Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
C |
6: 146,853,909 (GRCm39) |
I249M |
possibly damaging |
Het |
Abl1 |
G |
T |
2: 31,691,822 (GRCm39) |
A1114S |
probably damaging |
Het |
Acbd5 |
T |
C |
2: 22,989,733 (GRCm39) |
V452A |
probably damaging |
Het |
Armc12 |
A |
G |
17: 28,756,910 (GRCm39) |
D225G |
probably damaging |
Het |
Atad3a |
T |
A |
4: 155,840,139 (GRCm39) |
Q121H |
probably damaging |
Het |
Atosa |
A |
T |
9: 74,913,603 (GRCm39) |
T79S |
probably benign |
Het |
Bptf |
T |
A |
11: 106,963,873 (GRCm39) |
I1711F |
probably damaging |
Het |
C2cd4c |
A |
T |
10: 79,448,064 (GRCm39) |
I361N |
probably damaging |
Het |
Canx |
A |
G |
11: 50,199,221 (GRCm39) |
|
probably benign |
Het |
Ccdc127 |
C |
T |
13: 74,505,034 (GRCm39) |
T194I |
probably benign |
Het |
Cdc42ep3 |
T |
C |
17: 79,642,465 (GRCm39) |
K152E |
probably benign |
Het |
Cnbd2 |
T |
C |
2: 156,181,204 (GRCm39) |
|
probably null |
Het |
Cplane1 |
T |
A |
15: 8,248,853 (GRCm39) |
Y1801N |
possibly damaging |
Het |
Crybg1 |
T |
C |
10: 43,851,074 (GRCm39) |
N1599S |
probably benign |
Het |
Cyc1 |
T |
C |
15: 76,228,548 (GRCm39) |
V59A |
probably benign |
Het |
Cyp2j11 |
T |
C |
4: 96,183,117 (GRCm39) |
K484E |
probably benign |
Het |
Ddx60 |
T |
C |
8: 62,411,193 (GRCm39) |
|
probably benign |
Het |
Epg5 |
T |
C |
18: 78,005,642 (GRCm39) |
S711P |
probably damaging |
Het |
Espl1 |
A |
T |
15: 102,214,120 (GRCm39) |
Q649L |
probably benign |
Het |
Eya1 |
G |
A |
1: 14,374,638 (GRCm39) |
|
probably benign |
Het |
Fat2 |
T |
A |
11: 55,186,913 (GRCm39) |
Y1311F |
probably damaging |
Het |
Garin5b |
T |
A |
7: 4,760,687 (GRCm39) |
H675L |
possibly damaging |
Het |
Gins4 |
T |
C |
8: 23,717,144 (GRCm39) |
Y208C |
probably damaging |
Het |
Gsk3b |
T |
C |
16: 37,910,937 (GRCm39) |
V17A |
probably benign |
Het |
Gykl1 |
A |
T |
18: 52,827,833 (GRCm39) |
K347I |
probably benign |
Het |
Helz |
T |
A |
11: 107,483,666 (GRCm39) |
|
probably benign |
Het |
Hivep3 |
C |
T |
4: 119,953,772 (GRCm39) |
T696I |
possibly damaging |
Het |
Ifi27l2a |
G |
T |
12: 103,409,093 (GRCm39) |
|
probably benign |
Het |
Kif13a |
A |
G |
13: 46,944,987 (GRCm39) |
|
probably benign |
Het |
Kpna3 |
C |
T |
14: 61,620,669 (GRCm39) |
|
probably benign |
Het |
Mmp15 |
C |
G |
8: 96,096,190 (GRCm39) |
P327R |
probably benign |
Het |
Mrc1 |
A |
T |
2: 14,320,074 (GRCm39) |
T1003S |
probably benign |
Het |
Mtss1 |
T |
C |
15: 58,819,239 (GRCm39) |
D393G |
probably benign |
Het |
Olfm4 |
T |
A |
14: 80,258,843 (GRCm39) |
Y331N |
probably damaging |
Het |
Or10a49 |
T |
A |
7: 108,468,167 (GRCm39) |
N65Y |
probably damaging |
Het |
Or4c12b |
G |
C |
2: 89,646,725 (GRCm39) |
L12F |
probably damaging |
Het |
P2rx3 |
G |
C |
2: 84,855,294 (GRCm39) |
T54R |
possibly damaging |
Het |
Pacsin1 |
C |
T |
17: 27,924,937 (GRCm39) |
T217I |
probably damaging |
Het |
Phlpp1 |
A |
G |
1: 106,308,155 (GRCm39) |
|
probably null |
Het |
Pknox1 |
T |
C |
17: 31,811,066 (GRCm39) |
|
probably benign |
Het |
Plb1 |
A |
G |
5: 32,422,256 (GRCm39) |
R70G |
possibly damaging |
Het |
Rab3gap2 |
G |
A |
1: 184,980,101 (GRCm39) |
A340T |
probably damaging |
Het |
Rnf103 |
T |
A |
6: 71,485,983 (GRCm39) |
W205R |
probably damaging |
Het |
Rps6kc1 |
G |
A |
1: 190,530,923 (GRCm39) |
T936M |
probably damaging |
Het |
Spef2 |
T |
C |
15: 9,596,793 (GRCm39) |
|
probably benign |
Het |
Sstr4 |
A |
G |
2: 148,238,279 (GRCm39) |
S297G |
probably benign |
Het |
Timm8a1 |
C |
T |
X: 133,438,872 (GRCm39) |
E93K |
probably benign |
Het |
Uck1 |
A |
C |
2: 32,148,367 (GRCm39) |
Y150D |
probably damaging |
Het |
Yipf4 |
A |
G |
17: 74,805,300 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cdh15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Cdh15
|
APN |
8 |
123,592,062 (GRCm39) |
intron |
probably benign |
|
IGL01958:Cdh15
|
APN |
8 |
123,586,089 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02588:Cdh15
|
APN |
8 |
123,583,291 (GRCm39) |
nonsense |
probably null |
|
IGL02793:Cdh15
|
APN |
8 |
123,587,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Cdh15
|
APN |
8 |
123,592,111 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Cdh15
|
UTSW |
8 |
123,592,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:Cdh15
|
UTSW |
8 |
123,587,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Cdh15
|
UTSW |
8 |
123,588,188 (GRCm39) |
intron |
probably benign |
|
R0898:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Cdh15
|
UTSW |
8 |
123,591,939 (GRCm39) |
missense |
probably damaging |
0.98 |
R1054:Cdh15
|
UTSW |
8 |
123,591,076 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1072:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R1081:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1101:Cdh15
