Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg7 |
A |
G |
16: 56,761,945 (GRCm38) |
S277P |
possibly damaging |
Het |
Arl6ip4 |
T |
C |
5: 124,116,599 (GRCm38) |
S52P |
probably benign |
Het |
Barx2 |
T |
C |
9: 31,913,087 (GRCm38) |
H2R |
probably damaging |
Het |
Calhm3 |
T |
C |
19: 47,151,965 (GRCm38) |
T230A |
probably damaging |
Het |
Card11 |
C |
T |
5: 140,882,362 (GRCm38) |
V844M |
possibly damaging |
Het |
Dnah6 |
C |
T |
6: 73,149,173 (GRCm38) |
R1327Q |
probably benign |
Het |
Ehbp1 |
C |
A |
11: 22,089,524 (GRCm38) |
|
probably null |
Het |
Fgg |
T |
A |
3: 83,014,189 (GRCm38) |
I393N |
possibly damaging |
Het |
Foxq1 |
A |
T |
13: 31,558,533 (GRCm38) |
|
probably benign |
Het |
Hmgxb3 |
T |
C |
18: 61,147,494 (GRCm38) |
T646A |
probably benign |
Het |
Homer3 |
G |
A |
8: 70,293,056 (GRCm38) |
E324K |
possibly damaging |
Het |
Krt80 |
A |
G |
15: 101,359,503 (GRCm38) |
F183L |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 125,941,615 (GRCm38) |
K647* |
probably null |
Het |
Mcm3ap |
A |
G |
10: 76,490,057 (GRCm38) |
Y1067C |
probably damaging |
Het |
Myh1 |
G |
T |
11: 67,213,271 (GRCm38) |
Q921H |
probably benign |
Het |
Nme8 |
A |
G |
13: 19,677,859 (GRCm38) |
F200S |
probably damaging |
Het |
Nploc4 |
T |
C |
11: 120,418,317 (GRCm38) |
N153S |
possibly damaging |
Het |
Olfr1246 |
A |
G |
2: 89,590,773 (GRCm38) |
V114A |
probably benign |
Het |
Olfr173 |
C |
T |
16: 58,797,244 (GRCm38) |
V201I |
probably benign |
Het |
Olfr297 |
T |
C |
7: 86,527,383 (GRCm38) |
F209L |
probably damaging |
Het |
Olfr319 |
T |
C |
11: 58,702,126 (GRCm38) |
C142R |
probably damaging |
Het |
Pipox |
T |
A |
11: 77,892,117 (GRCm38) |
L86F |
probably damaging |
Het |
Polr3h |
G |
T |
15: 81,917,205 (GRCm38) |
L157I |
probably benign |
Het |
Prex2 |
G |
A |
1: 11,266,152 (GRCm38) |
V1525M |
possibly damaging |
Het |
Rapgef2 |
A |
T |
3: 79,088,772 (GRCm38) |
D561E |
possibly damaging |
Het |
Sacs |
A |
T |
14: 61,202,905 (GRCm38) |
D800V |
possibly damaging |
Het |
Sbsn |
A |
T |
7: 30,752,230 (GRCm38) |
L223F |
possibly damaging |
Het |
Slc16a9 |
TCCCC |
TCCCCC |
10: 70,256,081 (GRCm38) |
|
probably null |
Het |
Srrm3 |
G |
T |
5: 135,835,176 (GRCm38) |
E43* |
probably null |
Het |
Tcaf3 |
G |
A |
6: 42,593,729 (GRCm38) |
A363V |
probably damaging |
Het |
Tmem138 |
A |
G |
19: 10,574,904 (GRCm38) |
F78S |
probably damaging |
Het |
Tnfrsf17 |
G |
A |
16: 11,319,812 (GRCm38) |
D138N |
probably damaging |
Het |
Tubgcp6 |
C |
T |
15: 89,102,365 (GRCm38) |
V1344I |
probably benign |
Het |
Usp24 |
T |
A |
4: 106,409,645 (GRCm38) |
L1875* |
probably null |
Het |
Wdr78 |
T |
C |
4: 103,066,352 (GRCm38) |
I427V |
probably benign |
Het |
Zfp541 |
A |
G |
7: 16,076,448 (GRCm38) |
N137D |
possibly damaging |
Het |
|
Other mutations in Vmn2r109 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01313:Vmn2r109
|
APN |
17 |
20,550,157 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01383:Vmn2r109
|
APN |
17 |
