Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,055,701 (GRCm39) |
K408E |
probably damaging |
Het |
2010315B03Rik |
T |
A |
9: 124,055,783 (GRCm39) |
K380N |
probably damaging |
Het |
9230104M06Rik |
C |
T |
12: 112,964,359 (GRCm39) |
|
probably benign |
Het |
Ahi1 |
T |
A |
10: 20,846,810 (GRCm39) |
C413* |
probably null |
Het |
Alms1 |
T |
A |
6: 85,599,464 (GRCm39) |
M1430K |
possibly damaging |
Het |
Ankrd52 |
G |
T |
10: 128,225,220 (GRCm39) |
A894S |
probably benign |
Het |
Arhgap33 |
C |
A |
7: 30,226,654 (GRCm39) |
V494L |
probably damaging |
Het |
Atic |
G |
T |
1: 71,608,130 (GRCm39) |
V275F |
probably damaging |
Het |
Atoh1 |
T |
A |
6: 64,706,668 (GRCm39) |
V121E |
probably damaging |
Het |
Atp5pd |
T |
A |
11: 115,306,864 (GRCm39) |
|
probably null |
Het |
Baiap2l2 |
A |
T |
15: 79,146,174 (GRCm39) |
|
probably null |
Het |
Brca2 |
A |
T |
5: 150,465,227 (GRCm39) |
T1664S |
probably benign |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Celf3 |
ACAGCAGCAGCAGCAGCAGCAGCA |
ACAGCAGCAGCAGCAGCAGCA |
3: 94,395,537 (GRCm39) |
|
probably benign |
Het |
Cep350 |
A |
T |
1: 155,835,464 (GRCm39) |
|
probably null |
Het |
Ces2g |
T |
C |
8: 105,692,621 (GRCm39) |
|
probably null |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Cyp2d34 |
A |
G |
15: 82,500,368 (GRCm39) |
F457S |
probably damaging |
Het |
Disp3 |
T |
A |
4: 148,325,880 (GRCm39) |
T1293S |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,517,970 (GRCm39) |
I1348F |
possibly damaging |
Het |
Dsp |
A |
T |
13: 38,380,380 (GRCm39) |
H1776L |
probably damaging |
Het |
Efhd1 |
A |
T |
1: 87,237,477 (GRCm39) |
Q228L |
possibly damaging |
Het |
Entpd2 |
T |
A |
2: 25,289,295 (GRCm39) |
I259N |
probably benign |
Het |
Fam149b |
A |
T |
14: 20,425,578 (GRCm39) |
M138L |
probably damaging |
Het |
Fastkd5 |
T |
C |
2: 130,458,285 (GRCm39) |
K102E |
probably benign |
Het |
Fzd7 |
C |
A |
1: 59,523,695 (GRCm39) |
T526K |
possibly damaging |
Het |
G6pd2 |
T |
A |
5: 61,966,330 (GRCm39) |
I35N |
probably damaging |
Het |
Gars1 |
T |
A |
6: 55,042,548 (GRCm39) |
M427K |
probably damaging |
Het |
Gimap4 |
C |
T |
6: 48,667,799 (GRCm39) |
R57C |
probably damaging |
Het |
Gm11232 |
C |
A |
4: 71,676,022 (GRCm39) |
W41L |
probably benign |
Het |
Gm15737 |
T |
A |
6: 92,856,701 (GRCm39) |
C43* |
probably null |
Het |
Gpr180 |
T |
C |
14: 118,377,185 (GRCm39) |
V62A |
probably benign |
Het |
H2-M11 |
C |
T |
17: 36,859,042 (GRCm39) |
T194I |
possibly damaging |
Het |
Jakmip3 |
A |
T |
7: 138,591,197 (GRCm39) |
E27V |
possibly damaging |
Het |
Kcnq3 |
T |
C |
15: 65,903,276 (GRCm39) |
T145A |
probably damaging |
Het |
Krt8 |
A |
G |
15: 101,906,459 (GRCm39) |
M350T |
probably benign |
Het |
Krtap4-9 |
T |
A |
11: 99,676,492 (GRCm39) |
|
probably benign |
Het |
Lbr |
G |
T |
1: 181,663,692 (GRCm39) |
D109E |
probably damaging |
Het |
Ldc1 |
A |
T |
4: 130,103,681 (GRCm39) |
L420Q |
probably benign |
Het |
Med23 |
A |
G |
10: 24,764,473 (GRCm39) |
H42R |
probably damaging |
Het |
Mgat5 |
A |
T |
1: 127,234,741 (GRCm39) |
M77L |
probably benign |
Het |
Mlf1 |
A |
T |
3: 67,291,919 (GRCm39) |
N28I |
possibly damaging |
Het |
Mroh3 |
A |
C |
1: 136,125,864 (GRCm39) |
L343R |
probably damaging |
Het |
Mrpl37 |
T |
A |
4: 106,921,690 (GRCm39) |
I180F |
possibly damaging |
Het |
Mrps27 |
T |
A |
13: 99,536,836 (GRCm39) |
C116* |
probably null |
Het |
Muc6 |
A |
G |
7: 141,226,651 (GRCm39) |
S1354P |
possibly damaging |
Het |
Myh7 |
