Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933436I01Rik |
T |
A |
X: 66,964,308 (GRCm39) |
I184L |
probably benign |
Het |
9530002B09Rik |
T |
A |
4: 122,583,115 (GRCm39) |
|
probably benign |
Het |
Abca15 |
A |
T |
7: 119,960,127 (GRCm39) |
T637S |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,709,588 (GRCm39) |
K1135R |
possibly damaging |
Het |
Afap1l1 |
A |
T |
18: 61,872,193 (GRCm39) |
|
probably null |
Het |
AI467606 |
A |
G |
7: 126,692,009 (GRCm39) |
S195G |
probably damaging |
Het |
Alox12e |
G |
A |
11: 70,206,828 (GRCm39) |
R620W |
probably damaging |
Het |
Ascc2 |
A |
T |
11: 4,631,496 (GRCm39) |
M646L |
probably benign |
Het |
Ccnt1 |
A |
T |
15: 98,449,823 (GRCm39) |
H156Q |
probably benign |
Het |
Cic |
T |
A |
7: 24,972,876 (GRCm39) |
V869E |
probably damaging |
Het |
Cpsf2 |
A |
G |
12: 101,949,722 (GRCm39) |
D118G |
probably damaging |
Het |
Csnk1g1 |
A |
G |
9: 65,909,512 (GRCm39) |
S210G |
probably damaging |
Het |
Cyp4a12b |
A |
T |
4: 115,290,700 (GRCm39) |
D274V |
possibly damaging |
Het |
Dnaaf3 |
T |
C |
7: 4,526,798 (GRCm39) |
I426M |
possibly damaging |
Het |
Dnah3 |
C |
T |
7: 119,551,132 (GRCm39) |
M3062I |
probably damaging |
Het |
Dtx2 |
C |
T |
5: 136,059,431 (GRCm39) |
S493F |
probably damaging |
Het |
Elavl2 |
A |
T |
4: 91,141,687 (GRCm39) |
S278R |
possibly damaging |
Het |
Emilin2 |
T |
C |
17: 71,581,950 (GRCm39) |
S259G |
probably benign |
Het |
Endov |
T |
C |
11: 119,390,408 (GRCm39) |
F12S |
probably damaging |
Het |
Faim2 |
G |
A |
15: 99,412,314 (GRCm39) |
T140I |
probably damaging |
Het |
Fbxo21 |
T |
C |
5: 118,115,031 (GRCm39) |
S56P |
probably benign |
Het |
Fgb |
C |
A |
3: 82,956,996 (GRCm39) |
D25Y |
probably benign |
Het |
Foxj2 |
A |
T |
6: 122,817,200 (GRCm39) |
H509L |
probably benign |
Het |
Fth1 |
T |
A |
19: 9,961,576 (GRCm39) |
L49Q |
probably damaging |
Het |
Gbp11 |
C |
A |
5: 105,476,450 (GRCm39) |
E220* |
probably null |
Het |
Gm12695 |
T |
C |
4: 96,657,963 (GRCm39) |
T69A |
probably benign |
Het |
Gm1527 |
C |
A |
3: 28,980,796 (GRCm39) |
T632N |
probably benign |
Het |
Gm4787 |
A |
T |
12: 81,425,694 (GRCm39) |
S155T |
probably benign |
Het |
Gtf2f2 |
A |
G |
14: 76,155,136 (GRCm39) |
S142P |
possibly damaging |
Het |
Helb |
T |
C |
10: 119,941,671 (GRCm39) |
Y339C |
probably benign |
Het |
Hs3st4 |
A |
G |
7: 123,996,236 (GRCm39) |
I301V |
probably benign |
Het |
Hunk |
A |
G |
16: 90,290,368 (GRCm39) |
D382G |
probably damaging |
Het |
Ifnb1 |
T |
A |
4: 88,440,996 (GRCm39) |
I6F |
possibly damaging |
Het |
Il10 |
T |
C |
1: 130,947,770 (GRCm39) |
L41P |
probably damaging |
Het |
Il2rg |
A |
G |
X: 100,311,416 (GRCm39) |
L57P |
possibly damaging |
Het |
Invs |
T |
A |
4: 48,396,287 (GRCm39) |
L320Q |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,317,050 (GRCm39) |
M768I |
probably benign |
Het |
Krt90 |
T |
C |
15: 101,466,794 (GRCm39) |
E263G |
probably benign |
Het |
Lama2 |
C |
T |
10: 27,040,922 (GRCm39) |
C1467Y |
probably damaging |
Het |
Maco1 |
A |
T |
4: 134,555,590 (GRCm39) |
