Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
A |
G |
8: 120,880,706 (GRCm39) |
Y286C |
probably damaging |
Het |
Cacna1c |
T |
C |
6: 118,587,455 (GRCm39) |
T1657A |
|
Het |
Ccs |
A |
T |
19: 4,882,897 (GRCm39) |
D151E |
probably benign |
Het |
Cfap74 |
A |
G |
4: 155,509,133 (GRCm39) |
T295A |
|
Het |
Chmp4c |
A |
T |
3: 10,432,222 (GRCm39) |
E44V |
probably damaging |
Het |
Crybg2 |
A |
T |
4: 133,801,383 (GRCm39) |
K539* |
probably null |
Het |
Dgkg |
T |
C |
16: 22,441,011 (GRCm39) |
M1V |
probably null |
Het |
E2f2 |
T |
A |
4: 135,911,743 (GRCm39) |
Y251* |
probably null |
Het |
Fat2 |
T |
C |
11: 55,180,093 (GRCm39) |
Y1416C |
probably damaging |
Het |
Fgl2 |
T |
C |
5: 21,577,991 (GRCm39) |
S93P |
possibly damaging |
Het |
Hivep3 |
C |
T |
4: 119,989,786 (GRCm39) |
T2079I |
probably damaging |
Het |
Igfl3 |
A |
C |
7: 17,913,920 (GRCm39) |
K90T |
possibly damaging |
Het |
Lsamp |
A |
G |
16: 41,709,292 (GRCm39) |
D74G |
probably benign |
Het |
Mmrn2 |
C |
A |
14: 34,119,654 (GRCm39) |
T211K |
possibly damaging |
Het |
Mov10 |
A |
T |
3: 104,707,664 (GRCm39) |
V570D |
probably benign |
Het |
Mrc1 |
A |
T |
2: 14,313,517 (GRCm39) |
Y916F |
probably benign |
Het |
Myo10 |
CAGGTATAAAG |
CAG |
15: 25,776,401 (GRCm39) |
|
probably null |
Het |
Ndc1 |
T |
A |
4: 107,246,686 (GRCm39) |
C370S |
probably damaging |
Het |
Nln |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
13: 104,186,924 (GRCm39) |
|
probably null |
Het |
Nrp1 |
G |
A |
8: 129,229,029 (GRCm39) |
E836K |
probably benign |
Het |
Or2t29 |
C |
T |
11: 58,433,753 (GRCm39) |
C196Y |
probably damaging |
Het |
Or5b120 |
A |
T |
19: 13,479,943 (GRCm39) |
K79* |
probably null |
Het |
Or6c216 |
A |
T |
10: 129,678,625 (GRCm39) |
C95* |
probably null |
Het |
Or8b1d |
A |
G |
9: 38,558,620 (GRCm39) |
S67P |
probably damaging |
Het |
Pcca |
T |
C |
14: 122,901,717 (GRCm39) |
S287P |
probably damaging |
Het |
Pitpnm3 |
T |
A |
11: 71,955,069 (GRCm39) |
T482S |
probably benign |
Het |
Pld2 |
C |
T |
11: 70,445,893 (GRCm39) |
R676* |
probably null |
Het |
Ppm1k |
T |
C |
6: 57,491,057 (GRCm39) |
Y286C |
possibly damaging |
Het |
Rb1 |
T |
C |
14: 73,517,573 (GRCm39) |
N278D |
probably damaging |
Het |
Sema3g |
T |
C |
14: 30,943,783 (GRCm39) |
L221P |
probably damaging |
Het |
Skint2 |
C |
T |
4: 112,483,147 (GRCm39) |
T184I |
probably benign |
Het |
Slc38a2 |
A |
G |
15: 96,591,172 (GRCm39) |
F232S |
probably damaging |
Het |
Snx6 |
T |
C |
12: 54,814,811 (GRCm39) |
N170S |
probably benign |
Het |
Sox9 |
T |
A |
11: 112,673,416 (GRCm39) |
N2K |
probably damaging |
Het |
Sp140l1 |
G |
C |
1: 85,075,344 (GRCm39) |
|
probably null |
Het |
Srpk2 |
T |
C |
5: 23,729,604 (GRCm39) |
E345G |
probably benign |
Het |
Tbc1d21 |
T |
C |
9: 58,268,487 (GRCm39) |
M291V |
possibly damaging |
Het |
Tekt2 |
T |
C |
4: 126,218,693 (GRCm39) |
N20S |
probably benign |
Het |
Tnxb |
T |
G |
17: 34,914,578 (GRCm39) |
I1888S |
possibly damaging |
Het |
Tsnaxip1 |
G |
A |
8: 106,566,685 (GRCm39) |
E174K |
probably damaging |
Het |
Ttc28 |
G |
A |
