Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730480H06Rik |
C |
A |
5: 48,531,777 (GRCm39) |
T35K |
probably benign |
Het |
Abhd14a |
A |
G |
9: 106,317,446 (GRCm39) |
|
probably benign |
Het |
Abhd8 |
A |
G |
8: 71,914,506 (GRCm39) |
F41L |
possibly damaging |
Het |
Ace2 |
A |
T |
X: 162,939,524 (GRCm39) |
M123L |
possibly damaging |
Het |
Actr5 |
T |
C |
2: 158,477,949 (GRCm39) |
Y440H |
possibly damaging |
Het |
Akr1c6 |
T |
A |
13: 4,496,383 (GRCm39) |
N81K |
probably benign |
Het |
Aqp11 |
T |
A |
7: 97,386,725 (GRCm39) |
N157I |
possibly damaging |
Het |
Arhgap10 |
T |
C |
8: 78,071,282 (GRCm39) |
E568G |
probably damaging |
Het |
Asb7 |
T |
A |
7: 66,329,001 (GRCm39) |
Q13L |
probably benign |
Het |
Atf7ip |
C |
A |
6: 136,537,778 (GRCm39) |
A345E |
probably benign |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Bpifb4 |
A |
T |
2: 153,785,996 (GRCm39) |
I259F |
probably damaging |
Het |
Cand1 |
A |
T |
10: 119,038,925 (GRCm39) |
D1218E |
probably damaging |
Het |
Capg |
A |
G |
6: 72,535,236 (GRCm39) |
|
probably null |
Het |
Cep290 |
C |
T |
10: 100,333,815 (GRCm39) |
T289M |
possibly damaging |
Het |
Cfap69 |
T |
C |
5: 5,643,818 (GRCm39) |
Y548C |
probably damaging |
Het |
Cfap97d1 |
A |
T |
11: 101,877,989 (GRCm39) |
H17L |
probably damaging |
Het |
Cimip2b |
T |
A |
4: 43,427,586 (GRCm39) |
K220N |
probably damaging |
Het |
Clock |
A |
G |
5: 76,377,340 (GRCm39) |
L652P |
probably damaging |
Het |
Col3a1 |
C |
T |
1: 45,373,453 (GRCm39) |
|
probably benign |
Het |
Coro7 |
T |
C |
16: 4,446,596 (GRCm39) |
E843G |
probably benign |
Het |
Crebrf |
T |
C |
17: 26,961,442 (GRCm39) |
S188P |
probably damaging |
Het |
Crppa |
G |
A |
12: 36,440,367 (GRCm39) |
V92I |
probably benign |
Het |
Cul1 |
T |
C |
6: 47,485,289 (GRCm39) |
F307L |
probably benign |
Het |
Cyb561d2 |
G |
A |
9: 107,417,515 (GRCm39) |
R79W |
probably damaging |
Het |
Cyp3a59 |
T |
C |
5: 146,031,187 (GRCm39) |
S117P |
possibly damaging |
Het |
Ddias |
A |
G |
7: 92,507,830 (GRCm39) |
I695T |
probably benign |
Het |
Dhx29 |
G |
A |
13: 113,101,864 (GRCm39) |
G1311D |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,139,159 (GRCm39) |
|
probably null |
Het |
Ece2 |
T |
A |
16: 20,436,616 (GRCm39) |
V146E |
probably damaging |
Het |
Eml2 |
A |
G |
7: 18,937,889 (GRCm39) |
K586E |
possibly damaging |
Het |
Eps8l3 |
A |
G |
3: 107,791,708 (GRCm39) |
E316G |
probably benign |
Het |
Fam135b |
A |
T |
15: 71,493,863 (GRCm39) |
L22H |
probably damaging |
Het |
Focad |
T |
A |
4: 88,319,318 (GRCm39) |
M1K |
probably null |
Het |
Fryl |
A |
G |
5: 73,290,710 (GRCm39) |
S65P |
probably damaging |
Het |
Gm14190 |
C |
T |
11: 99,581,556 (GRCm39) |
C4Y |
unknown |
Het |
H2-T5 |
T |
A |
17: 36,478,899 (GRCm39) |
T117S |
probably damaging |
Het |
Ift74 |
T |
A |
4: 94,550,883 (GRCm39) |
M345K |
probably benign |
Het |
Jag1 |
C |
G |
2: 136,925,393 (GRCm39) |
V1070L |
possibly damaging |
Het |
Kcng1 |
T |
C |
2: 168,104,941 (GRCm39) |
T302A |
probably benign |
Het |
Kif20b |
T |
C |
19: 34,930,278 (GRCm39) |
V1221A |
possibly damaging |
Het |
Kif23 |
A |
T |
9: 61,853,892 (GRCm39) |
|
probably null |
Het |
Meiob |
A |
G |
17: 25,037,305 (GRCm39) |
H61R |
probably benign |
Het |
Mfhas1 |
C |
T |
8: 36,056,799 (GRCm39) |
L425F |
probably damaging |
Het |
Myo3a |
A |
T |
2: 22,401,126 (GRCm39) |
S632C |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,298,362 (GRCm39) |
