Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310061N02Rik |
T |
C |
16: 88,504,342 (GRCm39) |
T152A |
probably benign |
Het |
Abca1 |
T |
C |
4: 53,067,155 (GRCm39) |
I1351V |
probably benign |
Het |
Acap1 |
A |
T |
11: 69,778,043 (GRCm39) |
|
probably benign |
Het |
Als2cl |
T |
C |
9: 110,720,935 (GRCm39) |
L521P |
probably damaging |
Het |
Ankrd50 |
T |
C |
3: 38,510,384 (GRCm39) |
D661G |
probably benign |
Het |
Atp6v1b2 |
T |
A |
8: 69,556,112 (GRCm39) |
N262K |
probably damaging |
Het |
Baz1a |
T |
A |
12: 54,945,491 (GRCm39) |
D1288V |
possibly damaging |
Het |
Bbs1 |
A |
T |
19: 4,945,057 (GRCm39) |
D371E |
probably benign |
Het |
Bphl |
A |
G |
13: 34,248,029 (GRCm39) |
|
probably benign |
Het |
Caskin2 |
C |
A |
11: 115,691,820 (GRCm39) |
R988S |
probably damaging |
Het |
Cbr1 |
C |
A |
16: 93,406,875 (GRCm39) |
T197N |
probably damaging |
Het |
Ccdc88c |
T |
C |
12: 100,901,999 (GRCm39) |
E1213G |
possibly damaging |
Het |
Ccna1 |
A |
G |
3: 54,957,169 (GRCm39) |
F83L |
probably damaging |
Het |
Cep290 |
T |
A |
10: 100,372,787 (GRCm39) |
|
probably benign |
Het |
Cmtm7 |
T |
C |
9: 114,610,738 (GRCm39) |
M45V |
probably benign |
Het |
Col16a1 |
T |
A |
4: 129,946,650 (GRCm39) |
V91E |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,845,326 (GRCm39) |
N920S |
probably benign |
Het |
Cyp26b1 |
A |
G |
6: 84,554,190 (GRCm39) |
|
probably benign |
Het |
Dao |
T |
A |
5: 114,158,024 (GRCm39) |
H215Q |
probably damaging |
Het |
Dido1 |
T |
C |
2: 180,313,617 (GRCm39) |
D885G |
probably benign |
Het |
Dlx4 |
T |
G |
11: 95,032,055 (GRCm39) |
M240L |
probably benign |
Het |
Dnah5 |
C |
T |
15: 28,295,071 (GRCm39) |
P1351L |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,015,717 (GRCm39) |
|
probably benign |
Het |
Dock5 |
A |
T |
14: 68,083,491 (GRCm39) |
D139E |
probably benign |
Het |
Dynlt5 |
T |
C |
4: 102,859,649 (GRCm39) |
|
probably benign |
Het |
Fam234b |
T |
C |
6: 135,195,821 (GRCm39) |
|
probably benign |
Het |
Fat2 |
T |
C |
11: 55,180,112 (GRCm39) |
T1410A |
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,815,269 (GRCm39) |
N3667K |
probably benign |
Het |
Gm5114 |
T |
C |
7: 39,057,880 (GRCm39) |
I580V |
probably benign |
Het |
Hapln1 |
A |
T |
13: 89,755,988 (GRCm39) |
Y264F |
probably benign |
Het |
Heatr5a |
A |
G |
12: 51,972,188 (GRCm39) |
V694A |
probably benign |
Het |
Hps1 |
A |
G |
19: 42,759,550 (GRCm39) |
|
probably benign |
Het |
Igsf9b |
G |
T |
9: 27,245,681 (GRCm39) |
R1216L |
possibly damaging |
Het |
Il4ra |
G |
T |
7: 125,168,242 (GRCm39) |
C87F |
probably damaging |
Het |
Kmt5b |
A |
G |
19: 3,836,465 (GRCm39) |
M1V |
probably null |
Het |
Krit1 |
A |
G |
5: 3,872,178 (GRCm39) |
E401G |
probably damaging |
Het |
Lamp1 |
T |
C |
8: 13,224,491 (GRCm39) |
V385A |
probably damaging |
Het |
Ly6g5b |
A |
G |
17: 35,333,567 (GRCm39) |
Y82H |
probably damaging |
Het |
Mapre2 |
A |
G |
18: 23,937,232 (GRCm39) |
I25V |
probably benign |
Het |
Mep1a |
A |
G |
17: 43,808,777 (GRCm39) |
|
probably benign |
Het |
Mkrn1 |
A |
G |
6: 39,376,209 (GRCm39) |
W466R |
probably benign |
Het |
Muc2 |
C |
A |
7: 141,302,691 (GRCm39) |
F11L |
probably benign |
Het |
Nebl |
T |
A |
2: 17,397,794 (GRCm39) |
M501L |
probably benign |
Het |
Oga |
A |
T |
19: 45,760,327 (GRCm39) |
I277N |
probably damaging |
Het |
Or11g2 |
A |
G |
14: 50,855,789 (GRCm39) |
I37V |
probably benign |
Het |
Or4p18 |
A |
G |
2: 88,232,699 (GRCm39) |
V193A |
probably benign |
Het |
Or5w8 |
A |
G |
2: 87,687,827 (GRCm39) |
