Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn1 |
T |
A |
12: 80,224,023 (GRCm39) |
K478M |
probably benign |
Het |
Ankar |
G |
T |
1: 72,713,213 (GRCm39) |
S474* |
probably null |
Het |
Barx2 |
C |
A |
9: 31,758,199 (GRCm39) |
E246D |
probably benign |
Het |
Cdh20 |
A |
T |
1: 110,065,997 (GRCm39) |
Q757L |
probably damaging |
Het |
Cnr1 |
T |
C |
4: 33,944,751 (GRCm39) |
F380L |
probably damaging |
Het |
Cntnap5b |
G |
A |
1: 100,318,317 (GRCm39) |
A655T |
probably benign |
Het |
Col2a1 |
T |
A |
15: 97,898,451 (GRCm39) |
|
probably benign |
Het |
Crybg3 |
C |
T |
16: 59,370,838 (GRCm39) |
R2340Q |
possibly damaging |
Het |
Ctsb |
G |
T |
14: 63,379,305 (GRCm39) |
D306Y |
probably damaging |
Het |
Cyp2a22 |
A |
C |
7: 26,633,664 (GRCm39) |
Y349D |
probably damaging |
Het |
Dcpp2 |
T |
C |
17: 24,117,886 (GRCm39) |
L22S |
probably damaging |
Het |
Dnah8 |
G |
T |
17: 30,966,239 (GRCm39) |
M2476I |
probably damaging |
Het |
Dst |
A |
G |
1: 34,228,053 (GRCm39) |
E1882G |
probably damaging |
Het |
Esrp1 |
T |
C |
4: 11,357,580 (GRCm39) |
K511E |
possibly damaging |
Het |
Fat3 |
T |
A |
9: 16,289,113 (GRCm39) |
T137S |
probably benign |
Het |
Fbxw24 |
T |
A |
9: 109,436,079 (GRCm39) |
M318L |
probably benign |
Het |
Fpr-rs7 |
T |
A |
17: 20,333,477 (GRCm39) |
T338S |
probably benign |
Het |
Gcgr |
T |
C |
11: 120,425,584 (GRCm39) |
M1T |
probably null |
Het |
Grifin |
C |
A |
5: 140,549,311 (GRCm39) |
R135L |
possibly damaging |
Het |
Helz |
T |
C |
11: 107,504,946 (GRCm39) |
|
probably null |
Het |
Hivep3 |
C |
G |
4: 119,955,061 (GRCm39) |
Q1126E |
possibly damaging |
Het |
Htr3a |
T |
A |
9: 48,815,999 (GRCm39) |
H146L |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,707,311 (GRCm39) |
V3081E |
probably damaging |
Het |
Mgat5 |
T |
A |
1: 127,387,636 (GRCm39) |
C531S |
probably damaging |
Het |
Mical2 |
A |
G |
7: 111,979,619 (GRCm39) |
D106G |
probably benign |
Het |
Nectin2 |
C |
T |
7: 19,472,063 (GRCm39) |
A109T |
probably benign |
Het |
Olig3 |
T |
C |
10: 19,232,503 (GRCm39) |
S43P |
probably damaging |
Het |
Or5an9 |
A |
T |
19: 12,187,286 (GRCm39) |
M119L |
probably damaging |
Het |
Or8b39 |
T |
A |
9: 37,996,390 (GRCm39) |
V86E |
probably damaging |
Het |
Pcdh12 |
T |
C |
18: 38,414,558 (GRCm39) |
R856G |
probably damaging |
Het |
Phpt1 |
T |
A |
2: 25,464,851 (GRCm39) |
M1L |
probably benign |
Het |
Polr2m |
T |
C |
9: 71,391,080 (GRCm39) |
I41V |
probably damaging |
Het |
Pramel28 |
G |
T |
4: 143,692,631 (GRCm39) |
D123E |
probably benign |
Het |
Pzp |
A |
G |
6: 128,500,977 (GRCm39) |
V127A |
possibly damaging |
Het |
Rgs7 |
G |
T |
1: 174,977,226 (GRCm39) |
T126K |
probably damaging |
Het |
RP23-399J5.1 |
T |
C |
8: 71,542,571 (GRCm39) |
|
noncoding transcript |
Het |
Rras |
A |
T |
7: 44,669,820 (GRCm39) |
D112V |
probably damaging |
Het |
Sdcbp2 |
T |
A |
2: 151,424,646 (GRCm39) |
Y5* |
probably null |
Het |
Slc43a2 |
T |
C |
11: 75,461,433 (GRCm39) |
F462L |
