Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020A23Rik |
A |
G |
2: 130,247,482 (GRCm39) |
D6G |
probably benign |
Het |
Abl2 |
T |
G |
1: 156,469,084 (GRCm39) |
S783A |
probably damaging |
Het |
Adamtsl1 |
A |
T |
4: 86,117,543 (GRCm39) |
T169S |
probably benign |
Het |
Adcy9 |
A |
G |
16: 4,141,653 (GRCm39) |
V621A |
probably benign |
Het |
Ahnak2 |
T |
C |
12: 112,742,510 (GRCm39) |
S521G |
possibly damaging |
Het |
Ap2m1 |
G |
A |
16: 20,360,037 (GRCm39) |
G213R |
probably damaging |
Het |
Apol11b |
C |
T |
15: 77,524,771 (GRCm39) |
E5K |
possibly damaging |
Het |
Arl4d |
T |
C |
11: 101,558,032 (GRCm39) |
M186T |
possibly damaging |
Het |
Cep192 |
A |
G |
18: 67,952,109 (GRCm39) |
D428G |
probably damaging |
Het |
Ckap5 |
A |
C |
2: 91,387,953 (GRCm39) |
D266A |
probably damaging |
Het |
Crls1 |
A |
T |
2: 132,691,793 (GRCm39) |
N106I |
probably damaging |
Het |
Csmd3 |
T |
A |
15: 48,655,398 (GRCm39) |
|
probably benign |
Het |
Csnk1a1 |
A |
G |
18: 61,704,969 (GRCm39) |
R161G |
possibly damaging |
Het |
Cyp4f39 |
T |
A |
17: 32,702,196 (GRCm39) |
I231N |
probably damaging |
Het |
Ddx31 |
T |
A |
2: 28,750,034 (GRCm39) |
V352D |
probably damaging |
Het |
Dna2 |
A |
G |
10: 62,800,740 (GRCm39) |
D758G |
probably damaging |
Het |
Duxf4 |
G |
A |
10: 58,071,378 (GRCm39) |
L279F |
possibly damaging |
Het |
Gatad2a |
C |
A |
8: 70,370,381 (GRCm39) |
A172S |
probably benign |
Het |
Ghsr |
G |
T |
3: 27,426,664 (GRCm39) |
R240L |
probably benign |
Het |
Gli3 |
T |
A |
13: 15,900,858 (GRCm39) |
M1415K |
probably benign |
Het |
Glo1 |
G |
A |
17: 30,816,835 (GRCm39) |
T107I |
possibly damaging |
Het |
Gm10800 |
AAAGAAAACTGAA |
ACAAGAAAACTGAA |
2: 98,497,378 (GRCm39) |
|
probably null |
Het |
Gm17334 |
C |
T |
11: 53,663,760 (GRCm39) |
V34M |
unknown |
Het |
Habp4 |
T |
A |
13: 64,322,615 (GRCm39) |
M228K |
probably benign |
Het |
Hacl1 |
A |
G |
14: 31,344,838 (GRCm39) |
V257A |
possibly damaging |
Het |
Ift122 |
T |
G |
6: 115,857,628 (GRCm39) |
S125A |
possibly damaging |
Het |
Iqce |
C |
T |
5: 140,651,862 (GRCm39) |
D704N |
possibly damaging |
Het |
Jcad |
T |
A |
18: 4,673,252 (GRCm39) |
L338* |
probably null |
Het |
Kcnj13 |
T |
C |
1: 87,316,849 (GRCm39) |
D88G |
probably damaging |
Het |
Kif1b |
T |
C |
4: 149,305,098 (GRCm39) |
D942G |
probably damaging |
Het |
Marchf8 |
T |
A |
6: 116,383,237 (GRCm39) |
S271T |
probably benign |
Het |
Meis1 |
A |
G |
11: 18,961,378 (GRCm39) |
L165S |
probably damaging |
Het |
Morc2b |
T |
A |
17: 33,355,178 (GRCm39) |
T865S |
probably benign |
Het |
Morc3 |
T |
A |
16: 93,641,107 (GRCm39) |
N46K |
possibly damaging |
Het |
Mpzl1 |
C |
T |
1: 165,429,374 (GRCm39) |
C219Y |
probably benign |
Het |
Mup5 |
A |
G |
4: 61,750,787 (GRCm39) |
|
probably null |
Het |
Nol6 |
A |
T |
4: 41,120,156 (GRCm39) |
S491T |
probably benign |
Het |
Or4f53 |
A |
T |
2: 111,088,083 (GRCm39) |
I208F |
probably benign |
Het |
Or51g1 |
A |
G |
7: 102,634,221 (GRCm39) |
V50A |
probably benign |
Het |
Or5b121 |
T |
A |
19: 13,507,697 (GRCm39) |
I264N |
probably damaging |
Het |
Or6c205 |
C |
A |
10: 129,087,182 (GRCm39) |
P260T |