I103V |
probably benign |
Het |
Or8g32 |
A |
G |
9: 39,305,238 (GRCm39) |
I50M |
probably benign |
Het |
Pkd1l2 |
A |
G |
8: 117,776,787 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,418,001 (GRCm39) |
M2886V |
probably damaging |
Het |
Pop5 |
T |
A |
5: 115,378,230 (GRCm39) |
L58H |
probably damaging |
Het |
Prkch |
C |
A |
12: 73,768,561 (GRCm39) |
H444N |
possibly damaging |
Het |
Reln |
T |
C |
5: 22,209,134 (GRCm39) |
D1148G |
probably damaging |
Het |
Rffl |
G |
A |
11: 82,703,458 (GRCm39) |
T120M |
probably damaging |
Het |
Rmdn2 |
A |
T |
17: 79,977,998 (GRCm39) |
S320C |
probably damaging |
Het |
Rrbp1 |
C |
T |
2: 143,831,864 (GRCm39) |
R101H |
probably benign |
Het |
Rtf1 |
G |
A |
2: 119,557,224 (GRCm39) |
R443H |
probably damaging |
Het |
Serac1 |
G |
T |
17: 6,099,115 (GRCm39) |
L559I |
probably damaging |
Het |
Slc12a1 |
A |
G |
2: 125,061,682 (GRCm39) |
R958G |
probably damaging |
Het |
Slc15a3 |
T |
A |
19: 10,833,350 (GRCm39) |
W456R |
probably damaging |
Het |
Slc28a2b |
T |
A |
2: 122,347,550 (GRCm39) |
|
probably null |
Het |
Slc35f5 |
C |
T |
1: 125,503,942 (GRCm39) |
P290L |
probably damaging |
Het |
Slc35g2 |
C |
T |
9: 100,435,170 (GRCm39) |
R167Q |
probably benign |
Het |
Spag4 |
T |
C |
2: 155,909,962 (GRCm39) |
V302A |
probably damaging |
Het |
Spire2 |
A |
C |
8: 124,084,836 (GRCm39) |
|
probably benign |
Het |
Sptbn2 |
G |
T |
19: 4,774,772 (GRCm39) |
V142L |
probably damaging |
Het |
Syt17 |
T |
A |
7: 118,009,164 (GRCm39) |
D352V |
probably damaging |
Het |
Tars3 |
A |
T |
7: 65,314,717 (GRCm39) |
D425V |
probably benign |
Het |
Thsd7a |
A |
G |
6: 12,554,907 (GRCm39) |
S326P |
probably benign |
Het |
Tnpo2 |
T |
C |
8: 85,767,257 (GRCm39) |
S64P |
probably damaging |
Het |
Tonsl |
G |
T |
15: 76,517,685 (GRCm39) |
A678D |
probably benign |
Het |
Trim12c |
A |
G |
7: 103,990,113 (GRCm39) |
|
probably null |
Het |
Tsc22d1 |
A |
G |
14: 76,656,421 (GRCm39) |
T885A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,572,542 (GRCm39) |
D26117G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,707,355 (GRCm39) |
|
probably benign |
Het |
Ugt3a1 |
T |
C |
15: 9,306,342 (GRCm39) |
F164L |
probably benign |
Het |
Vmn2r89 |
A |
G |
14: 51,693,160 (GRCm39) |
N170S |
probably damaging |
Het |
Vrk2 |
G |
T |
11: 26,484,313 (GRCm39) |
|
probably benign |
Het |
Wt1 |
C |
A |
2: 104,963,802 (GRCm39) |
D207E |
probably damaging |
Het |
Zbtb46 |
G |
A |
2: 181,053,608 (GRCm39) |
A368V |
probably benign |
Het |
Zc3h13 |
A |
T |
14: 75,560,694 (GRCm39) |
D428V |
unknown |
Het |
Zcchc8 |
C |
G |
5: 123,845,400 (GRCm39) |
G320A |
probably damaging |
Het |
Znfx1 |
T |
C |
2: 166,886,130 (GRCm39) |
E810G |
possibly damaging |
Het |
|
Other mutations in Cep89 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00784:Cep89
|
APN |
7 |
35,105,132 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01546:Cep89
|
APN |
7 |
35,120,325 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02001:Cep89
|
APN |
7 |
35,102,432 (GRCm39) |
splice site |
probably benign |
|
IGL02141:Cep89
|
APN |
7 |
35,120,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02468:Cep89
|
APN |
7 |
35,102,577 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02507:Cep89
|
APN |
7 |
35,134,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02612:Cep89
|
APN |
7 |
35,124,080 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03324:Cep89
|
APN |
7 |
35,124,078 (GRCm39) |
intron |
probably benign |
|
IGL03396:Cep89
|
APN |
7 |
