Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933405L10Rik |
A |
T |
8: 106,435,563 (GRCm39) |
|
probably null |
Het |
Adamts3 |
G |
A |
5: 89,849,576 (GRCm39) |
Q615* |
probably null |
Het |
Adamtsl3 |
T |
A |
7: 82,114,907 (GRCm39) |
|
probably benign |
Het |
Anks1b |
T |
C |
10: 89,909,924 (GRCm39) |
S48P |
possibly damaging |
Het |
Aoc1l2 |
A |
C |
6: 48,908,122 (GRCm39) |
Q374P |
probably damaging |
Het |
Arfip2 |
T |
A |
7: 105,287,437 (GRCm39) |
K94N |
probably damaging |
Het |
Arhgap42 |
G |
T |
9: 9,009,314 (GRCm39) |
N524K |
probably damaging |
Het |
Arhgef28 |
T |
G |
13: 98,067,762 (GRCm39) |
T1388P |
probably damaging |
Het |
Arid4b |
T |
C |
13: 14,303,779 (GRCm39) |
V68A |
probably benign |
Het |
BC005537 |
T |
C |
13: 24,989,923 (GRCm39) |
F129L |
probably damaging |
Het |
Capn3 |
A |
T |
2: 120,333,010 (GRCm39) |
H592L |
possibly damaging |
Het |
Dglucy |
A |
T |
12: 100,804,910 (GRCm39) |
I134F |
possibly damaging |
Het |
Dhh |
T |
A |
15: 98,791,869 (GRCm39) |
M380L |
probably benign |
Het |
Dnai2 |
A |
C |
11: 114,645,158 (GRCm39) |
D531A |
probably benign |
Het |
Dthd1 |
A |
T |
5: 63,000,383 (GRCm39) |
R568S |
possibly damaging |
Het |
Efr3a |
A |
G |
15: 65,727,290 (GRCm39) |
N613S |
probably damaging |
Het |
Epb41l5 |
T |
A |
1: 119,551,641 (GRCm39) |
|
probably benign |
Het |
Ermp1 |
A |
G |
19: 29,608,788 (GRCm39) |
Y164H |
possibly damaging |
Het |
Fam120c |
CCAGCAGCAGCAGCAGCA |
CCAGCAGCAGCAGCA |
X: 150,127,341 (GRCm39) |
|
probably benign |
Het |
Fbrs |
C |
T |
7: 127,088,659 (GRCm39) |
A145V |
probably damaging |
Het |
Gm4736 |
T |
C |
6: 132,092,569 (GRCm39) |
|
noncoding transcript |
Het |
Gm9873 |
A |
T |
2: 168,863,029 (GRCm39) |
|
noncoding transcript |
Het |
Grik1 |
T |
C |
16: 87,831,114 (GRCm39) |
M219V |
possibly damaging |
Het |
Gtsf1l |
C |
T |
2: 162,929,456 (GRCm39) |
C9Y |
probably damaging |
Het |
Itih5 |
G |
A |
2: 10,256,189 (GRCm39) |
R885Q |
probably benign |
Het |
Kdm4c |
A |
G |
4: 74,275,580 (GRCm39) |
E752G |
probably damaging |
Het |
Ksr1 |
A |
G |
11: 78,929,073 (GRCm39) |
|
probably benign |
Het |
Lama1 |
T |
A |
17: 68,112,408 (GRCm39) |
F2283I |
probably benign |
Het |
Luc7l3 |
A |
G |
11: 94,192,320 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,277,583 (GRCm39) |
M122L |
probably benign |
Het |
Map1a |
A |
G |
2: 121,131,986 (GRCm39) |
E696G |
probably damaging |
Het |
Mrps34 |
A |
G |
17: 25,114,643 (GRCm39) |
D110G |
probably damaging |
Het |
Myh11 |
T |
A |
16: 14,022,231 (GRCm39) |
K1710M |
possibly damaging |
Het |
Myo1d |
A |
G |
11: 80,375,158 (GRCm39) |
L972P |
probably damaging |
Het |
Nos1ap |
T |
C |
1: 170,156,816 (GRCm39) |
D214G |
probably damaging |
Het |
Or4c119 |
A |
T |
2: 88,986,640 (GRCm39) |
M293K |
probably benign |
Het |
Or8b46 |
A |
T |
9: 38,450,832 (GRCm39) |
I214F |
probably damaging |
Het |
Pate4 |
T |
G |
9: 35,523,130 (GRCm39) |
T5P |
probably damaging |
Het |
Pygl |
A |
T |
12: 70,237,940 (GRCm39) |
|
probably benign |
Het |
Samd4 |
A |
T |