5: 111,433,140 (GRCm39) |
R2058Q |
probably benign |
Het |
Ttn |
C |
T |
2: 76,715,357 (GRCm39) |
E7912K |
unknown |
Het |
Ttyh2 |
T |
A |
11: 114,601,667 (GRCm39) |
D430E |
probably benign |
Het |
Ubr2 |
C |
T |
17: 47,245,020 (GRCm39) |
G1669R |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,853,491 (GRCm39) |
S490T |
probably damaging |
Het |
Vmn1r86 |
T |
A |
7: 12,836,741 (GRCm39) |
D45V |
probably damaging |
Het |
Wdr12 |
A |
G |
1: 60,127,226 (GRCm39) |
V143A |
possibly damaging |
Het |
Zbtb18 |
T |
A |
1: 177,274,989 (GRCm39) |
Y116* |
probably null |
Het |
Zdbf2 |
C |
T |
1: 63,342,536 (GRCm39) |
T305I |
possibly damaging |
Het |
Zfp384 |
T |
A |
6: 125,007,802 (GRCm39) |
M244K |
possibly damaging |
Het |
Zfp423 |
A |
T |
8: 88,414,595 (GRCm39) |
V1241D |
probably damaging |
Het |
Zfp574 |
A |
G |
7: 24,780,640 (GRCm39) |
Y554C |
probably damaging |
Het |
Zfp616 |
T |
C |
11: 73,976,220 (GRCm39) |
S830P |
probably damaging |
Het |
Zfp839 |
A |
G |
12: 110,834,776 (GRCm39) |
Y677C |
probably benign |
Het |
|
Other mutations in Nrcam |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01399:Nrcam
|
APN |
12 |
44,622,667 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01657:Nrcam
|
APN |
12 |
44,606,583 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02434:Nrcam
|
APN |
12 |
44,637,026 (GRCm39) |
splice site |
probably benign |
|
IGL02455:Nrcam
|
APN |
12 |
44,617,313 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02712:Nrcam
|
APN |
12 |
44,620,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02834:Nrcam
|
APN |
12 |
44,587,858 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03022:Nrcam
|
APN |
12 |
44,645,225 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03174:Nrcam
|
APN |
12 |
44,622,789 (GRCm39) |
splice site |
probably benign |
|
IGL03389:Nrcam
|
APN |
12 |
44,596,689 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03397:Nrcam
|
APN |
12 |
44,606,540 (GRCm39) |
missense |
probably damaging |
1.00 |
I2288:Nrcam
|
UTSW |
12 |
44,611,098 (GRCm39) |
missense |
probably benign |
0.06 |
I2289:Nrcam
|
UTSW |
12 |
44,611,098 (GRCm39) |
missense |
probably benign |
0.06 |
R0063:Nrcam
|
UTSW |
12 |
44,596,811 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0063:Nrcam
|
UTSW |
12 |
44,596,811 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0195:Nrcam
|
UTSW |
12 |
44,631,628 (GRCm39) |
missense |
probably benign |
0.00 |
R0463:Nrcam
|
UTSW |
12 |
44,598,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R0590:Nrcam
|
UTSW |
12 |
44,610,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Nrcam
|
UTSW |
12 |
44,611,105 (GRCm39) |
missense |
probably benign |
0.17 |
R0930:Nrcam
|
UTSW |
12 |
44,596,667 (GRCm39) |
missense |
probably benign |
|
R1241:Nrcam
|
UTSW |
12 |
44,636,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R1279:Nrcam
|
UTSW |
12 |
44,591,660 (GRCm39) |
splice site |
probably null |
|
R1523:Nrcam
|
UTSW |
12 |
44,619,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Nrcam
|
UTSW |
12 |
44,584,147 (GRCm39) |
