Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,909,681 (GRCm39) |
D28G |
probably benign |
Het |
Abcg1 |
T |
A |
17: 31,311,369 (GRCm39) |
S125T |
probably damaging |
Het |
Actbl2 |
T |
C |
13: 111,392,717 (GRCm39) |
S351P |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,575,569 (GRCm39) |
|
probably null |
Het |
BC051665 |
C |
T |
13: 60,930,468 (GRCm39) |
V295I |
probably benign |
Het |
C1qtnf2 |
A |
G |
11: 43,381,983 (GRCm39) |
N265S |
probably damaging |
Het |
Ccdc14 |
C |
T |
16: 34,542,220 (GRCm39) |
R573* |
probably null |
Het |
Cd55b |
A |
T |
1: 130,337,612 (GRCm39) |
Y247N |
probably damaging |
Het |
Celsr2 |
A |
T |
3: 108,320,907 (GRCm39) |
V635E |
probably benign |
Het |
Clec16a |
T |
C |
16: 10,377,551 (GRCm39) |
|
probably benign |
Het |
Clec4b1 |
A |
G |
6: 123,042,904 (GRCm39) |
Y41C |
probably damaging |
Het |
Cntn5 |
A |
T |
9: 10,172,126 (GRCm39) |
D19E |
probably benign |
Het |
Cop1 |
A |
G |
1: 159,060,375 (GRCm39) |
N53S |
probably damaging |
Het |
Cplane1 |
G |
A |
15: 8,248,700 (GRCm39) |
E1750K |
probably damaging |
Het |
Csad |
A |
T |
15: 102,097,102 (GRCm39) |
M1K |
probably null |
Het |
Cyb5rl |
A |
G |
4: 106,938,142 (GRCm39) |
I200V |
probably benign |
Het |
Cyp26a1 |
A |
G |
19: 37,686,790 (GRCm39) |
T81A |
probably damaging |
Het |
Cyp2d12 |
A |
T |
15: 82,443,237 (GRCm39) |
H433L |
probably benign |
Het |
D7Ertd443e |
T |
A |
7: 133,951,208 (GRCm39) |
|
probably null |
Het |
Dennd1b |
A |
G |
1: 139,097,908 (GRCm39) |
|
probably benign |
Het |
Dmap1 |
G |
T |
4: 117,532,495 (GRCm39) |
T357K |
probably damaging |
Het |
Dzip1 |
G |
T |
14: 119,118,456 (GRCm39) |
T759K |
probably benign |
Het |
Elmo2 |
A |
G |
2: 165,140,607 (GRCm39) |
V300A |
probably damaging |
Het |
Eml5 |
T |
C |
12: 98,810,364 (GRCm39) |
D864G |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,816,511 (GRCm39) |
V2670A |
probably damaging |
Het |
Epha3 |
T |
A |
16: 63,423,988 (GRCm39) |
I534F |
probably damaging |
Het |
Epha4 |
A |
C |
1: 77,359,628 (GRCm39) |
Y742D |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,106,272 (GRCm39) |
|
probably null |
Het |
Ero1a |
A |
T |
14: 45,536,545 (GRCm39) |
|
probably null |
Het |
Fam229a |
A |
G |
4: 129,385,279 (GRCm39) |
D70G |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,226,431 (GRCm39) |
R781Q |
probably damaging |
Het |
Fbxo16 |
A |
T |
14: 65,508,163 (GRCm39) |
|
probably benign |
Het |
Fbxo39 |
T |
A |
11: 72,208,111 (GRCm39) |
S154R |
probably benign |
Het |
Fer |
T |
A |
17: 64,298,575 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
T |
16: 57,391,410 (GRCm39) |
D428V |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,391,025 (GRCm39) |
I538V |
possibly damaging |
Het |
Fsip2 |
T |
C |
2: 82,809,954 (GRCm39) |
I2091T |
possibly damaging |
Het |
Glyat |
A |
C |
19: 12,628,762 (GRCm39) |
T186P |
possibly damaging |
Het |
Gm10604 |
A |
G |
4: 11,980,083 (GRCm39) |
S74P |
unknown |
Het |
Gm4787 |
T |
G |
12: 81,425,911 (GRCm39) |
K82N |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,358,683 (GRCm39) |
I50T |
unknown |
Het |
Hectd4 |
T |
C |
5: 121,402,030 (GRCm39) |
S373P |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,562,618 (GRCm39) |
C2313* |
probably null |
Het |
Hrob |
T |
C |
11: 102,146,122 (GRCm39) |
Y133H |
possibly damaging |
Het |
Igfn1 |
A |
T |
