Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c12 |
T |
C |
13: 4,320,206 (GRCm39) |
T295A |
probably benign |
Het |
Aldh2 |
C |
A |
5: 121,706,997 (GRCm39) |
V217L |
probably damaging |
Het |
Arap3 |
G |
A |
18: 38,123,844 (GRCm39) |
R392C |
probably damaging |
Het |
Aurkaip1 |
T |
G |
4: 155,916,977 (GRCm39) |
L75R |
probably damaging |
Het |
Blm |
C |
A |
7: 80,149,688 (GRCm39) |
K640N |
probably benign |
Het |
Brap |
A |
T |
5: 121,823,328 (GRCm39) |
T487S |
probably benign |
Het |
Ccser2 |
G |
A |
14: 36,601,632 (GRCm39) |
P276L |
probably damaging |
Het |
Cdc42bpg |
A |
G |
19: 6,361,503 (GRCm39) |
E343G |
probably damaging |
Het |
Cecr2 |
A |
G |
6: 120,738,647 (GRCm39) |
S1097G |
probably benign |
Het |
D7Ertd443e |
A |
T |
7: 133,951,514 (GRCm39) |
V53D |
probably damaging |
Het |
Ddx3y |
G |
A |
Y: 1,266,635 (GRCm39) |
T274I |
probably damaging |
Homo |
Dnah5 |
T |
A |
15: 28,335,773 (GRCm39) |
F2246L |
possibly damaging |
Het |
Dock3 |
T |
A |
9: 106,841,952 (GRCm39) |
H959L |
probably damaging |
Het |
Dpy19l1 |
A |
G |
9: 24,350,442 (GRCm39) |
S406P |
probably damaging |
Het |
Efcab8 |
T |
C |
2: 153,625,688 (GRCm39) |
L116P |
probably damaging |
Het |
Efnb2 |
T |
C |
8: 8,710,524 (GRCm39) |
I31V |
probably benign |
Het |
Fbxl12 |
A |
T |
9: 20,549,911 (GRCm39) |
L271Q |
probably damaging |
Het |
Fmn1 |
T |
A |
2: 113,426,683 (GRCm39) |
N1133K |
probably damaging |
Het |
Gm7298 |
A |
T |
6: 121,759,663 (GRCm39) |
R1187S |
probably damaging |
Het |
H6pd |
T |
C |
4: 150,080,414 (GRCm39) |
I136V |
probably benign |
Het |
Hyal2 |
A |
G |
9: 107,447,914 (GRCm39) |
N189S |
probably benign |
Het |
Jmjd1c |
C |
T |
10: 67,085,439 (GRCm39) |
P2410S |
probably damaging |
Het |
Larp1 |
A |
G |
11: 57,933,089 (GRCm39) |
D231G |
probably damaging |
Het |
Lilra5 |
T |
A |
7: 4,244,927 (GRCm39) |
S233T |
possibly damaging |
Het |
Lrrc43 |
T |
C |
5: 123,641,340 (GRCm39) |
F508S |
probably damaging |
Het |
Marchf4 |
T |
C |
1: 72,491,647 (GRCm39) |
Y208C |
probably damaging |
Het |
Mtarc2 |
T |
C |
1: 184,566,140 (GRCm39) |
R85G |
probably damaging |
Het |
Nr1h2 |
A |
T |
7: 44,201,476 (GRCm39) |
C45* |
probably null |
Het |
Or10ag2 |
T |
A |
2: 87,249,350 (GRCm39) |
S319R |
probably benign |
Het |
Or2n1e |
A |
G |
17: 38,586,039 (GRCm39) |
I126V |
probably benign |
Het |
Ppp2r5d |
G |
T |
17: 46,996,629 (GRCm39) |
|
probably null |
Het |
Prpf40a |
A |
T |
2: 53,046,639 (GRCm39) |
S324T |
probably benign |
Het |
Psmb7 |
T |
C |
2: 38,530,199 (GRCm39) |
D94G |
probably damaging |
Het |
Psmd11 |
A |
G |
11: 80,336,767 (GRCm39) |
T140A |
probably benign |
Het |
Pygm |
T |
C |
19: 6,448,169 (GRCm39) |
I737T |
probably damaging |
Het |
Rbp3 |
G |
A |
14: 33,676,418 (GRCm39) |
R122H |
probably benign |
Het |
Relch |
T |
G |
1: 105,659,007 (GRCm39) |
|
probably null |
Het |
Rrp8 |
T |
C |
7: 105,385,596 (GRCm39) |
E3G |
probably damaging |
Het |
Sacm1l |
T |
C |
9: 123,371,485 (GRCm39) |
S37P |
probably damaging |
Het |
Slc12a3 |
A |
G |
8: 95,085,099 (GRCm39) |
R939G |
possibly damaging |
Het |
Slc20a1 |
T |
C |
2: 129,051,814 (GRCm39) |
S608P |
possibly damaging |
Het |
Sntg1 |
T |
C |
1: 8,624,953 (GRCm39) |
Q281R |
possibly damaging |
Het |
Spata31d1e |
C |
T |
13: 59,890,126 (GRCm39) |
V147I |
probably benign |
Het |
Tefm |
A |
G |
11: 80,028,814 (GRCm39) |
L194P |
probably damaging |
Het |
Terf2ip |
T |
A |
8: 112,738,547 (GRCm39) |
V145E |
probably damaging |
Het |
Tmem231 |
T |
A |
8: 112,641,897 (GRCm39) |
E219V |
probably null |
Het |
Tmx3 |
T |
A |
18: 90,555,334 (GRCm39) |
|
probably null |
Het |
Tns3 |
G |