possibly damaging |
Het |
Osbpl6 |
T |
A |
2: 76,425,191 (GRCm39) |
M919K |
probably benign |
Het |
Otogl |
A |
T |
10: 107,598,364 (GRCm39) |
V2262E |
possibly damaging |
Het |
Pcbp2 |
A |
G |
15: 102,383,113 (GRCm39) |
D77G |
possibly damaging |
Het |
Pcsk7 |
G |
A |
9: 45,820,907 (GRCm39) |
R113Q |
possibly damaging |
Het |
Pds5b |
T |
C |
5: 150,645,971 (GRCm39) |
I143T |
probably damaging |
Het |
Polr2m |
T |
C |
9: 71,386,710 (GRCm39) |
E357G |
possibly damaging |
Het |
Prox2 |
G |
A |
12: 85,141,766 (GRCm39) |
Q146* |
probably null |
Het |
Ptprt |
A |
G |
2: 161,395,732 (GRCm39) |
V1167A |
probably benign |
Het |
Rbm11 |
G |
A |
16: 75,397,543 (GRCm39) |
E158K |
possibly damaging |
Het |
Sall2 |
A |
T |
14: 52,551,830 (GRCm39) |
V455E |
probably damaging |
Het |
Sar1b |
T |
A |
11: 51,680,064 (GRCm39) |
L130Q |
probably damaging |
Het |
Slc35f6 |
A |
G |
5: 30,815,180 (GRCm39) |
N369S |
possibly damaging |
Het |
Slc39a12 |
A |
T |
2: 14,412,380 (GRCm39) |
M351L |
probably benign |
Het |
Taf15 |
T |
A |
11: 83,395,487 (GRCm39) |
Y397* |
probably null |
Het |
Tmprss11e |
A |
T |
5: 86,875,149 (GRCm39) |
V39D |
probably damaging |
Het |
Trim71 |
T |
C |
9: 114,342,359 (GRCm39) |
D641G |
probably damaging |
Het |
Trpc3 |
T |
A |
3: 36,694,909 (GRCm39) |
T682S |
probably damaging |
Het |
Tsen54 |
T |
C |
11: 115,707,933 (GRCm39) |
|
probably null |
Het |
Usp6nl |
A |
G |
2: 6,445,960 (GRCm39) |
N646D |
possibly damaging |
Het |
Vip |
T |
C |
10: 5,590,661 (GRCm39) |
F12L |
probably benign |
Het |
Vmn1r39 |
A |
T |
6: 66,781,572 (GRCm39) |
F249I |
probably benign |
Het |
Vmn2r106 |
A |
T |
17: 20,505,641 (GRCm39) |
S18T |
probably benign |
Het |
Vmn2r97 |
G |
T |
17: 19,149,919 (GRCm39) |
V436L |
probably benign |
Het |
Washc2 |
T |
C |
6: 116,237,631 (GRCm39) |
|
probably null |
Het |
Ykt6 |
T |
C |
11: 5,914,613 (GRCm39) |
V171A |
possibly damaging |
Het |
Zfp658 |
A |
G |
7: 43,222,139 (GRCm39) |
D138G |
possibly damaging |
Het |
|
Other mutations in Ninl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Ninl
|
APN |
2 |
150,808,161 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01697:Ninl
|
APN |
2 |
150,781,867 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01756:Ninl
|
APN |
2 |
150,821,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01925:Ninl
|
APN |
2 |
150,812,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02341:Ninl
|
APN |
2 |
150,786,525 (GRCm39) |
nonsense |
probably null |
|
IGL02838:Ninl
|
APN |
2 |
150,797,631 (GRCm39) |
splice site |
probably null |
|
IGL02868:Ninl
|
APN |
2 |
150,778,974 (GRCm39) |
missense |
probably benign |
|
IGL03116:Ninl
|
APN |
2 |
150,806,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03396:Ninl
|
APN |
2 |
150,808,132 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0117:Ninl
|
UTSW |
2 |
150,779,593 (GRCm39) |
missense |
probably damaging |
0.98 |
R0685:Ninl
|
UTSW |
2 |
150,781,775 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0928:Ninl
|
UTSW |
2 |
150,805,395 (GRCm39) |
missense |
probably damaging |
0.99 |
R1051:Ninl
|
UTSW |
2 |
150,812,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R1441:Ninl
