Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
T |
A |
6: 124,333,882 (GRCm39) |
M33L |
probably benign |
Het |
2310003L06Rik |
A |
G |
5: 88,119,890 (GRCm39) |
T216A |
probably benign |
Het |
9330161L09Rik |
A |
C |
12: 103,373,837 (GRCm39) |
C12G |
unknown |
Het |
Ahdc1 |
T |
A |
4: 132,788,929 (GRCm39) |
F57I |
possibly damaging |
Het |
Amotl1 |
C |
A |
9: 14,461,787 (GRCm39) |
A809S |
possibly damaging |
Het |
Ankfn1 |
C |
T |
11: 89,414,011 (GRCm39) |
M121I |
probably benign |
Het |
Aspm |
A |
G |
1: 139,404,453 (GRCm39) |
D1261G |
probably damaging |
Het |
Axl |
T |
C |
7: 25,469,658 (GRCm39) |
T502A |
probably damaging |
Het |
Catsperd |
G |
A |
17: 56,968,252 (GRCm39) |
D546N |
probably benign |
Het |
Ccdc102a |
A |
G |
8: 95,639,748 (GRCm39) |
V182A |
possibly damaging |
Het |
Cdh23 |
C |
T |
10: 60,153,664 (GRCm39) |
A2309T |
probably benign |
Het |
Cfap69 |
A |
T |
5: 5,676,064 (GRCm39) |
N210K |
probably benign |
Het |
Cnot1 |
A |
G |
8: 96,500,054 (GRCm39) |
S147P |
probably benign |
Het |
Cntnap5c |
T |
C |
17: 58,600,912 (GRCm39) |
S752P |
probably benign |
Het |
Cyp3a41a |
A |
T |
5: 145,642,654 (GRCm39) |
M235K |
probably benign |
Het |
Cyp4f15 |
A |
G |
17: 32,919,185 (GRCm39) |
D336G |
possibly damaging |
Het |
Dagla |
A |
G |
19: 10,228,525 (GRCm39) |
I631T |
possibly damaging |
Het |
Dph6 |
C |
T |
2: 114,353,591 (GRCm39) |
C199Y |
probably damaging |
Het |
Ermard |
T |
A |
17: 15,273,495 (GRCm39) |
L360Q |
probably damaging |
Het |
F830045P16Rik |
T |
C |
2: 129,314,708 (GRCm39) |
T190A |
probably benign |
Het |
Fgfr3 |
G |
T |
5: 33,887,316 (GRCm39) |
V212L |
possibly damaging |
Het |
Flnb |
C |
A |
14: 7,887,541 (GRCm38) |
C450* |
probably null |
Het |
Gls |
T |
C |
1: 52,239,015 (GRCm39) |
Y362C |
probably damaging |
Het |
Gngt1 |
A |
G |
6: 3,994,246 (GRCm39) |
D8G |
possibly damaging |
Het |
Gns |
T |
C |
10: 121,216,080 (GRCm39) |
F276L |
|
Het |
Impa2 |
C |
T |
18: 67,422,473 (GRCm39) |
|
probably benign |
Het |
Itgal |
A |
T |
7: 126,905,883 (GRCm39) |
D355V |
probably benign |
Het |
Kdm6b |
A |
T |
11: 69,297,521 (GRCm39) |
|
probably null |
Het |
Klk1b1 |
T |
A |
7: 43,618,715 (GRCm39) |
C31S |
probably damaging |
Het |
Ldb3 |
A |
T |
14: 34,277,312 (GRCm39) |
V354E |
probably benign |
Het |
Mettl21c |
T |
A |
1: 44,049,142 (GRCm39) |
Y135F |
probably benign |
Het |
Mocs1 |
A |
G |
17: 49,740,303 (GRCm39) |
T77A |
probably damaging |
Het |
Ndufs1 |
T |
C |
1: 63,209,274 (GRCm39) |
N30D |
probably benign |
Het |
Or1j11 |
T |
C |
2: 36,312,126 (GRCm39) |
S239P |
probably damaging |
Het |
Or4a71 |
T |
A |
2: 89,358,494 (GRCm39) |
K87* |
probably null |
Het |
Otog |
C |
A |
7: 45,937,885 (GRCm39) |
P1865T |
possibly damaging |
Het |
Pabpc1l |
T |
C |
2: 163,873,140 (GRCm39) |
S137P |
probably damaging |
Het |
Pilrb1 |
C |
A |
5: 137,855,657 (GRCm39) |
W78L |
probably damaging |
Het |
Plekha6 |
A |
G |
1: 133,214,085 (GRCm39) |
Y832C |
possibly damaging |
Het |
Ppan |
C |
A |
9: 20,803,199 (GRCm39) |
Q424K |
probably benign |
Het |
Ppp1r12a |
T |
A |
10: 108,087,782 (GRCm39) |
N544K |
probably damaging |
Het |
Pramel16 |
T |
C |
4: 143,676,294 (GRCm39) |
E270G |
probably benign |
Het |
Pstpip2 |
A |
G |
18: 77,961,155 (GRCm39) |
D246G |
possibly damaging |
Het |
Rasef |
G |
A |
4: 73,662,356 (GRCm39) |
T198I |
probably damaging |
Het |
Rbm12 |
T |
C |
2: 155,938,463 (GRCm39) |
H603R |
probably benign |
Het |
Rims1 |
T |
C |
1: 22,482,490 (GRCm39) |
R179G |
probably damaging |
Het |
Scel |
T |
C |
14: 103,811,836 (GRCm39) |
L288P |
