Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
C |
A |
3: 59,947,235 (GRCm39) |
P311Q |
probably damaging |
Het |
Acoxl |
T |
A |
2: 127,814,526 (GRCm39) |
M314K |
probably damaging |
Het |
Agmat |
A |
T |
4: 141,483,214 (GRCm39) |
D216V |
probably damaging |
Het |
Aida |
A |
T |
1: 183,094,627 (GRCm39) |
E107D |
probably benign |
Het |
Ano5 |
A |
G |
7: 51,187,561 (GRCm39) |
K50R |
possibly damaging |
Het |
Anxa2 |
A |
T |
9: 69,391,098 (GRCm39) |
D95V |
probably damaging |
Het |
Aspm |
G |
A |
1: 139,419,403 (GRCm39) |
V3023M |
probably damaging |
Het |
Atg16l2 |
A |
G |
7: 100,939,568 (GRCm39) |
|
probably null |
Het |
B3galt4 |
G |
A |
17: 34,169,813 (GRCm39) |
R142C |
probably damaging |
Het |
B3galt5 |
A |
T |
16: 96,117,225 (GRCm39) |
K286M |
probably damaging |
Het |
Best3 |
A |
C |
10: 116,838,499 (GRCm39) |
I186L |
probably benign |
Het |
Blm |
G |
T |
7: 80,155,697 (GRCm39) |
|
probably null |
Het |
Cat |
A |
T |
2: 103,293,660 (GRCm39) |
D389E |
probably damaging |
Het |
Cert1 |
T |
A |
13: 96,771,394 (GRCm39) |
N550K |
probably damaging |
Het |
Cluh |
C |
A |
11: 74,550,355 (GRCm39) |
C222* |
probably null |
Het |
Cntnap2 |
G |
A |
6: 47,275,522 (GRCm39) |
E1325K |
probably damaging |
Het |
Col14a1 |
A |
T |
15: 55,313,336 (GRCm39) |
D1320V |
unknown |
Het |
Cpne7 |
A |
G |
8: 123,854,176 (GRCm39) |
K288E |
possibly damaging |
Het |
Cyp26b1 |
A |
G |
6: 84,552,032 (GRCm39) |
S369P |
possibly damaging |
Het |
Cyp2j9 |
T |
A |
4: 96,460,201 (GRCm39) |
K434M |
probably damaging |
Het |
Dpyd |
G |
C |
3: 118,858,601 (GRCm39) |
S605T |
probably benign |
Het |
Dst |
A |
G |
1: 34,229,339 (GRCm39) |
T1986A |
probably benign |
Het |
Ebf2 |
T |
A |
14: 67,625,391 (GRCm39) |
V233D |
probably damaging |
Het |
Ecm2 |
A |
G |
13: 49,683,732 (GRCm39) |
D570G |
probably benign |
Het |
Efhc1 |
T |
A |
1: 21,059,784 (GRCm39) |
C611* |
probably null |
Het |
Epop |
T |
C |
11: 97,519,480 (GRCm39) |
T210A |
probably benign |
Het |
Fdxacb1 |
A |
T |
9: 50,682,946 (GRCm39) |
N101I |
probably benign |
Het |
Fezf1 |
A |
G |
6: 23,247,331 (GRCm39) |
F248S |
possibly damaging |
Het |
Galnt16 |
A |
G |
12: 80,630,430 (GRCm39) |
D262G |
probably damaging |
Het |
Gm9507 |
T |
A |
10: 77,647,500 (GRCm39) |
|
probably benign |
Het |
Grin2b |
A |
T |
6: 135,757,138 (GRCm39) |
I441N |
probably benign |
Het |
H2-Eb2 |
A |
G |
17: 34,553,278 (GRCm39) |
I155V |
probably benign |
Het |
Hectd4 |
C |
A |
5: 121,493,692 (GRCm39) |
D3811E |
probably benign |
Het |
Herc4 |
T |
C |
10: 63,081,889 (GRCm39) |
S71P |
probably benign |
Het |
Hhipl1 |
A |
G |
12: 108,293,977 (GRCm39) |
T628A |
probably benign |
Het |
Hoga1 |
A |
C |
19: 42,048,459 (GRCm39) |
|
probably null |
Het |
Igf2bp1 |
A |
G |
11: 95,866,122 (GRCm39) |
V122A |
probably damaging |
Het |
Il10ra |
C |
A |
9: 45,167,109 (GRCm39) |
A481S |
probably benign |
Het |
Klk1b26 |
A |
T |
7: 43,666,324 (GRCm39) |
T256S |
probably damaging |
Het |
Kndc1 |
C |
T |
7: 139,501,150 (GRCm39) |
T813I |
probably benign |
Het |
Limch1 |
A |
G |
5: 67,156,072 (GRCm39) |
K394R |
probably benign |
Het |
Lrrc37a |
T |
C |
11: 103,391,087 (GRCm39) |
E1446G |
probably benign |
Het |
Lrrc47 |
C |
T |
4: 154,100,350 (GRCm39) |
