Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
A |
16: 4,682,454 (GRCm39) |
L195* |
probably null |
Het |
Ahnak |
T |
G |
19: 8,983,196 (GRCm39) |
D1493E |
possibly damaging |
Het |
Alox12e |
C |
A |
11: 70,212,111 (GRCm39) |
R162L |
probably benign |
Het |
Bax |
T |
G |
7: 45,115,539 (GRCm39) |
Q32P |
probably benign |
Het |
Chd9 |
T |
A |
8: 91,761,684 (GRCm39) |
Y2256* |
probably null |
Het |
Chuk |
A |
G |
19: 44,085,420 (GRCm39) |
I242T |
probably damaging |
Het |
Cic |
T |
C |
7: 24,987,715 (GRCm39) |
S1468P |
probably damaging |
Het |
Col27a1 |
A |
G |
4: 63,142,789 (GRCm39) |
H159R |
probably damaging |
Het |
Cux1 |
T |
C |
5: 136,311,815 (GRCm39) |
K1174E |
probably damaging |
Het |
Dnah2 |
C |
A |
11: 69,311,974 (GRCm39) |
|
probably null |
Het |
Dpp3 |
C |
A |
19: 4,967,052 (GRCm39) |
E351* |
probably null |
Het |
Dyrk1a |
A |
G |
16: 94,474,200 (GRCm39) |
Y319C |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,719,841 (GRCm39) |
S458P |
probably damaging |
Het |
Ehmt1 |
G |
A |
2: 24,746,708 (GRCm39) |
L425F |
probably damaging |
Het |
Emp2 |
C |
A |
16: 10,102,437 (GRCm39) |
R125L |
possibly damaging |
Het |
Farsb |
A |
G |
1: 78,435,200 (GRCm39) |
|
probably null |
Het |
Frk |
A |
T |
10: 34,360,021 (GRCm39) |
R7S |
possibly damaging |
Het |
Glb1l2 |
T |
C |
9: 26,678,720 (GRCm39) |
T483A |
probably benign |
Het |
Gm5773 |
T |
C |
3: 93,680,586 (GRCm39) |
V86A |
possibly damaging |
Het |
Gm7324 |
T |
G |
14: 43,952,003 (GRCm39) |
D215E |
probably benign |
Het |
Gng13 |
A |
T |
17: 25,937,932 (GRCm39) |
K44* |
probably null |
Het |
Gprin1 |
C |
T |
13: 54,887,263 (GRCm39) |
G337D |
possibly damaging |
Het |
Ighv1-84 |
G |
T |
12: 115,944,609 (GRCm39) |
Q22K |
probably benign |
Het |
Il20rb |
T |
C |
9: 100,348,304 (GRCm39) |
H210R |
probably benign |
Het |
Iqcm |
C |
T |
8: 76,304,578 (GRCm39) |
S113L |
probably benign |
Het |
Kat6b |
AGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGA |
14: 21,712,417 (GRCm39) |
|
probably benign |
Het |
Kmo |
G |
T |
1: 175,487,236 (GRCm39) |
G430W |
probably damaging |
Het |
Kti12 |
A |
C |
4: 108,705,443 (GRCm39) |
E119A |
probably benign |
Het |
Kti12 |
G |
T |
4: 108,705,444 (GRCm39) |
E119D |
probably benign |
Het |
Ldhd |
T |
G |
8: 112,356,023 (GRCm39) |
D120A |
possibly damaging |
Het |
Lyst |
T |
C |
13: 13,821,657 (GRCm39) |
S1344P |
possibly damaging |
Het |
Mb |
T |
A |
15: 76,900,257 (GRCm39) |
I112F |
probably damaging |
Het |
Mbd5 |
G |
A |
2: 49,147,118 (GRCm39) |
V443M |
probably damaging |
Het |
Milr1 |
A |
G |
11: 106,654,688 (GRCm39) |
K180R |
possibly damaging |
Het |
Mst1r |
T |
C |
9: 107,784,777 (GRCm39) |
F145S |
probably damaging |
Het |
Mthfd2 |
A |
T |
6: 83,286,455 (GRCm39) |
I251K |
possibly damaging |
Het |
Nfx1 |
T |
A |
4: 40,977,142 (GRCm39) |
M272K |
probably benign |
Het |
Nlrp3 |
A |
G |
11: 59,442,689 (GRCm39) |
D747G |
probably benign |
Het |
Odr4 |
C |
T |
1: 150,260,249 (GRCm39) |
R123K |
probably benign |
Het |
Or2y1 |
A |
T |
11: 49,385,543 (GRCm39) |
Y61F |
probably benign |
Het |
