Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adarb1 |
A |
T |
10: 77,157,626 (GRCm39) |
F274I |
probably damaging |
Het |
Adprhl1 |
C |
T |
8: 13,271,974 (GRCm39) |
V1595I |
probably benign |
Het |
Anxa6 |
A |
G |
11: 54,898,694 (GRCm39) |
V160A |
probably benign |
Het |
Appl1 |
T |
C |
14: 26,645,692 (GRCm39) |
E706G |
unknown |
Het |
Arhgap21 |
T |
C |
2: 20,860,469 (GRCm39) |
T1313A |
possibly damaging |
Het |
Armc2 |
T |
C |
10: 41,823,935 (GRCm39) |
Y511C |
probably damaging |
Het |
Atp1a1 |
A |
T |
3: 101,499,750 (GRCm39) |
C111S |
probably damaging |
Het |
Atp6v0d2 |
T |
A |
4: 19,878,374 (GRCm39) |
M300L |
probably benign |
Het |
C1ra |
T |
C |
6: 124,493,739 (GRCm39) |
C164R |
probably damaging |
Het |
Cacna1h |
T |
C |
17: 25,599,856 (GRCm39) |
Y1659C |
probably damaging |
Het |
Catsperb |
T |
C |
12: 101,516,053 (GRCm39) |
I563T |
probably benign |
Het |
Cblif |
G |
A |
19: 11,737,748 (GRCm39) |
W386* |
probably null |
Het |
Cd180 |
TA |
TAA |
13: 102,841,514 (GRCm39) |
|
probably null |
Het |
Cd55b |
A |
T |
1: 130,350,619 (GRCm39) |
L26* |
probably null |
Het |
Cdc42bpa |
A |
G |
1: 179,933,638 (GRCm39) |
N759S |
probably benign |
Het |
Cenpj |
C |
T |
14: 56,802,176 (GRCm39) |
E130K |
possibly damaging |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Chd7 |
C |
T |
4: 8,805,272 (GRCm39) |
S777L |
probably benign |
Het |
Chrm3 |
C |
A |
13: 9,928,479 (GRCm39) |
V186L |
probably benign |
Het |
Clrn2 |
A |
G |
5: 45,621,283 (GRCm39) |
T226A |
probably damaging |
Het |
Col3a1 |
C |
T |
1: 45,383,138 (GRCm39) |
P1071S |
unknown |
Het |
Dytn |
A |
T |
1: 63,686,611 (GRCm39) |
V353D |
probably benign |
Het |
Egfem1 |
G |
A |
3: 29,411,317 (GRCm39) |
E155K |
probably benign |
Het |
Eif3m |
A |
T |
2: 104,831,705 (GRCm39) |
M285K |
probably damaging |
Het |
Fam135b |
T |
C |
15: 71,335,856 (GRCm39) |
K446R |
probably benign |
Het |
Fam186a |
T |
C |
15: 99,853,384 (GRCm39) |
T119A |
unknown |
Het |
Frmd4a |
T |
C |
2: 4,612,844 (GRCm39) |
S1025P |
possibly damaging |
Het |
Fubp3 |
A |
G |
2: 31,502,564 (GRCm39) |
H449R |
probably benign |
Het |
Fyco1 |
A |
T |
9: 123,648,211 (GRCm39) |
I1241N |
probably damaging |
Het |
Gabpb2 |
A |
T |
3: 95,111,998 (GRCm39) |
M77K |
probably damaging |
Het |
Gfpt1 |
T |
A |
6: 87,027,906 (GRCm39) |
I4K |
probably damaging |
Het |
Glis1 |
T |
C |
4: 107,425,327 (GRCm39) |
S313P |
probably benign |
Het |
Golga4 |
T |
A |
9: 118,385,941 (GRCm39) |
M1021K |
possibly damaging |
Het |
Grid2ip |
G |
A |
5: 143,359,194 (GRCm39) |
R270Q |
probably damaging |
Het |
Hps4 |
G |
A |
5: 112,525,905 (GRCm39) |
S642N |
possibly damaging |
Het |
Ifit1 |
A |
G |
19: 34,625,236 (GRCm39) |
E124G |
possibly damaging |
Het |
Ifna14 |
T |
C |
4: 88,489,752 (GRCm39) |
D95G |
probably benign |
Het |
Ilkap |
A |
C |
1: 91,314,937 (GRCm39) |
I142S |
probably benign |
Het |
Inpp5e |
C |
T |
2: 26,288,616 (GRCm39) |
R588H |
probably damaging |
Het |
Kif1b |
A |
C |
4: 149,322,357 (GRCm39) |
M854R |
probably damaging |
Het |
Lcn6 |
A |
T |
2: 25,570,107 (GRCm39) |
K91M |
probably damaging |
Het |
Lpin1 |
A |
T |
12: 16,588,483 (GRCm39) |
S902R |
unknown |
Het |
Lrig1 |
C |
A |
6: 94,607,113 (GRCm39) |
C160F |
probably damaging |
Het |
Mapk13 |
T |
C |
17: 28,994,532 (GRCm39) |
I141T |
probably damaging |
Het |
Mapkapk3 |
A |
G |
9: 107,137,354 (GRCm39) |
L175P |
probably damaging |
Het |
Micall2 |
A |
G |
5: 139,701,827 (GRCm39) |
V472A |
unknown |
Het |
Mmp15 |
T |
C |
8: 96,092,959 (GRCm39) |
F113L |
probably benign |
Het |
Msh2 |
T |
G |
17: 88,026,717 (GRCm39) |
S738A |
probably benign |
Het |
Myb |
C |
T |
10: 21,030,612 (GRCm39) |
D62N |
probably benign |
Het |
Myo1f |
T |
C |
17: 33,795,424 (GRCm39) |
V53A |
probably damaging |
Het |
Ncf1 |
A |
T |
5: 134,250,718 (GRCm39) |
N367K |
probably benign |
Het |
Nim1k |
C |
A |
13: 120,174,118 (GRCm39) |
V259F |
probably damaging |
Het |
Nme8 |
T |
G |
13: 19,874,384 (GRCm39) |
I139L |
probably benign |
Het |
