Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
T |
C |
4: 53,085,092 (GRCm39) |
|
probably null |
Het |
Abca7 |
C |
T |
10: 79,840,617 (GRCm39) |
Q870* |
probably null |
Het |
Ambp |
C |
T |
4: 63,070,888 (GRCm39) |
V64M |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,622,212 (GRCm39) |
V1542A |
probably damaging |
Het |
Anln |
T |
C |
9: 22,287,797 (GRCm39) |
Y168C |
probably benign |
Het |
Apoa4 |
T |
A |
9: 46,152,803 (GRCm39) |
N29K |
probably benign |
Het |
Arfgef1 |
T |
C |
1: 10,283,334 (GRCm39) |
T192A |
probably damaging |
Het |
Atad2b |
G |
T |
12: 5,084,513 (GRCm39) |
D1420Y |
probably damaging |
Het |
Baiap3 |
A |
G |
17: 25,465,336 (GRCm39) |
W648R |
possibly damaging |
Het |
Bank1 |
A |
G |
3: 135,960,662 (GRCm39) |
L198P |
probably damaging |
Het |
Bicd2 |
A |
G |
13: 49,532,940 (GRCm39) |
K509E |
possibly damaging |
Het |
Cacna1e |
T |
C |
1: 154,289,739 (GRCm39) |
D1821G |
probably damaging |
Het |
Ccdc80 |
G |
A |
16: 44,936,650 (GRCm39) |
V692M |
possibly damaging |
Het |
Ccdc88a |
C |
T |
11: 29,432,133 (GRCm39) |
Q308* |
probably null |
Het |
Ccl8 |
T |
C |
11: 82,006,973 (GRCm39) |
V62A |
probably damaging |
Het |
Clspn |
C |
A |
4: 126,472,179 (GRCm39) |
P951Q |
probably damaging |
Het |
Cngb1 |
T |
A |
8: 95,985,785 (GRCm39) |
I858F |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Ctc1 |
C |
T |
11: 68,924,328 (GRCm39) |
A960V |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 31,009,221 (GRCm39) |
E1106G |
probably damaging |
Het |
Dido1 |
C |
T |
2: 180,302,606 (GRCm39) |
R1766H |
probably damaging |
Het |
Dipk1a |
A |
T |
5: 108,057,400 (GRCm39) |
L386* |
probably null |
Het |
Dnajc13 |
G |
T |
9: 104,063,922 (GRCm39) |
N1341K |
probably damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Homo |
E2f8 |
G |
A |
7: 48,524,918 (GRCm39) |
|
probably benign |
Het |
Entpd8 |
A |
G |
2: 24,972,967 (GRCm39) |
D91G |
possibly damaging |
Het |
Fars2 |
A |
G |
13: 36,388,564 (GRCm39) |
R18G |
possibly damaging |
Het |
Fcgbp |
A |
G |
7: 27,816,995 (GRCm39) |
S2486G |
probably benign |
Het |
Fibin |
C |
T |
2: 110,192,963 (GRCm39) |
D60N |
possibly damaging |
Het |
Fpgs |
A |
G |
2: 32,577,379 (GRCm39) |
|
probably benign |
Het |
Galnt15 |
A |
G |
14: 31,765,247 (GRCm39) |
D303G |
probably damaging |
Het |
Gli3 |
C |
A |
13: 15,899,049 (GRCm39) |
T812K |
possibly damaging |
Het |
Gpbar1 |
G |
C |
1: 74,318,404 (GRCm39) |
A216P |
probably benign |
Het |
Grin2d |
A |
G |
7: 45,507,357 (GRCm39) |
I448T |
probably benign |
Het |
Il21 |
C |
A |
3: 37,286,653 (GRCm39) |
S21I |
probably damaging |
Het |
Iqce |
G |
T |
5: 140,677,376 (GRCm39) |
D148E |
probably damaging |
Het |
Iqcg |
T |
A |
16: 32,839,884 (GRCm39) |
E354V |
probably damaging |
Het |
Iws1 |
T |
C |
18: 32,226,320 (GRCm39) |
|
probably benign |
Het |
Ly75 |
C |
T |
2: 60,206,238 (GRCm39) |
G144S |
probably damaging |
Het |
Marco |
C |
A |
1: 120,421,954 (GRCm39) |
M83I |
