Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
A |
G |
6: 91,905,707 (GRCm39) |
T493A |
probably damaging |
Het |
Aars1 |
A |
G |
8: 111,776,493 (GRCm39) |
K650E |
probably benign |
Het |
Abcb1b |
C |
T |
5: 8,882,258 (GRCm39) |
S793F |
probably benign |
Het |
Adamts18 |
T |
A |
8: 114,501,908 (GRCm39) |
I318F |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,571,322 (GRCm39) |
I1137T |
probably damaging |
Het |
Ambra1 |
T |
A |
2: 91,603,838 (GRCm39) |
F607L |
probably benign |
Het |
Ankrd46 |
A |
T |
15: 36,479,566 (GRCm39) |
V175D |
possibly damaging |
Het |
Arhgap28 |
C |
A |
17: 68,208,277 (GRCm39) |
E114* |
probably null |
Het |
Arrdc1 |
C |
T |
2: 24,816,158 (GRCm39) |
G282S |
probably damaging |
Het |
Atp1a3 |
A |
T |
7: 24,681,216 (GRCm39) |
L790Q |
probably damaging |
Het |
Bend5 |
T |
A |
4: 111,272,406 (GRCm39) |
V12D |
probably damaging |
Het |
Bod1l |
C |
T |
5: 41,976,608 (GRCm39) |
E1569K |
probably damaging |
Het |
Cdc123 |
T |
A |
2: 5,808,775 (GRCm39) |
I234L |
probably benign |
Het |
Cep126 |
T |
G |
9: 8,120,749 (GRCm39) |
E91D |
probably damaging |
Het |
Ces1d |
T |
C |
8: 93,897,765 (GRCm39) |
T442A |
probably benign |
Het |
Chsy3 |
C |
T |
18: 59,542,299 (GRCm39) |
A479V |
probably benign |
Het |
Clcn4 |
C |
A |
7: 7,296,060 (GRCm39) |
G261C |
probably damaging |
Het |
Clhc1 |
A |
T |
11: 29,507,651 (GRCm39) |
|
probably null |
Het |
Cnot3 |
T |
A |
7: 3,658,565 (GRCm39) |
|
probably null |
Het |
Col9a1 |
C |
A |
1: 24,276,261 (GRCm39) |
P723H |
probably damaging |
Het |
Crybg3 |
A |
T |
16: 59,375,605 (GRCm39) |
M169K |
probably benign |
Het |
Cxxc4 |
A |
G |
3: 133,963,814 (GRCm39) |
R353G |
probably benign |
Het |
Dennd3 |
A |
T |
15: 73,412,657 (GRCm39) |
I440F |
probably damaging |
Het |
Dnai3 |
A |
G |
3: 145,772,675 (GRCm39) |
L457P |
probably damaging |
Het |
Elmo3 |
G |
T |
8: 106,035,649 (GRCm39) |
S553I |
probably damaging |
Het |
Elovl2 |
A |
G |
13: 41,340,943 (GRCm39) |
Y198H |
probably benign |
Het |
Epm2aip1 |
A |
G |
9: 111,101,105 (GRCm39) |
Y26C |
probably damaging |
Het |
Ext1 |
A |
C |
15: 52,953,335 (GRCm39) |
C510G |
possibly damaging |
Het |
Extl3 |
A |
T |
14: 65,314,938 (GRCm39) |
D81E |
probably benign |
Het |
Fbxl5 |
T |
A |
5: 43,916,018 (GRCm39) |
T465S |
probably benign |
Het |
Fbxo31 |
G |
A |
8: 122,291,384 (GRCm39) |
|
probably null |
Het |
Gabrr2 |
A |
T |
4: 33,081,470 (GRCm39) |
K169* |
probably null |
Het |
Haus4 |
A |
G |
14: 54,779,602 (GRCm39) |
Y341H |
probably damaging |
Het |
Itgae |
A |
T |
11: 73,011,099 (GRCm39) |
|
probably null |
Het |
Jmjd7 |
C |
T |
2: 119,860,996 (GRCm39) |
H149Y |
possibly damaging |
Het |
Kcnh2 |
C |
T |
5: 24,529,561 (GRCm39) |
C725Y |
probably damaging |
Het |
Mroh1 |
C |
T |
15: 76,331,532 (GRCm39) |
P1252L |
probably benign |
Het |
Ms4a14 |
A |
G |
19: 11,280,308 (GRCm39) |
F750S |
probably benign |
Het |
Naf1 |
T |
A |
8: 67,313,165 (GRCm39) |
D49E |
unknown |
Het |
Notch3 |
T |
C |
17: 32,341,747 (GRCm39) |
T2002A |
possibly damaging |
Het |
Or10q12 |
T |
A |
19: 13,745,716 (GRCm39) |
D3E |
probably benign |