Odam |
T |
C |
5: 88,034,457 (GRCm39) |
F46L |
probably benign |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or7a42 |
G |
A |
10: 78,791,929 (GRCm39) |
D297N |
possibly damaging |
Het |
Pcare |
A |
G |
17: 72,057,217 (GRCm39) |
L820P |
probably damaging |
Het |
Pcdha9 |
A |
G |
18: 37,131,954 (GRCm39) |
E341G |
probably damaging |
Het |
Poglut1 |
A |
T |
16: 38,355,168 (GRCm39) |
D219E |
possibly damaging |
Het |
Racgap1 |
A |
G |
15: 99,534,078 (GRCm39) |
S145P |
possibly damaging |
Het |
Rasgef1a |
C |
T |
6: 118,066,110 (GRCm39) |
T441I |
possibly damaging |
Het |
Rbm6 |
T |
C |
9: 107,664,498 (GRCm39) |
T844A |
probably benign |
Het |
Rbmyf9 |
T |
G |
Y: 3,774,819 (GRCm39) |
D5E |
probably damaging |
Het |
Rell1 |
T |
C |
5: 64,097,105 (GRCm39) |
|
probably benign |
Het |
Ripk3 |
A |
G |
14: 56,023,303 (GRCm39) |
F134S |
probably benign |
Het |
Rnf169 |
T |
C |
7: 99,574,699 (GRCm39) |
D632G |
possibly damaging |
Het |
Sclt1 |
A |
T |
3: 41,665,631 (GRCm39) |
W146R |
probably benign |
Het |
Setd5 |
T |
C |
6: 113,098,755 (GRCm39) |
F796S |
possibly damaging |
Het |
Slc24a5 |
G |
T |
2: 124,922,568 (GRCm39) |
G110V |
probably damaging |
Het |
Slc30a10 |
T |
A |
1: 185,187,391 (GRCm39) |
M44K |
probably damaging |
Het |
Slc38a10 |
T |
A |
11: 119,996,781 (GRCm39) |
D772V |
probably benign |
Het |
Thy1 |
C |
T |
9: 43,958,004 (GRCm39) |
T44I |
probably damaging |
Het |
Tinagl1 |
G |
T |
4: 130,061,271 (GRCm39) |
S324Y |
probably benign |
Het |
Tll2 |
T |
A |
19: 41,093,436 (GRCm39) |
Y477F |
probably benign |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tmco6 |
T |
C |
18: 36,874,719 (GRCm39) |
L402P |
probably damaging |
Het |
Tnrc18 |
G |
T |
5: 142,773,392 (GRCm39) |
A479D |
|
Het |
Uba7 |
T |
C |
9: 107,853,001 (GRCm39) |
V12A |
possibly damaging |
Het |
Usp5 |
T |
C |
6: 124,795,599 (GRCm39) |
D598G |
probably damaging |
Het |
Vmn1r158 |
C |
T |
7: 22,489,469 (GRCm39) |
V247I |
probably benign |
Het |
Vpreb1b |
A |
G |
16: 17,798,801 (GRCm39) |
N96D |
probably damaging |
Het |
Zcchc17 |
A |
T |
4: 130,230,928 (GRCm39) |
M87K |
probably damaging |
Het |
|
Other mutations in Pmepa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1401:Pmepa1
|
UTSW |
2 |
173,070,368 (GRCm39) |
critical splice donor site |
probably null |
|
R1439:Pmepa1
|
UTSW |
2 |
173,069,874 (GRCm39) |
missense |
probably benign |
0.13 |
R1772:Pmepa1
|
UTSW |
2 |
173,076,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R2229:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R2380:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R2381:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R2382:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R2385:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R2386:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R3783:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R3785:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Pmepa1
|
UTSW |
2 |
173,069,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Pmepa1
|
UTSW |
2 |
173,070,120 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5368:Pmepa1
|
UTSW |
2 |
173,070,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R5982:Pmepa1
|
UTSW |
2 |
173,076,105 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7371:Pmepa1
|
UTSW |
2 |
173,076,212 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7640:Pmepa1
|
UTSW |
2 |
173,117,956 (GRCm39) |
missense |
probably benign |
0.02 |
R8221:Pmepa1
|
UTSW |
2 |
173,069,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Pmepa1
|
UTSW |
2 |
173,069,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R9228:Pmepa1
|
UTSW |
2 |
173,117,962 (GRCm39) |
missense |
probably benign |
0.06 |
R9229:Pmepa1
|
UTSW |
2 |
173,117,962 (GRCm39) |
missense |
probably benign |
0.06 |
R9260:Pmepa1
|
UTSW |
2 |
173,117,943 (GRCm39) |
small deletion |
probably benign |
|
R9568:Pmepa1
|
UTSW |
2 |
173,069,794 (GRCm39) |
missense |
probably damaging |
1.00 |
|