Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
A |
3: 121,921,786 (GRCm39) |
I1114N |
probably damaging |
Het |
Ache |
C |
A |
5: 137,288,449 (GRCm39) |
R52S |
possibly damaging |
Het |
AI182371 |
A |
T |
2: 34,975,714 (GRCm39) |
|
probably null |
Het |
Ankrd17 |
T |
C |
5: 90,406,325 (GRCm39) |
S1453G |
probably damaging |
Het |
Arvcf |
A |
G |
16: 18,218,845 (GRCm39) |
N508S |
probably damaging |
Het |
Aurkc |
A |
C |
7: 7,005,796 (GRCm39) |
D136A |
possibly damaging |
Het |
Bfsp2 |
A |
G |
9: 103,325,848 (GRCm39) |
M265T |
probably benign |
Het |
Bmpr1b |
T |
C |
3: 141,562,369 (GRCm39) |
T273A |
probably damaging |
Het |
Cacnb1 |
T |
C |
11: 97,896,578 (GRCm39) |
K406R |
probably damaging |
Het |
Calcoco2 |
C |
T |
11: 95,998,252 (GRCm39) |
|
probably benign |
Het |
Capza1 |
T |
C |
3: 104,748,209 (GRCm39) |
|
probably null |
Het |
Ccdc63 |
T |
A |
5: 122,251,265 (GRCm39) |
I382F |
probably damaging |
Het |
Cep350 |
A |
T |
1: 155,739,161 (GRCm39) |
N2227K |
probably benign |
Het |
Chia1 |
T |
A |
3: 106,036,333 (GRCm39) |
Y304* |
probably null |
Het |
Col5a2 |
G |
A |
1: 45,461,123 (GRCm39) |
P258L |
|
Het |
Cyp21a1 |
A |
G |
17: 35,023,285 (GRCm39) |
L30P |
probably damaging |
Het |
Dennd4b |
T |
A |
3: 90,186,523 (GRCm39) |
H1351Q |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,746,078 (GRCm39) |
I4012F |
possibly damaging |
Het |
Drd1 |
A |
G |
13: 54,207,290 (GRCm39) |
I301T |
possibly damaging |
Het |
Dzip1 |
T |
A |
14: 119,144,326 (GRCm39) |
H369L |
probably damaging |
Het |
Fgfrl1 |
T |
A |
5: 108,851,257 (GRCm39) |
M58K |
probably damaging |
Het |
Ftsj3 |
G |
T |
11: 106,141,660 (GRCm39) |
D529E |
probably benign |
Het |
Fut9 |
A |
T |
4: 25,619,861 (GRCm39) |
W318R |
probably damaging |
Het |
Gabrg3 |
A |
G |
7: 56,634,706 (GRCm39) |
I159T |
probably damaging |
Het |
Gabrr1 |
A |
T |
4: 33,146,972 (GRCm39) |
D53V |
probably benign |
Het |
Ggps1 |
A |
G |
13: 14,228,928 (GRCm39) |
V85A |
probably benign |
Het |
Gm5141 |
C |
T |
13: 62,924,854 (GRCm39) |
W18* |
probably null |
Het |
Grik5 |
T |
A |
7: 24,722,743 (GRCm39) |
T518S |
probably benign |
Het |
Hapln3 |
A |
T |
7: 78,767,378 (GRCm39) |
|
probably benign |
Het |
Hbs1l |
C |
T |
10: 21,243,584 (GRCm39) |
Q646* |
probably null |
Het |
Hmox1 |
T |
C |
8: 75,823,644 (GRCm39) |
I104T |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,413 (GRCm39) |
Y348C |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,920,131 (GRCm39) |
S1403T |
probably damaging |
Het |
Igf2r |
G |
A |
17: 12,923,524 (GRCm39) |
T1186M |
probably damaging |
Het |
Igfbp1 |
T |
C |
11: 7,148,333 (GRCm39) |
|
probably null |
Het |
Ikbip |
C |
A |
10: 90,919,092 (GRCm39) |
A35E |
probably benign |
Het |
Isca1 |
C |
T |
13: 59,917,497 (GRCm39) |
A8T |
probably damaging |
Het |
Itgb2 |
T |
C |
10: 77,401,022 (GRCm39) |
L754P |
probably damaging |
Het |
Itgb6 |
C |
T |
2: 60,458,247 (GRCm39) |
C502Y |
probably damaging |
Het |
Kdm3a |
A |
G |
6: 71,577,092 (GRCm39) |
V741A |
probably benign |
Het |
Kdsr |
T |
C |
1: 106,680,949 (GRCm39) |
D83G |
possibly damaging |
Het |
Kiz |
T |
A |
2: 146,784,037 (GRCm39) |
N523K |
|
Het |
Kmt2a |
T |
C |
9: 44,733,802 (GRCm39) |
|
probably benign |
Het |
Krt25 |
T |
C |
11: 99,212,064 (GRCm39) |
E191G |
probably benign |
Het |
Lipn |
A |
G |
19: 34,046,880 (GRCm39) |
I61V |
probably damaging |
Het |
Lmbr1l |
T |
A |
