Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061N02Rik |
C |
A |
16: 88,707,891 (GRCm38) |
R6L |
unknown |
Het |
Anxa11 |
A |
G |
14: 25,874,270 (GRCm38) |
Q235R |
possibly damaging |
Het |
Ap2b1 |
T |
A |
11: 83,308,239 (GRCm38) |
M1K |
probably null |
Het |
Atl2 |
G |
A |
17: 79,850,223 (GRCm38) |
T563I |
probably benign |
Het |
Azin1 |
A |
T |
15: 38,492,343 (GRCm38) |
S307R |
possibly damaging |
Het |
Ccdc153 |
A |
G |
9: 44,245,780 (GRCm38) |
T118A |
probably benign |
Het |
Chac1 |
G |
A |
2: 119,353,534 (GRCm38) |
V206I |
probably damaging |
Het |
Chrm3 |
A |
G |
13: 9,877,662 (GRCm38) |
V446A |
probably benign |
Het |
Cped1 |
T |
C |
6: 22,123,649 (GRCm38) |
F467S |
probably damaging |
Het |
Csmd3 |
G |
A |
15: 48,673,560 (GRCm38) |
P82L |
probably damaging |
Het |
Ddx60 |
T |
A |
8: 61,977,950 (GRCm38) |
S840T |
probably benign |
Het |
Ddx60 |
C |
T |
8: 61,998,681 (GRCm38) |
H1202Y |
probably benign |
Het |
Dnah8 |
T |
A |
17: 30,765,635 (GRCm38) |
N3102K |
probably benign |
Het |
Dst |
A |
T |
1: 34,116,128 (GRCm38) |
K85M |
probably damaging |
Het |
Ehbp1l1 |
T |
C |
19: 5,718,757 (GRCm38) |
I839M |
probably benign |
Het |
Frem2 |
T |
C |
3: 53,572,378 (GRCm38) |
T1965A |
probably benign |
Het |
Ftl1 |
A |
T |
7: 45,459,210 (GRCm38) |
D41E |
probably benign |
Het |
Garem2 |
G |
A |
5: 30,116,737 (GRCm38) |
W698* |
probably null |
Het |
Glt8d2 |
T |
C |
10: 82,652,906 (GRCm38) |
Y283C |
probably damaging |
Het |
Hars |
T |
C |
18: 36,773,590 (GRCm38) |
E109G |
possibly damaging |
Het |
Hspb9 |
T |
C |
11: 100,714,210 (GRCm38) |
S121P |
probably damaging |
Het |
Hus1b |
A |
T |
13: 30,947,205 (GRCm38) |
L157Q |
probably damaging |
Het |
Hykk |
A |
G |
9: 54,946,359 (GRCm38) |
M322V |
probably benign |
Het |
Igkv4-61 |
C |
A |
6: 69,417,154 (GRCm38) |
A31S |
possibly damaging |
Het |
Il17f |
T |
A |
1: 20,777,907 (GRCm38) |
M116L |
probably benign |
Het |
Kif22 |
T |
C |
7: 127,028,932 (GRCm38) |
K9E |
possibly damaging |
Het |
Krt90 |
T |
C |
15: 101,559,244 (GRCm38) |
E233G |
probably benign |
Het |
Lipg |
T |
C |
18: 74,957,236 (GRCm38) |
M81V |
probably benign |
Het |
Mocos |
C |
T |
18: 24,701,456 (GRCm38) |
S850L |
probably damaging |
Het |
Mug2 |
T |
A |
6: 122,082,754 (GRCm38) |
S1364T |
probably damaging |
Het |
Neb |
A |
T |
2: 52,185,328 (GRCm38) |
N208K |
probably benign |
Het |
Oca2 |
G |
T |
7: 56,328,767 (GRCm38) |
R561L |
probably benign |
Het |
Olfm5 |
A |
G |
7: 104,154,053 (GRCm38) |
L401P |
probably damaging |
Het |
Olfr109 |
T |
A |
17: 37,467,080 (GRCm38) |
Y291* |
probably null |
Het |
Olfr1238 |
C |
A |
2: 89,406,522 (GRCm38) |
A186S |
possibly damaging |
Het |
Olfr331 |
T |
C |
11: 58,502,340 (GRCm38) |
D72G |
probably damaging |
Het |
Olfr828 |
G |
A |
9: 18,815,892 (GRCm38) |
T134M |
probably benign |
Het |
Olfr952 |
T |
A |
9: 39,426,891 (GRCm38) |
Y60F |
probably damaging |
Het |
Oxgr1 |
T |
C |
14: 120,022,448 (GRCm38) |
N116D |
probably damaging |
Het |
Pcdha11 |
G |
T |
18: 37,012,169 (GRCm38) |
