Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
C |
3: 121,932,179 (GRCm39) |
S278P |
possibly damaging |
Het |
Adam11 |
A |
G |
11: 102,663,665 (GRCm39) |
Y281C |
probably damaging |
Het |
Adam6a |
G |
T |
12: 113,507,849 (GRCm39) |
R74L |
possibly damaging |
Het |
Adcy5 |
T |
C |
16: 35,091,368 (GRCm39) |
|
probably null |
Het |
Adrb2 |
A |
G |
18: 62,312,090 (GRCm39) |
L245P |
probably benign |
Het |
Aebp2 |
T |
C |
6: 140,589,800 (GRCm39) |
|
probably null |
Het |
Arhgap23 |
A |
G |
11: 97,343,070 (GRCm39) |
T240A |
probably benign |
Het |
Atp10a |
T |
C |
7: 58,423,794 (GRCm39) |
|
probably benign |
Het |
Atp13a4 |
T |
A |
16: 29,274,213 (GRCm39) |
Y416F |
probably damaging |
Het |
Atp5mc2 |
A |
C |
15: 102,571,492 (GRCm39) |
L133R |
probably damaging |
Het |
Bicral |
A |
T |
17: 47,136,233 (GRCm39) |
Y326N |
probably damaging |
Het |
Chst4 |
T |
C |
8: 110,757,297 (GRCm39) |
S189G |
probably damaging |
Het |
Cnot1 |
A |
T |
8: 96,489,772 (GRCm39) |
I477N |
probably damaging |
Het |
Col7a1 |
G |
T |
9: 108,796,574 (GRCm39) |
|
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,415,301 (GRCm39) |
|
probably benign |
Het |
Dcn |
A |
G |
10: 97,342,551 (GRCm39) |
N169S |
probably benign |
Het |
Dnajc6 |
T |
C |
4: 101,473,974 (GRCm39) |
|
probably benign |
Het |
Egln3 |
A |
G |
12: 54,228,432 (GRCm39) |
F225L |
probably benign |
Het |
Erap1 |
G |
A |
13: 74,816,171 (GRCm39) |
R100Q |
possibly damaging |
Het |
Erc2 |
A |
T |
14: 27,498,781 (GRCm39) |
|
probably null |
Het |
Fto |
G |
A |
8: 92,168,435 (GRCm39) |
|
probably null |
Het |
Gdap1l1 |
C |
T |
2: 163,288,011 (GRCm39) |
P80S |
probably damaging |
Het |
Gm1123 |
T |
C |
9: 98,905,405 (GRCm39) |
E35G |
possibly damaging |
Het |
Hhipl1 |
A |
G |
12: 108,288,156 (GRCm39) |
|
probably benign |
Het |
Ift80 |
A |
T |
3: 68,822,008 (GRCm39) |
L679Q |
probably damaging |
Het |
Il18 |
A |
G |
9: 50,488,013 (GRCm39) |
|
probably benign |
Het |
Inhbb |
T |
C |
1: 119,345,125 (GRCm39) |
Y388C |
probably damaging |
Het |
Kmt2d |
G |
T |
15: 98,742,360 (GRCm39) |
|
probably benign |
Het |
Krt20 |
A |
G |
11: 99,328,640 (GRCm39) |
V95A |
probably damaging |
Het |
Lck |
A |
T |
4: 129,449,474 (GRCm39) |
S274R |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,376,848 (GRCm39) |
N4243I |
probably damaging |
Het |
Lrrfip2 |
G |
A |
9: 111,043,311 (GRCm39) |
V506I |
probably damaging |
Het |
Ltbp2 |
A |
G |
12: 84,840,507 (GRCm39) |
C1000R |
probably damaging |
Het |
Matn3 |
G |
A |
12: 9,002,105 (GRCm39) |
D106N |
probably damaging |
Het |
Mical2 |
A |
G |
7: 111,980,503 (GRCm39) |
E49G |
probably benign |
Het |
Mmadhc |
A |
G |
2: 50,182,869 (GRCm39) |
S36P |
probably damaging |
Het |
Morn1 |
T |
C |
4: 155,229,629 (GRCm39) |
Y433H |
probably damaging |
Het |
Mpo |
A |
G |
11: 87,692,436 (GRCm39) |
M525V |
probably benign |
Het |
Myo5a |
C |
T |
9: 75,068,774 (GRCm39) |
R659C |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,568,364 (GRCm39) |
S171G |
probably benign |
Het |
Or1j18 |
A |
G |
2: 36,624,917 (GRCm39) |
N195D |
probably damaging |
Het |
Or4k36 |
T |
A |
2: 111,146,518 (GRCm39) |
D231E |
probably benign |
Het |
Or5g29 |
A |
T |
2: 85,421,696 (GRCm39) |
N271Y |
probably benign |
Het |
P2ry14 |
A |
G |
3: 59,023,314 (GRCm39) |
Y49H |
