Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522H14Rik |
T |
A |
4: 109,381,520 (GRCm39) |
Q86L |
probably null |
Het |
Abhd2 |
A |
G |
7: 79,000,561 (GRCm39) |
D262G |
possibly damaging |
Het |
Abhd5 |
T |
C |
9: 122,197,211 (GRCm39) |
F133L |
possibly damaging |
Het |
Ankrd12 |
T |
C |
17: 66,292,676 (GRCm39) |
K919R |
probably damaging |
Het |
Ap1m1 |
T |
C |
8: 73,006,738 (GRCm39) |
S245P |
probably benign |
Het |
Ap1m1 |
T |
C |
8: 73,010,568 (GRCm39) |
|
probably benign |
Het |
Apcdd1 |
A |
G |
18: 63,070,168 (GRCm39) |
Y145C |
possibly damaging |
Het |
Apob |
A |
T |
12: 8,060,136 (GRCm39) |
N2840Y |
probably damaging |
Het |
Arel1 |
A |
G |
12: 84,981,027 (GRCm39) |
S327P |
probably damaging |
Het |
Arhgap21 |
C |
A |
2: 20,885,944 (GRCm39) |
R421L |
probably damaging |
Het |
Ccdc85a |
A |
T |
11: 28,533,400 (GRCm39) |
I48N |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,856,244 (GRCm39) |
S672P |
probably damaging |
Het |
Ciz1 |
G |
C |
2: 32,267,375 (GRCm39) |
|
probably null |
Het |
Cmbl |
G |
A |
15: 31,585,588 (GRCm39) |
|
probably null |
Het |
Cmya5 |
A |
G |
13: 93,231,377 (GRCm39) |
V1237A |
possibly damaging |
Het |
Cntnap4 |
A |
T |
8: 113,583,143 (GRCm39) |
K1074* |
probably null |
Het |
Cntnap5b |
A |
G |
1: 100,202,193 (GRCm39) |
M347V |
probably benign |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cuzd1 |
A |
T |
7: 130,917,991 (GRCm39) |
M203K |
probably benign |
Het |
Cyp3a16 |
T |
C |
5: 145,392,689 (GRCm39) |
|
probably benign |
Het |
Dlgap3 |
A |
G |
4: 127,129,314 (GRCm39) |
E892G |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,275,948 (GRCm39) |
S2612P |
probably damaging |
Het |
Epas1 |
T |
G |
17: 87,113,276 (GRCm39) |
|
probably benign |
Het |
Etv5 |
G |
A |
16: 22,230,458 (GRCm39) |
A192V |
probably benign |
Het |
Fa2h |
T |
A |
8: 112,075,921 (GRCm39) |
H234L |
probably damaging |
Het |
Fcho1 |
T |
C |
8: 72,170,134 (GRCm39) |
Y47C |
probably damaging |
Het |
Flvcr1 |
T |
A |
1: 190,744,451 (GRCm39) |
|
probably benign |
Het |
Il1rl1 |
CTTGTTGTTGTTGTTGTTG |
CTTGTTGTTGTTGTTGTTGTTG |
1: 40,481,734 (GRCm39) |
|
probably benign |
Het |
Ino80 |
G |
A |
2: 119,213,441 (GRCm39) |
R1249C |
probably damaging |
Het |
Inpp4b |
T |
C |
8: 82,610,886 (GRCm39) |
|
probably benign |
Het |
Isy1 |
G |
A |
6: 87,796,167 (GRCm39) |
R257W |
probably damaging |
Het |
Kmt2a |
A |
G |
9: 44,721,010 (GRCm39) |
|
probably null |
Het |
Krt4 |
G |
A |
15: 101,833,081 (GRCm39) |
R9C |
possibly damaging |
Het |
Map1a |
T |
C |
2: 121,132,525 (GRCm39) |
S876P |
probably damaging |
Het |
Mettl21e |
A |
G |
1: 44,250,190 (GRCm39) |
|
probably null |
Het |
Msh2 |
C |
T |
17: 88,024,904 (GRCm39) |
T594M |
probably benign |
Het |
Mtmr3 |
A |
G |
11: 4,437,536 (GRCm39) |
S973P |
probably damaging |
Het |
Muc5ac |
A |
T |
7: 141,354,697 (GRCm39) |
M889L |
probably benign |
Het |
Ntn1 |
A |
G |
11: 68,276,369 (GRCm39) |
I193T |
probably benign |
Het |
Nudt13 |
A |
T |
14: 20,359,851 (GRCm39) |
I193F |
probably damaging |
Het |
Or2n1 |
A |
G |
17: 38,486,338 (GRCm39) |
D121G |
probably damaging |
Het |
Or3a1 |
C |
T |
11: 74,225,925 (GRCm39) |
G44D |
probably damaging |
Het |
Or4b1b |
A |
T |
2: 90,112,200 (GRCm39) |
S240T |
probably damaging |
Het |
Or5p73 |
A |
T |
7: 108,064,941 (GRCm39) |
