Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
C |
5: 64,056,011 (GRCm39) |
V249A |
possibly damaging |
Het |
9930111J21Rik2 |
C |
G |
11: 48,910,149 (GRCm39) |
L761F |
probably damaging |
Het |
Abca1 |
G |
A |
4: 53,090,291 (GRCm39) |
T386I |
probably damaging |
Het |
Abca14 |
T |
C |
7: 119,888,764 (GRCm39) |
Y1237H |
probably benign |
Het |
Abi3bp |
C |
T |
16: 56,471,088 (GRCm39) |
R578* |
probably null |
Het |
Abi3bp |
T |
G |
16: 56,433,566 (GRCm39) |
L550R |
probably benign |
Het |
Adamts7 |
A |
T |
9: 90,062,729 (GRCm39) |
K394N |
probably damaging |
Het |
Ahdc1 |
A |
G |
4: 132,793,220 (GRCm39) |
E1487G |
possibly damaging |
Het |
AI987944 |
T |
C |
7: 41,023,950 (GRCm39) |
E343G |
probably damaging |
Het |
Ankrd26 |
T |
A |
6: 118,500,843 (GRCm39) |
H876L |
possibly damaging |
Het |
Atg16l1 |
A |
C |
1: 87,694,737 (GRCm39) |
Q138P |
probably benign |
Het |
Atp1b1 |
G |
T |
1: 164,281,084 (GRCm39) |
T11K |
probably benign |
Het |
Calr3 |
A |
G |
8: 73,188,683 (GRCm39) |
L40S |
probably damaging |
Het |
Ccar1 |
A |
C |
10: 62,581,066 (GRCm39) |
D1119E |
unknown |
Het |
Cdan1 |
C |
A |
2: 120,551,241 (GRCm39) |
C1093F |
probably damaging |
Het |
Cdk12 |
T |
G |
11: 98,101,464 (GRCm39) |
S441A |
unknown |
Het |
Cfap61 |
T |
C |
2: 146,056,600 (GRCm39) |
L1193P |
probably damaging |
Het |
Chd2 |
A |
T |
7: 73,128,416 (GRCm39) |
D856E |
probably benign |
Het |
Chil3 |
T |
C |
3: 106,071,562 (GRCm39) |
D34G |
probably benign |
Het |
Cln3 |
T |
A |
7: 126,178,390 (GRCm39) |
H211L |
probably benign |
Het |
Cpa1 |
A |
G |
6: 30,641,818 (GRCm39) |
D214G |
probably damaging |
Het |
Cttnbp2 |
T |
G |
6: 18,408,693 (GRCm39) |
D976A |
probably benign |
Het |
Dcstamp |
T |
A |
15: 39,617,708 (GRCm39) |
V39E |
probably damaging |
Het |
Dicer1 |
C |
T |
12: 104,697,297 (GRCm39) |
V87M |
possibly damaging |
Het |
Duox1 |
A |
G |
2: 122,175,194 (GRCm39) |
T1331A |
probably benign |
Het |
Elapor1 |
C |
T |
3: 108,382,359 (GRCm39) |
G270E |
probably damaging |
Het |
Fam184a |
T |
A |
10: 53,528,530 (GRCm39) |
Q29L |
probably damaging |
Het |
Fcer2a |
T |
C |
8: 3,738,557 (GRCm39) |
E60G |
possibly damaging |
Het |
Flnc |
C |
T |
6: 29,459,507 (GRCm39) |
P2536S |
probably damaging |
Het |
Fnbp1l |
A |
T |
3: 122,340,611 (GRCm39) |
M463K |
probably benign |
Het |
Garem2 |
A |
G |
5: 30,319,762 (GRCm39) |
D408G |
probably benign |
Het |
Gm6370 |
T |
A |
5: 146,430,539 (GRCm39) |
D241E |
probably benign |
Het |
Gpc3 |
T |
A |
X: 51,486,083 (GRCm39) |
I344F |
probably damaging |
Het |
Gtf2e1 |
T |
A |
16: 37,331,904 (GRCm39) |
E390D |
possibly damaging |
Het |
Hmgcs2 |
T |
A |
3: 98,198,499 (GRCm39) |
I134N |
probably damaging |
Het |
Il15ra |
T |
A |
2: 11,723,155 (GRCm39) |
|
probably null |
Het |
Ints8 |
A |
T |
4: 11,225,712 (GRCm39) |
M615K |
possibly damaging |
Het |
Irak1 |
G |
A |
X: 73,060,744 (GRCm39) |
T193I |
probably damaging |
Het |
Jmjd1c |
A |
G |
10: 67,075,242 (GRCm39) |
|
probably null |
Het |
Knstrn |
T |
A |
2: 118,661,456 (GRCm39) |
|
probably null |
Het |
Letm1 |
C |
A |
5: 33,926,830 (GRCm39) |
V156L |
possibly damaging |
Het |
Lrrc24 |
G |
A |
15: 76,607,111 (GRCm39) |
P95L |
probably damaging |
Het |
Map2k2 |
T |
C |
10: 80,955,213 (GRCm39) |
S14P |
probably damaging |
Het |
Me3 |
T |
C |
7: 89,499,589 (GRCm39) |
Y535H |
probably damaging |
Het |
Nfatc2ip |
T |
C |