A |
T |
14: 55,220,699 (GRCm39) |
D1033E |
probably damaging |
Het |
Myo16 |
A |
T |
8: 10,644,820 (GRCm39) |
E1717D |
probably benign |
Het |
Myo1g |
T |
A |
11: 6,462,539 (GRCm39) |
|
probably null |
Het |
Or51ag1 |
A |
G |
7: 103,155,367 (GRCm39) |
M262T |
probably benign |
Het |
Or6c217 |
A |
C |
10: 129,737,964 (GRCm39) |
L205R |
probably damaging |
Het |
Parp8 |
A |
G |
13: 117,032,223 (GRCm39) |
S278P |
possibly damaging |
Het |
Pdk2 |
A |
G |
11: 94,918,028 (GRCm39) |
|
probably null |
Het |
Phf1 |
T |
C |
17: 27,156,062 (GRCm39) |
S450P |
probably damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,746,233 (GRCm39) |
Y1919C |
probably damaging |
Het |
Postn |
T |
A |
3: 54,284,374 (GRCm39) |
S614T |
probably damaging |
Het |
Psmg1 |
A |
T |
16: 95,783,395 (GRCm39) |
Y213* |
probably null |
Het |
Rab11b |
T |
A |
17: 33,966,692 (GRCm39) |
T203S |
probably benign |
Het |
Rad54l2 |
T |
A |
9: 106,580,825 (GRCm39) |
T899S |
possibly damaging |
Het |
Ramp2 |
TTGCTGCTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTG |
11: 101,137,371 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
A |
G |
11: 54,578,537 (GRCm39) |
T1028A |
possibly damaging |
Het |
Rbm6 |
A |
G |
9: 107,669,197 (GRCm39) |
S58P |
possibly damaging |
Het |
Rreb1 |
G |
T |
13: 38,113,768 (GRCm39) |
A376S |
possibly damaging |
Het |
Rsbn1l |
T |
A |
5: 21,124,767 (GRCm39) |
N345I |
probably benign |
Het |
Sf3b2 |
A |
T |
19: 5,325,118 (GRCm39) |
S785T |
possibly damaging |
Het |
Sh2b1 |
C |
T |
7: 126,068,098 (GRCm39) |
D519N |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,987,704 (GRCm39) |
T668A |
probably benign |
Het |
Stkld1 |
T |
A |
2: 26,840,650 (GRCm39) |
I444N |
probably damaging |
Het |
Sucla2 |
A |
T |
14: 73,790,244 (GRCm39) |
|
probably benign |
Het |
Tmem67 |
T |
A |
4: 12,079,918 (GRCm39) |
L190F |
probably damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trem2 |
G |
A |
17: 48,658,863 (GRCm39) |
W191* |
probably null |
Het |
Ube2d4 |
A |
T |
15: 58,718,528 (GRCm39) |
|
noncoding transcript |
Het |
Uimc1 |
G |
T |
13: 55,223,617 (GRCm39) |
D218E |
probably damaging |
Het |
Wdr62 |
A |
T |
7: 29,973,424 (GRCm39) |
V95E |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,310,203 (GRCm39) |
V862A |
probably damaging |
Het |
Zfp462 |
T |
A |
4: 55,008,522 (GRCm39) |
S163T |
probably benign |
Het |
Zfp704 |
T |
C |
3: 9,674,553 (GRCm39) |
D76G |
unknown |
Het |
|
Other mutations in Pan2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00164:Pan2
|
APN |
10 |
128,148,795 (GRCm39) |
nonsense |
probably null |
|
IGL02183:Pan2
|
APN |
10 |
128,144,944 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02219:Pan2
|
APN |
10 |
128,156,221 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02514:Pan2
|
APN |
10 |
128,146,610 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02552:Pan2
|
APN |
10 |
128,154,896 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Pan2
|
APN |
10 |
128,148,768 (GRCm39) |
missense |
probably benign |
|
IGL02860:Pan2
|
APN |
10 |
128,146,604 (GRCm39) |
nonsense |
probably null |
|
IGL03104:Pan2
|
APN |
10 |
128,151,532 (GRCm39) |
splice site |
probably benign |
|
IGL03372:Pan2
|
APN |
10 |
128,150,996 (GRCm39) |
missense |
probably benign |
0.09 |
R0541:Pan2
|
UTSW |
10 |
128,144,091 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0585:Pan2
|
UTSW |
10 |
128,146,384 (GRCm39) |
critical splice donor site |
probably null |
|
R1079:Pan2
|
UTSW |