probably benign |
Het |
Mettl6 |
A |
T |
14: 31,201,752 (GRCm39) |
L185H |
probably damaging |
Het |
Mppe1 |
C |
T |
18: 67,362,773 (GRCm39) |
G154D |
probably damaging |
Het |
Mrpl42 |
T |
C |
10: 95,326,237 (GRCm39) |
E85G |
probably benign |
Het |
Neb |
A |
G |
2: 52,079,921 (GRCm39) |
V5518A |
probably damaging |
Het |
Or12d13 |
A |
T |
17: 37,647,759 (GRCm39) |
F121L |
probably benign |
Het |
Or52p1 |
T |
A |
7: 104,267,812 (GRCm39) |
F317I |
probably null |
Het |
Or5b105 |
A |
T |
19: 13,080,053 (GRCm39) |
I199N |
probably damaging |
Het |
Or7a42 |
T |
A |
10: 78,791,766 (GRCm39) |
C242* |
probably null |
Het |
Or7d10 |
G |
T |
9: 19,831,655 (GRCm39) |
S50I |
probably benign |
Het |
Perm1 |
A |
G |
4: 156,302,034 (GRCm39) |
T193A |
probably benign |
Het |
Prkd2 |
T |
A |
7: 16,582,652 (GRCm39) |
C172S |
probably damaging |
Het |
Prr23a3 |
T |
A |
9: 98,747,431 (GRCm39) |
D128E |
possibly damaging |
Het |
Prss28 |
A |
G |
17: 25,528,711 (GRCm39) |
Y51C |
probably damaging |
Het |
Psmb1 |
A |
T |
17: 15,696,451 (GRCm39) |
M85K |
probably benign |
Het |
Rae1 |
T |
A |
2: 172,854,401 (GRCm39) |
|
probably benign |
Het |
Rasal1 |
A |
G |
5: 120,816,741 (GRCm39) |
D759G |
probably benign |
Het |
Rcvrn |
G |
A |
11: 67,586,246 (GRCm39) |
G2R |
probably damaging |
Het |
Robo3 |
C |
T |
9: 37,334,640 (GRCm39) |
A597T |
probably damaging |
Het |
Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Homo |
Sdcbp |
T |
A |
4: 6,378,980 (GRCm39) |
Y22* |
probably null |
Het |
Sin3a |
T |
C |
9: 57,025,360 (GRCm39) |
F1069L |
probably damaging |
Het |
Slitrk3 |
C |
T |
3: 72,957,129 (GRCm39) |
V548I |
possibly damaging |
Het |
Tbc1d22a |
A |
G |
15: 86,275,287 (GRCm39) |
H403R |
probably damaging |
Het |
Tbr1 |
G |
T |
2: 61,635,593 (GRCm39) |
|
probably null |
Het |
Tiam2 |
T |
A |
17: 3,555,985 (GRCm39) |
D65E |
probably damaging |
Het |
Tpcn2 |
A |
G |
7: 144,813,833 (GRCm39) |
S488P |
probably benign |
Het |
Trav9-2 |
T |
C |
14: 53,828,695 (GRCm39) |
S22P |
probably damaging |
Het |
Trim34a |
T |
A |
7: 103,897,069 (GRCm39) |
N44K |
probably benign |
Het |
Unc79 |
C |
G |
12: 103,078,691 (GRCm39) |
P1619A |
probably benign |
Het |
Usp22 |
A |
T |
11: 61,048,042 (GRCm39) |
V426E |
probably damaging |
Het |
Vhl |
A |
T |
6: 113,601,159 (GRCm39) |
M20L |
unknown |
Het |
Vmn1r215 |
G |
A |
13: 23,260,064 (GRCm39) |
A35T |
probably benign |
Het |
Vmn1r222 |
G |
A |
13: 23,416,602 (GRCm39) |
L204F |
possibly damaging |
Het |
Zfp871 |
A |
T |
17: 32,994,829 (GRCm39) |
H115Q |
probably damaging |
Het |
Zpr1 |
T |
A |
9: 46,189,640 (GRCm39) |
F340L |
probably benign |
Het |
|
Other mutations in 1700010I14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00988:1700010I14Rik
|
APN |
17 |
9,215,937 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01569:1700010I14Rik
|
APN |
17 |
9,215,827 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03024:1700010I14Rik
|
APN |
17 |