1: 135,897,054 (GRCm39) |
S1171T |
probably benign |
Het |
Ints8 |
T |
C |
4: 11,241,642 (GRCm39) |
D267G |
probably benign |
Het |
Itln1 |
A |
G |
1: 171,356,727 (GRCm39) |
C251R |
probably damaging |
Het |
Jcad |
C |
T |
18: 4,674,026 (GRCm39) |
T596M |
probably damaging |
Het |
Kcnj16 |
C |
T |
11: 110,916,409 (GRCm39) |
T357M |
probably benign |
Het |
Kif13a |
G |
A |
13: 46,967,676 (GRCm39) |
T346M |
probably damaging |
Het |
Klhl24 |
G |
A |
16: 19,938,917 (GRCm39) |
A491T |
probably benign |
Het |
Kntc1 |
C |
T |
5: 123,916,410 (GRCm39) |
Q748* |
probably null |
Het |
Krt25 |
T |
A |
11: 99,208,122 (GRCm39) |
K369* |
probably null |
Het |
Krt75 |
C |
T |
15: 101,476,466 (GRCm39) |
R433Q |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,793,293 (GRCm39) |
F582L |
unknown |
Het |
Lysmd1 |
G |
A |
3: 95,045,708 (GRCm39) |
V182I |
probably benign |
Het |
Mab21l2 |
T |
A |
3: 86,454,862 (GRCm39) |
E46V |
probably damaging |
Het |
Magi2 |
A |
T |
5: 20,563,934 (GRCm39) |
K355N |
probably damaging |
Het |
Marchf10 |
T |
C |
11: 105,276,398 (GRCm39) |
D630G |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,875,147 (GRCm39) |
I1215N |
probably damaging |
Het |
Nckap1 |
G |
A |
2: 80,360,562 (GRCm39) |
T523I |
probably benign |
Het |
Nexmif |
T |
A |
X: 103,127,999 (GRCm39) |
D1306V |
probably damaging |
Het |
Nfkb1 |
A |
C |
3: 135,295,090 (GRCm39) |
I918R |
possibly damaging |
Het |
Nt5el |
A |
G |
13: 105,246,250 (GRCm39) |
I270M |
probably benign |
Het |
Nup50 |
A |
T |
15: 84,817,859 (GRCm39) |
T93S |
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,961,717 (GRCm39) |
Y434H |
probably benign |
Het |
Or13a28 |
T |
C |
7: 140,218,397 (GRCm39) |
V261A |
probably benign |
Het |
Osbpl1a |
C |
A |
18: 13,038,088 (GRCm39) |
V288L |
probably benign |
Het |
Pan3 |
A |
G |
5: 147,463,846 (GRCm39) |
E562G |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,099,126 (GRCm39) |
Y548* |
probably null |
Het |
Phf3 |
A |
T |
1: 30,849,870 (GRCm39) |
L1181Q |
probably damaging |
Het |
Phip |
T |
C |
9: 82,797,392 (GRCm39) |
H537R |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,348,824 (GRCm39) |
I240T |
probably damaging |
Het |
Pole |
G |
A |
5: 110,438,368 (GRCm39) |
|
probably null |
Het |
Polq |
T |
A |
16: 36,832,304 (GRCm39) |
S15T |
unknown |
Het |
Prrt2 |
T |
C |
7: 126,619,396 (GRCm39) |
E23G |
possibly damaging |
Het |
Prss37 |
A |
T |
6: 40,494,760 (GRCm39) |
|
probably null |
Het |
Prune2 |
T |
C |
19: 16,977,400 (GRCm39) |
L45P |
probably damaging |
Het |
Psd |
A |
T |
19: 46,313,352 (GRCm39) |
M6K |
possibly damaging |
Het |
Psmd1 |
A |
G |
1: 86,017,719 (GRCm39) |
E510G |
possibly damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Pxdn |
T |
A |
12: 30,053,405 (GRCm39) |
I1194N |
probably damaging |
Het |
Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
Rgmb |
C |
A |
17: 16,027,909 (GRCm39) |
R270L |
probably benign |
Het |
Rpgrip1l |
A |
G |
8: 92,007,344 (GRCm39) |
|
probably null |
Het |
Rps2 |
G |
A |
17: 24,939,353 (GRCm39) |
|
probably benign |
Het |
Rsbn1l |
G |
T |
5: 21,107,364 (GRCm39) |
A550E |
probably damaging |
Het |
S1pr4 |
C |
T |
10: 81,335,138 (GRCm39) |
R112H |
probably benign |
Het |
Scfd2 |
T |
C |
5: 74,691,838 (GRCm39) |
N148S |
probably damaging |
Het |
Scin |
C |
T |
12: 40,131,705 (GRCm39) |
M276I |
probably benign |
