Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrb2 |
T |
C |
4: 129,907,419 (GRCm39) |
F977S |
probably damaging |
Het |
Ago4 |
A |
G |
4: 126,406,393 (GRCm39) |
Y306H |
probably benign |
Het |
Cblc |
T |
C |
7: 19,526,502 (GRCm39) |
T196A |
probably damaging |
Het |
Cfap52 |
T |
A |
11: 67,844,445 (GRCm39) |
|
probably null |
Het |
Cops3 |
T |
C |
11: 59,710,844 (GRCm39) |
N375S |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,685,557 (GRCm39) |
K153E |
probably benign |
Het |
Elovl1 |
C |
T |
4: 118,287,945 (GRCm39) |
S27F |
probably damaging |
Het |
Erc2 |
A |
G |
14: 27,863,185 (GRCm39) |
E804G |
probably damaging |
Het |
Fam110b |
G |
T |
4: 5,798,840 (GRCm39) |
C86F |
probably damaging |
Het |
Fbn1 |
T |
A |
2: 125,236,541 (GRCm39) |
R380W |
probably damaging |
Het |
Gatad2a |
C |
T |
8: 70,369,301 (GRCm39) |
R221Q |
probably damaging |
Het |
Gcn1 |
C |
T |
5: 115,727,174 (GRCm39) |
P677L |
probably damaging |
Het |
Gm6020 |
C |
T |
19: 61,172,391 (GRCm39) |
H22Y |
possibly damaging |
Het |
Gm9817 |
T |
C |
13: 45,232,605 (GRCm39) |
V136A |
unknown |
Het |
Gmip |
T |
A |
8: 70,273,622 (GRCm39) |
L971H |
probably damaging |
Het |
Gnptab |
G |
A |
10: 88,254,989 (GRCm39) |
E192K |
possibly damaging |
Het |
Grm7 |
G |
A |
6: 111,335,568 (GRCm39) |
V660I |
probably benign |
Het |
Helz2 |
G |
A |
2: 180,876,082 (GRCm39) |
P1471S |
probably damaging |
Het |
Herc1 |
G |
A |
9: 66,386,743 (GRCm39) |
G3786S |
probably damaging |
Het |
Isg20 |
T |
C |
7: 78,569,647 (GRCm39) |
V206A |
probably benign |
Het |
Jund |
T |
A |
8: 71,152,470 (GRCm39) |
I255N |
probably damaging |
Het |
Kcnt2 |
A |
T |
1: 140,353,079 (GRCm39) |
I263F |
probably damaging |
Het |
Kif2c |
A |
T |
4: 117,019,420 (GRCm39) |
L561Q |
probably benign |
Het |
Klhl3 |
T |
C |
13: 58,157,189 (GRCm39) |
D546G |
probably damaging |
Het |
Klk1b4 |
A |
T |
7: 43,859,054 (GRCm39) |
Q24L |
probably benign |
Het |
Ltbp2 |
A |
T |
12: 84,834,735 (GRCm39) |
C225S |
probably damaging |
Het |
Mcub |
T |
C |
3: 129,728,312 (GRCm39) |
H55R |
probably benign |
Het |
Mecp2 |
C |
T |
X: 73,080,781 (GRCm39) |
A79T |
probably damaging |
Het |
Med18 |
G |
A |
4: 132,187,242 (GRCm39) |
R86* |
probably null |
Het |
Mfsd2b |
T |
C |
12: 4,919,155 (GRCm39) |
E63G |
probably damaging |
Het |
Mtus1 |
C |
T |
8: 41,537,362 (GRCm39) |
S118N |
probably damaging |
Het |
Mybbp1a |
C |
T |
11: 72,336,863 (GRCm39) |
T565I |
probably benign |
Het |
Myo15b |
G |
A |
11: 115,777,899 (GRCm39) |
G1049S |
probably damaging |
Het |
Nfrkb |
T |
A |
9: 31,326,064 (GRCm39) |
V1169E |
probably benign |
Het |
Nr2f2 |
T |
A |
7: 70,004,419 (GRCm39) |
M411L |
probably benign |
Het |
Nup155 |
A |
T |
15: 8,187,244 (GRCm39) |
H1391L |
probably damaging |
Het |
Nup214 |
A |
T |
2: 31,886,392 (GRCm39) |
T585S |
possibly damaging |
Het |
Or5m13 |
C |
T |
2: 85,748,599 (GRCm39) |
T110I |
probably benign |
Het |
Or6c214 |
A |
T |
10: 129,590,943 (GRCm39) |
C125* |
probably null |
Het |
Or7e177 |
T |
C |
9: 20,211,633 (GRCm39) |
S47P |
probably benign |
Het |
Or8b12b |
T |
A |
9: 37,684,163 (GRCm39) |
D69E |
possibly damaging |
Het |
Pih1d1 |
T |
A |
7: 44,807,165 (GRCm39) |
I166N |
probably damaging |
Het |
Prl2c5 |
T |
C |
13: 13,366,263 (GRCm39) |
F181L |
probably benign |
Het |
Prx |
C |
T |
7: 27,218,535 (GRCm39) |
T1012I |
possibly damaging |
Het |
Rassf8 |
T |
A |
6: 145,754,199 (GRCm39) |
V5E |
probably damaging |
Het |
Rassf9 |
C |
A |
10: 102,380,755 (GRCm39) |
R44S |
possibly damaging |
Het |
Relch |
A |
T |
1: 105,592,301 (GRCm39) |
I157F |
probably benign |
Het |
Sde2 |
G |
A |
1: 180,687,573 (GRCm39) |
S153N |
probably benign |
Het |
Sec16b |
T |
A |
1: 157,380,545 (GRCm39) |
M372K |
possibly damaging |
Het |
Sgcd |
A |
T |
11: 47,085,937 (GRCm39) |
I71N |
probably damaging |
Het |
Slco5a1 |
C |
T |
1: 12,942,483 (GRCm39) |
C721Y |
probably damaging |
Het |
Slx4ip |
A |
T |
2: 136,910,038 (GRCm39) |
K344N |
probably benign |
Het |
Sorcs3 |
A |
T |
19: 48,782,713 (GRCm39) |
Q1076L |
probably benign |
Het |
Spata21 |
A |
T |
4: 140,838,692 (GRCm39) |
N581I |
possibly damaging |
Het |
Spata31d1d |
G |
T |
13: 59,875,936 (GRCm39) |
P533H |
