Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610507B11Rik |
G |
T |
11: 78,287,750 (GRCm38) |
V1993F |
probably damaging |
Het |
4933425L06Rik |
C |
A |
13: 105,082,194 (GRCm38) |
A12E |
unknown |
Het |
Acss2 |
T |
A |
2: 155,558,630 (GRCm38) |
Y530N |
probably damaging |
Het |
Adam4 |
T |
C |
12: 81,419,559 (GRCm38) |
I763V |
probably benign |
Het |
Aipl1 |
T |
G |
11: 72,030,499 (GRCm38) |
K190T |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,678,503 (GRCm38) |
S3344T |
possibly damaging |
Het |
Alpi |
A |
G |
1: 87,099,414 (GRCm38) |
V381A |
possibly damaging |
Het |
Ankfn1 |
A |
T |
11: 89,447,618 (GRCm38) |
S365R |
probably benign |
Het |
Aox2 |
G |
A |
1: 58,308,991 (GRCm38) |
A623T |
probably benign |
Het |
Apc |
T |
A |
18: 34,317,077 (GRCm38) |
L2308Q |
probably damaging |
Het |
Atp9b |
C |
T |
18: 80,778,883 (GRCm38) |
V501I |
probably benign |
Het |
Baz2b |
T |
C |
2: 59,901,819 (GRCm38) |
E1994G |
probably benign |
Het |
Cacna1a |
T |
C |
8: 84,581,357 (GRCm38) |
|
probably null |
Het |
Cacna1h |
C |
A |
17: 25,392,076 (GRCm38) |
V583L |
probably benign |
Het |
Cd55 |
T |
C |
1: 130,447,609 (GRCm38) |
|
probably benign |
Het |
Cep192 |
T |
A |
18: 67,804,424 (GRCm38) |
S75T |
possibly damaging |
Het |
Cfap54 |
T |
A |
10: 92,962,375 (GRCm38) |
D1674V |
probably benign |
Het |
Churc1 |
T |
C |
12: 76,773,297 (GRCm38) |
F27L |
possibly damaging |
Het |
Coro1c |
A |
G |
5: 113,848,543 (GRCm38) |
I280T |
probably benign |
Het |
Creb1 |
C |
T |
1: 64,550,950 (GRCm38) |
Q32* |
probably null |
Het |
Cyp2b9 |
A |
G |
7: 26,200,783 (GRCm38) |
T339A |
probably benign |
Het |
Dctn3 |
T |
C |
4: 41,720,813 (GRCm38) |
R51G |
probably damaging |
Het |
Ddb1 |
T |
C |
19: 10,626,593 (GRCm38) |
V888A |
probably damaging |
Het |
Disp1 |
A |
G |
1: 183,089,000 (GRCm38) |
Y619H |
probably damaging |
Het |
Dnajc9 |
T |
C |
14: 20,388,334 (GRCm38) |
D96G |
possibly damaging |
Het |
Eepd1 |
A |
G |
9: 25,482,868 (GRCm38) |
T143A |
possibly damaging |
Het |
Eps8 |
T |
A |
6: 137,522,279 (GRCm38) |
K204* |
probably null |
Het |
Ercc5 |
T |
A |
1: 44,180,875 (GRCm38) |
S1102R |
probably benign |
Het |
Ergic2 |
T |
A |
6: 148,189,581 (GRCm38) |
Y211F |
possibly damaging |
Het |
Fam135b |
G |
T |
15: 71,490,711 (GRCm38) |
L274M |
probably damaging |
Het |
Fat3 |
G |
A |
9: 15,998,088 (GRCm38) |
T2206I |
probably damaging |
Het |
Fat4 |
A |
G |
3: 38,983,571 (GRCm38) |
I3791V |
probably benign |
Het |
Gemin4 |
A |
G |
11: 76,213,296 (GRCm38) |
M213T |
possibly damaging |
Het |
Gnai3 |
T |
C |