20,541,121 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL01469:Vmn2r109
|
APN |
17 |
20,541,409 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01762:Vmn2r109
|
APN |
17 |
20,554,392 (GRCm38) |
missense |
probably benign |
|
IGL01864:Vmn2r109
|
APN |
17 |
20,541,134 (GRCm38) |
missense |
probably benign |
0.28 |
IGL02028:Vmn2r109
|
APN |
17 |
20,541,080 (GRCm38) |
missense |
probably benign |
0.28 |
IGL02074:Vmn2r109
|
APN |
17 |
20,554,341 (GRCm38) |
missense |
probably benign |
0.05 |
IGL02162:Vmn2r109
|
APN |
17 |
20,554,160 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02474:Vmn2r109
|
APN |
17 |
20,540,888 (GRCm38) |
missense |
probably benign |
|
IGL02490:Vmn2r109
|
APN |
17 |
20,540,984 (GRCm38) |
missense |
possibly damaging |
0.78 |
IGL02604:Vmn2r109
|
APN |
17 |
20,540,701 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02669:Vmn2r109
|
APN |
17 |
20,554,256 (GRCm38) |
missense |
possibly damaging |
0.64 |
IGL02705:Vmn2r109
|
APN |
17 |
20,553,800 (GRCm38) |
missense |
probably benign |
|
IGL02745:Vmn2r109
|
APN |
17 |
20,541,250 (GRCm38) |
missense |
probably damaging |
0.99 |
PIT4142001:Vmn2r109
|
UTSW |
17 |
20,554,577 (GRCm38) |
critical splice acceptor site |
probably null |
|
R0389:Vmn2r109
|
UTSW |
17 |
20,541,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R0470:Vmn2r109
|
UTSW |
17 |
20,552,886 (GRCm38) |
missense |
probably benign |
0.06 |
R0570:Vmn2r109
|
UTSW |
17 |
20,540,675 (GRCm38) |
missense |
probably damaging |
0.99 |
R0855:Vmn2r109
|
UTSW |
17 |
20,541,408 (GRCm38) |
nonsense |
probably null |
|
R0882:Vmn2r109
|
UTSW |
17 |
20,554,580 (GRCm38) |
splice site |
probably benign |
|
R1241:Vmn2r109
|
UTSW |
17 |
20,555,241 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1587:Vmn2r109
|
UTSW |
17 |
20,540,740 (GRCm38) |
missense |
probably damaging |
1.00 |
R1931:Vmn2r109
|
UTSW |
17 |
20,553,810 (GRCm38) |
nonsense |
probably null |
|
R1957:Vmn2r109
|
UTSW |
17 |
20,564,707 (GRCm38) |
missense |
probably benign |
0.11 |
R1962:Vmn2r109
|
UTSW |
17 |
20,553,923 (GRCm38) |
missense |
probably damaging |
0.99 |
R2020:Vmn2r109
|
UTSW |
17 |
20,541,186 (GRCm38) |
nonsense |
probably null |
|
R2073:Vmn2r109
|
UTSW |
17 |
20,564,712 (GRCm38) |
missense |
probably benign |
0.00 |
R3123:Vmn2r109
|
UTSW |
17 |
20,540,986 (GRCm38) |
missense |
probably damaging |
1.00 |
R3839:Vmn2r109
|
UTSW |
17 |
20,554,442 (GRCm38) |
missense |
probably damaging |
1.00 |
R4019:Vmn2r109
|
UTSW |
17 |
20,553,812 (GRCm38) |
missense |
probably benign |
|
R4428:Vmn2r109
|
UTSW |
17 |
20,553,024 (GRCm38) |
missense |
probably benign |
|
R4584:Vmn2r109
|
UTSW |
17 |
20,554,558 (GRCm38) |
nonsense |
probably null |
|
R4652:Vmn2r109
|
UTSW |
17 |
20,541,394 (GRCm38) |
missense |
probably damaging |
1.00 |
R4708:Vmn2r109
|
UTSW |
17 |
20,541,343 (GRCm38) |
missense |
probably damaging |
0.97 |
R4823:Vmn2r109
|
UTSW |
17 |
20,553,891 (GRCm38) |
missense |
probably damaging |
1.00 |
R4831:Vmn2r109
|