N294K |
possibly damaging |
Het |
Med24 |
A |
G |
11: 98,606,472 (GRCm39) |
L330P |
probably damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Mtcl1 |
T |
C |
17: 66,653,350 (GRCm39) |
R1065G |
probably damaging |
Het |
Mtmr14 |
G |
A |
6: 113,217,322 (GRCm39) |
G38D |
probably damaging |
Het |
Mtus1 |
T |
C |
8: 41,535,745 (GRCm39) |
E657G |
probably damaging |
Het |
Muc21 |
T |
A |
17: 35,932,297 (GRCm39) |
|
probably benign |
Het |
Myo5c |
A |
T |
9: 75,189,150 (GRCm39) |
Q1020L |
probably benign |
Het |
Nav1 |
C |
T |
1: 135,376,742 (GRCm39) |
R1694Q |
probably damaging |
Het |
Nckap1 |
T |
C |
2: 80,400,494 (GRCm39) |
K69R |
probably damaging |
Het |
Nlrp1b |
T |
C |
11: 71,051,912 (GRCm39) |
N1012D |
probably benign |
Het |
Ntrk2 |
A |
C |
13: 59,007,111 (GRCm39) |
K238Q |
probably damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or2ab1 |
A |
G |
11: 58,488,396 (GRCm39) |
N58S |
probably damaging |
Het |
Or52n2b |
T |
C |
7: 104,565,982 (GRCm39) |
N174D |
probably benign |
Het |
Pcdh8 |
A |
T |
14: 80,005,651 (GRCm39) |
S912R |
probably damaging |
Het |
Pfpl |
C |
T |
19: 12,407,237 (GRCm39) |
S496L |
probably damaging |
Het |
Phc2 |
T |
C |
4: 128,640,929 (GRCm39) |
F672S |
probably damaging |
Het |
Pkhd1l1 |
A |
T |
15: 44,414,148 (GRCm39) |
H2805L |
possibly damaging |
Het |
Pla2g4a |
T |
C |
1: 149,716,427 (GRCm39) |
N678S |
possibly damaging |
Het |
Plxnb3 |
T |
A |
X: 72,815,357 (GRCm39) |
Y1845* |
probably null |
Het |
Polr1a |
T |
G |
6: 71,913,269 (GRCm39) |
|
probably null |
Het |
Prl3d3 |
A |
C |
13: 27,346,304 (GRCm39) |
E180D |
probably benign |
Het |
Prl7a2 |
T |
A |
13: 27,844,870 (GRCm39) |
Y172F |
probably damaging |
Het |
Prpf3 |
A |
T |
3: 95,751,551 (GRCm39) |
D383E |
probably benign |
Het |
Psmc4 |
A |
T |
7: 27,748,322 (GRCm39) |
L73H |
probably damaging |
Het |
Rapgef3 |
C |
A |
15: 97,664,842 (GRCm39) |
G7V |
probably damaging |
Het |
Rasl12 |
G |
A |
9: 65,318,106 (GRCm39) |
G157R |
probably damaging |
Het |
Rnf38 |
A |
C |
4: 44,149,098 (GRCm39) |
V83G |
probably damaging |
Het |
Rnls |
A |
C |
19: 33,179,944 (GRCm39) |
S51A |
probably benign |
Het |
Siglecf |
A |
G |
7: 43,001,804 (GRCm39) |
T205A |
possibly damaging |
Het |
Skint1 |
T |
A |
4: 111,882,730 (GRCm39) |
V258D |
probably benign |
Het |
Slc12a5 |
C |
T |
2: 164,839,067 (GRCm39) |
R1072W |
probably damaging |
Het |
Spata13 |
GTTAGGCT |
GT |
14: 60,998,320 (GRCm39) |
|
probably benign |
Het |
Specc1 |
T |
G |
11: 62,009,122 (GRCm39) |
S293A |
probably benign |
Het |
Speer2 |
T |
G |
16: 69,657,385 (GRCm39) |
Q86P |
probably benign |
Het |
Tbc1d15 |
T |
C |
10: 115,065,078 (GRCm39) |
D169G |
probably benign |
Het |
Tbx20 |
C |
A |
9: 24,681,067 (GRCm39) |
E142* |
probably null |
Het |
Tcp1 |
T |
A |
17: 13,139,699 (GRCm39) |
L199H |
probably damaging |
Het |
Tex26 |
A |
T |
5: 149,363,204 (GRCm39) |
R5W |
probably damaging |
Het |
Tg |
C |
A |
15: 66,700,402 (GRCm39) |
A120E |
probably damaging |
Het |
Thrap3 |
T |
C |
4: 126,069,189 (GRCm39) |
Y654C |
possibly damaging |
