Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,336,830 (GRCm39) |
M45L |
probably benign |
Het |
Abcb1a |
T |
A |
5: 8,787,632 (GRCm39) |
V978D |
probably damaging |
Het |
Acsm4 |
T |
C |
7: 119,297,900 (GRCm39) |
V179A |
probably benign |
Het |
Agtr1a |
C |
A |
13: 30,565,842 (GRCm39) |
Y302* |
probably null |
Het |
Akap9 |
T |
C |
5: 4,058,382 (GRCm39) |
I1677T |
probably damaging |
Het |
Ankk1 |
T |
A |
9: 49,327,230 (GRCm39) |
M650L |
probably benign |
Het |
Apod |
T |
A |
16: 31,122,280 (GRCm39) |
N65Y |
probably damaging |
Het |
Bcl2l1 |
T |
A |
2: 152,624,178 (GRCm39) |
N197Y |
possibly damaging |
Het |
Brpf1 |
A |
T |
6: 113,292,072 (GRCm39) |
I373F |
probably damaging |
Het |
Car13 |
T |
C |
3: 14,726,615 (GRCm39) |
V257A |
probably damaging |
Het |
Ccdc150 |
A |
T |
1: 54,317,874 (GRCm39) |
H271L |
possibly damaging |
Het |
Cit |
T |
A |
5: 116,135,608 (GRCm39) |
I1836N |
probably damaging |
Het |
Clec12b |
A |
G |
6: 129,357,655 (GRCm39) |
S68P |
probably damaging |
Het |
Col4a4 |
A |
G |
1: 82,506,187 (GRCm39) |
F298L |
unknown |
Het |
Crct1 |
G |
A |
3: 92,922,093 (GRCm39) |
Q15* |
probably null |
Het |
Creld1 |
A |
G |
6: 113,469,208 (GRCm39) |
E346G |
probably benign |
Het |
Ctnnal1 |
T |
A |
4: 56,847,980 (GRCm39) |
H53L |
probably damaging |
Het |
Cyb5d1 |
T |
C |
11: 69,285,814 (GRCm39) |
D74G |
probably damaging |
Het |
Deptor |
A |
T |
15: 55,075,674 (GRCm39) |
S293C |
probably damaging |
Het |
Dnajb12 |
A |
G |
10: 59,728,592 (GRCm39) |
S187G |
probably benign |
Het |
Duoxa2 |
G |
T |
2: 122,131,072 (GRCm39) |
V78L |
possibly damaging |
Het |
Fem1al |
A |
T |
11: 29,775,454 (GRCm39) |
M1K |
probably null |
Het |
Fhod1 |
C |
A |
8: 106,074,443 (GRCm39) |
|
probably benign |
Het |
Foxf2 |
C |
T |
13: 31,810,172 (GRCm39) |
P37L |
unknown |
Het |
Gabbr2 |
T |
C |
4: 46,875,675 (GRCm39) |
N149S |
probably damaging |
Het |
Gckr |
G |
T |
5: 31,464,728 (GRCm39) |
M344I |
possibly damaging |
Het |
Herc6 |
G |
A |
6: 57,577,045 (GRCm39) |
|
probably null |
Het |
Igf1 |
A |
T |
10: 87,751,287 (GRCm39) |
E161V |
probably benign |
Het |
Ighv8-13 |
T |
A |
12: 115,729,268 (GRCm39) |
|
probably benign |
Het |
Igkv6-14 |
A |
T |
6: 70,412,426 (GRCm39) |
L12* |
probably null |
Het |
Lingo1 |
A |
G |
9: 56,527,209 (GRCm39) |
V460A |
probably benign |
Het |
Lsm6 |
T |
C |
8: 79,539,711 (GRCm39) |
|
probably null |
Het |
Mccc1 |
C |
T |
3: 36,050,066 (GRCm39) |
G42E |
probably benign |
Het |
Mga |
A |
G |
2: 119,734,120 (GRCm39) |
K323E |
possibly damaging |
Het |
Mks1 |
A |
G |
11: 87,753,850 (GRCm39) |
*562W |
probably null |
Het |
Mrgpra4 |
T |
A |
7: 47,630,686 (GRCm39) |
E305V |
probably damaging |
Het |
Msh4 |
T |
A |
3: 153,585,024 (GRCm39) |
H360L |
probably damaging |
Het |
Mthfsd |
C |
T |
8: 121,825,737 (GRCm39) |
|
probably null |
Het |
Myl12a |
A |
T |
17: 71,303,798 (GRCm39) |
F26L |
possibly damaging |
Het |
Nedd4l |
A |
G |
18: 65,298,676 (GRCm39) |
S343G |
probably damaging |
Het |
Nlgn1 |
T |
A |
3: 25,490,332 (GRCm39) |
D465V |
probably damaging |
Het |
Nlgn1 |
C |
T |
3: 25,490,507 (GRCm39) |
V407I |
possibly damaging |
Het |
Npsr1 |
T |
C |
9: 24,046,064 (GRCm39) |
V61A |
probably benign |
Het |
Nrxn2 |
A |
G |
19: 6,559,851 (GRCm39) |
D160G |
probably damaging |
Het |
Or2p2 |
T |
C |
13: 21,256,715 (GRCm39) |
Y252C |
probably damaging |
Het |
Or52d3 |
T |
C |
7: 104,229,404 (GRCm39) |
Y184H |
possibly damaging |
Het |
Or5b107 |
A |
C |
19: 13,143,277 (GRCm39) |
S300R |
probably benign |
Het |
Or5b113 |
G |
T |
19: 13,342,810 (GRCm39) |
A273S |
probably benign |
Het |
Or9g4 |
A |
G |
2: 85,504,664 (GRCm39) |
F277S |
probably damaging |
Het |
Pbx1 |
C |
A |
1: 168,023,450 (GRCm39) |
R235L |
probably damaging |
Het |
Pcnx4 |
T |
C |
12: 72,603,067 (GRCm39) |
V443A |
probably benign |
Het |
Pde7b |
T |
C |
10: 20,423,688 (GRCm39) |
T63A |
probably benign |
