Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
G |
7: 119,940,468 (GRCm39) |
I354M |
probably damaging |
Het |
Abca8a |
T |
C |
11: 109,917,731 (GRCm39) |
|
probably null |
Het |
Abca8b |
T |
C |
11: 109,870,724 (GRCm39) |
R143G |
probably benign |
Het |
Actn4 |
T |
C |
7: 28,594,047 (GRCm39) |
D840G |
probably damaging |
Het |
Agpat5 |
T |
C |
8: 18,928,026 (GRCm39) |
L197P |
probably damaging |
Het |
Akr1d1 |
T |
C |
6: 37,512,983 (GRCm39) |
V93A |
probably benign |
Het |
Arap2 |
T |
C |
5: 62,834,007 (GRCm39) |
K820R |
possibly damaging |
Het |
Armc9 |
T |
A |
1: 86,135,696 (GRCm39) |
C551S |
probably damaging |
Het |
Atg7 |
T |
C |
6: 114,683,191 (GRCm39) |
L418P |
probably damaging |
Het |
Awat2 |
G |
A |
X: 99,448,165 (GRCm39) |
P148S |
probably damaging |
Het |
Brms1 |
C |
T |
19: 5,096,027 (GRCm39) |
R34W |
probably damaging |
Het |
Cbx2 |
A |
G |
11: 118,919,395 (GRCm39) |
Q320R |
possibly damaging |
Het |
Ccdc106 |
G |
A |
7: 5,062,539 (GRCm39) |
D11N |
possibly damaging |
Het |
Ccdc30 |
C |
T |
4: 119,196,988 (GRCm39) |
R426Q |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,356,885 (GRCm39) |
V47E |
probably damaging |
Het |
Cep170b |
C |
T |
12: 112,704,495 (GRCm39) |
S751L |
probably damaging |
Het |
Cfap46 |
A |
T |
7: 139,246,957 (GRCm39) |
L328Q |
probably damaging |
Het |
Crtc3 |
A |
G |
7: 80,239,679 (GRCm39) |
F558L |
probably damaging |
Het |
Cyp2d34 |
A |
G |
15: 82,502,809 (GRCm39) |
V139A |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,413,408 (GRCm39) |
Y1136H |
probably damaging |
Het |
Dhrs4 |
T |
C |
14: 55,725,060 (GRCm39) |
V185A |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,281,263 (GRCm39) |
K2775E |
possibly damaging |
Het |
Dst |
C |
A |
1: 34,230,097 (GRCm39) |
S2238R |
possibly damaging |
Het |
Duox2 |
T |
C |
2: 122,127,853 (GRCm39) |
|
probably null |
Het |
Dusp16 |
G |
T |
6: 134,695,099 (GRCm39) |
Y577* |
probably null |
Het |
Dync1h1 |
G |
A |
12: 110,602,943 (GRCm39) |
E2195K |
probably benign |
Het |
Eml5 |
A |
G |
12: 98,842,570 (GRCm39) |
F176S |
probably damaging |
Het |
Esco2 |
C |
A |
14: 66,068,982 (GRCm39) |
R109S |
probably damaging |
Het |
Galnt7 |
C |
T |
8: 57,985,748 (GRCm39) |
E541K |
probably benign |
Het |
Gbf1 |
C |
T |
19: 46,255,658 (GRCm39) |
T707I |
probably damaging |
Het |
Gdf5 |
A |
G |
2: 155,783,672 (GRCm39) |
C427R |
probably damaging |
Het |
Glyctk |
T |
C |
9: 106,035,064 (GRCm39) |
M1V |
probably null |
Het |
Gm5478 |
T |
C |
15: 101,552,830 (GRCm39) |
E367G |
probably damaging |
Het |
Golga7b |
G |
A |
19: 42,251,768 (GRCm39) |
V5I |
probably benign |
Het |
Gpt2 |
T |
C |
8: 86,219,764 (GRCm39) |
L70P |
probably damaging |
Het |
Gsdmc3 |
C |
A |
15: 63,730,315 (GRCm39) |
Q416H |
probably damaging |
Het |
Hoxb5 |
A |
G |
11: 96,194,918 (GRCm39) |
E160G |
probably benign |
Het |
Ift81 |
A |
T |
5: 122,698,772 (GRCm39) |
Y532N |
probably benign |
Het |
Igf1 |
G |
A |
10: 87,700,726 (GRCm39) |
C66Y |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,857,023 (GRCm39) |