Het |
Skint11 |
T |
A |
4: 114,086,009 (GRCm39) |
F41I |
possibly damaging |
Het |
Slc15a4 |
A |
T |
5: 127,694,303 (GRCm39) |
F44Y |
possibly damaging |
Het |
Slc6a18 |
A |
G |
13: 73,823,925 (GRCm39) |
Y72H |
probably benign |
Het |
Slc7a11 |
A |
T |
3: 50,332,195 (GRCm39) |
|
probably null |
Het |
Slc7a14 |
G |
T |
3: 31,291,650 (GRCm39) |
N209K |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,257 (GRCm39) |
C59R |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,884,997 (GRCm39) |
|
probably null |
Het |
Stag1 |
G |
T |
9: 100,748,263 (GRCm39) |
S475I |
probably damaging |
Het |
Stxbp5l |
A |
G |
16: 36,936,029 (GRCm39) |
Y1183H |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,135,628 (GRCm39) |
|
probably null |
Het |
Tm9sf2 |
A |
G |
14: 122,396,096 (GRCm39) |
T653A |
probably benign |
Het |
Tmeff1 |
T |
C |
4: 48,662,059 (GRCm39) |
S366P |
possibly damaging |
Het |
Tnnt2 |
G |
T |
1: 135,779,803 (GRCm39) |
W300L |
probably damaging |
Het |
Traj32 |
A |
G |
14: 54,423,560 (GRCm39) |
|
probably benign |
Het |
Trp53bp2 |
A |
T |
1: 182,269,204 (GRCm39) |
M223L |
probably benign |
Het |
Tsga10 |
G |
A |
1: 37,854,758 (GRCm39) |
T246M |
probably damaging |
Het |
Txn2 |
A |
T |
15: 77,810,870 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,768,542 (GRCm39) |
F450I |
probably damaging |
Het |
Usp47 |
T |
C |
7: 111,703,677 (GRCm39) |
|
probably null |
Het |
Vars2 |
C |
T |
17: 35,975,685 (GRCm39) |
R244Q |
probably damaging |
Het |
Xrra1 |
T |
A |
7: 99,546,803 (GRCm39) |
F251L |
probably damaging |
Het |
Zfp804a |
G |
A |
2: 82,087,863 (GRCm39) |
R564Q |
probably benign |
Het |
Zfp983 |
T |
C |
17: 21,877,883 (GRCm39) |
C29R |
probably damaging |
Het |
|
Other mutations in Sec24d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01420:Sec24d
|
APN |
3 |
123,143,658 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01621:Sec24d
|
APN |
3 |
123,087,807 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01866:Sec24d
|
APN |
3 |
123,087,244 (GRCm39) |
nonsense |
probably null |
|
IGL02064:Sec24d
|
APN |
3 |
123,137,463 (GRCm39) |
splice site |
probably benign |
|
IGL02125:Sec24d
|
APN |
3 |
123,152,607 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02173:Sec24d
|
APN |
3 |
123,147,330 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03239:Sec24d
|
APN |
3 |
123,130,138 (GRCm39) |
missense |
probably benign |
0.00 |
Scanty
|
UTSW |
3 |
123,148,596 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Sec24d
|
UTSW |
3 |
123,147,279 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4531001:Sec24d
|
UTSW |
3 |
123,136,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Sec24d
|
UTSW |
3 |
123,144,525 (GRCm39) |
splice site |
probably benign |
|
R0838:Sec24d
|
UTSW |
3 |
123,099,485 (GRCm39) |
missense |
probably benign |
0.08 |
R1775:Sec24d
|
UTSW |
3 |
123,130,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1895:Sec24d
|
UTSW |
3 |
123,147,043 (GRCm39) |
missense |
probably benign |
0.04 |
R1946:Sec24d
|
UTSW |
3 |
123,147,043 (GRCm39) |
missense |
probably benign |
0.04 |
R2238:Sec24d
|
UTSW |
3 |
123,143,543 (GRCm39) |
splice site |
probably null |
|
R2846:Sec24d
|
UTSW |
3 |
123,144,395 (GRCm39) |
missense |
probably damaging |
0.98 |
R2895:Sec24d
|
UTSW |
3 |
123,136,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R3428:Sec24d
