Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
C |
A |
5: 125,514,977 (GRCm38) |
N576K |
probably benign |
Het |
Abca5 |
T |
A |
11: 110,299,986 (GRCm38) |
H766L |
possibly damaging |
Het |
Abca5 |
G |
T |
11: 110,299,978 (GRCm38) |
L769M |
probably damaging |
Het |
Acvr1c |
A |
G |
2: 58,287,884 (GRCm38) |
I191T |
probably damaging |
Het |
Agps |
A |
T |
2: 75,866,779 (GRCm38) |
E314D |
probably damaging |
Het |
Agxt |
G |
A |
1: 93,135,768 (GRCm38) |
G131R |
probably damaging |
Het |
Ak8 |
A |
G |
2: 28,742,746 (GRCm38) |
T326A |
probably benign |
Het |
Aldoart2 |
T |
A |
12: 55,566,277 (GRCm38) |
I329N |
probably benign |
Het |
Apaf1 |
T |
C |
10: 91,060,185 (GRCm38) |
I342V |
possibly damaging |
Het |
Arhgap40 |
T |
C |
2: 158,527,161 (GRCm38) |
S68P |
probably benign |
Het |
Arsi |
G |
A |
18: 60,916,651 (GRCm38) |
G202E |
probably benign |
Het |
AU022252 |
C |
T |
4: 119,228,097 (GRCm38) |
R71Q |
possibly damaging |
Het |
Baz1b |
T |
C |
5: 135,217,782 (GRCm38) |
L695P |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,962,024 (GRCm38) |
S587T |
probably benign |
Het |
Cep76 |
T |
C |
18: 67,624,958 (GRCm38) |
M421V |
probably benign |
Het |
Clk2 |
A |
G |
3: 89,168,703 (GRCm38) |
D60G |
probably damaging |
Het |
Clstn3 |
G |
T |
6: 124,462,169 (GRCm38) |
T6K |
probably damaging |
Het |
Cluap1 |
T |
A |
16: 3,919,558 (GRCm38) |
D180E |
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,699,552 (GRCm38) |
I530V |
probably benign |
Het |
Cpt1a |
T |
C |
19: 3,365,788 (GRCm38) |
|
probably benign |
Het |
Cr2 |
T |
G |
1: 195,155,272 (GRCm38) |
K797Q |
possibly damaging |
Het |
Crybg3 |
C |
A |
16: 59,554,112 (GRCm38) |
V2260L |
probably benign |
Het |
Csnk1a1 |
T |
A |
18: 61,585,250 (GRCm38) |
|
probably benign |
Het |
Cxcr1 |
T |
C |
1: 74,192,770 (GRCm38) |
D31G |
probably benign |
Het |
Cyp2a5 |
G |
T |
7: 26,835,936 (GRCm38) |
D108Y |
probably damaging |
Het |
Dnajc1 |
A |
G |
2: 18,222,727 (GRCm38) |
V376A |
possibly damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,236,278 (GRCm38) |
V462A |
probably benign |
Het |
Elmo1 |
A |
G |
13: 20,290,477 (GRCm38) |
K357R |
possibly damaging |
Het |
Eml6 |
T |
A |
11: 29,818,374 (GRCm38) |
H771L |
probably damaging |
Het |
Epb41l4a |
A |
G |
18: 33,832,664 (GRCm38) |
I370T |
probably benign |
Het |
Esp36 |
A |
T |
17: 38,417,281 (GRCm38) |
N79K |
possibly damaging |
Het |
Fam229b |
A |
G |
10: 39,118,919 (GRCm38) |
*81Q |
probably null |
Het |
Fat4 |
T |
C |
3: 38,983,076 (GRCm38) |
Y3626H |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,306,285 (GRCm38) |
F2681Y |
probably benign |
Het |
Gad1-ps |
A |
G |
10: 99,445,469 (GRCm38) |
|
noncoding transcript |
Het |
Galm |
C |
A |
17: 80,183,267 (GRCm38) |
N284K |
probably damaging |
Het |
Gtf3c2 |
A |
T |
5: 31,159,102 (GRCm38) |
S735T |
probably benign |
Het |
Hsph1 |
A |
T |
5: 149,630,383 (GRCm38) |
S207T |
probably benign |
Het |
Il33 |
C |
T |
19: 29,955,215 (GRCm38) |
R159C |
probably damaging |
Het |
Invs |
A |
G |
4: 48,382,148 (GRCm38) |
N106S |
possibly damaging |
Het |
Kif21b |
G |
T |
1: 136,169,324 (GRCm38) |
|
probably null |
Het |
Kirrel2 |
A |
G |
7: 30,456,498 (GRCm38) |
C42R |
probably damaging |
Het |
Letm1 |
A |
C |
5: 33,752,555 (GRCm38) |
C378W |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,745,484 (GRCm38) |
K160N |
probably benign |
Het |
Lrrtm3 |