V995A |
probably damaging |
Het |
Ip6k1 |
T |
C |
9: 107,918,287 (GRCm39) |
|
probably null |
Het |
Jaml |
T |
C |
9: 45,015,495 (GRCm39) |
I333T |
possibly damaging |
Het |
Kdm4c |
T |
C |
4: 74,225,253 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
T |
C |
11: 69,292,191 (GRCm39) |
|
probably benign |
Het |
Krt6a |
C |
T |
15: 101,599,900 (GRCm39) |
R404H |
probably damaging |
Het |
Larp4b |
C |
A |
13: 9,186,878 (GRCm39) |
H69N |
probably benign |
Het |
Lcat |
A |
T |
8: 106,668,355 (GRCm39) |
W222R |
probably damaging |
Het |
Lrrc40 |
T |
A |
3: 157,746,086 (GRCm39) |
C54S |
probably benign |
Het |
Mcpt9 |
T |
A |
14: 56,265,024 (GRCm39) |
H159L |
probably benign |
Het |
Megf8 |
T |
C |
7: 25,062,976 (GRCm39) |
V2444A |
probably damaging |
Het |
Memo1 |
T |
C |
17: 74,552,003 (GRCm39) |
T98A |
possibly damaging |
Het |
Mical2 |
A |
T |
7: 112,012,051 (GRCm39) |
I634L |
probably benign |
Het |
Mov10 |
C |
T |
3: 104,704,293 (GRCm39) |
R835Q |
probably damaging |
Het |
Mybpc1 |
A |
T |
10: 88,384,688 (GRCm39) |
L546Q |
probably damaging |
Het |
Myo6 |
T |
C |
9: 80,168,117 (GRCm39) |
V427A |
probably damaging |
Het |
Myom2 |
T |
A |
8: 15,182,599 (GRCm39) |
|
probably null |
Het |
Mzt2 |
G |
A |
16: 15,666,543 (GRCm39) |
R125C |
probably damaging |
Het |
Neb |
T |
A |
2: 52,162,949 (GRCm39) |
R2031* |
probably null |
Het |
Nphp3 |
T |
C |
9: 103,898,537 (GRCm39) |
S447P |
probably benign |
Het |
Nrp2 |
T |
A |
1: 62,758,090 (GRCm39) |
D25E |
probably benign |
Het |
Nts |
A |
G |
10: 102,320,918 (GRCm39) |
L57S |
probably damaging |
Het |
Nudt9 |
G |
A |
5: 104,212,971 (GRCm39) |
R348H |
probably benign |
Het |
Or10d5j |
T |
C |
9: 39,867,979 (GRCm39) |
Y84C |
probably benign |
Het |
Or13a1 |
C |
T |
6: 116,470,725 (GRCm39) |
P52S |
probably benign |
Het |
Or3a1b |
C |
A |
11: 74,012,650 (GRCm39) |
D178E |
probably benign |
Het |
Or4k49 |
T |
C |
2: 111,495,234 (GRCm39) |
I221T |
probably damaging |
Het |
Or5ac16 |
T |
A |
16: 59,022,271 (GRCm39) |
I173F |
possibly damaging |
Het |
Pafah1b1 |
T |
C |
11: 74,590,177 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
C |
A |
18: 63,211,911 (GRCm39) |
M1291I |
probably damaging |
Het |
Pik3ca |
T |
C |
3: 32,498,016 (GRCm39) |
F486S |
probably benign |
Het |
Podnl1 |
C |
T |
8: 84,853,926 (GRCm39) |
H99Y |
probably benign |
Het |
Prdm6 |
A |
T |
18: 53,701,233 (GRCm39) |
Y341F |
probably damaging |
Het |
Prr5l |
C |
T |
2: 101,588,854 (GRCm39) |
|
probably null |
Het |
Psmd4 |
G |
T |
3: 94,944,012 (GRCm39) |
T24N |
possibly damaging |
Het |
Rbbp8nl |
G |
A |
2: 179,922,667 (GRCm39) |
T242M |
probably benign |
Het |
Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
GGCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
GGCGGCGGCGGCGGCGGCGGCGGCGGCGGCGGC |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Scfd1 |
T |
C |
12: 51,469,769 (GRCm39) |
V438A |
probably benign |
Het |
Scn9a |
A |
G |
2: 66,314,655 (GRCm39) |
C1677R |
probably damaging |
Het |
Sgsm2 |
T |
A |
11: 74,782,854 (GRCm39) |
H34L |
