Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432M17Rik |
G |
A |
3: 121,465,053 (GRCm39) |
E30K |
unknown |
Het |
Abi3bp |
A |
T |
16: 56,491,670 (GRCm39) |
T1319S |
possibly damaging |
Het |
Adam18 |
T |
C |
8: 25,119,653 (GRCm39) |
|
probably null |
Het |
Adgre1 |
G |
A |
17: 57,713,839 (GRCm39) |
D175N |
possibly damaging |
Het |
Adgrf1 |
T |
C |
17: 43,614,679 (GRCm39) |
|
probably null |
Het |
Ankhd1 |
A |
G |
18: 36,777,652 (GRCm39) |
S1612G |
possibly damaging |
Het |
Anks1 |
A |
G |
17: 28,214,926 (GRCm39) |
R458G |
possibly damaging |
Het |
Cacna1g |
C |
T |
11: 94,350,523 (GRCm39) |
V441M |
probably damaging |
Het |
Cadps2 |
A |
T |
6: 23,321,781 (GRCm39) |
V1037E |
possibly damaging |
Het |
Casz1 |
T |
C |
4: 149,033,368 (GRCm39) |
V1380A |
possibly damaging |
Het |
Cenpq |
T |
C |
17: 41,244,085 (GRCm39) |
|
probably benign |
Het |
Chrac1 |
T |
C |
15: 72,965,376 (GRCm39) |
I93T |
possibly damaging |
Het |
Cntnap2 |
T |
A |
6: 45,986,571 (GRCm39) |
S359T |
probably benign |
Het |
Col6a6 |
C |
A |
9: 105,661,403 (GRCm39) |
M235I |
probably benign |
Het |
Crat |
T |
C |
2: 30,293,640 (GRCm39) |
|
probably benign |
Het |
Cyp1a2 |
T |
C |
9: 57,589,308 (GRCm39) |
N169D |
probably benign |
Het |
Dennd1c |
T |
A |
17: 57,374,649 (GRCm39) |
T499S |
probably benign |
Het |
Dst |
A |
G |
1: 34,333,631 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
G |
T |
9: 7,167,244 (GRCm39) |
|
probably null |
Het |
Eif3h |
C |
A |
15: 51,662,660 (GRCm39) |
V129F |
probably damaging |
Het |
Eno2 |
A |
G |
6: 124,739,654 (GRCm39) |
F380L |
probably damaging |
Het |
Ergic2 |
T |
A |
6: 148,084,700 (GRCm39) |
I34F |
probably benign |
Het |
Ergic3 |
G |
A |
2: 155,858,707 (GRCm39) |
V278M |
probably benign |
Het |
Fam185a |
C |
T |
5: 21,664,283 (GRCm39) |
T339M |
probably damaging |
Het |
Fam20b |
A |
T |
1: 156,509,023 (GRCm39) |
D396E |
probably benign |
Het |
Fasn |
G |
T |
11: 120,707,008 (GRCm39) |
D881E |
probably damaging |
Het |
Fat1 |
C |
A |
8: 45,403,385 (GRCm39) |
H45Q |
probably benign |
Het |
Fbxw16 |
A |
T |
9: 109,261,550 (GRCm39) |
C439S |
probably benign |
Het |
Garin1a |
T |
A |
6: 29,281,391 (GRCm39) |
V43E |
possibly damaging |
Het |
Gba2 |
A |
T |
4: 43,570,832 (GRCm39) |
F280Y |
probably damaging |
Het |
Gfm1 |
A |
G |
3: 67,365,251 (GRCm39) |
I517V |
probably benign |
Het |
Gng13 |
C |
T |
17: 25,937,696 (GRCm39) |
Q8* |
probably null |
Het |
Golga1 |
A |
T |
2: 38,908,453 (GRCm39) |
S749T |
probably damaging |
Het |
Gphn |
A |
T |
12: 78,637,433 (GRCm39) |
I381F |
probably damaging |
Het |
Grm3 |
T |
C |
5: 9,554,794 (GRCm39) |
N833D |
probably damaging |
Het |
Gstt2 |
G |
T |
10: 75,668,266 (GRCm39) |
T163K |
probably damaging |
Het |
Gusb |
A |
T |
5: 130,026,927 (GRCm39) |
V388E |
probably damaging |
Het |
Hcrtr2 |
A |
T |
9: 76,153,662 (GRCm39) |
Y243* |
probably null |
Het |
Hspg2 |
A |
G |
4: 137,242,734 (GRCm39) |
T650A |
possibly damaging |
Het |
Ints2 |
C |
T |
11: 86,139,677 (GRCm39) |
V306I |