|
probably null |
Het |
Pi4ka |
T |
C |
16: 17,358,322 (GRCm38) |
I418V |
probably benign |
Het |
Pih1d2 |
T |
C |
9: 50,618,609 (GRCm38) |
V62A |
probably benign |
Het |
Pkib |
T |
A |
10: 57,728,138 (GRCm38) |
V46E |
probably damaging |
Het |
Pum1 |
A |
G |
4: 130,728,287 (GRCm38) |
|
probably null |
Het |
Rbak |
G |
T |
5: 143,176,552 (GRCm38) |
Q19K |
possibly damaging |
Het |
Sema3c |
A |
G |
5: 17,576,961 (GRCm38) |
T32A |
probably damaging |
Het |
Shprh |
T |
C |
10: 11,167,873 (GRCm38) |
W835R |
probably damaging |
Het |
Sis |
T |
G |
3: 72,911,854 (GRCm38) |
K1456N |
probably damaging |
Het |
Slc4a4 |
A |
T |
5: 89,179,729 (GRCm38) |
N675I |
probably benign |
Het |
Slc8a3 |
C |
A |
12: 81,315,627 (GRCm38) |
M139I |
probably damaging |
Het |
Sorcs3 |
T |
C |
19: 48,802,759 (GRCm38) |
F1182S |
probably damaging |
Het |
St8sia2 |
A |
T |
7: 73,971,921 (GRCm38) |
I96N |
probably damaging |
Het |
Stx19 |
T |
C |
16: 62,822,057 (GRCm38) |
S79P |
probably damaging |
Het |
Tecta |
C |
T |
9: 42,375,267 (GRCm38) |
V698M |
probably damaging |
Het |
Timm22 |
T |
C |
11: 76,411,139 (GRCm38) |
S150P |
probably damaging |
Het |
Tjp1 |
C |
T |
7: 65,313,205 (GRCm38) |
D995N |
possibly damaging |
Het |
Tmem135 |
T |
A |
7: 89,147,794 (GRCm38) |
T365S |
probably benign |
Het |
Tmem174 |
T |
C |
13: 98,636,981 (GRCm38) |
T114A |
probably benign |
Het |
Tnc |
A |
G |
4: 64,007,816 (GRCm38) |
I909T |
probably benign |
Het |
Trcg1 |
A |
G |
9: 57,241,330 (GRCm38) |
I62V |
possibly damaging |
Het |
Tulp1 |
A |
T |
17: 28,356,031 (GRCm38) |
*487K |
probably null |
Het |
Unc79 |
T |
A |
12: 103,131,646 (GRCm38) |
V1826E |
possibly damaging |
Het |
Vmn2r13 |
A |
T |
5: 109,174,116 (GRCm38) |
N238K |
probably damaging |
Het |
Vmn2r22 |
T |
A |
6: 123,637,738 (GRCm38) |
N298Y |
probably damaging |
Het |
Vmn2r23 |
T |
A |
6: 123,712,902 (GRCm38) |
F246I |
probably damaging |
Het |
Vps9d1 |
A |
C |
8: 123,248,639 (GRCm38) |
V194G |
probably damaging |
Het |
Zfp260 |
A |
T |
7: 30,104,810 (GRCm38) |
H45L |
possibly damaging |
Het |
Zfp846 |
A |
T |
9: 20,593,720 (GRCm38) |
H292L |
possibly damaging |
Het |
|
Other mutations in Fam184b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Fam184b
|
APN |
5 |
45,539,749 (GRCm38) |
missense |
probably benign |
0.17 |
IGL00781:Fam184b
|
APN |
5 |
45,555,192 (GRCm38) |
splice site |
probably null |
|
IGL01636:Fam184b
|
APN |
5 |
45,584,295 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02008:Fam184b
|
APN |
5 |
45,532,823 (GRCm38) |
missense |
possibly damaging |
0.75 |
IGL02123:Fam184b
|
APN |
5 |
45,639,151 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL02177:Fam184b
|
APN |
5 |
45,532,815 (GRCm38) |
nonsense |
probably null |
|
IGL02192:Fam184b
|
APN |
5 |
45,537,720 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02478:Fam184b
|
APN |
5 |
45,537,697 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03368:Fam184b
|
APN |
5 |
45,531,824 (GRCm38) |
missense |
possibly damaging |
