Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300002M23Rik |
T |
C |
17: 35,878,508 (GRCm39) |
C20R |
probably benign |
Het |
6030468B19Rik |
A |
G |
11: 117,693,739 (GRCm39) |
K69E |
probably damaging |
Het |
9430015G10Rik |
T |
A |
4: 156,203,607 (GRCm39) |
|
probably null |
Het |
A2ml1 |
A |
G |
6: 128,545,726 (GRCm39) |
V467A |
probably damaging |
Het |
Abcc3 |
T |
C |
11: 94,259,446 (GRCm39) |
|
probably null |
Het |
Acad10 |
A |
T |
5: 121,760,881 (GRCm39) |
M941K |
probably benign |
Het |
Agrn |
A |
G |
4: 156,253,759 (GRCm39) |
L1649P |
probably damaging |
Het |
Arhgap12 |
T |
C |
18: 6,061,930 (GRCm39) |
R402G |
possibly damaging |
Het |
Atp4b |
T |
C |
8: 13,443,549 (GRCm39) |
Y43C |
probably damaging |
Het |
Btn2a2 |
T |
A |
13: 23,664,635 (GRCm39) |
T308S |
probably benign |
Het |
C8b |
G |
T |
4: 104,640,206 (GRCm39) |
A170S |
probably benign |
Het |
Cabyr |
T |
A |
18: 12,884,747 (GRCm39) |
D411E |
probably benign |
Het |
Capn3 |
T |
C |
2: 120,314,964 (GRCm39) |
|
probably benign |
Het |
Cd200r4 |
T |
C |
16: 44,641,313 (GRCm39) |
F19L |
probably benign |
Het |
Cflar |
T |
A |
1: 58,774,856 (GRCm39) |
Y218N |
probably benign |
Het |
Col11a2 |
T |
C |
17: 34,273,154 (GRCm39) |
Y630H |
probably damaging |
Het |
Coq6 |
T |
C |
12: 84,419,189 (GRCm39) |
|
probably benign |
Het |
Drg2 |
A |
G |
11: 60,350,334 (GRCm39) |
T98A |
possibly damaging |
Het |
Fry |
T |
A |
5: 150,419,884 (GRCm39) |
S1015R |
possibly damaging |
Het |
Gjb4 |
A |
G |
4: 127,245,222 (GRCm39) |
S240P |
probably benign |
Het |
Glmp |
G |
A |
3: 88,233,718 (GRCm39) |
V107I |
probably damaging |
Het |
Gls |
A |
C |
1: 52,272,147 (GRCm39) |
M2R |
possibly damaging |
Het |
Igfbp4 |
A |
G |
11: 98,939,061 (GRCm39) |
E27G |
probably damaging |
Het |
Ints8 |
A |
T |
4: 11,225,621 (GRCm39) |
Y645* |
probably null |
Het |
Kat6a |
G |
T |
8: 23,352,380 (GRCm39) |
V55F |
probably damaging |
Het |
Kat8 |
T |
A |
7: 127,523,654 (GRCm39) |
D292E |
possibly damaging |
Het |
Myo19 |
T |
A |
11: 84,776,505 (GRCm39) |
C54S |
probably damaging |
Het |
Myo5b |
C |
T |
18: 74,794,726 (GRCm39) |
H532Y |
probably benign |
Het |
Nckap1 |
T |
C |
2: 80,370,904 (GRCm39) |
K357E |
possibly damaging |
Het |
Ndufaf1 |
C |
T |
2: 119,490,752 (GRCm39) |
V105M |
probably benign |
Het |
Or2o1 |
A |
G |
11: 49,051,620 (GRCm39) |
S260G |
possibly damaging |
Het |
Or8b101 |
A |
T |
9: 38,020,134 (GRCm39) |
I51F |
possibly damaging |
Het |
Or8b1b |
T |
A |
9: 38,375,822 (GRCm39) |
C162S |
probably benign |
Het |
Or8c17 |
T |
G |
9: 38,179,814 (GRCm39) |
S2A |
probably benign |
Het |
Or8k30 |
T |
G |
2: 86,339,367 (GRCm39) |
L188R |
possibly damaging |
Het |
Palld |
T |
C |
8: 62,162,067 (GRCm39) |
D439G |
probably damaging |
Het |
Pcf11 |
T |
C |
7: 92,308,828 (GRCm39) |
|
probably benign |
Het |
Pigo |
A |
T |
4: 43,020,909 (GRCm39) |
W678R |
possibly damaging |
Het |
Pip5kl1 |
A |
T |
2: 32,473,283 (GRCm39) |
|
probably null |
Het |
Plscr3 |
G |
A |
11: 69,740,964 (GRCm39) |
V267M |
probably benign |
Het |
Pramel24 |
A |
T |
4: 143,453,255 (GRCm39) |
H121L |
probably benign |
Het |
Ptk7 |
A |
G |
17: 46,876,304 (GRCm39) |
I1049T |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,186,694 (GRCm39) |
I1743F |
probably benign |
Het |
Ptprm |
A |
G |
17: 67,116,570 (GRCm39) |
V894A |
probably benign |
Het |
Rack1 |
A |
G |
11: 48,693,131 (GRCm39) |
T105A |
probably benign |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
Sdk1 |
A |
G |
5: 141,921,804 (GRCm39) |
T267A |
probably benign |
Het |
Slco1a7 |
T |
C |
6: 141,700,100 (GRCm39) |
Q144R |
possibly damaging |
Het |
Sorcs3 |
T |
A |
19: 48,711,395 (GRCm39) |
D653E |
probably damaging |
Het |
Spata31e3 |
G |
A |
13: 50,399,548 (GRCm39) |
S926F |
possibly damaging |
Het |
Spata31f3 |
A |
G |
4: 42,873,492 (GRCm39) |
|
probably null |
Het |
St8sia1 |
A |
G |
6: 142,774,751 (GRCm39) |
L276P |
probably damaging |
Het |
Sync |
T |
C |
4: 129,188,156 (GRCm39) |
V396A |
possibly damaging |
Het |
Taok3 |
A |
G |
5: 117,394,002 (GRCm39) |
T592A |
probably benign |
Het |
Tas2r104 |
T |
A |
6: 131,662,002 (GRCm39) |
I236F |
possibly damaging |
Het |
Tas2r107 |
A |
C |
6: 131,636,293 (GRCm39) |
I252S |
probably benign |
Het |
Tmem259 |
T |
C |
10: 79,814,282 (GRCm39) |
N334S |
possibly damaging |
Het |
Tsga10 |
A |
T |
