Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930595D18Rik |
G |
A |
12: 111,141,369 (GRCm39) |
Q19* |
probably null |
Het |
6030468B19Rik |
T |
A |
11: 117,697,092 (GRCm39) |
C230* |
probably null |
Het |
Adcy10 |
A |
G |
1: 165,345,815 (GRCm39) |
E288G |
probably damaging |
Het |
Adnp |
T |
A |
2: 168,029,537 (GRCm39) |
T51S |
possibly damaging |
Het |
Agap3 |
C |
A |
5: 24,683,011 (GRCm39) |
A464D |
probably damaging |
Het |
Ago4 |
A |
C |
4: 126,400,635 (GRCm39) |
C693G |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,860,303 (GRCm39) |
R675G |
probably damaging |
Het |
Amigo1 |
T |
A |
3: 108,094,981 (GRCm39) |
L160Q |
probably damaging |
Het |
Ankrd35 |
T |
C |
3: 96,591,438 (GRCm39) |
S575P |
probably benign |
Het |
Ano3 |
T |
A |
2: 110,601,365 (GRCm39) |
T298S |
possibly damaging |
Het |
Ap2b1 |
T |
G |
11: 83,281,532 (GRCm39) |
F813V |
probably damaging |
Het |
Aplnr |
T |
G |
2: 84,967,261 (GRCm39) |
F95L |
probably damaging |
Het |
Apobec2 |
T |
C |
17: 48,730,153 (GRCm39) |
E171G |
probably benign |
Het |
Ascc1 |
A |
G |
10: 59,840,684 (GRCm39) |
N15S |
probably benign |
Het |
AY358078 |
T |
A |
14: 52,040,108 (GRCm39) |
Y73N |
unknown |
Het |
B3gnt8 |
C |
A |
7: 25,328,308 (GRCm39) |
P246Q |
probably damaging |
Het |
C2cd2l |
T |
C |
9: 44,227,857 (GRCm39) |
Q250R |
probably damaging |
Het |
Camk2d |
T |
C |
3: 126,577,624 (GRCm39) |
Y180H |
probably damaging |
Het |
Ccdc170 |
A |
G |
10: 4,468,971 (GRCm39) |
E167G |
probably damaging |
Het |
Cdyl2 |
A |
G |
8: 117,305,926 (GRCm39) |
M445T |
probably damaging |
Het |
Clca3a1 |
T |
C |
3: 144,721,605 (GRCm39) |
D322G |
probably benign |
Het |
Cnot10 |
C |
T |
9: 114,458,202 (GRCm39) |
M101I |
possibly damaging |
Het |
Cntrl |
C |
T |
2: 35,055,694 (GRCm39) |
T1196M |
probably benign |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Dcaf6 |
T |
C |
1: 165,247,774 (GRCm39) |
D153G |
probably damaging |
Het |
Dennd2c |
G |
A |
3: 103,039,140 (GRCm39) |
G96E |
probably benign |
Het |
Dhrs9 |
T |
C |
2: 69,231,752 (GRCm39) |
F304S |
probably damaging |
Het |
Dmxl1 |
T |
C |
18: 50,010,764 (GRCm39) |
S974P |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,169,659 (GRCm39) |
|
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,634,168 (GRCm39) |
L1049P |
probably damaging |
Het |
Dnajc2 |
T |
C |
5: 21,962,338 (GRCm39) |
K621E |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,096,592 (GRCm39) |
D299G |
probably benign |
Het |
Erap1 |
A |
G |
13: 74,794,647 (GRCm39) |
E102G |
probably benign |
Het |
Fasn |
T |
G |
11: 120,707,472 (GRCm39) |
N799T |
probably benign |
Het |
Fbxl20 |
T |
C |
11: 98,019,186 (GRCm39) |
D22G |
probably damaging |
Het |
Fgfr1 |
T |
C |
8: 26,053,542 (GRCm39) |
|
probably null |
Het |
Frzb |
A |
T |
2: 80,276,871 (GRCm39) |
I105N |
probably damaging |
Het |
Gabrb1 |
T |
A |
5: 72,026,764 (GRCm39) |
F55Y |
probably damaging |
Het |
Gatd1 |
G |
T |
7: 140,989,010 (GRCm39) |
C216* |
probably null |
Het |
Gnl2 |
A |
C |
4: 124,937,485 (GRCm39) |
N255T |
probably damaging |
Het |
Golgb1 |
A |
T |
