Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
CCACGACC |
CCACGACCACGACC |
16: 56,447,952 (GRCm39) |
|
probably benign |
Het |
Acan |
T |
G |
7: 78,742,148 (GRCm39) |
V515G |
possibly damaging |
Het |
Acap3 |
TGG |
TGGACTGCTGCATCCAGG |
4: 155,989,555 (GRCm39) |
|
probably benign |
Het |
AI837181 |
G |
GGCT |
19: 5,475,266 (GRCm39) |
|
probably benign |
Het |
Ankhd1 |
GGCGGC |
GGCGGCAGCGGC |
18: 36,693,977 (GRCm39) |
|
probably benign |
Het |
Anks1b |
G |
A |
10: 89,869,087 (GRCm39) |
G49D |
probably damaging |
Het |
Arid1b |
GCG |
GCGACG |
17: 5,045,869 (GRCm39) |
|
probably benign |
Het |
Arid1b |
CGG |
CGGAGG |
17: 5,045,870 (GRCm39) |
|
probably benign |
Het |
Begain |
G |
GCCGCCC |
12: 108,999,363 (GRCm39) |
|
probably null |
Het |
Cacna1e |
A |
G |
1: 154,317,882 (GRCm39) |
M1500T |
probably damaging |
Het |
Casp16 |
C |
A |
17: 23,774,201 (GRCm39) |
|
probably benign |
Het |
Ccdc174 |
T |
C |
6: 91,876,347 (GRCm39) |
S395P |
possibly damaging |
Het |
Ccdc7a |
T |
G |
8: 129,691,434 (GRCm39) |
Q396H |
probably damaging |
Het |
Ccdc85c |
CC |
CCGGC |
12: 108,240,887 (GRCm39) |
|
probably benign |
Het |
Cemip |
T |
C |
7: 83,610,843 (GRCm39) |
T704A |
probably damaging |
Het |
Cfap68 |
C |
T |
9: 50,677,067 (GRCm39) |
R8H |
probably benign |
Het |
Col7a1 |
C |
T |
9: 108,793,547 (GRCm39) |
P1370S |
unknown |
Het |
Cts8 |
T |
C |
13: 61,397,102 (GRCm39) |
I273V |
probably benign |
Het |
Cyp2c50 |
T |
A |
19: 40,078,268 (GRCm39) |
I42N |
probably damaging |
Het |
Dbt |
T |
G |
3: 116,341,717 (GRCm39) |
Y439* |
probably null |
Het |
Dennd1b |
T |
A |
1: 138,981,135 (GRCm39) |
D116E |
probably damaging |
Het |
Dkk2 |
T |
A |
3: 131,883,863 (GRCm39) |
H254Q |
probably damaging |
Het |
Dpy30 |
C |
A |
17: 74,622,902 (GRCm39) |
V27F |
possibly damaging |
Het |
Efhd2 |
GCCGCC |
GCCGCCCCCGCC |
4: 141,602,069 (GRCm39) |
|
probably benign |
Het |
Eif4g3 |
A |
T |
4: 137,903,235 (GRCm39) |
E1020V |
probably damaging |
Het |
Elmo1 |
T |
A |
13: 20,458,706 (GRCm39) |
S156T |
probably benign |
Het |
Fancd2os |
T |
C |
6: 113,574,881 (GRCm39) |
T42A |
probably damaging |
Het |
Fbrsl1 |
TGTGC |
TGTGCGGGTGTGGGTGC |
5: 110,525,984 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
T |
C |
2: 82,808,184 (GRCm39) |
V1501A |
probably benign |
Het |
Gabrb2 |
A |
G |
11: 42,517,705 (GRCm39) |
Y509C |
probably damaging |
Het |
Gm8369 |
GTGT |
GTGTTTGT |
19: 11,489,118 (GRCm39) |
|
probably null |
Het |
Gpr139 |
T |
C |
7: 118,744,090 (GRCm39) |
D165G |
probably benign |
Het |
Grik2 |
T |
C |
10: 49,120,480 (GRCm39) |
E603G |
probably damaging |
Het |
H13 |
G |
A |
2: 152,511,589 (GRCm39) |
E30K |
probably damaging |
Het |
Ifitm10 |
T |
A |
7: 141,882,330 (GRCm39) |
M147L |
unknown |
Het |
Itpkb |
C |
T |
1: 180,160,887 (GRCm39) |
R338W |
probably damaging |
Het |
Kif1b |
T |
A |
4: 149,336,195 (GRCm39) |
|
probably null |
Het |
Krtap28-10 |
ACCACAGCCACAGCCACCACAGCCACAGCCACCACAGC |
ACCACAGCCACAGCCACCACAGCCACAGCCACCACAGCCACAGCCACCACAGC |
1: 83,019,974 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
AGCCACCACAGC |
AGCCACCACAGCCACCGCCACCACAGC |
1: 83,020,000 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CAGCCA |
CAGCCATAGCCA |
1: 83,019,849 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
AGCCAC |
AGCCACCGCCAC |
1: 83,019,856 (GRCm39) |
|
probably benign |
Het |
Las1l |
AGTGG |
AGTGGTGG |
X: 94,984,422 (GRCm39) |
|
probably benign |
Het |
Mical2 |
T |
C |
7: 111,922,833 (GRCm39) |
Y613H |
probably damaging |
Het |
Mlf2 |
C |
A |
6: 124,911,259 (GRCm39) |
H91Q |
probably benign |
Het |
Nat9 |
A |
T |
11: 115,074,212 (GRCm39) |
I152N |
probably damaging |
Het |
Or10d4c |
T |
C |
9: 39,558,559 (GRCm39) |
M179T |
probably benign |
