Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
T |
6: 142,566,509 (GRCm39) |
|
probably null |
Het |
Abtb3 |
A |
C |
10: 85,487,526 (GRCm39) |
N998T |
probably benign |
Het |
Adamts20 |
T |
C |
15: 94,277,655 (GRCm39) |
H269R |
probably benign |
Het |
Adamtsl1 |
C |
T |
4: 86,342,410 (GRCm39) |
Q1642* |
probably null |
Het |
Adamtsl3 |
A |
C |
7: 82,216,185 (GRCm39) |
T863P |
probably damaging |
Het |
Adcy3 |
G |
T |
12: 4,184,896 (GRCm39) |
V191L |
probably benign |
Het |
Akap9 |
G |
T |
5: 4,007,664 (GRCm39) |
R244L |
probably benign |
Het |
Anapc1 |
C |
T |
2: 128,526,514 (GRCm39) |
V95M |
probably benign |
Het |
Arhgap17 |
G |
T |
7: 122,886,149 (GRCm39) |
|
probably benign |
Het |
Art2b |
T |
A |
7: 101,229,437 (GRCm39) |
Y154F |
probably damaging |
Het |
Atrn |
C |
T |
2: 130,836,967 (GRCm39) |
R1144* |
probably null |
Het |
Atxn3 |
T |
C |
12: 101,914,638 (GRCm39) |
S29G |
possibly damaging |
Het |
Batf3 |
C |
T |
1: 190,830,707 (GRCm39) |
P18S |
probably benign |
Het |
Bmal1 |
T |
A |
7: 112,898,642 (GRCm39) |
|
probably null |
Het |
Bmpr1b |
A |
T |
3: 141,576,546 (GRCm39) |
C96S |
probably damaging |
Het |
Bola1 |
A |
G |
3: 96,104,370 (GRCm39) |
S75P |
probably benign |
Het |
Cela3a |
G |
A |
4: 137,129,959 (GRCm39) |
R221* |
probably null |
Het |
Chat |
A |
G |
14: 32,142,771 (GRCm39) |
V406A |
possibly damaging |
Het |
Chd1 |
T |
A |
17: 15,962,493 (GRCm39) |
M750K |
probably damaging |
Het |
Clip1 |
T |
A |
5: 123,792,066 (GRCm39) |
K35* |
probably null |
Het |
Cnr2 |
G |
A |
4: 135,644,918 (GRCm39) |
G332D |
probably benign |
Het |
Cnrip1 |
A |
G |
11: 17,002,228 (GRCm39) |
D20G |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 97,874,030 (GRCm39) |
Y1384C |
unknown |
Het |
Col6a3 |
T |
A |
1: 90,731,940 (GRCm39) |
I831F |
probably damaging |
Het |
Cp |
G |
A |
3: 20,027,961 (GRCm39) |
V456I |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Ctbp2 |
T |
C |
7: 132,615,967 (GRCm39) |
I323V |
probably benign |
Het |
Ctnna2 |
C |
T |
6: 77,630,094 (GRCm39) |
R120H |
probably damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,733,575 (GRCm39) |
H318R |
probably benign |
Het |
Cyp2c66 |
A |
T |
19: 39,151,766 (GRCm39) |
|
probably null |
Het |
Cyp2j8 |
T |
C |
4: 96,395,614 (GRCm39) |
T4A |
probably benign |
Het |
Cyp4v3 |
A |
G |
8: 45,773,674 (GRCm39) |
V165A |
possibly damaging |
Het |
D5Ertd579e |
G |
A |
5: 36,773,571 (GRCm39) |
R275* |
probably null |
Het |
Deup1 |
G |
T |
9: 15,512,264 (GRCm39) |
Q160K |
possibly damaging |
Het |
Dhx36 |
A |
T |
3: 62,404,280 (GRCm39) |
I221K |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,272,886 (GRCm39) |
M2338K |
probably benign |
Het |
Dync2li1 |
T |
G |
17: 84,940,969 (GRCm39) |
L62V |
probably benign |
Het |
Ephb3 |
A |
G |
16: 21,039,245 (GRCm39) |
K367R |
probably benign |
Het |
Etv3 |
A |
G |
3: 87,435,368 (GRCm39) |
K80E |
probably damaging |
Het |
Flacc1 |
T |
A |
1: 58,706,965 (GRCm39) |
E234V |
probably damaging |
Het |
Gdap1l1 |
T |
C |
2: 163,295,779 (GRCm39) |
F346L |
probably benign |
Het |
Gm4787 |
C |
T |
12: 81,426,090 (GRCm39) |
V23M |
probably damaging |
Het |
Greb1l |
T |
A |
18: 10,547,306 (GRCm39) |
I1508N |
probably damaging |
Het |
Heatr5b |
G |
A |