R287W |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,738,712 (GRCm39) |
L3555Q |
possibly damaging |
Het |
Mei1 |
A |
G |
15: 81,987,405 (GRCm39) |
H399R |
possibly damaging |
Het |
Mei1 |
G |
T |
15: 81,991,237 (GRCm39) |
V472F |
probably damaging |
Het |
Mrps34 |
T |
A |
17: 25,114,464 (GRCm39) |
|
probably null |
Het |
Myom3 |
A |
G |
4: 135,503,723 (GRCm39) |
T391A |
probably benign |
Het |
Nfib |
G |
A |
4: 82,248,645 (GRCm39) |
T314I |
possibly damaging |
Het |
Or5p73 |
A |
G |
7: 108,064,810 (GRCm39) |
N93S |
probably benign |
Het |
Or6c5 |
T |
C |
10: 129,074,368 (GRCm39) |
S117P |
probably damaging |
Het |
Or9a2 |
A |
G |
6: 41,748,939 (GRCm39) |
I98T |
probably benign |
Het |
Pdia3 |
G |
C |
2: 121,264,474 (GRCm39) |
G346A |
probably damaging |
Het |
Plce1 |
T |
C |
19: 38,766,368 (GRCm39) |
F2117S |
probably damaging |
Het |
Plec |
A |
G |
15: 76,057,743 (GRCm39) |
F4055L |
probably damaging |
Het |
Ppip5k1 |
A |
T |
2: 121,152,134 (GRCm39) |
|
probably null |
Het |
Psma6 |
T |
C |
12: 55,454,842 (GRCm39) |
I57T |
probably benign |
Het |
Psme2 |
A |
T |
14: 55,828,297 (GRCm39) |
|
probably null |
Het |
Reln |
A |
T |
5: 22,174,358 (GRCm39) |
D1948E |
possibly damaging |
Het |
Rsf1 |
GGCG |
GGCGACGGCAGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Sbno1 |
G |
T |
5: 124,532,000 (GRCm39) |
S727R |
probably damaging |
Het |
Serpina3m |
C |
A |
12: 104,355,958 (GRCm39) |
Y208* |
probably null |
Het |
Serpind1 |
T |
C |
16: 17,160,808 (GRCm39) |
V446A |
probably benign |
Het |
Shc3 |
T |
A |
13: 51,596,872 (GRCm39) |
M384L |
probably benign |
Het |
Slc38a11 |
A |
G |
2: 65,160,683 (GRCm39) |
F304L |
probably benign |
Het |
Slc4a5 |
A |
C |
6: 83,201,663 (GRCm39) |
D4A |
probably benign |
Het |
Slc4a5 |
G |
A |
6: 83,274,360 (GRCm39) |
A1076T |
probably benign |
Het |
Slpi |
C |
T |
2: 164,197,463 (GRCm39) |
C28Y |
probably damaging |
Het |
Sptan1 |
T |
C |
2: 29,920,483 (GRCm39) |
S2320P |
probably damaging |
Het |
Stim2 |
A |
G |
5: 54,262,591 (GRCm39) |
T278A |
possibly damaging |
Het |
Sympk |
T |
A |
7: 18,788,041 (GRCm39) |
S1186T |
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,560,715 (GRCm39) |
D387G |
probably benign |
Het |
Tns2 |
A |
T |
15: 102,021,100 (GRCm39) |
|
probably null |
Het |
Tnxb |
A |
G |
17: 34,901,225 (GRCm39) |
Y1013C |
probably damaging |
Het |
Tpsg1 |
T |
C |
17: 25,592,267 (GRCm39) |
S41P |
possibly damaging |
Het |
Trim36 |
T |
C |
18: 46,329,149 (GRCm39) |
N85S |
probably benign |
Het |
Trpm6 |
A |
T |
19: 18,773,648 (GRCm39) |
H380L |
probably benign |
Het |
Tssk4 |
A |
G |
14: 55,888,997 (GRCm39) |
I174M |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,776,735 (GRCm39) |
|
probably null |
Het |
Vmn2r114 |
ATTT |
ATT |
17: 23,509,906 (GRCm39) |
|
probably null |
Het |
Vmn2r4 |
T |
A |
3: 64,322,704 (GRCm39) |
N5I |
possibly damaging |
Het |
Vps11 |
G |
A |
9: 44,270,524 (GRCm39) |
H183Y |
probably damaging |
Het |
Vsig10l |
A |
G |
7: 43,116,892 (GRCm39) |
T476A |
possibly damaging |
Het |
Vwa8 |
C |
T |
14: 79,145,670 (GRCm39) |
R116C |
probably damaging |
Het |
Vwf |
G |
A |
6: 125,623,293 (GRCm39) |
V1797I |
probably benign |
Het |
Wasl |
A |
T |