A |
11: 8,442,987 (GRCm39) |
P459S |
probably damaging |
Het |
Trav13d-1 |
T |
A |
14: 53,089,220 (GRCm39) |
S76R |
probably benign |
Het |
Trp63 |
A |
G |
16: 25,681,210 (GRCm39) |
N254S |
probably damaging |
Het |
Tsen34 |
A |
G |
7: 3,696,984 (GRCm39) |
|
probably benign |
Het |
Unc13d |
A |
G |
11: 115,959,064 (GRCm39) |
V701A |
probably damaging |
Het |
Usp36 |
A |
G |
11: 118,159,411 (GRCm39) |
S513P |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,141,176 (GRCm39) |
S392T |
probably damaging |
Het |
Vmn2r102 |
T |
A |
17: 19,899,007 (GRCm39) |
C450S |
probably benign |
Het |
Zfp128 |
T |
C |
7: 12,624,897 (GRCm39) |
Y422H |
possibly damaging |
Het |
Zkscan7 |
C |
T |
9: 122,724,299 (GRCm39) |
Q423* |
probably null |
Het |
|
Other mutations in Frmpd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
D4216:Frmpd2
|
UTSW |
14 |
33,274,014 (GRCm39) |
missense |
probably damaging |
0.97 |
FR4304:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4342:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4589:Frmpd2
|
UTSW |
14 |
33,232,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Frmpd2
|
UTSW |
14 |
33,244,820 (GRCm39) |
missense |
probably damaging |
0.98 |
R6562:Frmpd2
|
UTSW |
14 |
33,293,872 (GRCm39) |
missense |
probably benign |
0.22 |
R7138:Frmpd2
|
UTSW |
14 |
33,293,761 (GRCm39) |
missense |
probably benign |
0.01 |
R7220:Frmpd2
|
UTSW |
14 |
33,229,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7239:Frmpd2
|
UTSW |
14 |
33,274,034 (GRCm39) |
missense |
probably benign |
0.00 |
R7269:Frmpd2
|
UTSW |
14 |
33,244,838 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7412:Frmpd2
|
UTSW |
14 |
33,293,926 (GRCm39) |
missense |
probably benign |
0.00 |
R7432:Frmpd2
|
UTSW |
14 |
33,229,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R7635:Frmpd2
|
UTSW |
14 |
33,222,920 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7699:Frmpd2
|
UTSW |
14 |
33,264,895 (GRCm39) |
missense |
probably benign |
|
R7938:Frmpd2
|
UTSW |
14 |
33,260,246 (GRCm39) |
missense |
probably benign |
0.02 |
R7940:Frmpd2
|
UTSW |
14 |
33,276,850 (GRCm39) |
nonsense |
probably null |
|
R8134:Frmpd2
|
UTSW |
14 |
33,227,452 (GRCm39) |
missense |
probably benign |
0.02 |
R8152:Frmpd2
|
UTSW |
14 |
33,265,244 (GRCm39) |
splice site |
probably null |
|
R8232:Frmpd2
|
UTSW |
14 |
33,261,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Frmpd2
|
UTSW |
14 |
33,224,934 (GRCm39) |
missense |
probably benign |
0.23 |
R8304:Frmpd2
|
UTSW |
14 |
33,274,066 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8326:Frmpd2
|
UTSW |
14 |
33,232,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R8410:Frmpd2
|
UTSW |
14 |
33,217,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R8851:Frmpd2
|
UTSW |
14 |
33,217,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R8907:Frmpd2
|
UTSW |
14 |
33,248,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Frmpd2
|
UTSW |
14 |
33,252,407 (GRCm39) |
missense |
probably benign |
0.01 |
R9428:Frmpd2
|
UTSW |
14 |
33,272,010 (GRCm39) |
missense |
probably damaging |
0.98 |
R9468:Frmpd2
|
UTSW |
14 |
33,266,432 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9502:Frmpd2
|
UTSW |
14 |
33,227,404 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Frmpd2
|
UTSW |
14 |
33,252,462 (GRCm39) |
nonsense |
probably null |
|
Z1177:Frmpd2
|
UTSW |
14 |
33,252,461 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Frmpd2
|
UTSW |
14 |
33,252,408 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1177:Frmpd2
|
UTSW |
14 |
33,264,983 (GRCm39) |
missense |
probably benign |
0.02 |
|