E558G |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,307,100 (GRCm39) |
Y374* |
probably null |
Het |
Notch3 |
T |
C |
17: 32,372,826 (GRCm39) |
S582G |
probably benign |
Het |
Nphs1 |
A |
T |
7: 30,173,798 (GRCm39) |
Q985L |
probably damaging |
Het |
Oas1c |
T |
A |
5: 120,941,049 (GRCm39) |
H248L |
probably benign |
Het |
Or5c1 |
A |
T |
2: 37,221,896 (GRCm39) |
N46Y |
probably damaging |
Het |
Or5g26 |
T |
C |
2: 85,494,341 (GRCm39) |
I146V |
probably benign |
Het |
Or5h25 |
A |
T |
16: 58,930,157 (GRCm39) |
M272K |
probably benign |
Het |
Or8g35 |
A |
G |
9: 39,381,333 (GRCm39) |
S230P |
possibly damaging |
Het |
Pamr1 |
A |
T |
2: 102,472,617 (GRCm39) |
I639F |
possibly damaging |
Het |
Panx1 |
G |
T |
9: 14,918,980 (GRCm39) |
T293K |
possibly damaging |
Het |
Papss1 |
G |
T |
3: 131,305,632 (GRCm39) |
V226F |
probably benign |
Het |
Pax1 |
G |
T |
2: 147,209,809 (GRCm39) |
G301V |
possibly damaging |
Het |
Pdlim5 |
C |
A |
3: 141,950,742 (GRCm39) |
R557L |
possibly damaging |
Het |
Pdyn |
C |
A |
2: 129,531,729 (GRCm39) |
M20I |
probably benign |
Het |
Pelp1 |
G |
A |
11: 70,284,541 (GRCm39) |
|
probably null |
Het |
Pkd2 |
T |
C |
5: 104,626,790 (GRCm39) |
V324A |
probably damaging |
Het |
Pkdrej |
A |
G |
15: 85,703,368 (GRCm39) |
I856T |
probably benign |
Het |
Polr1a |
T |
C |
6: 71,913,536 (GRCm39) |
|
probably null |
Het |
Pot1a |
A |
T |
6: 25,753,323 (GRCm39) |
D404E |
probably benign |
Het |
Ppp2r2a |
A |
T |
14: 67,253,878 (GRCm39) |
I430N |
possibly damaging |
Het |
Prob1 |
C |
T |
18: 35,787,279 (GRCm39) |
R325Q |
possibly damaging |
Het |
Prrc2a |
T |
C |
17: 35,376,884 (GRCm39) |
D742G |
probably damaging |
Het |
Psmc1 |
C |
T |
12: 100,081,102 (GRCm39) |
P54S |
probably benign |
Het |
Rab22a |
A |
G |
2: 173,530,004 (GRCm39) |
T61A |
probably damaging |
Het |
Rims1 |
T |
A |
1: 22,358,754 (GRCm39) |
K184N |
probably damaging |
Het |
Rnf213 |
G |
A |
11: 119,322,511 (GRCm39) |
R1376H |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,683,848 (GRCm39) |
E3072G |
probably damaging |
Het |
Serpina1b |
T |
C |
12: 103,698,420 (GRCm39) |
K143R |
probably benign |
Het |
Slc22a15 |
T |
G |
3: 101,787,505 (GRCm39) |
|
probably null |
Het |
Slc25a14 |
G |
A |
X: 47,740,840 (GRCm39) |
V210I |
probably benign |
Het |
Slc25a48 |
A |
C |
13: 56,596,811 (GRCm39) |
T31P |
probably damaging |
Het |
Slc9a3 |
C |
T |
13: 74,314,175 (GRCm39) |
|
probably null |
Het |
Slx4 |
T |
C |
16: 3,805,030 (GRCm39) |
*105W |
probably null |
Het |
Smc6 |
A |
G |
12: 11,349,399 (GRCm39) |
N794S |
probably benign |
Het |
Spata18 |
G |
A |
5: 73,834,307 (GRCm39) |
R387Q |
probably damaging |
Het |
Sphkap |
C |
A |
1: 83,245,162 (GRCm39) |
E1486* |
probably null |
Het |
Srsf6 |
C |
T |
2: 162,776,403 (GRCm39) |
|
probably benign |
Het |
St8sia1 |
C |
T |
6: 142,909,398 (GRCm39) |
A33T |
probably damaging |
Het |
Tet2 |
T |
C |
3: 133,194,399 (GRCm39) |
T12A |
possibly damaging |
Het |
Tmem144 |
G |
T |
3: 79,732,611 (GRCm39) |
S222R |
probably damaging |
Het |
Tnrc6c |
A |
G |
11: 117,646,849 (GRCm39) |
D1450G |
possibly damaging |
Het |
Top1 |
A |
T |
2: 160,512,042 (GRCm39) |
K27N |
unknown |
Het |
Tox2 |
A |
G |
2: 163,067,476 (GRCm39) |
H30R |
probably benign |
Het |
Tra2b |
T |
C |
16: 22,065,993 (GRCm39) |
|
probably benign |
Het |
Trio |
A |
T |
15: 27,833,142 (GRCm39) |
