Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ank3 |
A |
G |
10: 69,809,602 (GRCm39) |
T260A |
probably damaging |
Het |
Arhgap21 |
A |
G |
2: 20,885,500 (GRCm39) |
V559A |
probably benign |
Het |
Arrdc5 |
G |
A |
17: 56,601,589 (GRCm39) |
Q179* |
probably null |
Het |
Atrnl1 |
T |
C |
19: 57,630,973 (GRCm39) |
Y247H |
probably benign |
Het |
Bend5 |
T |
A |
4: 111,311,468 (GRCm39) |
S361T |
probably benign |
Het |
Cdc20b |
A |
G |
13: 113,217,736 (GRCm39) |
D385G |
probably damaging |
Het |
Cep120 |
C |
T |
18: 53,842,208 (GRCm39) |
S709N |
probably benign |
Het |
Eif2b4 |
A |
G |
5: 31,347,355 (GRCm39) |
|
probably benign |
Het |
Eif2s1 |
T |
A |
12: 78,913,354 (GRCm39) |
D18E |
probably benign |
Het |
Etl4 |
G |
A |
2: 20,666,827 (GRCm39) |
S209N |
possibly damaging |
Het |
Farp2 |
T |
A |
1: 93,535,160 (GRCm39) |
F636L |
probably benign |
Het |
Fcgbp |
A |
T |
7: 27,789,342 (GRCm39) |
D636V |
possibly damaging |
Het |
Gm5082 |
T |
C |
13: 41,809,902 (GRCm39) |
|
noncoding transcript |
Het |
Gtf2ird1 |
C |
T |
5: 134,411,392 (GRCm39) |
G672D |
possibly damaging |
Het |
Heatr3 |
A |
G |
8: 88,876,738 (GRCm39) |
K143R |
probably benign |
Het |
Hrc |
A |
G |
7: 44,986,679 (GRCm39) |
E610G |
probably benign |
Het |
Ica1l |
G |
A |
1: 60,036,780 (GRCm39) |
S337F |
probably benign |
Het |
Ighv1-43 |
T |
C |
12: 114,909,625 (GRCm39) |
Y99C |
probably benign |
Het |
Kcna3 |
T |
A |
3: 106,944,521 (GRCm39) |
F261L |
probably benign |
Het |
Kdm4d |
T |
C |
9: 14,375,139 (GRCm39) |
R240G |
probably damaging |
Het |
Kif5c |
A |
G |
2: 49,591,104 (GRCm39) |
M55V |
probably damaging |
Het |
Oas1a |
A |
T |
5: 121,035,062 (GRCm39) |
L366Q |
possibly damaging |
Het |
Or5p68 |
T |
C |
7: 107,946,196 (GRCm39) |
|
probably benign |
Het |
Pds5b |
T |
C |
5: 150,711,796 (GRCm39) |
V918A |
probably damaging |
Het |
Plcz1 |
G |
A |
6: 139,936,490 (GRCm39) |
L580F |
possibly damaging |
Het |
Prlr |
C |
A |
15: 10,319,403 (GRCm39) |
P147T |
possibly damaging |
Het |
Ptpn18 |
A |
T |
1: 34,509,338 (GRCm39) |
|
probably null |
Het |
Ptprt |
A |
T |
2: 161,397,379 (GRCm39) |
C1109* |
probably null |
Het |
Ralgapa2 |
A |
T |
2: 146,199,907 (GRCm39) |
S1212R |
probably benign |
Het |
Scn2b |
T |
A |
9: 45,037,498 (GRCm39) |
C182S |
probably damaging |
Het |
Slc7a14 |
A |
T |
3: 31,277,664 (GRCm39) |
M647K |
probably damaging |
Het |
Sult2a6 |
G |
A |
7: 13,956,511 (GRCm39) |
T250I |
probably benign |
Het |
Syn3 |
A |
T |
10: 85,900,736 (GRCm39) |
M384K |
possibly damaging |
Het |
Tmem8b |
A |
G |
4: 43,685,561 (GRCm39) |
T596A |
probably benign |
Het |
Tnpo1 |
C |
T |
13: 99,000,348 (GRCm39) |
E340K |
probably damaging |
Het |
Vat1l |
A |
T |
8: 115,009,006 (GRCm39) |
I247F |
probably damaging |
Het |
Vmn2r110 |
T |
C |
17: 20,803,906 (GRCm39) |
D223G |
probably damaging |
Het |
Wdr11 |
T |
A |
7: 129,200,847 (GRCm39) |
D99E |
probably damaging |
Het |
Zan |
C |
T |
5: 137,462,477 (GRCm39) |
V901I |
unknown |
Het |
|
Other mutations in Kidins220 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00551:Kidins220
|
APN |
12 |
25,088,559 (GRCm39) |
splice site |
probably benign |
|
IGL00959:Kidins220
|
APN |
12 |
25,101,132 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL00978:Kidins220
|
APN |
12 |
25,107,473 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01144:Kidins220
|
APN |
12 |
25,060,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01326:Kidins220
|
APN |
12 |
25,088,498 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01545:Kidins220
|
APN |
12 |
25,090,459 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01802:Kidins220
|
APN |
12 |
