Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
A |
11: 110,011,522 (GRCm39) |
T1174S |
|
Het |
Aoc2 |
C |
T |
11: 101,216,262 (GRCm39) |
P115L |
possibly damaging |
Het |
Arhgef19 |
C |
T |
4: 140,973,738 (GRCm39) |
P75L |
probably benign |
Het |
Atad3a |
A |
G |
4: 155,838,052 (GRCm39) |
V240A |
possibly damaging |
Het |
AW551984 |
A |
T |
9: 39,508,973 (GRCm39) |
L317* |
probably null |
Het |
Bdkrb1 |
T |
C |
12: 105,570,700 (GRCm39) |
S89P |
probably damaging |
Het |
Bpifb4 |
T |
A |
2: 153,790,607 (GRCm39) |
L166* |
probably null |
Het |
Ccdc27 |
A |
G |
4: 154,124,014 (GRCm39) |
V173A |
unknown |
Het |
Ccl8 |
T |
C |
11: 82,006,877 (GRCm39) |
V30A |
probably benign |
Het |
Cdc16 |
C |
T |
8: 13,831,501 (GRCm39) |
A578V |
probably benign |
Het |
Cnksr1 |
T |
C |
4: 133,959,365 (GRCm39) |
Y423C |
probably damaging |
Het |
Cyp3a44 |
T |
C |
5: 145,727,519 (GRCm39) |
D270G |
probably damaging |
Het |
Ep300 |
A |
G |
15: 81,532,730 (GRCm39) |
E1656G |
unknown |
Het |
Eppk1 |
A |
G |
15: 75,992,472 (GRCm39) |
F1470L |
probably benign |
Het |
Fbxw16 |
T |
A |
9: 109,270,135 (GRCm39) |
D202V |
probably damaging |
Het |
Fndc3a |
G |
A |
14: 72,811,840 (GRCm39) |
T330I |
probably benign |
Het |
Gm36864 |
A |
T |
7: 43,887,028 (GRCm39) |
Q307L |
probably benign |
Het |
Gm37240 |
T |
C |
3: 84,426,946 (GRCm39) |
E38G |
probably damaging |
Het |
Gm6871 |
A |
T |
7: 41,195,262 (GRCm39) |
C492S |
probably damaging |
Het |
Gnaq |
T |
C |
19: 16,355,638 (GRCm39) |
Y285H |
probably benign |
Het |
Htt |
T |
A |
5: 35,023,920 (GRCm39) |
F1723I |
probably damaging |
Het |
Il21r |
G |
A |
7: 125,231,472 (GRCm39) |
S300N |
probably damaging |
Het |
Itm2b |
G |
A |
14: 73,605,856 (GRCm39) |
|
probably benign |
Het |
Kat6a |
T |
C |
8: 23,425,754 (GRCm39) |
S1100P |
probably damaging |
Het |
Kcnj2 |
T |
C |
11: 110,963,415 (GRCm39) |
I269T |
probably damaging |
Het |
Kmt2c |
G |
A |
5: 25,488,208 (GRCm39) |
A4635V |
probably damaging |
Het |
Kng2 |
A |
T |
16: 22,847,546 (GRCm39) |
D38E |
probably damaging |
Het |
Lgr5 |
A |
C |
10: 115,314,454 (GRCm39) |
L161R |
probably damaging |
Het |
Lrig2 |
A |
T |
3: 104,368,914 (GRCm39) |
I923N |
probably benign |
Het |
Mrgprh |
T |
C |
17: 13,096,200 (GRCm39) |
S147P |
probably damaging |
Het |
Mthfd1 |
C |
T |
12: 76,350,754 (GRCm39) |
T712M |
probably benign |
Het |
Nsmaf |
A |
T |
4: 6,418,523 (GRCm39) |
S427R |
probably damaging |
Het |
Or8g53 |
G |
T |
9: 39,684,038 (GRCm39) |
D19E |
probably benign |
Het |
Pdcd11 |
G |
T |
19: 47,101,658 (GRCm39) |
G948C |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,375,612 (GRCm39) |
Y1508H |
probably damaging |
Het |
Prmt5 |
G |
T |
14: 54,753,564 (GRCm39) |
A105E |
probably benign |
Het |
Prr23a3 |
T |
C |
9: 98,747,213 (GRCm39) |
S56P |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,265,077 (GRCm39) |
E705G |
probably damaging |
Het |
Sostdc1 |
A |
T |
12: 36,364,431 (GRCm39) |
N47Y |
probably benign |
Het |
Speg |
T |
C |
1: 75,405,882 (GRCm39) |
Y3029H |
probably damaging |
Het |
Srd5a1 |
G |
A |
13: 69,748,413 (GRCm39) |
R129* |
probably null |
Het |
Srrm4 |
A |
G |
5: 116,605,586 (GRCm39) |
S224P |
unknown |
Het |
Syne2 |
A |
G |
12: 75,999,618 (GRCm39) |
E2337G |
possibly damaging |
Het |
Topaz1 |
T |
C |
9: 122,619,192 (GRCm39) |
I1263T |
possibly damaging |
Het |
Ttc39d |
C |
T |
17: 80,523,349 (GRCm39) |
R3W |
probably benign |
Het |
Xylt1 |
T |
C |
7: 117,250,038 (GRCm39) |
|
probably null |
Het |
Zfp933 |
A |
T |
4: 147,911,021 (GRCm39) |
C192S |
probably damaging |
Het |
Zswim8 |
G |
A |
14: 20,761,119 (GRCm39) |
G129D |
probably damaging |
Het |
|
Other mutations in Tmem150c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00574:Tmem150c
|
APN |
5 |
100,240,810 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03088:Tmem150c
|
APN |
5 |
100,234,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R0331:Tmem150c
|
UTSW |
5 |
100,234,132 (GRCm39) |
splice site |
probably null |
|
R1193:Tmem150c
|
UTSW |
5 |
100,231,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Tmem150c
|
UTSW |
5 |
100,227,887 (GRCm39) |
missense |
probably damaging |
0.96 |
R5053:Tmem150c
|
UTSW |
5 |
100,231,599 (GRCm39) |
missense |
probably benign |
0.17 |
R5202:Tmem150c
|
UTSW |
5 |
100,227,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R5641:Tmem150c
|
UTSW |
5 |
100,231,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Tmem150c
|
UTSW |
5 |
100,243,524 (GRCm39) |
missense |
probably benign |
|
R6934:Tmem150c
|
UTSW |
5 |
100,243,465 (GRCm39) |
critical splice donor site |
probably null |
|
R6936:Tmem150c
|
UTSW |
5 |
100,231,577 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6982:Tmem150c
|
UTSW |
5 |
100,240,680 (GRCm39) |
missense |
probably benign |
0.00 |
R7889:Tmem150c
|
UTSW |
5 |
100,240,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R8827:Tmem150c
|
UTSW |
5 |
100,240,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R9434:Tmem150c
|
UTSW |
5 |
100,240,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|