Het |
Pdik1l |
CACCAC |
CACCACAACCAC |
4: 134,006,822 (GRCm39) |
|
probably benign |
Het |
Phldb2 |
T |
C |
16: 45,583,337 (GRCm39) |
S1054G |
probably damaging |
Het |
Pkhd1l1 |
TTTT |
TTTTTTTTTTGTTT |
15: 44,421,901 (GRCm39) |
|
probably benign |
Het |
Plcg2 |
T |
A |
8: 118,300,263 (GRCm39) |
|
probably null |
Het |
Polr1has |
CACCACCACCACCACCAC |
CACCACCACCACCACCACCACAACCACCACCACCACCAC |
17: 37,275,946 (GRCm39) |
|
probably benign |
Het |
Prdm16 |
T |
A |
4: 154,426,452 (GRCm39) |
R444S |
probably damaging |
Het |
Rgs6 |
T |
C |
12: 83,110,223 (GRCm39) |
F163L |
probably damaging |
Het |
Rnaseh2a |
A |
T |
8: 85,686,687 (GRCm39) |
L154* |
probably null |
Het |
Rpp38 |
A |
G |
2: 3,330,072 (GRCm39) |
S277P |
unknown |
Het |
Setd1a |
GGTAGTGGT |
GGTAGTGGTTGTAGTGGT |
7: 127,384,486 (GRCm39) |
|
probably benign |
Het |
Shisa6 |
CGACAGCAGCAGAG |
CG |
11: 66,416,749 (GRCm39) |
|
probably benign |
Het |
Slc27a2 |
T |
A |
2: 126,395,175 (GRCm39) |
L34Q |
possibly damaging |
Het |
Slc7a6 |
G |
A |
8: 106,922,030 (GRCm39) |
V386I |
probably benign |
Het |
Spry1 |
C |
T |
3: 37,697,264 (GRCm39) |
T169I |
possibly damaging |
Het |
Sry |
TGCTGCTGCTG |
TGCTGCTGCTGCTG |
Y: 2,662,826 (GRCm39) |
|
probably benign |
Het |
Stk24 |
A |
T |
14: 121,532,172 (GRCm39) |
I275N |
probably benign |
Het |
Strn |
TC |
TCCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCAGGC |
17: 78,984,716 (GRCm39) |
|
probably null |
Het |
Tcp11l2 |
C |
A |
10: 84,449,388 (GRCm39) |
P451Q |
probably damaging |
Het |
Tfeb |
AGC |
AGCTGC |
17: 48,097,027 (GRCm39) |
|
probably benign |
Het |
Trappc9 |
TGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
TGCTGCTGCTGCTGCGGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
15: 72,673,138 (GRCm39) |
|
probably benign |
Het |
V1ra8 |
A |
G |
6: 90,180,591 (GRCm39) |
T265A |
probably benign |
Het |
Zfp106 |
CTCCTGGCAGT |
CT |
2: 120,355,026 (GRCm39) |
|
probably benign |
Het |
Zfp612 |
C |
A |
8: 110,816,193 (GRCm39) |
H467N |
probably damaging |
Het |
Zfp777 |
A |
T |
6: 48,018,982 (GRCm39) |
Y317* |
probably null |
Het |
|
Other mutations in Or4a75 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02871:Or4a75
|
APN |
2 |
89,448,504 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4431001:Or4a75
|
UTSW |
2 |
89,448,201 (GRCm39) |
missense |
probably benign |
0.00 |
R0504:Or4a75
|
UTSW |
2 |
89,448,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Or4a75
|
UTSW |
2 |
89,448,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R2176:Or4a75
|
UTSW |
2 |
89,447,924 (GRCm39) |
missense |
possibly damaging |
0.54 |
R3722:Or4a75
|
UTSW |
2 |
89,448,503 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4030:Or4a75
|
UTSW |
2 |
89,448,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R4440:Or4a75
|
UTSW |
2 |
89,448,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R4756:Or4a75
|
UTSW |
2 |
89,447,814 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4981:Or4a75
|
UTSW |
2 |
89,447,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R5678:Or4a75
|
UTSW |
2 |
89,447,625 (GRCm39) |
missense |
probably benign |
|
R6503:Or4a75
|
UTSW |
2 |
89,447,922 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6569:Or4a75
|
UTSW |
2 |
89,448,359 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6770:Or4a75
|
UTSW |
2 |
89,448,206 (GRCm39) |
missense |
probably benign |
0.39 |
R7823:Or4a75
|
UTSW |
2 |
89,447,613 (GRCm39) |
makesense |
probably null |
|
R8423:Or4a75
|
UTSW |
2 |
89,448,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R8438:Or4a75
|
UTSW |
2 |
89,448,054 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9046:Or4a75
|
UTSW |
2 |
89,448,496 (GRCm39) |
unclassified |
probably benign |
|
|