Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410089E03Rik |
G |
A |
15: 8,219,216 |
E1750K |
probably damaging |
Het |
4933425L06Rik |
A |
G |
13: 105,109,742 |
I270M |
probably benign |
Het |
Aatk |
T |
C |
11: 120,018,855 |
D28G |
probably benign |
Het |
Abcg1 |
T |
A |
17: 31,092,395 |
S125T |
probably damaging |
Het |
Actbl2 |
T |
C |
13: 111,256,183 |
S351P |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,439,061 |
|
probably null |
Het |
BC030867 |
T |
C |
11: 102,255,296 |
Y133H |
possibly damaging |
Het |
BC051665 |
C |
T |
13: 60,782,654 |
V295I |
probably benign |
Het |
C1qtnf2 |
A |
G |
11: 43,491,156 |
N265S |
probably damaging |
Het |
Ccdc14 |
C |
T |
16: 34,721,850 |
R573* |
probably null |
Het |
Cd55b |
A |
T |
1: 130,409,875 |
Y247N |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,413,591 |
V635E |
probably benign |
Het |
Clec16a |
T |
C |
16: 10,559,687 |
|
probably benign |
Het |
Clec4b1 |
A |
G |
6: 123,065,945 |
Y41C |
probably damaging |
Het |
Cntn5 |
A |
T |
9: 10,172,121 |
D19E |
probably benign |
Het |
Cop1 |
A |
G |
1: 159,232,805 |
N53S |
probably damaging |
Het |
Csad |
A |
T |
15: 102,188,667 |
M1K |
probably null |
Het |
Cyb5rl |
A |
G |
4: 107,080,945 |
I200V |
probably benign |
Het |
Cyp26a1 |
A |
G |
19: 37,698,342 |
T81A |
probably damaging |
Het |
Cyp2d12 |
A |
T |
15: 82,559,036 |
H433L |
probably benign |
Het |
D7Ertd443e |
T |
A |
7: 134,349,479 |
|
probably null |
Het |
Dennd1b |
A |
G |
1: 139,170,170 |
|
probably benign |
Het |
Dmap1 |
G |
T |
4: 117,675,298 |
T357K |
probably damaging |
Het |
Dzip1 |
G |
T |
14: 118,881,044 |
T759K |
probably benign |
Het |
Elmo2 |
A |
G |
2: 165,298,687 |
V300A |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,844,105 |
D864G |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,668,645 |
V2670A |
probably damaging |
Het |
Epha3 |
T |
A |
16: 63,603,625 |
I534F |
probably damaging |
Het |
Epha4 |
A |
C |
1: 77,382,991 |
Y742D |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,204,774 |
|
probably null |
Het |
Ero1l |
A |
T |
14: 45,299,088 |
|
probably null |
Het |
Fam229a |
A |
G |
4: 129,491,486 |
D70G |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,093,359 |
R781Q |
probably damaging |
Het |
Fbxo16 |
A |
T |
14: 65,270,714 |
|
probably benign |
Het |
Fbxo39 |
T |
A |
11: 72,317,285 |
S154R |
probably benign |
Het |
Fer |
T |
A |
17: 63,991,580 |
|
probably null |
Het |
Filip1l |
A |
T |
16: 57,571,047 |
D428V |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,570,662 |
I538V |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,979,610 |
I2091T |
possibly damaging |
Het |
Glyat |
A |
C |
19: 12,651,398 |
T186P |
possibly damaging |
Het |
Gm10604 |
A |
G |
4: 11,980,083 |
S74P |
unknown |
Het |
Gm4787 |
T |
G |
12: 81,379,137 |
K82N |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,686,867 |
C2313* |
probably null |
Het |
Igfn1 |
A |
T |
1: 135,969,316 |
S1171T |
probably benign |
Het |
Ints8 |
T |
C |
4: 11,241,642 |
D267G |
probably benign |
Het |
Itln1 |
A |
G |
1: 171,529,159 |
C251R |
probably damaging |
Het |
Jcad |
C |
T |
18: 4,674,026 |
T596M |
probably damaging |
Het |
Kcnj16 |
C |
T |
11: 111,025,583 |
T357M |
probably benign |
Het |
Kif13a |
G |
A |
13: 46,814,200 |
T346M |
probably damaging |
Het |
Klhl24 |
G |
A |
16: 20,120,167 |
A491T |
probably benign |
Het |
Kntc1 |
C |
T |
5: 123,778,347 |
Q748* |
probably null |
Het |
Krt25 |
T |
A |
11: 99,317,296 |
K369* |
probably null |
Het |
Krt75 |
C |
T |
15: 101,568,031 |
R433Q |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,884,858 |
F582L |
unknown |
Het |
Lysmd1 |
G |
A |
3: 95,138,397 |
V182I |
probably benign |
Het |
Mab21l2 |
T |
A |