7: 125,990,467 (GRCm39) |
E178G |
probably benign |
Het |
Nop56 |
T |
A |
2: 130,119,488 (GRCm39) |
I51N |
probably damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Nudt5 |
A |
T |
2: 5,860,794 (GRCm39) |
I22F |
possibly damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,523 (GRCm39) |
W163R |
probably damaging |
Het |
Or2m12 |
C |
T |
16: 19,105,047 (GRCm39) |
A149T |
probably benign |
Het |
Or4p23 |
C |
G |
2: 88,576,953 (GRCm39) |
G93A |
probably benign |
Het |
Pbrm1 |
A |
G |
14: 30,754,406 (GRCm39) |
D142G |
possibly damaging |
Het |
Pdcl |
A |
T |
2: 37,242,056 (GRCm39) |
N231K |
probably benign |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pid1 |
T |
A |
1: 84,016,159 (GRCm39) |
I69F |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,607,584 (GRCm39) |
S1091P |
probably benign |
Het |
Plcb4 |
T |
C |
2: 135,844,514 (GRCm39) |
I144T |
probably benign |
Het |
Plxnd1 |
T |
C |
6: 115,939,725 (GRCm39) |
N1418S |
probably benign |
Het |
Pmm1 |
T |
C |
15: 81,840,601 (GRCm39) |
T82A |
probably benign |
Het |
Prrc2b |
C |
A |
2: 32,113,476 (GRCm39) |
Q1970K |
probably damaging |
Het |
Ptprz1 |
C |
T |
6: 23,000,649 (GRCm39) |
T913M |
possibly damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,659,585 (GRCm39) |
|
probably null |
Het |
Rbm8a2 |
T |
C |
1: 175,806,420 (GRCm39) |
E19G |
possibly damaging |
Het |
Rgs3 |
T |
C |
4: 62,608,741 (GRCm39) |
S336P |
probably damaging |
Het |
Saxo5 |
A |
T |
8: 3,529,028 (GRCm39) |
D201V |
probably benign |
Het |
Serpina11 |
G |
T |
12: 103,952,233 (GRCm39) |
T179K |
probably damaging |
Het |
Serpina1f |
T |
C |
12: 103,659,655 (GRCm39) |
N209S |
possibly damaging |
Het |
Serpinf2 |
G |
A |
11: 75,327,588 (GRCm39) |
T159I |
probably benign |
Het |
Slc19a1 |
T |
C |
10: 76,877,758 (GRCm39) |
C98R |
possibly damaging |
Het |
Slc22a20 |
A |
T |
19: 6,021,553 (GRCm39) |
I483N |
possibly damaging |
Het |
Spata31d1d |
A |
G |
13: 59,879,435 (GRCm39) |
C34R |
possibly damaging |
Het |
Stoml2 |
G |
T |
4: 43,030,243 (GRCm39) |
Y119* |
probably null |
Het |
Susd1 |
A |
G |
4: 59,349,843 (GRCm39) |
L531P |
possibly damaging |
Het |
Timd5 |
A |
G |
11: 46,419,394 (GRCm39) |
N70S |
probably benign |
Het |
Tln1 |
C |
T |
4: 43,553,083 (GRCm39) |
|
probably null |
Het |
Tmem39b |
A |
C |
4: 129,587,716 (GRCm39) |
S32A |
probably benign |
Het |
Tmx3 |
T |
C |
18: 90,546,037 (GRCm39) |
F206S |
probably damaging |
Het |
Tnfsf14 |
T |
C |
17: 57,497,638 (GRCm39) |
D198G |
possibly damaging |
Het |
Trappc10 |
A |
G |
10: 78,034,876 (GRCm39) |
|
probably null |
Het |
Tssk2 |
A |
G |
16: 17,716,603 (GRCm39) |
D2G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,601,985 (GRCm39) |
N18559S |
possibly damaging |
Het |
Ube3b |
G |
A |
5: 114,527,135 (GRCm39) |
V118M |
probably damaging |
Het |
Vmn1r23 |
T |
C |
6: 57,903,604 (GRCm39) |
D58G |
probably benign |
Het |
Vmn2r53 |
T |
A |
7: 12,335,366 (GRCm39) |
Y98F |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,513,594 (GRCm39) |
N350Y |
probably benign |
Het |
Vmn2r82 |
A |
T |
10: 79,192,519 (GRCm39) |
H32L |
probably benign |
Het |
Wsb1 |
T |
C |
11: 79,131,212 (GRCm39) |
I395V |
probably benign |
Het |
Zbtb47 |
A |
G |
9: 121,591,703 (GRCm39) |
T8A |
possibly damaging |
Het |
Zfat |
T |
C |
15: 68,051,709 (GRCm39) |
D695G |
probably benign |
Het |
Zfp358 |
G |
T |
8: 3,546,995 (GRCm39) |