probably damaging |
Het |
Shank1 |
T |
A |
7: 43,993,747 (GRCm39) |
|
probably null |
Het |
Smarca2 |
G |
T |
19: 26,650,124 (GRCm39) |
E24* |
probably null |
Het |
Sncaip |
C |
T |
18: 53,004,434 (GRCm39) |
H354Y |
probably damaging |
Het |
St8sia2 |
T |
A |
7: 73,593,057 (GRCm39) |
D333V |
probably damaging |
Het |
Stxbp2 |
C |
A |
8: 3,692,672 (GRCm39) |
R575S |
probably benign |
Het |
Syt9 |
T |
A |
7: 107,024,314 (GRCm39) |
V69D |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,689,558 (GRCm39) |
N240S |
probably benign |
Het |
Tcl1b1 |
T |
C |
12: 105,130,727 (GRCm39) |
L70S |
probably benign |
Het |
Tmem44 |
C |
T |
16: 30,362,219 (GRCm39) |
|
probably null |
Het |
Tor1b |
A |
G |
2: 30,846,931 (GRCm39) |
R293G |
probably benign |
Het |
Trim29 |
T |
C |
9: 43,222,615 (GRCm39) |
V148A |
probably benign |
Het |
Trmt10b |
C |
A |
4: 45,314,378 (GRCm39) |
Y271* |
probably null |
Het |
Ubqln5 |
A |
T |
7: 103,778,095 (GRCm39) |
V243E |
possibly damaging |
Het |
Ubqln5 |
T |
C |
7: 103,778,134 (GRCm39) |
D230G |
probably damaging |
Het |
Ugt2b37 |
A |
G |
5: 87,402,193 (GRCm39) |
F146S |
probably damaging |
Het |
Vmn1r160 |
T |
A |
7: 22,570,827 (GRCm39) |
V60E |
probably damaging |
Het |
Vmn2r109 |
T |
A |
17: 20,774,185 (GRCm39) |
D390V |
probably damaging |
Het |
Vmn2r27 |
C |
T |
6: 124,200,793 (GRCm39) |
R388Q |
possibly damaging |
Het |
Vmn2r72 |
A |
T |
7: 85,398,369 (GRCm39) |
V537D |
probably benign |
Het |
Vmn2r84 |
A |
G |
10: 130,226,591 (GRCm39) |
S416P |
probably damaging |
Het |
Vmn2r-ps158 |
T |
C |
7: 42,696,824 (GRCm39) |
V620A |
probably benign |
Het |
Xrra1 |
A |
C |
7: 99,560,227 (GRCm39) |
E401A |
probably damaging |
Het |
Zfp280d |
T |
A |
9: 72,242,362 (GRCm39) |
C688* |
probably null |
Het |
Zfp3 |
T |
A |
11: 70,662,954 (GRCm39) |
Y304* |
probably null |
Het |
Zfp407 |
A |
T |
18: 84,577,461 (GRCm39) |
D1217E |
probably benign |
Het |
Zfp658 |
T |
C |
7: 43,223,245 (GRCm39) |
Y507H |
possibly damaging |
Het |
Zfyve16 |
T |
C |
13: 92,659,252 (GRCm39) |
T220A |
possibly damaging |
Het |
Zmym4 |
C |
G |
4: 126,796,463 (GRCm39) |
K820N |
possibly damaging |
Het |
|
Other mutations in Vmn2r98 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Vmn2r98
|
APN |
17 |
19,286,007 (GRCm39) |
splice site |
probably benign |
|
IGL01296:Vmn2r98
|
APN |
17 |
19,285,447 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01363:Vmn2r98
|
APN |
17 |
19,286,020 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01618:Vmn2r98
|
APN |
17 |
19,285,521 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01746:Vmn2r98
|
APN |
17 |
19,286,713 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01747:Vmn2r98
|
APN |
17 |
19,286,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01770:Vmn2r98
|
APN |
17 |
19,286,702 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01868:Vmn2r98
|
APN |
17 |
19,286,548 (GRCm39) |
missense |
probably benign |
|
IGL02123:Vmn2r98
|
APN |
17 |
19,300,941 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02323:Vmn2r98