3: 86,547,555 |
E46V |
probably damaging |
Het |
Magi2 |
A |
T |
5: 20,358,936 |
K355N |
probably damaging |
Het |
March10 |
T |
C |
11: 105,385,572 |
D630G |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,738,639 |
I1215N |
probably damaging |
Het |
Nckap1 |
G |
A |
2: 80,530,218 |
T523I |
probably benign |
Het |
Nexmif |
T |
A |
X: 104,084,393 |
D1306V |
probably damaging |
Het |
Nfkb1 |
A |
C |
3: 135,589,329 |
I918R |
possibly damaging |
Het |
Nup50 |
A |
T |
15: 84,933,658 |
T93S |
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,804,374 |
Y434H |
probably benign |
Het |
Olfr61 |
T |
C |
7: 140,638,484 |
V261A |
probably benign |
Het |
Osbpl1a |
C |
A |
18: 12,905,031 |
V288L |
probably benign |
Het |
Pan3 |
A |
G |
5: 147,527,036 |
E562G |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,180,889 |
Y548* |
probably null |
Het |
Phf3 |
A |
T |
1: 30,810,789 |
L1181Q |
probably damaging |
Het |
Phip |
T |
C |
9: 82,915,339 |
H537R |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,485,428 |
I240T |
probably damaging |
Het |
Pole |
G |
A |
5: 110,290,502 |
|
probably null |
Het |
Polq |
T |
A |
16: 37,011,942 |
S15T |
unknown |
Het |
Prrt2 |
T |
C |
7: 127,020,224 |
E23G |
possibly damaging |
Het |
Prss37 |
A |
T |
6: 40,517,826 |
|
probably null |
Het |
Prune2 |
T |
C |
19: 17,000,036 |
L45P |
probably damaging |
Het |
Psd |
A |
T |
19: 46,324,913 |
M6K |
possibly damaging |
Het |
Psmd1 |
A |
G |
1: 86,089,997 |
E510G |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,524,959 |
E944A |
probably benign |
Het |
Pxdn |
T |
A |
12: 30,003,406 |
I1194N |
probably damaging |
Het |
Rbp3 |
C |
T |
14: 33,956,018 |
T641M |
probably damaging |
Het |
Rgmb |
C |
A |
17: 15,807,647 |
R270L |
probably benign |
Het |
Rpgrip1l |
A |
G |
8: 91,280,716 |
|
probably null |
Het |
Rps2 |
G |
A |
17: 24,720,379 |
|
probably benign |
Het |
Rsbn1l |
G |
T |
5: 20,902,366 |
A550E |
probably damaging |
Het |
S1pr4 |
C |
T |
10: 81,499,304 |
R112H |
probably benign |
Het |
Scfd2 |
T |
C |
5: 74,531,177 |
N148S |
probably damaging |
Het |
Scin |
C |
T |
12: 40,081,706 |
M276I |
probably benign |
Het |
Sec24d |
T |
C |
3: 123,353,606 |
I708T |
possibly damaging |
Het |
Skint11 |
T |
A |
4: 114,228,812 |
F41I |
possibly damaging |
Het |
Slc15a4 |
A |
T |
5: 127,617,239 |
F44Y |
possibly damaging |
Het |
Slc6a18 |
A |
G |
13: 73,675,806 |
Y72H |
probably benign |
Het |
Slc7a11 |
A |
T |
3: 50,377,746 |
|
probably null |
Het |
Slc7a14 |
G |
T |
3: 31,237,501 |
N209K |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,624,431 |
C59R |
probably damaging |
Het |
Stab1 |
A |
G |
14: 31,163,040 |
|
probably null |
Het |
Stag1 |
G |
T |
9: 100,866,210 |
S475I |
probably damaging |
Het |
Stxbp5l |
A |
G |
16: 37,115,667 |
Y1183H |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,135,628 |
|
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,158,684 |
T653A |
probably benign |
Het |
Tmeff1 |
T |
C |
4: 48,662,059 |
S366P |
possibly damaging |
Het |
Tnnt2 |
G |
T |
1: 135,852,065 |
W300L |
probably damaging |
Het |
Traj32 |
A |
G |
14: 54,186,103 |
|
probably benign |
Het |
Trp53bp2 |
A |
T |
1: 182,441,639 |
M223L |
probably benign |
Het |
Tsga10 |
G |
A |
1: 37,815,677 |
T246M |
probably damaging |
Het |
Txn2 |
A |
T |
15: 77,926,670 |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,938,198 |
F450I |
probably damaging |
Het |
Usp47 |
T |
C |
7: 112,104,470 |
|
probably null |
Het |
Vars2 |
C |
T |
17: 35,664,793 |
R244Q |
probably damaging |
Het |
Xrra1 |
T |
A |
7: 99,897,596 |
F251L |
probably damaging |
Het |
Zfp804a |
G |
A |
2: 82,257,519 |
R564Q |
probably benign |
Het |
Zfp983 |
T |
C |
17: 21,658,967 |
C29R |
probably damaging |
Het |
|