14: 47,301,754 (GRCm39) |
M252L |
possibly damaging |
Het |
Serpinb1c |
T |
A |
13: 33,070,266 (GRCm39) |
|
probably benign |
Het |
Sis |
A |
T |
3: 72,835,600 (GRCm39) |
W921R |
probably damaging |
Het |
Skint5 |
A |
T |
4: 113,454,965 (GRCm39) |
|
probably benign |
Het |
Slc27a6 |
T |
C |
18: 58,731,829 (GRCm39) |
|
probably benign |
Het |
Sycp2 |
G |
T |
2: 178,045,528 (GRCm39) |
Q31K |
probably damaging |
Het |
Tarm1 |
T |
C |
7: 3,546,067 (GRCm39) |
T79A |
probably benign |
Het |
Tektl1 |
T |
A |
10: 78,584,539 (GRCm39) |
I328L |
probably benign |
Het |
Trf |
A |
G |
9: 103,099,358 (GRCm39) |
F300L |
probably damaging |
Het |
Vmn1r69 |
T |
A |
7: 10,313,985 (GRCm39) |
I170F |
probably damaging |
Het |
Vmn2r105 |
A |
G |
17: 20,447,741 (GRCm39) |
F361S |
possibly damaging |
Het |
Vmn2r79 |
A |
G |
7: 86,686,527 (GRCm39) |
Y636C |
probably damaging |
Het |
Wdr59 |
T |
C |
8: 112,231,005 (GRCm39) |
N68D |
probably damaging |
Het |
Zfp345 |
T |
A |
2: 150,314,220 (GRCm39) |
H439L |
probably damaging |
Het |
|
Other mutations in Taar7f |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00936:Taar7f
|
APN |
10 |
23,926,066 (GRCm39) |
missense |
probably benign |
|
IGL01618:Taar7f
|
APN |
10 |
23,926,239 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02567:Taar7f
|
APN |
10 |
23,926,323 (GRCm39) |
missense |
probably damaging |
0.97 |
R0139:Taar7f
|
UTSW |
10 |
23,926,312 (GRCm39) |
missense |
probably benign |
0.04 |
R0363:Taar7f
|
UTSW |
10 |
23,925,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1776:Taar7f
|
UTSW |
10 |
23,925,546 (GRCm39) |
missense |
probably benign |
0.14 |
R1952:Taar7f
|
UTSW |
10 |
23,925,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Taar7f
|
UTSW |
10 |
23,926,323 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2280:Taar7f
|
UTSW |
10 |
23,925,417 (GRCm39) |
missense |
probably benign |
|
R3120:Taar7f
|
UTSW |
10 |
23,925,478 (GRCm39) |
missense |
probably benign |
|
R4210:Taar7f
|
UTSW |
10 |
23,925,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4211:Taar7f
|
UTSW |
10 |
23,925,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R4587:Taar7f
|
UTSW |
10 |
23,926,473 (GRCm39) |
missense |
probably damaging |
0.97 |
R5092:Taar7f
|
UTSW |
10 |
23,925,451 (GRCm39) |
missense |
probably benign |
|
R5512:Taar7f
|
UTSW |
10 |
23,926,321 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7439:Taar7f
|
UTSW |
10 |
23,925,885 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7441:Taar7f
|
UTSW |
10 |
23,925,885 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7839:Taar7f
|
UTSW |
10 |
23,925,967 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8326:Taar7f
|
UTSW |
10 |
23,925,811 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9443:Taar7f
|
UTSW |
10 |
23,926,311 (GRCm39) |
missense |
probably benign |
0.00 |
R9687:Taar7f
|
UTSW |
10 |
23,925,727 (GRCm39) |
missense |
probably benign |
0.19 |
RF021:Taar7f
|
UTSW |
10 |
23,926,321 (GRCm39) |
missense |
possibly damaging |
0.89 |
|