Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
A |
G |
12: 71,184,815 (GRCm39) |
|
probably benign |
Het |
4930407I10Rik |
T |
C |
15: 81,947,440 (GRCm39) |
W446R |
possibly damaging |
Het |
Aldh1l2 |
T |
A |
10: 83,326,479 (GRCm39) |
E912D |
probably damaging |
Het |
Apol9a |
T |
C |
15: 77,289,220 (GRCm39) |
D49G |
possibly damaging |
Het |
Bnc2 |
A |
T |
4: 84,194,582 (GRCm39) |
D847E |
possibly damaging |
Het |
Ccdc91 |
A |
G |
6: 147,437,114 (GRCm39) |
N100S |
possibly damaging |
Het |
Copb2 |
G |
T |
9: 98,450,072 (GRCm39) |
K10N |
possibly damaging |
Het |
Cyp4a14 |
A |
G |
4: 115,348,275 (GRCm39) |
S401P |
probably damaging |
Het |
Cyp4f15 |
A |
T |
17: 32,916,914 (GRCm39) |
Q277L |
probably benign |
Het |
Dmxl2 |
A |
T |
9: 54,354,217 (GRCm39) |
S410T |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,880,644 (GRCm39) |
N2651S |
probably benign |
Het |
Efhb |
A |
G |
17: 53,720,489 (GRCm39) |
|
probably null |
Het |
Eif4ebp1 |
T |
A |
8: 27,765,124 (GRCm39) |
F113L |
probably damaging |
Het |
Emilin2 |
C |
G |
17: 71,562,141 (GRCm39) |
D954H |
probably damaging |
Het |
Eng |
A |
G |
2: 32,569,005 (GRCm39) |
T511A |
probably benign |
Het |
Eps8l1 |
A |
G |
7: 4,474,817 (GRCm39) |
D266G |
probably damaging |
Het |
Fam120a |
T |
C |
13: 49,087,433 (GRCm39) |
H309R |
possibly damaging |
Het |
Gga3 |
A |
T |
11: 115,477,834 (GRCm39) |
S585T |
probably benign |
Het |
Gm12117 |
T |
C |
11: 33,226,126 (GRCm39) |
Q70R |
probably damaging |
Het |
Gpr158 |
A |
G |
2: 21,373,701 (GRCm39) |
H212R |
probably benign |
Het |
Hmgb1 |
A |
G |
5: 148,987,427 (GRCm39) |
F41L |
possibly damaging |
Het |
Iqcm |
T |
A |
8: 76,480,118 (GRCm39) |
|
probably benign |
Het |
Itgav |
T |
A |
2: 83,596,121 (GRCm39) |
I214N |
probably damaging |
Het |
Kcna1 |
T |
A |
6: 126,619,255 (GRCm39) |
H355L |
probably benign |
Het |
Lrrc37a |
C |
T |
11: 103,394,247 (GRCm39) |
V393I |
probably benign |
Het |
Mak16 |
T |
C |
8: 31,658,697 (GRCm39) |
D4G |
probably damaging |
Het |
Metap2 |
C |
T |
10: 93,697,384 (GRCm39) |
R432H |
possibly damaging |
Het |
Nlrc4 |
G |
A |
17: 74,753,540 (GRCm39) |
T281M |
probably damaging |
Het |
Ntrk1 |
T |
A |
3: 87,688,870 (GRCm39) |
Q561L |
probably damaging |
Het |
Or10ak7 |
A |
C |
4: 118,791,347 (GRCm39) |
S231A |
probably damaging |
Het |
Or10w3 |
A |
G |
19: 13,704,035 (GRCm39) |
T137A |
possibly damaging |
Het |
Pira1 |
T |
C |
7: 3,739,482 (GRCm39) |
D462G |
probably benign |
Het |
Polr2a |
T |
C |
11: 69,628,282 (GRCm39) |
I1304V |
probably null |
Het |
Ppp4r2 |
T |
C |
6: 100,843,343 (GRCm39) |
S354P |
probably benign |
Het |
Ptchd3 |
A |
G |
11: 121,727,299 (GRCm39) |
H391R |
possibly damaging |
Het |
Rchy1 |
T |
C |
5: 92,099,762 (GRCm39) |
D192G |
probably damaging |
Het |
Rmdn1 |
T |
C |
4: 19,575,329 (GRCm39) |
|
probably null |
Het |
Rp1 |
T |
A |
1: 4,418,572 (GRCm39) |
I847L |
probably benign |
Het |
Rtn1 |
T |
C |
12: 72,350,838 (GRCm39) |
E457G |
probably damaging |
Het |
Serpind1 |
G |
A |
16: 17,160,730 (GRCm39) |
