Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
A |
G |
11: 109,993,359 (GRCm39) |
L1584P |
probably damaging |
Het |
Abca9 |
G |
T |
11: 110,056,806 (GRCm39) |
H5N |
probably benign |
Het |
Acox1 |
A |
T |
11: 116,069,024 (GRCm39) |
I371N |
probably damaging |
Het |
Aopep |
C |
A |
13: 63,208,903 (GRCm39) |
A340E |
probably benign |
Het |
Bmp5 |
A |
G |
9: 75,805,833 (GRCm39) |
N445S |
probably damaging |
Het |
Cacna1b |
G |
T |
2: 24,568,927 (GRCm39) |
A999E |
probably benign |
Het |
Cdc27 |
A |
T |
11: 104,419,394 (GRCm39) |
|
probably benign |
Het |
Dmxl2 |
T |
C |
9: 54,308,349 (GRCm39) |
E2134G |
possibly damaging |
Het |
Dnttip2 |
A |
G |
3: 122,078,062 (GRCm39) |
N698S |
possibly damaging |
Het |
Duox1 |
A |
T |
2: 122,174,655 (GRCm39) |
K1271M |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,599,254 (GRCm39) |
Y1870H |
possibly damaging |
Het |
Edem3 |
A |
G |
1: 151,680,470 (GRCm39) |
T532A |
probably benign |
Het |
Epx |
A |
T |
11: 87,760,294 (GRCm39) |
L440Q |
probably damaging |
Het |
F11 |
A |
G |
8: 45,699,791 (GRCm39) |
F432L |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,822,204 (GRCm39) |
D5979G |
possibly damaging |
Het |
Furin |
A |
G |
7: 80,043,207 (GRCm39) |
S335P |
probably damaging |
Het |
Gtf3c1 |
T |
A |
7: 125,258,284 (GRCm39) |
Q1262L |
probably damaging |
Het |
Hmmr |
A |
T |
11: 40,598,256 (GRCm39) |
V652E |
probably benign |
Het |
Iapp |
A |
T |
6: 142,249,199 (GRCm39) |
N84I |
probably benign |
Het |
Katnip |
G |
A |
7: 125,413,993 (GRCm39) |
C379Y |
probably benign |
Het |
Mmp17 |
C |
T |
5: 129,675,752 (GRCm39) |
Q304* |
probably null |
Het |
Mpl |
T |
C |
4: 118,314,333 (GRCm39) |
T55A |
possibly damaging |
Het |
Mst1r |
G |
A |
9: 107,794,478 (GRCm39) |
R1219H |
probably damaging |
Het |
Muc6 |
T |
A |
7: 141,226,117 (GRCm39) |
|
probably benign |
Het |
Nalcn |
C |
T |
14: 123,831,915 (GRCm39) |
V120I |
probably benign |
Het |
Nt5dc1 |
A |
T |
10: 34,275,806 (GRCm39) |
C134* |
probably null |
Het |
Obscn |
A |
C |
11: 58,971,530 (GRCm39) |
N2228K |
probably damaging |
Het |
Or2n1c |
T |
A |
17: 38,520,074 (GRCm39) |
*313R |
probably null |
Het |
Osbpl10 |
T |
C |
9: 115,046,062 (GRCm39) |
M566T |
possibly damaging |
Het |
Pabpc1l |
G |
A |
2: 163,886,267 (GRCm39) |
V466I |
probably benign |
Het |
Pdcd11 |
T |
G |
19: 47,094,860 (GRCm39) |
V548G |
probably benign |
Het |
Prss27 |
G |
T |
17: 24,263,951 (GRCm39) |
K212N |
possibly damaging |
Het |
Ranbp2 |
T |
A |
10: 58,297,789 (GRCm39) |
S399T |
probably damaging |
Het |
Rgs19 |
A |
G |
2: 181,331,076 (GRCm39) |
S159P |
probably damaging |
Het |
Sh2b1 |
A |
G |
7: 126,068,465 (GRCm39) |
S449P |
probably damaging |
Het |
Slc6a18 |
T |
A |
13: 73,820,870 (GRCm39) |
Y238F |
probably benign |
Het |
Stx11 |
T |
C |
10: 12,817,224 (GRCm39) |
I167V |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,371 (GRCm39) |
M300V |
possibly damaging |
