Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
G |
3: 121,898,965 (GRCm39) |
I649S |
probably damaging |
Het |
Abcc2 |
T |
A |
19: 43,792,221 (GRCm39) |
L334* |
probably null |
Het |
Adam28 |
A |
T |
14: 68,872,325 (GRCm39) |
S306T |
probably benign |
Het |
Adam34 |
T |
A |
8: 44,104,349 (GRCm39) |
D432V |
probably damaging |
Het |
Adcy7 |
A |
G |
8: 89,050,264 (GRCm39) |
Y723C |
probably benign |
Het |
Adgre5 |
T |
A |
8: 84,451,089 (GRCm39) |
M713L |
probably benign |
Het |
Aebp2 |
C |
A |
6: 140,583,412 (GRCm39) |
C295* |
probably null |
Het |
Amn1 |
G |
T |
6: 149,072,357 (GRCm39) |
Q127K |
probably benign |
Het |
Atcay |
C |
T |
10: 81,046,383 (GRCm39) |
V314M |
probably damaging |
Het |
Atp1a1 |
T |
C |
3: 101,488,495 (GRCm39) |
E847G |
probably benign |
Het |
Atp2b1 |
A |
G |
10: 98,852,840 (GRCm39) |
E1039G |
probably benign |
Het |
Caskin1 |
A |
G |
17: 24,718,266 (GRCm39) |
Y292C |
probably damaging |
Het |
Cftr |
A |
G |
6: 18,214,105 (GRCm39) |
T94A |
probably damaging |
Het |
Ciart |
T |
A |
3: 95,787,788 (GRCm39) |
K182M |
probably damaging |
Het |
Col1a2 |
A |
C |
6: 4,527,079 (GRCm39) |
S603R |
possibly damaging |
Het |
Cspp1 |
C |
A |
1: 10,145,097 (GRCm39) |
S298R |
possibly damaging |
Het |
Cul7 |
T |
A |
17: 46,962,746 (GRCm39) |
C126S |
probably damaging |
Het |
Cyp2c55 |
A |
T |
19: 39,000,235 (GRCm39) |
I145F |
probably damaging |
Het |
Cypt4 |
G |
C |
9: 24,536,770 (GRCm39) |
A87P |
probably damaging |
Het |
Disp2 |
G |
A |
2: 118,618,125 (GRCm39) |
V224M |
probably benign |
Het |
Dlgap5 |
TTC |
T |
14: 47,638,979 (GRCm39) |
|
probably null |
Het |
Dock1 |
A |
G |
7: 134,754,029 (GRCm39) |
K1602R |
probably benign |
Het |
Ears2 |
T |
C |
7: 121,647,562 (GRCm39) |
I241V |
probably benign |
Het |
Eml6 |
T |
C |
11: 29,752,489 (GRCm39) |
T975A |
probably damaging |
Het |
Ephb2 |
T |
C |
4: 136,388,121 (GRCm39) |
T660A |
probably benign |
Het |
Fbxw7 |
G |
A |
3: 84,872,621 (GRCm39) |
V268M |
|
Het |
Gart |
A |
G |
16: 91,433,426 (GRCm39) |
F289S |
probably damaging |
Het |
Gmcl1 |
G |
T |
6: 86,681,520 (GRCm39) |
N391K |
probably benign |
Het |
Greb1l |
A |
C |
18: 10,533,031 (GRCm39) |
Q975P |
probably damaging |
Het |
Greb1l |
G |
T |
18: 10,533,032 (GRCm39) |
Q975H |
probably benign |
Het |
Grik5 |
C |
A |
7: 24,710,119 (GRCm39) |
R872L |
probably damaging |
Het |
Hmox2 |
T |
A |
16: 4,582,921 (GRCm39) |
I218N |
probably damaging |
Het |
Hook1 |
A |
T |
4: 95,903,089 (GRCm39) |
D526V |
probably damaging |
Het |
Ifna4 |
A |
T |
4: 88,760,191 (GRCm39) |
N32Y |
probably damaging |
Het |
Ighg2b |
T |
A |
12: 113,270,492 (GRCm39) |
N213Y |
unknown |
Het |
Itih4 |
G |
A |
14: 30,623,127 (GRCm39) |
V900I |
probably benign |
Het |
Itpr2 |
A |
T |
6: 146,274,671 (GRCm39) |
F837Y |
probably damaging |
Het |
Kif3a |
T |
C |
11: 53,469,941 (GRCm39) |
V147A |
probably benign |
Het |
Klra9 |
T |
A |
6: 130,168,284 (GRCm39) |
|
probably benign |
Het |
Lamp3 |
G |
T |
16: 19,492,210 (GRCm39) |
Q345K |
probably benign |
Het |
Ltbp3 |
G |
A |
19: 5,807,822 (GRCm39) |
E1188K |
probably damaging |
Het |
Med1 |
T |
A |
11: 98,049,243 (GRCm39) |
I518L |
probably benign |
Het |
Mis18bp1 |
T |
C |
12: 65,205,447 (GRCm39) |
T242A |
probably damaging |
Het |
Nemp1 |
T |
A |
10: 127,532,123 (GRCm39) |
F392Y |
probably benign |
Het |
Obscn |
C |
A |
