Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310034C09Rik |
T |
C |
16: 88,556,427 (GRCm39) |
C214R |
possibly damaging |
Het |
Ahnak |
A |
T |
19: 8,990,475 (GRCm39) |
K3920* |
probably null |
Het |
Alox12b |
A |
G |
11: 69,060,394 (GRCm39) |
D650G |
probably damaging |
Het |
Amt |
A |
T |
9: 108,178,684 (GRCm39) |
Y400F |
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,617,934 (GRCm39) |
S1973P |
possibly damaging |
Het |
Aoc1 |
A |
T |
6: 48,884,573 (GRCm39) |
T539S |
probably benign |
Het |
Arhgap44 |
CTGCT |
CTGCTTGCT |
11: 64,922,910 (GRCm39) |
|
probably null |
Het |
Ccdc15 |
C |
T |
9: 37,227,060 (GRCm39) |
G292S |
probably benign |
Het |
Ccdc162 |
C |
T |
10: 41,437,159 (GRCm39) |
C287Y |
possibly damaging |
Het |
Ccn6 |
T |
C |
10: 39,034,296 (GRCm39) |
Y102C |
probably damaging |
Het |
Cdk15 |
G |
A |
1: 59,328,818 (GRCm39) |
G244D |
probably damaging |
Het |
Cep290 |
T |
A |
10: 100,377,649 (GRCm39) |
Y1560N |
probably damaging |
Het |
Cfap251 |
A |
G |
5: 123,392,435 (GRCm39) |
|
probably benign |
Het |
Cic |
A |
C |
7: 24,971,423 (GRCm39) |
I385L |
probably benign |
Het |
Cobl |
A |
T |
11: 12,319,684 (GRCm39) |
F231L |
probably benign |
Het |
Cpeb1 |
T |
C |
7: 81,011,428 (GRCm39) |
D171G |
possibly damaging |
Het |
Csnk1g2 |
T |
A |
10: 80,474,778 (GRCm39) |
V305E |
probably damaging |
Het |
Cyp2c29 |
A |
G |
19: 39,296,050 (GRCm39) |
|
probably null |
Het |
Dner |
A |
T |
1: 84,361,650 (GRCm39) |
M653K |
possibly damaging |
Het |
Dst |
T |
A |
1: 34,251,304 (GRCm39) |
M4311K |
possibly damaging |
Het |
Ep400 |
A |
G |
5: 110,831,067 (GRCm39) |
S2200P |
unknown |
Het |
Ephb2 |
A |
T |
4: 136,411,341 (GRCm39) |
S440T |
possibly damaging |
Het |
Ercc1 |
A |
T |
7: 19,081,086 (GRCm39) |
|
probably benign |
Het |
Folh1 |
T |
A |
7: 86,375,142 (GRCm39) |
N615Y |
probably benign |
Het |
Gm7298 |
T |
C |
6: 121,742,038 (GRCm39) |
Y487H |
possibly damaging |
Het |
Gucy1b2 |
A |
T |
14: 62,656,499 (GRCm39) |
I286N |
probably benign |
Het |
Hr |
A |
G |
14: 70,805,273 (GRCm39) |
D1005G |
probably damaging |
Het |
Ifrd1 |
C |
A |
12: 40,266,243 (GRCm39) |
V117F |
possibly damaging |
Het |
Ift140 |
A |
T |
17: 25,255,934 (GRCm39) |
T210S |
probably benign |
Het |
Igll1 |
C |
A |
16: 16,681,805 (GRCm39) |
|
probably benign |
Het |
Ino80 |
G |
T |
2: 119,204,989 (GRCm39) |
S1512R |
probably benign |
Het |
Intu |
A |
T |
3: 40,608,578 (GRCm39) |
K197* |
probably null |
Het |
Kdm6b |
A |
G |
11: 69,294,424 (GRCm39) |
L1216P |
unknown |
Het |
Klrb1c |
T |
G |
6: 128,761,120 (GRCm39) |
D169A |
probably damaging |
Het |
Lamp3 |
T |
A |
16: 19,519,698 (GRCm39) |
T162S |
possibly damaging |
Het |
Mapk10 |
G |
A |
5: 103,114,342 (GRCm39) |
P319S |
probably damaging |
Het |
Mapk10 |
G |
A |
5: 103,114,341 (GRCm39) |
P319L |
probably damaging |
Het |
Mical3 |
T |
C |
6: 120,998,281 (GRCm39) |
T702A |
probably benign |
Het |
Nckap1l |
T |
C |
15: 103,387,242 (GRCm39) |
S706P |
probably benign |
Het |
Nckap5l |
G |
A |
15: 99,324,766 (GRCm39) |
T579I |
probably damaging |
Het |
Or13p3 |
A |
T |
4: 118,567,441 (GRCm39) |
N279I |
probably damaging |
Het |
Or4a27 |
C |
A |
2: 88,559,575 (GRCm39) |
A123S |
probably damaging |
Het |
Or8s16 |
G |
A |
15: 98,211,317 (GRCm39) |
T38I |
probably benign |
Het |
Pcdh18 |
A |
C |
3: 49,708,913 (GRCm39) |
S801A |
probably damaging |
Het |
Pde11a |
A |
T |
2: 75,848,204 (GRCm39) |
D874E |
probably damaging |
Het |
Pfdn6 |
G |
T |
17: 34,158,589 (GRCm39) |
P62T |
probably damaging |
Het |
Pkd1l1 |
A |
G |
11: 8,900,427 (GRCm39) |
I38T |
probably benign |
Het |
Prkdc |
A |
T |
16: 15,647,561 (GRCm39) |
I3662F |
possibly damaging |
Het |
