Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
T |
A |
2: 68,492,768 (GRCm39) |
|
probably null |
Het |
Adam28 |
A |
G |
14: 68,879,511 (GRCm39) |
L179P |
probably benign |
Het |
Amer2 |
G |
T |
14: 60,616,231 (GRCm39) |
G142V |
possibly damaging |
Het |
Ap2a1 |
A |
G |
7: 44,553,819 (GRCm39) |
|
probably null |
Het |
Arhgap32 |
A |
G |
9: 32,168,275 (GRCm39) |
T753A |
probably benign |
Het |
Capsl |
A |
G |
15: 9,461,874 (GRCm39) |
D90G |
probably damaging |
Het |
Cd96 |
A |
T |
16: 45,938,349 (GRCm39) |
S39T |
possibly damaging |
Het |
Cdx2 |
T |
A |
5: 147,240,044 (GRCm39) |
T211S |
probably damaging |
Het |
Chd9 |
A |
G |
8: 91,705,515 (GRCm39) |
Y251C |
probably damaging |
Het |
Chrna6 |
C |
T |
8: 27,896,774 (GRCm39) |
V368I |
probably benign |
Het |
Coro1a |
G |
T |
7: 126,302,252 (GRCm39) |
Q32K |
probably benign |
Het |
Cps1 |
T |
A |
1: 67,211,914 (GRCm39) |
V694E |
possibly damaging |
Het |
Eif3h |
A |
G |
15: 51,662,672 (GRCm39) |
Y125H |
probably benign |
Het |
Fbxw22 |
A |
C |
9: 109,210,750 (GRCm39) |
Y420* |
probably null |
Het |
Fgf21 |
T |
C |
7: 45,264,651 (GRCm39) |
Y27C |
probably benign |
Het |
Gm7356 |
A |
G |
17: 14,221,001 (GRCm39) |
S343P |
probably benign |
Het |
Hmcn2 |
A |
G |
2: 31,310,321 (GRCm39) |
D3305G |
probably damaging |
Het |
Ift70a1 |
T |
C |
2: 75,811,121 (GRCm39) |
T321A |
possibly damaging |
Het |
Kdm4c |
T |
A |
4: 74,323,206 (GRCm39) |
F1046Y |
possibly damaging |
Het |
Klk1b27 |
T |
A |
7: 43,705,114 (GRCm39) |
W94R |
probably benign |
Het |
Nwd2 |
A |
T |
5: 63,962,143 (GRCm39) |
M576L |
probably benign |
Het |
Or13c7d |
T |
C |
4: 43,770,063 (GRCm39) |
H316R |
probably benign |
Het |
Or4d2 |
A |
T |
11: 87,784,633 (GRCm39) |
V39E |
probably damaging |
Het |
Or5b122 |
T |
C |
19: 13,562,781 (GRCm39) |
|
probably benign |
Het |
Or5p54 |
A |
G |
7: 107,554,376 (GRCm39) |
H176R |
probably damaging |
Het |
Pappa |
T |
A |
4: 65,215,645 (GRCm39) |
V1184D |
probably damaging |
Het |
Pcyox1 |
T |
A |
6: 86,369,164 (GRCm39) |
M152L |
probably benign |
Het |
Pdha2 |
A |
G |
3: 140,917,457 (GRCm39) |
V17A |
probably benign |
Het |
Pi4k2b |
A |
T |
5: 52,914,247 (GRCm39) |
I328L |
probably benign |
Het |
Ppp1r13l |
T |
C |
7: 19,111,895 (GRCm39) |
F814L |
probably benign |
Het |
Prag1 |
A |
T |
8: 36,571,337 (GRCm39) |
H640L |
probably benign |
Het |
Rabgap1 |
A |
G |
2: 37,363,614 (GRCm39) |
T132A |
probably benign |
Het |
Sec31b |
T |
C |
19: 44,524,203 (GRCm39) |
I146V |
probably benign |
Het |
Slc30a9 |
A |
G |
5: 67,499,460 (GRCm39) |
Y306C |
probably damaging |
Het |
Stat3 |
A |
G |
11: 100,794,569 (GRCm39) |
S247P |
probably benign |
Het |
Tbc1d1 |
C |
A |
5: 64,490,776 (GRCm39) |
L747I |
probably damaging |
Het |
Tbc1d24 |
A |
T |
17: 24,402,761 (GRCm39) |
M1K |
probably null |
Het |
Vezt |
A |
C |
10: 93,836,336 (GRCm39) |
V104G |
probably damaging |
Het |
Zbtb41 |
A |
G |
1: 139,351,397 (GRCm39) |
D170G |
probably damaging |
Het |
Zswim2 |
C |
A |
2: 83,746,032 (GRCm39) |
D469Y |
probably damaging |
Het |
|
Other mutations in Prl5a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01638:Prl5a1
|
APN |
13 |
28,329,422 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01820:Prl5a1
|
APN |
13 |
28,332,683 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02682:Prl5a1
|
APN |
13 |
28,329,403 (GRCm39) |
missense |
probably benign |
0.32 |
R0266:Prl5a1
|
UTSW |
13 |
28,333,970 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1022:Prl5a1
|
UTSW |
13 |
28,333,880 (GRCm39) |
missense |
probably damaging |
0.97 |
R1024:Prl5a1
|
UTSW |
13 |
28,333,880 (GRCm39) |
missense |
probably damaging |
0.97 |
R2098:Prl5a1
|
UTSW |
13 |
28,329,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R5467:Prl5a1
|
UTSW |
13 |
28,333,994 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6026:Prl5a1
|
UTSW |
13 |
28,335,247 (GRCm39) |
missense |
probably benign |
0.43 |
R6242:Prl5a1
|
UTSW |
13 |
28,326,538 (GRCm39) |
nonsense |
probably null |
|
R6616:Prl5a1
|
UTSW |
13 |
28,333,839 (GRCm39) |
missense |
probably benign |
0.00 |
R6733:Prl5a1
|
UTSW |
13 |
28,333,919 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6979:Prl5a1
|
UTSW |
13 |
28,335,189 (GRCm39) |
missense |
probably benign |
0.32 |
R7692:Prl5a1
|
UTSW |
13 |
28,333,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Prl5a1
|
UTSW |
13 |
28,329,492 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9611:Prl5a1
|
UTSW |
13 |
28,329,492 (GRCm39) |
missense |
possibly damaging |
0.71 |
|