V526F |
possibly damaging |
Het |
Zmat1 |
A |
G |
X: 133,873,861 (GRCm39) |
L476P |
possibly damaging |
Het |
|
Other mutations in Ces4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00584:Ces4a
|
APN |
8 |
105,871,795 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01574:Ces4a
|
APN |
8 |
105,871,859 (GRCm39) |
splice site |
probably benign |
|
IGL01655:Ces4a
|
APN |
8 |
105,873,806 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03092:Ces4a
|
APN |
8 |
105,874,836 (GRCm39) |
splice site |
probably benign |
|
IGL03151:Ces4a
|
APN |
8 |
105,874,829 (GRCm39) |
critical splice donor site |
probably null |
|
F6893:Ces4a
|
UTSW |
8 |
105,873,859 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0266:Ces4a
|
UTSW |
8 |
105,868,598 (GRCm39) |
missense |
probably benign |
|
R0659:Ces4a
|
UTSW |
8 |
105,871,554 (GRCm39) |
splice site |
probably benign |
|
R1239:Ces4a
|
UTSW |
8 |
105,876,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Ces4a
|
UTSW |
8 |
105,864,667 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1467:Ces4a
|
UTSW |
8 |
105,864,667 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1505:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1598:Ces4a
|
UTSW |
8 |
105,869,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1736:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1737:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1738:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1744:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2126:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R4512:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R4865:Ces4a
|
UTSW |
8 |
105,873,790 (GRCm39) |
missense |
probably benign |
0.05 |
R4934:Ces4a
|
UTSW |
8 |
105,864,613 (GRCm39) |
missense |
probably benign |
0.30 |
R4936:Ces4a
|
UTSW |
8 |
105,864,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R5255:Ces4a
|
UTSW |
8 |
105,869,121 (GRCm39) |
missense |
probably benign |
0.00 |
R5342:Ces4a
|
UTSW |
8 |
105,872,775 (GRCm39) |
missense |
probably benign |
0.07 |
R5647:Ces4a
|
UTSW |
8 |
105,872,712 (GRCm39) |
missense |
probably benign |
0.10 |
R6062:Ces4a
|
UTSW |
8 |
105,864,806 (GRCm39) |
critical splice donor site |
probably null |
|
R6490:Ces4a
|
UTSW |
8 |
105,876,090 (GRCm39) |
missense |
probably benign |
0.09 |
R6606:Ces4a
|
UTSW |
8 |
105,876,010 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6876:Ces4a
|
UTSW |
8 |
105,871,624 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6901:Ces4a
|
UTSW |
8 |
105,873,330 (GRCm39) |
missense |
probably benign |
|
R7519:Ces4a
|
UTSW |
8 |
105,871,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R7682:Ces4a
|
UTSW |
8 |
105,873,297 (GRCm39) |
missense |
probably benign |
0.00 |
R8171:Ces4a
|
UTSW |
8 |
105,873,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Ces4a
|
UTSW |
8 |
105,874,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R8833:Ces4a
|
UTSW |
8 |
105,858,614 (GRCm39) |
missense |
probably benign |
0.00 |
R9168:Ces4a
|
UTSW |
8 |
105,876,050 (GRCm39) |
missense |
probably benign |
0.00 |
R9557:Ces4a
|
UTSW |
8 |
105,869,527 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9758:Ces4a
|
UTSW |
8 |
105,869,054 (GRCm39) |
missense |
possibly damaging |
0.50 |
Z1176:Ces4a
|
UTSW |
8 |
105,858,609 (GRCm39) |
missense |
probably benign |
0.00 |
|