Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
G |
2: 25,332,322 (GRCm39) |
N1452D |
possibly damaging |
Het |
Abhd15 |
T |
C |
11: 77,409,273 (GRCm39) |
L329P |
probably benign |
Het |
Add3 |
T |
C |
19: 53,225,205 (GRCm39) |
S442P |
probably damaging |
Het |
Arhgef18 |
T |
C |
8: 3,484,980 (GRCm39) |
F228L |
probably damaging |
Het |
Bptf |
A |
T |
11: 107,001,688 (GRCm39) |
Y475N |
probably damaging |
Het |
C3 |
T |
C |
17: 57,518,612 (GRCm39) |
N1257S |
probably null |
Het |
Cdkl1 |
A |
T |
12: 69,803,338 (GRCm39) |
Y179* |
probably null |
Het |
Ceacam1 |
T |
C |
7: 25,174,025 (GRCm39) |
N210S |
possibly damaging |
Het |
Celf3 |
T |
A |
3: 94,386,433 (GRCm39) |
I7N |
probably damaging |
Het |
Clxn |
T |
A |
16: 14,738,300 (GRCm39) |
L155H |
probably damaging |
Het |
Cmpk1 |
A |
G |
4: 114,844,167 (GRCm39) |
V55A |
possibly damaging |
Het |
Csrnp1 |
C |
T |
9: 119,802,144 (GRCm39) |
G305D |
possibly damaging |
Het |
Dnah3 |
A |
G |
7: 119,638,585 (GRCm39) |
S1266P |
possibly damaging |
Het |
Edc4 |
T |
C |
8: 106,617,499 (GRCm39) |
L1077P |
probably damaging |
Het |
Fam174a |
G |
A |
1: 95,252,868 (GRCm39) |
G157S |
probably damaging |
Het |
Fubp3 |
T |
A |
2: 31,488,622 (GRCm39) |
D159E |
probably benign |
Het |
Garem2 |
C |
T |
5: 30,319,288 (GRCm39) |
T250M |
probably damaging |
Het |
H2-Eb1 |
C |
T |
17: 34,528,745 (GRCm39) |
P92L |
probably benign |
Het |
Ifnl3 |
G |
T |
7: 28,222,936 (GRCm39) |
C69F |
probably damaging |
Het |
Itga2b |
C |
A |
11: 102,348,427 (GRCm39) |
|
probably benign |
Het |
Klhl33 |
A |
T |
14: 51,130,335 (GRCm39) |
D386E |
probably damaging |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Loricrin |
G |
A |
3: 91,987,846 (GRCm39) |
A480V |
unknown |
Het |
Msh3 |
G |
T |
13: 92,352,030 (GRCm39) |
Q1041K |
probably benign |
Het |
Mtrex |
G |
A |
13: 113,045,486 (GRCm39) |
R349W |
probably damaging |
Het |
Myo1e |
G |
A |
9: 70,291,086 (GRCm39) |
G959E |
probably benign |
Het |
Nfat5 |
G |
T |
8: 108,074,359 (GRCm39) |
V338L |
probably damaging |
Het |
Nrf1 |
A |
G |
6: 30,089,975 (GRCm39) |
H18R |
possibly damaging |
Het |
Nup160 |
A |
G |
2: 90,537,382 (GRCm39) |
D752G |
probably benign |
Het |
Obscn |
A |
T |
11: 58,885,526 (GRCm39) |
L2489* |
probably null |
Het |
Or4p22 |
A |
G |
2: 88,317,204 (GRCm39) |
I43V |
possibly damaging |
Het |
Or51q1c |
A |
G |
7: 103,652,659 (GRCm39) |
E59G |
probably benign |
Het |
Paip1 |
T |
C |
13: 119,577,301 (GRCm39) |
S215P |
possibly damaging |
Het |
Pate2 |
T |
A |
9: 35,581,797 (GRCm39) |
Y26* |
probably null |
Het |
Pcdhb10 |
A |
G |
18: 37,545,811 (GRCm39) |
I296V |
probably benign |
Het |
Pdzph1 |
T |
G |
17: 59,280,741 (GRCm39) |
T514P |
probably benign |
Het |
Pnlip |
G |
A |
19: 58,662,224 (GRCm39) |
W123* |
probably null |
Het |
Prmt2 |
C |
A |
10: 76,072,574 (GRCm39) |
C9F |
possibly damaging |
Het |
Rbl1 |
T |
A |
2: 157,009,245 (GRCm39) |
K763N |
probably benign |
Het |
Rfk |
C |
T |
19: 17,372,562 (GRCm39) |
A28V |
probably damaging |
Het |
Scart1 |
C |
T |
7: 139,807,940 (GRCm39) |
P704S |
possibly damaging |
Het |
Sele |
A |
G |
1: 163,877,143 (GRCm39) |
K140E |
probably benign |
Het |
Sla |
G |
A |
15: 66,655,572 (GRCm39) |
T189I |
probably damaging |
Het |
Slc46a2 |
A |
G |
4: 59,913,906 (GRCm39) |
V339A |
probably damaging |
Het |
Slc5a9 |
A |
G |
4: 111,742,797 (GRCm39) |
F432L |
probably benign |
Het |
Slc6a19 |
A |
G |
13: 73,839,859 (GRCm39) |
F141S |
possibly damaging |
Het |
Tas2r123 |
T |
C |
6: 132,824,271 (GRCm39) |
L56S |
probably damaging |
Het |
Tektip1 |
A |
T |
10: 81,200,711 (GRCm39) |
|
probably null |
Het |
Tmem245 |
T |
C |
4: 56,916,770 (GRCm39) |
I53V |
probably benign |
Het |
Tor2a |
A |
T |
2: 32,651,619 (GRCm39) |
Q278L |
probably benign |
Het |
Trav6-3 |
A |
G |
14: 53,667,572 (GRCm39) |
M15V |
probably benign |
Het |
Ttc28 |
G |
A |
5: 111,383,335 (GRCm39) |
|
probably benign |