probably benign |
Het |
Spice1 |
T |
G |
16: 44,185,989 (GRCm39) |
S111A |
probably damaging |
Het |
Tex14 |
T |
G |
11: 87,365,274 (GRCm39) |
F61V |
probably damaging |
Het |
Timp3 |
C |
T |
10: 86,181,716 (GRCm39) |
R196* |
probably null |
Het |
Tll2 |
A |
G |
19: 41,077,110 (GRCm39) |
|
probably null |
Het |
Tppp |
A |
G |
13: 74,169,326 (GRCm39) |
D22G |
possibly damaging |
Het |
Trim24 |
G |
T |
6: 37,934,013 (GRCm39) |
R652L |
probably damaging |
Het |
Uaca |
T |
C |
9: 60,777,718 (GRCm39) |
S702P |
possibly damaging |
Het |
Uggt2 |
T |
C |
14: 119,287,130 (GRCm39) |
E146G |
probably damaging |
Het |
Vmn1r233 |
T |
C |
17: 21,213,994 (GRCm39) |
S319G |
probably benign |
Het |
Wdr47 |
A |
T |
3: 108,530,692 (GRCm39) |
Q395L |
possibly damaging |
Het |
Wrnip1 |
A |
G |
13: 32,989,319 (GRCm39) |
|
probably null |
Het |
Zfp420 |
A |
T |
7: 29,573,933 (GRCm39) |
H51L |
probably damaging |
Het |
|
Other mutations in Crb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00593:Crb1
|
APN |
1 |
139,250,983 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01591:Crb1
|
APN |
1 |
139,165,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01644:Crb1
|
APN |
1 |
139,165,368 (GRCm39) |
nonsense |
probably null |
|
IGL01769:Crb1
|
APN |
1 |
139,264,806 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02172:Crb1
|
APN |
1 |
139,164,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02294:Crb1
|
APN |
1 |
139,162,520 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02382:Crb1
|
APN |
1 |
139,165,352 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02411:Crb1
|
APN |
1 |
139,176,213 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03070:Crb1
|
APN |
1 |
139,168,996 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02984:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL02988:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL02991:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL02991:Crb1
|
UTSW |
1 |
139,164,822 (GRCm39) |
frame shift |
probably null |
|
IGL03014:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03050:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03054:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03055:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03097:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03098:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03134:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03138:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
IGL03147:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
P0017:Crb1
|
UTSW |
1 |
139,176,678 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0276:Crb1
|
UTSW |
1 |
139,251,073 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0325:Crb1
|
UTSW |
1 |
139,168,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Crb1
|
UTSW |
1 |
139,126,529 (GRCm39) |
splice site |
probably benign |
|
R0479:Crb1
|
UTSW |
1 |
139,126,352 (GRCm39) |
missense |
probably damaging |
0.98 |
R0734:Crb1
|
UTSW |
1 |
139,264,822 (GRCm39) |
missense |
probably benign |
0.25 |
R1573:Crb1
|
UTSW |
1 |
139,265,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1728:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1729:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1730:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1730:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1739:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1762:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1762:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1762:Crb1
|
UTSW |
1 |
139,165,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1783:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1784:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Crb1
|
UTSW |
1 |
139,170,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Crb1
|
UTSW |
1 |
139,171,155 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Crb1
|
UTSW |
1 |
139,162,517 (GRCm39) |
missense |
probably benign |
|
R1785:Crb1
|
UTSW |
1 |
139,165,360 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Crb1
|
UTSW |
1 |
139,168,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Crb1