Het |
Or14c44 |
A |
G |
7: 86,057,119 (GRCm39) |
|
probably benign |
Het |
Or1e33 |
A |
T |
11: 73,738,333 (GRCm39) |
I206N |
probably benign |
Het |
Or2d3c |
A |
T |
7: 106,525,777 (GRCm39) |
D296E |
probably benign |
Het |
Or2l13b |
A |
T |
16: 19,349,167 (GRCm39) |
C168S |
probably damaging |
Het |
Or7e175 |
A |
T |
9: 20,048,871 (GRCm39) |
N153I |
probably benign |
Het |
Or9s23 |
G |
A |
1: 92,501,810 (GRCm39) |
D306N |
probably benign |
Het |
Pck1 |
A |
G |
2: 172,997,743 (GRCm39) |
T271A |
possibly damaging |
Het |
Penk |
A |
G |
4: 4,133,976 (GRCm39) |
W224R |
possibly damaging |
Het |
Per2 |
C |
A |
1: 91,372,481 (GRCm39) |
V198F |
probably damaging |
Het |
Phf11d |
A |
G |
14: 59,599,280 (GRCm39) |
M23T |
probably damaging |
Het |
Pla2g4d |
A |
G |
2: 120,097,211 (GRCm39) |
V796A |
probably benign |
Het |
Pramel51 |
A |
T |
12: 88,143,122 (GRCm39) |
N360K |
possibly damaging |
Het |
Prdx6 |
A |
T |
1: 161,069,428 (GRCm39) |
|
probably null |
Het |
Prep |
A |
T |
10: 44,967,108 (GRCm39) |
N47I |
probably damaging |
Het |
Prodh2 |
A |
T |
7: 30,212,064 (GRCm39) |
|
probably null |
Het |
Prss38 |
G |
T |
11: 59,265,996 (GRCm39) |
H96N |
probably damaging |
Het |
Rab11a |
C |
A |
9: 64,635,613 (GRCm39) |
E47* |
probably null |
Het |
Rad18 |
C |
T |
6: 112,626,798 (GRCm39) |
G369D |
probably benign |
Het |
Rragc |
T |
C |
4: 123,823,717 (GRCm39) |
V330A |
probably damaging |
Het |
Serpina9 |
A |
T |
12: 103,967,680 (GRCm39) |
H238Q |
probably benign |
Het |
Serpinb3b |
T |
A |
1: 107,085,467 (GRCm39) |
K91N |
probably damaging |
Het |
Slc16a12 |
T |
G |
19: 34,652,730 (GRCm39) |
S139R |
probably benign |
Het |
Slc22a27 |
T |
A |
19: 7,887,472 (GRCm39) |
|
probably null |
Het |
Slc25a11 |
A |
G |
11: 70,536,005 (GRCm39) |
V243A |
probably benign |
Het |
Slc38a9 |
A |
T |
13: 112,868,148 (GRCm39) |
I545F |
probably benign |
Het |
Slc39a8 |
A |
T |
3: 135,590,157 (GRCm39) |
H349L |
probably damaging |
Het |
Slk |
C |
T |
19: 47,630,510 (GRCm39) |
T1227I |
possibly damaging |
Het |
Spdye4b |
A |
G |
5: 143,180,609 (GRCm39) |
E25G |
possibly damaging |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
St3gal1 |
A |
G |
15: 66,983,114 (GRCm39) |
V214A |
probably benign |
Het |
St7l |
T |
A |
3: 104,833,893 (GRCm39) |
M550K |
probably benign |
Het |
Tbk1 |
A |
C |
10: 121,388,151 (GRCm39) |
F638C |
possibly damaging |
Het |
Tex101 |
A |
T |
7: 24,369,190 (GRCm39) |
C114S |
probably damaging |
Het |
Ttll13 |
A |
G |
7: 79,905,135 (GRCm39) |
M384V |
probably benign |
Het |
Ugt2b37 |
A |
T |
5: 87,402,189 (GRCm39) |
D147E |
probably damaging |
Het |
Vmn1r10 |
A |
T |
6: 57,090,686 (GRCm39) |
T93S |
probably benign |
Het |
Wasl |
G |
A |
6: 24,619,396 (GRCm39) |
P375S |
unknown |
Het |
Zfp236 |
C |
A |
18: 82,692,481 (GRCm39) |
E165* |
probably null |
Het |
Zfp839 |
A |
T |
12: 110,822,060 (GRCm39) |
R291S |
probably 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 |
|
R0127:Cep89
|
UTSW |
7 |
35,127,687 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
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 |
|
|