Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aim2 |
C |
G |
1: 173,291,546 (GRCm39) |
T317R |
probably damaging |
Het |
Aqp9 |
T |
A |
9: 71,019,498 (GRCm39) |
M321L |
probably benign |
Het |
Avil |
G |
A |
10: 126,849,431 (GRCm39) |
D576N |
probably benign |
Het |
Bbs1 |
C |
T |
19: 4,953,880 (GRCm39) |
M94I |
possibly damaging |
Het |
Bms1 |
A |
G |
6: 118,393,455 (GRCm39) |
V139A |
probably benign |
Het |
Bscl2 |
A |
T |
19: 8,818,745 (GRCm39) |
M57L |
probably damaging |
Het |
C2cd5 |
A |
G |
6: 142,975,364 (GRCm39) |
I794T |
possibly damaging |
Het |
Cacna1s |
C |
T |
1: 136,012,175 (GRCm39) |
T539I |
possibly damaging |
Het |
Cand1 |
T |
C |
10: 119,045,935 (GRCm39) |
K990R |
probably benign |
Het |
Capn7 |
A |
G |
14: 31,076,130 (GRCm39) |
I311V |
possibly damaging |
Het |
Cd180 |
A |
G |
13: 102,839,239 (GRCm39) |
N41D |
probably benign |
Het |
Cdin1 |
T |
C |
2: 115,607,471 (GRCm39) |
F275L |
possibly damaging |
Het |
Celsr1 |
G |
A |
15: 85,823,395 (GRCm39) |
T1671I |
probably benign |
Het |
Cep135 |
A |
T |
5: 76,780,062 (GRCm39) |
Q798L |
probably damaging |
Het |
Cfap65 |
T |
C |
1: 74,971,180 (GRCm39) |
D46G |
probably benign |
Het |
Cracd |
A |
T |
5: 77,006,056 (GRCm39) |
T806S |
unknown |
Het |
Ddx46 |
G |
T |
13: 55,787,748 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
C |
1: 46,230,948 (GRCm39) |
L1402P |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,929,525 (GRCm39) |
E1402G |
probably damaging |
Het |
Dock9 |
A |
G |
14: 121,784,008 (GRCm39) |
Y1989H |
possibly damaging |
Het |
Ereg |
A |
G |
5: 91,236,323 (GRCm39) |
D50G |
probably benign |
Het |
Evi5 |
G |
T |
5: 107,990,027 (GRCm39) |
T64K |
possibly damaging |
Het |
Frem3 |
A |
C |
8: 81,338,660 (GRCm39) |
T318P |
probably damaging |
Het |
Gpx1 |
A |
G |
9: 108,217,139 (GRCm39) |
D81G |
possibly damaging |
Het |
Gramd1a |
T |
C |
7: 30,833,929 (GRCm39) |
I499V |
probably benign |
Het |
H4c12 |
A |
T |
13: 21,934,375 (GRCm39) |
F101I |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,758,526 (GRCm39) |
D804E |
probably damaging |
Het |
Hk1 |
T |
C |
10: 62,107,437 (GRCm39) |
E846G |
probably damaging |
Het |
Iars2 |
G |
A |
1: 185,061,342 (GRCm39) |
A48V |
probably damaging |
Het |
Invs |
C |
T |
4: 48,283,278 (GRCm39) |
T10M |
possibly damaging |
Het |
Ism2 |
A |
T |
12: 87,326,975 (GRCm39) |
D321E |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,448,152 (GRCm39) |
S231P |
possibly damaging |
Het |
Kif17 |
A |
T |
4: 138,005,710 (GRCm39) |
|
probably null |
Het |
Lvrn |
A |
G |
18: 47,023,947 (GRCm39) |
I765V |
possibly damaging |
Het |
Map4k4 |
T |
A |
1: 40,015,882 (GRCm39) |
C108S |
probably damaging |
Het |
Mapk13 |
G |
T |
17: 28,996,535 (GRCm39) |
|
probably null |
Het |
Mapkapk2 |
T |
A |
1: 130,985,740 (GRCm39) |
K95* |
probably null |
Het |
Mau2 |
A |
T |
8: 70,491,947 (GRCm39) |
|
probably null |
Het |
Mex3a |
A |
G |
3: 88,444,084 (GRCm39) |
T387A |
probably benign |
Het |
Myo5a |
T |
C |
9: 75,061,165 (GRCm39) |
|
probably null |
Het |
Nod2 |
A |
C |
8: 89,397,086 (GRCm39) |
E810A |
possibly damaging |
Het |
Nol3 |
A |
T |
8: 106,006,207 (GRCm39) |
E152V |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,567,664 (GRCm39) |
E261G |
possibly damaging |
Het |
Or2h1 |
A |
T |
17: 37,404,058 (GRCm39) |
L236* |
probably null |
Het |
Or8b12b |
A |
C |
9: 37,684,348 (GRCm39) |
Y131S |
possibly damaging |
Het |
P3h2 |
T |
C |
16: 25,924,034 (GRCm39) |
S134G |
possibly damaging |
Het |
Plxna2 |
A |
T |
1: 194,487,222 (GRCm39) |
R1592S |
possibly damaging |
Het |
Ppp1r12a |
C |
T |
10: 108,097,137 (GRCm39) |
S250L |
possibly damaging |
Het |
Rab38 |
A |
G |
7: 88,099,917 (GRCm39) |
D144G |
possibly damaging |
Het |
Septin1 |
T |
C |
7: 126,815,894 (GRCm39) |
M176V |
probably benign |
Het |
Spata22 |