Het |
Troap |
T |
C |
15: 98,980,344 (GRCm39) |
L508P |
probably benign |
Het |
Ubap2 |
C |
T |
4: 41,199,872 (GRCm39) |
A752T |
probably benign |
Het |
Ush1c |
T |
C |
7: 45,878,905 (GRCm39) |
Y74C |
probably damaging |
Het |
Vmn1r55 |
A |
G |
7: 5,150,048 (GRCm39) |
V125A |
possibly damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,553 (GRCm39) |
H412L |
possibly damaging |
Het |
Vps54 |
C |
T |
11: 21,227,955 (GRCm39) |
T176I |
probably damaging |
Het |
Wdr95 |
T |
C |
5: 149,502,627 (GRCm39) |
|
probably null |
Het |
Zfp81 |
T |
C |
17: 33,554,278 (GRCm39) |
T179A |
probably benign |
Het |
|
Other mutations in Cyp2c40 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01384:Cyp2c40
|
APN |
19 |
39,801,027 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01660:Cyp2c40
|
APN |
19 |
39,775,254 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01897:Cyp2c40
|
APN |
19 |
39,792,217 (GRCm39) |
nonsense |
probably null |
|
IGL01926:Cyp2c40
|
APN |
19 |
39,791,099 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02078:Cyp2c40
|
APN |
19 |
39,755,926 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02259:Cyp2c40
|
APN |
19 |
39,792,246 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02716:Cyp2c40
|
APN |
19 |
39,795,980 (GRCm39) |
missense |
possibly damaging |
0.49 |
cypriot
|
UTSW |
19 |
39,755,899 (GRCm39) |
missense |
probably damaging |
0.98 |
R0269:Cyp2c40
|
UTSW |
19 |
39,762,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R0308:Cyp2c40
|
UTSW |
19 |
39,766,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R0309:Cyp2c40
|
UTSW |
19 |
39,766,495 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0441:Cyp2c40
|
UTSW |
19 |
39,795,607 (GRCm39) |
splice site |
probably benign |
|
R1068:Cyp2c40
|
UTSW |
19 |
39,801,025 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1123:Cyp2c40
|
UTSW |
19 |
39,801,121 (GRCm39) |
missense |
probably benign |
0.00 |
R1443:Cyp2c40
|
UTSW |
19 |
39,766,415 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1506:Cyp2c40
|
UTSW |
19 |
39,766,443 (GRCm39) |
missense |
probably damaging |
0.96 |
R1567:Cyp2c40
|
UTSW |
19 |
39,792,215 (GRCm39) |
missense |
probably null |
0.99 |
R1731:Cyp2c40
|
UTSW |
19 |
39,801,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Cyp2c40
|
UTSW |
19 |
39,775,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R1861:Cyp2c40
|
UTSW |
19 |
39,775,319 (GRCm39) |
missense |
probably benign |
0.11 |
R1977:Cyp2c40
|
UTSW |
19 |
39,766,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R2022:Cyp2c40
|
UTSW |
19 |
39,801,224 (GRCm39) |
unclassified |
probably benign |
|
R2359:Cyp2c40
|
UTSW |
19 |
39,766,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R2413:Cyp2c40
|
UTSW |
19 |
39,792,331 (GRCm39) |
nonsense |
probably null |
|
R3685:Cyp2c40
|
UTSW |
19 |
39,775,223 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4080:Cyp2c40
|
UTSW |
19 |
39,790,973 (GRCm39) |
missense |
probably benign |
0.01 |
R4614:Cyp2c40
|
UTSW |
19 |
