Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
A |
11: 110,030,446 (GRCm39) |
D767V |
probably damaging |
Het |
Add1 |
T |
A |
5: 34,763,197 (GRCm39) |
N128K |
probably damaging |
Het |
Ado |
A |
T |
10: 67,384,058 (GRCm39) |
D182E |
probably benign |
Het |
Anapc4 |
T |
A |
5: 53,002,761 (GRCm39) |
|
probably benign |
Het |
Ano10 |
A |
G |
9: 122,088,661 (GRCm39) |
|
probably benign |
Het |
Apba2 |
A |
G |
7: 64,364,263 (GRCm39) |
|
probably null |
Het |
Apc2 |
A |
G |
10: 80,150,417 (GRCm39) |
T1795A |
probably benign |
Het |
Atp4a |
A |
G |
7: 30,418,424 (GRCm39) |
N571D |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,887,344 (GRCm39) |
N891D |
probably benign |
Het |
Bltp2 |
G |
A |
11: 78,159,283 (GRCm39) |
E494K |
probably damaging |
Het |
Car3 |
G |
T |
3: 14,931,864 (GRCm39) |
M78I |
probably benign |
Het |
Cc2d2a |
A |
T |
5: 43,887,371 (GRCm39) |
H1267L |
probably benign |
Het |
Cdk18 |
A |
G |
1: 132,046,610 (GRCm39) |
L192P |
probably damaging |
Het |
Cdk9 |
A |
T |
2: 32,599,836 (GRCm39) |
Y134N |
probably damaging |
Het |
Ceacam5 |
A |
T |
7: 17,448,888 (GRCm39) |
T85S |
probably benign |
Het |
Cenpe |
A |
G |
3: 134,952,347 (GRCm39) |
T1403A |
probably benign |
Het |
Chd8 |
C |
T |
14: 52,457,214 (GRCm39) |
G918D |
possibly damaging |
Het |
Csnk1e |
T |
A |
15: 79,304,098 (GRCm39) |
|
probably benign |
Het |
Dctpp1 |
A |
T |
7: 126,856,365 (GRCm39) |
I119N |
probably damaging |
Het |
Defb34 |
T |
A |
8: 19,173,784 (GRCm39) |
F6Y |
unknown |
Het |
Dnai4 |
T |
C |
4: 102,930,054 (GRCm39) |
|
probably benign |
Het |
Dvl1 |
C |
G |
4: 155,939,232 (GRCm39) |
N248K |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,618,181 (GRCm39) |
|
probably benign |
Het |
Dync2i1 |
T |
C |
12: 116,211,910 (GRCm39) |
D199G |
probably damaging |
Het |
Eml5 |
T |
A |
12: 98,831,738 (GRCm39) |
R407W |
probably damaging |
Het |
Epb41l5 |
T |
C |
1: 119,551,688 (GRCm39) |
D99G |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,504,205 (GRCm39) |
N4566I |
possibly damaging |
Het |
Gm21834 |
T |
C |
17: 58,049,015 (GRCm39) |
E67G |
possibly damaging |
Het |
Gsap |
T |
A |
5: 21,458,949 (GRCm39) |
|
probably null |
Het |
Guf1 |
T |
C |
5: 69,715,923 (GRCm39) |
I108T |
probably damaging |
Het |
Hsd3b5 |
T |
C |
3: 98,526,720 (GRCm39) |
D242G |
probably damaging |
Het |
Kcna7 |
A |
G |
7: 45,059,114 (GRCm39) |
D467G |
probably null |
Het |
Lars1 |
A |
G |
18: 42,375,849 (GRCm39) |
|
probably benign |
Het |
Lrrc56 |
A |
T |
7: 140,786,366 (GRCm39) |
D248V |
probably damaging |
Het |
Map3k14 |
T |
A |
11: 103,133,117 (GRCm39) |
E27V |
possibly damaging |
Het |
Med12l |
G |
A |
3: 58,945,123 (GRCm39) |
W116* |
probably null |
Het |
Mgll |
A |
G |
6: 88,702,799 (GRCm39) |
R33G |
probably damaging |
Het |
Mmp13 |
A |
G |
9: 7,280,221 (GRCm39) |
S384G |
possibly damaging |
Het |
Nalcn |
C |
T |
14: 123,607,444 (GRCm39) |
C675Y |
probably benign |
Het |
Nrxn1 |
A |
G |
17: 91,396,117 (GRCm39) |
L13P |
unknown |
Het |
Ocstamp |
A |
G |
2: 165,239,772 (GRCm39) |
V138A |
probably damaging |
Het |
Or12e8 |
T |
G |
2: 87,188,026 (GRCm39) |
Y79* |
probably null |
Het |
Or2z8 |
T |
A |
8: 72,812,006 (GRCm39) |
S161T |
possibly damaging |
Het |
Or4a68 |
