Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
T |
C |
8: 124,694,737 (GRCm39) |
|
probably null |
Het |
Abt1 |
T |
C |
13: 23,606,225 (GRCm39) |
E243G |
possibly damaging |
Het |
Afap1l1 |
A |
G |
18: 61,876,771 (GRCm39) |
S361P |
probably damaging |
Het |
Alms1 |
T |
C |
6: 85,596,694 (GRCm39) |
S507P |
probably benign |
Het |
Atp13a3 |
A |
G |
16: 30,181,518 (GRCm39) |
V34A |
probably benign |
Het |
Atpaf2 |
A |
T |
11: 60,296,708 (GRCm39) |
|
probably benign |
Het |
Bbs1 |
A |
C |
19: 4,943,022 (GRCm39) |
L456R |
probably benign |
Het |
Bri3bp |
G |
T |
5: 125,529,217 (GRCm39) |
G84* |
probably null |
Het |
Bri3bp |
G |
C |
5: 125,529,218 (GRCm39) |
|
probably benign |
Het |
Car10 |
A |
C |
11: 93,381,439 (GRCm39) |
H134P |
probably damaging |
Het |
Cntrl |
A |
G |
2: 35,006,691 (GRCm39) |
E119G |
probably damaging |
Het |
Cxcl3 |
C |
T |
5: 90,934,175 (GRCm39) |
|
probably benign |
Het |
Dppa4 |
T |
C |
16: 48,111,471 (GRCm39) |
V100A |
possibly damaging |
Het |
Elmo1 |
G |
T |
13: 20,474,553 (GRCm39) |
E105* |
probably null |
Het |
Esrp2 |
T |
G |
8: 106,859,565 (GRCm39) |
|
probably benign |
Het |
Exoc3l4 |
A |
G |
12: 111,388,835 (GRCm39) |
K108R |
possibly damaging |
Het |
Exph5 |
G |
A |
9: 53,286,522 (GRCm39) |
R1201H |
probably benign |
Het |
Galnt3 |
A |
C |
2: 65,914,500 (GRCm39) |
|
probably benign |
Het |
Gm14486 |
C |
T |
2: 30,548,813 (GRCm39) |
|
noncoding transcript |
Het |
Gna12 |
T |
A |
5: 140,746,717 (GRCm39) |
I243F |
probably damaging |
Het |
Itga5 |
A |
T |
15: 103,265,212 (GRCm39) |
W232R |
probably damaging |
Het |
Lekr1 |
A |
T |
3: 65,680,498 (GRCm39) |
|
noncoding transcript |
Het |
Lrp1 |
C |
T |
10: 127,425,423 (GRCm39) |
|
probably null |
Het |
Mast4 |
T |
C |
13: 102,872,148 (GRCm39) |
M2215V |
probably benign |
Het |
Mfap5 |
T |
C |
6: 122,502,945 (GRCm39) |
Y52H |
probably damaging |
Het |
Mrps31 |
A |
G |
8: 22,904,991 (GRCm39) |
K127E |
possibly damaging |
Het |
Mto1 |
C |
T |
9: 78,368,311 (GRCm39) |
T485M |
probably damaging |
Het |
Mybbp1a |
G |
A |
11: 72,333,257 (GRCm39) |
C107Y |
probably damaging |
Het |
Nedd4 |
G |
A |
9: 72,638,132 (GRCm39) |
|
probably benign |
Het |
Notch1 |
T |
A |
2: 26,352,540 (GRCm39) |
|
probably benign |
Het |
Nubp1 |
T |
C |
16: 10,238,050 (GRCm39) |
|
probably benign |
Het |
Pcdhb1 |
G |
A |
18: 37,399,726 (GRCm39) |
R559H |
possibly damaging |
Het |
Pdcd11 |
G |
A |
19: 47,117,702 (GRCm39) |
V1684I |
probably benign |
Het |
Pggt1b |
G |
T |
18: 46,382,007 (GRCm39) |
N258K |
probably benign |
Het |
Pou6f1 |
C |
T |
15: 100,484,001 (GRCm39) |
V166M |
possibly damaging |
Het |
Pprc1 |
A |
G |
19: 46,052,111 (GRCm39) |
D546G |
possibly damaging |
Het |
Psapl1 |
T |
C |
5: 36,361,651 (GRCm39) |
V81A |
probably benign |
Het |
Rin2 |
T |
A |
2: 145,686,863 (GRCm39) |
|
probably benign |
Het |
Rpf1 |
A |
G |
3: 146,212,299 (GRCm39) |
F347S |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,859,247 (GRCm39) |
|
probably null |
Het |
Ryr1 |
A |
T |
7: 28,771,349 (GRCm39) |
L2557Q |
probably null |
Het |
Slc1a7 |
T |
C |
4: 107,867,497 (GRCm39) |
|