16: 36,736,480 (GRCm39) |
Q1909L |
probably benign |
Het |
Gpnmb |
T |
C |
6: 49,028,904 (GRCm39) |
L474P |
probably damaging |
Het |
H60b |
T |
C |
10: 22,163,115 (GRCm39) |
V230A |
possibly damaging |
Het |
Hmcn2 |
T |
A |
2: 31,250,992 (GRCm39) |
V818D |
probably damaging |
Het |
Irag2 |
C |
A |
6: 145,111,027 (GRCm39) |
S277R |
probably damaging |
Het |
Itprid1 |
C |
T |
6: 55,955,175 (GRCm39) |
P928S |
possibly damaging |
Het |
Jade2 |
G |
T |
11: 51,707,909 (GRCm39) |
T768K |
probably benign |
Het |
Kif28 |
T |
C |
1: 179,530,085 (GRCm39) |
H692R |
probably benign |
Het |
Kmt2b |
T |
C |
7: 30,277,942 (GRCm39) |
N1634S |
probably damaging |
Het |
Knop1 |
A |
G |
7: 118,445,299 (GRCm39) |
W222R |
probably damaging |
Het |
Map1b |
T |
C |
13: 99,569,808 (GRCm39) |
D971G |
unknown |
Het |
Mapk7 |
G |
T |
11: 61,384,475 (GRCm39) |
T77K |
probably damaging |
Het |
Mcm6 |
A |
G |
1: 128,276,714 (GRCm39) |
L292P |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,039,089 (GRCm39) |
L900P |
probably benign |
Het |
Meis1 |
G |
A |
11: 18,831,776 (GRCm39) |
H421Y |
possibly damaging |
Het |
Minar2 |
A |
T |
18: 59,205,277 (GRCm39) |
I22F |
probably damaging |
Het |
Mllt1 |
T |
C |
17: 57,206,813 (GRCm39) |
T344A |
probably benign |
Het |
Mta1 |
T |
A |
12: 113,100,160 (GRCm39) |
S657T |
probably benign |
Het |
Mtus1 |
C |
A |
8: 41,453,838 (GRCm39) |
K998N |
probably damaging |
Het |
Ncdn |
G |
A |
4: 126,643,731 (GRCm39) |
L364F |
possibly damaging |
Het |
Ndufb7 |
T |
C |
8: 84,297,534 (GRCm39) |
L63P |
probably damaging |
Het |
Nfix |
T |
C |
8: 85,498,458 (GRCm39) |
I172V |
probably benign |
Het |
Nos1 |
T |
C |
5: 118,085,635 (GRCm39) |
|
probably null |
Het |
Nrp1 |
C |
A |
8: 129,229,285 (GRCm39) |
S921* |
probably null |
Het |
Oma1 |
T |
C |
4: 103,176,727 (GRCm39) |
|
probably null |
Het |
Or3a1b |
A |
T |
11: 74,012,705 (GRCm39) |
I197F |
probably benign |
Het |
Or5b106 |
T |
A |
19: 13,123,355 (GRCm39) |
I223L |
possibly damaging |
Het |
Pcp2 |
T |
A |
8: 3,675,534 (GRCm39) |
|
probably benign |
Het |
Pdk4 |
T |
A |
6: 5,489,157 (GRCm39) |
H250L |
possibly damaging |
Het |
Phldb3 |
A |
G |
7: 24,323,716 (GRCm39) |
H449R |
probably benign |
Het |
Pip4k2c |
T |
C |
10: 127,035,196 (GRCm39) |
T391A |
possibly damaging |
Het |
Polrmt |
A |
G |
10: 79,582,385 (GRCm39) |
M1T |
probably null |
Het |
Ppfia2 |
G |
C |
10: 106,597,978 (GRCm39) |
L180F |
probably damaging |
Het |
Prkcg |
T |
G |
7: 3,378,781 (GRCm39) |
Y624* |
probably null |
Het |
Psmg2 |
A |
G |
18: 67,781,926 (GRCm39) |
E164G |
probably damaging |
Het |
Rb1 |
A |
T |
14: 73,454,131 (GRCm39) |
L589H |
probably damaging |
Het |
Rcvrn |
A |
T |
11: 67,586,591 (GRCm39) |
I117F |
probably damaging |
Het |
Rere |
T |
A |
4: 150,703,601 (GRCm39) |
W1528R |
probably damaging |
Het |
Robo2 |
A |
G |
16: 73,695,803 (GRCm39) |
S1447P |
possibly damaging |
Het |
Scfd2 |
C |
A |
5: 74,623,319 (GRCm39) |
G405W |
probably damaging |
Het |
Scin |
T |
A |
12: 40,119,373 (GRCm39) |
I552F |
possibly damaging |
Het |
Serpina3k |
G |
A |
12: 104,309,269 (GRCm39) |
V238M |
