Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Aadat |
C |
T |
8: 60,979,663 (GRCm39) |
P175L |
probably damaging |
Het |
Acot7 |
G |
T |
4: 152,270,664 (GRCm39) |
|
probably benign |
Het |
Adad1 |
T |
G |
3: 37,130,813 (GRCm39) |
F259V |
possibly damaging |
Het |
Adora2a |
A |
G |
10: 75,161,879 (GRCm39) |
Y6C |
probably null |
Het |
Ahnak |
A |
G |
19: 8,990,118 (GRCm39) |
|
probably benign |
Het |
Ankar |
A |
T |
1: 72,737,966 (GRCm39) |
M72K |
probably damaging |
Het |
Ankrd45 |
A |
G |
1: 160,988,270 (GRCm39) |
K176R |
possibly damaging |
Het |
Ap3m2 |
T |
C |
8: 23,293,997 (GRCm39) |
K18E |
probably damaging |
Het |
Apol10b |
C |
T |
15: 77,473,006 (GRCm39) |
R16Q |
possibly damaging |
Het |
Atp2b2 |
T |
A |
6: 113,819,147 (GRCm39) |
T49S |
possibly damaging |
Het |
B3gntl1 |
T |
G |
11: 121,520,795 (GRCm39) |
Y206S |
possibly damaging |
Het |
BC061237 |
G |
A |
14: 44,738,666 (GRCm39) |
E22K |
possibly damaging |
Het |
Bmp1 |
A |
G |
14: 70,712,655 (GRCm39) |
V959A |
probably benign |
Het |
Cep295 |
T |
C |
9: 15,263,056 (GRCm39) |
E169G |
probably damaging |
Het |
Cfap20dc |
G |
A |
14: 8,578,394 (GRCm38) |
T116I |
probably damaging |
Het |
Cfap65 |
T |
G |
1: 74,942,283 (GRCm39) |
E1757A |
possibly damaging |
Het |
Cgrrf1 |
T |
A |
14: 47,090,912 (GRCm39) |
I216N |
possibly damaging |
Het |
Clstn2 |
T |
A |
9: 97,681,448 (GRCm39) |
D64V |
probably damaging |
Het |
Col27a1 |
T |
A |
4: 63,194,197 (GRCm39) |
D851E |
possibly damaging |
Het |
Coq9 |
C |
T |
8: 95,579,822 (GRCm39) |
P259L |
probably benign |
Het |
Cps1 |
A |
G |
1: 67,216,183 (GRCm39) |
N836S |
probably benign |
Het |
Cracd |
A |
T |
5: 76,996,682 (GRCm39) |
I47F |
probably damaging |
Het |
Crebbp |
T |
C |
16: 3,906,239 (GRCm39) |
K1588E |
probably damaging |
Het |
Cspg4 |
T |
C |
9: 56,805,353 (GRCm39) |
W2055R |
probably benign |
Het |
Cyp3a44 |
A |
T |
5: 145,714,792 (GRCm39) |
M453K |
probably damaging |
Het |
Dhx36 |
T |
G |
3: 62,391,681 (GRCm39) |
D555A |
probably damaging |
Het |
Dock2 |
A |
T |
11: 34,216,248 (GRCm39) |
Y1219N |
probably damaging |
Het |
Dpy19l2 |
A |
T |
9: 24,539,476 (GRCm39) |
C492* |
probably null |
Het |
Dusp22 |
A |
G |
13: 30,852,813 (GRCm39) |
N16S |
probably benign |
Het |
Epha1 |
A |
G |
6: 42,337,668 (GRCm39) |
M805T |
probably damaging |
Het |
Espl1 |
C |
T |
15: 102,232,505 (GRCm39) |
A2071V |
possibly damaging |
Het |
Fbxo11 |
T |
A |
17: 88,299,761 (GRCm39) |
D863V |
probably damaging |
Het |
Fbxo7 |
T |
A |
10: 85,865,014 (GRCm39) |
Y106N |
probably damaging |
Het |
Fhip1a |
A |
C |
3: 85,590,918 (GRCm39) |
C178G |
probably damaging |
Het |
Fst |
A |
G |
13: 114,590,920 (GRCm39) |
V282A |
probably damaging |
Het |
Gfra3 |
T |
A |
18: 34,844,304 (GRCm39) |
M79L |
probably benign |
Het |
Glp1r |
T |
C |
17: 31,155,240 (GRCm39) |
V409A |
probably damaging |
Het |
Gm10799 |
T |
A |
2: 103,898,552 (GRCm39) |
D51V |
probably damaging |
Het |
Gm572 |
C |
A |
4: 148,751,819 (GRCm39) |
T228N |
possibly damaging |
Het |
Grip1 |
C |
T |
10: 119,911,211 (GRCm39) |
T643M |
probably damaging |
Het |
Hdgfl2 |
C |
T |
17: 56,403,265 (GRCm39) |
R222C |
possibly damaging |
Het |
Hecw2 |
T |
A |
1: 53,990,000 (GRCm39) |
I125F |
probably benign |
Het |
Hipk1 |
A |
G |
3: 103,651,338 (GRCm39) |
S1153P |
possibly damaging |
Het |
Insm2 |
T |
C |
12: 55,646,546 (GRCm39) |
S97P |
probably damaging |
Het |
Iqca1 |
A |
G |
1: 90,067,759 (GRCm39) |
V164A |
probably benign |
Het |
Kcna6 |
T |
C |
6: 126,715,689 (GRCm39) |
D400G |
probably benign |
