Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa1b |
T |
C |
9: 118,977,450 (GRCm39) |
T411A |
possibly damaging |
Het |
Ace |
A |
G |
11: 105,876,887 (GRCm39) |
H1123R |
probably damaging |
Het |
Acot12 |
T |
A |
13: 91,889,651 (GRCm39) |
M1K |
probably null |
Het |
Actr2 |
A |
T |
11: 20,022,544 (GRCm39) |
M309K |
probably damaging |
Het |
Ahsa2 |
G |
T |
11: 23,440,558 (GRCm39) |
T279K |
probably benign |
Het |
Ak8 |
A |
G |
2: 28,702,947 (GRCm39) |
Y437C |
possibly damaging |
Het |
Atp1a3 |
T |
A |
7: 24,700,577 (GRCm39) |
K5* |
probably null |
Het |
Bbs2 |
T |
A |
8: 94,814,033 (GRCm39) |
E195V |
possibly damaging |
Het |
C4b |
T |
A |
17: 34,949,446 (GRCm39) |
Y1505F |
probably damaging |
Het |
Camkk1 |
C |
G |
11: 72,917,873 (GRCm39) |
N147K |
probably damaging |
Het |
Cdh18 |
G |
A |
15: 23,227,036 (GRCm39) |
V166I |
possibly damaging |
Het |
Cep135 |
T |
A |
5: 76,754,592 (GRCm39) |
C356* |
probably null |
Het |
Cilp |
A |
T |
9: 65,187,527 (GRCm39) |
R1207S |
probably benign |
Het |
Clcnkb |
A |
G |
4: 141,137,923 (GRCm39) |
I291T |
possibly damaging |
Het |
Clrn3 |
G |
T |
7: 135,130,198 (GRCm39) |
S12Y |
probably damaging |
Het |
Clstn2 |
G |
T |
9: 97,343,422 (GRCm39) |
A675D |
probably benign |
Het |
Cyp2c68 |
A |
G |
19: 39,677,634 (GRCm39) |
I452T |
probably damaging |
Het |
Dhh |
A |
G |
15: 98,792,291 (GRCm39) |
V239A |
probably damaging |
Het |
Edar |
T |
G |
10: 58,446,376 (GRCm39) |
H183P |
probably damaging |
Het |
Epha2 |
T |
A |
4: 141,035,764 (GRCm39) |
S67T |
probably benign |
Het |
Gapdh |
A |
G |
6: 125,139,900 (GRCm39) |
L168P |
probably benign |
Het |
Grm4 |
C |
T |
17: 27,653,798 (GRCm39) |
W717* |
probably null |
Het |
Gtf3c1 |
T |
C |
7: 125,303,055 (GRCm39) |
I127V |
probably benign |
Het |
Igkv4-72 |
C |
T |
6: 69,204,087 (GRCm39) |
A35T |
probably damaging |
Het |
Il6st |
T |
A |
13: 112,630,185 (GRCm39) |
S344T |
probably benign |
Het |
Ip6k1 |
A |
G |
9: 107,922,452 (GRCm39) |
D168G |
possibly damaging |
Het |
Itpr1 |
G |
A |
6: 108,415,292 (GRCm39) |
R1742H |
probably benign |
Het |
Lat2 |
T |
A |
5: 134,635,641 (GRCm39) |
T58S |
probably damaging |
Het |
Limk2 |
T |
C |
11: 3,296,311 (GRCm39) |
K566E |
probably benign |
Het |
Lonp2 |
C |
A |
8: 87,358,022 (GRCm39) |
T81K |
probably damaging |
Het |
Mdn1 |
C |
A |
4: 32,723,685 (GRCm39) |
N2540K |
probably benign |
Het |
Myt1l |
T |
A |
12: 29,901,553 (GRCm39) |
D769E |
unknown |
Het |
Neb |
C |
T |
2: 52,079,715 (GRCm39) |
V5780M |
possibly damaging |
Het |
Or1j18 |
T |
A |
2: 36,625,057 (GRCm39) |
C241* |
probably null |
Het |
Or5d35 |
C |
A |
2: 87,855,265 (GRCm39) |
H66Q |
possibly damaging |
Het |
Or6c8b |
C |
T |
10: 128,882,333 (GRCm39) |
V200M |
probably damaging |
Het |
Or7g25 |
T |
A |
9: 19,160,567 (GRCm39) |
I43F |
probably benign |
Het |
Pcdhga12 |
T |
C |
18: 37,901,439 (GRCm39) |
V757A |
probably damaging |
Het |
Prpf31 |
A |
G |
7: 3,642,854 (GRCm39) |
T448A |
probably damaging |
Het |
Rbm6 |
A |
T |
9: 107,668,244 (GRCm39) |
M694K |
possibly damaging |
Het |
Ropn1l |
T |
C |
15: 31,451,349 (GRCm39) |
Y45C |
|
Het |
Selenbp1 |
T |
A |
3: 94,847,021 (GRCm39) |
D182E |
probably benign |
Het |
Son |
TACCATGGACTCCCAGATGTTAGCCTCTAGCACCATGGACTCCCAGATGTTAGCCTCTAGCACCATGGACTCCCAGATGTTAGCAACTAGCACCATGGACTCCCAGATGTTAGC |
TACCATGGACTCCCAGATGTTAGCCTCTAGCACCATGGACTCCCAGATGTTAGCAACTAGCACCATGGACTCCCAGATGTTAGC |
16: 91,453,486 (GRCm39) |
|
probably benign |
Het |
Spef1 |
G |
A |
2: 131,014,653 (GRCm39) |
R90W |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,452,396 (GRCm39) |
S2787G |
probably benign |
Het |
Stox2 |
A |
G |
8: 47,645,271 (GRCm39) |
S730P |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,078,434 (GRCm39) |
