Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
A |
G |
17: 9,005,220 (GRCm38) |
N435S |
probably damaging |
Het |
Aip |
A |
T |
19: 4,115,381 (GRCm38) |
V195E |
probably benign |
Het |
Amer3 |
A |
T |
1: 34,588,788 (GRCm38) |
I703F |
probably benign |
Het |
Amfr |
T |
C |
8: 94,012,009 (GRCm38) |
E7G |
probably benign |
Het |
Angel1 |
A |
G |
12: 86,726,384 (GRCm38) |
S4P |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,464,651 (GRCm38) |
I146T |
probably damaging |
Het |
Atp6v0e |
A |
G |
17: 26,695,416 (GRCm38) |
T72A |
probably benign |
Het |
Bahcc1 |
T |
C |
11: 120,272,646 (GRCm38) |
V590A |
possibly damaging |
Het |
Bcl6 |
T |
C |
16: 23,972,902 (GRCm38) |
D234G |
probably damaging |
Het |
Bcl6 |
A |
G |
16: 23,972,614 (GRCm38) |
V330A |
possibly damaging |
Het |
Btaf1 |
C |
T |
19: 36,949,102 (GRCm38) |
T58I |
probably damaging |
Het |
Ccdc175 |
A |
T |
12: 72,128,409 (GRCm38) |
|
probably null |
Het |
Cdca4 |
C |
A |
12: 112,821,569 (GRCm38) |
V180L |
probably benign |
Het |
Ces1g |
C |
A |
8: 93,317,037 (GRCm38) |
G425C |
possibly damaging |
Het |
Chl1 |
T |
C |
6: 103,706,448 (GRCm38) |
L745P |
probably damaging |
Het |
Clec4g |
T |
A |
8: 3,719,518 (GRCm38) |
T42S |
possibly damaging |
Het |
Ctsg |
A |
C |
14: 56,100,032 (GRCm38) |
I238S |
probably damaging |
Het |
Cyb5rl |
A |
T |
4: 107,087,316 (GRCm38) |
E41V |
unknown |
Het |
Dcdc2a |
A |
G |
13: 25,107,698 (GRCm38) |
E222G |
probably benign |
Het |
Dnaaf1 |
G |
T |
8: 119,596,799 (GRCm38) |
G509V |
possibly damaging |
Het |
Dnah5 |
A |
G |
15: 28,453,264 (GRCm38) |
I4394V |
probably benign |
Het |
Dot1l |
T |
G |
10: 80,790,726 (GRCm38) |
S1260R |
probably damaging |
Het |
Dst |
T |
G |
1: 34,169,260 (GRCm38) |
I1089S |
probably damaging |
Het |
Eps8l3 |
A |
G |
3: 107,884,485 (GRCm38) |
|
probably null |
Het |
Fam135b |
A |
G |
15: 71,622,068 (GRCm38) |
V4A |
possibly damaging |
Het |
Fnip2 |
T |
C |
3: 79,481,006 (GRCm38) |
E806G |
probably benign |
Het |
Fryl |
T |
A |
5: 73,073,908 (GRCm38) |
I1609F |
probably benign |
Het |
Gdi1 |
G |
A |
X: 74,306,855 (GRCm38) |
R55H |
probably benign |
Het |
Gm11639 |
A |
T |
11: 105,008,961 (GRCm38) |
I4350F |
possibly damaging |
Het |
Gsn |
A |
T |
2: 35,295,049 (GRCm38) |
K339* |
probably null |
Het |
Hecw2 |
T |
A |
1: 53,865,124 (GRCm38) |
Y1155F |
possibly damaging |
Het |
Kif20b |
T |
A |
19: 34,974,492 (GRCm38) |
N1723K |
probably damaging |
Het |
Kif2b |
T |
C |
11: 91,576,824 (GRCm38) |
D211G |
probably benign |
Het |
Lhfpl4 |
C |
T |
6: 113,176,671 (GRCm38) |
V140I |
probably benign |
Het |
Med16 |
C |
T |
10: 79,903,343 (GRCm38) |
G203D |
probably damaging |
Het |
Mrgpra3 |
T |
A |
7: 47,589,641 (GRCm38) |
Y179F |
probably benign |
Het |
Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,634,450 (GRCm38) |
|
probably null |
Het |
Myo18b |
A |
G |
5: 112,874,405 (GRCm38) |
S374P |
unknown |
Het |
Myoz1 |
A |
G |
14: 20,649,409 (GRCm38) |
I287T |
possibly damaging |
Het |
Ncoa6 |
T |
C |
2: 155,438,063 (GRCm38) |
D11G |
probably benign |
Het |
Nlrp9c |
A |
G |
7: 26,385,621 (GRCm38) |
Y178H |
probably damaging |
Het |
Nmur1 |
T |
C |
1: 86,387,508 (GRCm38) |
T212A |
probably damaging |
Het |
Oacyl |
A |
G |
18: 65,720,252 (GRCm38) |
D143G |
probably benign |
Het |
Obox5 |
A |
G |
7: 15,758,807 (GRCm38) |
Y229C |
probably damaging |
Het |
Olfr340 |
A |
G |
2: 36,452,690 (GRCm38) |
Y35C |
probably damaging |
Het |
Olfr347 |
G |
T |
2: 36,734,424 (GRCm38) |
M34I |
probably benign |
Het |
Olfr54 |
C |
A |
11: 51,027,601 (GRCm38) |
L200I |
probably benign |