probably damaging |
Het |
Slc1a6 |
G |
A |
10: 78,632,085 (GRCm39) |
V304M |
probably damaging |
Het |
Slc20a2 |
C |
T |
8: 23,051,020 (GRCm39) |
S351L |
probably damaging |
Het |
Slc31a2 |
T |
C |
4: 62,215,325 (GRCm39) |
V124A |
probably damaging |
Het |
Slc38a3 |
T |
C |
9: 107,533,426 (GRCm39) |
N244S |
probably benign |
Het |
Slc4a1 |
A |
G |
11: 102,243,279 (GRCm39) |
V784A |
probably damaging |
Het |
Slc6a5 |
T |
C |
7: 49,598,004 (GRCm39) |
F623L |
probably benign |
Het |
Slf2 |
T |
G |
19: 44,960,100 (GRCm39) |
D1022E |
probably damaging |
Het |
Slfn8 |
G |
A |
11: 82,907,704 (GRCm39) |
H280Y |
probably damaging |
Het |
Smpdl3a |
A |
T |
10: 57,677,127 (GRCm39) |
D45V |
probably damaging |
Het |
Ssh3 |
T |
C |
19: 4,315,170 (GRCm39) |
E342G |
probably damaging |
Het |
Tacr1 |
A |
T |
6: 82,531,922 (GRCm39) |
I273F |
probably benign |
Het |
Tfg |
T |
A |
16: 56,514,759 (GRCm39) |
|
probably null |
Het |
Tmem179 |
A |
G |
12: 112,468,268 (GRCm39) |
L71P |
probably damaging |
Het |
Tmem63a |
T |
A |
1: 180,794,086 (GRCm39) |
I541N |
probably benign |
Het |
Traj20 |
G |
A |
14: 54,436,924 (GRCm39) |
|
probably benign |
Het |
Trappc13 |
A |
T |
13: 104,290,802 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Tulp1 |
A |
G |
17: 28,578,109 (GRCm39) |
L310P |
probably damaging |
Het |
Ube3d |
A |
G |
9: 86,304,925 (GRCm39) |
Y306H |
probably damaging |
Het |
Urb1 |
A |
T |
16: 90,580,216 (GRCm39) |
V649E |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,709,963 (GRCm39) |
L4211P |
probably damaging |
Het |
Vwa5b1 |
T |
A |
4: 138,321,573 (GRCm39) |
I407F |
possibly damaging |
Het |
Vwce |
G |
T |
19: 10,624,243 (GRCm39) |
C378F |
probably damaging |
Het |
Zfp791 |
T |
A |
8: 85,837,580 (GRCm39) |
I95L |
probably benign |
Het |
|
Other mutations in Cdcp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Cdcp3
|
APN |
7 |
130,839,823 (GRCm39) |
splice site |
probably null |
|
IGL00848:Cdcp3
|
APN |
7 |
130,848,453 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00966:Cdcp3
|
APN |
7 |
130,844,836 (GRCm39) |
nonsense |
probably null |
|
IGL01286:Cdcp3
|
APN |
7 |
130,848,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Cdcp3
|
APN |
7 |
130,796,060 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01585:Cdcp3
|
APN |
7 |
130,846,487 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01665:Cdcp3
|
APN |
7 |
130,848,386 (GRCm39) |
nonsense |
probably null |
|
IGL01953:Cdcp3
|
APN |
7 |
130,826,709 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02427:Cdcp3
|
APN |
7 |
130,846,517 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02508:Cdcp3
|
APN |
7 |
130,824,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02678:Cdcp3
|
APN |
7 |
130,830,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03092:Cdcp3
|
APN |
7 |
130,803,527 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03122:Cdcp3
|
APN |
7 |
130,798,243 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03343:Cdcp3
|
APN |
7 |
130,848,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Cdcp3
|
UTSW |
7 |