17: 79,139,013 (GRCm39) |
T43I |
probably benign |
Het |
Hephl1 |
T |
C |
9: 14,997,586 (GRCm39) |
Y360C |
probably damaging |
Het |
Itgam |
A |
C |
7: 127,715,012 (GRCm39) |
T865P |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 24,054,186 (GRCm39) |
|
probably benign |
Het |
Kidins220 |
T |
A |
12: 25,042,259 (GRCm39) |
C185* |
probably null |
Het |
Klhl35 |
G |
T |
7: 99,118,275 (GRCm39) |
G273V |
probably damaging |
Het |
Lama5 |
A |
G |
2: 179,850,045 (GRCm39) |
|
probably null |
Het |
Lamc3 |
A |
G |
2: 31,805,966 (GRCm39) |
Q689R |
probably benign |
Het |
Lnx2 |
C |
T |
5: 146,955,850 (GRCm39) |
V649I |
probably benign |
Het |
Lrrc43 |
A |
G |
5: 123,637,675 (GRCm39) |
I281V |
probably benign |
Het |
Ly6g6d |
C |
A |
17: 35,290,730 (GRCm39) |
A67S |
probably benign |
Het |
Map1b |
A |
G |
13: 99,568,720 (GRCm39) |
S1334P |
probably benign |
Het |
Mast1 |
T |
A |
8: 85,644,500 (GRCm39) |
T810S |
probably benign |
Het |
Matcap1 |
G |
T |
8: 106,009,843 (GRCm39) |
R369S |
probably damaging |
Het |
Mbnl1 |
A |
G |
3: 60,503,117 (GRCm39) |
M1V |
probably null |
Het |
Mc5r |
T |
G |
18: 68,471,890 (GRCm39) |
M83R |
possibly damaging |
Het |
Mkln1 |
T |
C |
6: 31,435,941 (GRCm39) |
F300S |
probably damaging |
Het |
Mrgpre |
A |
T |
7: 143,335,088 (GRCm39) |
C138* |
probably null |
Het |
Mtarc2 |
T |
A |
1: 184,566,116 (GRCm39) |
M186L |
probably benign |
Het |
Ncbp1 |
C |
T |
4: 46,165,273 (GRCm39) |
Q529* |
probably null |
Het |
Nherf1 |
A |
G |
11: 115,067,289 (GRCm39) |
D180G |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,613,082 (GRCm39) |
D591G |
probably benign |
Het |
Nrxn3 |
A |
T |
12: 88,761,971 (GRCm39) |
H6L |
possibly damaging |
Het |
Nsmaf |
T |
A |
4: 6,423,342 (GRCm39) |
D342V |
probably damaging |
Het |
Oip5 |
TGAGAAA |
T |
2: 119,448,342 (GRCm39) |
|
probably benign |
Het |
Omt2a |
T |
A |
9: 78,220,305 (GRCm39) |
E31D |
possibly damaging |
Het |
Or4f62 |
A |
G |
2: 111,986,697 (GRCm39) |
T134A |
probably benign |
Het |
Or52n2b |
A |
G |
7: 104,565,915 (GRCm39) |
I196T |
probably benign |
Het |
Or5ac20 |
A |
G |
16: 59,104,348 (GRCm39) |
S171P |
probably benign |
Het |
Or6c88 |
A |
C |
10: 129,406,895 (GRCm39) |
I124L |
probably damaging |
Het |
Phyhipl |
A |
G |
10: 70,404,815 (GRCm39) |
V131A |
probably benign |
Het |
Pik3r5 |
A |
G |
11: 68,384,464 (GRCm39) |
M619V |
probably benign |
Het |
Pramel19 |
T |
C |
4: 101,798,661 (GRCm39) |
Y211H |
probably benign |
Het |
Ptprg |
A |
T |
14: 12,237,837 (GRCm38) |
E1431D |
probably benign |
Het |
Rnf20 |
A |
G |
4: 49,638,029 (GRCm39) |
T85A |
probably damaging |
Het |
Rtn3 |
A |
T |
19: 7,433,886 (GRCm39) |
I683K |
probably damaging |
Het |
Rwdd3 |
A |
G |
3: 120,952,470 (GRCm39) |
F174L |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,778,208 (GRCm39) |
Q2096R |
possibly damaging |
Het |
Scrn1 |
T |
C |
6: 54,511,407 (GRCm39) |
D111G |
probably damaging |
Het |
Sema3e |
A |
G |
5: 14,302,646 (GRCm39) |
R724G |
possibly damaging |
Het |
She |
A |
G |
3: 89,741,544 (GRCm39) |
M232V |
possibly damaging |
Het |
Skic3 |
T |
A |
13: 76,333,275 (GRCm39) |
V1508E |
possibly damaging |
Het |
Slc25a54 |
A |
T |
3: 109,020,132 (GRCm39) |
N382I |
possibly damaging |
Het |
Slc26a2 |
T |
C |