A |
G |
2: 89,270,482 (GRCm39) |
V47A |
possibly damaging |
Het |
Or4f7 |
T |
C |
2: 111,645,056 (GRCm39) |
N5S |
probably damaging |
Het |
Or5p51 |
A |
G |
7: 107,444,323 (GRCm39) |
S206P |
possibly damaging |
Het |
Or9i1b |
T |
G |
19: 13,896,808 (GRCm39) |
C141W |
probably damaging |
Het |
Patj |
T |
C |
4: 98,569,472 (GRCm39) |
|
probably benign |
Het |
Pcdhb22 |
A |
G |
18: 37,651,780 (GRCm39) |
I83V |
probably benign |
Het |
Pclo |
A |
G |
5: 14,719,670 (GRCm39) |
E1269G |
unknown |
Het |
Plagl2 |
T |
C |
2: 153,077,973 (GRCm39) |
T3A |
probably benign |
Het |
Plcb1 |
C |
T |
2: 135,136,831 (GRCm39) |
P309S |
possibly damaging |
Het |
Pld3 |
A |
T |
7: 27,239,000 (GRCm39) |
L175Q |
possibly damaging |
Het |
Prrx1 |
A |
G |
1: 163,075,974 (GRCm39) |
|
probably benign |
Het |
Psap |
T |
G |
10: 60,135,345 (GRCm39) |
|
probably benign |
Het |
Ptgfr |
G |
A |
3: 151,540,839 (GRCm39) |
T223M |
probably damaging |
Het |
Reep2 |
A |
T |
18: 34,973,824 (GRCm39) |
I6F |
probably benign |
Het |
Rraga |
A |
G |
4: 86,494,454 (GRCm39) |
E100G |
probably benign |
Het |
Rrm2b |
T |
C |
15: 37,931,889 (GRCm39) |
D37G |
probably benign |
Het |
Rtl1 |
T |
C |
12: 109,559,153 (GRCm39) |
I895M |
probably damaging |
Het |
Ryr1 |
G |
A |
7: 28,774,034 (GRCm39) |
A2445V |
probably damaging |
Het |
Sbf1 |
C |
T |
15: 89,186,532 (GRCm39) |
D898N |
possibly damaging |
Het |
Sh3d19 |
G |
A |
3: 86,022,213 (GRCm39) |
V548I |
possibly damaging |
Het |
Shf |
C |
A |
2: 122,199,116 (GRCm39) |
|
probably benign |
Het |
Sipa1l3 |
T |
C |
7: 29,086,676 (GRCm39) |
E638G |
probably damaging |
Het |
Slc13a3 |
G |
T |
2: 165,253,807 (GRCm39) |
P449T |
probably damaging |
Het |
Slc2a13 |
C |
T |
15: 91,234,215 (GRCm39) |
V374I |
possibly damaging |
Het |
Slc4a7 |
T |
C |
14: 14,794,059 (GRCm38) |
|
probably null |
Het |
Slc7a2 |
T |
A |
8: 41,361,568 (GRCm39) |
S414T |
probably benign |
Het |
Slc9c1 |
A |
G |
16: 45,393,719 (GRCm39) |
E554G |
probably benign |
Het |
Smad2 |
T |
C |
18: 76,433,064 (GRCm39) |
I332T |
probably damaging |
Het |
Snrnp40 |
C |
T |
4: 130,256,451 (GRCm39) |
P59S |
probably damaging |
Het |
Sorcs2 |
A |
T |
5: 36,222,777 (GRCm39) |
I154N |
probably damaging |
Het |
Sox10 |
T |
C |
15: 79,043,586 (GRCm39) |
D149G |
possibly damaging |
Het |
Spn |
C |
T |
7: 126,735,380 (GRCm39) |
V376M |
possibly damaging |
Het |
Tacc2 |
A |
G |
7: 130,179,239 (GRCm39) |
D9G |
probably damaging |
Het |
Tapt1 |
T |
G |
5: 44,334,448 (GRCm39) |
L514F |
possibly damaging |
Het |
Tcf3 |
A |
G |
10: 80,249,168 (GRCm39) |
L480P |
probably damaging |
Het |
Tenm4 |
G |
C |
7: 96,423,227 (GRCm39) |
G637A |
probably damaging |
Het |
Tex14 |
T |
A |
11: 87,411,525 (GRCm39) |
N950K |
probably benign |
Het |
Tgfbrap1 |
T |
G |
1: 43,098,289 (GRCm39) |
H497P |
probably benign |
Het |
Tnfrsf18 |
A |
T |
4: 156,110,986 (GRCm39) |
Y48F |
possibly damaging |
Het |
Tnxb |
A |
C |
17: 34,902,522 (GRCm39) |
H1002P |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,593,571 (GRCm39) |
|
probably benign |
Het |
Ugt2b34 |
C |
G |
5: 87,041,591 (GRCm39) |
|
probably null |
Het |
Vldlr |
A |
G |
19: 27,215,663 (GRCm39) |
D220G |
possibly damaging |
Het |
Vmn1r33 |
A |
T |
6: 66,589,121 (GRCm39) |