S420N |
possibly damaging |
Het |
Sirpa |
T |
C |
2: 129,458,143 (GRCm39) |
V253A |
probably damaging |
Het |
Snapc4 |
A |
T |
2: 26,268,546 (GRCm39) |
F38L |
probably benign |
Het |
Spata31g1 |
T |
C |
4: 42,973,169 (GRCm39) |
V834A |
probably benign |
Het |
Srcap |
T |
C |
7: 127,156,969 (GRCm39) |
F2321S |
probably damaging |
Het |
Stat4 |
A |
T |
1: 52,142,075 (GRCm39) |
I641F |
probably damaging |
Het |
Tmem216 |
A |
T |
19: 10,529,191 (GRCm39) |
F65Y |
probably benign |
Het |
Tmem37 |
C |
T |
1: 119,995,982 (GRCm39) |
V32M |
possibly damaging |
Het |
Tmprss11c |
T |
G |
5: 86,383,412 (GRCm39) |
Q338P |
probably damaging |
Het |
Tonsl |
C |
T |
15: 76,517,463 (GRCm39) |
S752N |
probably benign |
Het |
Vps13b |
T |
A |
15: 35,887,100 (GRCm39) |
V3229D |
probably benign |
Het |
Vwa5b2 |
C |
T |
16: 20,409,972 (GRCm39) |
R21W |
probably damaging |
Het |
Wdr37 |
T |
C |
13: 8,903,609 (GRCm39) |
R165G |
unknown |
Het |
Yars2 |
T |
C |
16: 16,125,147 (GRCm39) |
F388L |
probably benign |
Het |
Ykt6 |
T |
A |
11: 5,912,366 (GRCm39) |
D106E |
probably benign |
Het |
Zc3h12a |
A |
C |
4: 125,020,788 (GRCm39) |
S18R |
possibly damaging |
Het |
|
Other mutations in Vmn1r26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02517:Vmn1r26
|
APN |
6 |
57,986,127 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02609:Vmn1r26
|
APN |
6 |
57,985,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R1121:Vmn1r26
|
UTSW |
6 |
57,985,647 (GRCm39) |
missense |
probably benign |
0.43 |
R1881:Vmn1r26
|
UTSW |
6 |
57,985,650 (GRCm39) |
missense |
probably benign |
0.20 |
R1958:Vmn1r26
|
UTSW |
6 |
57,985,286 (GRCm39) |
missense |
probably benign |
0.01 |
R1978:Vmn1r26
|
UTSW |
6 |
57,986,111 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2106:Vmn1r26
|
UTSW |
6 |
57,985,710 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2117:Vmn1r26
|
UTSW |
6 |
57,985,335 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2323:Vmn1r26
|
UTSW |
6 |
57,985,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Vmn1r26
|
UTSW |
6 |
57,985,808 (GRCm39) |
missense |
probably damaging |
0.99 |
R5695:Vmn1r26
|
UTSW |
6 |
57,985,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6355:Vmn1r26
|
UTSW |
6 |
57,985,536 (GRCm39) |
missense |
probably benign |
0.02 |
R6948:Vmn1r26
|
UTSW |
6 |
57,985,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R7114:Vmn1r26
|
UTSW |
6 |
57,985,755 (GRCm39) |
missense |
probably benign |
0.02 |
R7977:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R7987:Vmn1r26
|
UTSW |
6 |
57,985,264 (GRCm39) |
nonsense |
probably null |
|
R8442:Vmn1r26
|
UTSW |
6 |
57,985,728 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8784:Vmn1r26
|
UTSW |
6 |
57,985,440 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9129:Vmn1r26
|
UTSW |
6 |
57,985,373 (GRCm39) |
missense |
|
|
RF020:Vmn1r26
|
UTSW |
6 |
57,985,705 (GRCm39) |
missense |
probably benign |
0.35 |
Z1176:Vmn1r26
|
UTSW |
6 |
57,985,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|