3: 108,118,407 (GRCm38) |
M119V |
probably benign |
Het |
Heatr5b |
A |
T |
17: 78,773,563 (GRCm38) |
L1420Q |
probably damaging |
Het |
Herc2 |
G |
T |
7: 56,206,765 (GRCm38) |
G3918* |
probably null |
Het |
Ints9 |
A |
G |
14: 65,032,256 (GRCm38) |
Y465C |
probably damaging |
Het |
Ist1 |
A |
G |
8: 109,678,883 (GRCm38) |
V175A |
probably damaging |
Het |
Kcnj12 |
T |
C |
11: 61,069,557 (GRCm38) |
L227P |
possibly damaging |
Het |
Kcnq5 |
T |
C |
1: 21,466,387 (GRCm38) |
S416G |
probably benign |
Het |
Kdm3a |
T |
A |
6: 71,613,956 (GRCm38) |
T295S |
probably benign |
Het |
Kif1c |
T |
A |
11: 70,708,971 (GRCm38) |
M479K |
probably damaging |
Het |
Kif20b |
T |
C |
19: 34,956,038 (GRCm38) |
L83P |
probably damaging |
Het |
Kndc1 |
A |
G |
7: 139,927,711 (GRCm38) |
E1194G |
probably damaging |
Het |
Llgl1 |
A |
G |
11: 60,704,730 (GRCm38) |
M81V |
probably benign |
Het |
Map4k5 |
C |
A |
12: 69,824,662 (GRCm38) |
M495I |
probably damaging |
Het |
Mest |
C |
T |
6: 30,742,791 (GRCm38) |
R146C |
probably benign |
Het |
Mettl24 |
T |
A |
10: 40,737,816 (GRCm38) |
|
probably null |
Het |
Mical1 |
T |
C |
10: 41,483,535 (GRCm38) |
S586P |
probably benign |
Het |
Mss51 |
A |
T |
14: 20,483,178 (GRCm38) |
C408* |
probably null |
Het |
Myh6 |
T |
C |
14: 54,957,401 (GRCm38) |
T666A |
probably benign |
Het |
Myo10 |
T |
C |
15: 25,805,587 (GRCm38) |
C1685R |
possibly damaging |
Het |
Naip5 |
A |
T |
13: 100,223,218 (GRCm38) |
Y503* |
probably null |
Het |
Neil1 |
A |
C |
9: 57,146,604 (GRCm38) |
F144C |
probably damaging |
Het |
Nipbl |
T |
A |
15: 8,343,517 (GRCm38) |
I1082F |
possibly damaging |
Het |
Nkiras1 |
T |
C |
14: 18,276,732 (GRCm38) |
V7A |
probably damaging |
Het |
Ntng2 |
G |
A |
2: 29,197,057 (GRCm38) |
Q384* |
probably null |
Het |
Ocrl |
T |
A |
X: 47,962,116 (GRCm38) |
I74N |
probably damaging |
Het |
Olfr137 |
A |
T |
17: 38,305,312 (GRCm38) |
S50T |
probably benign |
Het |
Olfr1385 |
A |
T |
11: 49,494,670 (GRCm38) |
I46F |
probably damaging |
Het |
Olfr1408 |
A |
G |
1: 173,130,815 (GRCm38) |
V134A |
probably benign |
Het |
Olfr381 |
A |
C |
11: 73,486,374 (GRCm38) |
V150G |
probably benign |
Het |
Olfr535 |
A |
G |
7: 140,492,709 (GRCm38) |
S24G |
probably benign |
Het |
Olfr761 |
C |
T |
17: 37,952,385 (GRCm38) |
G213E |
possibly damaging |
Het |
Patj |
A |
G |
4: 98,491,590 (GRCm38) |
D151G |
probably benign |
Het |
Plpbp |
T |
C |
8: 27,049,231 (GRCm38) |
V126A |
probably damaging |
Het |
Pold2 |
A |
G |
11: 5,873,454 (GRCm38) |
L325P |
possibly damaging |
Het |
Ppp1r12c |