|
UTSW |
3 |
123,137,572 (GRCm39) |
splice site |
probably benign |
|
R4573:Sec24d
|
UTSW |
3 |
123,152,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4668:Sec24d
|
UTSW |
3 |
123,149,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R4706:Sec24d
|
UTSW |
3 |
123,149,427 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4896:Sec24d
|
UTSW |
3 |
123,148,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Sec24d
|
UTSW |
3 |
123,093,255 (GRCm39) |
missense |
probably benign |
0.29 |
R5030:Sec24d
|
UTSW |
3 |
123,152,550 (GRCm39) |
missense |
probably damaging |
0.98 |
R5041:Sec24d
|
UTSW |
3 |
123,087,880 (GRCm39) |
missense |
probably damaging |
0.96 |
R5078:Sec24d
|
UTSW |
3 |
123,084,201 (GRCm39) |
missense |
probably benign |
0.00 |
R5108:Sec24d
|
UTSW |
3 |
123,099,434 (GRCm39) |
splice site |
probably null |
|
R5174:Sec24d
|
UTSW |
3 |
123,158,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R5661:Sec24d
|
UTSW |
3 |
123,136,791 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5661:Sec24d
|
UTSW |
3 |
123,136,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Sec24d
|
UTSW |
3 |
123,084,109 (GRCm39) |
missense |
probably benign |
0.00 |
R5859:Sec24d
|
UTSW |
3 |
123,072,961 (GRCm39) |
unclassified |
probably benign |
|
R5944:Sec24d
|
UTSW |
3 |
123,087,230 (GRCm39) |
missense |
probably benign |
0.01 |
R6053:Sec24d
|
UTSW |
3 |
123,072,871 (GRCm39) |
nonsense |
probably null |
|
R6515:Sec24d
|
UTSW |
3 |
123,136,719 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6552:Sec24d
|
UTSW |
3 |
123,084,201 (GRCm39) |
missense |
probably benign |
0.00 |
R6557:Sec24d
|
UTSW |
3 |
123,136,736 (GRCm39) |
missense |
probably damaging |
1.00 |
R6593:Sec24d
|
UTSW |
3 |
123,147,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6594:Sec24d
|
UTSW |
3 |
123,087,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6842:Sec24d
|
UTSW |
3 |
123,136,868 (GRCm39) |
missense |
probably benign |
0.00 |
R7072:Sec24d
|
UTSW |
3 |
123,124,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R7481:Sec24d
|
UTSW |
3 |
123,144,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R7554:Sec24d
|
UTSW |
3 |
123,149,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R8270:Sec24d
|
UTSW |
3 |
123,099,535 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8481:Sec24d
|
UTSW |
3 |
123,147,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Sec24d
|
UTSW |
3 |
123,137,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8872:Sec24d
|
UTSW |
3 |
123,148,585 (GRCm39) |
splice site |
probably benign |
|
R8922:Sec24d
|
UTSW |
3 |
123,144,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R8974:Sec24d
|
UTSW |
3 |
123,099,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R9015:Sec24d
|
UTSW |
3 |
123,121,287 (GRCm39) |
missense |
probably benign |
0.43 |
R9050:Sec24d
|
UTSW |
3 |
123,144,374 (GRCm39) |
missense |
probably benign |
0.00 |
R9065:Sec24d
|
UTSW |
3 |
123,149,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R9128:Sec24d
|
UTSW |
3 |
123,087,810 (GRCm39) |
missense |
probably benign |
|
R9447:Sec24d
|
UTSW |
3 |
123,084,162 (GRCm39) |
missense |
probably benign |
0.00 |
R9701:Sec24d
|
UTSW |
3 |
123,063,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R9758:Sec24d
|
UTSW |
3 |
123,136,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|