Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6b |
A |
T |
12: 113,455,278 (GRCm39) |
K698N |
possibly damaging |
Het |
Adcy8 |
A |
T |
15: 64,694,044 (GRCm39) |
V411D |
probably damaging |
Het |
Arfgef3 |
T |
A |
10: 18,475,036 (GRCm39) |
E1550V |
probably damaging |
Het |
Asb3 |
T |
A |
11: 31,011,406 (GRCm39) |
I306K |
probably damaging |
Het |
Asic4 |
T |
A |
1: 75,445,746 (GRCm39) |
|
probably benign |
Het |
Basp1 |
G |
T |
15: 25,364,948 (GRCm39) |
D16E |
unknown |
Het |
Cbll1 |
A |
T |
12: 31,540,539 (GRCm39) |
I123N |
probably damaging |
Het |
Ccdc141 |
A |
T |
2: 76,869,837 (GRCm39) |
H889Q |
probably benign |
Het |
Ccdc65 |
T |
C |
15: 98,618,930 (GRCm39) |
V303A |
probably benign |
Het |
Ceacam20 |
T |
A |
7: 19,720,593 (GRCm39) |
M60K |
probably damaging |
Het |
Chd9 |
T |
A |
8: 91,725,223 (GRCm39) |
V711D |
probably damaging |
Het |
Clcn1 |
T |
A |
6: 42,289,979 (GRCm39) |
|
probably null |
Het |
Col16a1 |
A |
T |
4: 129,962,268 (GRCm39) |
|
probably benign |
Het |
Col4a3 |
C |
A |
1: 82,694,084 (GRCm39) |
P1568Q |
possibly damaging |
Het |
Colec12 |
C |
A |
18: 9,858,650 (GRCm39) |
P478T |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,407,985 (GRCm39) |
H1949R |
probably damaging |
Het |
Dgka |
A |
G |
10: 128,572,876 (GRCm39) |
|
probably null |
Het |
Dlgap4 |
A |
G |
2: 156,588,111 (GRCm39) |
I669V |
probably benign |
Het |
Dsg1c |
T |
A |
18: 20,412,298 (GRCm39) |
D543E |
probably benign |
Het |
Egflam |
A |
T |
15: 7,271,906 (GRCm39) |
C677* |
probably null |
Het |
Eml5 |
A |
C |
12: 98,791,031 (GRCm39) |
|
probably null |
Het |
Fbn1 |
G |
A |
2: 125,231,169 (GRCm39) |
R466C |
probably damaging |
Het |
Fnbp1 |
C |
A |
2: 30,948,990 (GRCm39) |
D198Y |
probably damaging |
Het |
Gfra3 |
T |
A |
18: 34,824,668 (GRCm39) |
M272L |
probably benign |
Het |
Gm5422 |
T |
A |
10: 31,126,156 (GRCm39) |
|
noncoding transcript |
Het |
Gpr21 |
T |
A |
2: 37,407,556 (GRCm39) |
I34N |
probably damaging |
Het |
Hspb2 |
G |
T |
9: 50,662,664 (GRCm39) |
T155K |
probably benign |
Het |
Il21r |
A |
G |
7: 125,224,457 (GRCm39) |
T24A |
probably benign |
Het |
Mmadhc |
T |
A |
2: 50,182,847 (GRCm39) |
H43L |
possibly damaging |
Het |
Morn1 |
T |
A |
4: 155,195,473 (GRCm39) |
D278E |
possibly damaging |
Het |
Myoc |
T |
C |
1: 162,476,243 (GRCm39) |
Y316H |
probably damaging |
Het |
Nags |
A |
G |
11: 102,037,805 (GRCm39) |
D266G |
probably damaging |
Het |
Nlrp4b |
A |
G |
7: 10,448,142 (GRCm39) |
N115S |
probably benign |
Het |
Nlrp5 |
T |
A |
7: 23,117,056 (GRCm39) |
I260N |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,926,905 (GRCm39) |
R6190C |
probably damaging |
Het |
Or5b24 |
T |
C |
19: 12,912,624 (GRCm39) |
V174A |
possibly damaging |
Het |
Or5be3 |
A |
G |
2: 86,863,812 (GRCm39) |
F251S |
probably damaging |
Het |
Orc4 |
C |
T |
2: 48,807,285 (GRCm39) |
M215I |
probably benign |
Het |
Osbpl6 |
A |
T |
2: 76,420,735 (GRCm39) |
H770L |
probably damaging |
Het |
Otogl |
A |
C |
10: 107,616,849 (GRCm39) |
N1809K |
probably benign |
Het |
Pde3a |
G |
T |
6: 141,437,957 (GRCm39) |
V1009L |
probably damaging |
Het |
Pign |
T |
C |
1: 105,580,902 (GRCm39) |
Y159C |
probably damaging |
Het |
Pik3cg |
C |
A |
12: 32,247,196 (GRCm39) |
M842I |
probably damaging |
Het |
Pramel17 |
A |
C |
4: 101,692,611 (GRCm39) |
V463G |
probably damaging |
Het |
Prpf8 |
A |
G |
11: 75,381,480 (GRCm39) |
N239D |
probably damaging |
Het |
Psd2 |
T |
A |
18: 36,113,546 (GRCm39) |
|
probably benign |
Het |
Ptprt |
T |
C |
2: 161,393,668 (GRCm39) |
D1251G |
probably damaging |
Het |
Pwp2 |
G |
A |
10: 78,018,520 (GRCm39) |