probably damaging |
Het |
Smchd1 |
T |
A |
17: 71,684,052 (GRCm39) |
K1436* |
probably null |
Het |
Snrnp27 |
A |
C |
6: 86,659,902 (GRCm39) |
S31A |
unknown |
Het |
Sqstm1 |
A |
C |
11: 50,098,251 (GRCm39) |
F172V |
probably benign |
Het |
Stk32b |
T |
A |
5: 37,806,458 (GRCm39) |
I29F |
probably damaging |
Het |
Syt10 |
G |
A |
15: 89,725,824 (GRCm39) |
T50I |
probably benign |
Het |
Syt16 |
T |
C |
12: 74,313,504 (GRCm39) |
Y477H |
probably damaging |
Het |
Tacr3 |
A |
T |
3: 134,638,153 (GRCm39) |
T437S |
probably benign |
Het |
Tg |
G |
A |
15: 66,555,842 (GRCm39) |
D845N |
probably benign |
Het |
Uqcc1 |
G |
T |
2: 155,763,564 (GRCm39) |
S36R |
possibly damaging |
Het |
Xpo7 |
T |
A |
14: 70,933,103 (GRCm39) |
Q263L |
possibly damaging |
Het |
Zfp442 |
T |
C |
2: 150,250,016 (GRCm39) |
K572E |
probably damaging |
Het |
Zswim5 |
A |
C |
4: 116,819,818 (GRCm39) |
S408R |
probably benign |
Het |
|
Other mutations in Vmn1r20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01761:Vmn1r20
|
APN |
6 |
57,408,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02622:Vmn1r20
|
APN |
6 |
57,409,583 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02636:Vmn1r20
|
APN |
6 |
57,408,746 (GRCm39) |
missense |
probably benign |
|
R0006:Vmn1r20
|
UTSW |
6 |
57,409,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R0079:Vmn1r20
|
UTSW |
6 |
57,408,777 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0200:Vmn1r20
|
UTSW |
6 |
57,409,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R1675:Vmn1r20
|
UTSW |
6 |
57,408,937 (GRCm39) |
missense |
probably benign |
0.00 |
R1734:Vmn1r20
|
UTSW |
6 |
57,409,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R1883:Vmn1r20
|
UTSW |
6 |
57,409,306 (GRCm39) |
missense |
probably benign |
0.14 |
R2049:Vmn1r20
|
UTSW |
6 |
57,408,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R2307:Vmn1r20
|
UTSW |
6 |
57,409,121 (GRCm39) |
missense |
probably benign |
0.03 |
R2346:Vmn1r20
|
UTSW |
6 |
57,408,931 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4405:Vmn1r20
|
UTSW |
6 |
57,409,042 (GRCm39) |
missense |
probably benign |
0.02 |
R4946:Vmn1r20
|
UTSW |
6 |
57,409,159 (GRCm39) |
missense |
probably damaging |
0.98 |
R5259:Vmn1r20
|
UTSW |
6 |
57,409,050 (GRCm39) |
nonsense |
probably null |
|
R5321:Vmn1r20
|
UTSW |
6 |
57,409,427 (GRCm39) |
missense |
probably benign |
0.21 |
R5911:Vmn1r20
|
UTSW |
6 |
57,408,774 (GRCm39) |
missense |
probably benign |
0.16 |
R6298:Vmn1r20
|
UTSW |
6 |
57,409,112 (GRCm39) |
missense |
probably benign |
|
R6314:Vmn1r20
|
UTSW |
6 |
57,409,042 (GRCm39) |
missense |
probably benign |
0.00 |
R6331:Vmn1r20
|
UTSW |
6 |
57,408,655 (GRCm39) |
splice site |
probably null |
|
R6482:Vmn1r20
|
UTSW |
6 |
57,409,093 (GRCm39) |
missense |
probably benign |
0.01 |
R9161:Vmn1r20
|
UTSW |
6 |
57,408,759 (GRCm39) |
missense |
probably benign |
0.00 |
R9165:Vmn1r20
|
UTSW |
6 |
57,409,246 (GRCm39) |
missense |
probably damaging |
0.99 |
|