18: 61,331,875 (GRCm39) |
M519V |
probably damaging |
Het |
Slc9a1 |
T |
A |
4: 133,097,967 (GRCm39) |
L38H |
probably damaging |
Het |
Snap47 |
A |
T |
11: 59,319,369 (GRCm39) |
D256E |
probably damaging |
Het |
Tacc3 |
A |
G |
5: 33,829,326 (GRCm39) |
T610A |
probably benign |
Het |
Tbc1d30 |
G |
A |
10: 121,103,121 (GRCm39) |
T637M |
probably benign |
Het |
Tbcd |
T |
A |
11: 121,464,681 (GRCm39) |
M572K |
probably benign |
Het |
Thoc7 |
A |
T |
14: 13,953,460 (GRCm38) |
D68E |
probably benign |
Het |
Tmpo |
G |
A |
10: 90,989,171 (GRCm39) |
T250M |
probably damaging |
Het |
Tmtc1 |
TGTCCGCCAGGCCCTTGCCCCAGAAGTC |
TGTC |
6: 148,345,445 (GRCm39) |
|
probably benign |
Het |
Tnfaip1 |
A |
T |
11: 78,418,396 (GRCm39) |
C224S |
possibly damaging |
Het |
Tshz1 |
T |
C |
18: 84,032,987 (GRCm39) |
T474A |
probably benign |
Het |
Tspoap1 |
C |
T |
11: 87,657,222 (GRCm39) |
Q345* |
probably null |
Het |
Ttc21a |
A |
G |
9: 119,774,067 (GRCm39) |
E258G |
possibly damaging |
Het |
Ttyh1 |
T |
C |
7: 4,131,225 (GRCm39) |
L232P |
probably damaging |
Het |
Usp2 |
T |
A |
9: 43,987,110 (GRCm39) |
L136Q |
probably damaging |
Het |
Usp31 |
T |
C |
7: 121,247,868 (GRCm39) |
S1192G |
probably damaging |
Het |
|
Other mutations in Or9a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00896:Or9a2
|
APN |
6 |
41,749,047 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01460:Or9a2
|
APN |
6 |
41,749,216 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02465:Or9a2
|
APN |
6 |
41,748,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R0352:Or9a2
|
UTSW |
6 |
41,749,058 (GRCm39) |
missense |
probably damaging |
0.99 |
R0443:Or9a2
|
UTSW |
6 |
41,748,829 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0480:Or9a2
|
UTSW |
6 |
41,749,198 (GRCm39) |
missense |
probably benign |
0.01 |
R1491:Or9a2
|
UTSW |
6 |
41,748,456 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1495:Or9a2
|
UTSW |
6 |
41,748,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R2103:Or9a2
|
UTSW |
6 |
41,748,939 (GRCm39) |
missense |
probably benign |
0.36 |
R3688:Or9a2
|
UTSW |
6 |
41,749,160 (GRCm39) |
nonsense |
probably null |
|
R3910:Or9a2
|
UTSW |
6 |
41,749,083 (GRCm39) |
missense |
probably benign |
0.00 |
R4709:Or9a2
|
UTSW |
6 |
41,748,442 (GRCm39) |
missense |
probably benign |
0.06 |
R4710:Or9a2
|
UTSW |
6 |
41,748,442 (GRCm39) |
missense |
probably benign |
0.06 |
R5162:Or9a2
|
UTSW |
6 |
41,748,706 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5236:Or9a2
|
UTSW |
6 |
41,749,045 (GRCm39) |
missense |
probably benign |
0.00 |
R5441:Or9a2
|
UTSW |
6 |
41,748,782 (GRCm39) |
missense |
probably benign |
0.00 |
R7171:Or9a2
|
UTSW |
6 |
41,748,961 (GRCm39) |
missense |
probably benign |
0.09 |
R7400:Or9a2
|
UTSW |
6 |
41,748,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R8115:Or9a2
|
UTSW |
6 |
41,748,472 (GRCm39) |
missense |
probably benign |
0.00 |
R8346:Or9a2
|
UTSW |
6 |
41,749,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R8363:Or9a2
|
UTSW |
6 |
41,748,684 (GRCm39) |
missense |
probably benign |
0.06 |
R9573:Or9a2
|
UTSW |
6 |
41,748,940 (GRCm39) |
missense |
probably benign |
0.00 |
R9700:Or9a2
|
UTSW |
6 |
41,749,076 (GRCm39) |
missense |
probably benign |
0.00 |
|