A |
C |
7: 4,483,651 (GRCm38) |
S480A |
probably damaging |
Het |
Pum1 |
T |
C |
4: 130,701,048 (GRCm38) |
S124P |
possibly damaging |
Het |
Pwp2 |
C |
G |
10: 78,179,091 (GRCm38) |
G353A |
probably damaging |
Het |
Reln |
C |
A |
5: 21,979,002 (GRCm38) |
Q1666H |
probably damaging |
Het |
Rnf19a |
T |
C |
15: 36,265,925 (GRCm38) |
I9V |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,769,878 (GRCm38) |
H1063R |
probably benign |
Het |
Samd14 |
C |
G |
11: 95,023,600 (GRCm38) |
D361E |
probably damaging |
Het |
Samd15 |
A |
T |
12: 87,201,843 (GRCm38) |
N365I |
probably damaging |
Het |
Sec16b |
A |
G |
1: 157,531,312 (GRCm38) |
H105R |
probably benign |
Het |
Sez6 |
T |
C |
11: 77,953,503 (GRCm38) |
S51P |
probably benign |
Het |
Sh3bp1 |
T |
A |
15: 78,905,150 (GRCm38) |
L236Q |
probably damaging |
Het |
Sspo |
C |
T |
6: 48,457,340 (GRCm38) |
T991I |
probably damaging |
Het |
Suco |
A |
T |
1: 161,859,500 (GRCm38) |
L97* |
probably null |
Het |
Tab1 |
C |
A |
15: 80,148,296 (GRCm38) |
R35S |
probably benign |
Het |
Tet3 |
C |
A |
6: 83,404,163 (GRCm38) |
S341I |
possibly damaging |
Het |
Tlr1 |
A |
T |
5: 64,925,700 (GRCm38) |
D511E |
probably benign |
Het |
Tmem132b |
A |
C |
5: 125,785,899 (GRCm38) |
D656A |
probably damaging |
Het |
Tmtc4 |
T |
A |
14: 122,941,988 (GRCm38) |
|
probably null |
Het |
Trmo |
T |
C |
4: 46,380,158 (GRCm38) |
T404A |
probably damaging |
Het |
Trpm1 |
A |
G |
7: 64,230,268 (GRCm38) |
K790E |
probably damaging |
Het |
Ulk4 |
C |
A |
9: 121,168,184 (GRCm38) |
R774M |
probably null |
Het |
Ush2a |
C |
T |
1: 188,451,818 (GRCm38) |
L1440F |
probably benign |
Het |
Usp16 |
A |
G |
16: 87,480,907 (GRCm38) |
K682E |
probably damaging |
Het |
Virma |
T |
C |
4: 11,540,511 (GRCm38) |
S1471P |
probably benign |
Het |
Vmn1r177 |
A |
T |
7: 23,865,686 (GRCm38) |
I255N |
probably damaging |
Het |
Vmn2r61 |
A |
T |
7: 42,266,652 (GRCm38) |
R230* |
probably null |
Het |
Vps13c |
T |
A |
9: 67,993,013 (GRCm38) |
F3671L |
probably benign |
Het |
Washc5 |
T |
C |
15: 59,359,340 (GRCm38) |
N358S |
possibly damaging |
Het |
Wdr72 |
A |
G |
9: 74,151,617 (GRCm38) |
K331E |
probably damaging |
Het |
Zfp986 |
A |
T |
4: 145,899,235 (GRCm38) |
K155I |
probably benign |
Het |
|
Other mutations in Mrgpra3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00162:Mrgpra3
|
APN |
7 |
47,589,519 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02097:Mrgpra3
|
APN |
7 |
47,589,456 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL02101:Mrgpra3
|
APN |
7 |
