Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
A |
16: 4,685,323 (GRCm39) |
S1142T |
possibly damaging |
Het |
Aadacl4fm5 |
T |
C |
4: 144,512,938 (GRCm39) |
I54V |
probably benign |
Het |
Actr3b |
T |
G |
5: 26,037,433 (GRCm39) |
V215G |
probably damaging |
Het |
Adam9 |
C |
T |
8: 25,460,634 (GRCm39) |
V617M |
probably damaging |
Het |
Adgrl2 |
G |
T |
3: 148,596,241 (GRCm39) |
P32T |
probably damaging |
Het |
Afg2a |
G |
T |
3: 37,518,694 (GRCm39) |
G743W |
probably damaging |
Het |
Ago3 |
A |
T |
4: 126,261,580 (GRCm39) |
|
probably benign |
Het |
Allc |
A |
C |
12: 28,623,206 (GRCm39) |
I20M |
probably benign |
Het |
Asic3 |
G |
A |
5: 24,621,972 (GRCm39) |
W361* |
probably null |
Het |
Atf7ip |
A |
G |
6: 136,583,577 (GRCm39) |
K1203E |
probably damaging |
Het |
Babam2 |
C |
A |
5: 32,162,116 (GRCm39) |
H272Q |
possibly damaging |
Het |
Baz2b |
G |
A |
2: 59,807,872 (GRCm39) |
T129I |
probably benign |
Het |
C130073F10Rik |
A |
T |
4: 101,747,590 (GRCm39) |
Y146* |
probably null |
Het |
Cd247 |
A |
G |
1: 165,684,986 (GRCm39) |
E74G |
probably damaging |
Het |
Cdh17 |
A |
T |
4: 11,814,908 (GRCm39) |
Q778L |
probably benign |
Het |
Ceacam1 |
T |
C |
7: 25,175,966 (GRCm39) |
D76G |
probably benign |
Het |
Cela3a |
T |
C |
4: 137,131,145 (GRCm39) |
K198E |
probably benign |
Het |
Cemip2 |
T |
A |
19: 21,789,241 (GRCm39) |
D558E |
probably damaging |
Het |
Ces2a |
T |
A |
8: 105,465,691 (GRCm39) |
D281E |
probably damaging |
Het |
Cetn2 |
A |
T |
X: 71,958,527 (GRCm39) |
D116E |
probably damaging |
Het |
Cracd |
A |
G |
5: 77,006,890 (GRCm39) |
K1084E |
unknown |
Het |
Ctu2 |
G |
T |
8: 123,205,530 (GRCm39) |
|
probably null |
Het |
Cybb |
T |
C |
X: 9,308,828 (GRCm39) |
N469D |
probably benign |
Het |
Cygb |
C |
T |
11: 116,540,749 (GRCm39) |
R79Q |
probably damaging |
Het |
Cyp2d10 |
C |
T |
15: 82,288,069 (GRCm39) |
V186M |
possibly damaging |
Het |
Defb29 |
T |
A |
2: 152,380,942 (GRCm39) |
|
probably null |
Het |
Depdc7 |
T |
G |
2: 104,560,694 (GRCm39) |
Q100P |
probably damaging |
Het |
Dhx30 |
A |
C |
9: 109,926,251 (GRCm39) |
I91R |
probably damaging |
Het |
Dnm1l |
T |
A |
16: 16,159,288 (GRCm39) |
K105* |
probably null |
Het |
Eddm13 |
T |
C |
7: 6,272,898 (GRCm39) |
|
probably benign |
Het |
Efhc1 |
T |
C |
1: 21,037,567 (GRCm39) |
I248T |
probably damaging |
Het |
Elapor1 |
A |
G |
3: 108,380,182 (GRCm39) |
I309T |
probably benign |
Het |
Entpd2 |
A |
G |
2: 25,288,120 (GRCm39) |
T115A |
probably damaging |
Het |
Epb42 |
G |
T |
2: 120,856,227 (GRCm39) |
A439E |
probably benign |
Het |
Esm1 |
T |
G |
13: 113,346,618 (GRCm39) |
L81R |
probably damaging |
Het |
F8 |
T |
C |
X: 74,330,987 (GRCm39) |
S968G |
probably benign |
Het |
Fam234b |
T |
G |
6: 135,202,201 (GRCm39) |
Y308D |
probably damaging |
Het |
Fbxo46 |
T |
G |
7: 18,871,139 (GRCm39) |
V586G |
probably damaging |
Het |
Foxp1 |
C |
A |
6: 98,907,044 (GRCm39) |
|
probably benign |
Het |
Gm10754 |
A |
T |
10: 97,518,136 (GRCm39) |
|
probably benign |
Het |
Gm12695 |
A |
C |
4: 96,650,370 (GRCm39) |
|
probably benign |
Het |
Gm5468 |
T |
C |
15: 25,414,726 (GRCm39) |
|
probably benign |
Het |
Grhl1 |
T |
C |
12: 24,631,490 (GRCm39) |
S66P |
probably damaging |
