Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl7a |
A |
G |
4: 56,743,870 (GRCm39) |
I132M |
possibly damaging |
Het |
Agap2 |
A |
T |
10: 126,926,779 (GRCm39) |
I939F |
probably damaging |
Het |
Ahctf1 |
A |
G |
1: 179,623,378 (GRCm39) |
V80A |
possibly damaging |
Het |
Atxn3 |
T |
C |
12: 101,914,285 (GRCm39) |
D67G |
probably damaging |
Het |
Avl9 |
G |
A |
6: 56,730,375 (GRCm39) |
V573M |
possibly damaging |
Het |
Baz1b |
G |
A |
5: 135,246,305 (GRCm39) |
E585K |
possibly damaging |
Het |
Camk2d |
G |
A |
3: 126,591,363 (GRCm39) |
V278I |
possibly damaging |
Het |
Car10 |
A |
G |
11: 93,490,149 (GRCm39) |
I297V |
possibly damaging |
Het |
Cfap65 |
C |
T |
1: 74,962,190 (GRCm39) |
C677Y |
probably damaging |
Het |
Cfap74 |
T |
A |
4: 155,538,495 (GRCm39) |
D872E |
possibly damaging |
Het |
Cgrrf1 |
A |
C |
14: 47,091,158 (GRCm39) |
Q227H |
probably damaging |
Het |
Chil4 |
A |
G |
3: 106,121,711 (GRCm39) |
I46T |
probably damaging |
Het |
Chpf2 |
A |
T |
5: 24,796,917 (GRCm39) |
H621L |
probably damaging |
Het |
Cluap1 |
C |
T |
16: 3,755,437 (GRCm39) |
R351W |
possibly damaging |
Het |
Cnot6 |
A |
T |
11: 49,574,066 (GRCm39) |
Y201* |
probably null |
Het |
Col15a1 |
T |
C |
4: 47,245,630 (GRCm39) |
V127A |
probably benign |
Het |
Col6a3 |
C |
T |
1: 90,701,219 (GRCm39) |
V2566I |
unknown |
Het |
Cope |
T |
A |
8: 70,761,162 (GRCm39) |
M88K |
probably damaging |
Het |
Cops4 |
A |
G |
5: 100,691,776 (GRCm39) |
I358M |
possibly damaging |
Het |
Coro7 |
T |
C |
16: 4,487,820 (GRCm39) |
E130G |
possibly damaging |
Het |
Csrp3 |
A |
G |
7: 48,485,213 (GRCm39) |
|
probably null |
Het |
Cyp4f39 |
T |
C |
17: 32,701,160 (GRCm39) |
F217L |
probably damaging |
Het |
Dmac1 |
A |
G |
4: 75,196,473 (GRCm39) |
S6P |
unknown |
Het |
Drd4 |
A |
T |
7: 140,874,709 (GRCm39) |
I367F |
probably damaging |
Het |
Efcc1 |
T |
A |
6: 87,730,711 (GRCm39) |
|
probably null |
Het |
Emid1 |
A |
T |
11: 5,085,389 (GRCm39) |
M119K |
possibly damaging |
Het |
Fbn2 |
C |
T |
18: 58,202,596 (GRCm39) |
D1237N |
probably benign |
Het |
Fbxl18 |
C |
A |
5: 142,858,153 (GRCm39) |
R761L |
probably damaging |
Het |
Gbp10 |
A |
C |
5: 105,372,205 (GRCm39) |
L185R |
probably damaging |
Het |
Gm7247 |
C |
T |
14: 51,601,805 (GRCm39) |
S26F |
probably benign |
Het |
Gucd1 |
G |
T |
10: 75,256,600 (GRCm39) |
|
probably benign |
Het |
Helb |
G |
A |
10: 119,941,788 (GRCm39) |
T300M |
probably damaging |
Het |
Ifna11 |
A |
T |
4: 88,738,278 (GRCm39) |
H28L |
probably benign |
Het |
Kalrn |
T |
A |
16: 33,830,950 (GRCm39) |
N723I |
probably benign |
Het |
Kcnb2 |
C |
T |
1: 15,780,790 (GRCm39) |
S554F |
possibly damaging |
Het |
Med1 |
A |
C |
11: 98,049,188 (GRCm39) |
V536G |
probably damaging |
Het |
Nanog |
A |
C |
6: 122,690,255 (GRCm39) |
N195T |
probably benign |
Het |
Neu1 |
C |
T |
17: 35,151,031 (GRCm39) |
S94F |
probably damaging |
Het |
Nop58 |
T |
A |
1: 59,740,071 (GRCm39) |
S154R |
probably damaging |
Het |
Npl |
A |
T |
1: 153,388,314 (GRCm39) |
L239* |
probably null |
Het |
Nrg1 |
G |
A |
8: 32,308,600 (GRCm39) |
T483M |
probably damaging |
Het |
Nup98 |
G |
T |
7: 101,829,636 (GRCm39) |
F391L |
probably damaging |
Het |
Or4c122 |
A |
T |
2: 89,079,087 (GRCm39) |
I305K |
probably benign |
Het |
Or5ar1 |
T |
C |
2: 85,671,905 (GRCm39) |
I77V |
probably benign |
Het |
Or5d47 |
A |
T |
2: 87,804,886 (GRCm39) |
V41E |
probably damaging |
Het |
Or5g26 |
T |
C |
2: 85,494,374 (GRCm39) |
I135V |
probably benign |
Het |
Pacsin2 |
A |
G |
15: 83,266,020 (GRCm39) |
V59A |
possibly damaging |
Het |
Pcsk9 |
C |
T |
4: 106,311,469 (GRCm39) |
R254H |
possibly damaging |
Het |
Pierce2 |
A |
T |
9: 72,887,488 (GRCm39) |
|
probably null |
Het |
Psme2 |
C |
A |
14: 55,824,980 (GRCm39) |
|
probably null |