11: 58,951,802 (GRCm39) |
G3984W |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,960,660 (GRCm39) |
H3217L |
possibly damaging |
Het |
Or10ak7 |
A |
G |
4: 118,791,823 (GRCm39) |
M74T |
probably benign |
Het |
Or13j1 |
A |
G |
4: 43,706,464 (GRCm39) |
Y35H |
probably damaging |
Het |
Or2d3b |
C |
T |
7: 106,514,136 (GRCm39) |
H244Y |
probably damaging |
Het |
Or2d3c |
T |
C |
7: 106,526,049 (GRCm39) |
I206V |
probably benign |
Het |
Or5l14 |
C |
T |
2: 87,792,802 (GRCm39) |
V145M |
possibly damaging |
Het |
P4ha1 |
G |
T |
10: 59,186,294 (GRCm39) |
A258S |
probably benign |
Het |
Pcdh20 |
C |
A |
14: 88,704,744 (GRCm39) |
S852I |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,722,784 (GRCm39) |
|
probably null |
Het |
Pcsk1 |
A |
T |
13: 75,260,769 (GRCm39) |
I331F |
probably damaging |
Het |
Pkd1l2 |
G |
T |
8: 117,748,761 (GRCm39) |
S1803R |
probably benign |
Het |
Pkd1l3 |
C |
A |
8: 110,387,433 (GRCm39) |
N1792K |
probably damaging |
Het |
Plekhg1 |
C |
A |
10: 3,913,469 (GRCm39) |
Q1119K |
|
Het |
Prr30 |
T |
A |
14: 101,436,371 (GRCm39) |
T64S |
probably benign |
Het |
Rec114 |
T |
C |
9: 58,567,653 (GRCm39) |
N111S |
probably benign |
Het |
Reck |
G |
A |
4: 43,895,850 (GRCm39) |
V79I |
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,386,231 (GRCm39) |
F276L |
probably damaging |
Het |
Rgs6 |
T |
C |
12: 83,138,553 (GRCm39) |
Y296H |
probably damaging |
Het |
Sdk1 |
A |
G |
5: 142,197,793 (GRCm39) |
R2149G |
probably benign |
Het |
Slc20a2 |
C |
A |
8: 23,025,398 (GRCm39) |
F33L |
probably damaging |
Het |
Spopl |
T |
A |
2: 23,435,461 (GRCm39) |
T25S |
probably damaging |
Het |
Srcap |
A |
T |
7: 127,148,492 (GRCm39) |
I1947F |
possibly damaging |
Het |
Srek1 |
A |
C |
13: 103,881,291 (GRCm39) |
|
probably null |
Het |
St8sia1 |
C |
T |
6: 142,774,978 (GRCm39) |
W200* |
probably null |
Het |
Tas2r106 |
A |
T |
6: 131,655,465 (GRCm39) |
F129I |
possibly damaging |
Het |
Tbrg4 |
A |
T |
11: 6,570,857 (GRCm39) |
L205Q |
probably damaging |
Het |
Tchh |
C |
A |
3: 93,353,187 (GRCm39) |
R876S |
unknown |
Het |
Thap12 |
G |
T |
7: 98,364,245 (GRCm39) |
A138S |
probably benign |
Het |
Tjp1 |
C |
T |
7: 64,993,362 (GRCm39) |
|
probably null |
Het |
Traf4 |
G |
A |
11: 78,052,360 (GRCm39) |
P95L |
probably benign |
Het |
Trappc9 |
ATCTC |
ATCTCTC |
15: 72,903,447 (GRCm39) |
|
probably null |
Het |
Usp20 |
G |
A |
2: 30,907,498 (GRCm39) |
V677M |
possibly damaging |
Het |
Usp50 |
C |
A |
2: 126,625,236 (GRCm39) |
|
probably benign |
Het |
Vmn1r21 |
T |
C |
6: 57,821,307 (GRCm39) |
T46A |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,363,669 (GRCm39) |
H408L |
probably benign |
Het |
Zfp266 |
T |
C |
9: 20,417,299 (GRCm39) |
T30A |
probably benign |
Het |
Zfp536 |
T |
C |
7: 37,179,182 (GRCm39) |
H1141R |
probably benign |
Het |
|
Other mutations in Parn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00987:Parn
|
APN |
16 |
13,485,467 (GRCm39) |
missense |
probably benign |
|
IGL02030:Parn
|
APN |
16 |
13,482,514 (GRCm39) |
splice site |
probably null |
|
IGL02179:Parn
|
APN |
16 |
13,485,456 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02336:Parn
|
APN |
16 |
13,384,567 (GRCm39) |
missense |
probably damaging |
1.00 |
arlette
|
UTSW |
16 |
13,424,035 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4651001:Parn
|
UTSW |
16 |
13,449,431 (GRCm39) |
