Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam26a |
T |
A |
8: 44,023,190 (GRCm39) |
H100L |
probably benign |
Het |
Adgrf2 |
T |
C |
17: 43,022,263 (GRCm39) |
N187S |
probably damaging |
Het |
Adipoq |
T |
A |
16: 22,976,332 (GRCm39) |
H244Q |
probably damaging |
Het |
Arhgap40 |
T |
A |
2: 158,373,845 (GRCm39) |
S209T |
probably benign |
Het |
Arrdc3 |
C |
T |
13: 81,037,212 (GRCm39) |
L123F |
probably damaging |
Het |
Aspscr1 |
A |
G |
11: 120,579,865 (GRCm39) |
N212D |
probably benign |
Het |
Ccr9 |
A |
T |
9: 123,608,371 (GRCm39) |
S18C |
probably damaging |
Het |
Cdc42bpa |
T |
A |
1: 179,892,646 (GRCm39) |
V270D |
probably damaging |
Het |
Clic4 |
A |
G |
4: 134,944,516 (GRCm39) |
Y220H |
probably damaging |
Het |
Cntln |
A |
C |
4: 84,897,577 (GRCm39) |
H388P |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,538,925 (GRCm39) |
V2457A |
probably damaging |
Het |
Ctsk |
A |
G |
3: 95,408,925 (GRCm39) |
N103D |
probably benign |
Het |
Ddx60 |
T |
C |
8: 62,428,826 (GRCm39) |
S779P |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,246,378 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
A |
1: 46,148,462 (GRCm39) |
D279E |
probably benign |
Het |
Eif1ad10 |
T |
C |
12: 88,216,524 (GRCm39) |
N116S |
probably benign |
Het |
Fam117a |
A |
G |
11: 95,269,660 (GRCm39) |
N308S |
probably benign |
Het |
Fasn |
A |
G |
11: 120,704,245 (GRCm39) |
V1419A |
probably damaging |
Het |
Fhad1 |
A |
G |
4: 141,678,802 (GRCm39) |
S625P |
probably benign |
Het |
Gemin5 |
A |
G |
11: 58,038,754 (GRCm39) |
V585A |
probably benign |
Het |
Gm5145 |
C |
A |
17: 20,790,646 (GRCm39) |
P8Q |
probably benign |
Het |
Herc1 |
C |
A |
9: 66,323,629 (GRCm39) |
T1381K |
probably damaging |
Het |
Herc6 |
T |
C |
6: 57,637,107 (GRCm39) |
I824T |
probably damaging |
Het |
Klrb1 |
C |
T |
6: 128,687,050 (GRCm39) |
V161I |
probably benign |
Het |
Krtap31-1 |
A |
G |
11: 99,799,258 (GRCm39) |
N154D |
not run |
Het |
Lcp1 |
A |
T |
14: 75,437,871 (GRCm39) |
I94F |
probably benign |
Het |
Lin7a |
A |
T |
10: 107,218,552 (GRCm39) |
Q154L |
possibly damaging |
Het |
Lnx1 |
T |
C |
5: 74,846,351 (GRCm39) |
Y33C |
probably damaging |
Het |
Myo5b |
T |
C |
18: 74,834,517 (GRCm39) |
V859A |
probably benign |
Het |
Ncbp1 |
A |
G |
4: 46,170,015 (GRCm39) |
Q696R |
probably damaging |
Het |
Neurl1b |
C |
G |
17: 26,657,720 (GRCm39) |
H219Q |
probably benign |
Het |
Nme8 |
T |
C |
13: 19,842,999 (GRCm39) |
E392G |
probably benign |
Het |
Nufip1 |
CAAAACAGAAAACAGAAAAC |
CAAAACAGAAAACAGAAAACAGAAAAC |
14: 76,349,414 (GRCm39) |
|
probably null |
Het |
Nuggc |
A |
G |
14: 65,850,975 (GRCm39) |
I298V |
probably damaging |
Het |
Nup155 |
A |
C |
15: 8,183,180 (GRCm39) |
K1247Q |
probably damaging |
Het |
Or1a1 |
A |
G |
11: 74,087,033 (GRCm39) |
K235E |
probably damaging |
Het |
Or5c1 |
A |
T |
2: 37,221,771 (GRCm39) |
E4V |
probably benign |
Het |
Otud4 |
T |
A |
8: 80,382,493 (GRCm39) |
|
probably null |
Het |
Pacc1 |
A |
G |
1: 191,073,065 (GRCm39) |
N162S |
probably benign |
Het |
Pcdhb18 |
T |
C |
18: 37,624,749 (GRCm39) |
V693A |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,727,210 (GRCm39) |
F1108L |
probably benign |
Het |
Prkca |
A |
T |
11: 107,905,170 (GRCm39) |
N189K |
probably damaging |
Het |
Rbm24 |
A |
G |
13: 46,582,683 (GRCm39) |
I201V |
probably benign |
Het |
Reep6 |
T |
C |
10: 80,169,627 (GRCm39) |
L105P |
probably damaging |
Het |
Retreg1 |
T |
C |
15: 25,941,126 (GRCm39) |
|
probably benign |
Het |
Rev3l |
C |
T |
10: 39,712,718 (GRCm39) |
T2382I |
probably benign |
Het |
Rreb1 |
T |
C |
13: 38,115,548 (GRCm39) |
L969P |
probably benign |
Het |
Rsph4a |
T |
A |
10: 33,785,029 (GRCm39) |
N313K |
probably damaging |
Het |
Serpina3f |
T |
A |
12: 104,183,525 (GRCm39) |
L129Q |
probably damaging |
Het |
Slc9a2 |
T |
A |
1: 40,758,157 (GRCm39) |
V232D |
probably damaging |
Het |
Stmn2 |
T |
C |
3: 8,619,925 (GRCm39) |
L121P |
probably damaging |
Het |
Svep1 |
C |
T |
4: 58,097,424 (GRCm39) |