|
UTSW |
1 |
139,164,750 (GRCm39) |
missense |
probably damaging |
0.97 |
R2057:Crb1
|
UTSW |
1 |
139,242,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Crb1
|
UTSW |
1 |
139,265,163 (GRCm39) |
missense |
probably benign |
0.03 |
R2140:Crb1
|
UTSW |
1 |
139,164,750 (GRCm39) |
missense |
probably benign |
0.01 |
R2363:Crb1
|
UTSW |
1 |
139,265,016 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3605:Crb1
|
UTSW |
1 |
139,165,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R3817:Crb1
|
UTSW |
1 |
139,175,835 (GRCm39) |
missense |
probably benign |
|
R3942:Crb1
|
UTSW |
1 |
139,265,211 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4272:Crb1
|
UTSW |
1 |
139,251,049 (GRCm39) |
missense |
probably benign |
0.04 |
R4301:Crb1
|
UTSW |
1 |
139,176,568 (GRCm39) |
missense |
probably benign |
0.01 |
R4403:Crb1
|
UTSW |
1 |
139,176,117 (GRCm39) |
missense |
probably benign |
0.00 |
R4700:Crb1
|
UTSW |
1 |
139,126,509 (GRCm39) |
missense |
probably damaging |
0.96 |
R4771:Crb1
|
UTSW |
1 |
139,255,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R4845:Crb1
|
UTSW |
1 |
139,170,772 (GRCm39) |
missense |
probably benign |
0.06 |
R4867:Crb1
|
UTSW |
1 |
139,170,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:Crb1
|
UTSW |
1 |
139,170,756 (GRCm39) |
missense |
probably damaging |
0.99 |
R5270:Crb1
|
UTSW |
1 |
139,164,602 (GRCm39) |
missense |
probably damaging |
0.97 |
R5347:Crb1
|
UTSW |
1 |
139,265,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R5513:Crb1
|
UTSW |
1 |
139,164,559 (GRCm39) |
critical splice donor site |
probably null |
|
R5641:Crb1
|
UTSW |
1 |
139,176,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R5754:Crb1
|
UTSW |
1 |
139,159,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R5968:Crb1
|
UTSW |
1 |
139,170,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:Crb1
|
UTSW |
1 |
139,176,686 (GRCm39) |
nonsense |
probably null |
|
R6369:Crb1
|
UTSW |
1 |
139,165,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Crb1
|
UTSW |
1 |
139,170,864 (GRCm39) |
missense |
probably benign |
0.00 |
R7020:Crb1
|
UTSW |
1 |
139,159,341 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7072:Crb1
|
UTSW |
1 |
139,165,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R7073:Crb1
|
UTSW |
1 |
139,176,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R7135:Crb1
|
UTSW |
1 |
139,171,105 (GRCm39) |
missense |
probably damaging |
0.97 |
R7493:Crb1
|
UTSW |
1 |
139,164,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Crb1
|
UTSW |
1 |
139,175,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R7554:Crb1
|
UTSW |
1 |
139,265,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Crb1
|
UTSW |
1 |
139,164,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R7740:Crb1
|
UTSW |
1 |
139,165,428 (GRCm39) |
missense |
probably benign |
0.01 |
R7912:Crb1
|
UTSW |
1 |
139,170,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R8036:Crb1
|
UTSW |
1 |
139,165,122 (GRCm39) |
missense |
probably benign |
0.07 |
R8042:Crb1
|
UTSW |
1 |
139,242,392 (GRCm39) |
missense |
probably damaging |
0.99 |
R8329:Crb1
|
UTSW |
1 |
139,165,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R8332:Crb1
|
UTSW |
1 |
139,165,152 (GRCm39) |
missense |
probably damaging |
0.96 |
R8880:Crb1
|
UTSW |
1 |
139,164,886 (GRCm39) |
missense |
probably benign |
0.19 |
R8894:Crb1
|
UTSW |
1 |
139,175,750 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9052:Crb1
|
UTSW |
1 |
139,171,161 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9138:Crb1
|
UTSW |
1 |
139,162,468 (GRCm39) |
missense |
|
|
R9209:Crb1
|
UTSW |
1 |
139,171,051 (GRCm39) |
missense |
probably damaging |
0.98 |
R9567:Crb1
|
UTSW |
1 |
139,171,208 (GRCm39) |
missense |
probably benign |
0.04 |
X0066:Crb1
|
UTSW |
1 |
139,175,983 (GRCm39) |
missense |
probably benign |
0.10 |
Z1176:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
Z1177:Crb1
|
UTSW |
1 |
139,264,766 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Crb1
|
UTSW |
1 |
139,176,639 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:Crb1
|
UTSW |
1 |
139,164,824 (GRCm39) |
frame shift |
probably null |
|
|