|
APN |
17 |
19,286,113 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02543:Vmn2r98
|
APN |
17 |
19,286,083 (GRCm39) |
missense |
probably benign |
|
IGL02650:Vmn2r98
|
APN |
17 |
19,301,223 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02676:Vmn2r98
|
APN |
17 |
19,285,521 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02803:Vmn2r98
|
APN |
17 |
19,286,275 (GRCm39) |
missense |
probably benign |
|
IGL02807:Vmn2r98
|
APN |
17 |
19,301,283 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03307:Vmn2r98
|
APN |
17 |
19,286,242 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL03396:Vmn2r98
|
APN |
17 |
19,290,107 (GRCm39) |
missense |
possibly damaging |
0.92 |
PIT4131001:Vmn2r98
|
UTSW |
17 |
19,301,223 (GRCm39) |
missense |
probably benign |
0.00 |
R0122:Vmn2r98
|
UTSW |
17 |
19,286,662 (GRCm39) |
missense |
probably benign |
0.06 |
R0329:Vmn2r98
|
UTSW |
17 |
19,286,609 (GRCm39) |
missense |
probably benign |
0.21 |
R0330:Vmn2r98
|
UTSW |
17 |
19,286,609 (GRCm39) |
missense |
probably benign |
0.21 |
R0368:Vmn2r98
|
UTSW |
17 |
19,286,089 (GRCm39) |
nonsense |
probably null |
|
R0545:Vmn2r98
|
UTSW |
17 |
19,273,875 (GRCm39) |
missense |
probably benign |
0.15 |
R0635:Vmn2r98
|
UTSW |
17 |
19,300,759 (GRCm39) |
missense |
probably benign |
0.00 |
R0689:Vmn2r98
|
UTSW |
17 |
19,300,782 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1035:Vmn2r98
|
UTSW |
17 |
19,301,011 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1243:Vmn2r98
|
UTSW |
17 |
19,286,210 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1421:Vmn2r98
|
UTSW |
17 |
19,285,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Vmn2r98
|
UTSW |
17 |
19,287,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1643:Vmn2r98
|
UTSW |
17 |
19,301,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Vmn2r98
|
UTSW |
17 |
19,286,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Vmn2r98
|
UTSW |
17 |
19,286,680 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2165:Vmn2r98
|
UTSW |
17 |
19,301,553 (GRCm39) |
missense |
unknown |
|
R2238:Vmn2r98
|
UTSW |
17 |
19,286,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Vmn2r98
|
UTSW |
17 |
19,300,698 (GRCm39) |
missense |
probably benign |
0.00 |
R2323:Vmn2r98
|
UTSW |
17 |
19,286,081 (GRCm39) |
missense |
probably benign |
0.18 |
R2887:Vmn2r98
|
UTSW |
17 |
19,301,439 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2909:Vmn2r98
|
UTSW |
17 |
19,287,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R3001:Vmn2r98
|
UTSW |
17 |
19,286,125 (GRCm39) |
missense |
probably benign |
0.01 |
R3002:Vmn2r98
|
UTSW |
17 |
19,286,125 (GRCm39) |
missense |
probably benign |
0.01 |
R3003:Vmn2r98
|
UTSW |
17 |
19,286,125 (GRCm39) |
missense |
probably benign |
0.01 |
R3788:Vmn2r98
|
UTSW |
17 |
19,300,887 (GRCm39) |
missense |
probably benign |
0.31 |
R4570:Vmn2r98
|
UTSW |
17 |
19,286,354 (GRCm39) |
missense |
probably benign |
0.11 |
R4706:Vmn2r98
|
UTSW |
17 |
19,290,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4723:Vmn2r98