Het |
Ptprc |
T |
A |
1: 138,028,794 (GRCm39) |
H468L |
probably benign |
Het |
Rbp3 |
T |
A |
14: 33,676,604 (GRCm39) |
I184N |
probably damaging |
Het |
Serpinb1c |
A |
G |
13: 33,066,042 (GRCm39) |
L301P |
probably damaging |
Het |
Smim6 |
G |
T |
11: 115,804,219 (GRCm39) |
G2V |
probably damaging |
Het |
Snrpb2 |
A |
G |
2: 142,912,815 (GRCm39) |
D146G |
possibly damaging |
Het |
Svep1 |
T |
A |
4: 58,115,832 (GRCm39) |
S954C |
possibly damaging |
Het |
Telo2 |
G |
T |
17: 25,323,852 (GRCm39) |
T568N |
possibly damaging |
Het |
Tpp2 |
T |
C |
1: 43,990,373 (GRCm39) |
|
probably null |
Het |
Upf1 |
A |
G |
8: 70,789,675 (GRCm39) |
V720A |
probably damaging |
Het |
Vmn1r81 |
T |
C |
7: 11,994,349 (GRCm39) |
I86M |
possibly damaging |
Het |
Vps8 |
T |
A |
16: 21,363,955 (GRCm39) |
|
probably benign |
Het |
Wdr70 |
T |
C |
15: 7,916,900 (GRCm39) |
|
probably null |
Het |
Zfp385c |
A |
T |
11: 100,548,363 (GRCm39) |
S30T |
probably benign |
Het |
Zfp607a |
T |
A |
7: 27,577,254 (GRCm39) |
L108* |
probably null |
Het |
|
Other mutations in Brms1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00922:Brms1l
|
APN |
12 |
55,892,111 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00951:Brms1l
|
APN |
12 |
55,912,834 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02199:Brms1l
|
APN |
12 |
55,907,957 (GRCm39) |
critical splice donor site |
probably benign |
|
IGL02669:Brms1l
|
APN |
12 |
55,888,401 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03158:Brms1l
|
APN |
12 |
55,883,320 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03184:Brms1l
|
APN |
12 |
55,915,062 (GRCm39) |
makesense |
probably null |
|
R0445:Brms1l
|
UTSW |
12 |
55,908,191 (GRCm39) |
nonsense |
probably null |
|
R0568:Brms1l
|
UTSW |
12 |
55,908,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0942:Brms1l
|
UTSW |
12 |
55,912,742 (GRCm39) |
missense |
probably benign |
0.00 |
R0968:Brms1l
|
UTSW |
12 |
55,912,798 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1240:Brms1l
|
UTSW |
12 |
55,891,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R1580:Brms1l
|
UTSW |
12 |
55,915,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Brms1l
|
UTSW |
12 |
55,888,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R1926:Brms1l
|
UTSW |
12 |
55,909,946 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4626:Brms1l
|
UTSW |
12 |
55,909,958 (GRCm39) |
missense |
probably benign |
0.01 |
R4669:Brms1l
|
UTSW |
12 |
55,888,356 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4987:Brms1l
|
UTSW |
12 |
55,912,800 (GRCm39) |
missense |
probably benign |
0.15 |
R6129:Brms1l
|
UTSW |
12 |
55,914,970 (GRCm39) |
missense |
probably benign |
0.03 |
R7429:Brms1l
|
UTSW |
12 |
55,892,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R7430:Brms1l
|
UTSW |
12 |
55,892,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Brms1l
|
UTSW |
12 |
55,892,107 (GRCm39) |
nonsense |
probably null |
|
R7543:Brms1l
|
UTSW |
12 |
55,914,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R7855:Brms1l
|
UTSW |
12 |
55,912,838 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8200:Brms1l
|
UTSW |
12 |
55,891,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R8376:Brms1l
|
UTSW |
12 |
55,888,414 (GRCm39) |
missense |
probably benign |
0.03 |
R8532:Brms1l
|
UTSW |
12 |
55,891,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R9131:Brms1l
|
UTSW |
12 |
55,906,913 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9335:Brms1l
|
UTSW |
12 |
55,888,431 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9433:Brms1l
|
UTSW |
12 |
55,912,863 (GRCm39) |
critical splice donor site |
probably null |
|
R9577:Brms1l
|
UTSW |
12 |
55,906,876 (GRCm39) |
missense |
probably damaging |
1.00 |
|