A |
G |
10: 64,089,025 (GRCm38) |
I121T |
probably damaging |
Het |
Lztr1 |
T |
A |
16: 17,509,670 (GRCm38) |
V79E |
probably damaging |
Het |
Mmp8 |
T |
G |
9: 7,566,278 (GRCm38) |
D378E |
probably damaging |
Het |
Mpzl3 |
A |
G |
9: 45,066,529 (GRCm38) |
E145G |
probably damaging |
Het |
Mrps2 |
C |
T |
2: 28,469,664 (GRCm38) |
L178F |
probably damaging |
Het |
Mzb1 |
A |
G |
18: 35,647,822 (GRCm38) |
|
probably null |
Het |
Nckap1 |
T |
C |
2: 80,553,415 (GRCm38) |
D135G |
probably damaging |
Het |
Ndst1 |
A |
G |
18: 60,697,170 (GRCm38) |
F623L |
possibly damaging |
Het |
Nlrp5 |
A |
T |
7: 23,413,347 (GRCm38) |
D143V |
probably damaging |
Het |
Olfr1241 |
T |
C |
2: 89,482,248 (GRCm38) |
M296V |
probably null |
Het |
Olfr1311 |
A |
G |
2: 112,021,404 (GRCm38) |
V150A |
probably benign |
Het |
Olfr146 |
T |
C |
9: 39,019,025 (GRCm38) |
D172G |
probably benign |
Het |
Olfr307 |
T |
C |
7: 86,336,345 (GRCm38) |
D17G |
possibly damaging |
Het |
Olfr32 |
A |
G |
2: 90,138,404 (GRCm38) |
V245A |
probably benign |
Het |
Olfr548-ps1 |
T |
C |
7: 102,542,125 (GRCm38) |
L63P |
probably damaging |
Het |
Olfr907 |
A |
G |
9: 38,498,818 (GRCm38) |
I50V |
probably benign |
Het |
Parp14 |
T |
G |
16: 35,857,224 (GRCm38) |
E791D |
probably benign |
Het |
Pcdh8 |
C |
T |
14: 79,769,389 (GRCm38) |
R578H |
possibly damaging |
Het |
Phrf1 |
T |
A |
7: 141,259,801 (GRCm38) |
|
probably benign |
Het |
Polr3b |
C |
A |
10: 84,680,385 (GRCm38) |
H626N |
probably benign |
Het |
Ppp1r12a |
A |
G |
10: 108,251,859 (GRCm38) |
T58A |
probably benign |
Het |
Ppp4r3b |
T |
A |
11: 29,182,460 (GRCm38) |
V33D |
probably damaging |
Het |
Ppp5c |
A |
G |
7: 17,009,982 (GRCm38) |
Y176H |
probably damaging |
Het |
R3hdm1 |
A |
G |
1: 128,197,005 (GRCm38) |
Y343C |
probably damaging |
Het |
Rabac1 |
C |
T |
7: 24,972,130 (GRCm38) |
V122M |
probably damaging |
Het |
Rasef |
G |
T |
4: 73,735,748 (GRCm38) |
Q561K |
probably damaging |
Het |
Rbl1 |
A |
G |
2: 157,195,634 (GRCm38) |
S198P |
probably damaging |
Het |
Rbm12 |
A |
T |
2: 156,097,536 (GRCm38) |
M272K |
probably damaging |
Het |
Rexo1 |
T |
G |
10: 80,550,050 (GRCm38) |
K391N |
possibly damaging |
Het |
Rnf43 |
T |
C |
11: 87,731,347 (GRCm38) |
S384P |
probably benign |
Het |
Rpsa |
A |
T |
9: 120,131,000 (GRCm38) |
I210F |
possibly damaging |
Het |
Rslcan18 |
A |
G |
13: 67,098,952 (GRCm38) |
Y75H |
possibly damaging |
Het |
Scn9a |
T |
A |
2: 66,526,813 (GRCm38) |
D1048V |
probably benign |
Het |
Sec11a |
T |
C |
7: 80,927,734 (GRCm38) |
|
probably null |
Het |
Sidt2 |
A |
G |
9: 45,950,089 (GRCm38) |
V19A |
probably damaging |
Het |
Snx14 |
G |
A |
9: 88,398,364 (GRCm38) |
Q522* |
probably null |
Het |
Stx1b |
A |
G |
7: 127,814,972 (GRCm38) |
L74S |
probably damaging |
Het |
Tm7sf3 |
A |
T |
6: 146,609,878 (GRCm38) |
M371K |
probably benign |
Het |
Tmem115 |
T |
C |
9: 107,534,975 (GRCm38) |
V166A |
probably benign |
Het |
Traf5 |
T |
A |
1: 191,999,951 (GRCm38) |
T310S |
probably benign |
Het |
Trdn |
A |
G |
10: 33,466,452 (GRCm38) |
K619E |
probably benign |
Het |
Trmt10a |
T |
A |
3: 138,152,184 (GRCm38) |
|
probably null |
Het |
Txk |
A |
C |
5: 72,707,671 (GRCm38) |
I287R |
probably damaging |
Het |
Txndc16 |
T |
C |
14: 45,151,887 (GRCm38) |
D452G |
probably damaging |
Het |
Ube2f |
G |
A |
1: 91,262,301 (GRCm38) |
|
probably null |
Het |
Ubtfl1 |
T |
G |
9: 18,410,193 (GRCm38) |
