Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,331,850 (GRCm39) |
I88F |
possibly damaging |
Het |
4930407I10Rik |
T |
C |
15: 81,943,471 (GRCm39) |
S28P |
probably benign |
Het |
a |
A |
T |
2: 154,889,602 (GRCm39) |
N56I |
probably damaging |
Het |
Apoe |
C |
A |
7: 19,432,305 (GRCm39) |
|
probably benign |
Het |
Aspm |
C |
A |
1: 139,406,977 (GRCm39) |
R1955S |
possibly damaging |
Het |
Boc |
G |
A |
16: 44,319,911 (GRCm39) |
L358F |
possibly damaging |
Het |
Cadm2 |
A |
T |
16: 66,612,195 (GRCm39) |
|
probably null |
Het |
Ccdc183 |
T |
C |
2: 25,499,764 (GRCm39) |
E384G |
probably benign |
Het |
Ccl12 |
A |
G |
11: 81,993,943 (GRCm39) |
T67A |
probably damaging |
Het |
Cep120 |
T |
C |
18: 53,857,529 (GRCm39) |
D312G |
probably benign |
Het |
Cmya5 |
A |
G |
13: 93,229,952 (GRCm39) |
V1712A |
possibly damaging |
Het |
Cmya5 |
A |
G |
13: 93,233,784 (GRCm39) |
S435P |
possibly damaging |
Het |
Dmbt1 |
A |
T |
7: 130,699,361 (GRCm39) |
N997Y |
probably damaging |
Het |
Dock2 |
T |
A |
11: 34,453,396 (GRCm39) |
I86F |
probably damaging |
Het |
Duox1 |
A |
G |
2: 122,150,275 (GRCm39) |
Q168R |
probably benign |
Het |
Epb41l4a |
T |
A |
18: 33,965,718 (GRCm39) |
I370L |
probably benign |
Het |
Erc2 |
T |
A |
14: 28,039,208 (GRCm39) |
D950E |
probably damaging |
Het |
Exoc6b |
A |
G |
6: 84,832,479 (GRCm39) |
V405A |
probably damaging |
Het |
F13a1 |
T |
C |
13: 37,209,752 (GRCm39) |
D71G |
probably benign |
Het |
Fam151a |
A |
T |
4: 106,602,696 (GRCm39) |
Y205F |
possibly damaging |
Het |
Fcnb |
C |
A |
2: 27,969,202 (GRCm39) |
R165M |
possibly damaging |
Het |
Fndc3a |
C |
T |
14: 72,827,401 (GRCm39) |
V50I |
probably damaging |
Het |
Gm13276 |
C |
T |
4: 88,704,096 (GRCm39) |
Q51* |
probably null |
Het |
Grik1 |
T |
C |
16: 87,852,959 (GRCm39) |
T75A |
probably benign |
Het |
Grip2 |
A |
G |
6: 91,740,514 (GRCm39) |
L1015P |
probably damaging |
Het |
Hnrnpk |
A |
G |
13: 58,541,967 (GRCm39) |
F339L |
probably benign |
Het |
Iqgap3 |
A |
G |
3: 88,006,200 (GRCm39) |
D537G |
probably benign |
Het |
Kars1 |
C |
T |
8: 112,735,113 (GRCm39) |
|
probably null |
Het |
Kpna7 |
G |
T |
5: 144,929,654 (GRCm39) |
N390K |
probably damaging |
Het |
Krt36 |
A |
T |
11: 99,993,246 (GRCm39) |
S410T |
probably benign |
Het |
Lingo4 |
A |
G |
3: 94,310,157 (GRCm39) |
E365G |
probably damaging |
Het |
Liph |
T |
C |
16: 21,803,018 (GRCm39) |
D17G |
probably benign |
Het |
Lmbrd1 |
C |
A |
1: 24,750,626 (GRCm39) |
N166K |
probably benign |
Het |
Lypd9 |
T |
C |
11: 58,337,182 (GRCm39) |
E97G |
probably benign |
Het |
Nup155 |
T |
C |
15: 8,139,059 (GRCm39) |
S44P |
probably damaging |
Het |
Or2m12 |
A |
G |
16: 19,105,307 (GRCm39) |
M62T |
probably damaging |
Het |
Or4a72 |
A |
T |
2: 89,405,538 (GRCm39) |
C177* |
probably null |
Het |
Or5a3 |
A |
G |
19: 12,399,974 (GRCm39) |
I100M |
probably benign |
Het |
Pcdhga6 |
T |
C |
18: 37,841,324 (GRCm39) |
V348A |
probably benign |
Het |
Phc3 |
G |
A |
3: 30,991,198 (GRCm39) |
Q295* |
probably null |
Het |
Phyh |
A |
G |
2: 4,932,301 (GRCm39) |
E129G |
probably damaging |
Het |
Polb |
A |
G |
8: 23,137,463 (GRCm39) |
S96P |
probably damaging |
Het |
Ppp1r9a |
A |
T |
6: 5,158,113 (GRCm39) |
K1174* |
probably null |
Het |
Ppp1r9b |
C |
T |
11: 94,882,662 (GRCm39) |
R97W |
probably damaging |
Het |
Pttg1ip |
T |
C |
10: 77,418,342 (GRCm39) |
|
probably null |
Het |
Pygm |
G |
A |
19: 6,447,967 (GRCm39) |
|
probably null |
Het |
Rgs20 |
GGAGAGAG |
GGAGAG |
1: 5,091,106 (GRCm39) |
|
probably null |
Het |
Rlf |
T |
C |
4: 121,027,963 (GRCm39) |
H111R |
probably damaging |
Het |
Rmdn3 |
A |
G |
2: 118,969,831 (GRCm39) |
|
probably null |
Het |
Ror2 |
T |
A |
13: 53,265,347 (GRCm39) |
T570S |
probably damaging |
