Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aqr |
A |
T |
2: 113,992,147 (GRCm39) |
Y76* |
probably null |
Het |
Armc5 |
C |
A |
7: 127,837,717 (GRCm39) |
A140E |
probably benign |
Het |
Auts2 |
T |
C |
5: 131,468,476 (GRCm39) |
H947R |
probably damaging |
Het |
Bag2 |
T |
C |
1: 33,786,074 (GRCm39) |
T83A |
probably damaging |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
Bean1 |
A |
G |
8: 104,937,799 (GRCm39) |
Y126C |
probably damaging |
Het |
Cars1 |
T |
C |
7: 143,129,697 (GRCm39) |
E330G |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,122,332 (GRCm39) |
I45V |
probably benign |
Het |
Cd320 |
G |
A |
17: 34,067,152 (GRCm39) |
G214R |
probably null |
Het |
Ckm |
G |
A |
7: 19,153,419 (GRCm39) |
V237M |
probably damaging |
Het |
Cplane1 |
T |
C |
15: 8,247,939 (GRCm39) |
V1496A |
probably benign |
Het |
Cspg4 |
T |
C |
9: 56,793,960 (GRCm39) |
V565A |
possibly damaging |
Het |
Dnaaf10 |
T |
C |
11: 17,182,853 (GRCm39) |
V338A |
probably benign |
Het |
Eddm13 |
T |
G |
7: 6,261,624 (GRCm39) |
I35S |
possibly damaging |
Het |
Ephb6 |
A |
G |
6: 41,594,799 (GRCm39) |
Y638C |
probably damaging |
Het |
Fat2 |
G |
C |
11: 55,187,039 (GRCm39) |
S1269* |
probably null |
Het |
Fbxo3 |
T |
C |
2: 103,883,820 (GRCm39) |
V348A |
probably damaging |
Het |
Gas6 |
G |
A |
8: 13,520,254 (GRCm39) |
P478L |
probably damaging |
Het |
Herc1 |
T |
C |
9: 66,340,660 (GRCm39) |
S1670P |
probably damaging |
Het |
Hnrnpk |
C |
A |
13: 58,542,331 (GRCm39) |
R281L |
probably damaging |
Het |
Ifih1 |
C |
A |
2: 62,439,563 (GRCm39) |
C488F |
probably benign |
Het |
Ift172 |
T |
C |
5: 31,441,559 (GRCm39) |
K192E |
probably benign |
Het |
Ighv5-9 |
T |
A |
12: 113,625,440 (GRCm39) |
Q101L |
probably benign |
Het |
Igkv3-2 |
G |
T |
6: 70,675,863 (GRCm39) |
M57I |
probably benign |
Het |
Insyn2a |
A |
T |
7: 134,500,877 (GRCm39) |
Y409* |
probably null |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
L3mbtl3 |
T |
C |
10: 26,213,715 (GRCm39) |
Y237C |
unknown |
Het |
Lats1 |
G |
A |
10: 7,588,347 (GRCm39) |
C988Y |
probably damaging |
Het |
Lgals3 |
T |
A |
14: 47,619,079 (GRCm39) |
|
probably null |
Het |
Lrrc3b |
G |
T |
14: 15,358,220 (GRCm38) |
H129N |
probably benign |
Het |
Lrriq1 |
T |
C |
10: 102,899,273 (GRCm39) |
H1656R |
possibly damaging |
Het |
Lypd6 |
T |
G |
2: 50,063,623 (GRCm39) |
Y43* |
probably null |
Het |
Mettl25b |
A |
G |
3: 87,835,055 (GRCm39) |
S82P |
probably damaging |
Het |
Mical2 |
A |
G |
7: 111,927,884 (GRCm39) |
D674G |
possibly damaging |
Het |
Msi1 |
G |
A |
5: 115,588,334 (GRCm39) |
R284Q |
probably damaging |
Het |
Mybpc2 |
T |
C |
7: 44,155,066 (GRCm39) |
E947G |
probably damaging |
Het |
Nat14 |
T |
A |
7: 4,927,446 (GRCm39) |
L206Q |
probably damaging |
Het |
Nup88 |
A |
T |
11: 70,856,672 (GRCm39) |
|
probably null |
Het |
Or11g27 |
A |
T |
14: 50,771,061 (GRCm39) |
Y64F |
probably damaging |
Het |
Or4k15 |
A |
G |
14: 50,364,939 (GRCm39) |
R302G |
probably benign |
Het |
Or8g19 |
A |
T |
9: 39,056,145 (GRCm39) |
I250F |
probably damaging |
Het |
Pdcl |
T |
C |
2: 37,245,778 (GRCm39) |
E75G |
probably damaging |
Het |
Phf14 |
A |
G |
6: 11,953,421 (GRCm39) |
I387V |
possibly damaging |
Het |
Phf3 |
G |
A |
1: 30,860,296 (GRCm39) |
R845W |
probably damaging |
Het |
Prkd1 |
C |
T |
12: 50,466,631 (GRCm39) |
|
probably null |
Het |
Psmb2 |
T |
C |
4: 126,571,558 (GRCm39) |
L4P |
probably damaging |
Het |
Pttg1 |
T |
A |
11: 43,315,677 (GRCm39) |
K46* |
probably null |
Het |
Ryr2 |
T |
C |
13: 11,764,395 (GRCm39) |
H1401R |
possibly damaging |
Het |
Septin4 |
T |
A |
11: 87,458,429 (GRCm39) |
Y268N |
probably damaging |
Het |
Sh3d19 |
G |
A |
3: 86,030,570 (GRCm39) |
D696N |
probably benign |
Het |
Slc16a2 |
T |
C |
X: 102,751,585 (GRCm39) |