39,792,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R4661:Cyp2c40
|
UTSW |
19 |
39,775,290 (GRCm39) |
missense |
probably benign |
0.00 |
R4716:Cyp2c40
|
UTSW |
19 |
39,791,105 (GRCm39) |
splice site |
probably null |
|
R4799:Cyp2c40
|
UTSW |
19 |
39,762,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Cyp2c40
|
UTSW |
19 |
39,795,663 (GRCm39) |
missense |
probably benign |
0.02 |
R5191:Cyp2c40
|
UTSW |
19 |
39,791,035 (GRCm39) |
missense |
probably damaging |
0.96 |
R5310:Cyp2c40
|
UTSW |
19 |
39,766,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Cyp2c40
|
UTSW |
19 |
39,792,236 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5619:Cyp2c40
|
UTSW |
19 |
39,792,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R5989:Cyp2c40
|
UTSW |
19 |
39,796,024 (GRCm39) |
missense |
probably benign |
0.45 |
R6175:Cyp2c40
|
UTSW |
19 |
39,801,004 (GRCm39) |
missense |
probably benign |
0.00 |
R6622:Cyp2c40
|
UTSW |
19 |
39,790,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R6987:Cyp2c40
|
UTSW |
19 |
39,801,211 (GRCm39) |
unclassified |
probably benign |
|
R7057:Cyp2c40
|
UTSW |
19 |
39,796,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Cyp2c40
|
UTSW |
19 |
39,796,050 (GRCm39) |
nonsense |
probably null |
|
R7560:Cyp2c40
|
UTSW |
19 |
39,795,658 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7648:Cyp2c40
|
UTSW |
19 |
39,792,289 (GRCm39) |
makesense |
probably null |
|
R7718:Cyp2c40
|
UTSW |
19 |
39,755,782 (GRCm39) |
missense |
probably benign |
0.00 |
R7763:Cyp2c40
|
UTSW |
19 |
39,795,612 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7893:Cyp2c40
|
UTSW |
19 |
39,775,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R8094:Cyp2c40
|
UTSW |
19 |
39,791,015 (GRCm39) |
missense |
probably benign |
0.00 |
R8094:Cyp2c40
|
UTSW |
19 |
39,791,009 (GRCm39) |
missense |
probably benign |
0.17 |
R8264:Cyp2c40
|
UTSW |
19 |
39,795,971 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8287:Cyp2c40
|
UTSW |
19 |
39,755,899 (GRCm39) |
missense |
probably damaging |
0.98 |
R8302:Cyp2c40
|
UTSW |
19 |
39,796,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R8848:Cyp2c40
|
UTSW |
19 |
39,801,244 (GRCm39) |
missense |
unknown |
|
R8915:Cyp2c40
|
UTSW |
19 |
39,795,991 (GRCm39) |
missense |
probably benign |
0.31 |
R8963:Cyp2c40
|
UTSW |
19 |
39,755,926 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9132:Cyp2c40
|
UTSW |
19 |
39,762,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R9159:Cyp2c40
|
UTSW |
19 |
39,762,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R9168:Cyp2c40
|
UTSW |
19 |
39,755,819 (GRCm39) |
missense |
probably benign |
|
R9486:Cyp2c40
|
UTSW |
19 |
39,796,050 (GRCm39) |
nonsense |
probably null |
|
R9486:Cyp2c40
|
UTSW |
19 |
39,755,808 (GRCm39) |
missense |
probably benign |
0.00 |
R9489:Cyp2c40
|
UTSW |
19 |
39,766,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R9605:Cyp2c40
|
UTSW |
19 |
39,766,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R9772:Cyp2c40
|
UTSW |
19 |
39,792,348 (GRCm39) |
missense |
probably benign |
|
|