probably damaging |
Het |
Itga1 |
T |
A |
13: 115,128,996 (GRCm39) |
D554V |
probably benign |
Het |
Itgam |
C |
T |
7: 127,680,806 (GRCm39) |
A245V |
probably damaging |
Het |
Kcnk15 |
A |
G |
2: 163,700,243 (GRCm39) |
T161A |
probably benign |
Het |
Klhl18 |
A |
T |
9: 110,257,749 (GRCm39) |
C564S |
probably benign |
Het |
Krt40 |
T |
A |
11: 99,432,540 (GRCm39) |
R159* |
probably null |
Het |
L3mbtl4 |
G |
A |
17: 68,762,775 (GRCm39) |
V103M |
probably damaging |
Het |
Lnx2 |
C |
A |
5: 146,955,850 (GRCm39) |
V649L |
possibly damaging |
Het |
Lpp |
A |
T |
16: 24,426,991 (GRCm39) |
Q39H |
probably damaging |
Het |
Lrpprc |
A |
T |
17: 85,060,540 (GRCm39) |
|
probably null |
Het |
Map3k19 |
A |
T |
1: 127,750,152 (GRCm39) |
N1066K |
probably benign |
Het |
Mbtps2 |
G |
T |
X: 156,351,364 (GRCm39) |
T134K |
probably benign |
Het |
Mfng |
C |
T |
15: 78,648,637 (GRCm39) |
V147M |
possibly damaging |
Het |
Mks1 |
T |
C |
11: 87,748,754 (GRCm39) |
S273P |
probably benign |
Het |
Myh2 |
T |
C |
11: 67,071,647 (GRCm39) |
L488P |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,369,364 (GRCm39) |
N708S |
probably benign |
Het |
Myo6 |
A |
T |
9: 80,199,748 (GRCm39) |
N1019I |
probably damaging |
Het |
Myrf |
G |
C |
19: 10,195,526 (GRCm39) |
T428S |
probably benign |
Het |
Ncoa1 |
T |
G |
12: 4,345,976 (GRCm39) |
N457T |
probably benign |
Het |
Neb |
T |
C |
2: 52,051,489 (GRCm39) |
|
probably null |
Het |
Nlrp4e |
C |
A |
7: 23,054,628 (GRCm39) |
N927K |
probably damaging |
Het |
Npffr2 |
T |
C |
5: 89,730,613 (GRCm39) |
M181T |
probably benign |
Het |
Nxf7 |
A |
T |
X: 134,485,132 (GRCm39) |
C495S |
possibly damaging |
Het |
Oas1g |
T |
C |
5: 121,025,592 (GRCm39) |
T12A |
probably benign |
Het |
Or11g2 |
T |
A |
14: 50,856,036 (GRCm39) |
L119Q |
probably damaging |
Het |
Or1e17 |
T |
A |
11: 73,831,879 (GRCm39) |
V269E |
probably benign |
Het |
Or2g7 |
C |
G |
17: 38,378,562 (GRCm39) |
R167G |
possibly damaging |
Het |
Or52s1b |
A |
T |
7: 102,822,490 (GRCm39) |
V118E |
possibly damaging |
Het |
Or5p60 |
A |
G |
7: 107,724,023 (GRCm39) |
V149A |
probably benign |
Het |
Papln |
C |
T |
12: 83,830,153 (GRCm39) |
Q1008* |
probably null |
Het |
Pcdhb10 |
A |
C |
18: 37,545,485 (GRCm39) |
D187A |
probably damaging |
Het |
Phf2 |
T |
A |
13: 48,957,965 (GRCm39) |
E1016D |
unknown |
Het |
Phf8 |
T |
A |
X: 150,335,618 (GRCm39) |
D197E |
probably benign |
Het |
Pikfyve |
A |
G |
1: 65,235,865 (GRCm39) |
H179R |
probably damaging |
Het |
Prkcz |
T |
A |
4: 155,353,597 (GRCm39) |
D250V |
probably damaging |
Het |
Prpf4 |
A |
G |
4: 62,340,842 (GRCm39) |
Y419C |
probably damaging |
Het |
Prr15l |
C |
A |
11: 96,825,440 (GRCm39) |
Y23* |
probably null |
Het |
Prr5 |
T |
A |
15: 84,587,152 (GRCm39) |
S301T |
probably benign |
Het |
Psg16 |
T |
A |
7: 16,829,088 (GRCm39) |
I224N |
probably benign |
Het |
Radil |
A |
G |
5: 142,529,226 (GRCm39) |
F186L |
probably damaging |
Het |
Reg3g |
A |
T |
6: 78,445,544 (GRCm39) |
M1K |
probably null |
Het |