Het |
Ubap2 |
G |
A |
4: 41,206,268 (GRCm39) |
Q534* |
probably null |
Het |
Yju2 |
C |
T |
17: 56,274,582 (GRCm39) |
S298F |
probably damaging |
Het |
Zfp954 |
C |
A |
7: 7,118,624 (GRCm39) |
E307* |
probably null |
Het |
Zscan21 |
A |
G |
5: 138,124,740 (GRCm39) |
K219E |
probably benign |
Het |
|
Other mutations in Sdk1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00498:Sdk1
|
APN |
5 |
142,071,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00945:Sdk1
|
APN |
5 |
142,070,368 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00946:Sdk1
|
APN |
5 |
142,070,368 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01394:Sdk1
|
APN |
5 |
141,598,970 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01398:Sdk1
|
APN |
5 |
141,923,332 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01410:Sdk1
|
APN |
5 |
142,197,875 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01525:Sdk1
|
APN |
5 |
141,985,675 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01548:Sdk1
|
APN |
5 |
142,071,520 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01672:Sdk1
|
APN |
5 |
142,170,930 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01676:Sdk1
|
APN |
5 |
142,113,591 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01679:Sdk1
|
APN |
5 |
142,031,919 (GRCm39) |
missense |
probably benign |
|
IGL01929:Sdk1
|
APN |
5 |
141,938,785 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01970:Sdk1
|
APN |
5 |
142,071,437 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02016:Sdk1
|
APN |
5 |
142,020,184 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02060:Sdk1
|
APN |
5 |
141,938,767 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02457:Sdk1
|
APN |
5 |
141,938,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02634:Sdk1
|
APN |
5 |
141,595,787 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02637:Sdk1
|
APN |
5 |
142,080,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02731:Sdk1
|
APN |
5 |
142,158,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Sdk1
|
APN |
5 |
142,071,497 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03259:Sdk1
|
APN |
5 |
141,938,788 (GRCm39) |
nonsense |
probably null |
|
PIT4453001:Sdk1
|
UTSW |
5 |
142,197,793 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4544001:Sdk1
|
UTSW |
5 |
141,941,987 (GRCm39) |
missense |
probably benign |
0.08 |
R0149:Sdk1
|
UTSW |
5 |
141,842,809 (GRCm39) |
intron |
probably benign |
|
R0173:Sdk1
|
UTSW |
5 |
142,159,564 (GRCm39) |
splice site |
probably benign |
|
R0240:Sdk1
|
UTSW |
5 |
141,984,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Sdk1
|
UTSW |
5 |
141,984,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Sdk1
|
UTSW |
5 |
142,129,677 (GRCm39) |
splice site |
probably benign |
|
R0245:Sdk1
|
UTSW |
5 |
141,940,713 (GRCm39) |
missense |
probably benign |
0.02 |
R0270:Sdk1
|
UTSW |
5 |
142,070,321 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0398:Sdk1
|
UTSW |
5 |
141,948,476 (GRCm39) |
missense |
probably benign |
0.05 |
R0401:Sdk1
|
UTSW |
5 |
142,031,916 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0501:Sdk1
|
UTSW |
5 |
141,923,473 (GRCm39) |
missense |
probably benign |
|
R0558:Sdk1
|
UTSW |
5 |
142,117,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Sdk1
|
UTSW |
5 |
141,940,713 (GRCm39) |
missense |
probably benign |
0.02 |
R0834:Sdk1
|
UTSW |
5 |
141,227,779 (GRCm39) |
missense |
probably benign |
|
R0962:Sdk1
|
UTSW |
5 |
142,147,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R1424:Sdk1
|
UTSW |
5 |
142,147,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R1438:Sdk1
|
UTSW |
5 |
142,024,078 (GRCm39) |
missense |
probably damaging |
0.96 |
R1517:Sdk1
|
UTSW |
5 |
142,113,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R1519:Sdk1
|
UTSW |
5 |
141,985,705 (GRCm39) |
missense |
probably benign |
0.00 |
R1539:Sdk1
|
UTSW |