15: 98,807,150 (GRCm39) |
|
probably null |
Het |
Lrrc4c |
A |
G |
2: 97,459,826 (GRCm39) |
K151E |
probably benign |
Het |
Mab21l3 |
T |
C |
3: 101,730,774 (GRCm39) |
Q155R |
probably benign |
Het |
Mtfr2 |
G |
A |
10: 20,233,274 (GRCm39) |
R281H |
possibly damaging |
Het |
Muc5ac |
A |
G |
7: 141,343,493 (GRCm39) |
Y35C |
possibly damaging |
Het |
Myadm |
C |
T |
7: 3,345,433 (GRCm39) |
T65I |
probably benign |
Het |
Nap1l1 |
T |
C |
10: 111,328,710 (GRCm39) |
V213A |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,111,705 (GRCm39) |
D737G |
probably damaging |
Het |
Ndst4 |
T |
A |
3: 125,405,155 (GRCm39) |
V470D |
probably damaging |
Het |
Nek5 |
T |
A |
8: 22,601,226 (GRCm39) |
Y165F |
probably damaging |
Het |
Nek5 |
A |
T |
8: 22,610,859 (GRCm39) |
V48E |
probably damaging |
Het |
Nr6a1 |
T |
C |
2: 38,650,400 (GRCm39) |
I77V |
probably damaging |
Het |
Nvl |
A |
T |
1: 180,966,638 (GRCm39) |
D93E |
probably benign |
Het |
Or11a4 |
C |
A |
17: 37,536,346 (GRCm39) |
T110K |
possibly damaging |
Het |
Or2q1 |
A |
G |
6: 42,794,950 (GRCm39) |
T182A |
probably benign |
Het |
Or52e5 |
A |
G |
7: 104,718,599 (GRCm39) |
|
probably benign |
Het |
Or52k2 |
A |
T |
7: 102,253,637 (GRCm39) |
L25F |
probably damaging |
Het |
Or52p1 |
A |
T |
7: 104,266,873 (GRCm39) |
T4S |
probably benign |
Het |
Or6c68 |
A |
T |
10: 129,158,259 (GRCm39) |
I256F |
probably damaging |
Het |
Pla2g4c |
G |
A |
7: 13,073,627 (GRCm39) |
V225I |
probably benign |
Het |
Ptpn13 |
A |
G |
5: 103,727,671 (GRCm39) |
R2051G |
probably benign |
Het |
Rbm45 |
T |
C |
2: 76,209,068 (GRCm39) |
S346P |
probably damaging |
Het |
Samd14 |
A |
C |
11: 94,912,027 (GRCm39) |
D168A |
probably damaging |
Het |
Slc15a1 |
C |
T |
14: 121,724,091 (GRCm39) |
G172R |
probably benign |
Het |
Slco3a1 |
G |
T |
7: 73,934,248 (GRCm39) |
Y641* |
probably null |
Het |
Srcap |
G |
A |
7: 127,151,566 (GRCm39) |
R2027H |
probably damaging |
Het |
Stra8 |
A |
T |
6: 34,904,624 (GRCm39) |
|
probably benign |
Het |
Syt11 |
T |
C |
3: 88,655,011 (GRCm39) |
Y430C |
probably damaging |
Het |
Tanc1 |
T |
G |
2: 59,615,800 (GRCm39) |
V269G |
possibly damaging |
Het |
Tead1 |
A |
G |
7: 112,497,818 (GRCm39) |
N342S |
probably benign |
Het |
Tenm3 |
C |
T |
8: 48,732,095 (GRCm39) |
A1254T |
possibly damaging |
Het |
Txlnb |
A |
T |
10: 17,682,546 (GRCm39) |
N156I |
probably damaging |
Het |
Ufl1 |
A |
T |
4: 25,262,258 (GRCm39) |
S409R |
possibly damaging |
Het |
Usp17la |
A |
G |
7: 104,510,307 (GRCm39) |
H304R |
probably benign |
Het |
Vmn1r203 |
T |
A |
13: 22,708,691 (GRCm39) |
H157Q |
possibly damaging |
Het |
Vmn1r37 |
C |
T |
6: 66,709,231 (GRCm39) |
R249* |
probably null |
Het |
Vmn2r96 |
A |
G |
17: 18,804,241 (GRCm39) |
Q497R |
probably benign |
Het |
Vps39 |
A |
G |
2: 120,169,066 (GRCm39) |
S292P |
probably benign |
Het |
Wnk1 |
A |
G |
6: 120,013,959 (GRCm39) |
V212A |
probably damaging |
Het |
Xbp1 |
T |
C |
11: 5,474,741 (GRCm39) |
V161A |
probably benign |
Het |
Zfp113 |
T |
C |
5: 138,143,092 (GRCm39) |
Q386R |
probably damaging |
Het |
|
Other mutations in Plppr4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Plppr4
|
APN |
3 |
117,115,869 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01969:Plppr4
|
APN |
3 |
117,122,008 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02014:Plppr4
|
APN |
3 |
117,129,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02068:Plppr4