Rps6ka3 |
A |
G |
X: 158,100,963 (GRCm39) |
Y76C |
probably damaging |
Het |
Rtl1 |
C |
T |
12: 109,556,797 (GRCm39) |
V1681I |
possibly damaging |
Het |
Sfmbt1 |
C |
T |
14: 30,533,464 (GRCm39) |
R614C |
probably damaging |
Het |
Slc12a4 |
A |
G |
8: 106,678,599 (GRCm39) |
S244P |
probably benign |
Het |
Sp140l2 |
T |
A |
1: 85,247,773 (GRCm39) |
N5Y |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,089,250 (GRCm39) |
T671A |
possibly damaging |
Het |
Supt16 |
A |
T |
14: 52,411,570 (GRCm39) |
N604K |
probably damaging |
Het |
Synj2 |
G |
A |
17: 6,080,058 (GRCm39) |
V1096I |
probably benign |
Het |
Tas2r129 |
G |
T |
6: 132,928,159 (GRCm39) |
C32F |
probably benign |
Het |
Tbc1d25 |
T |
C |
X: 8,039,108 (GRCm39) |
Y140C |
probably damaging |
Het |
Tdrd7 |
A |
G |
4: 46,016,987 (GRCm39) |
D709G |
probably benign |
Het |
Tfap2d |
C |
T |
1: 19,174,591 (GRCm39) |
R15C |
possibly damaging |
Het |
Tgfbi |
C |
A |
13: 56,777,515 (GRCm39) |
T333N |
probably benign |
Het |
Tnk1 |
T |
C |
11: 69,746,508 (GRCm39) |
Y235C |
probably damaging |
Het |
Ttc17 |
A |
G |
2: 94,208,439 (GRCm39) |
F144S |
probably benign |
Het |
Twnk |
G |
T |
19: 44,996,578 (GRCm39) |
G337V |
possibly damaging |
Het |
Unc13a |
A |
G |
8: 72,110,676 (GRCm39) |
F464L |
probably benign |
Het |
Usp17le |
C |
A |
7: 104,417,667 (GRCm39) |
A492S |
probably damaging |
Het |
Vmn1r213 |
A |
T |
13: 23,195,932 (GRCm39) |
M172L |
probably benign |
Het |
Vmn1r71 |
G |
A |
7: 10,482,238 (GRCm39) |
T84I |
probably benign |
Het |
Vmn2r109 |
C |
T |
17: 20,761,336 (GRCm39) |
V674M |
probably damaging |
Het |
Vmn2r19 |
A |
T |
6: 123,312,945 (GRCm39) |
I672F |
possibly damaging |
Het |
Xdh |
T |
A |
17: 74,205,357 (GRCm39) |
H1036L |
probably damaging |
Het |
Zfp930 |
T |
A |
8: 69,680,948 (GRCm39) |
Y214* |
probably null |
Het |
|
Other mutations in Vmn2r77 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00954:Vmn2r77
|
APN |
7 |
86,449,975 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01105:Vmn2r77
|
APN |
7 |
86,460,872 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01367:Vmn2r77
|
APN |
7 |
86,461,124 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01634:Vmn2r77
|
APN |
7 |
86,460,857 (GRCm39) |
missense |
probably benign |
|
IGL01805:Vmn2r77
|
APN |
7 |
86,460,395 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01868:Vmn2r77
|
APN |
7 |
86,452,224 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01980:Vmn2r77
|
APN |
7 |
86,450,678 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02055:Vmn2r77
|
APN |
7 |
86,450,763 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02066:Vmn2r77
|
APN |
7 |
86,452,836 (GRCm39) |
nonsense |
probably null |
|
IGL02185:Vmn2r77
|
APN |
7 |
86,444,360 (GRCm39) |
missense |
unknown |
|
IGL02200:Vmn2r77
|
APN |
7 |
86,451,187 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02336:Vmn2r77
|
APN |
7 |
86,451,224 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02445:Vmn2r77
|
APN |
7 |
86,452,848 (GRCm39) |