6: 24,618,377 (GRCm39) |
S447T |
unknown |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Zfp874a |
T |
A |
13: 67,590,623 (GRCm39) |
I354F |
probably benign |
Het |
|
Other mutations in Or5b99 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Or5b99
|
APN |
19 |
12,976,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01301:Or5b99
|
APN |
19 |
12,976,781 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01369:Or5b99
|
APN |
19 |
12,977,125 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02098:Or5b99
|
APN |
19 |
12,976,937 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02106:Or5b99
|
APN |
19 |
12,976,929 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02369:Or5b99
|
APN |
19 |
12,977,072 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU18:Or5b99
|
UTSW |
19 |
12,976,781 (GRCm39) |
missense |
probably damaging |
0.99 |
R0316:Or5b99
|
UTSW |
19 |
12,976,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R0926:Or5b99
|
UTSW |
19 |
12,976,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R0988:Or5b99
|
UTSW |
19 |
12,977,151 (GRCm39) |
missense |
probably benign |
0.39 |
R1268:Or5b99
|
UTSW |
19 |
12,976,625 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1509:Or5b99
|
UTSW |
19 |
12,976,815 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1991:Or5b99
|
UTSW |
19 |
12,976,866 (GRCm39) |
missense |
possibly damaging |
0.60 |
R2132:Or5b99
|
UTSW |
19 |
12,976,402 (GRCm39) |
missense |
probably benign |
0.21 |
R2206:Or5b99
|
UTSW |
19 |
12,976,404 (GRCm39) |
missense |
probably benign |
0.06 |
R3687:Or5b99
|
UTSW |
19 |
12,976,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R4077:Or5b99
|
UTSW |
19 |
12,977,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R4803:Or5b99
|
UTSW |
19 |
12,976,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R4948:Or5b99
|
UTSW |
19 |
12,977,195 (GRCm39) |
missense |
probably benign |
0.06 |
R4999:Or5b99
|
UTSW |
19 |
12,976,583 (GRCm39) |
missense |
probably benign |
0.03 |
R6274:Or5b99
|
UTSW |
19 |
12,977,234 (GRCm39) |
missense |
probably damaging |
0.97 |
R6843:Or5b99
|
UTSW |
19 |
12,976,362 (GRCm39) |
missense |
probably benign |
0.09 |
R6928:Or5b99
|
UTSW |
19 |
12,977,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R6941:Or5b99
|
UTSW |
19 |
12,976,861 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7485:Or5b99
|
UTSW |
19 |
12,976,922 (GRCm39) |
missense |
probably benign |
0.03 |
R7611:Or5b99
|
UTSW |
19 |
12,976,431 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7823:Or5b99
|
UTSW |
19 |
12,976,781 (GRCm39) |
missense |
probably damaging |
0.99 |
R8948:Or5b99
|
UTSW |
19 |
12,976,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Or5b99
|
UTSW |
19 |
12,976,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:Or5b99
|
UTSW |
19 |
12,976,353 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9155:Or5b99
|
UTSW |
19 |
12,976,428 (GRCm39) |
missense |
probably benign |
0.00 |
R9236:Or5b99
|
UTSW |
19 |
12,976,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R9556:Or5b99
|
UTSW |
19 |
12,976,938 (GRCm39) |
missense |
probably benign |
0.12 |
R9563:Or5b99
|
UTSW |
19 |
12,976,983 (GRCm39) |
missense |
probably damaging |
0.97 |
|