|
UTSW |
8 |
123,587,585 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1208:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1208:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1209:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1210:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1312:Cdh15
|
UTSW |
8 |
123,588,188 (GRCm39) |
intron |
probably benign |
|
R1317:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1318:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1393:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1429:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Cdh15
|
UTSW |
8 |
123,588,755 (GRCm39) |
missense |
probably benign |
0.05 |
R2157:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2170:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2178:Cdh15
|
UTSW |
8 |
123,591,715 (GRCm39) |
splice site |
probably null |
|
R2252:Cdh15
|
UTSW |
8 |
123,584,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Cdh15
|
UTSW |
8 |
123,586,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R2317:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2330:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2345:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2349:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2353:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2354:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2893:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2894:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2937:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2938:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2990:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2992:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2993:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3029:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3030:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3195:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R3441:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3442:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3608:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3686:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Cdh15
|
UTSW |
8 |
123,590,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Cdh15
|
UTSW |
8 |
123,590,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4477:Cdh15
|
UTSW |
8 |
123,591,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4478:Cdh15
|
UTSW |
8 |
123,591,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4480:Cdh15
|
UTSW |
8 |
123,591,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4580:Cdh15
|
UTSW |
8 |
123,591,897 (GRCm39) |
missense |
probably damaging |
0.99 |
R4583:Cdh15
|
UTSW |
8 |
123,591,767 (GRCm39) |
missense |
probably damaging |
0.98 |
R4619:Cdh15
|
UTSW |
8 |
123,587,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4694:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R5076:Cdh15
|
UTSW |
8 |
123,591,087 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5347:Cdh15
|
UTSW |
8 |
123,588,802 (GRCm39) |
missense |
probably null |
1.00 |
R5375:Cdh15
|
UTSW |
8 |
123,591,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5498:Cdh15
|
UTSW |
8 |
123,591,917 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5778:Cdh15
|
UTSW |
8 |
123,583,326 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6320:Cdh15
|
UTSW |
8 |
123,591,086 (GRCm39) |
missense |
probably benign |
0.01 |
R6570:Cdh15
|
UTSW |
8 |
123,584,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R6708:Cdh15
|
UTSW |
8 |
123,590,294 (GRCm39) |
missense |
probably benign |
0.32 |
R7505:Cdh15
|
UTSW |
8 |
123,575,231 (GRCm39) |
missense |
probably benign |
0.01 |
R7527:Cdh15
|
UTSW |
8 |
123,588,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R7724:Cdh15
|
UTSW |
8 |
123,593,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R8093:Cdh15
|
UTSW |
8 |
123,593,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R8485:Cdh15
|
UTSW |
8 |
123,584,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Cdh15
|
UTSW |
8 |
123,587,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8910:Cdh15
|
UTSW |
8 |
123,575,240 (GRCm39) |
missense |
probably benign |
0.04 |
R9017:Cdh15
|
UTSW |
8 |
123,584,256 (GRCm39) |
critical splice donor site |
probably null |
|
R9453:Cdh15
|
UTSW |
8 |
123,586,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R9699:Cdh15
|
UTSW |
8 |
123,588,769 (GRCm39) |
missense |
probably benign |
0.00 |
R9705:Cdh15
|
UTSW |
8 |
123,591,024 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cdh15
|
UTSW |
8 |
123,590,998 (GRCm39) |
missense |
probably damaging |
1.00 |
|