Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk2 |
T |
A |
18: 65,433,212 (GRCm39) |
I1765F |
probably damaging |
Het |
Ano5 |
T |
A |
7: 51,237,414 (GRCm39) |
I696N |
probably damaging |
Het |
Areg |
A |
T |
5: 91,291,375 (GRCm39) |
N106I |
probably damaging |
Het |
Atad2b |
A |
G |
12: 5,035,710 (GRCm39) |
N759D |
probably benign |
Het |
B4galnt4 |
T |
C |
7: 140,641,239 (GRCm39) |
L18P |
probably damaging |
Het |
Boc |
T |
C |
16: 44,312,247 (GRCm39) |
D605G |
probably damaging |
Het |
Cfap46 |
G |
T |
7: 139,246,203 (GRCm39) |
Q387K |
possibly damaging |
Het |
Cfap74 |
C |
A |
4: 155,547,529 (GRCm39) |
H1238Q |
probably benign |
Het |
Clip2 |
A |
G |
5: 134,564,051 (GRCm39) |
|
probably benign |
Het |
Cog4 |
T |
C |
8: 111,585,244 (GRCm39) |
I303T |
probably damaging |
Het |
Col18a1 |
C |
T |
10: 76,932,001 (GRCm39) |
V363I |
unknown |
Het |
Crip3 |
A |
T |
17: 46,742,156 (GRCm39) |
K184* |
probably null |
Het |
Ddi1 |
A |
G |
9: 6,265,799 (GRCm39) |
M190T |
probably benign |
Het |
Dnah3 |
G |
A |
7: 119,628,248 (GRCm39) |
Q1459* |
probably null |
Het |
Dpp8 |
A |
G |
9: 64,962,205 (GRCm39) |
D415G |
probably benign |
Het |
Ehhadh |
T |
G |
16: 21,581,438 (GRCm39) |
D518A |
probably damaging |
Het |
Erbb2 |
A |
G |
11: 98,318,869 (GRCm39) |
K549R |
probably benign |
Het |
Fbxl3 |
G |
A |
14: 103,326,854 (GRCm39) |
S176L |
probably damaging |
Het |
Gm1979 |
T |
C |
5: 26,206,119 (GRCm39) |
T154A |
probably benign |
Het |
Gm6871 |
G |
T |
7: 41,195,204 (GRCm39) |
T511K |
probably damaging |
Het |
Gtf2h1 |
C |
T |
7: 46,454,489 (GRCm39) |
A157V |
probably benign |
Het |
Hexb |
T |
C |
13: 97,313,259 (GRCm39) |
|
probably benign |
Het |
Ifi214 |
A |
T |
1: 173,352,509 (GRCm39) |
S307T |
possibly damaging |
Het |
Ighv3-4 |
A |
T |
12: 114,217,533 (GRCm39) |
D19E |
probably benign |
Het |
Klk6 |
A |
G |
7: 43,478,597 (GRCm39) |
H168R |
probably benign |
Het |
Large2 |
A |
G |
2: 92,196,950 (GRCm39) |
|
probably benign |
Het |
Myo5c |
T |
C |
9: 75,191,224 (GRCm39) |
I1086T |
probably benign |
Het |
Nes |
C |
A |
3: 87,886,666 (GRCm39) |
P1598T |
probably damaging |
Het |
Or13a25 |
A |
G |
7: 140,247,496 (GRCm39) |
N99D |
probably benign |
Het |
Or51f1d |
T |
C |
7: 102,701,003 (GRCm39) |
V166A |
probably benign |
Het |
Or5g25 |
T |
A |
2: 85,478,647 (GRCm39) |
Q6L |
probably damaging |
Het |
Otud7a |
A |
G |
7: 63,300,702 (GRCm39) |
D47G |
probably damaging |
Het |
Phactr1 |
T |
A |
13: 43,248,363 (GRCm39) |
N437K |
possibly damaging |
Het |
Plcb1 |
A |
T |
2: 135,186,078 (GRCm39) |
I682F |
probably damaging |
Het |
Plcz1 |
T |
A |
6: 139,986,344 (GRCm39) |
|
probably null |
Het |
Prl7a1 |
T |
A |
13: 27,821,549 (GRCm39) |
Q129L |
possibly damaging |
Het |
Prrt4 |
T |
C |
6: 29,170,163 (GRCm39) |
Y763C |
probably damaging |
Het |
Psma7 |
T |
C |
2: 179,681,304 (GRCm39) |
|
probably benign |
Het |
Serpinb6b |
G |
C |
13: 33,156,246 (GRCm39) |
C112S |
probably damaging |
Het |
Slc14a2 |
G |
A |
18: 78,250,283 (GRCm39) |
R62C |
probably damaging |
Het |
Slc35f5 |
G |
A |
1: 125,500,211 (GRCm39) |
A242T |
possibly damaging |
Het |
Speer4b |
T |
C |
5: 27,706,311 (GRCm39) |
R19G |
probably benign |
Het |
Trank1 |
A |
G |