T137S |
possibly damaging |
Het |
Otulin |
A |
G |
15: 27,606,381 (GRCm39) |
V344A |
probably damaging |
Het |
P2rx7 |
C |
T |
5: 122,795,093 (GRCm39) |
Q128* |
probably null |
Het |
Pcdhb22 |
G |
A |
18: 37,652,213 (GRCm39) |
R227H |
probably benign |
Het |
Plekha5 |
G |
A |
6: 140,537,473 (GRCm39) |
R646K |
possibly damaging |
Het |
Pltp |
C |
T |
2: 164,682,056 (GRCm39) |
R394H |
probably benign |
Het |
Ppip5k1 |
C |
G |
2: 121,177,836 (GRCm39) |
A324P |
probably damaging |
Het |
Pramel14 |
C |
T |
4: 143,718,221 (GRCm39) |
M407I |
probably benign |
Het |
Prdm13 |
A |
C |
4: 21,679,737 (GRCm39) |
V251G |
unknown |
Het |
Prkg1 |
T |
C |
19: 31,641,596 (GRCm39) |
E29G |
probably damaging |
Het |
Prrc2c |
A |
G |
1: 162,525,380 (GRCm39) |
S409P |
unknown |
Het |
Rp1 |
T |
A |
1: 4,417,941 (GRCm39) |
D1057V |
probably damaging |
Het |
Rttn |
G |
A |
18: 89,029,079 (GRCm39) |
C599Y |
probably damaging |
Het |
Shisa6 |
C |
T |
11: 66,416,153 (GRCm39) |
R213Q |
probably benign |
Het |
Slc3a1 |
T |
C |
17: 85,340,273 (GRCm39) |
Y232H |
probably damaging |
Het |
Slx4 |
G |
A |
16: 3,797,953 (GRCm39) |
A1477V |
probably damaging |
Het |
Ssrp1 |
T |
G |
2: 84,871,018 (GRCm39) |
I218S |
probably damaging |
Het |
St6galnac1 |
A |
C |
11: 116,659,756 (GRCm39) |
S186A |
probably benign |
Het |
Stab1 |
A |
G |
14: 30,880,965 (GRCm39) |
|
probably benign |
Het |
Sycp2 |
T |
C |
2: 177,988,204 (GRCm39) |
|
probably benign |
Het |
Syne2 |
T |
A |
12: 76,118,981 (GRCm39) |
I5867N |
probably damaging |
Het |
Taar7f |
T |
A |
10: 23,925,839 (GRCm39) |
D144E |
probably damaging |
Het |
Tlcd5 |
A |
T |
9: 43,023,048 (GRCm39) |
M84K |
probably damaging |
Het |
Tmem87b |
T |
A |
2: 128,673,153 (GRCm39) |
S196T |
probably damaging |
Het |
Tnfrsf21 |
A |
G |
17: 43,348,768 (GRCm39) |
T127A |
probably benign |
Het |
Trp73 |
A |
G |
4: 154,148,406 (GRCm39) |
I336T |
probably benign |
Het |
Ttl |
A |
G |
2: 128,917,981 (GRCm39) |
I148V |
probably damaging |
Het |
Ttll7 |
T |
C |
3: 146,649,970 (GRCm39) |
Y667H |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,119,171 (GRCm39) |
T152A |
probably damaging |
Het |
Vmn1r58 |
A |
T |
7: 5,413,636 (GRCm39) |
V198E |
probably damaging |
Het |
Vps52 |
T |
A |
17: 34,181,091 (GRCm39) |
F376L |
probably benign |
Het |
Zfp1007 |
T |
C |
5: 109,824,754 (GRCm39) |
E232G |
probably benign |
Het |
|
Other mutations in Agap2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01385:Agap2
|
APN |
10 |
126,923,865 (GRCm39) |
missense |
unknown |
|
IGL01690:Agap2
|
APN |
10 |
126,918,827 (GRCm39) |
splice site |
probably benign |
|
IGL01765:Agap2
|
APN |
10 |
126,919,104 (GRCm39) |
missense |
unknown |
|
IGL02029:Agap2
|
APN |
10 |
126,916,152 (GRCm39) |
missense |
unknown |
|
IGL02525:Agap2
|
APN |
10 |
126,919,070 (GRCm39) |
splice site |
probably null |
|
IGL03019:Agap2
|
APN |
10 |
126,927,431 (GRCm39) |
splice site |
probably benign |
|
R0086:Agap2
|
UTSW |
10 |
126,923,751 (GRCm39) |
splice site |
probably null |
|
R0197:Agap2
|
UTSW |
10 |
126,927,571 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0345:Agap2
|
UTSW |
10 |
126,923,764 (GRCm39) |
missense |
unknown |
|
R0682:Agap2
|
UTSW |
10 |
126,919,351 (GRCm39) |
missense |
unknown |
|
R0787:Agap2
|
UTSW |
10 |
126,921,019 (GRCm39) |
missense |