130,831,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R0011:Cdcp3
|
UTSW |
7 |
130,831,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R0234:Cdcp3
|
UTSW |
7 |
130,796,032 (GRCm39) |
splice site |
probably null |
|
R0234:Cdcp3
|
UTSW |
7 |
130,796,032 (GRCm39) |
splice site |
probably null |
|
R0268:Cdcp3
|
UTSW |
7 |
130,839,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:Cdcp3
|
UTSW |
7 |
130,841,268 (GRCm39) |
missense |
probably benign |
0.05 |
R0973:Cdcp3
|
UTSW |
7 |
130,839,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Cdcp3
|
UTSW |
7 |
130,839,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Cdcp3
|
UTSW |
7 |
130,839,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Cdcp3
|
UTSW |
7 |
130,846,560 (GRCm39) |
nonsense |
probably null |
|
R1911:Cdcp3
|
UTSW |
7 |
130,839,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R2032:Cdcp3
|
UTSW |
7 |
130,844,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R2097:Cdcp3
|
UTSW |
7 |
130,783,693 (GRCm39) |
nonsense |
probably null |
|
R2221:Cdcp3
|
UTSW |
7 |
130,849,186 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2223:Cdcp3
|
UTSW |
7 |
130,849,186 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2254:Cdcp3
|
UTSW |
7 |
130,824,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R2913:Cdcp3
|
UTSW |
7 |
130,783,753 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2991:Cdcp3
|
UTSW |
7 |
130,848,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R3439:Cdcp3
|
UTSW |
7 |
130,790,508 (GRCm39) |
critical splice donor site |
probably null |
|
R4418:Cdcp3
|
UTSW |
7 |
130,849,194 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5488:Cdcp3
|
UTSW |
7 |
130,848,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R5594:Cdcp3
|
UTSW |
7 |
130,841,252 (GRCm39) |
missense |
probably benign |
0.12 |
R5897:Cdcp3
|
UTSW |
7 |
130,798,280 (GRCm39) |
splice site |
probably null |
|
R5898:Cdcp3
|
UTSW |
7 |
130,843,696 (GRCm39) |
splice site |
probably null |
|
R5940:Cdcp3
|
UTSW |
7 |
130,839,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Cdcp3
|
UTSW |
7 |
130,776,216 (GRCm39) |
splice site |
probably null |
|
R6187:Cdcp3
|
UTSW |
7 |
130,872,328 (GRCm39) |
intron |
probably benign |
|
R6321:Cdcp3
|
UTSW |
7 |
130,858,735 (GRCm39) |
critical splice donor site |
probably null |
|
R6409:Cdcp3
|
UTSW |
7 |
130,863,800 (GRCm39) |
intron |
probably benign |
|
R6432:Cdcp3
|
UTSW |
7 |
130,846,601 (GRCm39) |
critical splice donor site |
probably null |
|
R6481:Cdcp3
|
UTSW |
7 |
130,858,530 (GRCm39) |
missense |
probably benign |
0.05 |
R6750:Cdcp3
|
UTSW |
7 |
130,889,974 (GRCm39) |
intron |
probably benign |
|
R6783:Cdcp3
|
UTSW |
7 |
130,828,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R6836:Cdcp3
|
UTSW |
7 |
130,798,233 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6925:Cdcp3
|
UTSW |
7 |
130,824,436 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6995:Cdcp3
|
UTSW |
7 |
130,824,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Cdcp3
|
UTSW |
7 |
130,837,641 (GRCm39) |
nonsense |
probably null |
|
R7205:Cdcp3
