Other mutations in this stock |
Total: 150 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,775,632 (GRCm39) |
L1607P |
probably damaging |
Het |
1700016H13Rik |
T |
C |
5: 103,796,687 (GRCm39) |
*118W |
probably null |
Het |
4930595M18Rik |
G |
T |
X: 80,464,537 (GRCm39) |
T390N |
possibly damaging |
Het |
Abca13 |
C |
T |
11: 9,241,238 (GRCm39) |
Q1034* |
probably null |
Het |
Acsbg3 |
A |
T |
17: 57,190,835 (GRCm39) |
N468Y |
probably benign |
Het |
Adgra3 |
T |
C |
5: 50,118,065 (GRCm39) |
H1161R |
probably damaging |
Het |
Aff1 |
T |
C |
5: 103,974,004 (GRCm39) |
|
probably benign |
Het |
Agap2 |
A |
G |
10: 126,927,571 (GRCm39) |
T1131A |
possibly damaging |
Het |
Ankrd12 |
A |
G |
17: 66,292,127 (GRCm39) |
V1102A |
probably benign |
Het |
Ankrd54 |
A |
T |
15: 78,946,931 (GRCm39) |
C23S |
probably damaging |
Het |
Anxa10 |
C |
T |
8: 62,531,001 (GRCm39) |
V70I |
probably benign |
Het |
Asap3 |
T |
C |
4: 135,961,636 (GRCm39) |
|
probably benign |
Het |
Asb13 |
T |
C |
13: 3,695,052 (GRCm39) |
|
probably null |
Het |
Atp6v1a |
A |
T |
16: 43,922,055 (GRCm39) |
|
probably benign |
Het |
Atp8b1 |
T |
G |
18: 64,697,612 (GRCm39) |
I411L |
probably benign |
Het |
Baiap3 |
T |
A |
17: 25,468,075 (GRCm39) |
N313I |
probably damaging |
Het |
Bok |
T |
C |
1: 93,614,209 (GRCm39) |
I14T |
probably benign |
Het |
Bri3bp |
T |
A |
5: 125,518,808 (GRCm39) |
|
probably null |
Het |
C2cd2l |
A |
G |
9: 44,227,499 (GRCm39) |
L186P |
probably damaging |
Het |
Cadm2 |
A |
T |
16: 66,679,702 (GRCm39) |
C44S |
probably damaging |
Het |
Capn11 |
T |
C |
17: 45,949,807 (GRCm39) |
|
probably benign |
Het |
Carm1 |
T |
A |
9: 21,480,887 (GRCm39) |
|
probably benign |
Het |
Ccdc27 |
T |
C |
4: 154,120,941 (GRCm39) |
E285G |
unknown |
Het |
Cct3 |
T |
A |
3: 88,220,864 (GRCm39) |
D298E |
probably damaging |
Het |
Cd59b |
T |
A |
2: 103,911,331 (GRCm39) |
|
probably benign |
Het |
Cdh2 |
T |
C |
18: 16,762,633 (GRCm39) |
N437S |
probably benign |
Het |
Celsr3 |
T |
A |
9: 108,719,832 (GRCm39) |
I2470N |
probably damaging |
Het |
Cfap100 |
G |
A |
6: 90,392,888 (GRCm39) |
|
probably benign |
Het |
Cfap119 |
T |
C |
7: 127,184,034 (GRCm39) |
E261G |
probably damaging |
Het |
Cfap45 |
A |
T |
1: 172,359,756 (GRCm39) |
R98S |
possibly damaging |
Het |
Cfap54 |
T |
A |
10: 92,706,531 (GRCm39) |
H2757L |
unknown |
Het |
Chd1 |
C |
A |
17: 15,945,693 (GRCm39) |
N72K |
probably benign |
Het |
Cntn4 |
A |
T |
6: 106,644,501 (GRCm39) |
|
probably benign |
Het |
Cstf2t |
A |
T |
19: 31,062,026 (GRCm39) |
M521L |
probably benign |
Het |
Daam2 |
A |
T |
17: 49,805,911 (GRCm39) |
|
probably benign |
Het |
Ddias |
A |
T |
7: 92,508,545 (GRCm39) |
W457R |
probably benign |
Het |
Ddr2 |
C |
T |
1: 169,822,198 (GRCm39) |
V417I |
probably benign |
Het |
Dhx57 |
T |
C |
17: 80,577,800 (GRCm39) |