1: 37,873,278 (GRCm39) |
N200K |
possibly damaging |
Het |
Usp24 |
G |
A |
4: 106,236,263 (GRCm39) |
V984I |
probably benign |
Het |
Vmn1r189 |
T |
A |
13: 22,286,382 (GRCm39) |
T152S |
probably benign |
Het |
Vmn1r2 |
A |
T |
4: 3,172,413 (GRCm39) |
T111S |
probably damaging |
Het |
Vmn2r74 |
T |
G |
7: 85,607,466 (GRCm39) |
N86H |
probably damaging |
Het |
Zfp12 |
T |
C |
5: 143,226,077 (GRCm39) |
V72A |
probably benign |
Het |
|
Other mutations in Prom2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Prom2
|
APN |
2 |
127,383,059 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01140:Prom2
|
APN |
2 |
127,373,125 (GRCm39) |
splice site |
probably benign |
|
IGL01300:Prom2
|
APN |
2 |
127,377,009 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01445:Prom2
|
APN |
2 |
127,381,433 (GRCm39) |
splice site |
probably benign |
|
IGL01472:Prom2
|
APN |
2 |
127,374,802 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01541:Prom2
|
APN |
2 |
127,371,050 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01991:Prom2
|
APN |
2 |
127,371,142 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02421:Prom2
|
APN |
2 |
127,373,802 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02557:Prom2
|
APN |
2 |
127,371,391 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02724:Prom2
|
APN |
2 |
127,380,577 (GRCm39) |
splice site |
probably benign |
|
IGL02826:Prom2
|
APN |
2 |
127,373,036 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02830:Prom2
|
APN |
2 |
127,376,989 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02990:Prom2
|
APN |
2 |
127,370,734 (GRCm39) |
missense |
probably benign |
0.10 |
R0110:Prom2
|
UTSW |
2 |
127,373,033 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0133:Prom2
|
UTSW |
2 |
127,380,258 (GRCm39) |
splice site |
probably benign |
|
R0165:Prom2
|
UTSW |
2 |
127,381,434 (GRCm39) |
splice site |
probably benign |
|
R0220:Prom2
|
UTSW |
2 |
127,383,027 (GRCm39) |
missense |
probably benign |
0.03 |
R0466:Prom2
|
UTSW |
2 |
127,370,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R0505:Prom2
|
UTSW |
2 |
127,374,787 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0605:Prom2
|
UTSW |
2 |
127,381,915 (GRCm39) |
critical splice donor site |
probably null |
|
R0633:Prom2
|
UTSW |
2 |
127,381,445 (GRCm39) |
missense |
probably benign |
0.19 |
R0947:Prom2
|
UTSW |
2 |
127,380,183 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1682:Prom2
|
UTSW |
2 |
127,382,082 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1806:Prom2
|
UTSW |
2 |
127,374,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Prom2
|
UTSW |
2 |
127,383,017 (GRCm39) |
missense |
probably damaging |
0.97 |
R1864:Prom2
|
UTSW |
2 |
127,381,707 (GRCm39) |
missense |
probably benign |
0.00 |
R1866:Prom2
|
UTSW |
2 |
127,378,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R4472:Prom2
|
UTSW |
2 |
127,382,111 (GRCm39) |
missense |
probably benign |
0.06 |
R5078:Prom2
|
UTSW |
2 |
127,373,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5889:Prom2
|
UTSW |
2 |
127,371,331 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5930:Prom2
|
UTSW |
2 |
127,372,053 (GRCm39) |
nonsense |
probably null |
|
R6214:Prom2
|
UTSW |
2 |
127,381,695 (GRCm39) |
critical splice donor site |
probably null |
|
R6215:Prom2
|
UTSW |
2 |
127,381,695 (GRCm39) |
critical splice donor site |
probably null |
|
R6914:Prom2
|
UTSW |
2 |
127,372,295 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7099:Prom2
|
UTSW |
2 |
127,381,698 (GRCm39) |
missense |
probably benign |
|
R7427:Prom2
|
UTSW |
2 |
127,381,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R7428:Prom2
|
UTSW |
2 |
127,381,731 (GRCm39) |
missense |
probably damaging |
0.99 |
R7525:Prom2
|
UTSW |
2 |
127,374,701 (GRCm39) |
missense |
probably benign |
|
R8477:Prom2
|
UTSW |
2 |
127,381,124 (GRCm39) |
missense |
probably benign |
0.01 |
R9287:Prom2
|
UTSW |
2 |
127,380,185 (GRCm39) |
missense |
probably damaging |
0.98 |
R9337:Prom2
|
UTSW |
2 |
127,371,094 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Prom2
|
UTSW |
2 |
127,374,695 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Prom2
|
UTSW |
2 |
127,381,446 (GRCm39) |
missense |
probably benign |
0.19 |
Z1177:Prom2
|
UTSW |
2 |
127,380,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|