25,044,999 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01875:Kidins220
|
APN |
12 |
25,107,728 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02160:Kidins220
|
APN |
12 |
25,054,110 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02383:Kidins220
|
APN |
12 |
25,047,332 (GRCm39) |
splice site |
probably benign |
|
IGL02673:Kidins220
|
APN |
12 |
25,044,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02800:Kidins220
|
APN |
12 |
25,053,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03345:Kidins220
|
APN |
12 |
25,053,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03412:Kidins220
|
APN |
12 |
25,049,344 (GRCm39) |
missense |
probably damaging |
1.00 |
P0043:Kidins220
|
UTSW |
12 |
25,058,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Kidins220
|
UTSW |
12 |
25,049,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R0011:Kidins220
|
UTSW |
12 |
25,049,351 (GRCm39) |
missense |
probably damaging |
0.99 |
R0269:Kidins220
|
UTSW |
12 |
25,090,511 (GRCm39) |
missense |
probably damaging |
0.98 |
R0280:Kidins220
|
UTSW |
12 |
25,060,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Kidins220
|
UTSW |
12 |
25,058,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R1601:Kidins220
|
UTSW |
12 |
25,055,087 (GRCm39) |
missense |
probably benign |
0.35 |
R1778:Kidins220
|
UTSW |
12 |
25,063,445 (GRCm39) |
splice site |
probably benign |
|
R1808:Kidins220
|
UTSW |
12 |
25,053,008 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Kidins220
|
UTSW |
12 |
25,106,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R1965:Kidins220
|
UTSW |
12 |
25,044,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Kidins220
|
UTSW |
12 |
25,101,193 (GRCm39) |
missense |
probably benign |
0.01 |
R2069:Kidins220
|
UTSW |
12 |
25,037,005 (GRCm39) |
splice site |
probably benign |
|
R2101:Kidins220
|
UTSW |
12 |
25,107,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Kidins220
|
UTSW |
12 |
25,091,302 (GRCm39) |
critical splice donor site |
probably null |
|
R2371:Kidins220
|
UTSW |
12 |
25,107,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R2405:Kidins220
|
UTSW |
12 |
25,061,508 (GRCm39) |
missense |
probably damaging |
0.99 |
R3522:Kidins220
|
UTSW |
12 |
25,040,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R3877:Kidins220
|
UTSW |
12 |
25,051,564 (GRCm39) |
splice site |
probably benign |
|
R3915:Kidins220
|
UTSW |
12 |
25,103,957 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4023:Kidins220
|
UTSW |
12 |
25,107,143 (GRCm39) |
splice site |
probably null |
|
R4287:Kidins220
|
UTSW |
12 |
25,106,845 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4476:Kidins220
|
UTSW |
12 |
25,061,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Kidins220
|
UTSW |
12 |
25,088,301 (GRCm39) |
splice site |
probably null |
|
R4627:Kidins220
|
UTSW |
12 |
25,107,041 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4807:Kidins220
|
UTSW |
12 |
25,107,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Kidins220
|
UTSW |
12 |
25,063,442 (GRCm39) |
critical splice donor site |
probably null |
|
R4960:Kidins220
|
UTSW |
12 |
25,042,259 (GRCm39) |
nonsense |
probably null |
|
R5118:Kidins220
|
UTSW |
12 |
25,042,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Kidins220
|
UTSW |
12 |
25,101,125 (GRCm39) |
missense |
probably benign |
0.17 |
R5238:Kidins220
|
UTSW |
12 |
25,053,009 (GRCm39) |
missense |
probably benign |
0.31 |
R5580:Kidins220
|
UTSW |
12 |
25,097,896 (GRCm39) |
missense |
probably benign |
0.00 |
R5707:Kidins220
|
UTSW |
12 |
25,063,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Kidins220
|
UTSW |
12 |
25,107,139 (GRCm39) |
nonsense |