Het |
Gstt3 |
A |
T |
10: 75,612,576 (GRCm39) |
|
probably null |
Het |
Gtf2i |
A |
G |
5: 134,308,281 (GRCm39) |
|
probably benign |
Het |
Gzmk |
C |
A |
13: 113,308,560 (GRCm39) |
G175C |
probably damaging |
Het |
Helz2 |
T |
C |
2: 180,872,939 (GRCm39) |
|
probably benign |
Het |
Ift20 |
T |
C |
11: 78,430,780 (GRCm39) |
|
probably benign |
Het |
Intu |
A |
G |
3: 40,642,216 (GRCm39) |
D491G |
probably damaging |
Het |
Itch |
G |
T |
2: 155,015,853 (GRCm39) |
|
probably null |
Het |
Itgb5 |
A |
G |
16: 33,665,362 (GRCm39) |
N26S |
possibly damaging |
Het |
Lama2 |
A |
T |
10: 26,891,534 (GRCm39) |
S2526R |
probably damaging |
Het |
Lat2 |
A |
G |
5: 134,637,027 (GRCm39) |
I40T |
probably damaging |
Het |
Lipa |
T |
A |
19: 34,471,397 (GRCm39) |
M393L |
probably benign |
Het |
Lipa |
G |
T |
19: 34,471,371 (GRCm39) |
|
probably benign |
Het |
Lpcat1 |
T |
A |
13: 73,632,417 (GRCm39) |
L10H |
probably damaging |
Het |
Lpcat3 |
T |
C |
6: 124,679,970 (GRCm39) |
Y348H |
possibly damaging |
Het |
Lrp1b |
A |
T |
2: 40,591,842 (GRCm39) |
N50K |
unknown |
Het |
Lrrk2 |
T |
A |
15: 91,634,480 (GRCm39) |
Y1415N |
probably damaging |
Het |
Lsamp |
A |
T |
16: 41,965,078 (GRCm39) |
T312S |
probably benign |
Het |
Man2a2 |
T |
C |
7: 80,013,689 (GRCm39) |
E454G |
probably benign |
Het |
Mcm3 |
T |
C |
1: 20,879,063 (GRCm39) |
K570R |
probably damaging |
Het |
Mctp2 |
C |
A |
7: 71,878,219 (GRCm39) |
|
probably null |
Het |
Msantd2 |
T |
G |
9: 37,434,796 (GRCm39) |
C345W |
probably damaging |
Het |
Musk |
T |
C |
4: 58,354,078 (GRCm39) |
I362T |
probably benign |
Het |
Myh15 |
A |
T |
16: 48,965,767 (GRCm39) |
N1224I |
probably benign |
Het |
Myo18a |
A |
G |
11: 77,755,612 (GRCm39) |
Y1983C |
probably damaging |
Het |
Myo18a |
C |
T |
11: 77,720,699 (GRCm39) |
|
probably benign |
Het |
Myrfl |
G |
T |
10: 116,664,909 (GRCm39) |
Q374K |
probably damaging |
Het |
Ndrg1 |
T |
A |
15: 66,818,346 (GRCm39) |
Q87H |
probably benign |
Het |
Nol9 |
G |
A |
4: 152,131,030 (GRCm39) |
C351Y |
probably damaging |
Het |
Nr5a1 |
A |
G |
2: 38,598,141 (GRCm39) |
S219P |
probably benign |
Het |
Or8b43 |
T |
C |
9: 38,360,489 (GRCm39) |
F107S |
possibly damaging |
Het |
Or8g28 |
A |
T |
9: 39,169,520 (GRCm39) |
Y149* |
probably null |
Het |
Pcdhb19 |
A |
G |
18: 37,631,690 (GRCm39) |
D495G |
probably damaging |
Het |
Pfkm |
A |
G |
15: 98,026,123 (GRCm39) |
M573V |
probably damaging |
Het |
Plec |
A |
T |
15: 76,065,516 (GRCm39) |
L1586Q |
probably damaging |
Het |
Prelp |
C |
A |
1: 133,843,005 (GRCm39) |
E47* |
probably null |
Het |
Rbm33 |
T |
A |
5: 28,615,753 (GRCm39) |
I32N |
probably damaging |
Het |
Rgs12 |
A |
T |
5: 35,183,227 (GRCm39) |
D310V |
probably damaging |
Het |
Sh3d21 |
T |
C |
4: 126,056,034 (GRCm39) |
E124G |
probably benign |
Het |
Shroom2 |
C |
T |
X: 151,442,549 (GRCm39) |
S872N |
probably benign |
Het |
Slc44a5 |
A |
G |
3: 153,956,651 (GRCm39) |
Y301C |
probably damaging |
Het |
Smap1 |
A |
T |
1: 23,930,995 (GRCm39) |
H66Q |
possibly damaging |
Het |
Smyd1 |
G |
T |
6: 71,198,007 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
T |
A |
7: 27,093,573 (GRCm39) |
|
probably benign |
Het |
Srsf3-ps |
T |
A |
11: 98,516,146 (GRCm39) |