|
UTSW |
2 |
150,813,044 (GRCm39) |
missense |
probably benign |
0.10 |
R1493:Ninl
|
UTSW |
2 |
150,822,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Ninl
|
UTSW |
2 |
150,822,096 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1539:Ninl
|
UTSW |
2 |
150,817,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1658:Ninl
|
UTSW |
2 |
150,806,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R2038:Ninl
|
UTSW |
2 |
150,817,763 (GRCm39) |
nonsense |
probably null |
|
R2156:Ninl
|
UTSW |
2 |
150,786,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Ninl
|
UTSW |
2 |
150,791,970 (GRCm39) |
missense |
probably benign |
0.00 |
R2373:Ninl
|
UTSW |
2 |
150,822,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R3743:Ninl
|
UTSW |
2 |
150,792,168 (GRCm39) |
missense |
probably benign |
0.01 |
R3906:Ninl
|
UTSW |
2 |
150,822,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R3950:Ninl
|
UTSW |
2 |
150,794,408 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4283:Ninl
|
UTSW |
2 |
150,795,336 (GRCm39) |
unclassified |
probably benign |
|
R4798:Ninl
|
UTSW |
2 |
150,801,801 (GRCm39) |
nonsense |
probably null |
|
R4963:Ninl
|
UTSW |
2 |
150,781,829 (GRCm39) |
missense |
probably benign |
0.04 |
R4998:Ninl
|
UTSW |
2 |
150,795,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R5343:Ninl
|
UTSW |
2 |
150,813,110 (GRCm39) |
missense |
probably benign |
0.01 |
R5810:Ninl
|
UTSW |
2 |
150,792,088 (GRCm39) |
missense |
probably benign |
0.31 |
R5825:Ninl
|
UTSW |
2 |
150,782,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R6436:Ninl
|
UTSW |
2 |
150,808,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R6728:Ninl
|
UTSW |
2 |
150,817,777 (GRCm39) |
nonsense |
probably null |
|
R6734:Ninl
|
UTSW |
2 |
150,787,003 (GRCm39) |
critical splice donor site |
probably null |
|
R6997:Ninl
|
UTSW |
2 |
150,808,145 (GRCm39) |
missense |
probably benign |
0.08 |
R7135:Ninl
|
UTSW |
2 |
150,797,524 (GRCm39) |
missense |
probably benign |
0.00 |
R7157:Ninl
|
UTSW |
2 |
150,791,263 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7315:Ninl
|
UTSW |
2 |
150,791,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7840:Ninl
|
UTSW |
2 |
150,808,016 (GRCm39) |
missense |
probably benign |
0.00 |
R8134:Ninl
|
UTSW |
2 |
150,792,234 (GRCm39) |
missense |
probably benign |
0.01 |
R8319:Ninl
|
UTSW |
2 |
150,801,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8802:Ninl
|
UTSW |
2 |
150,777,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8997:Ninl
|
UTSW |
2 |
150,801,816 (GRCm39) |
missense |
probably damaging |
0.98 |
R9231:Ninl
|
UTSW |
2 |
150,792,129 (GRCm39) |
missense |
probably benign |
|
R9465:Ninl
|
UTSW |
2 |
150,782,726 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9474:Ninl
|
UTSW |
2 |
150,782,726 (GRCm39) |
missense |
probably benign |
0.27 |
R9789:Ninl
|
UTSW |
2 |
150,791,701 (GRCm39) |
missense |
probably benign |
0.05 |
X0062:Ninl
|
UTSW |
2 |
150,811,966 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ninl
|
UTSW |
2 |
150,795,318 (GRCm39) |
missense |
probably damaging |
1.00 |
|