UTSW |
17 |
20,541,232 (GRCm38) |
missense |
probably benign |
0.01 |
R4907:Vmn2r109
|
UTSW |
17 |
20,550,086 (GRCm38) |
missense |
probably damaging |
1.00 |
R5011:Vmn2r109
|
UTSW |
17 |
20,555,189 (GRCm38) |
missense |
probably damaging |
1.00 |
R5296:Vmn2r109
|
UTSW |
17 |
20,554,341 (GRCm38) |
missense |
possibly damaging |
0.90 |
R5600:Vmn2r109
|
UTSW |
17 |
20,540,927 (GRCm38) |
missense |
probably damaging |
1.00 |
R5602:Vmn2r109
|
UTSW |
17 |
20,540,671 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5652:Vmn2r109
|
UTSW |
17 |
20,540,519 (GRCm38) |
makesense |
probably null |
|
R5702:Vmn2r109
|
UTSW |
17 |
20,554,145 (GRCm38) |
missense |
probably benign |
0.42 |
R5706:Vmn2r109
|
UTSW |
17 |
20,554,305 (GRCm38) |
missense |
probably benign |
0.16 |
R5714:Vmn2r109
|
UTSW |
17 |
20,552,859 (GRCm38) |
missense |
probably damaging |
1.00 |
R5832:Vmn2r109
|
UTSW |
17 |
20,541,056 (GRCm38) |
missense |
probably benign |
0.10 |
R6008:Vmn2r109
|
UTSW |
17 |
20,540,719 (GRCm38) |
missense |
probably damaging |
1.00 |
R6334:Vmn2r109
|
UTSW |
17 |
20,541,178 (GRCm38) |
missense |
probably benign |
0.18 |
R6377:Vmn2r109
|
UTSW |
17 |
20,564,534 (GRCm38) |
critical splice donor site |
probably null |
|
R6738:Vmn2r109
|
UTSW |
17 |
20,554,523 (GRCm38) |
missense |
possibly damaging |
0.52 |
R6857:Vmn2r109
|
UTSW |
17 |
20,540,670 (GRCm38) |
missense |
probably benign |
0.45 |
R6953:Vmn2r109
|
UTSW |
17 |
20,540,711 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7108:Vmn2r109
|
UTSW |
17 |
20,564,744 (GRCm38) |
missense |
probably benign |
0.03 |
R7229:Vmn2r109
|
UTSW |
17 |
20,540,963 (GRCm38) |
missense |
possibly damaging |
0.80 |
R7238:Vmn2r109
|
UTSW |
17 |
20,541,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R7244:Vmn2r109
|
UTSW |
17 |
20,540,683 (GRCm38) |
missense |
possibly damaging |
0.70 |
R7292:Vmn2r109
|
UTSW |
17 |
20,541,438 (GRCm38) |
missense |
probably benign |
0.05 |
R7354:Vmn2r109
|
UTSW |
17 |
20,540,781 (GRCm38) |
missense |
probably damaging |
1.00 |
R7357:Vmn2r109
|
UTSW |
17 |
20,541,274 (GRCm38) |
missense |
probably damaging |
1.00 |
R7522:Vmn2r109
|
UTSW |
17 |
20,554,403 (GRCm38) |
missense |
probably benign |
0.11 |
R7596:Vmn2r109
|
UTSW |
17 |
20,540,680 (GRCm38) |
missense |
probably damaging |
0.98 |
R7728:Vmn2r109
|
UTSW |
17 |
20,552,855 (GRCm38) |
missense |
probably damaging |
0.99 |
R7859:Vmn2r109
|
UTSW |
17 |
20,541,174 (GRCm38) |
missense |
probably damaging |
1.00 |
R7871:Vmn2r109
|
UTSW |
17 |
20,540,520 (GRCm38) |
missense |
probably benign |
0.08 |
R8113:Vmn2r109
|
UTSW |
17 |
20,554,467 (GRCm38) |
missense |
probably benign |
0.01 |
R8153:Vmn2r109
|
UTSW |
17 |
20,564,707 (GRCm38) |
missense |
probably benign |
0.11 |
R8977:Vmn2r109
|
UTSW |
17 |
20,554,269 (GRCm38) |
missense |
possibly damaging |
0.96 |
R9687:Vmn2r109
|
UTSW |
17 |
20,555,070 (GRCm38) |
missense |
|
|
Z1176:Vmn2r109
|
UTSW |
17 |
20,552,994 (GRCm38) |
missense |
probably benign |
0.00 |
|