T274A |
probably benign |
Het |
Slc26a6 |
G |
A |
9: 108,735,106 (GRCm39) |
A335T |
probably damaging |
Het |
Slc49a3 |
T |
C |
5: 108,590,011 (GRCm39) |
M464V |
probably benign |
Het |
Slc6a5 |
C |
A |
7: 49,588,146 (GRCm39) |
Y493* |
probably null |
Het |
Slf1 |
A |
T |
13: 77,274,723 (GRCm39) |
S37R |
probably damaging |
Het |
Smoc1 |
G |
A |
12: 81,214,376 (GRCm39) |
G264S |
probably damaging |
Het |
Snapc4 |
T |
C |
2: 26,264,193 (GRCm39) |
E280G |
possibly damaging |
Het |
Snx25 |
G |
A |
8: 46,488,616 (GRCm39) |
T913M |
probably damaging |
Het |
Snx7 |
T |
C |
3: 117,594,528 (GRCm39) |
T408A |
probably benign |
Het |
Spdya |
T |
A |
17: 71,885,339 (GRCm39) |
S264R |
probably benign |
Het |
Spg11 |
A |
T |
2: 121,928,580 (GRCm39) |
|
probably null |
Het |
Suz12 |
T |
A |
11: 79,904,350 (GRCm39) |
L230Q |
probably damaging |
Het |
Szt2 |
A |
G |
4: 118,234,881 (GRCm39) |
|
probably benign |
Het |
Tenm3 |
C |
A |
8: 48,689,005 (GRCm39) |
R2194L |
probably damaging |
Het |
Tmed8 |
T |
A |
12: 87,221,005 (GRCm39) |
I194F |
probably damaging |
Het |
Tmem79 |
T |
A |
3: 88,240,751 (GRCm39) |
T66S |
probably damaging |
Het |
Trappc1 |
T |
A |
11: 69,216,337 (GRCm39) |
S118T |
probably benign |
Het |
Ttn |
C |
T |
2: 76,569,225 (GRCm39) |
V27223I |
probably benign |
Het |
Ttn |
T |
C |
2: 76,606,839 (GRCm39) |
T18024A |
probably damaging |
Het |
Vmn2r15 |
C |
T |
5: 109,441,940 (GRCm39) |
M164I |
probably benign |
Het |
Vmn2r53 |
T |
A |
7: 12,334,901 (GRCm39) |
Y253F |
probably benign |
Het |
Zfand6 |
C |
T |
7: 84,267,093 (GRCm39) |
R163H |
probably benign |
Het |
|
Other mutations in Pm20d1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Pm20d1
|
APN |
1 |
131,741,738 (GRCm39) |
splice site |
probably benign |
|
IGL02026:Pm20d1
|
APN |
1 |
131,729,497 (GRCm39) |
nonsense |
probably null |
|
IGL02684:Pm20d1
|
APN |
1 |
131,732,697 (GRCm39) |
missense |
probably benign |
0.01 |
R1725:Pm20d1
|
UTSW |
1 |
131,743,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R1808:Pm20d1
|
UTSW |
1 |
131,730,165 (GRCm39) |
missense |
probably benign |
0.02 |
R2010:Pm20d1
|
UTSW |
1 |
131,739,852 (GRCm39) |
missense |
probably benign |
0.02 |
R4790:Pm20d1
|
UTSW |
1 |
131,739,777 (GRCm39) |
missense |
probably benign |
0.08 |
R5211:Pm20d1
|
UTSW |
1 |
131,734,647 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5578:Pm20d1
|
UTSW |
1 |
131,743,760 (GRCm39) |
missense |
probably benign |
0.01 |
R6314:Pm20d1
|
UTSW |
1 |
131,743,754 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6410:Pm20d1
|
UTSW |
1 |
131,726,334 (GRCm39) |
missense |
probably benign |
0.30 |
R6880:Pm20d1
|
UTSW |
1 |
131,731,839 (GRCm39) |
missense |
probably benign |
0.00 |
R7128:Pm20d1
|
UTSW |
1 |
131,725,292 (GRCm39) |
missense |
probably benign |
0.01 |
R8088:Pm20d1
|
UTSW |
1 |
131,729,501 (GRCm39) |
missense |
probably benign |
0.37 |
R8922:Pm20d1
|
UTSW |
1 |
131,728,853 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8942:Pm20d1
|
UTSW |
1 |
131,739,785 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9026:Pm20d1
|
UTSW |
1 |
131,739,822 (GRCm39) |
missense |
probably benign |
0.04 |
R9093:Pm20d1
|
UTSW |
1 |
131,743,753 (GRCm39) |
missense |
probably benign |
0.16 |
R9094:Pm20d1
|
UTSW |
1 |
131,730,481 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9165:Pm20d1
|
UTSW |
1 |
131,743,825 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9189:Pm20d1
|
UTSW |
1 |
131,730,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R9562:Pm20d1
|
UTSW |
1 |
131,730,501 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Pm20d1
|
UTSW |
1 |
131,725,296 (GRCm39) |
missense |
possibly damaging |
0.89 |
Z1177:Pm20d1
|
UTSW |
1 |
131,729,006 (GRCm39) |
missense |
probably benign |
0.15 |
|