|
UTSW |
17 |
19,286,602 (GRCm39) |
missense |
probably benign |
0.01 |
R5036:Vmn2r98
|
UTSW |
17 |
19,286,419 (GRCm39) |
missense |
probably benign |
0.00 |
R5072:Vmn2r98
|
UTSW |
17 |
19,286,306 (GRCm39) |
missense |
probably benign |
0.07 |
R5121:Vmn2r98
|
UTSW |
17 |
19,273,815 (GRCm39) |
missense |
probably benign |
0.13 |
R5283:Vmn2r98
|
UTSW |
17 |
19,300,981 (GRCm39) |
missense |
probably benign |
0.05 |
R5294:Vmn2r98
|
UTSW |
17 |
19,290,016 (GRCm39) |
nonsense |
probably null |
|
R5371:Vmn2r98
|
UTSW |
17 |
19,290,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R5532:Vmn2r98
|
UTSW |
17 |
19,287,645 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5598:Vmn2r98
|
UTSW |
17 |
19,301,161 (GRCm39) |
missense |
probably benign |
0.37 |
R5800:Vmn2r98
|
UTSW |
17 |
19,286,260 (GRCm39) |
missense |
probably benign |
0.17 |
R6089:Vmn2r98
|
UTSW |
17 |
19,286,336 (GRCm39) |
missense |
probably benign |
0.29 |
R6155:Vmn2r98
|
UTSW |
17 |
19,286,143 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6853:Vmn2r98
|
UTSW |
17 |
19,286,063 (GRCm39) |
missense |
probably benign |
0.00 |
R6920:Vmn2r98
|
UTSW |
17 |
19,285,510 (GRCm39) |
missense |
probably damaging |
0.98 |
R7012:Vmn2r98
|
UTSW |
17 |
19,286,530 (GRCm39) |
missense |
probably benign |
0.06 |
R7042:Vmn2r98
|
UTSW |
17 |
19,301,184 (GRCm39) |
missense |
probably benign |
|
R7068:Vmn2r98
|
UTSW |
17 |
19,285,575 (GRCm39) |
missense |
probably benign |
|
R7607:Vmn2r98
|
UTSW |
17 |
19,287,570 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7763:Vmn2r98
|
UTSW |
17 |
19,300,797 (GRCm39) |
missense |
probably benign |
0.00 |
R7771:Vmn2r98
|
UTSW |
17 |
19,287,460 (GRCm39) |
splice site |
probably null |
|
R7915:Vmn2r98
|
UTSW |
17 |
19,287,493 (GRCm39) |
missense |
probably benign |
0.10 |
R8028:Vmn2r98
|
UTSW |
17 |
19,273,912 (GRCm39) |
missense |
probably benign |
0.00 |
R8205:Vmn2r98
|
UTSW |
17 |
19,301,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R8241:Vmn2r98
|
UTSW |
17 |
19,301,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R8906:Vmn2r98
|
UTSW |
17 |
19,286,532 (GRCm39) |
missense |
probably benign |
|
R8952:Vmn2r98
|
UTSW |
17 |
19,285,531 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9147:Vmn2r98
|
UTSW |
17 |
19,286,383 (GRCm39) |
missense |
probably benign |
0.04 |
R9148:Vmn2r98
|
UTSW |
17 |
19,286,383 (GRCm39) |
missense |
probably benign |
0.04 |
R9187:Vmn2r98
|
UTSW |
17 |
19,301,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R9344:Vmn2r98
|
UTSW |
17 |
19,286,777 (GRCm39) |
missense |
probably benign |
0.14 |
R9467:Vmn2r98
|
UTSW |
17 |
19,287,517 (GRCm39) |
missense |
probably benign |
0.01 |
R9487:Vmn2r98
|
UTSW |
17 |
19,301,496 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9753:Vmn2r98
|
UTSW |
17 |
19,285,665 (GRCm39) |
missense |
probably benign |
0.27 |
Z1177:Vmn2r98
|
UTSW |
17 |
19,287,685 (GRCm39) |
nonsense |
probably null |
|
Z1177:Vmn2r98
|
UTSW |
17 |
19,285,398 (GRCm39) |
critical splice acceptor site |
probably null |
|
|