Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
A |
T |
15: 64,787,358 |
W528R |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,421,917 |
E329G |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 30,903,059 |
R141Q |
probably damaging |
Het |
AI182371 |
A |
T |
2: 35,085,215 |
I334N |
probably benign |
Het |
Aldh1b1 |
A |
G |
4: 45,803,383 |
|
probably null |
Het |
Armc9 |
G |
A |
1: 86,186,116 |
M298I |
probably benign |
Het |
Atp8a1 |
T |
A |
5: 67,815,723 |
K27N |
probably benign |
Het |
BC004004 |
G |
A |
17: 29,294,415 |
|
probably null |
Het |
Ccdc83 |
A |
T |
7: 90,250,529 |
F45Y |
probably damaging |
Het |
Cct8l1 |
G |
A |
5: 25,516,883 |
V199I |
probably benign |
Het |
Cdc23 |
C |
A |
18: 34,651,689 |
V7L |
unknown |
Het |
Cdh17 |
G |
T |
4: 11,810,325 |
G672V |
probably damaging |
Het |
Cdh5 |
C |
A |
8: 104,140,702 |
T537K |
probably damaging |
Het |
Chd1 |
T |
A |
17: 15,762,405 |
S1377R |
probably benign |
Het |
Chd2 |
T |
C |
7: 73,429,689 |
N1821S |
probably benign |
Het |
Cnot3 |
A |
G |
7: 3,650,861 |
K4R |
probably damaging |
Het |
Colq |
T |
A |
14: 31,528,832 |
I339F |
possibly damaging |
Het |
Coq2 |
A |
T |
5: 100,667,950 |
L121Q |
probably damaging |
Het |
Csnk1e |
G |
A |
15: 79,420,872 |
R342* |
probably null |
Het |
Cstl1 |
A |
T |
2: 148,750,927 |
M1L |
probably benign |
Het |
Cwh43 |
A |
G |
5: 73,423,913 |
|
probably null |
Het |
Cyp2a22 |
A |
T |
7: 26,932,481 |
F450Y |
probably benign |
Het |
Cyp2d10 |
C |
T |
15: 82,403,753 |
R383H |
probably benign |
Het |
Cyp4a29 |
A |
G |
4: 115,247,663 |
T123A |
probably benign |
Het |
Dgkh |
T |
C |
14: 78,604,532 |
K417E |
probably damaging |
Het |
Edn1 |
A |
G |
13: 42,303,677 |
E62G |
probably damaging |
Het |
Eef1akmt1 |
A |
G |
14: 57,566,007 |
L30P |
probably damaging |
Het |
Fbxo42 |
T |
C |
4: 141,198,945 |
W313R |
probably damaging |
Het |
Fign |
A |
T |
2: 63,979,693 |
L411* |
probably null |
Het |
Fitm1 |
T |
A |
14: 55,575,773 |
V31E |
possibly damaging |
Het |
Fryl |
G |
A |
5: 73,074,767 |
P1550L |
probably damaging |
Het |
Gabrd |
A |
C |
4: 155,387,162 |
F228C |
probably damaging |
Het |
Gm5916 |
A |
C |
9: 36,128,668 |
L8R |
probably benign |
Het |
Gm9573 |
G |
A |
17: 35,620,552 |
|
probably benign |
Het |
Gpr108 |
A |
G |
17: 57,235,335 |
S557P |
probably damaging |
Het |
Gpr75 |
C |
A |
11: 30,892,380 |
N428K |
probably damaging |
Het |
H2-M5 |
T |
G |
17: 36,987,184 |
|
probably null |
Het |
Hdac6 |
A |
G |
X: 7,944,797 |
F104L |
probably damaging |
Homo |
Homer3 |
T |
C |
8: 70,291,355 |
V243A |
probably benign |
Het |
Hspg2 |
T |
C |
4: 137,540,230 |
S2050P |
probably damaging |
Het |
Hydin |
A |
G |
8: 110,538,473 |
N2763D |
probably benign |
Het |
Ifi203 |
T |
C |
1: 173,935,110 |
Q152R |
possibly damaging |
Het |
Ifi44 |
T |
C |
3: 151,749,632 |
|
probably benign |
Het |
Ifi47 |
A |
G |
11: 49,095,534 |
T43A |
probably benign |
Het |
Ighv1-24 |
A |
G |
12: 114,773,128 |
Y51H |
probably benign |
Het |
Inf2 |
A |
T |
12: 112,612,039 |
|
probably null |
Het |
Insl6 |
T |
C |
19: 29,325,255 |
R21G |
probably benign |
Het |
Kif19a |
G |
A |