5 |
142,080,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R1574:Sdk1
|
UTSW |
5 |
141,984,634 (GRCm39) |
missense |
probably benign |
0.03 |
R1574:Sdk1
|
UTSW |
5 |
141,984,634 (GRCm39) |
missense |
probably benign |
0.03 |
R1673:Sdk1
|
UTSW |
5 |
141,934,261 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1686:Sdk1
|
UTSW |
5 |
142,020,292 (GRCm39) |
missense |
probably benign |
0.00 |
R1806:Sdk1
|
UTSW |
5 |
142,147,681 (GRCm39) |
missense |
probably benign |
|
R1806:Sdk1
|
UTSW |
5 |
141,598,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Sdk1
|
UTSW |
5 |
142,171,040 (GRCm39) |
missense |
probably benign |
0.09 |
R1956:Sdk1
|
UTSW |
5 |
142,080,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Sdk1
|
UTSW |
5 |
142,129,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Sdk1
|
UTSW |
5 |
142,170,943 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2152:Sdk1
|
UTSW |
5 |
141,778,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R2186:Sdk1
|
UTSW |
5 |
142,032,047 (GRCm39) |
missense |
probably benign |
0.00 |
R2187:Sdk1
|
UTSW |
5 |
142,100,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2306:Sdk1
|
UTSW |
5 |
141,948,455 (GRCm39) |
missense |
probably benign |
0.00 |
R2520:Sdk1
|
UTSW |
5 |
142,071,526 (GRCm39) |
missense |
probably benign |
0.19 |
R2698:Sdk1
|
UTSW |
5 |
142,197,805 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2763:Sdk1
|
UTSW |
5 |
142,070,306 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3023:Sdk1
|
UTSW |
5 |
142,031,991 (GRCm39) |
missense |
probably benign |
|
R3500:Sdk1
|
UTSW |
5 |
141,992,371 (GRCm39) |
splice site |
probably benign |
|
R3613:Sdk1
|
UTSW |
5 |
142,105,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R3824:Sdk1
|
UTSW |
5 |
141,921,804 (GRCm39) |
missense |
probably benign |
|
R3916:Sdk1
|
UTSW |
5 |
142,036,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R3917:Sdk1
|
UTSW |
5 |
142,036,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R4158:Sdk1
|
UTSW |
5 |
142,100,154 (GRCm39) |
missense |
probably benign |
0.00 |
R4160:Sdk1
|
UTSW |
5 |
142,100,154 (GRCm39) |
missense |
probably benign |
0.00 |
R4161:Sdk1
|
UTSW |
5 |
142,100,154 (GRCm39) |
missense |
probably benign |
0.00 |
R4386:Sdk1
|
UTSW |
5 |
142,080,381 (GRCm39) |
missense |
probably damaging |
0.99 |
R4649:Sdk1
|
UTSW |
5 |
141,992,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Sdk1
|
UTSW |
5 |
142,170,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R4780:Sdk1
|
UTSW |
5 |
141,944,993 (GRCm39) |
missense |
probably damaging |
0.97 |
R4787:Sdk1
|
UTSW |
5 |
141,568,168 (GRCm39) |
missense |
probably benign |
|
R4825:Sdk1
|
UTSW |
5 |
141,568,049 (GRCm39) |
missense |
probably benign |
0.11 |
R4853:Sdk1
|
UTSW |
5 |
142,132,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Sdk1
|
UTSW |
5 |
142,147,531 (GRCm39) |
missense |
probably benign |
0.01 |
R4928:Sdk1
|
UTSW |
5 |
141,842,758 (GRCm39) |
intron |
probably benign |
|
R5111:Sdk1
|
UTSW |
5 |
142,113,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R5188:Sdk1
|
UTSW |
5 |
141,942,015 (GRCm39) |
critical splice donor site |
probably null |
|
R5246:Sdk1
|
UTSW |
5 |
142,100,317 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5273:Sdk1
|
UTSW |
5 |
141,984,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R5484:Sdk1
|
UTSW |
5 |
142,085,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5525:Sdk1
|
UTSW |
5 |
142,171,020 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5578:Sdk1
|
UTSW |
5 |
141,598,880 (GRCm39) |
nonsense |
probably null |
|
R5593:Sdk1
|
UTSW |
5 |
141,941,879 (GRCm39) |
missense |
probably damaging |
0.98 |
R5654:Sdk1
|
UTSW |
5 |
141,921,853 (GRCm39) |
missense |
probably damaging |
0.96 |
R5672:Sdk1
|
UTSW |
5 |
142,173,900 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5768:Sdk1
|
UTSW |
5 |
142,129,626 (GRCm39) |