probably null |
|
R6131:Kidins220
|
UTSW |
12 |
25,042,313 (GRCm39) |
splice site |
probably null |
|
R6146:Kidins220
|
UTSW |
12 |
25,102,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Kidins220
|
UTSW |
12 |
25,106,908 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6160:Kidins220
|
UTSW |
12 |
25,047,310 (GRCm39) |
missense |
probably damaging |
1.00 |
R6187:Kidins220
|
UTSW |
12 |
25,101,307 (GRCm39) |
splice site |
probably null |
|
R6289:Kidins220
|
UTSW |
12 |
25,106,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R6321:Kidins220
|
UTSW |
12 |
25,107,533 (GRCm39) |
missense |
probably benign |
0.09 |
R6450:Kidins220
|
UTSW |
12 |
25,107,190 (GRCm39) |
missense |
probably benign |
|
R6513:Kidins220
|
UTSW |
12 |
25,088,434 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6652:Kidins220
|
UTSW |
12 |
25,060,059 (GRCm39) |
splice site |
probably null |
|
R6711:Kidins220
|
UTSW |
12 |
25,048,750 (GRCm39) |
missense |
probably damaging |
0.96 |
R6858:Kidins220
|
UTSW |
12 |
25,058,542 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7102:Kidins220
|
UTSW |
12 |
25,107,662 (GRCm39) |
missense |
probably benign |
0.00 |
R7112:Kidins220
|
UTSW |
12 |
25,054,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R7139:Kidins220
|
UTSW |
12 |
25,044,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Kidins220
|
UTSW |
12 |
25,086,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R7271:Kidins220
|
UTSW |
12 |
25,061,570 (GRCm39) |
missense |
probably benign |
0.21 |
R7361:Kidins220
|
UTSW |
12 |
25,106,999 (GRCm39) |
missense |
probably benign |
0.01 |
R7509:Kidins220
|
UTSW |
12 |
25,032,360 (GRCm39) |
missense |
probably damaging |
0.98 |
R7510:Kidins220
|
UTSW |
12 |
25,042,268 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7783:Kidins220
|
UTSW |
12 |
25,038,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R7796:Kidins220
|
UTSW |
12 |
25,032,350 (GRCm39) |
missense |
probably damaging |
0.96 |
R7831:Kidins220
|
UTSW |
12 |
25,111,230 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8074:Kidins220
|
UTSW |
12 |
25,107,715 (GRCm39) |
missense |
probably benign |
0.29 |
R8214:Kidins220
|
UTSW |
12 |
25,044,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R8304:Kidins220
|
UTSW |
12 |
25,107,127 (GRCm39) |
missense |
probably benign |
0.01 |
R8313:Kidins220
|
UTSW |
12 |
25,054,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8346:Kidins220
|
UTSW |
12 |
25,086,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Kidins220
|
UTSW |
12 |
25,040,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R8482:Kidins220
|
UTSW |
12 |
25,090,527 (GRCm39) |
missense |
probably benign |
0.00 |
R8722:Kidins220
|
UTSW |
12 |
25,051,593 (GRCm39) |
missense |
probably benign |
|
R8831:Kidins220
|
UTSW |
12 |
25,086,454 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8960:Kidins220
|
UTSW |
12 |
25,106,914 (GRCm39) |
missense |
probably benign |
0.05 |
R9193:Kidins220
|
UTSW |
12 |
25,036,966 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9267:Kidins220
|
UTSW |
12 |
25,038,558 (GRCm39) |
missense |
probably benign |
0.29 |
R9303:Kidins220
|
UTSW |
12 |
25,107,110 (GRCm39) |
missense |
probably benign |
0.36 |
R9343:Kidins220
|
UTSW |
12 |
25,058,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Kidins220
|
UTSW |
12 |
25,088,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R9644:Kidins220
|
UTSW |
12 |
25,061,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Kidins220
|
UTSW |
12 |
25,047,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R9664:Kidins220
|
UTSW |
12 |
25,106,895 (GRCm39) |
missense |
probably benign |
0.39 |
|