Het |
Phf3 |
C |
T |
1: 30,859,908 (GRCm39) |
G873D |
probably damaging |
Het |
Phox2b |
A |
T |
5: 67,256,197 (GRCm39) |
Y30N |
probably damaging |
Het |
Plch2 |
T |
A |
4: 155,080,690 (GRCm39) |
I599F |
possibly damaging |
Het |
Plekha8 |
A |
G |
6: 54,599,213 (GRCm39) |
E249G |
probably benign |
Het |
Pou2af1 |
T |
A |
9: 51,144,439 (GRCm39) |
Y118N |
possibly damaging |
Het |
Ppp3cc |
T |
A |
14: 70,455,635 (GRCm39) |
K489N |
possibly damaging |
Het |
Sema4b |
T |
C |
7: 79,866,577 (GRCm39) |
L219P |
probably damaging |
Het |
Slc6a5 |
T |
G |
7: 49,609,030 (GRCm39) |
V745G |
probably benign |
Het |
Slf2 |
A |
G |
19: 44,923,497 (GRCm39) |
M104V |
probably benign |
Het |
Slx1b |
A |
G |
7: 126,291,701 (GRCm39) |
V121A |
probably benign |
Het |
Speer4e2 |
T |
A |
5: 15,026,222 (GRCm39) |
H145L |
probably benign |
Het |
Spen |
T |
A |
4: 141,200,390 (GRCm39) |
K2746* |
probably null |
Het |
Stxbp5l |
T |
C |
16: 37,008,996 (GRCm39) |
Y681C |
probably damaging |
Het |
Sv2b |
T |
C |
7: 74,773,918 (GRCm39) |
T518A |
probably benign |
Het |
Tgm7 |
A |
T |
2: 120,926,870 (GRCm39) |
H426Q |
possibly damaging |
Het |
Tlx2 |
A |
G |
6: 83,046,900 (GRCm39) |
F54S |
probably benign |
Het |
Trp53bp2 |
A |
T |
1: 182,286,339 (GRCm39) |
M1060L |
probably benign |
Het |
Trpv5 |
T |
A |
6: 41,630,148 (GRCm39) |
E647D |
probably damaging |
Het |
Tut1 |
G |
T |
19: 8,936,672 (GRCm39) |
K165N |
possibly damaging |
Het |
Tyro3 |
A |
G |
2: 119,641,419 (GRCm39) |
K543E |
probably damaging |
Het |
Vmn2r69 |
T |
A |
7: 85,061,575 (GRCm39) |
Y133F |
probably damaging |
Het |
Zfhx4 |
T |
A |
3: 5,465,122 (GRCm39) |
V1785D |
possibly damaging |
Het |
Zfp451 |
A |
G |
1: 33,804,939 (GRCm39) |
L1037P |
probably damaging |
Het |
Zscan29 |
A |
T |
2: 120,991,392 (GRCm39) |
F799I |
possibly damaging |
Het |
|
Other mutations in Kpnb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01284:Kpnb1
|
APN |
11 |
97,056,928 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01919:Kpnb1
|
APN |
11 |
97,055,556 (GRCm39) |
missense |
probably benign |
|
IGL02161:Kpnb1
|
APN |
11 |
97,059,762 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02679:Kpnb1
|
APN |
11 |
97,068,086 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02866:Kpnb1
|
APN |
11 |
97,068,112 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02899:Kpnb1
|
APN |
11 |
97,066,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Kpnb1
|
UTSW |
11 |
97,075,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R0542:Kpnb1
|
UTSW |
11 |
97,078,398 (GRCm39) |
missense |
probably benign |
0.12 |
R0724:Kpnb1
|
UTSW |
11 |
97,069,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0825:Kpnb1
|
UTSW |
11 |
97,062,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R0853:Kpnb1
|
UTSW |
11 |
97,078,237 (GRCm39) |
missense |
probably damaging |
0.97 |
R1481:Kpnb1
|
UTSW |
11 |
97,069,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R3802:Kpnb1
|
UTSW |
11 |
97,056,955 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4458:Kpnb1
|
UTSW |
11 |
97,059,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R4490:Kpnb1
|
UTSW |
11 |
97,062,424 (GRCm39) |
missense |
probably benign |
|
R5500:Kpnb1
|
UTSW |
11 |
97,063,937 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6360:Kpnb1
|
UTSW |
11 |
97,064,096 (GRCm39) |
missense |
probably benign |
|
R6494:Kpnb1
|
UTSW |
11 |
97,072,474 (GRCm39) |
missense |
probably benign |
0.04 |
R7678:Kpnb1
|
UTSW |
11 |
97,059,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R8171:Kpnb1
|
UTSW |
11 |
97,066,573 (GRCm39) |
critical splice donor site |
probably null |
|
R8874:Kpnb1
|
UTSW |
11 |
97,056,209 (GRCm39) |
missense |
probably benign |
0.25 |
R9318:Kpnb1
|
UTSW |
11 |
97,054,284 (GRCm39) |
missense |
probably benign |
|
R9621:Kpnb1
|
UTSW |
11 |
97,058,460 (GRCm39) |
missense |
probably benign |
0.04 |
|