Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
T |
A |
7: 119,130,983 (GRCm39) |
|
probably null |
Het |
Alb |
T |
A |
5: 90,610,665 (GRCm39) |
S82T |
probably benign |
Het |
Arf4 |
A |
G |
14: 26,374,248 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
T |
C |
14: 33,084,500 (GRCm39) |
C260R |
probably damaging |
Het |
Arhgap32 |
A |
G |
9: 32,081,441 (GRCm39) |
E153G |
probably benign |
Het |
Arhgef18 |
T |
A |
8: 3,484,897 (GRCm39) |
M200K |
probably damaging |
Het |
Atp1a4 |
T |
A |
1: 172,062,567 (GRCm39) |
N647Y |
probably benign |
Het |
Atp5f1c |
A |
T |
2: 10,064,428 (GRCm39) |
L226Q |
probably damaging |
Het |
Bcas1 |
T |
C |
2: 170,226,245 (GRCm39) |
K310R |
probably damaging |
Het |
Cadm3 |
T |
A |
1: 173,174,013 (GRCm39) |
T67S |
probably damaging |
Het |
Cartpt |
C |
T |
13: 100,036,588 (GRCm39) |
|
probably null |
Het |
Cenpj |
A |
T |
14: 56,790,840 (GRCm39) |
V403E |
possibly damaging |
Het |
Chst7 |
C |
A |
X: 19,927,110 (GRCm39) |
R386S |
probably damaging |
Het |
Cyp4f37 |
A |
T |
17: 32,844,126 (GRCm39) |
M77L |
probably benign |
Het |
Dnah7b |
A |
T |
1: 46,117,684 (GRCm39) |
D50V |
probably damaging |
Het |
Galnt4 |
A |
G |
10: 98,945,160 (GRCm39) |
D295G |
possibly damaging |
Het |
Gm6471 |
G |
A |
7: 142,385,360 (GRCm39) |
|
noncoding transcript |
Het |
Gm6818 |
T |
A |
7: 38,101,981 (GRCm39) |
|
noncoding transcript |
Het |
Gm9271 |
T |
A |
7: 39,013,734 (GRCm39) |
|
noncoding transcript |
Het |
Gpam |
A |
G |
19: 55,084,551 (GRCm39) |
|
probably null |
Het |
Gpr183 |
T |
C |
14: 122,192,149 (GRCm39) |
D124G |
probably damaging |
Het |
Ift140 |
C |
A |
17: 25,317,935 (GRCm39) |
|
probably benign |
Het |
Itih5 |
A |
C |
2: 10,195,180 (GRCm39) |
I191L |
probably benign |
Het |
Jcad |
A |
G |
18: 4,674,175 (GRCm39) |
T646A |
probably benign |
Het |
Kank1 |
T |
C |
19: 25,387,944 (GRCm39) |
M511T |
probably benign |
Het |
Krt74 |
A |
T |
15: 101,667,304 (GRCm39) |
|
noncoding transcript |
Het |
Lrrc37a |
A |
G |
11: 103,395,363 (GRCm39) |
S21P |
probably benign |
Het |
Lrrc8c |
G |
A |
5: 105,756,240 (GRCm39) |
V672I |
probably benign |
Het |
Lypd4 |
T |
C |
7: 24,566,151 (GRCm39) |
R58G |
probably benign |
Het |
Magi1 |
A |
T |
6: 93,663,624 (GRCm39) |
|
probably null |
Het |
Mefv |
T |
A |
16: 3,526,071 (GRCm39) |
L745F |
possibly damaging |
Het |
Myh13 |
A |
T |
11: 67,255,564 (GRCm39) |
K1645* |
probably null |
Het |
Naip6 |
A |
G |
13: 100,431,239 (GRCm39) |
|
probably null |
Het |
Nlrp1c-ps |
T |
C |
11: 71,171,382 (GRCm39) |
|
noncoding transcript |
Het |
Nsmce3 |
A |
T |
7: 64,522,530 (GRCm39) |
L46Q |
probably benign |
Het |
Or51aa2 |
A |
G |
7: 103,188,393 (GRCm39) |
V16A |
possibly damaging |
Het |
Or6k6 |
T |
A |
1: 173,945,427 (GRCm39) |
M52L |
probably benign |
Het |
Or8k37 |
T |
C |
2: 86,469,512 (GRCm39) |
D180G |
possibly damaging |
Het |
P2ry12 |
T |
C |
3: 59,125,325 (GRCm39) |
|
probably null |
Het |
Pcx |
T |
A |
19: 4,669,916 (GRCm39) |
V861E |
probably damaging |
Het |
Pkp3 |
C |
T |
7: 140,662,612 (GRCm39) |
P75S |
probably benign |
Het |
Plscr4 |
T |
C |
9: 92,364,920 (GRCm39) |
|
probably null |
Het |
Pole |
A |
G |
5: 110,454,253 (GRCm39) |
T923A |
probably benign |
Het |
Ptgir |
A |
G |
7: 16,640,794 (GRCm39) |
M29V |
possibly damaging |
Het |
Rhot2 |
A |
C |
17: 26,060,305 (GRCm39) |
|
probably benign |
Het |
Rsrp1 |
A |
G |
4: 134,651,488 (GRCm39) |
Y84C |
unknown |
Het |
Sbf2 |
T |
C |
7: 109,934,606 (GRCm39) |
K1348E |
probably damaging |
Het |
Sgip1 |
A |
T |
4: 102,726,951 (GRCm39) |
N53Y |
probably damaging |
Het |
Snapc2 |
A |
G |
8: 4,304,998 (GRCm39) |
T127A |
possibly damaging |