10 |
128,154,107 (GRCm39) |
missense |
probably damaging |
0.99 |
R1650:Pan2
|
UTSW |
10 |
128,153,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R1847:Pan2
|
UTSW |
10 |
128,140,247 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1867:Pan2
|
UTSW |
10 |
128,149,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Pan2
|
UTSW |
10 |
128,144,237 (GRCm39) |
missense |
probably damaging |
0.98 |
R1975:Pan2
|
UTSW |
10 |
128,156,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R1976:Pan2
|
UTSW |
10 |
128,156,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R1977:Pan2
|
UTSW |
10 |
128,156,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R2136:Pan2
|
UTSW |
10 |
128,149,506 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2162:Pan2
|
UTSW |
10 |
128,140,091 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2512:Pan2
|
UTSW |
10 |
128,140,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R2900:Pan2
|
UTSW |
10 |
128,144,211 (GRCm39) |
missense |
probably benign |
|
R3957:Pan2
|
UTSW |
10 |
128,151,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R4571:Pan2
|
UTSW |
10 |
128,144,512 (GRCm39) |
missense |
probably benign |
0.05 |
R5112:Pan2
|
UTSW |
10 |
128,151,464 (GRCm39) |
nonsense |
probably null |
|
R5120:Pan2
|
UTSW |
10 |
128,150,864 (GRCm39) |
critical splice donor site |
probably null |
|
R5183:Pan2
|
UTSW |
10 |
128,153,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R5325:Pan2
|
UTSW |
10 |
128,153,503 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5539:Pan2
|
UTSW |
10 |
128,144,002 (GRCm39) |
missense |
probably benign |
0.16 |
R5642:Pan2
|
UTSW |
10 |
128,143,969 (GRCm39) |
missense |
probably benign |
0.00 |
R5740:Pan2
|
UTSW |
10 |
128,144,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R5822:Pan2
|
UTSW |
10 |
128,156,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R6766:Pan2
|
UTSW |
10 |
128,150,381 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6902:Pan2
|
UTSW |
10 |
128,151,506 (GRCm39) |
missense |
probably benign |
0.33 |
R6946:Pan2
|
UTSW |
10 |
128,151,506 (GRCm39) |
missense |
probably benign |
0.33 |
R7206:Pan2
|
UTSW |
10 |
128,150,414 (GRCm39) |
nonsense |
probably null |
|
R7490:Pan2
|
UTSW |
10 |
128,144,309 (GRCm39) |
missense |
probably benign |
0.00 |
R7715:Pan2
|
UTSW |
10 |
128,153,592 (GRCm39) |
missense |
probably benign |
0.00 |
R7794:Pan2
|
UTSW |
10 |
128,152,396 (GRCm39) |
splice site |
probably null |
|
R8286:Pan2
|
UTSW |
10 |
128,154,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R9038:Pan2
|
UTSW |
10 |
128,153,810 (GRCm39) |
nonsense |
probably null |
|
R9057:Pan2
|
UTSW |
10 |
128,156,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R9072:Pan2
|
UTSW |
10 |
128,151,050 (GRCm39) |
missense |
probably damaging |
0.98 |
R9073:Pan2
|
UTSW |
10 |
128,151,050 (GRCm39) |
missense |
probably damaging |
0.98 |
R9077:Pan2
|
UTSW |
10 |
128,148,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Pan2
|
UTSW |
10 |
128,140,135 (GRCm39) |
missense |
probably benign |
|
R9787:Pan2
|
UTSW |
10 |
128,144,223 (GRCm39) |
missense |
probably benign |
0.05 |
RF005:Pan2
|
UTSW |
10 |
128,151,404 (GRCm39) |
missense |
probably benign |
0.00 |
RF024:Pan2
|
UTSW |
10 |
128,151,404 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Pan2
|
UTSW |
10 |
128,150,368 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Pan2
|
UTSW |
10 |
128,140,279 (GRCm39) |
missense |
possibly damaging |
0.94 |
|