probably benign |
Het |
Slc35e2 |
T |
A |
4: 155,696,171 (GRCm39) |
M186K |
possibly damaging |
Het |
Slc49a4 |
T |
C |
16: 35,550,676 (GRCm39) |
T308A |
probably benign |
Het |
Snx6 |
G |
T |
12: 54,817,549 (GRCm39) |
S116* |
probably null |
Het |
Sptan1 |
T |
C |
2: 29,884,379 (GRCm39) |
|
probably null |
Het |
Sucla2 |
T |
A |
14: 73,830,109 (GRCm39) |
M382K |
probably damaging |
Het |
Susd5 |
T |
C |
9: 113,886,659 (GRCm39) |
L16P |
possibly damaging |
Het |
Tmem260 |
G |
A |
14: 48,724,258 (GRCm39) |
A369T |
possibly damaging |
Het |
Tmprss6 |
A |
G |
15: 78,336,722 (GRCm39) |
Y393H |
probably damaging |
Het |
Tnrc6c |
A |
T |
11: 117,613,345 (GRCm39) |
Q501L |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,856,369 (GRCm39) |
Y142C |
probably damaging |
Het |
Trim65 |
T |
C |
11: 116,019,108 (GRCm39) |
R144G |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 63,873,547 (GRCm39) |
T601A |
probably benign |
Het |
Ttn |
A |
T |
2: 76,564,688 (GRCm39) |
V28483E |
probably damaging |
Het |
Ube2l3 |
T |
C |
16: 17,019,340 (GRCm39) |
|
probably null |
Het |
Ube2l3 |
G |
T |
16: 17,019,336 (GRCm39) |
|
probably benign |
Het |
Yme1l1 |
T |
C |
2: 23,085,318 (GRCm39) |
|
probably benign |
Het |
Zfat |
A |
G |
15: 68,051,806 (GRCm39) |
S663P |
probably benign |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
|
Other mutations in Nek2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00509:Nek2
|
APN |
1 |
191,559,490 (GRCm39) |
splice site |
probably benign |
|
IGL01753:Nek2
|
APN |
1 |
191,557,598 (GRCm39) |
nonsense |
probably null |
|
IGL02086:Nek2
|
APN |
1 |
191,563,401 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02164:Nek2
|
APN |
1 |
191,559,416 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02550:Nek2
|
APN |
1 |
191,554,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R0398:Nek2
|
UTSW |
1 |
191,559,473 (GRCm39) |
missense |
probably benign |
|
R0610:Nek2
|
UTSW |
1 |
191,554,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R0629:Nek2
|
UTSW |
1 |
191,563,429 (GRCm39) |
missense |
probably benign |
0.14 |
R0646:Nek2
|
UTSW |
1 |
191,554,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R0976:Nek2
|
UTSW |
1 |
191,559,349 (GRCm39) |
missense |
probably benign |
0.10 |
R2054:Nek2
|
UTSW |
1 |
191,553,764 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2112:Nek2
|
UTSW |
1 |
191,559,320 (GRCm39) |
missense |
probably benign |
0.08 |
R3873:Nek2
|
UTSW |
1 |
191,559,320 (GRCm39) |
missense |
probably benign |
0.08 |
R4461:Nek2
|
UTSW |
1 |
191,554,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6807:Nek2
|
UTSW |
1 |
191,554,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R8032:Nek2
|
UTSW |
1 |
191,558,457 (GRCm39) |
missense |
probably damaging |
0.96 |
R8692:Nek2
|
UTSW |
1 |
191,554,745 (GRCm39) |
missense |
probably benign |
0.00 |
R9709:Nek2
|
UTSW |
1 |
191,563,289 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9780:Nek2
|
UTSW |
1 |
191,554,738 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Nek2
|
UTSW |
1 |
191,559,351 (GRCm39) |
missense |
probably benign |
0.05 |
|