R76* |
probably null |
Het |
Stag3 |
A |
G |
5: 138,280,955 (GRCm39) |
K49R |
probably damaging |
Het |
Stim1 |
C |
A |
7: 101,917,758 (GRCm39) |
A46E |
unknown |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Tbc1d19 |
A |
G |
5: 53,992,559 (GRCm39) |
T114A |
probably benign |
Het |
Tln2 |
G |
A |
9: 67,128,807 (GRCm39) |
|
probably benign |
Het |
Trmt10a |
T |
A |
3: 137,857,945 (GRCm39) |
|
probably null |
Het |
Vwde |
G |
A |
6: 13,187,136 (GRCm39) |
H784Y |
probably damaging |
Het |
Zfp773 |
T |
C |
7: 7,137,232 (GRCm39) |
T121A |
probably benign |
Het |
|
Other mutations in Ripor2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01099:Ripor2
|
APN |
13 |
24,885,190 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02145:Ripor2
|
APN |
13 |
24,901,554 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02351:Ripor2
|
APN |
13 |
24,915,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02358:Ripor2
|
APN |
13 |
24,915,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Ripor2
|
APN |
13 |
24,879,549 (GRCm39) |
splice site |
probably benign |
|
IGL02533:Ripor2
|
APN |
13 |
24,885,378 (GRCm39) |
nonsense |
probably null |
|
IGL02798:Ripor2
|
APN |
13 |
24,858,649 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02852:Ripor2
|
APN |
13 |
24,879,681 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03219:Ripor2
|
APN |
13 |
24,907,702 (GRCm39) |
missense |
probably damaging |
1.00 |
gentleman
|
UTSW |
13 |
24,878,128 (GRCm39) |
missense |
probably damaging |
1.00 |
Jack
|
UTSW |
13 |
24,861,824 (GRCm39) |
nonsense |
probably null |
|
whitechapel
|
UTSW |
13 |
24,857,095 (GRCm39) |
critical splice donor site |
probably null |
|
R0045:Ripor2
|
UTSW |
13 |
24,878,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R0101:Ripor2
|
UTSW |
13 |
24,864,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Ripor2
|
UTSW |
13 |
24,864,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R0827:Ripor2
|
UTSW |
13 |
24,878,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R1331:Ripor2
|
UTSW |
13 |
24,861,824 (GRCm39) |
nonsense |
probably null |
|
R1374:Ripor2
|
UTSW |
13 |
24,857,095 (GRCm39) |
critical splice donor site |
probably null |
|
R1564:Ripor2
|
UTSW |
13 |
24,859,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1773:Ripor2
|
UTSW |
13 |
24,885,237 (GRCm39) |
missense |
probably benign |
0.10 |
R1889:Ripor2
|
UTSW |
13 |
24,877,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Ripor2
|
UTSW |
13 |
24,897,701 (GRCm39) |
missense |
probably damaging |
0.98 |
R2137:Ripor2
|
UTSW |
13 |
24,905,817 (GRCm39) |
critical splice donor site |
probably null |
|
R2209:Ripor2
|
UTSW |
13 |
24,885,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R2242:Ripor2
|
UTSW |
13 |
24,855,755 (GRCm39) |
missense |
probably benign |
0.08 |
R2392:Ripor2
|
UTSW |
13 |
24,890,206 (GRCm39) |
missense |
probably benign |
0.00 |
R2994:Ripor2
|
UTSW |
13 |
24,885,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R4008:Ripor2
|
UTSW |
13 |
24,880,521 (GRCm39) |
missense |
probably benign |
|
R4287:Ripor2
|
UTSW |
13 |
24,908,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R4364:Ripor2
|
UTSW |
13 |
24,905,694 (GRCm39) |
missense |