probably benign |
Het |
Papss2 |
C |
T |
19: 32,611,302 (GRCm39) |
T17I |
possibly damaging |
Het |
Pcid2 |
T |
C |
8: 13,135,392 (GRCm39) |
T206A |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,022,844 (GRCm39) |
E140G |
probably damaging |
Het |
Prdx2 |
T |
G |
8: 85,698,330 (GRCm39) |
|
probably benign |
Het |
Ptbp2 |
A |
T |
3: 119,514,310 (GRCm39) |
L471Q |
probably damaging |
Het |
Rbm33 |
T |
A |
5: 28,557,604 (GRCm39) |
D232E |
possibly damaging |
Het |
Rnf214 |
T |
A |
9: 45,809,791 (GRCm39) |
|
probably null |
Het |
Rora |
G |
A |
9: 69,281,330 (GRCm39) |
R314H |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,168,095 (GRCm39) |
|
probably benign |
Het |
Sag |
T |
C |
1: 87,742,402 (GRCm39) |
V58A |
probably damaging |
Het |
Serpina3i |
C |
T |
12: 104,231,423 (GRCm39) |
T20M |
probably damaging |
Het |
Slc4a5 |
A |
G |
6: 83,254,537 (GRCm39) |
N578S |
probably benign |
Het |
Soat2 |
A |
G |
15: 102,066,574 (GRCm39) |
Y285C |
probably damaging |
Het |
Syk |
A |
G |
13: 52,794,769 (GRCm39) |
Y478C |
probably damaging |
Het |
Syne4 |
G |
A |
7: 30,018,344 (GRCm39) |
G362E |
probably damaging |
Het |
Tas2r126 |
A |
T |
6: 42,412,036 (GRCm39) |
M190L |
probably benign |
Het |
Tnfrsf21 |
C |
T |
17: 43,349,104 (GRCm39) |
H239Y |
probably benign |
Het |
Ttc19 |
A |
G |
11: 62,199,910 (GRCm39) |
D218G |
probably damaging |
Het |
Tut1 |
T |
C |
19: 8,942,800 (GRCm39) |
V629A |
probably damaging |
Het |
Txndc11 |
T |
C |
16: 10,905,968 (GRCm39) |
N521D |
probably benign |
Het |
Ushbp1 |
T |
C |
8: 71,841,614 (GRCm39) |
E405G |
possibly damaging |
Het |
Usp46 |
C |
T |
5: 74,163,918 (GRCm39) |
R246Q |
probably benign |
Het |
Utrn |
T |
C |
10: 12,610,948 (GRCm39) |
D469G |
probably damaging |
Het |
Vmn2r104 |
T |
A |
17: 20,262,075 (GRCm39) |
I352F |
possibly damaging |
Het |
Wdr4 |
G |
A |
17: 31,715,890 (GRCm39) |
T398I |
probably benign |
Het |
Ythdc1 |
T |
A |
5: 86,968,560 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ppp1r3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Ppp1r3b
|
APN |
8 |
35,851,476 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01417:Ppp1r3b
|
APN |
8 |
35,851,566 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01526:Ppp1r3b
|
APN |
8 |
35,851,872 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02286:Ppp1r3b
|
APN |
8 |
35,851,515 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02429:Ppp1r3b
|
APN |
8 |
35,851,769 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03371:Ppp1r3b
|
APN |
8 |
35,851,403 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0234:Ppp1r3b
|
UTSW |
8 |
35,851,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R0234:Ppp1r3b
|
UTSW |
8 |
35,851,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R0512:Ppp1r3b
|
UTSW |
8 |
35,851,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R2212:Ppp1r3b
|
UTSW |
8 |
35,851,379 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6008:Ppp1r3b
|
UTSW |
8 |
35,851,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Ppp1r3b
|
UTSW |
8 |
35,851,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R7873:Ppp1r3b
|
UTSW |
8 |
35,851,329 (GRCm39) |
missense |
probably benign |
0.01 |
R8832:Ppp1r3b
|
UTSW |
8 |
35,851,419 (GRCm39) |
missense |
probably damaging |
0.98 |
|