T570A |
probably damaging |
Het |
Dmp1 |
A |
G |
5: 104,355,496 (GRCm39) |
E32G |
possibly damaging |
Het |
Dtymk |
C |
T |
1: 93,729,510 (GRCm39) |
V14M |
possibly damaging |
Het |
Dync2li1 |
G |
A |
17: 84,956,699 (GRCm39) |
M286I |
probably benign |
Het |
Eea1 |
G |
A |
10: 95,857,529 (GRCm39) |
D664N |
possibly damaging |
Het |
Esp6 |
G |
T |
17: 40,876,287 (GRCm39) |
V112L |
probably benign |
Het |
Fam83h |
G |
T |
15: 75,878,018 (GRCm39) |
Q127K |
probably damaging |
Het |
Gabbr2 |
G |
A |
4: 46,677,474 (GRCm39) |
T802I |
probably benign |
Het |
Gart |
C |
A |
16: 91,420,291 (GRCm39) |
D851Y |
possibly damaging |
Het |
Gemin6 |
T |
A |
17: 80,535,524 (GRCm39) |
H161Q |
probably damaging |
Het |
Gm10912 |
T |
C |
2: 103,896,875 (GRCm39) |
S5P |
probably benign |
Het |
Gm5941 |
G |
A |
X: 91,533,817 (GRCm39) |
A62T |
possibly damaging |
Het |
Gng2 |
G |
T |
14: 19,941,363 (GRCm39) |
D26E |
probably benign |
Het |
Gpr33 |
A |
G |
12: 52,070,418 (GRCm39) |
V207A |
probably benign |
Het |
Gstm3 |
T |
A |
3: 107,873,586 (GRCm39) |
|
probably benign |
Het |
Havcr1 |
T |
C |
11: 46,643,259 (GRCm39) |
C60R |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,268,751 (GRCm39) |
S2157P |
probably benign |
Het |
Ift140 |
A |
G |
17: 25,309,907 (GRCm39) |
T1105A |
probably benign |
Het |
Igsf8 |
C |
A |
1: 172,143,826 (GRCm39) |
A56D |
possibly damaging |
Het |
Kat6a |
G |
T |
8: 23,352,230 (GRCm39) |
A5S |
probably damaging |
Het |
Kctd16 |
A |
G |
18: 40,663,828 (GRCm39) |
E319G |
probably damaging |
Het |
Kmo |
T |
C |
1: 175,474,706 (GRCm39) |
V157A |
possibly damaging |
Het |
Lrp5 |
T |
A |
19: 3,655,308 (GRCm39) |
I1071F |
probably damaging |
Het |
Lrrc17 |
A |
G |
5: 21,766,276 (GRCm39) |
T253A |
probably benign |
Het |
Mast2 |
T |
A |
4: 116,168,964 (GRCm39) |
H769L |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,990,408 (GRCm39) |
K50E |
probably damaging |
Het |
Mbd5 |
A |
G |
2: 49,146,701 (GRCm39) |
T304A |
possibly damaging |
Het |
Mbp |
T |
C |
18: 82,590,995 (GRCm39) |
S73P |
probably damaging |
Het |
Mc5r |
T |
A |
18: 68,472,163 (GRCm39) |
V174E |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,197,864 (GRCm39) |
T736S |
probably benign |
Het |
Med13l |
T |
C |
5: 118,809,067 (GRCm39) |
|
probably benign |
Het |
Minar1 |
T |
C |
9: 89,484,470 (GRCm39) |
H309R |
probably benign |
Het |
Mlh3 |
C |
G |
12: 85,282,488 (GRCm39) |
A1382P |
possibly damaging |
Het |
Mpdz |
T |
C |
4: 81,278,228 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
A |
G |
7: 141,350,002 (GRCm39) |
T582A |
possibly damaging |
Het |
Nalcn |
A |
G |
14: 123,702,152 (GRCm39) |
F453S |
probably damaging |
Het |
Nrap |
T |
A |
19: 56,333,906 (GRCm39) |
M902L |
probably damaging |
Het |
Nup85 |
C |
T |
11: 115,459,196 (GRCm39) |
R100* |
probably null |
Het |
Nxf1 |
T |