G1373D |
probably damaging |
Het |
Tex55 |
C |
T |
16: 38,648,453 (GRCm39) |
D219N |
possibly damaging |
Het |
Tns1 |
C |
A |
1: 73,991,636 (GRCm39) |
R1014L |
possibly damaging |
Het |
Top2b |
T |
C |
14: 16,416,620 (GRCm38) |
S1127P |
possibly damaging |
Het |
Txndc16 |
A |
T |
14: 45,373,324 (GRCm39) |
C768* |
probably null |
Het |
Ubl7 |
A |
T |
9: 57,837,052 (GRCm39) |
E354D |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,516,905 (GRCm39) |
L3205P |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,340,917 (GRCm39) |
T1053A |
possibly damaging |
Het |
Zbtb21 |
A |
G |
16: 97,753,077 (GRCm39) |
L402P |
probably damaging |
Het |
Zfp27 |
T |
A |
7: 29,594,221 (GRCm39) |
K581N |
possibly damaging |
Het |
Zfp62 |
A |
T |
11: 49,105,903 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Rnf31 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00158:Rnf31
|
APN |
14 |
55,829,776 (GRCm39) |
splice site |
probably null |
|
IGL01532:Rnf31
|
APN |
14 |
55,840,080 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02118:Rnf31
|
APN |
14 |
55,836,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02272:Rnf31
|
APN |
14 |
55,836,239 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02893:Rnf31
|
APN |
14 |
55,836,566 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Rnf31
|
APN |
14 |
55,833,131 (GRCm39) |
missense |
probably benign |
0.30 |
R0285:Rnf31
|
UTSW |
14 |
55,838,846 (GRCm39) |
missense |
probably damaging |
0.96 |
R0678:Rnf31
|
UTSW |
14 |
55,839,170 (GRCm39) |
nonsense |
probably null |
|
R0924:Rnf31
|
UTSW |
14 |
55,830,459 (GRCm39) |
unclassified |
probably benign |
|
R1386:Rnf31
|
UTSW |
14 |
55,834,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1507:Rnf31
|
UTSW |
14 |
55,836,439 (GRCm39) |
nonsense |
probably null |
|
R2122:Rnf31
|
UTSW |
14 |
55,833,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R2164:Rnf31
|
UTSW |
14 |
55,829,994 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3714:Rnf31
|
UTSW |
14 |
55,840,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R3921:Rnf31
|
UTSW |
14 |
55,838,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4348:Rnf31
|
UTSW |
14 |
55,838,555 (GRCm39) |
frame shift |
probably null |
|
R4349:Rnf31
|
UTSW |
14 |
55,838,555 (GRCm39) |
frame shift |
probably null |
|
R4350:Rnf31
|
UTSW |
14 |
55,838,555 (GRCm39) |
frame shift |
probably null |
|
R4351:Rnf31
|
UTSW |
14 |
55,838,555 (GRCm39) |
frame shift |
probably null |
|
R4353:Rnf31
|
UTSW |
14 |
55,838,555 (GRCm39) |
frame shift |
probably null |
|
R4472:Rnf31
|
UTSW |
14 |
55,840,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Rnf31
|
UTSW |
14 |
55,829,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5245:Rnf31
|
UTSW |
14 |
55,839,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R5286:Rnf31
|
UTSW |
14 |
55,829,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R5669:Rnf31
|
UTSW |
14 |
55,834,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R5750:Rnf31
|
UTSW |
14 |
55,836,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R6377:Rnf31
|
UTSW |
14 |
55,832,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Rnf31
|
UTSW |
14 |
55,830,008 (GRCm39) |
missense |
probably benign |
0.00 |
R7018:Rnf31
|
UTSW |
14 |
55,829,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R7876:Rnf31
|
UTSW |
14 |
55,830,534 (GRCm39) |
critical splice donor site |
probably null |
|
R8490:Rnf31
|
UTSW |
14 |
55,833,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8818:Rnf31
|
UTSW |
14 |
55,832,396 (GRCm39) |
missense |
probably benign |
0.10 |
R8900:Rnf31
|
UTSW |
14 |
55,833,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Rnf31
|
UTSW |
14 |
55,833,698 (GRCm39) |
missense |
probably benign |
0.01 |
R9454:Rnf31
|
UTSW |
14 |
55,833,609 (GRCm39) |
missense |
|
|
R9526:Rnf31
|
UTSW |
14 |
55,836,269 (GRCm39) |
critical splice donor site |
probably null |
|
R9756:Rnf31
|
UTSW |
14 |
55,836,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|