missense |
probably benign |
0.25 |
R0388:Parn
|
UTSW |
16 |
13,472,340 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0485:Parn
|
UTSW |
16 |
13,472,299 (GRCm39) |
splice site |
probably benign |
|
R0625:Parn
|
UTSW |
16 |
13,458,158 (GRCm39) |
missense |
probably benign |
0.02 |
R1104:Parn
|
UTSW |
16 |
13,485,449 (GRCm39) |
missense |
probably damaging |
0.99 |
R1299:Parn
|
UTSW |
16 |
13,482,593 (GRCm39) |
missense |
probably benign |
0.10 |
R1356:Parn
|
UTSW |
16 |
13,468,538 (GRCm39) |
nonsense |
probably null |
|
R2067:Parn
|
UTSW |
16 |
13,420,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Parn
|
UTSW |
16 |
13,420,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R2397:Parn
|
UTSW |
16 |
13,384,518 (GRCm39) |
missense |
probably benign |
|
R4473:Parn
|
UTSW |
16 |
13,482,549 (GRCm39) |
missense |
probably benign |
0.00 |
R4474:Parn
|
UTSW |
16 |
13,482,549 (GRCm39) |
missense |
probably benign |
0.00 |
R4475:Parn
|
UTSW |
16 |
13,482,549 (GRCm39) |
missense |
probably benign |
0.00 |
R4476:Parn
|
UTSW |
16 |
13,482,549 (GRCm39) |
missense |
probably benign |
0.00 |
R4665:Parn
|
UTSW |
16 |
13,358,967 (GRCm39) |
missense |
probably benign |
0.19 |
R4795:Parn
|
UTSW |
16 |
13,424,066 (GRCm39) |
missense |
probably benign |
0.06 |
R5122:Parn
|
UTSW |
16 |
13,472,311 (GRCm39) |
critical splice donor site |
probably null |
|
R5226:Parn
|
UTSW |
16 |
13,443,416 (GRCm39) |
missense |
probably benign |
|
R5355:Parn
|
UTSW |
16 |
13,485,886 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5570:Parn
|
UTSW |
16 |
13,483,794 (GRCm39) |
missense |
probably damaging |
0.98 |
R5979:Parn
|
UTSW |
16 |
13,424,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Parn
|
UTSW |
16 |
13,485,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R6173:Parn
|
UTSW |
16 |
13,469,675 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6493:Parn
|
UTSW |
16 |
13,474,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7055:Parn
|
UTSW |
16 |
13,443,998 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7278:Parn
|
UTSW |
16 |
13,443,927 (GRCm39) |
splice site |
probably null |
|
R7391:Parn
|
UTSW |
16 |
13,485,870 (GRCm39) |
splice site |
probably null |
|
R7706:Parn
|
UTSW |
16 |
13,425,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R8188:Parn
|
UTSW |
16 |
13,359,020 (GRCm39) |
missense |
probably benign |
0.01 |
R8317:Parn
|
UTSW |
16 |
13,358,964 (GRCm39) |
missense |
probably damaging |
0.96 |
R8326:Parn
|
UTSW |
16 |
13,483,835 (GRCm39) |
missense |
probably benign |
0.00 |
R8419:Parn
|
UTSW |
16 |
13,466,338 (GRCm39) |
missense |
probably benign |
0.11 |
R8433:Parn
|
UTSW |
16 |
13,485,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R8475:Parn
|
UTSW |
16 |
13,425,113 (GRCm39) |
critical splice donor site |
probably null |
|
R8847:Parn
|
UTSW |
16 |
13,446,270 (GRCm39) |
nonsense |
probably null |
|
R8958:Parn
|
UTSW |
16 |
13,466,322 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8988:Parn
|
UTSW |
16 |
13,466,281 (GRCm39) |
critical splice donor site |
probably null |
|
R9277:Parn
|
UTSW |
16 |
13,482,519 (GRCm39) |
critical splice donor site |
probably null |
|
R9476:Parn
|
UTSW |
16 |
13,358,942 (GRCm39) |
missense |
probably benign |
0.10 |
R9510:Parn
|
UTSW |
16 |
13,358,942 (GRCm39) |
missense |
probably benign |
0.10 |
|