G |
19: 8,741,955 (GRCm39) |
N296K |
probably damaging |
Het |
Ogg1 |
A |
G |
6: 113,305,381 (GRCm39) |
T65A |
probably damaging |
Het |
Ogt |
A |
G |
X: 100,687,805 (GRCm39) |
|
probably benign |
Het |
Or4c10 |
A |
G |
2: 89,760,545 (GRCm39) |
T131A |
probably benign |
Het |
Or4k48 |
C |
T |
2: 111,476,136 (GRCm39) |
V69I |
probably benign |
Het |
Or51e1 |
T |
A |
7: 102,359,202 (GRCm39) |
H245Q |
probably damaging |
Het |
Ovol2 |
T |
C |
2: 144,173,710 (GRCm39) |
D24G |
probably damaging |
Het |
Pabpc1 |
A |
G |
15: 36,599,298 (GRCm39) |
|
probably benign |
Het |
Pak6 |
T |
C |
2: 118,524,168 (GRCm39) |
L441P |
probably damaging |
Het |
Pappa |
T |
A |
4: 65,107,552 (GRCm39) |
C654* |
probably null |
Het |
Paqr6 |
T |
A |
3: 88,273,298 (GRCm39) |
S97T |
probably damaging |
Het |
Parp14 |
T |
C |
16: 35,678,888 (GRCm39) |
N360S |
probably benign |
Het |
Pclo |
G |
T |
5: 14,727,873 (GRCm39) |
G2244* |
probably null |
Het |
Pdzrn3 |
A |
T |
6: 101,132,903 (GRCm39) |
|
probably null |
Het |
Pes1 |
T |
C |
11: 3,925,557 (GRCm39) |
M220T |
probably damaging |
Het |
Phip |
A |
T |
9: 82,758,274 (GRCm39) |
V1473E |
probably benign |
Het |
Pkd2l2 |
T |
A |
18: 34,563,321 (GRCm39) |
|
probably null |
Het |
Plch1 |
T |
C |
3: 63,660,677 (GRCm39) |
D302G |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,925,459 (GRCm39) |
T1419A |
probably benign |
Het |
Ppara |
A |
T |
15: 85,682,372 (GRCm39) |
E356V |
probably damaging |
Het |
Ppp1r37 |
G |
A |
7: 19,266,102 (GRCm39) |
P555S |
probably benign |
Het |
Ppp6r1 |
T |
C |
7: 4,642,709 (GRCm39) |
E545G |
possibly damaging |
Het |
Proser3 |
G |
A |
7: 30,240,124 (GRCm39) |
H327Y |
probably damaging |
Het |
Prss43 |
T |
A |
9: 110,658,576 (GRCm39) |
I292N |
probably damaging |
Het |
Pwwp3b |
T |
A |
X: 138,136,444 (GRCm39) |
D327E |
probably damaging |
Het |
Pygl |
G |
C |
12: 70,253,178 (GRCm39) |
N271K |
probably damaging |
Het |
Rassf7 |
T |
A |
7: 140,796,903 (GRCm39) |
|
probably benign |
Het |
Rfx2 |
T |
C |
17: 57,110,722 (GRCm39) |
Y88C |
probably damaging |
Het |
Rpl6 |
T |
C |
5: 121,346,541 (GRCm39) |
V214A |
probably benign |
Het |
Rspo1 |
T |
A |
4: 124,885,225 (GRCm39) |
|
probably null |
Het |
Sav1 |
A |
C |
12: 70,012,979 (GRCm39) |
L366V |
probably benign |
Het |
Sema3b |
T |
G |
9: 107,481,355 (GRCm39) |
T52P |
possibly damaging |
Het |
Senp6 |
A |
G |
9: 80,023,841 (GRCm39) |
D40G |
probably damaging |
Het |
Sh3pxd2a |
A |
G |
19: 47,256,646 (GRCm39) |
S719P |
probably damaging |
Het |
Shank1 |
C |
T |
7: 44,001,718 (GRCm39) |
R1146W |
unknown |
Het |
Slc34a3 |
G |
T |
2: 25,121,245 (GRCm39) |
D307E |
probably benign |
Het |
Slc35b3 |
T |
C |
13: 39,121,251 (GRCm39) |
I330V |
probably benign |
Het |
Slc4a10 |
G |
A |
2: 62,073,742 (GRCm39) |
C268Y |
probably benign |
Het |
Slco6d1 |
A |
G |