Y144* |
probably null |
Het |
Xrcc4 |
T |
C |
13: 90,140,594 (GRCm39) |
E205G |
possibly damaging |
Het |
|
Other mutations in Sort1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00227:Sort1
|
APN |
3 |
108,263,623 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01677:Sort1
|
APN |
3 |
108,252,201 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02532:Sort1
|
APN |
3 |
108,233,036 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03354:Sort1
|
APN |
3 |
108,256,022 (GRCm39) |
missense |
probably benign |
0.00 |
R0266:Sort1
|
UTSW |
3 |
108,252,247 (GRCm39) |
missense |
probably benign |
0.09 |
R0277:Sort1
|
UTSW |
3 |
108,231,908 (GRCm39) |
splice site |
probably benign |
|
R0559:Sort1
|
UTSW |
3 |
108,263,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Sort1
|
UTSW |
3 |
108,246,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Sort1
|
UTSW |
3 |
108,233,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Sort1
|
UTSW |
3 |
108,248,011 (GRCm39) |
missense |
probably benign |
0.01 |
R1986:Sort1
|
UTSW |
3 |
108,253,043 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2130:Sort1
|
UTSW |
3 |
108,259,002 (GRCm39) |
missense |
probably benign |
|
R2131:Sort1
|
UTSW |
3 |
108,259,002 (GRCm39) |
missense |
probably benign |
|
R2133:Sort1
|
UTSW |
3 |
108,259,002 (GRCm39) |
missense |
probably benign |
|
R2362:Sort1
|
UTSW |
3 |
108,253,981 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3436:Sort1
|
UTSW |
3 |
108,245,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R3548:Sort1
|
UTSW |
3 |
108,245,225 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3700:Sort1
|
UTSW |
3 |
108,263,955 (GRCm39) |
nonsense |
probably null |
|
R4496:Sort1
|
UTSW |
3 |
108,217,461 (GRCm39) |
missense |
probably benign |
0.17 |
R4616:Sort1
|
UTSW |
3 |
108,262,857 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4632:Sort1
|
UTSW |
3 |
108,253,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Sort1
|
UTSW |
3 |
108,263,639 (GRCm39) |
nonsense |
probably null |
|
R4994:Sort1
|
UTSW |
3 |
108,235,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5187:Sort1
|
UTSW |
3 |
108,231,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5753:Sort1
|
UTSW |
3 |
108,253,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Sort1
|
UTSW |
3 |
108,264,549 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6262:Sort1
|
UTSW |
3 |
108,217,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7369:Sort1
|
UTSW |
3 |
108,258,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R7484:Sort1
|
UTSW |
3 |
108,246,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Sort1
|
UTSW |
3 |
108,233,323 (GRCm39) |
splice site |
probably null |
|
R8076:Sort1
|
UTSW |
3 |
108,246,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R8222:Sort1
|
UTSW |
3 |
108,241,951 (GRCm39) |
missense |
probably benign |
|
R8871:Sort1
|
UTSW |
3 |
108,262,887 (GRCm39) |
critical splice donor site |
probably null |
|
R8894:Sort1
|
UTSW |
3 |
108,246,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R9169:Sort1
|
UTSW |
3 |
108,247,994 (GRCm39) |
nonsense |
probably null |
|
Z1177:Sort1
|
UTSW |
3 |
108,191,696 (GRCm39) |
missense |
probably benign |
0.00 |
|