Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox1 |
T |
A |
1: 58,145,184 (GRCm39) |
|
probably null |
Het |
Aspm |
C |
T |
1: 139,410,182 (GRCm39) |
T1359I |
probably benign |
Het |
Atp13a2 |
A |
G |
4: 140,719,509 (GRCm39) |
D26G |
probably benign |
Het |
Atrnl1 |
G |
A |
19: 58,119,536 (GRCm39) |
A1343T |
probably damaging |
Het |
Ccsap |
A |
C |
8: 124,585,969 (GRCm39) |
S61A |
probably damaging |
Het |
Cdh1 |
A |
T |
8: 107,384,485 (GRCm39) |
M318L |
probably benign |
Het |
Cfap69 |
G |
A |
5: 5,696,979 (GRCm39) |
P106S |
probably damaging |
Het |
Cfp |
G |
A |
X: 20,795,963 (GRCm39) |
T88I |
probably damaging |
Het |
Chst1 |
A |
T |
2: 92,444,475 (GRCm39) |
I316F |
probably damaging |
Het |
Col7a1 |
A |
T |
9: 108,793,686 (GRCm39) |
D1382V |
unknown |
Het |
Cr2 |
T |
A |
1: 194,845,542 (GRCm39) |
M514L |
possibly damaging |
Het |
Cubn |
G |
A |
2: 13,470,719 (GRCm39) |
H558Y |
probably benign |
Het |
Cul9 |
A |
T |
17: 46,839,572 (GRCm39) |
M802K |
probably damaging |
Het |
Dennd2d |
A |
T |
3: 106,398,542 (GRCm39) |
I169L |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 118,010,991 (GRCm39) |
K162* |
probably null |
Het |
Dnah3 |
T |
A |
7: 119,566,943 (GRCm39) |
T2428S |
possibly damaging |
Het |
Dock11 |
T |
A |
X: 35,301,296 (GRCm39) |
H1284Q |
probably damaging |
Het |
Flrt2 |
T |
A |
12: 95,745,966 (GRCm39) |
D101E |
probably damaging |
Het |
Gabrr2 |
G |
A |
4: 33,085,626 (GRCm39) |
V349M |
probably damaging |
Het |
Gli2 |
C |
A |
1: 118,764,621 (GRCm39) |
V1177L |
probably benign |
Het |
Gm16506 |
A |
G |
14: 43,961,630 (GRCm39) |
Y206H |
probably benign |
Het |
Gm5612 |
C |
T |
9: 18,338,869 (GRCm39) |
|
probably benign |
Het |
Gvin3 |
C |
T |
7: 106,202,258 (GRCm39) |
|
noncoding transcript |
Het |
Heg1 |
C |
T |
16: 33,545,936 (GRCm39) |
T460I |
possibly damaging |
Het |
Lgals9 |
T |
G |
11: 78,863,977 (GRCm39) |
D56A |
probably damaging |
Het |
Lpgat1 |
A |
T |
1: 191,508,544 (GRCm39) |
|
probably null |
Het |
Megf6 |
T |
A |
4: 154,337,020 (GRCm39) |
|
probably null |
Het |
Megf8 |
G |
A |
7: 25,059,296 (GRCm39) |
M2265I |
probably benign |
Het |
Memo1 |
G |
A |
17: 74,548,976 (GRCm39) |
R121* |
probably null |
Het |
Morc1 |
T |
C |
16: 48,432,677 (GRCm39) |
V715A |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,466,928 (GRCm39) |
|
probably null |
Het |
Ncapg2 |
T |
A |
12: 116,388,270 (GRCm39) |
V318D |
possibly damaging |
Het |
Ndst1 |
T |
C |
18: 60,833,517 (GRCm39) |
Y498C |
probably damaging |
Het |
Nod1 |
C |
T |
6: 54,921,341 (GRCm39) |
A326T |
probably damaging |
Het |
Or2ag15 |
A |
G |
7: 106,340,706 (GRCm39) |
V145A |
probably benign |
Het |
Or4c11 |
T |
A |
2: 88,695,864 (GRCm39) |
M305K |
probably benign |
Het |
Peg3 |
T |
C |
7: 6,710,624 (GRCm39) |
S1533G |
probably benign |
Het |
Pgc |
G |
T |
17: 48,045,165 (GRCm39) |
G361V |
probably damaging |
Het |
Phka1 |
C |
T |
X: 101,629,712 (GRCm39) |
R477H |
probably damaging |
Het |
Plagl2 |
C |
T |
2: 153,074,574 (GRCm39) |
R109Q |
probably damaging |
Het |
Prr36 |
T |
A |
8: 4,266,230 (GRCm39) |
I107F |
probably benign |
Het |
Ptpdc1 |
T |
A |
13: 48,740,080 (GRCm39) |
R450S |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,138,179 (GRCm39) |
D361V |
possibly damaging |
Het |
Rbm44 |
A |
G |
1: 91,096,551 (GRCm39) |
D970G |
probably benign |
Het |
Scrn2 |
T |
G |
11: 96,921,396 (GRCm39) |
V52G |
probably benign |
Het |
Serpina1d |
T |
A |
12: 103,729,993 (GRCm39) |
E396D |
probably benign |
Het |
Slc38a5 |
A |
C |
X: 8,146,070 (GRCm39) |
Q465P |
probably benign |
Het |
Slc38a5 |
G |
T |
X: 8,146,071 (GRCm39) |
Q465H |
probably benign |
Het |
Smarca1 |
T |
C |
X: 46,981,255 (GRCm39) |
T48A |
possibly damaging |
Het |
Trak2 |
A |
T |
1: 58,962,766 (GRCm39) |
I132N |
probably damaging |
Het |
Trank1 |
A |
G |
9: 111,194,117 (GRCm39) |
T714A |
probably benign |
Het |
Trank1 |
T |
C |
9: 111,194,327 (GRCm39) |
S784P |
probably benign |
Het |
Trp53i13 |
G |
A |
11: 77,399,083 (GRCm39) |
|
probably benign |
Het |
Trrap |
A |
C |
5: 144,767,831 (GRCm39) |
D2596A |
probably benign |
Het |
Ttyh1 |
A |
T |
7: 4,127,656 (GRCm39) |
T19S |
probably damaging |
Het |
Tyk2 |
C |
T |
9: 21,020,660 (GRCm39) |
V947M |
probably damaging |
Het |
Ugt2b34 |
G |
A |
5: 87,040,689 (GRCm39) |
A411V |
possibly damaging |
Het |
Virma |
T |
A |
4: 11,518,929 (GRCm39) |
Y725* |
probably null |
Het |
Vmn1r192 |
A |
G |
13: 22,372,079 (GRCm39) |
L47P |
probably damaging |
Het |
Vmn2r74 |
T |
C |
7: 85,610,500 (GRCm39) |
D64G |
possibly damaging |
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 |
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 |
R5851:Sdk1
|
UTSW |
5 |
141,948,424 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|