1: 98,349,124 (GRCm39) |
E65G |
probably benign |
Het |
Slit2 |
A |
G |
5: 48,402,915 (GRCm39) |
|
probably benign |
Het |
Smcr8 |
T |
C |
11: 60,668,941 (GRCm39) |
Y30H |
probably damaging |
Het |
Snap47 |
A |
G |
11: 59,329,326 (GRCm39) |
|
probably benign |
Het |
Snrnp25 |
G |
A |
11: 32,156,960 (GRCm39) |
V15I |
probably damaging |
Het |
Spns2 |
T |
C |
11: 72,345,223 (GRCm39) |
Y449C |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,760,314 (GRCm39) |
|
probably benign |
Het |
Strip1 |
C |
A |
3: 107,521,929 (GRCm39) |
D750Y |
probably damaging |
Het |
Taf1c |
A |
T |
8: 120,326,722 (GRCm39) |
I438N |
probably damaging |
Het |
Tbc1d2 |
T |
A |
4: 46,609,003 (GRCm39) |
K745* |
probably null |
Het |
Tctn1 |
T |
C |
5: 122,402,207 (GRCm39) |
T76A |
probably damaging |
Het |
Tesl1 |
A |
T |
X: 23,773,290 (GRCm39) |
I264F |
probably benign |
Het |
Tfpi |
T |
C |
2: 84,273,664 (GRCm39) |
|
probably benign |
Het |
Timm44 |
A |
T |
8: 4,316,592 (GRCm39) |
H317Q |
probably benign |
Het |
Tnfaip1 |
A |
T |
11: 78,420,840 (GRCm39) |
|
probably benign |
Het |
Tnpo3 |
A |
T |
6: 29,554,992 (GRCm39) |
|
probably benign |
Het |
Top3b |
T |
C |
16: 16,697,301 (GRCm39) |
|
probably benign |
Het |
Trak1 |
T |
A |
9: 121,282,351 (GRCm39) |
M410K |
possibly damaging |
Het |
Trpm3 |
C |
A |
19: 22,956,018 (GRCm39) |
P1160Q |
probably damaging |
Het |
Tyk2 |
T |
A |
9: 21,022,433 (GRCm39) |
T799S |
possibly damaging |
Het |
Ubfd1 |
G |
A |
7: 121,666,714 (GRCm39) |
|
probably benign |
Het |
Unc13a |
G |
A |
8: 72,094,817 (GRCm39) |
R1272* |
probably null |
Het |
Unc45b |
T |
A |
11: 82,831,031 (GRCm39) |
L797Q |
possibly damaging |
Het |
Urb2 |
C |
T |
8: 124,757,709 (GRCm39) |
Q1139* |
probably null |
Het |
Vmn2r66 |
A |
T |
7: 84,657,070 (GRCm39) |
S112T |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,272,842 (GRCm39) |
D552V |
probably benign |
Het |
Vmn2r76 |
A |
G |
7: 85,877,904 (GRCm39) |
Y498H |
probably benign |
Het |
Vmn2r84 |
A |
C |
10: 130,226,984 (GRCm39) |
W285G |
probably damaging |
Het |
Vps72 |
G |
T |
3: 95,029,894 (GRCm39) |
L304F |
probably damaging |
Het |
Wiz |
A |
T |
17: 32,575,415 (GRCm39) |
I907N |
probably damaging |
Het |
Yaf2 |
T |
C |
15: 93,183,417 (GRCm39) |
K131R |
probably damaging |
Het |
Zfp141 |
A |
T |
7: 42,125,480 (GRCm39) |
Y331N |
possibly damaging |
Het |
Zfp324 |
G |
T |
7: 12,704,951 (GRCm39) |
C380F |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,978,119 (GRCm39) |
T765A |
probably benign |
Het |
Zfp616 |
A |
T |
11: 73,976,500 (GRCm39) |
H923L |
probably damaging |
Het |
Zfpm1 |
C |
T |
8: 123,062,585 (GRCm39) |
T548M |
probably damaging |
Het |
Zp2 |
A |
T |
7: 119,742,799 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or56b1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01358:Or56b1b
|
APN |
7 |
