Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600014C10Rik |
A |
G |
7: 37,894,272 (GRCm39) |
T102A |
probably benign |
Het |
1700109H08Rik |
A |
G |
5: 3,632,161 (GRCm39) |
K164E |
possibly damaging |
Het |
2610042L04Rik |
C |
T |
14: 4,350,013 (GRCm38) |
Q74* |
probably null |
Het |
Aadacl4fm4 |
T |
A |
4: 144,401,256 (GRCm39) |
H76L |
probably benign |
Het |
Adgrb2 |
T |
A |
4: 129,915,363 (GRCm39) |
M1381K |
probably damaging |
Het |
Adgrv1 |
C |
A |
13: 81,620,523 (GRCm39) |
D3975Y |
probably damaging |
Het |
Ano10 |
C |
T |
9: 122,090,168 (GRCm39) |
E382K |
possibly damaging |
Het |
Ascc3 |
T |
C |
10: 50,535,015 (GRCm39) |
V636A |
probably damaging |
Het |
AU040320 |
T |
C |
4: 126,729,332 (GRCm39) |
V498A |
possibly damaging |
Het |
Bahcc1 |
C |
T |
11: 120,165,885 (GRCm39) |
T1047I |
possibly damaging |
Het |
BC004004 |
A |
T |
17: 29,501,682 (GRCm39) |
T74S |
possibly damaging |
Het |
Bend3 |
A |
G |
10: 43,387,419 (GRCm39) |
D604G |
possibly damaging |
Het |
Brinp3 |
T |
A |
1: 146,707,455 (GRCm39) |
V373E |
probably damaging |
Het |
Bsph2 |
A |
T |
7: 13,290,764 (GRCm39) |
D38E |
probably benign |
Het |
Castor1 |
T |
C |
11: 4,170,423 (GRCm39) |
F140L |
probably benign |
Het |
Catsperd |
A |
G |
17: 56,965,074 (GRCm39) |
I474V |
possibly damaging |
Het |
Ccdc180 |
A |
G |
4: 45,902,447 (GRCm39) |
N292S |
possibly damaging |
Het |
Cd1d1 |
A |
T |
3: 86,905,459 (GRCm39) |
V178E |
possibly damaging |
Het |
Cdca2 |
T |
A |
14: 67,931,131 (GRCm39) |
R521W |
probably damaging |
Het |
Champ1 |
A |
G |
8: 13,929,392 (GRCm39) |
K517E |
probably damaging |
Het |
Chrna9 |
T |
C |
5: 66,128,569 (GRCm39) |
F259S |
probably damaging |
Het |
Chuk |
A |
T |
19: 44,085,422 (GRCm39) |
C241* |
probably null |
Het |
Clns1a |
A |
G |
7: 97,363,240 (GRCm39) |
Y204C |
probably benign |
Het |
Cplane1 |
A |
G |
15: 8,215,692 (GRCm39) |
D416G |
probably damaging |
Het |
Cyp2j7 |
A |
T |
4: 96,115,869 (GRCm39) |
N192K |
probably damaging |
Het |
Ddr2 |
A |
G |
1: 169,829,504 (GRCm39) |
V250A |
probably benign |
Het |
Dlgap2 |
A |
G |
8: 14,777,441 (GRCm39) |
S229G |
probably damaging |
Het |
Dmrt1 |
A |
T |
19: 25,523,231 (GRCm39) |
H194L |
probably damaging |
Het |
Dock7 |
A |
T |
4: 98,968,064 (GRCm39) |
F138I |
|
Het |
Dsg2 |
T |
C |
18: 20,715,847 (GRCm39) |
V263A |
possibly damaging |
Het |
Dusp16 |
A |
G |
6: 134,716,902 (GRCm39) |
L135P |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,050,895 (GRCm39) |
N414S |
probably damaging |
Het |
Efhc1 |
A |
G |
1: 21,030,598 (GRCm39) |
Y177C |
probably damaging |
Het |
Fam83e |
A |
T |
7: 45,372,912 (GRCm39) |
R174S |
probably benign |
Het |
Fgf4 |
C |
T |
7: 144,416,664 (GRCm39) |
L199F |
probably damaging |
Het |
Fignl2 |
A |
G |
15: 100,951,271 (GRCm39) |
L337P |
unknown |
Het |
Gm4353 |
T |
C |
7: 115,682,724 (GRCm39) |
R286G |
probably damaging |
Het |
Gm5142 |
T |
C |
14: 59,416,126 (GRCm39) |
S11G |
probably benign |
Het |
Gpr151 |
A |
G |
18: 42,712,270 (GRCm39) |
V136A |
probably damaging |
Het |
Ift80 |
T |
A |
3: 68,847,483 (GRCm39) |
I338F |
probably damaging |
Het |
Itgb4 |
A |
G |