nonsense |
probably null |
|
IGL02557:Vmn2r77
|
APN |
7 |
86,444,342 (GRCm39) |
unclassified |
probably benign |
|
IGL02659:Vmn2r77
|
APN |
7 |
86,449,979 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02978:Vmn2r77
|
APN |
7 |
86,460,555 (GRCm39) |
missense |
probably benign |
|
IGL03180:Vmn2r77
|
APN |
7 |
86,450,843 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03255:Vmn2r77
|
APN |
7 |
86,461,131 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03273:Vmn2r77
|
APN |
7 |
86,460,494 (GRCm39) |
missense |
probably damaging |
0.99 |
R0046:Vmn2r77
|
UTSW |
7 |
86,451,146 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0047:Vmn2r77
|
UTSW |
7 |
86,460,858 (GRCm39) |
missense |
probably benign |
0.01 |
R0066:Vmn2r77
|
UTSW |
7 |
86,449,964 (GRCm39) |
missense |
probably benign |
0.17 |
R0066:Vmn2r77
|
UTSW |
7 |
86,449,964 (GRCm39) |
missense |
probably benign |
0.17 |
R0635:Vmn2r77
|
UTSW |
7 |
86,460,383 (GRCm39) |
missense |
probably benign |
|
R0689:Vmn2r77
|
UTSW |
7 |
86,460,872 (GRCm39) |
missense |
probably damaging |
0.99 |
R0827:Vmn2r77
|
UTSW |
7 |
86,451,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R1167:Vmn2r77
|
UTSW |
7 |
86,450,954 (GRCm39) |
missense |
probably benign |
0.02 |
R1228:Vmn2r77
|
UTSW |
7 |
86,450,242 (GRCm39) |
critical splice donor site |
probably null |
|
R1353:Vmn2r77
|
UTSW |
7 |
86,451,394 (GRCm39) |
missense |
probably benign |
0.29 |
R1392:Vmn2r77
|
UTSW |
7 |
86,450,830 (GRCm39) |
missense |
probably benign |
0.00 |
R1392:Vmn2r77
|
UTSW |
7 |
86,450,830 (GRCm39) |
missense |
probably benign |
0.00 |
R1613:Vmn2r77
|
UTSW |
7 |
86,460,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Vmn2r77
|
UTSW |
7 |
86,461,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Vmn2r77
|
UTSW |
7 |
86,444,543 (GRCm39) |
missense |
probably benign |
0.35 |
R1827:Vmn2r77
|
UTSW |
7 |
86,450,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R1911:Vmn2r77
|
UTSW |
7 |
86,461,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Vmn2r77
|
UTSW |
7 |
86,449,964 (GRCm39) |
missense |
probably benign |
0.17 |
R2008:Vmn2r77
|
UTSW |
7 |
86,450,921 (GRCm39) |
missense |
probably benign |
0.31 |
R2093:Vmn2r77
|
UTSW |
7 |
86,450,702 (GRCm39) |
missense |
probably benign |
0.29 |
R2143:Vmn2r77
|
UTSW |
7 |
86,461,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Vmn2r77
|
UTSW |
7 |
86,460,897 (GRCm39) |
missense |
probably benign |
0.03 |
R2972:Vmn2r77
|
UTSW |
7 |
86,452,893 (GRCm39) |
missense |
probably benign |
0.01 |
R2974:Vmn2r77
|
UTSW |
7 |
86,452,893 (GRCm39) |
missense |
probably benign |
0.01 |
R3037:Vmn2r77
|
UTSW |
7 |
86,450,191 (GRCm39) |
missense |
probably benign |
|
R3694:Vmn2r77
|
UTSW |
7 |
86,450,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R3695:Vmn2r77
|
UTSW |
7 |
86,450,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R3805:Vmn2r77
|
UTSW |
7 |
86,444,368 (GRCm39) |
nonsense |
probably null |
|
R3870:Vmn2r77
|
UTSW |
7 |