Or5p60 |
C |
A |
7: 107,724,329 (GRCm39) |
S47I |
possibly damaging |
Het |
Or8k18 |
A |
T |
2: 86,085,202 (GRCm39) |
Y278* |
probably null |
Het |
Pcdha11 |
A |
G |
18: 37,140,441 (GRCm39) |
E690G |
probably benign |
Het |
Pcdhga4 |
T |
A |
18: 37,818,502 (GRCm39) |
I17N |
probably benign |
Het |
Peg10 |
T |
TCCG |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Phf20 |
A |
G |
2: 156,129,858 (GRCm39) |
K477E |
probably damaging |
Het |
Pik3c2b |
T |
A |
1: 133,028,642 (GRCm39) |
I1377N |
probably benign |
Het |
Polr3h |
T |
C |
15: 81,806,613 (GRCm39) |
K69E |
probably benign |
Het |
Rpgrip1 |
A |
G |
14: 52,368,641 (GRCm39) |
H280R |
possibly damaging |
Het |
Rpp40 |
C |
A |
13: 36,086,034 (GRCm39) |
R132L |
probably benign |
Het |
Ryr1 |
G |
A |
7: 28,790,364 (GRCm39) |
Q1488* |
probably null |
Het |
Sh3bp1 |
A |
G |
15: 78,791,421 (GRCm39) |
M403V |
probably benign |
Het |
Slc20a1 |
G |
A |
2: 129,049,757 (GRCm39) |
D340N |
probably benign |
Het |
Snrnp200 |
T |
A |
2: 127,074,979 (GRCm39) |
N1517K |
possibly damaging |
Het |
Srek1ip1 |
T |
A |
13: 104,973,981 (GRCm39) |
H129Q |
possibly damaging |
Het |
Thumpd2 |
A |
T |
17: 81,334,116 (GRCm39) |
C491S |
probably benign |
Het |
Tle3 |
A |
T |
9: 61,314,410 (GRCm39) |
N204I |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,862,167 (GRCm39) |
V677A |
probably benign |
Het |
Topaz1 |
T |
G |
9: 122,576,499 (GRCm39) |
L30R |
probably benign |
Het |
Trim35 |
T |
A |
14: 66,546,309 (GRCm39) |
C359S |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,774,865 (GRCm39) |
V2105G |
unknown |
Het |
Ube2o |
A |
G |
11: 116,471,884 (GRCm39) |
V119A |
probably benign |
Het |
Ubr2 |
A |
T |
17: 47,279,308 (GRCm39) |
|
probably null |
Het |
Uhmk1 |
A |
G |
1: 170,032,757 (GRCm39) |
V347A |
possibly damaging |
Het |
Utp4 |
C |
T |
8: 107,649,497 (GRCm39) |
P649S |
probably damaging |
Het |
Vmn2r28 |
G |
A |
7: 5,483,818 (GRCm39) |
T794I |
probably damaging |
Het |
Vmn2r61 |
T |
G |
7: 41,949,935 (GRCm39) |
F785C |
probably damaging |
Het |
Xpot |
C |
A |
10: 121,458,848 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
C |
T |
13: 67,768,294 (GRCm39) |
R645H |
probably benign |
Het |
|
Other mutations in Cand1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00850:Cand1
|
APN |
10 |
119,047,040 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00917:Cand1
|
APN |
10 |
119,046,841 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01383:Cand1
|
APN |
10 |
119,044,072 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02016:Cand1
|
APN |
10 |
119,048,473 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02271:Cand1
|
APN |
10 |
119,047,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02282:Cand1
|
APN |
10 |
119,046,614 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02494:Cand1
|
APN |
10 |
119,049,522 (GRCm39) |
missense |
probably benign |
|
IGL02527:Cand1
|
APN |
10 |
119,042,712 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02675:Cand1
|
APN |
10 |
119,055,602 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02796:Cand1