9,212,464 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03410:1700010I14Rik
|
APN |
17 |
9,220,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R0017:1700010I14Rik
|
UTSW |
17 |
9,226,938 (GRCm39) |
utr 3 prime |
probably benign |
|
R0017:1700010I14Rik
|
UTSW |
17 |
9,226,938 (GRCm39) |
utr 3 prime |
probably benign |
|
R0324:1700010I14Rik
|
UTSW |
17 |
9,219,989 (GRCm39) |
missense |
probably benign |
0.33 |
R0361:1700010I14Rik
|
UTSW |
17 |
9,211,378 (GRCm39) |
missense |
probably benign |
0.39 |
R0482:1700010I14Rik
|
UTSW |
17 |
9,207,255 (GRCm39) |
critical splice donor site |
probably null |
|
R0529:1700010I14Rik
|
UTSW |
17 |
9,211,228 (GRCm39) |
missense |
probably benign |
0.32 |
R1102:1700010I14Rik
|
UTSW |
17 |
9,211,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1964:1700010I14Rik
|
UTSW |
17 |
9,211,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R3620:1700010I14Rik
|
UTSW |
17 |
9,226,864 (GRCm39) |
missense |
probably benign |
0.15 |
R4259:1700010I14Rik
|
UTSW |
17 |
9,214,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:1700010I14Rik
|
UTSW |
17 |
9,214,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:1700010I14Rik
|
UTSW |
17 |
9,210,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:1700010I14Rik
|
UTSW |
17 |
9,224,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:1700010I14Rik
|
UTSW |
17 |
9,226,845 (GRCm39) |
missense |
probably benign |
0.41 |
R5225:1700010I14Rik
|
UTSW |
17 |
9,226,839 (GRCm39) |
nonsense |
probably null |
|
R5383:1700010I14Rik
|
UTSW |
17 |
9,211,532 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6031:1700010I14Rik
|
UTSW |
17 |
9,214,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6031:1700010I14Rik
|
UTSW |
17 |
9,214,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6505:1700010I14Rik
|
UTSW |
17 |
9,220,772 (GRCm39) |
missense |
probably benign |
0.08 |
R6736:1700010I14Rik
|
UTSW |
17 |
9,211,100 (GRCm39) |
missense |
probably benign |
0.01 |
R7089:1700010I14Rik
|
UTSW |
17 |
9,226,927 (GRCm39) |
missense |
probably benign |
0.00 |
R7097:1700010I14Rik
|
UTSW |
17 |
9,224,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:1700010I14Rik
|
UTSW |
17 |
9,215,861 (GRCm39) |
nonsense |
probably null |
|
R7405:1700010I14Rik
|
UTSW |
17 |
9,220,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R7567:1700010I14Rik
|
UTSW |
17 |
9,226,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:1700010I14Rik
|
UTSW |
17 |
9,220,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:1700010I14Rik
|
UTSW |
17 |
9,226,939 (GRCm39) |
missense |
unknown |
|
R8805:1700010I14Rik
|
UTSW |
17 |
9,226,737 (GRCm39) |
nonsense |
probably null |
|
R9007:1700010I14Rik
|
UTSW |
17 |
9,226,935 (GRCm39) |
missense |
probably benign |
0.01 |
R9308:1700010I14Rik
|
UTSW |
17 |
9,220,667 (GRCm39) |
nonsense |
probably null |
|
R9400:1700010I14Rik
|
UTSW |
17 |
9,211,118 (GRCm39) |
missense |
probably benign |
0.01 |
|