|
UTSW |
7 |
130,879,352 (GRCm39) |
critical splice donor site |
probably null |
|
R7340:Cdcp3
|
UTSW |
7 |
130,879,344 (GRCm39) |
missense |
unknown |
|
R7354:Cdcp3
|
UTSW |
7 |
130,873,762 (GRCm39) |
missense |
unknown |
|
R7354:Cdcp3
|
UTSW |
7 |
130,858,458 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7434:Cdcp3
|
UTSW |
7 |
130,881,212 (GRCm39) |
missense |
unknown |
|
R7485:Cdcp3
|
UTSW |
7 |
130,830,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R7513:Cdcp3
|
UTSW |
7 |
130,873,800 (GRCm39) |
missense |
unknown |
|
R7562:Cdcp3
|
UTSW |
7 |
130,904,426 (GRCm39) |
missense |
unknown |
|
R7623:Cdcp3
|
UTSW |
7 |
130,879,295 (GRCm39) |
splice site |
probably null |
|
R7782:Cdcp3
|
UTSW |
7 |
130,904,466 (GRCm39) |
splice site |
probably null |
|
R7879:Cdcp3
|
UTSW |
7 |
130,844,871 (GRCm39) |
missense |
probably damaging |
0.98 |
R7935:Cdcp3
|
UTSW |
7 |
130,852,205 (GRCm39) |
missense |
probably damaging |
0.96 |
R7949:Cdcp3
|
UTSW |
7 |
130,895,324 (GRCm39) |
splice site |
probably null |
|
R7964:Cdcp3
|
UTSW |
7 |
130,899,963 (GRCm39) |
missense |
unknown |
|
R7980:Cdcp3
|
UTSW |
7 |
130,836,506 (GRCm39) |
missense |
probably damaging |
0.98 |
R8145:Cdcp3
|
UTSW |
7 |
130,898,045 (GRCm39) |
missense |
unknown |
|
R8673:Cdcp3
|
UTSW |
7 |
130,844,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R8684:Cdcp3
|
UTSW |
7 |
130,837,688 (GRCm39) |
nonsense |
probably null |
|
R8721:Cdcp3
|
UTSW |
7 |
130,879,335 (GRCm39) |
missense |
unknown |
|
R8725:Cdcp3
|
UTSW |
7 |
130,875,485 (GRCm39) |
missense |
unknown |
|
R8727:Cdcp3
|
UTSW |
7 |
130,875,485 (GRCm39) |
missense |
unknown |
|
R8742:Cdcp3
|
UTSW |
7 |
130,783,741 (GRCm39) |
missense |
unknown |
|
R8807:Cdcp3
|
UTSW |
7 |
130,846,507 (GRCm39) |
missense |
probably damaging |
0.97 |
R8822:Cdcp3
|
UTSW |
7 |
130,843,706 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8861:Cdcp3
|
UTSW |
7 |
130,861,690 (GRCm39) |
nonsense |
probably null |
|
R8897:Cdcp3
|
UTSW |
7 |
130,867,566 (GRCm39) |
missense |
unknown |
|
R8900:Cdcp3
|
UTSW |
7 |
130,904,197 (GRCm39) |
intron |
probably benign |
|
R9214:Cdcp3
|
UTSW |
7 |
130,824,481 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9218:Cdcp3
|
UTSW |
7 |
130,863,728 (GRCm39) |
missense |
unknown |
|
R9311:Cdcp3
|
UTSW |
7 |
130,859,490 (GRCm39) |
missense |
unknown |
|
R9323:Cdcp3
|
UTSW |
7 |
130,828,401 (GRCm39) |
missense |
probably damaging |
0.96 |
R9384:Cdcp3
|
UTSW |
7 |
130,904,404 (GRCm39) |
missense |
unknown |
|
R9387:Cdcp3
|
UTSW |
7 |
130,863,620 (GRCm39) |
missense |
unknown |
|
R9417:Cdcp3
|
UTSW |
7 |
130,852,218 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9502:Cdcp3
|
UTSW |
7 |
130,836,815 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9603:Cdcp3
|
UTSW |
7 |
130,830,643 (GRCm39) |
missense |
probably damaging |
0.98 |
R9642:Cdcp3
|
UTSW |
7 |
130,848,257 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Cdcp3
|
UTSW |
7 |
130,848,362 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cdcp3
|
UTSW |
7 |
130,867,595 (GRCm39) |
missense |
unknown |
|
|