86,461,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Vmn2r77
|
UTSW |
7 |
86,450,195 (GRCm39) |
missense |
probably benign |
0.00 |
R4733:Vmn2r77
|
UTSW |
7 |
86,450,195 (GRCm39) |
missense |
probably benign |
0.00 |
R5009:Vmn2r77
|
UTSW |
7 |
86,451,015 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5201:Vmn2r77
|
UTSW |
7 |
86,460,846 (GRCm39) |
missense |
probably damaging |
0.98 |
R5218:Vmn2r77
|
UTSW |
7 |
86,451,341 (GRCm39) |
missense |
probably damaging |
0.98 |
R5469:Vmn2r77
|
UTSW |
7 |
86,451,271 (GRCm39) |
missense |
probably benign |
0.01 |
R5673:Vmn2r77
|
UTSW |
7 |
86,461,214 (GRCm39) |
missense |
probably benign |
0.05 |
R5771:Vmn2r77
|
UTSW |
7 |
86,461,235 (GRCm39) |
missense |
probably benign |
0.06 |
R5832:Vmn2r77
|
UTSW |
7 |
86,460,670 (GRCm39) |
nonsense |
probably null |
|
R5899:Vmn2r77
|
UTSW |
7 |
86,460,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Vmn2r77
|
UTSW |
7 |
86,450,878 (GRCm39) |
missense |
probably benign |
0.00 |
R6182:Vmn2r77
|
UTSW |
7 |
86,460,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Vmn2r77
|
UTSW |
7 |
86,451,031 (GRCm39) |
missense |
probably benign |
|
R6419:Vmn2r77
|
UTSW |
7 |
86,460,767 (GRCm39) |
missense |
probably damaging |
0.99 |
R6549:Vmn2r77
|
UTSW |
7 |
86,450,065 (GRCm39) |
missense |
probably benign |
0.06 |
R6874:Vmn2r77
|
UTSW |
7 |
86,451,286 (GRCm39) |
missense |
probably benign |
0.00 |
R6972:Vmn2r77
|
UTSW |
7 |
86,452,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R7056:Vmn2r77
|
UTSW |
7 |
86,451,023 (GRCm39) |
missense |
probably benign |
0.06 |
R7185:Vmn2r77
|
UTSW |
7 |
86,451,035 (GRCm39) |
missense |
probably benign |
0.00 |
R7261:Vmn2r77
|
UTSW |
7 |
86,460,518 (GRCm39) |
nonsense |
probably null |
|
R7298:Vmn2r77
|
UTSW |
7 |
86,449,979 (GRCm39) |
missense |
probably benign |
0.00 |
R7662:Vmn2r77
|
UTSW |
7 |
86,460,492 (GRCm39) |
nonsense |
probably null |
|
R8182:Vmn2r77
|
UTSW |
7 |
86,460,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R8327:Vmn2r77
|
UTSW |
7 |
86,450,680 (GRCm39) |
missense |
probably benign |
0.08 |
R8387:Vmn2r77
|
UTSW |
7 |
86,450,947 (GRCm39) |
missense |
probably benign |
0.00 |
R8825:Vmn2r77
|
UTSW |
7 |
86,452,855 (GRCm39) |
missense |
probably benign |
|
R8898:Vmn2r77
|
UTSW |
7 |
86,444,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8973:Vmn2r77
|
UTSW |
7 |
86,452,150 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9258:Vmn2r77
|
UTSW |
7 |
86,452,302 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9338:Vmn2r77
|
UTSW |
7 |
86,460,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R9358:Vmn2r77
|
UTSW |
7 |
86,452,236 (GRCm39) |
missense |
probably benign |
0.00 |
R9377:Vmn2r77
|
UTSW |
7 |
86,444,442 (GRCm39) |
missense |
probably benign |
0.05 |
R9404:Vmn2r77
|
UTSW |
7 |
86,451,247 (GRCm39) |
missense |
probably benign |
|
R9673:Vmn2r77
|
UTSW |
7 |
86,450,171 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9679:Vmn2r77
|
UTSW |
7 |
86,460,741 (GRCm39) |
missense |
probably benign |
0.07 |
|