0.91 |
R0003:Fam184b
|
UTSW |
5 |
45,555,194 (GRCm38) |
splice site |
probably benign |
|
R0129:Fam184b
|
UTSW |
5 |
45,532,778 (GRCm38) |
missense |
probably damaging |
1.00 |
R0420:Fam184b
|
UTSW |
5 |
45,584,512 (GRCm38) |
missense |
probably damaging |
1.00 |
R0647:Fam184b
|
UTSW |
5 |
45,584,590 (GRCm38) |
missense |
probably benign |
|
R1215:Fam184b
|
UTSW |
5 |
45,584,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R1374:Fam184b
|
UTSW |
5 |
45,555,143 (GRCm38) |
missense |
probably benign |
|
R1466:Fam184b
|
UTSW |
5 |
45,580,509 (GRCm38) |
splice site |
probably benign |
|
R1773:Fam184b
|
UTSW |
5 |
45,584,334 (GRCm38) |
missense |
possibly damaging |
0.60 |
R1865:Fam184b
|
UTSW |
5 |
45,531,889 (GRCm38) |
missense |
possibly damaging |
0.91 |
R3615:Fam184b
|
UTSW |
5 |
45,582,815 (GRCm38) |
missense |
possibly damaging |
0.56 |
R3616:Fam184b
|
UTSW |
5 |
45,582,815 (GRCm38) |
missense |
possibly damaging |
0.56 |
R4180:Fam184b
|
UTSW |
5 |
45,539,764 (GRCm38) |
missense |
probably benign |
0.00 |
R4375:Fam184b
|
UTSW |
5 |
45,542,343 (GRCm38) |
missense |
probably benign |
|
R4674:Fam184b
|
UTSW |
5 |
45,582,888 (GRCm38) |
nonsense |
probably null |
|
R4942:Fam184b
|
UTSW |
5 |
45,573,307 (GRCm38) |
missense |
probably damaging |
0.97 |
R5021:Fam184b
|
UTSW |
5 |
45,573,262 (GRCm38) |
missense |
probably benign |
0.01 |
R5450:Fam184b
|
UTSW |
5 |
45,539,801 (GRCm38) |
missense |
probably benign |
|
R5731:Fam184b
|
UTSW |
5 |
45,553,129 (GRCm38) |
missense |
probably benign |
0.00 |
R5858:Fam184b
|
UTSW |
5 |
45,639,119 (GRCm38) |
missense |
probably damaging |
0.99 |
R6032:Fam184b
|
UTSW |
5 |
45,582,896 (GRCm38) |
missense |
probably benign |
0.01 |
R6032:Fam184b
|
UTSW |
5 |
45,582,896 (GRCm38) |
missense |
probably benign |
0.01 |
R6060:Fam184b
|
UTSW |
5 |
45,553,147 (GRCm38) |
missense |
probably damaging |
0.99 |
R6088:Fam184b
|
UTSW |
5 |
45,584,012 (GRCm38) |
missense |
probably damaging |
1.00 |
R6932:Fam184b
|
UTSW |
5 |
45,532,901 (GRCm38) |
splice site |
probably null |
|
R6956:Fam184b
|
UTSW |
5 |
45,530,757 (GRCm38) |
missense |
probably damaging |
0.97 |
R6965:Fam184b
|
UTSW |
5 |
45,555,135 (GRCm38) |
missense |
probably benign |
|
R7229:Fam184b
|
UTSW |
5 |
45,584,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R7303:Fam184b
|
UTSW |
5 |
45,542,226 (GRCm38) |
critical splice donor site |
probably null |
|
R7429:Fam184b
|
UTSW |
5 |
45,540,888 (GRCm38) |
missense |
probably benign |
|
R7522:Fam184b
|
UTSW |
5 |
45,530,751 (GRCm38) |
missense |
probably damaging |
1.00 |
R7541:Fam184b
|
UTSW |
5 |
45,542,232 (GRCm38) |
missense |
probably damaging |
0.99 |
R7942:Fam184b
|
UTSW |
5 |
45,584,253 (GRCm38) |
missense |
probably benign |
0.16 |
R8172:Fam184b
|
UTSW |
5 |
45,584,367 (GRCm38) |
missense |
possibly damaging |
0.86 |
R9470:Fam184b
|
UTSW |
5 |
45,584,512 (GRCm38) |
missense |
probably damaging |
1.00 |
R9649:Fam184b
|
UTSW |
5 |
45,639,142 (GRCm38) |
missense |
probably damaging |
1.00 |
|