108,164,409 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01447:Or56b1b
|
APN |
7 |
108,164,216 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01845:Or56b1b
|
APN |
7 |
108,164,343 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02110:Or56b1b
|
APN |
7 |
108,164,286 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03196:Or56b1b
|
APN |
7 |
108,164,061 (GRCm39) |
missense |
probably benign |
|
R0282:Or56b1b
|
UTSW |
7 |
108,164,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Or56b1b
|
UTSW |
7 |
108,164,721 (GRCm39) |
missense |
probably benign |
0.01 |
R0514:Or56b1b
|
UTSW |
7 |
108,164,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R0727:Or56b1b
|
UTSW |
7 |
108,164,315 (GRCm39) |
missense |
probably benign |
0.00 |
R0744:Or56b1b
|
UTSW |
7 |
108,164,205 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0836:Or56b1b
|
UTSW |
7 |
108,164,205 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0840:Or56b1b
|
UTSW |
7 |
108,164,823 (GRCm39) |
missense |
probably benign |
0.00 |
R1750:Or56b1b
|
UTSW |
7 |
108,164,564 (GRCm39) |
nonsense |
probably null |
|
R1827:Or56b1b
|
UTSW |
7 |
108,164,282 (GRCm39) |
missense |
probably benign |
0.35 |
R1933:Or56b1b
|
UTSW |
7 |
108,164,730 (GRCm39) |
missense |
possibly damaging |
0.57 |
R3004:Or56b1b
|
UTSW |
7 |
108,164,151 (GRCm39) |
missense |
probably benign |
0.42 |
R3766:Or56b1b
|
UTSW |
7 |
108,164,402 (GRCm39) |
missense |
probably benign |
0.00 |
R5179:Or56b1b
|
UTSW |
7 |
108,164,433 (GRCm39) |
missense |
probably benign |
|
R5408:Or56b1b
|
UTSW |
7 |
108,164,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R5493:Or56b1b
|
UTSW |
7 |
108,164,774 (GRCm39) |
missense |
probably benign |
0.24 |
R5569:Or56b1b
|
UTSW |
7 |
108,164,772 (GRCm39) |
missense |
probably benign |
0.01 |
R6520:Or56b1b
|
UTSW |
7 |
108,164,046 (GRCm39) |
makesense |
probably null |
|
R6798:Or56b1b
|
UTSW |
7 |
108,164,967 (GRCm39) |
nonsense |
probably null |
|
R6803:Or56b1b
|
UTSW |
7 |
108,164,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R7242:Or56b1b
|
UTSW |
7 |
108,164,919 (GRCm39) |
missense |
probably benign |
0.03 |
R7559:Or56b1b
|
UTSW |
7 |
108,164,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R7644:Or56b1b
|
UTSW |
7 |
108,164,649 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8498:Or56b1b
|
UTSW |
7 |
108,164,833 (GRCm39) |
nonsense |
probably null |
|
R8970:Or56b1b
|
UTSW |
7 |
108,164,997 (GRCm39) |
missense |
probably benign |
0.00 |
R9014:Or56b1b
|
UTSW |
7 |
108,164,882 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9093:Or56b1b
|
UTSW |
7 |
108,164,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R9103:Or56b1b
|
UTSW |
7 |
108,164,780 (GRCm39) |
missense |
probably benign |
0.02 |
R9548:Or56b1b
|
UTSW |
7 |
108,164,334 (GRCm39) |
missense |
possibly damaging |
0.75 |
|