Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
C |
T |
6: 128,548,948 (GRCm39) |
C278Y |
probably damaging |
Het |
Abcc2 |
A |
T |
19: 43,815,174 (GRCm39) |
Q1187L |
probably benign |
Het |
Adcy9 |
A |
T |
16: 4,236,683 (GRCm39) |
Y6N |
probably damaging |
Het |
Adh1 |
T |
C |
3: 137,992,559 (GRCm39) |
I225T |
probably benign |
Het |
Akap11 |
A |
T |
14: 78,749,939 (GRCm39) |
I816K |
probably benign |
Het |
Ap1b1 |
T |
A |
11: 4,969,364 (GRCm39) |
M240K |
possibly damaging |
Het |
Apex1 |
A |
T |
14: 51,162,982 (GRCm39) |
T17S |
probably benign |
Het |
Arhgap21 |
C |
T |
2: 20,886,616 (GRCm39) |
G26D |
probably damaging |
Het |
Bahcc1 |
A |
G |
11: 120,180,615 (GRCm39) |
Y2613C |
probably benign |
Het |
Baz1b |
C |
T |
5: 135,246,248 (GRCm39) |
R566W |
probably damaging |
Het |
Casp8ap2 |
A |
T |
4: 32,641,400 (GRCm39) |
Y818F |
probably damaging |
Het |
Col3a1 |
T |
A |
1: 45,360,739 (GRCm39) |
C56* |
probably null |
Het |
Coro2a |
G |
A |
4: 46,542,261 (GRCm39) |
P371S |
probably damaging |
Het |
Cyp2a22 |
T |
A |
7: 26,638,605 (GRCm39) |
|
probably null |
Het |
Dpysl3 |
T |
A |
18: 43,494,132 (GRCm39) |
I183F |
probably damaging |
Het |
Drc1 |
A |
T |
5: 30,502,993 (GRCm39) |
N172I |
probably damaging |
Het |
Dst |
T |
C |
1: 34,303,915 (GRCm39) |
Y1378H |
probably damaging |
Het |
Dync2i2 |
C |
T |
2: 29,921,763 (GRCm39) |
A533T |
probably benign |
Het |
Eml2 |
G |
A |
7: 18,935,088 (GRCm39) |
V432I |
probably damaging |
Het |
Epb41l3 |
A |
T |
17: 69,590,955 (GRCm39) |
T91S |
probably damaging |
Het |
Exoc4 |
T |
C |
6: 33,452,932 (GRCm39) |
V474A |
probably benign |
Het |
Fam229b |
G |
A |
10: 38,994,989 (GRCm39) |
T56I |
probably damaging |
Het |
Gfm2 |
A |
G |
13: 97,288,169 (GRCm39) |
|
probably null |
Het |
Git2 |
C |
T |
5: 114,871,938 (GRCm39) |
E152K |
probably benign |
Het |
Golt1b |
T |
A |
6: 142,341,943 (GRCm39) |
I109N |
probably damaging |
Het |
Grid2ip |
T |
A |
5: 143,373,578 (GRCm39) |
M783K |
possibly damaging |
Het |
Inpp5a |
A |
G |
7: 139,154,898 (GRCm39) |
Y339C |
probably damaging |
Het |
Isoc2a |
T |
C |
7: 4,894,625 (GRCm39) |
S103P |
probably damaging |
Het |
Itih4 |
C |
A |
14: 30,614,586 (GRCm39) |
Q483K |
probably benign |
Het |
Kansl2 |
A |
G |
15: 98,418,197 (GRCm39) |
|
probably null |
Het |
Kdm5d |
G |
A |
Y: 921,528 (GRCm39) |
A509T |
probably benign |
Het |
Krt13 |
A |
T |
11: 100,008,437 (GRCm39) |
D433E |
unknown |
Het |
Lat2 |
C |
T |
5: 134,632,308 (GRCm39) |
V142M |
probably damaging |
Het |
Lemd1 |
A |
C |
1: 132,184,463 (GRCm39) |
*102S |
probably null |
Het |
Lrfn2 |
T |
C |
17: 49,376,934 (GRCm39) |
L5P |
possibly damaging |
Het |
Lrrc4c |
T |
G |
2: 97,459,557 (GRCm39) |
|
probably null |
Het |
Lypla1 |
T |
A |
1: 4,878,594 (GRCm39) |
|
probably null |
Het |
Magi2 |
G |
A |
5: 20,816,091 (GRCm39) |
G744R |
probably damaging |
Het |
Myh14 |
T |
A |
7: 44,274,502 (GRCm39) |
E948V |
probably null |
Het |
Myo5a |
C |
A |
9: 75,074,489 (GRCm39) |
Y799* |
probably null |
Het |
Nacc1 |
A |
C |
8: 85,401,700 (GRCm39) |
M371R |
possibly damaging |
Het |
Nlrp5 |
T |
G |
7: 23,109,372 (GRCm39) |
M106R |
probably benign |
Het |
Oas1h |
C |
T |
5: 121,005,229 (GRCm39) |
H226Y |
possibly damaging |
Het |
Obscn |
A |
C |
11: 58,929,690 (GRCm39) |
I5175R |
probably damaging |
Het |
Pcdh7 |
T |
A |
5: 57,878,497 (GRCm39) |
I684N |
probably damaging |
Het |
Pcdhb3 |
T |
A |
18: 37,435,706 (GRCm39) |
N557K |
probably damaging |
Het |
Pde3b |
T |
C |
7: 114,015,675 (GRCm39) |
L297S |
probably damaging |
Het |