unknown |
|
R0882:Agap2
|
UTSW |
10 |
126,923,319 (GRCm39) |
missense |
unknown |
|
R0883:Agap2
|
UTSW |
10 |
126,927,571 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1445:Agap2
|
UTSW |
10 |
126,926,981 (GRCm39) |
splice site |
probably benign |
|
R1800:Agap2
|
UTSW |
10 |
126,927,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1854:Agap2
|
UTSW |
10 |
126,916,385 (GRCm39) |
missense |
unknown |
|
R1925:Agap2
|
UTSW |
10 |
126,926,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Agap2
|
UTSW |
10 |
126,918,913 (GRCm39) |
nonsense |
probably null |
|
R2050:Agap2
|
UTSW |
10 |
126,916,130 (GRCm39) |
nonsense |
probably null |
|
R2267:Agap2
|
UTSW |
10 |
126,918,297 (GRCm39) |
splice site |
probably benign |
|
R2269:Agap2
|
UTSW |
10 |
126,918,297 (GRCm39) |
splice site |
probably benign |
|
R4174:Agap2
|
UTSW |
10 |
126,926,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R4397:Agap2
|
UTSW |
10 |
126,926,352 (GRCm39) |
missense |
unknown |
|
R4418:Agap2
|
UTSW |
10 |
126,927,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R4472:Agap2
|
UTSW |
10 |
126,927,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Agap2
|
UTSW |
10 |
126,915,965 (GRCm39) |
missense |
unknown |
|
R4690:Agap2
|
UTSW |
10 |
126,927,244 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4744:Agap2
|
UTSW |
10 |
126,926,072 (GRCm39) |
critical splice donor site |
probably null |
|
R5316:Agap2
|
UTSW |
10 |
126,918,296 (GRCm39) |
splice site |
probably null |
|
R5533:Agap2
|
UTSW |
10 |
126,918,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R5680:Agap2
|
UTSW |
10 |
126,923,880 (GRCm39) |
missense |
unknown |
|
R6010:Agap2
|
UTSW |
10 |
126,926,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Agap2
|
UTSW |
10 |
126,925,229 (GRCm39) |
critical splice donor site |
probably null |
|
R6356:Agap2
|
UTSW |
10 |
126,918,865 (GRCm39) |
missense |
unknown |
|
R7138:Agap2
|
UTSW |
10 |
126,923,154 (GRCm39) |
missense |
unknown |
|
R7154:Agap2
|
UTSW |
10 |
126,927,524 (GRCm39) |
missense |
probably benign |
0.34 |
R7497:Agap2
|
UTSW |
10 |
126,926,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R7718:Agap2
|
UTSW |
10 |
126,915,734 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7720:Agap2
|
UTSW |
10 |
126,926,957 (GRCm39) |
missense |
probably damaging |
0.96 |
R7893:Agap2
|
UTSW |
10 |
126,916,064 (GRCm39) |
missense |
unknown |
|
R7933:Agap2
|
UTSW |
10 |
126,922,789 (GRCm39) |
splice site |
probably benign |
|
R8337:Agap2
|
UTSW |
10 |
126,924,194 (GRCm39) |
missense |
unknown |
|
R8372:Agap2
|
UTSW |
10 |
126,925,185 (GRCm39) |
missense |
unknown |
|
R8428:Agap2
|
UTSW |
10 |
126,923,175 (GRCm39) |
missense |
unknown |
|
R8861:Agap2
|
UTSW |
10 |
126,926,383 (GRCm39) |
missense |
unknown |
|
R9082:Agap2
|
UTSW |
10 |
126,918,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9341:Agap2
|
UTSW |
10 |
126,927,559 (GRCm39) |
missense |
unknown |
|
R9354:Agap2
|
UTSW |
10 |
126,923,104 (GRCm39) |
missense |
unknown |
|
R9650:Agap2
|
UTSW |
10 |
126,927,653 (GRCm39) |
missense |
unknown |
|
R9745:Agap2
|
UTSW |
10 |
126,919,380 (GRCm39) |
missense |
unknown |
|
Z1088:Agap2
|
UTSW |
10 |
126,924,111 (GRCm39) |
missense |
unknown |
|
Z1176:Agap2
|
UTSW |
10 |
126,916,094 (GRCm39) |
missense |
unknown |
|
|