Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5830454E08Rik |
T |
C |
9: 120,406,772 (GRCm39) |
|
probably benign |
Het |
Anxa4 |
G |
A |
6: 86,730,865 (GRCm39) |
T104M |
probably damaging |
Het |
BC048562 |
G |
T |
9: 108,313,777 (GRCm39) |
W9L |
probably damaging |
Het |
Cachd1 |
T |
A |
4: 100,838,203 (GRCm39) |
M822K |
probably damaging |
Het |
Clec4g |
C |
A |
8: 3,768,441 (GRCm39) |
V97L |
probably benign |
Het |
Ddx19a |
G |
A |
8: 111,707,263 (GRCm39) |
Q176* |
probably null |
Het |
Eml6 |
T |
C |
11: 29,710,096 (GRCm39) |
H1413R |
probably damaging |
Het |
Fam161b |
C |
T |
12: 84,395,408 (GRCm39) |
V512M |
probably damaging |
Het |
Glcci1 |
A |
T |
6: 8,537,835 (GRCm39) |
Q151L |
probably benign |
Het |
Gm10801 |
TC |
TCGAC |
2: 98,494,151 (GRCm39) |
|
probably benign |
Het |
Gpnmb |
A |
T |
6: 49,024,775 (GRCm39) |
D269V |
probably damaging |
Het |
Gpx3 |
A |
T |
11: 54,800,375 (GRCm39) |
D191V |
probably damaging |
Het |
Grm4 |
C |
T |
17: 27,653,712 (GRCm39) |
C491Y |
probably damaging |
Het |
Hrc |
T |
A |
7: 44,984,909 (GRCm39) |
L20Q |
probably damaging |
Het |
Hsd17b6 |
T |
A |
10: 127,827,308 (GRCm39) |
M255L |
probably benign |
Het |
Hydin |
A |
T |
8: 111,322,099 (GRCm39) |
I4584L |
probably benign |
Het |
Ift70a2 |
A |
T |
2: 75,807,630 (GRCm39) |
L294Q |
probably damaging |
Het |
Ints5 |
T |
A |
19: 8,873,931 (GRCm39) |
I630K |
possibly damaging |
Het |
Kctd10 |
A |
G |
5: 114,503,764 (GRCm39) |
I296T |
possibly damaging |
Het |
Ltv1 |
G |
A |
10: 13,058,103 (GRCm39) |
R234C |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,365,546 (GRCm39) |
S1507P |
probably damaging |
Het |
Megf8 |
G |
A |
7: 25,039,714 (GRCm39) |
G936D |
possibly damaging |
Het |
Ms4a4d |
T |
C |
19: 11,526,004 (GRCm39) |
|
probably null |
Het |
Net1 |
C |
T |
13: 3,943,379 (GRCm39) |
A3T |
probably benign |
Het |
Nlrp2 |
T |
C |
7: 5,303,908 (GRCm39) |
M206V |
probably benign |
Het |
Or1j1 |
C |
T |
2: 36,702,444 (GRCm39) |
R220H |
probably benign |
Het |
Or5an1b |
T |
A |
19: 12,299,505 (GRCm39) |
I229F |
probably damaging |
Het |
Pcyox1l |
T |
C |
18: 61,832,433 (GRCm39) |
I205V |
probably benign |
Het |
Pigo |
A |
G |
4: 43,019,645 (GRCm39) |
|
probably null |
Het |
Pla2g6 |
A |
T |
15: 79,173,893 (GRCm39) |
S590T |
possibly damaging |
Het |
Pwp2 |
T |
C |
10: 78,013,605 (GRCm39) |
T539A |
possibly damaging |
Het |
Rag1 |
T |
C |
2: 101,473,079 (GRCm39) |
T688A |
probably benign |
Het |
Senp7 |
A |
G |
16: 55,990,279 (GRCm39) |
T676A |
probably benign |
Het |
Slc26a6 |
T |
C |
9: 108,738,499 (GRCm39) |
|
probably benign |
Het |
Slc45a2 |
C |
T |
15: 11,027,871 (GRCm39) |
T480I |
probably damaging |
Het |
Sorbs2 |
A |
G |
8: 46,272,778 (GRCm39) |
H653R |
probably damaging |
Het |
Stk3 |
T |
A |
15: 35,114,706 (GRCm39) |
K67* |
probably null |
Het |
Tctn2 |
A |
ACC |
5: 124,762,400 (GRCm39) |
|
probably benign |
Homo |
Ttn |
T |
C |
2: 76,540,395 (GRCm39) |
Y34197C |
probably damaging |
Het |
Ufc1 |
A |
C |
1: 171,117,746 (GRCm39) |
L56R |
probably damaging |
Het |
Usp34 |
T |
A |
11: 23,394,202 (GRCm39) |
|
probably null |
Het |
Vnn3 |
T |
A |
10: 23,727,483 (GRCm39) |
M1K |
probably null |
Het |
Zfp653 |
C |
A |
9: 21,969,099 (GRCm39) |
|
probably null |
Het |
|
Other mutations in H2-M10.4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02329:H2-M10.4
|
APN |
17 |
36,771,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02651:H2-M10.4
|
APN |
17 |
36,771,548 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02821:H2-M10.4
|
APN |
17 |
36,771,323 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03123:H2-M10.4
|
APN |
17 |
36,772,812 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03171:H2-M10.4
|
APN |
17 |
36,772,142 (GRCm39) |
missense |
probably damaging |
0.98 |
R0206:H2-M10.4
|
UTSW |
17 |
36,771,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:H2-M10.4
|
UTSW |
17 |
36,771,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:H2-M10.4
|
UTSW |
17 |
36,772,877 (GRCm39) |
missense |
probably benign |
0.23 |
R4535:H2-M10.4
|
UTSW |
17 |
36,772,736 (GRCm39) |
missense |
probably damaging |
0.97 |
R4685:H2-M10.4
|
UTSW |
17 |
36,772,688 (GRCm39) |
missense |
probably benign |
0.23 |
R4702:H2-M10.4
|
UTSW |
17 |
36,772,874 (GRCm39) |
missense |
probably benign |
0.25 |
R5945:H2-M10.4
|
UTSW |
17 |
36,771,518 (GRCm39) |
missense |
probably benign |
0.01 |
R8135:H2-M10.4
|
UTSW |
17 |
36,772,662 (GRCm39) |
missense |
probably benign |
|
R8956:H2-M10.4
|
UTSW |
17 |
36,772,245 (GRCm39) |
missense |
probably benign |
0.08 |
R9342:H2-M10.4
|
UTSW |
17 |
36,771,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:H2-M10.4
|
UTSW |
17 |
36,771,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|