N997S |
probably benign |
Het |
Tipin |
A |
G |
9: 64,195,508 (GRCm39) |
D38G |
probably benign |
Het |
Tshz1 |
T |
A |
18: 84,032,956 (GRCm39) |
K484M |
probably damaging |
Het |
Ttll3 |
CAAAGTAA |
CAAAGTAAAGTAA |
6: 113,376,118 (GRCm39) |
|
probably null |
Het |
Ttll3 |
A |
AAGTAC |
6: 113,376,125 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,747,355 (GRCm39) |
V4565I |
probably benign |
Het |
Ubr7 |
A |
G |
12: 102,741,971 (GRCm39) |
I402V |
probably damaging |
Het |
Ucn3 |
A |
T |
13: 3,991,216 (GRCm39) |
N145K |
possibly damaging |
Het |
Utp18 |
A |
T |
11: 93,772,899 (GRCm39) |
|
probably null |
Het |
Utp20 |
GAA |
GA |
10: 88,623,424 (GRCm39) |
|
probably null |
Het |
Vmn1r189 |
A |
G |
13: 22,286,711 (GRCm39) |
I42T |
possibly damaging |
Het |
Vmn2r91 |
T |
C |
17: 18,326,429 (GRCm39) |
M238T |
probably damaging |
Het |
Washc5 |
G |
T |
15: 59,205,516 (GRCm39) |
A1125D |
probably benign |
Het |
Wsb2 |
A |
G |
5: 117,508,827 (GRCm39) |
E87G |
probably damaging |
Het |
Zfat |
G |
A |
15: 68,084,600 (GRCm39) |
P97L |
probably benign |
Het |
Zfp87 |
T |
G |
13: 74,523,153 (GRCm39) |
T22P |
probably damaging |
Het |
|
Other mutations in Cpvl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01338:Cpvl
|
APN |
6 |
53,951,640 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01340:Cpvl
|
APN |
6 |
53,873,436 (GRCm39) |
nonsense |
probably null |
|
IGL02596:Cpvl
|
APN |
6 |
53,908,995 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4472001:Cpvl
|
UTSW |
6 |
53,873,464 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0242:Cpvl
|
UTSW |
6 |
53,909,485 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0242:Cpvl
|
UTSW |
6 |
53,909,485 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1586:Cpvl
|
UTSW |
6 |
53,903,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Cpvl
|
UTSW |
6 |
53,931,596 (GRCm39) |
missense |
probably benign |
0.01 |
R4609:Cpvl
|
UTSW |
6 |
53,951,605 (GRCm39) |
critical splice donor site |
probably null |
|
R4664:Cpvl
|
UTSW |
6 |
53,908,918 (GRCm39) |
missense |
probably benign |
0.00 |
R4665:Cpvl
|
UTSW |
6 |
53,908,918 (GRCm39) |
missense |
probably benign |
0.00 |
R4666:Cpvl
|
UTSW |
6 |
53,908,918 (GRCm39) |
missense |
probably benign |
0.00 |
R5863:Cpvl
|
UTSW |
6 |
53,850,413 (GRCm39) |
missense |
probably damaging |
0.99 |
R5909:Cpvl
|
UTSW |
6 |
53,909,413 (GRCm39) |
missense |
probably damaging |
0.98 |
R6163:Cpvl
|
UTSW |
6 |
53,850,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6948:Cpvl
|
UTSW |
6 |
53,873,468 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7023:Cpvl
|
UTSW |
6 |
53,944,797 (GRCm39) |
missense |
probably benign |
0.00 |
R7262:Cpvl
|
UTSW |
6 |
53,909,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7488:Cpvl
|
UTSW |
6 |
53,924,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R7694:Cpvl
|
UTSW |
6 |
53,909,502 (GRCm39) |
nonsense |
probably null |
|
R7728:Cpvl
|
UTSW |
6 |
53,902,275 (GRCm39) |
missense |
probably benign |
0.00 |
R7750:Cpvl
|
UTSW |
6 |
53,903,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Cpvl
|
UTSW |
6 |
53,873,476 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7773:Cpvl
|
UTSW |
6 |
53,908,890 (GRCm39) |
critical splice donor site |
probably null |
|
R7868:Cpvl
|
UTSW |
6 |
53,951,745 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8670:Cpvl
|
UTSW |
6 |
53,951,780 (GRCm39) |
start codon destroyed |
probably null |
0.69 |
R9228:Cpvl
|
UTSW |
6 |
53,951,779 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R9337:Cpvl
|
UTSW |
6 |
53,909,479 (GRCm39) |
missense |
probably damaging |
1.00 |
X0062:Cpvl
|
UTSW |
6 |
53,903,837 (GRCm39) |
missense |
possibly damaging |
0.88 |
|