possibly damaging |
Het |
Sel1l |
A |
T |
12: 91,778,726 (GRCm39) |
D696E |
probably benign |
Het |
Slc4a8 |
A |
G |
15: 100,689,482 (GRCm39) |
K416R |
possibly damaging |
Het |
Tmem132b |
A |
T |
5: 125,700,115 (GRCm39) |
M218L |
probably benign |
Het |
Tnrc6a |
T |
C |
7: 122,791,881 (GRCm39) |
S1800P |
probably benign |
Het |
Tpcn1 |
A |
C |
5: 120,680,015 (GRCm39) |
L576R |
probably damaging |
Het |
Vmn2r34 |
T |
G |
7: 7,675,723 (GRCm39) |
Q555P |
possibly damaging |
Het |
Vwa8 |
C |
T |
14: 79,335,801 (GRCm39) |
T1419I |
probably benign |
Het |
Xrn2 |
T |
C |
2: 146,855,081 (GRCm39) |
Y14H |
probably benign |
Het |
Zfp1007 |
A |
G |
5: 109,823,708 (GRCm39) |
C581R |
probably damaging |
Het |
Zfyve28 |
A |
T |
5: 34,382,376 (GRCm39) |
D241E |
probably benign |
Het |
|
Other mutations in Grin2d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01097:Grin2d
|
APN |
7 |
45,502,716 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01772:Grin2d
|
APN |
7 |
45,507,890 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01952:Grin2d
|
APN |
7 |
45,511,704 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01994:Grin2d
|
APN |
7 |
45,507,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Grin2d
|
APN |
7 |
45,503,846 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03180:Grin2d
|
APN |
7 |
45,502,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R1121:Grin2d
|
UTSW |
7 |
45,503,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R1934:Grin2d
|
UTSW |
7 |
45,506,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2915:Grin2d
|
UTSW |
7 |
45,482,781 (GRCm39) |
unclassified |
probably benign |
|
R4162:Grin2d
|
UTSW |
7 |
45,507,042 (GRCm39) |
missense |
probably damaging |
0.98 |
R4753:Grin2d
|
UTSW |
7 |
45,483,330 (GRCm39) |
missense |
probably damaging |
0.98 |
R4781:Grin2d
|
UTSW |
7 |
45,511,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Grin2d
|
UTSW |
7 |
45,506,205 (GRCm39) |
missense |
probably damaging |
0.96 |
R4820:Grin2d
|
UTSW |
7 |
45,507,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R4877:Grin2d
|
UTSW |
7 |
45,504,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R4979:Grin2d
|
UTSW |
7 |
45,507,357 (GRCm39) |
missense |
probably benign |
0.03 |
R5092:Grin2d
|
UTSW |
7 |
45,503,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R6364:Grin2d
|
UTSW |
7 |
45,507,878 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6565:Grin2d
|
UTSW |
7 |
45,484,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R6747:Grin2d
|
UTSW |
7 |
45,511,692 (GRCm39) |
missense |
probably damaging |
0.99 |
R6816:Grin2d
|
UTSW |
7 |
45,483,106 (GRCm39) |
unclassified |
probably benign |
|
R7072:Grin2d
|
UTSW |
7 |
45,506,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7237:Grin2d
|
UTSW |
7 |
45,515,600 (GRCm39) |
nonsense |
probably null |
|
R7243:Grin2d
|
UTSW |
7 |
45,515,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7385:Grin2d
|
UTSW |
7 |
45,506,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R7577:Grin2d
|
UTSW |
7 |
45,511,803 (GRCm39) |
missense |
probably benign |
0.01 |
R8100:Grin2d
|
UTSW |
7 |
45,483,171 (GRCm39) |
missense |
unknown |
|
R8179:Grin2d
|
UTSW |
7 |
45,507,452 (GRCm39) |
nonsense |
probably null |
|
R8877:Grin2d
|
UTSW |
7 |
45,503,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R8988:Grin2d
|
UTSW |
7 |
45,483,425 (GRCm39) |
nonsense |
probably null |
|
R9643:Grin2d
|
UTSW |
7 |
45,506,948 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1177:Grin2d
|
UTSW |
7 |
45,482,601 (GRCm39) |
missense |
unknown |
|
|