S88L |
probably benign |
Het |
Rassf4 |
C |
T |
6: 116,624,516 (GRCm39) |
|
probably benign |
Het |
Rexo1 |
A |
G |
10: 80,380,684 (GRCm39) |
S884P |
probably damaging |
Het |
Rgs20 |
C |
A |
1: 5,091,037 (GRCm39) |
R131L |
possibly damaging |
Het |
Setd4 |
A |
G |
16: 93,386,834 (GRCm39) |
V288A |
probably benign |
Het |
Stx3 |
G |
T |
19: 11,763,110 (GRCm39) |
T160K |
probably damaging |
Het |
Tas2r102 |
T |
A |
6: 132,739,636 (GRCm39) |
S181R |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 49,127,434 (GRCm39) |
|
probably benign |
Het |
Tmem33 |
T |
C |
5: 67,421,603 (GRCm39) |
|
probably benign |
Het |
Trim33 |
A |
G |
3: 103,259,306 (GRCm39) |
|
probably benign |
Het |
Trip11 |
A |
G |
12: 101,853,119 (GRCm39) |
I491T |
probably benign |
Het |
Trp53bp1 |
A |
G |
2: 121,058,653 (GRCm39) |
|
probably benign |
Het |
Tuba4a |
T |
C |
1: 75,193,017 (GRCm39) |
D199G |
probably benign |
Het |
Zcchc4 |
A |
G |
5: 52,953,321 (GRCm39) |
Y110C |
probably damaging |
Het |
Zp2 |
C |
T |
7: 119,734,693 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Pnliprp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00495:Pnliprp1
|
APN |
19 |
58,723,162 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02367:Pnliprp1
|
APN |
19 |
58,726,601 (GRCm39) |
missense |
probably benign |
|
R0463:Pnliprp1
|
UTSW |
19 |
58,726,628 (GRCm39) |
nonsense |
probably null |
|
R0591:Pnliprp1
|
UTSW |
19 |
58,723,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Pnliprp1
|
UTSW |
19 |
58,726,628 (GRCm39) |
nonsense |
probably null |
|
R1169:Pnliprp1
|
UTSW |
19 |
58,723,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1575:Pnliprp1
|
UTSW |
19 |
58,728,901 (GRCm39) |
missense |
probably benign |
0.07 |
R1723:Pnliprp1
|
UTSW |
19 |
58,720,574 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1879:Pnliprp1
|
UTSW |
19 |
58,732,516 (GRCm39) |
missense |
probably benign |
0.07 |
R1955:Pnliprp1
|
UTSW |
19 |
58,723,404 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2090:Pnliprp1
|
UTSW |
19 |
58,728,901 (GRCm39) |
missense |
probably benign |
0.03 |
R2092:Pnliprp1
|
UTSW |
19 |
58,729,616 (GRCm39) |
missense |
probably benign |
0.02 |
R2342:Pnliprp1
|
UTSW |
19 |
58,729,691 (GRCm39) |
splice site |
probably benign |
|
R2421:Pnliprp1
|
UTSW |
19 |
58,732,517 (GRCm39) |
missense |
probably benign |
0.21 |
R4716:Pnliprp1
|
UTSW |
19 |
58,728,901 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5463:Pnliprp1
|
UTSW |
19 |
58,723,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5478:Pnliprp1
|
UTSW |
19 |
58,723,423 (GRCm39) |
splice site |
probably null |
|
R6155:Pnliprp1
|
UTSW |
19 |
58,718,565 (GRCm39) |
critical splice donor site |
probably null |
|
R6284:Pnliprp1
|
UTSW |
19 |
58,723,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Pnliprp1
|
UTSW |
19 |
58,717,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R7454:Pnliprp1
|
UTSW |
19 |
58,729,532 (GRCm39) |
missense |
probably benign |
0.29 |
R7470:Pnliprp1
|
UTSW |
19 |
58,720,457 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7574:Pnliprp1
|
UTSW |
19 |
58,726,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R7601:Pnliprp1
|
UTSW |
19 |
58,720,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R8782:Pnliprp1
|
UTSW |
19 |
58,719,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R9081:Pnliprp1
|
UTSW |
19 |
58,723,406 (GRCm39) |
missense |
probably benign |
|
R9445:Pnliprp1
|
UTSW |
19 |
58,720,628 (GRCm39) |
intron |
probably benign |
|
R9466:Pnliprp1
|
UTSW |
19 |
58,723,081 (GRCm39) |
missense |
probably damaging |
1.00 |
|