Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgra2 |
T |
C |
8: 27,610,929 (GRCm39) |
|
probably null |
Het |
Ap2a2 |
G |
A |
7: 141,178,777 (GRCm39) |
A148T |
probably benign |
Het |
Arhgef3 |
A |
T |
14: 27,123,664 (GRCm39) |
N442Y |
probably damaging |
Het |
B3gat3 |
A |
G |
19: 8,903,216 (GRCm39) |
Y191C |
probably damaging |
Het |
B430306N03Rik |
A |
T |
17: 48,629,483 (GRCm39) |
K203* |
probably null |
Het |
C1qtnf6 |
T |
A |
15: 78,409,283 (GRCm39) |
Y188F |
probably benign |
Het |
Capn10 |
T |
C |
1: 92,872,993 (GRCm39) |
V573A |
possibly damaging |
Het |
Cbx4 |
T |
C |
11: 118,972,754 (GRCm39) |
Y207C |
probably damaging |
Het |
Ccdc43 |
G |
T |
11: 102,579,695 (GRCm39) |
|
probably null |
Het |
Ccng2 |
C |
A |
5: 93,416,614 (GRCm39) |
P45Q |
probably benign |
Het |
Cd86 |
T |
C |
16: 36,441,263 (GRCm39) |
H68R |
probably benign |
Het |
Cmtm4 |
A |
G |
8: 105,081,827 (GRCm39) |
Y187H |
probably damaging |
Het |
Cst11 |
T |
C |
2: 148,610,649 (GRCm39) |
N134S |
probably benign |
Het |
Cyp3a25 |
A |
T |
5: 145,939,855 (GRCm39) |
F51I |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,342,973 (GRCm39) |
E1439G |
probably benign |
Het |
Dock4 |
T |
C |
12: 40,686,158 (GRCm39) |
V131A |
probably benign |
Het |
Dpysl2 |
A |
G |
14: 67,099,982 (GRCm39) |
S85P |
probably benign |
Het |
Dync1i2 |
A |
G |
2: 71,078,283 (GRCm39) |
H324R |
probably benign |
Het |
Elf1 |
A |
G |
14: 79,804,710 (GRCm39) |
D162G |
probably benign |
Het |
Eri3 |
G |
A |
4: 117,506,604 (GRCm39) |
|
probably null |
Het |
Fbxl21 |
T |
C |
13: 56,680,145 (GRCm39) |
S203P |
probably damaging |
Het |
Foxi1 |
G |
A |
11: 34,155,758 (GRCm39) |
R291C |
probably damaging |
Het |
Gprin3 |
C |
T |
6: 59,332,128 (GRCm39) |
A60T |
possibly damaging |
Het |
Hecw1 |
A |
G |
13: 14,491,118 (GRCm39) |
C212R |
probably benign |
Het |
Hivep3 |
T |
C |
4: 119,954,318 (GRCm39) |
L878P |
probably damaging |
Het |
Hs6st3 |
A |
T |
14: 119,376,514 (GRCm39) |
N230Y |
probably damaging |
Het |
Htr3b |
A |
G |
9: 48,848,441 (GRCm39) |
V268A |
possibly damaging |
Het |
Ip6k3 |
T |
C |
17: 27,363,969 (GRCm39) |
T360A |
probably damaging |
Het |
Izumo1 |
A |
G |
7: 45,275,536 (GRCm39) |
T282A |
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,086,623 (GRCm39) |
I1019N |
probably damaging |
Het |
Med13l |
T |
C |
5: 118,880,037 (GRCm39) |
V1043A |
probably benign |
Het |
Mon2 |
C |
T |
10: 122,871,358 (GRCm39) |
V420I |
probably benign |
Het |
Naip6 |
T |
A |
13: 100,436,708 (GRCm39) |
Y605F |
possibly damaging |
Het |
Notch3 |
A |
G |
17: 32,375,351 (GRCm39) |
V357A |
possibly damaging |
Het |
Nrxn1 |
G |
A |
17: 91,396,192 (GRCm39) |
|
probably benign |
Het |
Nutm1 |
G |
A |
2: 112,080,401 (GRCm39) |
R505C |
probably damaging |
Het |
Or2w4 |
C |
T |
13: 21,795,297 (GRCm39) |
V281M |
possibly damaging |
Het |
Or4a67 |
G |
A |
2: 88,598,308 (GRCm39) |
A117V |
probably damaging |
Het |
Or5g9 |
T |
A |
2: 85,551,818 (GRCm39) |
L23Q |
probably damaging |
Het |
Or6c74 |
T |
G |
10: 129,870,083 (GRCm39) |
M196R |
possibly damaging |
Het |
Ostm1 |
C |
T |
10: 42,559,268 (GRCm39) |
A176V |
probably null |
Het |
Pabpc6 |
C |
A |
17: 9,887,357 (GRCm39) |
S398I |
possibly damaging |
Het |
Pcdhac2 |
C |
A |
18: 37,277,239 (GRCm39) |
P73H |
possibly damaging |
Het |
Pcdhga9 |
A |
G |
18: 37,872,184 (GRCm39) |
D671G |
possibly damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pigu |
A |
C |
2: 155,143,160 (GRCm39) |
L248R |
possibly damaging |
Het |
Pinx1 |
C |
A |
14: 64,097,834 (GRCm39) |
|
probably null |
Het |
Pon3 |
T |
C |
6: 5,221,664 (GRCm39) |
