Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap13 |
C |
T |
7: 75,335,002 (GRCm39) |
S455L |
probably damaging |
Het |
Apbb1ip |
T |
G |
2: 22,757,005 (GRCm39) |
|
probably null |
Het |
Arhgap18 |
A |
T |
10: 26,722,061 (GRCm39) |
I11F |
probably damaging |
Het |
Arl14epl |
A |
T |
18: 47,059,409 (GRCm39) |
N8I |
possibly damaging |
Het |
Atp4a |
T |
A |
7: 30,414,781 (GRCm39) |
I190N |
possibly damaging |
Het |
Bfar |
T |
C |
16: 13,519,997 (GRCm39) |
F285S |
probably damaging |
Het |
Carf |
C |
T |
1: 60,180,699 (GRCm39) |
Q409* |
probably null |
Het |
Cd244a |
T |
C |
1: 171,404,889 (GRCm39) |
V247A |
probably damaging |
Het |
Ceacam12 |
T |
A |
7: 17,803,326 (GRCm39) |
I244K |
probably damaging |
Het |
Cmya5 |
T |
C |
13: 93,228,698 (GRCm39) |
E2130G |
probably damaging |
Het |
Cyp2b23 |
T |
G |
7: 26,381,150 (GRCm39) |
H69P |
probably damaging |
Het |
Dixdc1 |
T |
C |
9: 50,595,253 (GRCm39) |
Q183R |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,553,573 (GRCm39) |
|
probably null |
Het |
Fam20c |
T |
C |
5: 138,752,450 (GRCm39) |
F279S |
probably damaging |
Het |
Hcn4 |
C |
T |
9: 58,766,327 (GRCm39) |
T665I |
unknown |
Het |
Helz2 |
C |
T |
2: 180,875,260 (GRCm39) |
E1745K |
probably damaging |
Het |
Kdm7a |
A |
T |
6: 39,128,145 (GRCm39) |
|
probably null |
Het |
Ksr1 |
A |
C |
11: 78,910,490 (GRCm39) |
L814R |
possibly damaging |
Het |
Lmnb1 |
A |
G |
18: 56,876,310 (GRCm39) |
I473V |
probably benign |
Het |
Mllt3 |
T |
C |
4: 87,759,445 (GRCm39) |
K201R |
probably damaging |
Het |
Myo1b |
C |
T |
1: 51,823,666 (GRCm39) |
C413Y |
probably damaging |
Het |
Myom3 |
A |
T |
4: 135,533,362 (GRCm39) |
N1185I |
probably benign |
Het |
Nrde2 |
A |
G |
12: 100,098,565 (GRCm39) |
S701P |
probably benign |
Het |
Ntn4 |
A |
T |
10: 93,480,723 (GRCm39) |
D112V |
probably damaging |
Het |
Nup43 |
T |
A |
10: 7,550,826 (GRCm39) |
V232D |
probably damaging |
Het |
Pcdha6 |
G |
A |
18: 37,101,113 (GRCm39) |
C102Y |
probably damaging |
Het |
Pcdhgb8 |
T |
C |
18: 37,895,131 (GRCm39) |
L67P |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,358,016 (GRCm39) |
H836R |
probably damaging |
Het |
Plekha1 |
T |
A |
7: 130,479,512 (GRCm39) |
I10N |
probably benign |
Het |
Psmb5 |
C |
A |
14: 54,854,130 (GRCm39) |
R116L |
probably damaging |
Het |
Rsf1 |
A |
AGGGCGACGG |
7: 97,229,111 (GRCm39) |
|
probably null |
Het |
Secisbp2 |
C |
T |
13: 51,833,923 (GRCm39) |
H688Y |
probably damaging |
Het |
Senp5 |
A |
G |
16: 31,802,665 (GRCm39) |
Y508H |
probably damaging |
Het |
Shc3 |
T |
A |
13: 51,605,651 (GRCm39) |
T210S |
possibly damaging |
Het |
Slc27a2 |
G |
A |
2: 126,429,800 (GRCm39) |
V467M |
probably damaging |
Het |
Slc27a5 |
T |
A |
7: 12,724,899 (GRCm39) |
E487V |
possibly damaging |
Het |
Snx1 |
T |
C |
9: 66,001,930 (GRCm39) |
T298A |
possibly damaging |
Het |
Trir |
A |
G |
8: 85,753,643 (GRCm39) |
D39G |
possibly damaging |
Het |
Ubd |
C |
T |
17: 37,506,242 (GRCm39) |
Q43* |
probably null |
Het |
Ube2o |
T |
C |
11: 116,432,194 (GRCm39) |
E924G |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,659,578 (GRCm39) |
I1650V |
possibly damaging |
Het |
Xirp2 |
C |
A |
2: 67,346,425 (GRCm39) |
R2889S |
probably benign |
Het |
Zfp804b |
T |
C |
5: 6,820,534 (GRCm39) |
E843G |
probably benign |
Het |
|
Other mutations in Prss29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01120:Prss29
|
APN |
17 |
25,541,107 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01619:Prss29
|
APN |
17 |
25,540,113 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01670:Prss29
|
APN |
17 |
25,541,437 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02516:Prss29
|
APN |
17 |
25,539,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1538:Prss29
|
UTSW |
17 |
25,539,257 (GRCm39) |
start codon destroyed |
possibly damaging |
0.93 |
R4285:Prss29
|
UTSW |
17 |
25,541,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R5148:Prss29
|
UTSW |
17 |
25,539,881 (GRCm39) |
missense |
probably benign |
0.00 |
R5468:Prss29
|
UTSW |
17 |
25,540,020 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5483:Prss29
|
UTSW |
17 |
25,541,177 (GRCm39) |
missense |
probably benign |
0.00 |
R5852:Prss29
|
UTSW |
17 |
25,541,408 (GRCm39) |
missense |
probably benign |
0.01 |
R6226:Prss29
|
UTSW |
17 |
25,539,513 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7430:Prss29
|
UTSW |
17 |
25,540,113 (GRCm39) |
critical splice donor site |
probably null |
|
R7547:Prss29
|
UTSW |
17 |
25,539,896 (GRCm39) |
missense |
probably damaging |
1.00 |
|