C |
T |
11: 73,236,759 (GRCm39) |
T355M |
probably benign |
Het |
Tango6 |
A |
G |
8: 107,468,706 (GRCm39) |
N734S |
probably benign |
Het |
Tbc1d17 |
C |
A |
7: 44,493,738 (GRCm39) |
R295L |
probably damaging |
Het |
Thsd7a |
G |
T |
6: 12,504,074 (GRCm39) |
P360Q |
probably damaging |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Tnnt1 |
T |
C |
7: 4,510,406 (GRCm39) |
N239S |
possibly damaging |
Het |
Tpst1 |
A |
T |
5: 130,131,279 (GRCm39) |
M250L |
probably benign |
Het |
Urb1 |
T |
A |
16: 90,578,994 (GRCm39) |
D689V |
possibly damaging |
Het |
Usp28 |
T |
A |
9: 48,911,730 (GRCm39) |
|
probably null |
Het |
Vldlr |
G |
A |
19: 27,225,370 (GRCm39) |
D816N |
probably damaging |
Het |
Vmn1r257 |
T |
A |
7: 22,391,142 (GRCm39) |
M201L |
probably benign |
Het |
Wdr1 |
A |
G |
5: 38,687,374 (GRCm39) |
V219A |
probably damaging |
Het |
Xndc1 |
T |
C |
7: 101,722,476 (GRCm39) |
V47A |
possibly damaging |
Het |
Zfp366 |
C |
T |
13: 99,365,015 (GRCm39) |
P59S |
possibly damaging |
Het |
Zfp366 |
A |
G |
13: 99,382,685 (GRCm39) |
E616G |
possibly damaging |
Het |
Zfp937 |
T |
A |
2: 150,081,266 (GRCm39) |
I432K |
probably benign |
Het |
|
Other mutations in Ncbp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Ncbp3
|
APN |
11 |
72,964,355 (GRCm39) |
splice site |
probably benign |
|
R0180:Ncbp3
|
UTSW |
11 |
72,955,804 (GRCm39) |
splice site |
probably null |
|
R0464:Ncbp3
|
UTSW |
11 |
72,960,647 (GRCm39) |
splice site |
probably benign |
|
R0620:Ncbp3
|
UTSW |
11 |
72,940,671 (GRCm39) |
splice site |
probably benign |
|
R2024:Ncbp3
|
UTSW |
11 |
72,944,346 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2121:Ncbp3
|
UTSW |
11 |
72,944,304 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4610:Ncbp3
|
UTSW |
11 |
72,969,844 (GRCm39) |
missense |
probably damaging |
0.98 |
R4693:Ncbp3
|
UTSW |
11 |
72,966,503 (GRCm39) |
missense |
probably benign |
0.00 |
R4883:Ncbp3
|
UTSW |
11 |
72,960,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R4974:Ncbp3
|
UTSW |
11 |
72,944,355 (GRCm39) |
critical splice donor site |
probably null |
|
R5212:Ncbp3
|
UTSW |
11 |
72,944,373 (GRCm39) |
intron |
probably benign |
|
R5740:Ncbp3
|
UTSW |
11 |
72,944,323 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5906:Ncbp3
|
UTSW |
11 |
72,964,327 (GRCm39) |
missense |
probably benign |
0.04 |
R6026:Ncbp3
|
UTSW |
11 |
72,958,548 (GRCm39) |
missense |
probably benign |
0.00 |
R6154:Ncbp3
|
UTSW |
11 |
72,940,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R6403:Ncbp3
|
UTSW |
11 |
72,969,802 (GRCm39) |
missense |
probably benign |
0.00 |
R6626:Ncbp3
|
UTSW |
11 |
72,964,210 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7155:Ncbp3
|
UTSW |
11 |
72,938,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R7369:Ncbp3
|
UTSW |
11 |
72,968,747 (GRCm39) |
missense |
probably benign |
0.00 |
R7587:Ncbp3
|
UTSW |
11 |
72,957,591 (GRCm39) |
splice site |
probably null |
|
R7657:Ncbp3
|
UTSW |
11 |
72,964,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Ncbp3
|
UTSW |
11 |
72,938,808 (GRCm39) |
missense |
probably benign |
|
R8774-TAIL:Ncbp3
|
UTSW |
11 |
72,938,808 (GRCm39) |
missense |
probably benign |
|
R9063:Ncbp3
|
UTSW |
11 |
72,964,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R9478:Ncbp3
|
UTSW |
11 |
72,968,768 (GRCm39) |
missense |
probably damaging |
0.99 |
R9513:Ncbp3
|
UTSW |
11 |
72,938,727 (GRCm39) |
start codon destroyed |
probably null |
0.95 |
R9670:Ncbp3
|
UTSW |
11 |
72,944,323 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9762:Ncbp3
|
UTSW |
11 |
72,961,668 (GRCm39) |
missense |
probably benign |
0.35 |
Y5379:Ncbp3
|
UTSW |
11 |
72,964,086 (GRCm39) |
small deletion |
probably benign |
|
Z1177:Ncbp3
|
UTSW |
11 |
72,938,794 (GRCm39) |
frame shift |
probably null |
|
|