N322S |
possibly damaging |
Het |
Pramel23 |
T |
G |
4: 143,425,002 (GRCm39) |
H147P |
probably benign |
Het |
Rnft1 |
A |
G |
11: 86,382,586 (GRCm39) |
I270V |
probably benign |
Het |
Scgb2b11 |
A |
G |
7: 31,910,006 (GRCm39) |
F27L |
probably damaging |
Het |
Slc5a4b |
C |
T |
10: 75,910,943 (GRCm39) |
V298I |
probably damaging |
Het |
Slco1a6 |
T |
A |
6: 142,048,745 (GRCm39) |
H345L |
probably benign |
Het |
Sox1 |
C |
T |
8: 12,447,405 (GRCm39) |
P349S |
possibly damaging |
Het |
Spata31 |
A |
G |
13: 65,068,913 (GRCm39) |
N354D |
probably benign |
Het |
Speg |
T |
C |
1: 75,383,414 (GRCm39) |
|
probably null |
Het |
Stpg1 |
T |
C |
4: 135,261,033 (GRCm39) |
I281T |
probably benign |
Het |
Sult3a1 |
T |
C |
10: 33,753,283 (GRCm39) |
L193P |
probably damaging |
Het |
Tenm3 |
A |
T |
8: 48,745,271 (GRCm39) |
C1097S |
probably damaging |
Het |
Tfap2a |
A |
G |
13: 40,883,523 (GRCm39) |
S7P |
probably benign |
Het |
Tlr1 |
T |
C |
5: 65,083,021 (GRCm39) |
I519V |
probably benign |
Het |
Tmem238 |
A |
G |
7: 4,792,072 (GRCm39) |
V157A |
possibly damaging |
Het |
Tmem45b |
A |
T |
9: 31,345,780 (GRCm39) |
|
probably null |
Het |
Togaram2 |
A |
T |
17: 72,021,761 (GRCm39) |
H742L |
probably benign |
Het |
Trpc7 |
A |
T |
13: 56,937,487 (GRCm39) |
Y656* |
probably null |
Het |
Wdr35 |
T |
A |
12: 9,072,785 (GRCm39) |
Y920N |
probably damaging |
Het |
Xab2 |
G |
A |
8: 3,668,117 (GRCm39) |
R154C |
possibly damaging |
Het |
Zfp759 |
A |
T |
13: 67,288,177 (GRCm39) |
H576L |
possibly damaging |
Het |
Zfp958 |
G |
T |
8: 4,678,481 (GRCm39) |
A169S |
probably benign |
Het |
|
Other mutations in Nek7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02151:Nek7
|
APN |
1 |
138,414,838 (GRCm39) |
missense |
probably damaging |
1.00 |
Beauties
|
UTSW |
1 |
138,462,127 (GRCm39) |
missense |
probably damaging |
1.00 |
Cuties
|
UTSW |
1 |
138,471,980 (GRCm39) |
nonsense |
probably null |
|
Doubletake
|
UTSW |
1 |
138,443,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Nek7
|
UTSW |
1 |
138,471,942 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0103:Nek7
|
UTSW |
1 |
138,471,980 (GRCm39) |
nonsense |
probably null |
|
R0103:Nek7
|
UTSW |
1 |
138,471,980 (GRCm39) |
nonsense |
probably null |
|
R0646:Nek7
|
UTSW |
1 |
138,443,431 (GRCm39) |
frame shift |
probably null |
|
R3953:Nek7
|
UTSW |
1 |
138,462,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R3955:Nek7
|
UTSW |
1 |
138,462,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R3957:Nek7
|
UTSW |
1 |
138,462,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R4638:Nek7
|
UTSW |
1 |
138,472,038 (GRCm39) |
missense |
probably benign |
0.22 |
R4750:Nek7
|
UTSW |
1 |
138,426,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Nek7
|
UTSW |
1 |
138,443,431 (GRCm39) |
missense |
probably benign |
0.04 |
R5331:Nek7
|
UTSW |
1 |
138,426,312 (GRCm39) |
critical splice donor site |
probably null |
|
R5838:Nek7
|
UTSW |
1 |
138,462,101 (GRCm39) |
critical splice donor site |
probably null |
|
R6083:Nek7
|
UTSW |
1 |
138,443,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Nek7
|
UTSW |
1 |
138,426,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R6855:Nek7
|
UTSW |
1 |
138,443,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6857:Nek7
|
UTSW |
1 |
138,443,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Nek7
|
UTSW |
1 |
138,430,376 (GRCm39) |
missense |
probably damaging |
0.97 |
R7808:Nek7
|
UTSW |
1 |
138,489,509 (GRCm39) |
start gained |
probably benign |
|
Z1088:Nek7
|
UTSW |
1 |
138,443,363 (GRCm39) |
missense |
probably null |
0.81 |
|