Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
G |
A |
5: 109,885,370 (GRCm39) |
Q163* |
probably null |
Het |
Anxa6 |
T |
A |
11: 54,898,725 (GRCm39) |
T150S |
probably damaging |
Het |
Bpifb6 |
T |
A |
2: 153,744,929 (GRCm39) |
L45Q |
probably damaging |
Het |
Brwd1 |
T |
C |
16: 95,828,568 (GRCm39) |
D1121G |
probably damaging |
Het |
C1ql3 |
A |
G |
2: 13,015,483 (GRCm39) |
I59T |
possibly damaging |
Het |
Ccdc80 |
A |
G |
16: 44,924,888 (GRCm39) |
H674R |
possibly damaging |
Het |
Cdhr1 |
T |
G |
14: 36,811,337 (GRCm39) |
E258A |
probably damaging |
Het |
Ces2g |
T |
A |
8: 105,692,962 (GRCm39) |
F333L |
probably damaging |
Het |
Chn2 |
C |
T |
6: 54,277,156 (GRCm39) |
T445I |
probably benign |
Het |
Cpe |
T |
C |
8: 65,050,562 (GRCm39) |
D382G |
possibly damaging |
Het |
Cyp4a14 |
A |
T |
4: 115,350,806 (GRCm39) |
V156D |
probably damaging |
Het |
Ddx23 |
A |
T |
15: 98,556,315 (GRCm39) |
M1K |
probably null |
Het |
Dnajc7 |
T |
C |
11: 100,482,387 (GRCm39) |
I202V |
probably benign |
Het |
Dsn1 |
T |
A |
2: 156,839,636 (GRCm39) |
D255V |
possibly damaging |
Het |
Dvl3 |
A |
T |
16: 20,346,000 (GRCm39) |
|
probably null |
Het |
Epm2a |
A |
G |
10: 11,266,684 (GRCm39) |
D143G |
possibly damaging |
Het |
Erc1 |
T |
A |
6: 119,738,149 (GRCm39) |
M565L |
probably benign |
Het |
Fancm |
T |
C |
12: 65,173,321 (GRCm39) |
C1878R |
possibly damaging |
Het |
Gapvd1 |
T |
C |
2: 34,590,834 (GRCm39) |
E946G |
probably damaging |
Het |
Gm9195 |
C |
T |
14: 72,678,113 (GRCm39) |
R2352K |
possibly damaging |
Het |
Greb1 |
C |
A |
12: 16,790,122 (GRCm39) |
|
probably benign |
Het |
Haus5 |
G |
A |
7: 30,362,678 (GRCm39) |
A44V |
possibly damaging |
Het |
Herc4 |
A |
G |
10: 63,105,457 (GRCm39) |
Y146C |
probably benign |
Het |
Herc6 |
T |
G |
6: 57,636,802 (GRCm39) |
|
probably null |
Het |
Hivep2 |
G |
T |
10: 14,003,414 (GRCm39) |
G4V |
probably damaging |
Het |
Hsdl2 |
G |
T |
4: 59,612,724 (GRCm39) |
G425V |
probably damaging |
Het |
Igkv1-110 |
C |
T |
6: 68,247,974 (GRCm39) |
L28F |
probably benign |
Het |
Il21r |
T |
A |
7: 125,231,727 (GRCm39) |
L385Q |
possibly damaging |
Het |
Krtap5-1 |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
7: 141,850,333 (GRCm39) |
|
probably benign |
Het |
Krtap5-2 |
C |
T |
7: 141,728,699 (GRCm39) |
C149Y |
unknown |
Het |
Lingo2 |
T |
A |
4: 35,709,248 (GRCm39) |
N244I |
probably damaging |
Het |
Lrrk2 |
C |
T |
15: 91,651,527 (GRCm39) |
R1728C |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,578,096 (GRCm39) |
|
probably benign |
Het |
Malrd1 |
G |
A |
2: 15,619,026 (GRCm39) |
V297I |
not run |
Het |
Mars1 |
T |
A |
10: 127,136,444 (GRCm39) |
E460D |
probably benign |
Het |
Nr1i3 |
A |
G |
1: 171,044,396 (GRCm39) |
I174V |
probably benign |
Het |
Odf2 |
C |
T |
2: 29,820,636 (GRCm39) |
T814M |
probably damaging |
Het |
Or10q1 |
T |
C |
19: 13,727,328 (GRCm39) |
V286A |
probably benign |
Het |
Or4k1 |
T |
C |
14: 50,377,803 (GRCm39) |
M98V |
probably benign |
Het |
Or4k52 |
A |
T |
2: 111,610,793 (GRCm39) |
I43F |
possibly damaging |
Het |
Pcdhga8 |
T |
C |
18: 37,860,470 (GRCm39) |
S509P |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,374,102 (GRCm39) |
L2011S |
probably benign |
Het |
Pole |
T |
A |
5: 110,478,907 (GRCm39) |
S1930T |
probably benign |
Het |
Poteg |
T |
A |
8: 27,952,052 (GRCm39) |
|
probably null |
Het |
Ptprk |
T |
A |
10: 28,372,920 (GRCm39) |
C724S |
probably damaging |
Het |
Rabgap1l |
T |
C |
1: 160,509,673 (GRCm39) |
E468G |
probably benign |
Het |
Rbm12b1 |
G |
T |
4: 12,145,954 (GRCm39) |
R642L |
probably benign |
Het |
Relch |
T |
C |
1: 105,658,986 (GRCm39) |
V914A |
probably damaging |
Het |
S1pr4 |
A |
T |
10: 81,334,855 (GRCm39) |
Y206* |
probably null |
Het |
Sim2 |
A |
G |
16: 93,915,819 (GRCm39) |
I261V |
probably benign |
Het |
Slc22a12 |
C |
A |
19: 6,587,199 (GRCm39) |
A448S |
probably benign |
Het |
Slc4a2 |
A |
G |
5: 24,636,666 (GRCm39) |
|
probably null |
Het |
Slc6a7 |
T |
C |
18: 61,133,495 (GRCm39) |
E567G |
possibly damaging |
Het |
St6gal1 |
T |
C |
16: 23,139,785 (GRCm39) |
|
probably benign |
Het |
Syne3 |
T |
C |
12: 104,920,546 (GRCm39) |
K550R |
probably benign |
Het |
Tekt1 |
T |
A |
11: 72,250,544 (GRCm39) |
T51S |
probably benign |
Het |
Tm9sf4 |
T |
A |
2: 153,050,663 (GRCm39) |
V640E |
probably damaging |
Het |
Tnfsf8 |
G |
T |
4: 63,752,683 (GRCm39) |
H127Q |
possibly damaging |
Het |
Tomm20 |
A |
G |
8: 127,666,633 (GRCm39) |
L80S |
probably damaging |
Het |
Top2a |
T |
C |
11: 98,884,640 (GRCm39) |
D1526G |
probably benign |
Het |
Trmt1l |
T |
C |
1: 151,316,639 (GRCm39) |
V200A |
possibly damaging |
Het |
Trpa1 |
A |
G |
1: 14,982,625 (GRCm39) |
V77A |
possibly damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,239,615 (GRCm39) |
V316D |
probably damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,368,324 (GRCm39) |
L223M |
probably benign |
Het |
Zfp2 |
T |
C |
11: 50,791,605 (GRCm39) |
H146R |
probably damaging |
Het |
Zfp52 |
T |
C |
17: 21,781,252 (GRCm39) |
S367P |
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 |
R1894:Crb1
|
UTSW |
1 |
139,170,931 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
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 |
|
|