11: 115,880,625 (GRCm39) |
S693G |
probably benign |
Het |
Kif13a |
T |
A |
13: 46,951,838 (GRCm39) |
I812F |
probably damaging |
Het |
Krit1 |
T |
C |
5: 3,862,577 (GRCm39) |
|
probably null |
Het |
Mapk6 |
T |
C |
9: 75,305,252 (GRCm39) |
D55G |
possibly damaging |
Het |
Matn3 |
A |
G |
12: 9,002,033 (GRCm39) |
I82V |
possibly damaging |
Het |
Mecom |
T |
A |
3: 30,063,994 (GRCm39) |
D32V |
unknown |
Het |
Nacad |
T |
C |
11: 6,552,417 (GRCm39) |
H258R |
possibly damaging |
Het |
Ndufaf5 |
T |
A |
2: 140,030,752 (GRCm39) |
S213T |
possibly damaging |
Het |
Nphp1 |
C |
T |
2: 127,582,892 (GRCm39) |
D674N |
possibly damaging |
Het |
Nsmaf |
A |
G |
4: 6,426,412 (GRCm39) |
L250P |
probably damaging |
Het |
Ogdh |
T |
C |
11: 6,297,838 (GRCm39) |
S571P |
probably benign |
Het |
Or1e31 |
T |
C |
11: 73,690,478 (GRCm39) |
Y35C |
probably damaging |
Het |
Or51i2 |
T |
A |
7: 103,689,268 (GRCm39) |
D88E |
|
Het |
Or8g27 |
T |
C |
9: 39,129,175 (GRCm39) |
I174T |
probably damaging |
Het |
Osbpl11 |
A |
G |
16: 33,047,245 (GRCm39) |
I403V |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pira13 |
T |
A |
7: 3,827,580 (GRCm39) |
R192S |
unknown |
Het |
Plat |
A |
G |
8: 23,268,133 (GRCm39) |
R300G |
probably damaging |
Het |
Ppid |
T |
C |
3: 79,505,059 (GRCm39) |
I134T |
probably damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,772 (GRCm39) |
I565V |
probably benign |
Het |
Rasa1 |
T |
C |
13: 85,403,575 (GRCm39) |
|
probably null |
Het |
Sema4a |
C |
T |
3: 88,345,613 (GRCm39) |
W490* |
probably null |
Het |
Septin3 |
A |
G |
15: 82,173,439 (GRCm39) |
Y257C |
probably damaging |
Het |
Sh3rf2 |
C |
A |
18: 42,274,161 (GRCm39) |
F442L |
probably benign |
Het |
Sipa1l1 |
A |
G |
12: 82,388,792 (GRCm39) |
I339M |
possibly damaging |
Het |
Six2 |
T |
C |
17: 85,995,196 (GRCm39) |
N62S |
possibly damaging |
Het |
Slc44a5 |
T |
C |
3: 153,964,678 (GRCm39) |
I526T |
probably benign |
Het |
Smarca5 |
T |
C |
8: 81,447,378 (GRCm39) |
S402G |
probably benign |
Het |
Son |
T |
A |
16: 91,452,645 (GRCm39) |
V464E |
possibly damaging |
Het |
Sorcs3 |
A |
G |
19: 48,785,950 (GRCm39) |
K1144E |
probably damaging |
Het |
Stxbp6 |
A |
G |
12: 44,902,659 (GRCm39) |
L204P |
probably damaging |
Het |
Tchh |
A |
G |
3: 93,351,570 (GRCm39) |
R337G |
unknown |
Het |
Tgm4 |
T |
C |
9: 122,885,697 (GRCm39) |
V413A |
possibly damaging |
Het |
Tmem131 |
G |
A |
1: 36,858,236 (GRCm39) |
Q704* |
probably null |
Het |
Trim75 |
G |
T |
8: 65,435,315 (GRCm39) |
N378K |
probably benign |
Het |
Tspan18 |
T |
A |
2: 93,036,065 (GRCm39) |
I227F |
probably benign |
Het |
Ttn |
C |
T |
2: 76,541,526 (GRCm39) |
W33820* |
probably null |
Het |
Urb2 |
T |
A |
8: 124,774,034 (GRCm39) |
Y1522N |
probably damaging |
Het |
Zbtb40 |
T |
C |
4: 136,745,620 (GRCm39) |
N138D |
probably benign |
Het |
Zfp715 |
A |
T |
7: 42,947,328 (GRCm39) |
H877Q |
possibly damaging |
Het |
|
Other mutations in Tmpo |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00768:Tmpo
|
APN |
10 |
91,000,068 (GRCm39) |
splice site |
probably benign |
|
IGL00791:Tmpo
|
APN |
10 |
90,998,420 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00919:Tmpo