V1165E |
probably damaging |
Het |
Troap |
T |
A |
15: 98,975,269 (GRCm39) |
S145R |
probably damaging |
Het |
Ttc34 |
G |
A |
4: 154,950,139 (GRCm39) |
A1031T |
possibly damaging |
Het |
Ttc6 |
C |
T |
12: 57,663,109 (GRCm39) |
P302S |
probably benign |
Het |
Ubiad1 |
A |
G |
4: 148,528,468 (GRCm39) |
L147P |
probably damaging |
Het |
Ugt2b35 |
G |
T |
5: 87,149,141 (GRCm39) |
V131F |
probably damaging |
Het |
Utp25 |
A |
T |
1: 192,804,401 (GRCm39) |
D200E |
probably damaging |
Het |
Vmn1r167 |
G |
A |
7: 23,204,452 (GRCm39) |
T188I |
probably benign |
Het |
Vmn1r46 |
G |
T |
6: 89,953,716 (GRCm39) |
M188I |
probably benign |
Het |
Vmn2r115 |
T |
A |
17: 23,578,388 (GRCm39) |
N620K |
probably damaging |
Het |
Vmn2r66 |
A |
G |
7: 84,644,344 (GRCm39) |
S689P |
probably damaging |
Het |
Wipf2 |
C |
T |
11: 98,783,236 (GRCm39) |
R221* |
probably null |
Het |
Zbtb16 |
T |
C |
9: 48,571,078 (GRCm39) |
S563G |
probably benign |
Het |
Zfp319 |
T |
C |
8: 96,055,199 (GRCm39) |
T335A |
probably damaging |
Het |
Zfp418 |
A |
G |
7: 7,185,401 (GRCm39) |
R455G |
possibly damaging |
Het |
|
Other mutations in Lpxn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01895:Lpxn
|
APN |
19 |
12,810,450 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03088:Lpxn
|
APN |
19 |
12,810,575 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03203:Lpxn
|
APN |
19 |
12,796,770 (GRCm39) |
missense |
probably benign |
0.01 |
mascherano
|
UTSW |
19 |
12,810,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R0848:Lpxn
|
UTSW |
19 |
12,781,401 (GRCm39) |
missense |
probably benign |
|
R1514:Lpxn
|
UTSW |
19 |
12,801,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Lpxn
|
UTSW |
19 |
12,781,456 (GRCm39) |
critical splice donor site |
probably null |
|
R1880:Lpxn
|
UTSW |
19 |
12,781,452 (GRCm39) |
missense |
probably benign |
0.17 |
R2182:Lpxn
|
UTSW |
19 |
12,810,122 (GRCm39) |
critical splice donor site |
probably null |
|
R2897:Lpxn
|
UTSW |
19 |
12,796,722 (GRCm39) |
missense |
probably benign |
0.01 |
R4194:Lpxn
|
UTSW |
19 |
12,810,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Lpxn
|
UTSW |
19 |
12,810,654 (GRCm39) |
missense |
probably benign |
0.17 |
R4844:Lpxn
|
UTSW |
19 |
12,810,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R5567:Lpxn
|
UTSW |
19 |
12,810,023 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5570:Lpxn
|
UTSW |
19 |
12,810,023 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6060:Lpxn
|
UTSW |
19 |
12,810,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R6366:Lpxn
|
UTSW |
19 |
12,802,163 (GRCm39) |
missense |
probably benign |
0.12 |
R6615:Lpxn
|
UTSW |
19 |
12,802,163 (GRCm39) |
missense |
probably benign |
0.12 |
R7116:Lpxn
|
UTSW |
19 |
12,788,622 (GRCm39) |
missense |
probably benign |
0.28 |
R7135:Lpxn
|
UTSW |
19 |
12,810,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Lpxn
|
UTSW |
19 |
12,802,185 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8290:Lpxn
|
UTSW |
19 |
12,810,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Lpxn
|
UTSW |
19 |
12,802,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8983:Lpxn
|
UTSW |
19 |
12,810,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9415:Lpxn
|
UTSW |
19 |
12,802,336 (GRCm39) |
missense |
probably benign |
0.40 |
Z1176:Lpxn
|
UTSW |
19 |
12,802,311 (GRCm39) |
missense |
probably damaging |
1.00 |
|