35,128,603 (GRCm39) |
missense |
probably benign |
0.05 |
3-1:Cep89
|
UTSW |
7 |
35,124,147 (GRCm39) |
missense |
probably damaging |
0.99 |
FR4304:Cep89
|
UTSW |
7 |
35,109,066 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4976:Cep89
|
UTSW |
7 |
35,109,066 (GRCm39) |
utr 3 prime |
probably benign |
|
K2124:Cep89
|
UTSW |
7 |
35,120,397 (GRCm39) |
splice site |
probably benign |
|
R0416:Cep89
|
UTSW |
7 |
35,115,827 (GRCm39) |
unclassified |
probably benign |
|
R0609:Cep89
|
UTSW |
7 |
35,134,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:Cep89
|
UTSW |
7 |
35,117,636 (GRCm39) |
splice site |
probably benign |
|
R1468:Cep89
|
UTSW |
7 |
35,120,388 (GRCm39) |
splice site |
probably null |
|
R1468:Cep89
|
UTSW |
7 |
35,120,388 (GRCm39) |
splice site |
probably null |
|
R1661:Cep89
|
UTSW |
7 |
35,117,105 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3981:Cep89
|
UTSW |
7 |
35,137,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R4414:Cep89
|
UTSW |
7 |
35,115,822 (GRCm39) |
unclassified |
probably benign |
|
R4700:Cep89
|
UTSW |
7 |
35,137,862 (GRCm39) |
missense |
probably benign |
0.05 |
R4963:Cep89
|
UTSW |
7 |
35,102,577 (GRCm39) |
missense |
probably benign |
0.35 |
R4968:Cep89
|
UTSW |
7 |
35,109,055 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4972:Cep89
|
UTSW |
7 |
35,131,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Cep89
|
UTSW |
7 |
35,109,067 (GRCm39) |
unclassified |
probably benign |
|
R5767:Cep89
|
UTSW |
7 |
35,117,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R5809:Cep89
|
UTSW |
7 |
35,117,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R5890:Cep89
|
UTSW |
7 |
35,128,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R6290:Cep89
|
UTSW |
7 |
35,119,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R6361:Cep89
|
UTSW |
7 |
35,097,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R6627:Cep89
|
UTSW |
7 |
35,127,172 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7272:Cep89
|
UTSW |
7 |
35,137,888 (GRCm39) |
missense |
probably benign |
0.03 |
R7340:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7341:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7347:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7348:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7365:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7366:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7394:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7399:Cep89
|
UTSW |
7 |
35,137,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7422:Cep89
|
UTSW |
7 |
35,127,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7792:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7793:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R7819:Cep89
|
UTSW |
7 |
35,131,968 (GRCm39) |
missense |
probably benign |
0.07 |
R7860:Cep89
|
UTSW |
7 |
35,113,570 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7899:Cep89
|
UTSW |
7 |
35,129,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R8336:Cep89
|
UTSW |
7 |
35,127,141 (GRCm39) |
nonsense |
probably null |
|
R8669:Cep89
|
UTSW |
7 |
35,128,602 (GRCm39) |
missense |
probably benign |
0.04 |
R8974:Cep89
|
UTSW |
7 |
35,097,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R9580:Cep89
|
UTSW |
7 |
35,102,538 (GRCm39) |
missense |
possibly damaging |
0.63 |
V7732:Cep89
|
UTSW |
7 |
35,102,523 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cep89
|
UTSW |
7 |
35,096,506 (GRCm39) |
unclassified |
probably benign |
|
|