Het |
Kctd1 |
T |
C |
18: 15,107,311 (GRCm39) |
Y122C |
probably damaging |
Het |
Klk14 |
G |
A |
7: 43,341,501 (GRCm39) |
C51Y |
probably damaging |
Het |
Klra2 |
T |
C |
6: 131,207,165 (GRCm39) |
Y148C |
probably damaging |
Het |
Krtap31-1 |
G |
A |
11: 99,799,310 (GRCm39) |
C171Y |
unknown |
Het |
Ldlrap1 |
C |
T |
4: 134,486,282 (GRCm39) |
R59Q |
probably benign |
Het |
Ltb |
T |
C |
17: 35,414,234 (GRCm39) |
I3T |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,348,802 (GRCm39) |
I2477V |
probably benign |
Het |
Mpdz |
A |
T |
4: 81,279,713 (GRCm39) |
I39N |
probably damaging |
Het |
Mtcl3 |
A |
T |
10: 29,072,537 (GRCm39) |
N610Y |
probably damaging |
Het |
Mycbp2 |
A |
G |
14: 103,448,731 (GRCm39) |
I1776T |
probably damaging |
Het |
Myof |
T |
A |
19: 37,930,805 (GRCm39) |
E994V |
probably damaging |
Het |
Myom3 |
A |
G |
4: 135,510,366 (GRCm39) |
E553G |
possibly damaging |
Het |
Mysm1 |
A |
T |
4: 94,847,185 (GRCm39) |
C504S |
probably damaging |
Het |
Nectin3 |
A |
T |
16: 46,269,249 (GRCm39) |
H384Q |
probably benign |
Het |
Net1 |
G |
A |
13: 3,934,252 (GRCm39) |
R482* |
probably null |
Het |
Nit1 |
T |
C |
1: 171,171,263 (GRCm39) |
K193R |
probably null |
Het |
Nlgn1 |
A |
G |
3: 25,966,838 (GRCm39) |
V205A |
probably damaging |
Het |
Nr3c2 |
A |
T |
8: 77,635,438 (GRCm39) |
I180F |
possibly damaging |
Het |
Nup50l |
A |
T |
6: 96,141,793 (GRCm39) |
M417K |
probably damaging |
Het |
Nup62 |
T |
A |
7: 44,478,289 (GRCm39) |
S101R |
probably damaging |
Het |
Or13c7 |
T |
C |
4: 43,854,890 (GRCm39) |
S194P |
probably damaging |
Het |
Or1l8 |
G |
T |
2: 36,818,024 (GRCm39) |
T34K |
possibly damaging |
Het |
Or4c3 |
A |
G |
2: 89,851,987 (GRCm39) |
V141A |
probably benign |
Het |
Or51b17 |
T |
A |
7: 103,542,862 (GRCm39) |
I27F |
probably benign |
Het |
Or56b2j |
T |
A |
7: 104,353,068 (GRCm39) |
I98N |
probably damaging |
Het |
Or5b111 |
A |
T |
19: 13,291,034 (GRCm39) |
I205N |
probably benign |
Het |
Or5b124 |
A |
T |
19: 13,611,391 (GRCm39) |
K305N |
probably benign |
Het |
Or5p80 |
A |
T |
7: 108,229,819 (GRCm39) |
I207F |
probably damaging |
Het |
Osbpl6 |
A |
T |
2: 76,379,883 (GRCm39) |
I158F |
probably damaging |
Het |
Pcbp4 |
A |
G |
9: 106,339,301 (GRCm39) |
T103A |
probably benign |
Het |
Pcdha2 |
T |
A |
18: 37,073,953 (GRCm39) |
L528Q |
probably damaging |
Het |
Pcdhga5 |
T |
C |
18: 37,827,680 (GRCm39) |
S43P |
probably damaging |
Het |
Pdgfra |
C |
A |
5: 75,349,973 (GRCm39) |
N952K |
probably benign |
Het |
Pla2r1 |
A |
G |
2: 60,365,328 (GRCm39) |
S81P |
probably damaging |
Het |
Rabggtb |
A |
T |
3: 153,617,568 (GRCm39) |
D43E |
possibly damaging |
Het |
Rexo5 |
T |
A |
7: 119,424,774 (GRCm39) |
C43* |
probably null |
Het |
Robo1 |
T |
A |
16: 72,701,639 (GRCm39) |
D168E |
probably damaging |
Het |
Scimp |
A |
G |
11: 70,688,865 (GRCm39) |
M49T |
unknown |
Het |
Sema3e |
T |
A |
5: 14,275,579 (GRCm39) |
V228E |
probably damaging |
Het |
Sema6d |
A |
G |
2: 124,498,738 (GRCm39) |
|
probably null |
Het |
Serpinb6d |
A |
T |
13: 33,850,428 (GRCm39) |
D85V |
possibly damaging |
Het |
Slc24a2 |
C |
T |
4: 86,909,745 (GRCm39) |
V658I |
probably damaging |
Het |
Snd1 |
T |
C |
6: 28,526,911 (GRCm39) |
I198T |
possibly damaging |
Het |
Snx33 |
C |
T |
9: 56,833,464 (GRCm39) |
V202M |
probably damaging |
Het |
Srcap |
A |
G |
7: 127,121,189 (GRCm39) |
E174G |
probably damaging |
Het |
Srgap2 |
C |
A |
1: 131,220,314 (GRCm39) |
|
probably null |
Het |
Stxbp5 |
A |
T |
10: 9,688,085 (GRCm39) |
Y405* |