missense |
probably benign |
0.00 |
R5781:Sdk1
|
UTSW |
5 |
141,921,803 (GRCm39) |
missense |
probably benign |
0.00 |
R5846:Sdk1
|
UTSW |
5 |
142,100,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Sdk1
|
UTSW |
5 |
142,117,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Sdk1
|
UTSW |
5 |
142,020,181 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6364:Sdk1
|
UTSW |
5 |
141,948,464 (GRCm39) |
missense |
probably benign |
0.00 |
R6453:Sdk1
|
UTSW |
5 |
142,082,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R6892:Sdk1
|
UTSW |
5 |
142,032,053 (GRCm39) |
missense |
probably benign |
0.00 |
R6996:Sdk1
|
UTSW |
5 |
142,197,769 (GRCm39) |
missense |
probably benign |
0.16 |
R7003:Sdk1
|
UTSW |
5 |
142,082,489 (GRCm39) |
missense |
probably benign |
0.01 |
R7022:Sdk1
|
UTSW |
5 |
142,080,412 (GRCm39) |
splice site |
probably null |
|
R7027:Sdk1
|
UTSW |
5 |
142,082,481 (GRCm39) |
splice site |
probably null |
|
R7098:Sdk1
|
UTSW |
5 |
142,082,625 (GRCm39) |
missense |
probably damaging |
0.96 |
R7107:Sdk1
|
UTSW |
5 |
142,067,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7203:Sdk1
|
UTSW |
5 |
142,031,931 (GRCm39) |
missense |
probably benign |
0.08 |
R7313:Sdk1
|
UTSW |
5 |
141,923,377 (GRCm39) |
missense |
probably damaging |
0.97 |
R7363:Sdk1
|
UTSW |
5 |
142,173,897 (GRCm39) |
missense |
probably benign |
0.05 |
R7375:Sdk1
|
UTSW |
5 |
141,984,598 (GRCm39) |
missense |
probably benign |
0.01 |
R7446:Sdk1
|
UTSW |
5 |
142,130,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Sdk1
|
UTSW |
5 |
141,778,731 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7598:Sdk1
|
UTSW |
5 |
141,595,753 (GRCm39) |
nonsense |
probably null |
|
R7747:Sdk1
|
UTSW |
5 |
142,070,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R7810:Sdk1
|
UTSW |
5 |
141,923,434 (GRCm39) |
missense |
probably benign |
|
R7985:Sdk1
|
UTSW |
5 |
142,113,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Sdk1
|
UTSW |
5 |
142,177,648 (GRCm39) |
missense |
probably benign |
0.10 |
R8217:Sdk1
|
UTSW |
5 |
142,197,713 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8249:Sdk1
|
UTSW |
5 |
142,173,770 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8376:Sdk1
|
UTSW |
5 |
142,144,376 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8779:Sdk1
|
UTSW |
5 |
141,948,457 (GRCm39) |
missense |
probably benign |
0.00 |
R8807:Sdk1
|
UTSW |
5 |
142,071,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R8907:Sdk1
|
UTSW |
5 |
142,070,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R8942:Sdk1
|
UTSW |
5 |
142,082,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R8945:Sdk1
|
UTSW |
5 |
141,598,935 (GRCm39) |
missense |
probably benign |
|
R9006:Sdk1
|
UTSW |
5 |
141,923,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R9249:Sdk1
|
UTSW |
5 |
142,129,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Sdk1
|
UTSW |
5 |
141,941,953 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9345:Sdk1
|
UTSW |
5 |
142,147,708 (GRCm39) |
missense |
probably benign |
|
R9463:Sdk1
|
UTSW |
5 |
141,948,548 (GRCm39) |
missense |
probably benign |
0.31 |
R9549:Sdk1
|
UTSW |
5 |
141,940,657 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9572:Sdk1
|
UTSW |
5 |
141,595,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R9602:Sdk1
|
UTSW |
5 |
142,071,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R9703:Sdk1
|
UTSW |
5 |
142,100,283 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9720:Sdk1
|
UTSW |
5 |
142,197,796 (GRCm39) |
missense |
probably damaging |
0.96 |
R9771:Sdk1
|
UTSW |
5 |
142,082,624 (GRCm39) |
missense |
probably damaging |
0.99 |
X0017:Sdk1
|
UTSW |
5 |
141,984,535 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Sdk1
|
UTSW |
5 |
141,945,065 (GRCm39) |
missense |
probably null |
0.58 |
Z1177:Sdk1
|
UTSW |
5 |
141,948,463 (GRCm39) |
missense |
possibly damaging |
0.87 |
|