Het |
Snx8 |
A |
G |
5: 140,341,713 (GRCm39) |
|
probably null |
Het |
Spag8 |
A |
G |
4: 43,653,378 (GRCm39) |
|
probably benign |
Het |
Srebf2 |
T |
C |
15: 82,076,503 (GRCm39) |
F718L |
probably damaging |
Het |
Szt2 |
C |
G |
4: 118,233,026 (GRCm39) |
|
probably benign |
Het |
Traf3ip2 |
C |
T |
10: 39,515,256 (GRCm39) |
P345S |
possibly damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,004,146 (GRCm39) |
Y62* |
probably null |
Het |
Usp29 |
T |
A |
7: 6,965,914 (GRCm39) |
S586T |
possibly damaging |
Het |
Vasp |
T |
C |
7: 18,998,350 (GRCm39) |
N108S |
probably benign |
Het |
Vmn1r214 |
A |
G |
13: 23,219,141 (GRCm39) |
M212V |
probably benign |
Het |
Wipi2 |
G |
C |
5: 142,645,345 (GRCm39) |
A194P |
probably benign |
Het |
Zbtb4 |
T |
A |
11: 69,667,355 (GRCm39) |
I220N |
probably damaging |
Het |
Zcchc2 |
A |
T |
1: 105,917,996 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
T |
A |
13: 67,769,534 (GRCm39) |
K232* |
probably null |
Het |
Zfp995 |
A |
T |
17: 22,106,320 (GRCm39) |
M1K |
probably null |
Het |
|
Other mutations in Gin1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01479:Gin1
|
APN |
1 |
97,720,097 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01508:Gin1
|
APN |
1 |
97,705,162 (GRCm39) |
missense |
probably benign |
|
IGL01874:Gin1
|
APN |
1 |
97,710,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R0136:Gin1
|
UTSW |
1 |
97,710,741 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0299:Gin1
|
UTSW |
1 |
97,710,741 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1302:Gin1
|
UTSW |
1 |
97,703,314 (GRCm39) |
nonsense |
probably null |
|
R1607:Gin1
|
UTSW |
1 |
97,713,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1675:Gin1
|
UTSW |
1 |
97,713,780 (GRCm39) |
nonsense |
probably null |
|
R1739:Gin1
|
UTSW |
1 |
97,713,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R1769:Gin1
|
UTSW |
1 |
97,720,162 (GRCm39) |
missense |
probably benign |
0.02 |
R1817:Gin1
|
UTSW |
1 |
97,712,951 (GRCm39) |
splice site |
probably null |
|
R1818:Gin1
|
UTSW |
1 |
97,712,951 (GRCm39) |
splice site |
probably null |
|
R1819:Gin1
|
UTSW |
1 |
97,712,951 (GRCm39) |
splice site |
probably null |
|
R1907:Gin1
|
UTSW |
1 |
97,703,172 (GRCm39) |
unclassified |
probably benign |
|
R2325:Gin1
|
UTSW |
1 |
97,720,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R4206:Gin1
|
UTSW |
1 |
97,720,145 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4571:Gin1
|
UTSW |
1 |
97,712,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Gin1
|
UTSW |
1 |
97,720,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Gin1
|
UTSW |
1 |
97,712,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5659:Gin1
|
UTSW |
1 |
97,703,257 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6360:Gin1
|
UTSW |
1 |
97,720,264 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7035:Gin1
|
UTSW |
1 |
97,720,100 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7229:Gin1
|
UTSW |
1 |
97,712,876 (GRCm39) |
missense |
probably benign |
0.02 |
R8269:Gin1
|
UTSW |
1 |
97,710,929 (GRCm39) |
missense |
probably damaging |
0.98 |
R8877:Gin1
|
UTSW |
1 |
97,710,941 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9149:Gin1
|
UTSW |
1 |
97,710,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R9480:Gin1
|
UTSW |
1 |
97,705,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R9643:Gin1
|
UTSW |
1 |
97,712,498 (GRCm39) |
missense |
probably benign |
0.08 |
R9697:Gin1
|
UTSW |
1 |
97,712,897 (GRCm39) |
missense |
probably benign |
0.00 |
R9787:Gin1
|
UTSW |
1 |
97,703,211 (GRCm39) |
missense |
probably damaging |
1.00 |
|