9: 111,196,103 (GRCm39) |
I1376V |
probably benign |
Het |
Trbv12-2 |
A |
G |
6: 41,095,831 (GRCm39) |
N12D |
probably benign |
Het |
Uba7 |
T |
C |
9: 107,854,001 (GRCm39) |
|
probably null |
Het |
Upf3a |
A |
G |
8: 13,846,591 (GRCm39) |
R324G |
probably benign |
Het |
Usp46 |
T |
G |
5: 74,192,928 (GRCm39) |
|
probably benign |
Het |
Vmn2r14 |
T |
G |
5: 109,364,277 (GRCm39) |
|
probably null |
Het |
Wbp2 |
G |
A |
11: 115,971,373 (GRCm39) |
|
probably benign |
Het |
Wdpcp |
T |
A |
11: 21,645,269 (GRCm39) |
N232K |
probably damaging |
Het |
Wdpcp |
T |
A |
11: 21,645,271 (GRCm39) |
M233K |
probably benign |
Het |
Zfp157 |
A |
G |
5: 138,445,803 (GRCm39) |
I53V |
probably damaging |
Het |
|
Other mutations in 4930563M21Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02721:4930563M21Rik
|
APN |
9 |
55,888,124 (GRCm39) |
missense |
probably benign |
0.14 |
R2471:4930563M21Rik
|
UTSW |
9 |
55,888,147 (GRCm39) |
missense |
probably benign |
0.03 |
R3831:4930563M21Rik
|
UTSW |
9 |
55,880,992 (GRCm39) |
missense |
unknown |
|
R4237:4930563M21Rik
|
UTSW |
9 |
55,888,126 (GRCm39) |
missense |
probably benign |
0.29 |
R4238:4930563M21Rik
|
UTSW |
9 |
55,888,126 (GRCm39) |
missense |
probably benign |
0.29 |
R5412:4930563M21Rik
|
UTSW |
9 |
55,886,036 (GRCm39) |
missense |
probably damaging |
0.97 |
R6191:4930563M21Rik
|
UTSW |
9 |
55,909,807 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6368:4930563M21Rik
|
UTSW |
9 |
55,897,416 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6415:4930563M21Rik
|
UTSW |
9 |
55,881,296 (GRCm39) |
missense |
probably benign |
0.00 |
R6700:4930563M21Rik
|
UTSW |
9 |
55,881,140 (GRCm39) |
missense |
unknown |
|
R6727:4930563M21Rik
|
UTSW |
9 |
55,896,760 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7346:4930563M21Rik
|
UTSW |
9 |
55,914,587 (GRCm39) |
missense |
unknown |
|
R7470:4930563M21Rik
|
UTSW |
9 |
55,898,622 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7499:4930563M21Rik
|
UTSW |
9 |
55,907,186 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7609:4930563M21Rik
|
UTSW |
9 |
55,896,744 (GRCm39) |
missense |
probably benign |
0.00 |
R7616:4930563M21Rik
|
UTSW |
9 |
55,896,738 (GRCm39) |
missense |
probably benign |
0.03 |
R7662:4930563M21Rik
|
UTSW |
9 |
55,885,999 (GRCm39) |
missense |
probably benign |
0.00 |
R8018:4930563M21Rik
|
UTSW |
9 |
55,880,991 (GRCm39) |
missense |
unknown |
|
R8057:4930563M21Rik
|
UTSW |
9 |
55,916,564 (GRCm39) |
missense |
unknown |
|
R8077:4930563M21Rik
|
UTSW |
9 |
55,895,250 (GRCm39) |
missense |
probably damaging |
0.97 |
R8782:4930563M21Rik
|
UTSW |
9 |
55,910,242 (GRCm39) |
critical splice donor site |
probably null |
|
R9178:4930563M21Rik
|
UTSW |
9 |
55,880,992 (GRCm39) |
missense |
unknown |
|
R9214:4930563M21Rik
|
UTSW |
9 |
55,890,653 (GRCm39) |
missense |
probably benign |
0.03 |
R9293:4930563M21Rik
|
UTSW |
9 |
55,916,568 (GRCm39) |
missense |
unknown |
|
R9441:4930563M21Rik
|
UTSW |
9 |
55,917,776 (GRCm39) |
missense |
unknown |
|
R9602:4930563M21Rik
|
UTSW |
9 |
55,910,261 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9667:4930563M21Rik
|
UTSW |
9 |
55,890,645 (GRCm39) |
nonsense |
probably null |
|
|