probably null |
Het |
Thsd4 |
C |
T |
9: 59,895,320 (GRCm39) |
R710H |
probably benign |
Het |
Trp53inp1 |
T |
A |
4: 11,165,130 (GRCm39) |
D51E |
probably benign |
Het |
Ttc41 |
A |
G |
10: 86,566,882 (GRCm39) |
D516G |
probably benign |
Het |
Tut7 |
A |
T |
13: 59,937,266 (GRCm39) |
L775H |
probably damaging |
Het |
Uap1l1 |
A |
G |
2: 25,252,840 (GRCm39) |
V400A |
probably damaging |
Het |
Vit |
T |
C |
17: 78,932,182 (GRCm39) |
S430P |
probably damaging |
Het |
Vmn1r9 |
T |
A |
6: 57,048,294 (GRCm39) |
M123K |
possibly damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,369,384 (GRCm39) |
|
probably null |
Het |
Vwa3a |
A |
G |
7: 120,390,924 (GRCm39) |
T746A |
probably benign |
Het |
Wdfy4 |
G |
T |
14: 32,710,852 (GRCm39) |
Y2578* |
probably null |
Het |
Wdr53 |
A |
T |
16: 32,075,796 (GRCm39) |
K334* |
probably null |
Het |
Xpot |
G |
T |
10: 121,442,713 (GRCm39) |
H495Q |
probably damaging |
Het |
Zfp109 |
T |
C |
7: 23,928,570 (GRCm39) |
T288A |
probably benign |
Het |
Zfp277 |
T |
A |
12: 40,413,152 (GRCm39) |
E276V |
probably damaging |
Het |
Zfp703 |
A |
G |
8: 27,468,729 (GRCm39) |
D131G |
probably benign |
Het |
Zfp985 |
T |
A |
4: 147,667,801 (GRCm39) |
I223N |
probably benign |
Het |
Zrsr2-ps1 |
T |
C |
11: 22,923,805 (GRCm39) |
V193A |
possibly damaging |
Het |
Zscan20 |
A |
G |
4: 128,481,958 (GRCm39) |
I568T |
possibly damaging |
Het |
|
Other mutations in Saxo4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00959:Saxo4
|
APN |
19 |
10,454,887 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00979:Saxo4
|
APN |
19 |
10,451,863 (GRCm39) |
makesense |
probably null |
|
IGL02405:Saxo4
|
APN |
19 |
10,451,930 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02664:Saxo4
|
APN |
19 |
10,459,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Saxo4
|
APN |
19 |
10,454,384 (GRCm39) |
splice site |
probably benign |
|
R0255:Saxo4
|
UTSW |
19 |
10,452,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Saxo4
|
UTSW |
19 |
10,454,449 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1018:Saxo4
|
UTSW |
19 |
10,456,824 (GRCm39) |
splice site |
probably benign |
|
R1559:Saxo4
|
UTSW |
19 |
10,458,770 (GRCm39) |
missense |
probably benign |
0.01 |
R2384:Saxo4
|
UTSW |
19 |
10,458,646 (GRCm39) |
critical splice donor site |
probably null |
|
R4362:Saxo4
|
UTSW |
19 |
10,452,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R5998:Saxo4
|
UTSW |
19 |
10,458,716 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6130:Saxo4
|
UTSW |
19 |
10,455,128 (GRCm39) |
missense |
probably benign |
0.16 |
R6360:Saxo4
|
UTSW |
19 |
10,456,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R6388:Saxo4
|
UTSW |
19 |
10,459,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6625:Saxo4
|
UTSW |
19 |
10,459,100 (GRCm39) |
missense |
probably damaging |
0.97 |
R6754:Saxo4
|
UTSW |
19 |
10,454,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R7188:Saxo4
|
UTSW |
19 |
10,459,702 (GRCm39) |
missense |
probably benign |
0.15 |
R7361:Saxo4
|
UTSW |
19 |
10,456,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Saxo4
|
UTSW |
19 |
10,459,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Saxo4
|
UTSW |
19 |
10,455,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R8797:Saxo4
|
UTSW |
19 |
10,455,602 (GRCm39) |
missense |
probably benign |
0.43 |
R8859:Saxo4
|
UTSW |
19 |
10,459,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9315:Saxo4
|
UTSW |
19 |
10,458,767 (GRCm39) |
missense |
probably damaging |
1.00 |
|