Het |
Sel1l3 |
A |
C |
5: 53,313,061 (GRCm39) |
I542R |
possibly damaging |
Het |
Serpinb3d |
A |
G |
1: 107,006,237 (GRCm39) |
F284L |
probably damaging |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Slc38a2 |
A |
G |
15: 96,590,397 (GRCm39) |
|
probably null |
Het |
Spata31e2 |
T |
A |
1: 26,724,784 (GRCm39) |
Y132F |
probably damaging |
Het |
Spata31h1 |
A |
G |
10: 82,121,091 (GRCm39) |
I3973T |
probably damaging |
Het |
Tet2 |
T |
C |
3: 133,186,087 (GRCm39) |
S1117G |
probably benign |
Het |
Trav15-1-dv6-1 |
C |
T |
14: 53,797,414 (GRCm39) |
A21V |
probably damaging |
Het |
Tsr3 |
G |
T |
17: 25,460,835 (GRCm39) |
D234Y |
probably null |
Het |
Vmn1r220 |
A |
T |
13: 23,368,084 (GRCm39) |
L204H |
probably damaging |
Het |
Vmn1r3 |
A |
T |
4: 3,185,017 (GRCm39) |
S97T |
probably damaging |
Het |
Zfp983 |
A |
G |
17: 21,877,935 (GRCm39) |
Y46C |
probably damaging |
Het |
|
Other mutations in Zfp599 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Zfp599
|
APN |
9 |
22,160,768 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00845:Zfp599
|
APN |
9 |
22,162,814 (GRCm39) |
splice site |
probably benign |
|
R0136:Zfp599
|
UTSW |
9 |
22,161,038 (GRCm39) |
missense |
probably benign |
0.13 |
R0239:Zfp599
|
UTSW |
9 |
22,161,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Zfp599
|
UTSW |
9 |
22,161,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0421:Zfp599
|
UTSW |
9 |
22,161,843 (GRCm39) |
splice site |
probably benign |
|
R1699:Zfp599
|
UTSW |
9 |
22,161,700 (GRCm39) |
missense |
probably benign |
0.20 |
R1723:Zfp599
|
UTSW |
9 |
22,169,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Zfp599
|
UTSW |
9 |
22,162,845 (GRCm39) |
missense |
probably benign |
0.00 |
R4231:Zfp599
|
UTSW |
9 |
22,161,041 (GRCm39) |
nonsense |
probably null |
|
R4233:Zfp599
|
UTSW |
9 |
22,161,041 (GRCm39) |
nonsense |
probably null |
|
R4236:Zfp599
|
UTSW |
9 |
22,161,041 (GRCm39) |
nonsense |
probably null |
|
R4931:Zfp599
|
UTSW |
9 |
22,169,419 (GRCm39) |
missense |
probably damaging |
0.98 |
R5117:Zfp599
|
UTSW |
9 |
22,161,396 (GRCm39) |
nonsense |
probably null |
|
R5615:Zfp599
|
UTSW |
9 |
22,165,165 (GRCm39) |
missense |
probably benign |
|
R5759:Zfp599
|
UTSW |
9 |
22,160,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R5915:Zfp599
|
UTSW |
9 |
22,161,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R6184:Zfp599
|
UTSW |
9 |
22,160,947 (GRCm39) |
missense |
probably benign |
0.18 |
R6657:Zfp599
|
UTSW |
9 |
22,161,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R6736:Zfp599
|
UTSW |
9 |
22,161,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Zfp599
|
UTSW |
9 |
22,160,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R7071:Zfp599
|
UTSW |
9 |
22,169,392 (GRCm39) |
missense |
probably benign |
0.38 |
R7643:Zfp599
|
UTSW |
9 |
22,161,188 (GRCm39) |
missense |
probably benign |
0.19 |
R7714:Zfp599
|
UTSW |
9 |
22,161,811 (GRCm39) |
missense |
probably benign |
0.07 |
R7951:Zfp599
|
UTSW |
9 |
22,160,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7967:Zfp599
|
UTSW |
9 |
22,160,830 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8014:Zfp599
|
UTSW |
9 |
22,160,777 (GRCm39) |
missense |
probably benign |
0.03 |
R8187:Zfp599
|
UTSW |
9 |
22,161,111 (GRCm39) |
nonsense |
probably null |
|
R9562:Zfp599
|
UTSW |
9 |
22,160,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R9684:Zfp599
|
UTSW |
9 |
22,160,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9722:Zfp599
|
UTSW |
9 |
22,160,741 (GRCm39) |
missense |
probably damaging |
0.96 |
RF005:Zfp599
|
UTSW |
9 |
22,165,180 (GRCm39) |
missense |
probably benign |
0.03 |
RF024:Zfp599
|
UTSW |
9 |
22,165,180 (GRCm39) |
missense |
probably benign |
0.03 |
|