,276 (GRCm39) |
M458K |
probably benign |
Het |
Kl |
A |
G |
5: 150,904,409 (GRCm39) |
K387R |
possibly damaging |
Het |
L3mbtl2 |
C |
A |
15: 81,568,487 (GRCm39) |
|
probably benign |
Het |
Lamb1 |
A |
C |
12: 31,348,914 (GRCm39) |
I649L |
probably benign |
Het |
Lipm |
A |
C |
19: 34,093,906 (GRCm39) |
L274F |
probably benign |
Het |
Lrfn3 |
A |
G |
7: 30,060,216 (GRCm39) |
V3A |
probably benign |
Het |
Lrrc8c |
A |
C |
5: 105,754,894 (GRCm39) |
D223A |
probably damaging |
Het |
Ltn1 |
C |
A |
16: 87,212,898 (GRCm39) |
K554N |
probably benign |
Het |
Mertk |
T |
C |
2: 128,613,403 (GRCm39) |
I473T |
probably benign |
Het |
Mfsd12 |
C |
A |
10: 81,197,243 (GRCm39) |
N245K |
probably benign |
Het |
Mmp16 |
A |
G |
4: 17,987,705 (GRCm39) |
D89G |
probably damaging |
Het |
Myo5a |
T |
A |
9: 75,087,394 (GRCm39) |
N1083K |
probably benign |
Het |
Ncapd3 |
C |
T |
9: 26,999,294 (GRCm39) |
A1290V |
probably benign |
Het |
Nefm |
A |
G |
14: 68,362,070 (GRCm39) |
S65P |
probably damaging |
Het |
Nt5c2 |
C |
T |
19: 46,886,064 (GRCm39) |
R220H |
probably damaging |
Het |
Or4c102 |
T |
A |
2: 88,422,353 (GRCm39) |
D68E |
probably benign |
Het |
Osbpl1a |
A |
T |
18: 12,892,501 (GRCm39) |
S438R |
probably damaging |
Het |
Pcdhb5 |
T |
C |
18: 37,453,820 (GRCm39) |
S67P |
possibly damaging |
Het |
Per3 |
A |
T |
4: 151,118,409 (GRCm39) |
I228N |
probably damaging |
Het |
Pnpla7 |
T |
G |
2: 24,870,129 (GRCm39) |
|
probably benign |
Het |
Ppp1r15b |
G |
T |
1: 133,064,391 (GRCm39) |
|
probably benign |
Het |
Psmd2 |
G |
T |
16: 20,479,176 (GRCm39) |
L678F |
probably null |
Het |
Ptch2 |
A |
G |
4: 116,963,340 (GRCm39) |
|
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,312,158 (GRCm39) |
D959E |
probably benign |
Het |
Rph3al |
C |
T |
11: 75,724,227 (GRCm39) |
|
probably null |
Het |
Sec31b |
T |
A |
19: 44,512,992 (GRCm39) |
E499V |
probably damaging |
Het |
Sel1l |
T |
C |
12: 91,778,663 (GRCm39) |
I667M |
probably benign |
Het |
Sel1l |
C |
A |
12: 91,780,719 (GRCm39) |
V641L |
possibly damaging |
Het |
Slc7a1 |
T |
A |
5: 148,288,879 (GRCm39) |
I123F |
probably damaging |
Het |
Smarca2 |
G |
A |
19: 26,659,275 (GRCm39) |
R855Q |
possibly damaging |
Het |
Sphk1 |
G |
T |
11: 116,427,184 (GRCm39) |
|
probably benign |
Het |
Spink12 |
C |
A |
18: 44,237,755 (GRCm39) |
S11* |
probably null |
Het |
Sstr2 |
A |
T |
11: 113,516,445 (GRCm39) |
I342F |
probably benign |
Het |
Stxbp1 |
T |
C |
2: 32,709,860 (GRCm39) |
T78A |
probably benign |
Het |
Trim11 |
T |
A |
11: 58,881,410 (GRCm39) |
S434R |
probably damaging |
Het |
Ubr2 |
T |
C |
17: 47,266,812 (GRCm39) |
E1113G |
probably damaging |
Het |
Upb1 |
T |
A |
10: 75,264,188 (GRCm39) |
|
probably benign |
Het |
Vit |
T |
A |
17: 78,932,266 (GRCm39) |
C458S |
probably damaging |
Het |
Vmn1r58 |
T |
C |
7: 5,414,165 (GRCm39) |
I22V |
probably benign |
Het |
Vps25 |
T |
C |
11: 101,149,731 (GRCm39) |
|
probably benign |
Het |
Wbp2 |
G |
T |
11: 115,973,211 (GRCm39) |
D65E |
possibly damaging |
Het |
Wdr72 |
A |
G |
9: 74,124,588 (GRCm39) |
D980G |
probably benign |
Het |
Xkr8 |
A |
C |
4: 132,458,228 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ipo7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01796:Ipo7
|
APN |
7 |
109,629,055 (GRCm39) |
intron |
probably benign |
|
IGL02472:Ipo7
|
APN |
7 |
109,640,060 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02502:Ipo7