Psg26 |
A |
T |
7: 18,216,617 (GRCm39) |
L74* |
probably null |
Het |
Rassf6 |
A |
G |
5: 90,751,736 (GRCm39) |
V341A |
probably damaging |
Het |
Rsad2 |
C |
A |
12: 26,497,150 (GRCm39) |
|
probably null |
Het |
Rwdd3 |
A |
G |
3: 120,950,162 (GRCm39) |
Y95H |
probably damaging |
Het |
Scfd1 |
A |
G |
12: 51,492,457 (GRCm39) |
I589V |
possibly damaging |
Het |
Sgsm1 |
A |
T |
5: 113,434,704 (GRCm39) |
I131N |
probably damaging |
Het |
Tecpr1 |
A |
G |
5: 144,148,239 (GRCm39) |
S389P |
probably benign |
Het |
Tle3 |
T |
A |
9: 61,281,296 (GRCm39) |
I29N |
probably damaging |
Het |
Tmem63c |
C |
A |
12: 87,103,971 (GRCm39) |
N73K |
probably damaging |
Het |
Tpm2 |
T |
A |
4: 43,518,301 (GRCm39) |
|
probably null |
Het |
Trak2 |
A |
T |
1: 58,950,971 (GRCm39) |
D405E |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,575,516 (GRCm39) |
A23380S |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,715,495 (GRCm39) |
|
probably benign |
Het |
Tub |
T |
C |
7: 108,628,857 (GRCm39) |
S391P |
probably damaging |
Het |
Ush2a |
G |
T |
1: 187,999,223 (GRCm39) |
E178* |
probably null |
Het |
Vamp9 |
G |
T |
5: 100,089,226 (GRCm39) |
A164S |
probably benign |
Het |
Ylpm1 |
C |
A |
12: 85,044,030 (GRCm39) |
T256K |
unknown |
Het |
Zfp1007 |
A |
G |
5: 109,824,730 (GRCm39) |
V240A |
probably benign |
Het |
|
Other mutations in Mstn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01070:Mstn
|
APN |
1 |
53,101,156 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL01432:Mstn
|
APN |
1 |
53,105,689 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02009:Mstn
|
APN |
1 |
53,101,309 (GRCm39) |
splice site |
probably benign |
|
IGL02547:Mstn
|
APN |
1 |
53,103,284 (GRCm39) |
missense |
probably benign |
0.08 |
PIT4403001:Mstn
|
UTSW |
1 |
53,100,944 (GRCm39) |
missense |
probably benign |
0.00 |
R0499:Mstn
|
UTSW |
1 |
53,103,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R0556:Mstn
|
UTSW |
1 |
53,103,284 (GRCm39) |
missense |
probably benign |
0.08 |
R0730:Mstn
|
UTSW |
1 |
53,100,953 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1180:Mstn
|
UTSW |
1 |
53,103,167 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1472:Mstn
|
UTSW |
1 |
53,101,157 (GRCm39) |
missense |
probably damaging |
0.99 |
R1659:Mstn
|
UTSW |
1 |
53,103,236 (GRCm39) |
nonsense |
probably null |
|
R1676:Mstn
|
UTSW |
1 |
53,101,224 (GRCm39) |
missense |
probably benign |
0.08 |
R1753:Mstn
|
UTSW |
1 |
53,105,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R3852:Mstn
|
UTSW |
1 |
53,101,130 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4773:Mstn
|
UTSW |
1 |
53,101,267 (GRCm39) |
missense |
probably benign |
0.18 |
R4938:Mstn
|
UTSW |
1 |
53,105,582 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6393:Mstn
|
UTSW |
1 |
53,105,648 (GRCm39) |
missense |
probably benign |
0.00 |
R6991:Mstn
|
UTSW |
1 |
53,101,100 (GRCm39) |
missense |
probably benign |
0.02 |
R7018:Mstn
|
UTSW |
1 |
53,103,243 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7077:Mstn
|
UTSW |
1 |
53,103,408 (GRCm39) |
missense |
probably benign |
0.30 |
R7170:Mstn
|
UTSW |
1 |
53,105,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7300:Mstn
|
UTSW |
1 |
53,103,239 (GRCm39) |
missense |
probably benign |
0.13 |
R7486:Mstn
|
UTSW |
1 |
53,103,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R8063:Mstn
|
UTSW |
1 |
53,105,607 (GRCm39) |
missense |
probably benign |
0.10 |
R8966:Mstn
|
UTSW |
1 |
53,105,641 (GRCm39) |
missense |
probably benign |
0.00 |
R9009:Mstn
|
UTSW |
1 |
53,103,131 (GRCm39) |
nonsense |
probably null |
|
R9564:Mstn
|
UTSW |
1 |
53,103,367 (GRCm39) |
missense |
probably benign |
0.01 |
|