|
APN |
3 |
117,125,433 (GRCm39) |
splice site |
probably benign |
|
IGL02426:Plppr4
|
APN |
3 |
117,115,944 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03203:Plppr4
|
APN |
3 |
117,119,540 (GRCm39) |
missense |
possibly damaging |
0.89 |
PIT4445001:Plppr4
|
UTSW |
3 |
117,153,957 (GRCm39) |
unclassified |
probably benign |
|
R0376:Plppr4
|
UTSW |
3 |
117,116,740 (GRCm39) |
missense |
probably benign |
0.05 |
R0755:Plppr4
|
UTSW |
3 |
117,116,319 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0831:Plppr4
|
UTSW |
3 |
117,125,295 (GRCm39) |
critical splice donor site |
probably null |
|
R1518:Plppr4
|
UTSW |
3 |
117,129,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R1523:Plppr4
|
UTSW |
3 |
117,116,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R1581:Plppr4
|
UTSW |
3 |
117,121,915 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1628:Plppr4
|
UTSW |
3 |
117,121,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Plppr4
|
UTSW |
3 |
117,125,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R2511:Plppr4
|
UTSW |
3 |
117,125,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R4332:Plppr4
|
UTSW |
3 |
117,116,474 (GRCm39) |
missense |
probably benign |
|
R4380:Plppr4
|
UTSW |
3 |
117,116,046 (GRCm39) |
missense |
probably benign |
0.40 |
R4787:Plppr4
|
UTSW |
3 |
117,115,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R4829:Plppr4
|
UTSW |
3 |
117,129,240 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5511:Plppr4
|
UTSW |
3 |
117,119,551 (GRCm39) |
missense |
probably benign |
0.39 |
R5819:Plppr4
|
UTSW |
3 |
117,119,513 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6149:Plppr4
|
UTSW |
3 |
117,116,043 (GRCm39) |
missense |
probably benign |
0.22 |
R6257:Plppr4
|
UTSW |
3 |
117,116,228 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6974:Plppr4
|
UTSW |
3 |
117,116,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Plppr4
|
UTSW |
3 |
117,153,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7102:Plppr4
|
UTSW |
3 |
117,116,832 (GRCm39) |
missense |
probably damaging |
0.98 |
R7507:Plppr4
|
UTSW |
3 |
117,115,754 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7820:Plppr4
|
UTSW |
3 |
117,115,598 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8179:Plppr4
|
UTSW |
3 |
117,125,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:Plppr4
|
UTSW |
3 |
117,116,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R8391:Plppr4
|
UTSW |
3 |
117,129,060 (GRCm39) |
missense |
probably benign |
0.02 |
R8531:Plppr4
|
UTSW |
3 |
117,115,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R8762:Plppr4
|
UTSW |
3 |
117,119,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R8784:Plppr4
|
UTSW |
3 |
117,116,190 (GRCm39) |
nonsense |
probably null |
|
R9251:Plppr4
|
UTSW |
3 |
117,115,608 (GRCm39) |
missense |
probably benign |
0.22 |
R9311:Plppr4
|
UTSW |
3 |
117,119,518 (GRCm39) |
missense |
probably damaging |
0.99 |
R9385:Plppr4
|
UTSW |
3 |
117,116,377 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9474:Plppr4
|
UTSW |
3 |
117,116,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R9612:Plppr4
|
UTSW |
3 |
117,115,610 (GRCm39) |
missense |
probably benign |
0.07 |
R9709:Plppr4
|
UTSW |
3 |
117,121,976 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1176:Plppr4
|
UTSW |
3 |
117,116,498 (GRCm39) |
missense |
probably damaging |
1.00 |
|