47,589,552 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL03071:Mrgpra3
|
APN |
7 |
47,589,181 (GRCm38) |
utr 3 prime |
probably benign |
|
PIT4445001:Mrgpra3
|
UTSW |
7 |
47,590,160 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0828:Mrgpra3
|
UTSW |
7 |
47,590,136 (GRCm38) |
missense |
probably benign |
0.12 |
R1118:Mrgpra3
|
UTSW |
7 |
47,589,291 (GRCm38) |
missense |
possibly damaging |
0.83 |
R2258:Mrgpra3
|
UTSW |
7 |
47,590,094 (GRCm38) |
missense |
probably benign |
0.35 |
R2393:Mrgpra3
|
UTSW |
7 |
47,589,617 (GRCm38) |
missense |
possibly damaging |
0.92 |
R3437:Mrgpra3
|
UTSW |
7 |
47,589,566 (GRCm38) |
missense |
probably damaging |
1.00 |
R3973:Mrgpra3
|
UTSW |
7 |
47,589,666 (GRCm38) |
missense |
probably benign |
0.22 |
R4273:Mrgpra3
|
UTSW |
7 |
47,589,432 (GRCm38) |
missense |
probably benign |
0.01 |
R4495:Mrgpra3
|
UTSW |
7 |
47,590,065 (GRCm38) |
missense |
probably benign |
0.00 |
R4768:Mrgpra3
|
UTSW |
7 |
47,589,728 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4822:Mrgpra3
|
UTSW |
7 |
47,589,968 (GRCm38) |
missense |
possibly damaging |
0.69 |
R4967:Mrgpra3
|
UTSW |
7 |
47,589,519 (GRCm38) |
missense |
probably benign |
0.33 |
R5207:Mrgpra3
|
UTSW |
7 |
47,590,161 (GRCm38) |
missense |
probably benign |
0.06 |
R5569:Mrgpra3
|
UTSW |
7 |
47,590,011 (GRCm38) |
missense |
probably benign |
0.00 |
R5763:Mrgpra3
|
UTSW |
7 |
47,589,607 (GRCm38) |
nonsense |
probably null |
|
R6102:Mrgpra3
|
UTSW |
7 |
47,590,149 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6612:Mrgpra3
|
UTSW |
7 |
47,590,035 (GRCm38) |
missense |
probably benign |
0.00 |
R6718:Mrgpra3
|
UTSW |
7 |
47,589,696 (GRCm38) |
missense |
probably benign |
0.25 |
R6859:Mrgpra3
|
UTSW |
7 |
47,590,033 (GRCm38) |
missense |
probably benign |
0.04 |
R7029:Mrgpra3
|
UTSW |
7 |
47,589,542 (GRCm38) |
missense |
probably benign |
0.00 |
R7034:Mrgpra3
|
UTSW |
7 |
47,590,090 (GRCm38) |
missense |
possibly damaging |
0.49 |
R7036:Mrgpra3
|
UTSW |
7 |
47,590,090 (GRCm38) |
missense |
possibly damaging |
0.49 |
R7097:Mrgpra3
|
UTSW |
7 |
47,589,641 (GRCm38) |
missense |
probably benign |
|
R7475:Mrgpra3
|
UTSW |
7 |
47,589,947 (GRCm38) |
missense |
probably damaging |
1.00 |
R8289:Mrgpra3
|
UTSW |
7 |
47,589,720 (GRCm38) |
missense |
possibly damaging |
0.76 |
R8315:Mrgpra3
|
UTSW |
7 |
47,601,303 (GRCm38) |
start codon destroyed |
probably null |
0.93 |
R9500:Mrgpra3
|
UTSW |
7 |
47,589,652 (GRCm38) |
nonsense |
probably null |
|
Z1177:Mrgpra3
|
UTSW |
7 |
47,601,301 (GRCm38) |
nonsense |
probably null |
|
|