splice site |
probably benign |
|
R1629:Nrcam
|
UTSW |
12 |
44,610,769 (GRCm39) |
missense |
probably benign |
0.00 |
R1651:Nrcam
|
UTSW |
12 |
44,623,462 (GRCm39) |
missense |
probably damaging |
0.97 |
R1729:Nrcam
|
UTSW |
12 |
44,620,633 (GRCm39) |
missense |
probably benign |
|
R1739:Nrcam
|
UTSW |
12 |
44,618,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Nrcam
|
UTSW |
12 |
44,618,991 (GRCm39) |
missense |
probably benign |
|
R1884:Nrcam
|
UTSW |
12 |
44,591,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Nrcam
|
UTSW |
12 |
44,610,776 (GRCm39) |
missense |
probably benign |
0.05 |
R1992:Nrcam
|
UTSW |
12 |
44,587,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Nrcam
|
UTSW |
12 |
44,623,471 (GRCm39) |
missense |
probably benign |
0.00 |
R2106:Nrcam
|
UTSW |
12 |
44,617,073 (GRCm39) |
missense |
probably benign |
0.12 |
R3854:Nrcam
|
UTSW |
12 |
44,622,667 (GRCm39) |
missense |
probably benign |
0.27 |
R4005:Nrcam
|
UTSW |
12 |
44,579,429 (GRCm39) |
missense |
probably benign |
|
R4088:Nrcam
|
UTSW |
12 |
44,618,985 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4115:Nrcam
|
UTSW |
12 |
44,613,109 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4428:Nrcam
|
UTSW |
12 |
44,623,558 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4458:Nrcam
|
UTSW |
12 |
44,606,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Nrcam
|
UTSW |
12 |
44,609,323 (GRCm39) |
critical splice donor site |
probably null |
|
R4601:Nrcam
|
UTSW |
12 |
44,637,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Nrcam
|
UTSW |
12 |
44,594,020 (GRCm39) |
missense |
probably benign |
|
R4825:Nrcam
|
UTSW |
12 |
44,622,769 (GRCm39) |
nonsense |
probably null |
|
R4838:Nrcam
|
UTSW |
12 |
44,620,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4950:Nrcam
|
UTSW |
12 |
44,645,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:Nrcam
|
UTSW |
12 |
44,613,082 (GRCm39) |
missense |
probably benign |
0.01 |
R5081:Nrcam
|
UTSW |
12 |
44,617,136 (GRCm39) |
missense |
probably benign |
0.00 |
R5297:Nrcam
|
UTSW |
12 |
44,591,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R5504:Nrcam
|
UTSW |
12 |
44,610,915 (GRCm39) |
critical splice donor site |
probably null |
|
R5593:Nrcam
|
UTSW |
12 |
44,606,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R5654:Nrcam
|
UTSW |
12 |
44,610,841 (GRCm39) |
missense |
probably benign |
|
R5691:Nrcam
|
UTSW |
12 |
44,611,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Nrcam
|
UTSW |
12 |
44,623,554 (GRCm39) |
missense |
probably benign |
|
R5937:Nrcam
|
UTSW |
12 |
44,619,074 (GRCm39) |
missense |
probably benign |
0.00 |
R5980:Nrcam
|
UTSW |
12 |
44,618,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R6132:Nrcam
|
UTSW |
12 |
44,617,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R6213:Nrcam
|
UTSW |
12 |
44,609,215 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6334:Nrcam
|
UTSW |
12 |
44,619,083 (GRCm39) |
missense |
probably benign |
|
R6617:Nrcam
|
UTSW |
12 |
44,587,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R6666:Nrcam