Het |
Olfr891 |
A |
T |
9: 38,180,336 (GRCm38) |
C162* |
probably null |
Het |
Pcdhb17 |
A |
C |
18: 37,486,513 (GRCm38) |
N452T |
probably benign |
Het |
Pear1 |
T |
G |
3: 87,751,445 (GRCm38) |
H901P |
probably benign |
Het |
Pi16 |
A |
G |
17: 29,326,339 (GRCm38) |
Y192C |
probably damaging |
Het |
Pip5k1b |
T |
G |
19: 24,358,060 (GRCm38) |
E362D |
probably damaging |
Het |
Pla2g5 |
T |
C |
4: 138,804,519 (GRCm38) |
D58G |
probably damaging |
Het |
Pole |
T |
A |
5: 110,325,102 (GRCm38) |
|
probably null |
Het |
Prdm16 |
G |
T |
4: 154,345,468 (GRCm38) |
T348K |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,689,343 (GRCm38) |
F896I |
probably damaging |
Het |
Prmt7 |
T |
C |
8: 106,235,100 (GRCm38) |
F215S |
unknown |
Het |
Prss23 |
T |
A |
7: 89,510,184 (GRCm38) |
T226S |
probably damaging |
Het |
Ptpn14 |
G |
A |
1: 189,863,398 (GRCm38) |
W739* |
probably null |
Het |
Rfx5 |
G |
T |
3: 94,956,539 (GRCm38) |
G135C |
probably damaging |
Het |
Scmh1 |
A |
G |
4: 120,525,055 (GRCm38) |
H573R |
probably benign |
Het |
Serpina5 |
G |
T |
12: 104,102,295 (GRCm38) |
|
probably null |
Het |
Sh3rf2 |
G |
A |
18: 42,104,162 (GRCm38) |
|
probably null |
Het |
Slc38a2 |
T |
C |
15: 96,693,301 (GRCm38) |
M229V |
probably damaging |
Het |
Slc6a17 |
C |
G |
3: 107,493,148 (GRCm38) |
G222R |
probably damaging |
Het |
Sp110 |
C |
T |
1: 85,579,685 (GRCm38) |
G367D |
possibly damaging |
Het |
Srcap |
C |
A |
7: 127,539,041 (GRCm38) |
L1128M |
probably damaging |
Het |
Tmem189 |
C |
G |
2: 167,661,478 (GRCm38) |
A7P |
probably benign |
Het |
Tpra1 |
T |
A |
6: 88,908,294 (GRCm38) |
I76N |
probably damaging |
Het |
Trav6-4 |
A |
T |
14: 53,454,592 (GRCm38) |
Y52F |
probably benign |
Het |
Trp63 |
C |
A |
16: 25,820,477 (GRCm38) |
H138Q |
probably damaging |
Het |
Trub2 |
A |
G |
2: 29,779,826 (GRCm38) |
V177A |
possibly damaging |
Het |
Ugt2a2 |
T |
C |
5: 87,460,396 (GRCm38) |
D528G |
possibly damaging |
Het |
Wnk2 |
C |
A |
13: 49,102,838 (GRCm38) |
R269L |
possibly damaging |
Het |
Zc3h12c |
T |
A |
9: 52,115,926 (GRCm38) |
Q731L |
possibly damaging |
Het |
|
Other mutations in Olfr934 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02156:Olfr934
|
APN |
9 |
38,982,546 (GRCm38) |
missense |
possibly damaging |
0.71 |
R1061:Olfr934
|
UTSW |
9 |
38,982,483 (GRCm38) |
missense |
probably damaging |
1.00 |
R1604:Olfr934
|
UTSW |
9 |
38,982,618 (GRCm38) |
missense |
probably benign |
0.01 |
R1776:Olfr934
|
UTSW |
9 |
38,982,894 (GRCm38) |
missense |
probably damaging |
1.00 |
R3499:Olfr934
|
UTSW |
9 |
38,982,465 (GRCm38) |
missense |
probably damaging |
1.00 |
R3761:Olfr934
|
UTSW |
9 |
38,982,366 (GRCm38) |
missense |
possibly damaging |
0.94 |
R3876:Olfr934
|
UTSW |
9 |
38,982,870 (GRCm38) |
missense |
probably damaging |
1.00 |
R4191:Olfr934
|
UTSW |
9 |
38,983,017 (GRCm38) |
missense |
probably benign |
0.01 |
R4192:Olfr934
|
UTSW |
9 |
38,983,017 (GRCm38) |
missense |
probably benign |
0.01 |
R4333:Olfr934
|
UTSW |
9 |
38,982,588 (GRCm38) |
missense |
possibly damaging |
0.85 |
R4876:Olfr934
|
UTSW |
9 |
38,982,626 (GRCm38) |
nonsense |
probably null |
|
R5539:Olfr934
|
UTSW |
9 |
38,982,277 (GRCm38) |
missense |
possibly damaging |
0.85 |
R6916:Olfr934
|
UTSW |
9 |
38,982,904 (GRCm38) |
missense |
probably benign |
0.14 |
R7338:Olfr934
|
UTSW |
9 |
38,982,520 (GRCm38) |
missense |
probably damaging |
0.99 |
R8116:Olfr934
|
UTSW |
9 |
38,982,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R9350:Olfr934
|
UTSW |
9 |
38,982,785 (GRCm38) |
missense |
probably benign |
0.04 |
|