Pigv |
G |
T |
4: 133,392,740 (GRCm39) |
H143Q |
probably benign |
Het |
Ptk2 |
T |
G |
15: 73,176,293 (GRCm39) |
Y251S |
possibly damaging |
Het |
Ralgds |
A |
G |
2: 28,433,673 (GRCm39) |
N219S |
probably damaging |
Het |
Sardh |
C |
A |
2: 27,087,540 (GRCm39) |
|
probably null |
Het |
Serpina3b |
A |
T |
12: 104,097,356 (GRCm39) |
K212N |
possibly damaging |
Het |
Sh3bp2 |
A |
G |
5: 34,716,971 (GRCm39) |
N461D |
probably benign |
Het |
Shisa2 |
A |
T |
14: 59,867,357 (GRCm39) |
Q203L |
probably damaging |
Het |
Shmt1 |
C |
A |
11: 60,688,383 (GRCm39) |
G255V |
probably damaging |
Het |
Socs1 |
T |
A |
16: 10,602,357 (GRCm39) |
I127F |
possibly damaging |
Het |
Srcap |
A |
T |
7: 127,137,922 (GRCm39) |
T1091S |
probably benign |
Het |
Syt14 |
A |
G |
1: 192,613,003 (GRCm39) |
I599T |
probably damaging |
Het |
Tep1 |
A |
T |
14: 51,084,457 (GRCm39) |
N907K |
probably benign |
Het |
Themis2 |
A |
G |
4: 132,513,291 (GRCm39) |
Y312H |
probably benign |
Het |
Tubgcp5 |
T |
G |
7: 55,473,357 (GRCm39) |
S812A |
probably benign |
Het |
Ush2a |
A |
T |
1: 188,582,237 (GRCm39) |
I3767F |
probably damaging |
Het |
Usp40 |
T |
A |
1: 87,907,738 (GRCm39) |
E626V |
probably damaging |
Het |
Utrn |
T |
C |
10: 12,566,620 (GRCm39) |
R1181G |
probably benign |
Het |
Vmn2r117 |
T |
A |
17: 23,698,535 (GRCm39) |
I13F |
probably damaging |
Het |
Wdr48 |
G |
T |
9: 119,753,775 (GRCm39) |
V646F |
probably damaging |
Het |
Wdr64 |
T |
C |
1: 175,633,556 (GRCm39) |
F936L |
possibly damaging |
Het |
|
Other mutations in 4930568D16Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01376:4930568D16Rik
|
APN |
2 |
35,245,640 (GRCm39) |
missense |
probably benign |
0.36 |
IGL01701:4930568D16Rik
|
APN |
2 |
35,254,776 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02049:4930568D16Rik
|
APN |
2 |
35,254,801 (GRCm39) |
missense |
probably benign |
0.03 |
R0112:4930568D16Rik
|
UTSW |
2 |
35,244,815 (GRCm39) |
missense |
probably benign |
0.06 |
R1778:4930568D16Rik
|
UTSW |
2 |
35,244,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R2398:4930568D16Rik
|
UTSW |
2 |
35,244,872 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3846:4930568D16Rik
|
UTSW |
2 |
35,244,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:4930568D16Rik
|
UTSW |
2 |
35,244,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:4930568D16Rik
|
UTSW |
2 |
35,244,848 (GRCm39) |
missense |
probably benign |
0.38 |
R5418:4930568D16Rik
|
UTSW |
2 |
35,244,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5889:4930568D16Rik
|
UTSW |
2 |
35,244,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R5951:4930568D16Rik
|
UTSW |
2 |
35,244,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:4930568D16Rik
|
UTSW |
2 |
35,252,348 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7363:4930568D16Rik
|
UTSW |
2 |
35,244,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:4930568D16Rik
|
UTSW |
2 |
35,244,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R8776:4930568D16Rik
|
UTSW |
2 |
35,245,002 (GRCm39) |
missense |
probably benign |
0.01 |
R8776-TAIL:4930568D16Rik
|
UTSW |
2 |
35,245,002 (GRCm39) |
missense |
probably benign |
0.01 |
R9108:4930568D16Rik
|
UTSW |
2 |
35,244,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R9367:4930568D16Rik
|
UTSW |
2 |
35,244,939 (GRCm39) |
missense |
probably benign |
0.03 |
R9566:4930568D16Rik
|
UTSW |
2 |
35,244,645 (GRCm39) |
nonsense |
probably null |
|
R9673:4930568D16Rik
|
UTSW |
2 |
35,244,399 (GRCm39) |
missense |
probably benign |
0.00 |
|