11: 114,767,227 |
M37I |
probably benign |
Het |
Ltbp3 |
T |
C |
19: 5,756,823 |
C1043R |
probably damaging |
Het |
Mkl1 |
A |
G |
15: 81,022,426 |
V91A |
probably damaging |
Het |
Mpeg1 |
T |
A |
19: 12,461,181 |
M1K |
probably null |
Het |
Ncald |
A |
T |
15: 37,397,234 |
H67Q |
probably damaging |
Het |
Nek9 |
C |
A |
12: 85,327,459 |
R268L |
possibly damaging |
Het |
Nudt5 |
T |
A |
2: 5,864,387 |
H141Q |
probably benign |
Het |
Numbl |
G |
A |
7: 27,280,990 |
D466N |
probably damaging |
Het |
Olfr1100 |
A |
T |
2: 86,978,322 |
V158D |
possibly damaging |
Het |
Olfr1186 |
T |
C |
2: 88,526,041 |
S153P |
probably damaging |
Het |
Olfr167 |
A |
G |
16: 19,515,027 |
I203T |
probably benign |
Het |
Olfr310 |
A |
G |
7: 86,269,591 |
I66T |
probably damaging |
Het |
Olfr606 |
A |
T |
7: 103,451,410 |
E24D |
probably benign |
Het |
Olfr668 |
A |
C |
7: 104,925,493 |
N90K |
probably benign |
Het |
Olfr986 |
T |
C |
9: 40,187,664 |
L183S |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,720,147 |
C65S |
probably null |
Het |
Plagl1 |
A |
G |
10: 13,127,261 |
Y91C |
probably damaging |
Het |
Polr1a |
A |
G |
6: 71,931,709 |
N506S |
possibly damaging |
Het |
Pomt2 |
A |
C |
12: 87,133,460 |
C256G |
probably damaging |
Het |
Psg29 |
T |
A |
7: 17,211,838 |
D444E |
probably damaging |
Het |
Ptgs1 |
A |
T |
2: 36,251,260 |
N573I |
probably damaging |
Het |
Ptprf |
C |
A |
4: 118,211,999 |
G1624W |
probably damaging |
Het |
Rbm38 |
C |
T |
2: 173,022,082 |
P15S |
probably benign |
Het |
Rc3h1 |
A |
G |
1: 160,959,477 |
D814G |
possibly damaging |
Het |
Rnf40 |
T |
C |
7: 127,597,286 |
L802P |
probably damaging |
Het |
Rusc2 |
A |
G |
4: 43,415,240 |
D182G |
probably benign |
Het |
Setd1b |
A |
G |
5: 123,160,914 |
|
probably benign |
Het |
Slc4a2 |
G |
A |
5: 24,438,762 |
S855N |
probably benign |
Het |
Slc8a2 |
T |
C |
7: 16,150,583 |
L626P |
possibly damaging |
Het |
Slirp |
A |
G |
12: 87,444,014 |
T29A |
probably damaging |
Het |
Smarcc2 |
A |
G |
10: 128,463,940 |
D158G |
probably damaging |
Het |
Sptbn1 |
A |
G |
11: 30,113,854 |
|
probably null |
Het |
St3gal5 |
T |
C |
6: 72,132,053 |
C42R |
probably damaging |
Het |
Syt7 |
T |
C |
19: 10,443,428 |
S397P |
possibly damaging |
Het |
Tenm2 |
T |
A |
11: 36,068,381 |
T1114S |
probably damaging |
Het |
Thada |
T |
A |
17: 84,386,532 |
D1263V |
probably damaging |
Het |
Tmco3 |
G |
T |
8: 13,292,860 |
E199* |
probably null |
Het |
Tpcn1 |
A |
T |
5: 120,548,269 |
|
probably null |
Het |
Tppp2 |
G |
A |
14: 51,920,455 |
R119Q |
probably benign |
Het |
Trim30d |
A |
C |
7: 104,487,958 |
V13G |
probably damaging |
Het |
Ubxn2b |
A |
T |
4: 6,214,746 |
Q260L |
probably damaging |
Het |
Ufl1 |
A |
G |
4: 25,254,780 |
Y559H |
probably benign |
Het |
Usp5 |
A |
G |
6: 124,826,379 |
F7L |
probably benign |
Het |
Utrn |
A |
T |
10: 12,384,204 |
|
probably null |
Het |
Vmn1r28 |
A |
T |
6: 58,265,909 |
I246F |
probably benign |
Het |
Vmn2r2 |
C |
A |
3: 64,116,900 |
M753I |
probably benign |
Het |
Zbtb26 |
T |
C |
2: 37,435,929 |
H365R |
probably benign |
Het |
Zfp976 |
A |
T |
7: 42,612,930 |
Y494* |
probably null |
Het |
|