Het |
Synj2 |
A |
G |
17: 6,040,628 (GRCm39) |
T235A |
probably damaging |
Het |
Ubxn2b |
T |
A |
4: 6,214,749 (GRCm39) |
I261N |
probably damaging |
Het |
Vmn2r43 |
G |
A |
7: 8,260,512 (GRCm39) |
|
probably benign |
Het |
Vmn2r45 |
A |
G |
7: 8,484,443 (GRCm39) |
M454T |
probably damaging |
Het |
Vsig2 |
T |
A |
9: 37,451,251 (GRCm39) |
S51T |
probably damaging |
Het |
Wdr41 |
T |
C |
13: 95,153,964 (GRCm39) |
|
probably benign |
Het |
Wdr6 |
A |
C |
9: 108,453,752 (GRCm39) |
L44V |
probably damaging |
Het |
Zfp1001 |
T |
C |
2: 150,165,634 (GRCm39) |
Y5H |
probably damaging |
Het |
Zfp592 |
T |
C |
7: 80,674,796 (GRCm39) |
Y587H |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,602,254 (GRCm39) |
K399N |
probably benign |
Het |
|
Other mutations in Fam185a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00726:Fam185a
|
APN |
5 |
21,685,340 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01980:Fam185a
|
APN |
5 |
21,664,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02264:Fam185a
|
APN |
5 |
21,685,392 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02553:Fam185a
|
APN |
5 |
21,634,839 (GRCm39) |
splice site |
probably benign |
|
IGL02553:Fam185a
|
APN |
5 |
21,660,829 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03082:Fam185a
|
APN |
5 |
21,660,836 (GRCm39) |
missense |
possibly damaging |
0.49 |
famine
|
UTSW |
5 |
21,630,452 (GRCm39) |
missense |
probably benign |
0.00 |
R0389:Fam185a
|
UTSW |
5 |
21,664,283 (GRCm39) |
missense |
probably damaging |
0.99 |
R1872:Fam185a
|
UTSW |
5 |
21,685,328 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1883:Fam185a
|
UTSW |
5 |
21,630,242 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3775:Fam185a
|
UTSW |
5 |
21,660,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R4190:Fam185a
|
UTSW |
5 |
21,630,122 (GRCm39) |
unclassified |
probably benign |
|
R4192:Fam185a
|
UTSW |
5 |
21,630,122 (GRCm39) |
unclassified |
probably benign |
|
R4194:Fam185a
|
UTSW |
5 |
21,630,452 (GRCm39) |
missense |
probably benign |
0.00 |
R4704:Fam185a
|
UTSW |
5 |
21,685,471 (GRCm39) |
utr 3 prime |
probably benign |
|
R4724:Fam185a
|
UTSW |
5 |
21,660,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Fam185a
|
UTSW |
5 |
21,685,375 (GRCm39) |
missense |
probably benign |
0.00 |
R6225:Fam185a
|
UTSW |
5 |
21,630,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R6438:Fam185a
|
UTSW |
5 |
21,663,970 (GRCm39) |
splice site |
probably null |
|
R6475:Fam185a
|
UTSW |
5 |
21,630,281 (GRCm39) |
missense |
probably benign |
0.01 |
R7512:Fam185a
|
UTSW |
5 |
21,652,356 (GRCm39) |
critical splice donor site |
probably null |
|
R8400:Fam185a
|
UTSW |
5 |
21,643,814 (GRCm39) |
missense |
probably benign |
0.14 |
R8690:Fam185a
|
UTSW |
5 |
21,638,766 (GRCm39) |
missense |
probably benign |
0.32 |
R9157:Fam185a
|
UTSW |
5 |
21,660,837 (GRCm39) |
missense |
probably damaging |
1.00 |
|