|
APN |
10 |
90,998,662 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01382:Tmpo
|
APN |
10 |
91,001,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01806:Tmpo
|
APN |
10 |
90,999,104 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01813:Tmpo
|
APN |
10 |
90,999,104 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01838:Tmpo
|
APN |
10 |
90,999,104 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01952:Tmpo
|
APN |
10 |
90,999,104 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02110:Tmpo
|
APN |
10 |
90,998,727 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02122:Tmpo
|
APN |
10 |
90,999,998 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02191:Tmpo
|
APN |
10 |
90,997,741 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02338:Tmpo
|
APN |
10 |
90,999,104 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4366001:Tmpo
|
UTSW |
10 |
90,999,172 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4544001:Tmpo
|
UTSW |
10 |
90,997,976 (GRCm39) |
missense |
probably benign |
|
R0133:Tmpo
|
UTSW |
10 |
90,999,900 (GRCm39) |
splice site |
probably benign |
|
R0450:Tmpo
|
UTSW |
10 |
90,998,958 (GRCm39) |
missense |
probably benign |
0.45 |
R0469:Tmpo
|
UTSW |
10 |
90,998,958 (GRCm39) |
missense |
probably benign |
0.45 |
R0836:Tmpo
|
UTSW |
10 |
90,997,815 (GRCm39) |
nonsense |
probably null |
|
R2405:Tmpo
|
UTSW |
10 |
90,999,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Tmpo
|
UTSW |
10 |
90,988,548 (GRCm39) |
missense |
probably benign |
0.23 |
R4059:Tmpo
|
UTSW |
10 |
90,998,123 (GRCm39) |
missense |
probably benign |
0.00 |
R4296:Tmpo
|
UTSW |
10 |
90,998,818 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4741:Tmpo
|
UTSW |
10 |
90,998,506 (GRCm39) |
missense |
probably benign |
0.18 |
R4881:Tmpo
|
UTSW |
10 |
90,998,503 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4915:Tmpo
|
UTSW |
10 |
90,985,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Tmpo
|
UTSW |
10 |
90,985,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:Tmpo
|
UTSW |
10 |
90,989,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R5002:Tmpo
|
UTSW |
10 |
90,999,976 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5301:Tmpo
|
UTSW |
10 |
90,985,650 (GRCm39) |
intron |
probably benign |
|
R6167:Tmpo
|
UTSW |
10 |
90,998,800 (GRCm39) |
missense |
probably benign |
|
R6190:Tmpo
|
UTSW |
10 |
91,000,069 (GRCm39) |
splice site |
probably null |
|
R6979:Tmpo
|
UTSW |
10 |
90,988,359 (GRCm39) |
splice site |
probably null |
|
R7880:Tmpo
|
UTSW |
10 |
91,001,892 (GRCm39) |
nonsense |
probably null |
|
R8343:Tmpo
|
UTSW |
10 |
90,997,974 (GRCm39) |
missense |
probably benign |
0.00 |
R8492:Tmpo
|
UTSW |
10 |
90,997,720 (GRCm39) |
missense |
probably benign |
0.04 |
R8870:Tmpo
|
UTSW |
10 |
90,987,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Tmpo
|
UTSW |
10 |
90,989,138 (GRCm39) |
critical splice donor site |
probably null |
|
R9598:Tmpo
|
UTSW |
10 |
90,994,608 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Tmpo
|
UTSW |
10 |
90,998,722 (GRCm39) |
missense |
probably benign |
0.30 |
|