I339R |
probably benign |
Het |
Upf1 |
A |
G |
8: 70,338,505 (GRCm38) |
I529T |
probably damaging |
Het |
Vmn1r197 |
A |
G |
13: 22,328,653 (GRCm38) |
D248G |
possibly damaging |
Het |
Vmn1r5 |
A |
T |
6: 56,985,786 (GRCm38) |
T149S |
probably benign |
Het |
Vmn1r83 |
C |
T |
7: 12,321,270 (GRCm38) |
V287I |
possibly damaging |
Het |
Vmn2r118 |
G |
A |
17: 55,608,496 (GRCm38) |
R485* |
probably null |
Het |
Vmn2r-ps130 |
A |
G |
17: 23,063,801 (GRCm38) |
T152A |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,839,975 (GRCm38) |
F2448L |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,841,573 (GRCm38) |
N2583S |
probably benign |
Het |
Wscd1 |
C |
T |
11: 71,788,675 (GRCm38) |
P458L |
probably damaging |
Het |
Xylt2 |
T |
A |
11: 94,670,433 (GRCm38) |
D168V |
probably damaging |
Het |
Zdhhc2 |
A |
G |
8: 40,467,972 (GRCm38) |
T306A |
probably benign |
Het |
Zfp804b |
A |
T |
5: 6,769,771 (GRCm38) |
D1097E |
possibly damaging |
Het |
Zfp93 |
T |
A |
7: 24,275,731 (GRCm38) |
C380* |
probably null |
Het |
Zfp960 |
T |
A |
17: 17,088,256 (GRCm38) |
C411S |
probably damaging |
Het |
Zmynd15 |
T |
A |
11: 70,464,793 (GRCm38) |
V430E |
probably damaging |
Het |
|
Other mutations in Olfr1225 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03230:Olfr1225
|
APN |
2 |
89,171,089 (GRCm38) |
missense |
possibly damaging |
0.53 |
IGL03381:Olfr1225
|
APN |
2 |
89,171,179 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL03147:Olfr1225
|
UTSW |
2 |
89,170,972 (GRCm38) |
missense |
probably benign |
0.03 |
PIT4458001:Olfr1225
|
UTSW |
2 |
89,170,633 (GRCm38) |
missense |
probably benign |
0.02 |
R0100:Olfr1225
|
UTSW |
2 |
89,171,087 (GRCm38) |
missense |
probably benign |
0.00 |
R0373:Olfr1225
|
UTSW |
2 |
89,170,413 (GRCm38) |
missense |
probably benign |
0.02 |
R0482:Olfr1225
|
UTSW |
2 |
89,170,631 (GRCm38) |
missense |
probably benign |
0.37 |
R0491:Olfr1225
|
UTSW |
2 |
89,170,360 (GRCm38) |
missense |
probably benign |
0.07 |
R0548:Olfr1225
|
UTSW |
2 |
89,170,648 (GRCm38) |
missense |
probably damaging |
1.00 |
R1123:Olfr1225
|
UTSW |
2 |
89,170,868 (GRCm38) |
missense |
possibly damaging |
0.89 |
R1565:Olfr1225
|
UTSW |
2 |
89,170,627 (GRCm38) |
missense |
probably benign |
0.01 |
R4204:Olfr1225
|
UTSW |
2 |
89,170,780 (GRCm38) |
missense |
probably benign |
0.13 |
R4580:Olfr1225
|
UTSW |
2 |
89,171,200 (GRCm38) |
missense |
probably benign |
0.01 |
R4669:Olfr1225
|
UTSW |
2 |
89,170,901 (GRCm38) |
missense |
probably damaging |
1.00 |
R5137:Olfr1225
|
UTSW |
2 |
89,170,400 (GRCm38) |
missense |
probably benign |
0.00 |
R6391:Olfr1225
|
UTSW |
2 |
89,170,598 (GRCm38) |
missense |
probably benign |
0.03 |
R6396:Olfr1225
|
UTSW |
2 |
89,170,690 (GRCm38) |
missense |
probably damaging |
0.99 |
R7103:Olfr1225
|
UTSW |
2 |
89,170,483 (GRCm38) |
missense |
possibly damaging |
0.77 |
R7187:Olfr1225
|
UTSW |
2 |
89,171,370 (GRCm38) |
start gained |
probably benign |
|
R7394:Olfr1225
|
UTSW |
2 |
89,170,361 (GRCm38) |
missense |
probably benign |
|
R7758:Olfr1225
|
UTSW |
2 |
89,171,141 (GRCm38) |
missense |
probably benign |
0.00 |
R8073:Olfr1225
|
UTSW |
2 |
89,170,940 (GRCm38) |
missense |
probably damaging |
0.99 |
R9012:Olfr1225
|
UTSW |
2 |
89,170,585 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9632:Olfr1225
|
UTSW |
2 |
89,171,408 (GRCm38) |
start gained |
probably benign |
|
|