Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810004N23Rik |
T |
C |
8: 124,862,914 |
D20G |
possibly damaging |
Het |
5430401F13Rik |
T |
C |
6: 131,552,667 |
S75P |
probably benign |
Het |
9530003J23Rik |
T |
C |
10: 117,237,742 |
N62S |
probably benign |
Het |
Acad8 |
A |
T |
9: 26,978,454 |
F315I |
probably damaging |
Het |
Adcy5 |
A |
G |
16: 35,298,534 |
Y1085C |
probably damaging |
Het |
Aldh1a7 |
T |
C |
19: 20,716,018 |
K179R |
probably damaging |
Het |
Arhgap10 |
C |
T |
8: 77,250,954 |
G776R |
probably damaging |
Het |
Arhgap35 |
A |
C |
7: 16,562,566 |
F858C |
probably damaging |
Het |
Ash1l |
C |
T |
3: 89,077,074 |
R2957W |
probably damaging |
Het |
Atp6ap1l |
G |
T |
13: 90,883,729 |
A278E |
probably damaging |
Het |
Btn1a1 |
A |
T |
13: 23,459,351 |
D309E |
probably damaging |
Het |
Casd1 |
C |
T |
6: 4,624,211 |
R335C |
probably benign |
Het |
Ceacam3 |
A |
G |
7: 17,151,562 |
Q30R |
|
Het |
Cfap20 |
C |
T |
8: 95,422,167 |
C119Y |
probably damaging |
Het |
Cntrl |
A |
T |
2: 35,165,445 |
|
probably null |
Het |
Crot |
A |
G |
5: 8,987,878 |
V146A |
probably damaging |
Het |
Cx3cl1 |
A |
G |
8: 94,779,963 |
S199G |
probably damaging |
Het |
D5Ertd577e |
A |
G |
5: 95,482,821 |
I186V |
possibly damaging |
Het |
Ddhd1 |
A |
T |
14: 45,657,806 |
L69Q |
probably damaging |
Het |
Dpy19l3 |
A |
T |
7: 35,708,630 |
D450E |
probably benign |
Het |
Ercc3 |
A |
T |
18: 32,257,272 |
N538I |
probably damaging |
Het |
Fzd1 |
A |
T |
5: 4,756,145 |
V479E |
probably benign |
Het |
Gart |
T |
C |
16: 91,628,463 |
Y638C |
possibly damaging |
Het |
Gm2381 |
C |
A |
7: 42,820,464 |
V79L |
probably benign |
Het |
Gucy1b1 |
T |
C |
3: 82,043,162 |
Y312C |
probably damaging |
Het |
Hecw1 |
T |
A |
13: 14,434,460 |
M1L |
probably benign |
Het |
Ip6k2 |
A |
G |
9: 108,796,731 |
I99V |
unknown |
Het |
Itgb5 |
C |
T |
16: 33,940,643 |
T616I |
probably benign |
Het |
Kmt2c |
A |
C |
5: 25,300,362 |
V3316G |
possibly damaging |
Het |
Lama3 |
C |
T |
18: 12,468,289 |
R1008C |
probably damaging |
Het |
Lin54 |
T |
C |
5: 100,485,300 |
D175G |
possibly damaging |
Het |
Lrp2 |
A |
G |
2: 69,488,051 |
S2019P |
probably damaging |
Het |
Lrrc9 |
A |
G |
12: 72,466,952 |
E528G |
probably benign |
Het |
Mto1 |
A |
G |
9: 78,457,283 |
H299R |
probably damaging |
Het |
Myo19 |
G |
A |
11: 84,905,613 |
G684R |
probably benign |
Het |
Olfr297 |
A |
C |
7: 86,527,114 |
D119A |
probably damaging |
Het |
Olfr851 |
A |
T |
9: 19,496,849 |
M34L |
probably benign |
Het |
Pcdh18 |
C |
A |
3: 49,754,694 |
C724F |
probably benign |
Het |
Pcdha3 |
A |
T |
18: 36,947,112 |
K302N |
probably benign |
Het |
Pcdhgb2 |
T |
C |
18: 37,692,247 |
F764L |
possibly damaging |
Het |
Pik3cb |
C |
A |
9: 99,093,090 |
G246W |
probably damaging |
Het |
Polr2m |
A |
T |
9: 71,483,344 |
I192N |
probably damaging |
Het |
Polr2m |
G |
T |
9: 71,483,533 |
T129K |
probably benign |
Het |
Ptpn4 |
C |
T |
1: 119,691,745 |
|
probably null |
Het |
Scgb1b19 |
A |
T |
7: 33,287,515 |
K30N |
possibly damaging |
Het |
Shpk |
A |
G |
11: 73,213,489 |
T155A |
probably damaging |
Het |
Slit3 |
T |
C |
11: 35,570,719 |
Y261H |
probably damaging |
Het |
Sox13 |
A |
G |
1: 133,385,505 |
F438L |
possibly damaging |
Het |
Sphk1 |
A |
T |
11: 116,535,081 |
E61D |
probably benign |
Het |
St18 |
A |
G |
1: 6,803,019 |
D326G |
probably damaging |
Het |
Syde1 |
G |
A |
10: 78,586,198 |
Q566* |
probably null |
Het |
Tacc2 |
A |
G |
7: 130,729,077 |
T254A |
probably benign |
Het |
Tbc1d1 |
A |
G |
5: 64,173,484 |
E2G |
probably damaging |
Het |
Trim5 |
A |
T |
7: 104,276,810 |
N181K |
probably damaging |
Het |
Trpc7 |
A |
T |
13: 56,783,696 |
I730K |
probably benign |
Het |
Uqcrc1 |
T |
A |
9: 108,947,858 |
M377K |
probably benign |
Het |
Vmn2r4 |
T |
C |
3: 64,398,477 |
N508S |
probably benign |
Het |
Vmp1 |
A |
T |
11: 86,586,576 |
S333T |
probably benign |
Het |
Vps50 |
T |
A |
6: 3,578,854 |
M639K |
possibly damaging |
Het |
Zfp874b |
A |
T |
13: 67,474,503 |
C225* |
probably null |
Het |
|