probably benign |
0.07 |
R4365:Ripor2
|
UTSW |
13 |
24,905,694 (GRCm39) |
missense |
probably benign |
0.07 |
R4366:Ripor2
|
UTSW |
13 |
24,905,694 (GRCm39) |
missense |
probably benign |
0.07 |
R4868:Ripor2
|
UTSW |
13 |
24,878,124 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5304:Ripor2
|
UTSW |
13 |
24,858,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R6119:Ripor2
|
UTSW |
13 |
24,798,627 (GRCm39) |
start gained |
probably benign |
|
R6157:Ripor2
|
UTSW |
13 |
24,885,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Ripor2
|
UTSW |
13 |
24,894,113 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6382:Ripor2
|
UTSW |
13 |
24,861,828 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6664:Ripor2
|
UTSW |
13 |
24,859,803 (GRCm39) |
missense |
probably damaging |
0.98 |
R6908:Ripor2
|
UTSW |
13 |
24,890,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R7023:Ripor2
|
UTSW |
13 |
24,855,829 (GRCm39) |
missense |
probably benign |
0.00 |
R7041:Ripor2
|
UTSW |
13 |
24,877,749 (GRCm39) |
missense |
probably benign |
0.18 |
R7196:Ripor2
|
UTSW |
13 |
24,888,808 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7216:Ripor2
|
UTSW |
13 |
24,855,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R7248:Ripor2
|
UTSW |
13 |
24,878,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Ripor2
|
UTSW |
13 |
24,908,984 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7301:Ripor2
|
UTSW |
13 |
24,908,984 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7343:Ripor2
|
UTSW |
13 |
24,885,427 (GRCm39) |
nonsense |
probably null |
|
R7417:Ripor2
|
UTSW |
13 |
24,880,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Ripor2
|
UTSW |
13 |
24,878,188 (GRCm39) |
missense |
probably benign |
0.01 |
R7448:Ripor2
|
UTSW |
13 |
24,854,054 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7462:Ripor2
|
UTSW |
13 |
24,880,290 (GRCm39) |
missense |
unknown |
|
R7499:Ripor2
|
UTSW |
13 |
24,877,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R8081:Ripor2
|
UTSW |
13 |
24,897,683 (GRCm39) |
missense |
probably benign |
0.01 |
R8157:Ripor2
|
UTSW |
13 |
24,879,600 (GRCm39) |
missense |
probably benign |
0.05 |
R8364:Ripor2
|
UTSW |
13 |
24,894,176 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8447:Ripor2
|
UTSW |
13 |
24,907,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R8465:Ripor2
|
UTSW |
13 |
24,849,451 (GRCm39) |
intron |
probably benign |
|
R8751:Ripor2
|
UTSW |
13 |
24,885,050 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8818:Ripor2
|
UTSW |
13 |
24,901,651 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8867:Ripor2
|
UTSW |
13 |
24,822,760 (GRCm39) |
intron |
probably benign |
|
R9079:Ripor2
|
UTSW |
13 |
24,915,637 (GRCm39) |
missense |
probably benign |
0.35 |
R9187:Ripor2
|
UTSW |
13 |
24,897,632 (GRCm39) |
missense |
probably benign |
0.01 |
R9316:Ripor2
|
UTSW |
13 |
24,905,719 (GRCm39) |
missense |
probably benign |
0.09 |
R9320:Ripor2
|
UTSW |
13 |
24,915,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R9355:Ripor2
|
UTSW |
13 |
24,885,694 (GRCm39) |
missense |
probably benign |
0.00 |
R9655:Ripor2
|
UTSW |
13 |
24,908,983 (GRCm39) |
missense |
possibly damaging |
0.67 |
|