|
APN |
7 |
109,650,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02514:Ipo7
|
APN |
7 |
109,648,035 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02535:Ipo7
|
APN |
7 |
109,653,233 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02961:Ipo7
|
APN |
7 |
109,646,223 (GRCm39) |
missense |
probably benign |
0.02 |
R0089:Ipo7
|
UTSW |
7 |
109,649,972 (GRCm39) |
intron |
probably benign |
|
R0355:Ipo7
|
UTSW |
7 |
109,648,868 (GRCm39) |
missense |
probably benign |
0.00 |
R1342:Ipo7
|
UTSW |
7 |
109,629,011 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1405:Ipo7
|
UTSW |
7 |
109,638,456 (GRCm39) |
missense |
probably damaging |
0.97 |
R1405:Ipo7
|
UTSW |
7 |
109,638,456 (GRCm39) |
missense |
probably damaging |
0.97 |
R1405:Ipo7
|
UTSW |
7 |
109,629,048 (GRCm39) |
missense |
probably benign |
0.03 |
R1405:Ipo7
|
UTSW |
7 |
109,629,048 (GRCm39) |
missense |
probably benign |
0.03 |
R1791:Ipo7
|
UTSW |
7 |
109,626,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R1838:Ipo7
|
UTSW |
7 |
109,641,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Ipo7
|
UTSW |
7 |
109,650,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R2120:Ipo7
|
UTSW |
7 |
109,648,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R4366:Ipo7
|
UTSW |
7 |
109,647,423 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4366:Ipo7
|
UTSW |
7 |
109,628,919 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4805:Ipo7
|
UTSW |
7 |
109,650,691 (GRCm39) |
missense |
probably benign |
0.16 |
R5228:Ipo7
|
UTSW |
7 |
109,645,969 (GRCm39) |
missense |
probably benign |
0.00 |
R5903:Ipo7
|
UTSW |
7 |
109,650,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Ipo7
|
UTSW |
7 |
109,648,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Ipo7
|
UTSW |
7 |
109,648,267 (GRCm39) |
missense |
probably benign |
0.00 |
R6335:Ipo7
|
UTSW |
7 |
109,617,675 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6360:Ipo7
|
UTSW |
7 |
109,626,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Ipo7
|
UTSW |
7 |
109,646,272 (GRCm39) |
missense |
probably damaging |
0.98 |
R7132:Ipo7
|
UTSW |
7 |
109,653,254 (GRCm39) |
missense |
probably benign |
0.17 |
R7329:Ipo7
|
UTSW |
7 |
109,648,224 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7491:Ipo7
|
UTSW |
7 |
109,638,401 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7763:Ipo7
|
UTSW |
7 |
109,652,006 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8070:Ipo7
|
UTSW |
7 |
109,652,014 (GRCm39) |
missense |
probably benign |
0.01 |
R8479:Ipo7
|
UTSW |
7 |
109,638,452 (GRCm39) |
missense |
probably benign |
0.23 |
R8547:Ipo7
|
UTSW |
7 |
109,652,000 (GRCm39) |
missense |
probably benign |
0.01 |
R8839:Ipo7
|
UTSW |
7 |
109,641,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Ipo7
|
UTSW |
7 |
109,643,943 (GRCm39) |
critical splice donor site |
probably null |
|
R9024:Ipo7
|
UTSW |
7 |
109,643,943 (GRCm39) |
critical splice donor site |
probably null |
|
R9089:Ipo7
|
UTSW |
7 |
109,643,666 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9245:Ipo7
|
UTSW |
7 |
109,643,826 (GRCm39) |
missense |
probably damaging |
1.00 |
RF017:Ipo7
|
UTSW |
7 |
109,648,001 (GRCm39) |
missense |
probably benign |
0.00 |
X0062:Ipo7
|
UTSW |
7 |
109,652,093 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Ipo7
|
UTSW |
7 |
109,651,941 (GRCm39) |
missense |
probably damaging |
0.97 |
|