|
UTSW |
12 |
44,618,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R7191:Nrcam
|
UTSW |
12 |
44,619,027 (GRCm39) |
missense |
probably benign |
0.01 |
R7284:Nrcam
|
UTSW |
12 |
44,610,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Nrcam
|
UTSW |
12 |
44,610,809 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7388:Nrcam
|
UTSW |
12 |
44,645,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Nrcam
|
UTSW |
12 |
44,594,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R7734:Nrcam
|
UTSW |
12 |
44,584,034 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7757:Nrcam
|
UTSW |
12 |
44,596,681 (GRCm39) |
nonsense |
probably null |
|
R7840:Nrcam
|
UTSW |
12 |
44,587,858 (GRCm39) |
critical splice donor site |
probably null |
|
R7917:Nrcam
|
UTSW |
12 |
44,620,546 (GRCm39) |
splice site |
probably null |
|
R7935:Nrcam
|
UTSW |
12 |
44,631,644 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7955:Nrcam
|
UTSW |
12 |
44,631,737 (GRCm39) |
missense |
probably benign |
0.26 |
R8117:Nrcam
|
UTSW |
12 |
44,618,371 (GRCm39) |
missense |
probably benign |
0.04 |
R8117:Nrcam
|
UTSW |
12 |
44,645,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R8153:Nrcam
|
UTSW |
12 |
44,631,755 (GRCm39) |
missense |
probably benign |
|
R8189:Nrcam
|
UTSW |
12 |
44,617,291 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8215:Nrcam
|
UTSW |
12 |
44,610,896 (GRCm39) |
missense |
probably benign |
0.02 |
R8719:Nrcam
|
UTSW |
12 |
44,586,325 (GRCm39) |
missense |
probably benign |
|
R8738:Nrcam
|
UTSW |
12 |
44,619,075 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8794:Nrcam
|
UTSW |
12 |
44,624,958 (GRCm39) |
missense |
probably benign |
0.01 |
R8831:Nrcam
|
UTSW |
12 |
44,591,680 (GRCm39) |
critical splice donor site |
probably null |
|
R8858:Nrcam
|
UTSW |
12 |
44,644,554 (GRCm39) |
splice site |
probably benign |
|
R8885:Nrcam
|
UTSW |
12 |
44,610,908 (GRCm39) |
missense |
probably benign |
0.10 |
R8912:Nrcam
|
UTSW |
12 |
44,645,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R9178:Nrcam
|
UTSW |
12 |
44,615,329 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9243:Nrcam
|
UTSW |
12 |
44,620,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R9257:Nrcam
|
UTSW |
12 |
44,610,837 (GRCm39) |
missense |
probably benign |
0.27 |
R9266:Nrcam
|
UTSW |
12 |
44,636,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Nrcam
|
UTSW |
12 |
44,636,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R9681:Nrcam
|
UTSW |
12 |
44,598,133 (GRCm39) |
missense |
probably null |
1.00 |
R9747:Nrcam
|
UTSW |
12 |
44,645,192 (GRCm39) |
missense |
probably damaging |
1.00 |
U24488:Nrcam
|
UTSW |
12 |
44,584,042 (GRCm39) |
missense |
probably damaging |
1.00 |
X0057:Nrcam
|
UTSW |
12 |
44,598,199 (GRCm39) |
missense |
probably benign |
|
X0066:Nrcam
|
UTSW |
12 |
44,596,812 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Nrcam
|
UTSW |
12 |
44,618,353 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nrcam
|
UTSW |
12 |
44,620,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|