|
UTSW |
10 |
119,049,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R0114:Cand1
|
UTSW |
10 |
119,052,427 (GRCm39) |
missense |
probably benign |
|
R0667:Cand1
|
UTSW |
10 |
119,052,425 (GRCm39) |
missense |
probably benign |
0.00 |
R1589:Cand1
|
UTSW |
10 |
119,049,471 (GRCm39) |
missense |
probably damaging |
0.97 |
R1591:Cand1
|
UTSW |
10 |
119,047,774 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1626:Cand1
|
UTSW |
10 |
119,045,919 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1771:Cand1
|
UTSW |
10 |
119,044,211 (GRCm39) |
missense |
probably benign |
0.05 |
R1937:Cand1
|
UTSW |
10 |
119,038,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Cand1
|
UTSW |
10 |
119,043,925 (GRCm39) |
splice site |
probably benign |
|
R1990:Cand1
|
UTSW |
10 |
119,045,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R3522:Cand1
|
UTSW |
10 |
119,075,102 (GRCm39) |
missense |
probably benign |
0.01 |
R4207:Cand1
|
UTSW |
10 |
119,047,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R4209:Cand1
|
UTSW |
10 |
119,047,463 (GRCm39) |
missense |
probably benign |
0.24 |
R4502:Cand1
|
UTSW |
10 |
119,052,572 (GRCm39) |
missense |
probably benign |
|
R4791:Cand1
|
UTSW |
10 |
119,046,607 (GRCm39) |
missense |
probably benign |
0.02 |
R4841:Cand1
|
UTSW |
10 |
119,049,451 (GRCm39) |
critical splice donor site |
probably null |
|
R4842:Cand1
|
UTSW |
10 |
119,049,451 (GRCm39) |
critical splice donor site |
probably null |
|
R5326:Cand1
|
UTSW |
10 |
119,047,933 (GRCm39) |
missense |
probably benign |
|
R5606:Cand1
|
UTSW |
10 |
119,047,359 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5613:Cand1
|
UTSW |
10 |
119,051,228 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5768:Cand1
|
UTSW |
10 |
119,046,910 (GRCm39) |
missense |
probably benign |
0.06 |
R5884:Cand1
|
UTSW |
10 |
119,049,670 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6006:Cand1
|
UTSW |
10 |
119,045,933 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6062:Cand1
|
UTSW |
10 |
119,053,915 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6734:Cand1
|
UTSW |
10 |
119,047,897 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6838:Cand1
|
UTSW |
10 |
119,045,935 (GRCm39) |
missense |
probably benign |
0.21 |
R7058:Cand1
|
UTSW |
10 |
119,047,659 (GRCm39) |
missense |
probably benign |
0.00 |
R7342:Cand1
|
UTSW |
10 |
119,047,692 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7425:Cand1
|
UTSW |
10 |
119,052,148 (GRCm39) |
missense |
probably benign |
0.00 |
R7705:Cand1
|
UTSW |
10 |
119,048,343 (GRCm39) |
critical splice donor site |
probably null |
|
R7812:Cand1
|
UTSW |
10 |
119,053,864 (GRCm39) |
missense |
probably benign |
0.04 |
R7982:Cand1
|
UTSW |
10 |
119,052,378 (GRCm39) |
missense |
probably damaging |
0.97 |
R8117:Cand1
|
UTSW |
10 |
119,042,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Cand1
|
UTSW |
10 |
119,047,213 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1176:Cand1
|
UTSW |
10 |
119,075,099 (GRCm39) |
missense |
probably benign |
|
|