Other mutations in this stock |
Total: 26 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcyap1r1 |
T |
C |
6: 55,438,605 (GRCm39) |
|
probably benign |
Het |
Adig |
T |
A |
2: 158,344,709 (GRCm39) |
F16Y |
possibly damaging |
Het |
Alox12e |
T |
C |
11: 70,211,880 (GRCm39) |
T210A |
probably benign |
Het |
Ankfy1 |
T |
A |
11: 72,646,724 (GRCm39) |
|
probably benign |
Het |
Aoc1 |
T |
A |
6: 48,885,598 (GRCm39) |
I701N |
possibly damaging |
Het |
Armc1 |
A |
C |
3: 19,198,584 (GRCm39) |
N125K |
probably benign |
Het |
Bcl2a1c |
A |
T |
9: 114,159,560 (GRCm39) |
T113S |
probably benign |
Het |
Cdh10 |
A |
T |
15: 19,013,490 (GRCm39) |
I697L |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,829,137 (GRCm39) |
S256T |
probably damaging |
Het |
Chd6 |
T |
C |
2: 160,883,999 (GRCm39) |
N82S |
probably benign |
Het |
Gart |
T |
C |
16: 91,435,608 (GRCm39) |
|
probably benign |
Het |
Gtf3c6 |
A |
G |
10: 40,130,470 (GRCm39) |
|
probably benign |
Het |
Igf1r |
T |
C |
7: 67,851,100 (GRCm39) |
|
probably benign |
Het |
Mtmr6 |
T |
A |
14: 60,517,666 (GRCm39) |
Y92* |
probably null |
Het |
Muc13 |
A |
T |
16: 33,628,329 (GRCm39) |
K360* |
probably null |
Het |
Nfyc |
A |
G |
4: 120,638,744 (GRCm39) |
|
probably benign |
Het |
Pole |
T |
A |
5: 110,449,875 (GRCm39) |
V774E |
possibly damaging |
Het |
Rnf217 |
A |
G |
10: 31,379,770 (GRCm39) |
L484P |
probably damaging |
Het |
Slc18a2 |
A |
T |
19: 59,272,816 (GRCm39) |
I373F |
probably benign |
Het |
Slc5a9 |
A |
G |
4: 111,750,887 (GRCm39) |
|
probably benign |
Het |
Tbc1d30 |
T |
C |
10: 121,132,750 (GRCm39) |
I205V |
probably damaging |
Het |
Tfap2d |
A |
T |
1: 19,189,430 (GRCm39) |
D270V |
probably damaging |
Het |
Tmem63c |
G |
A |
12: 87,123,971 (GRCm39) |
S483N |
probably benign |
Het |
Tor1aip1 |
T |
A |
1: 155,882,662 (GRCm39) |
|
probably benign |
Het |
Tsga10 |
A |
C |
1: 37,840,992 (GRCm39) |
|
probably benign |
Het |
Wdr89 |
A |
T |
12: 75,679,825 (GRCm39) |
L143* |
probably null |
Het |
|
Other mutations in Ttc21b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Ttc21b
|
APN |
2 |
66,073,119 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00467:Ttc21b
|
APN |
2 |
66,018,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00721:Ttc21b
|
APN |
2 |
66,057,122 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01317:Ttc21b
|
APN |
2 |
66,018,700 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01485:Ttc21b
|
APN |
2 |
66,082,234 (GRCm39) |
splice site |
probably benign |
|
IGL01739:Ttc21b
|
APN |
2 |
66,068,200 (GRCm39) |
missense |
probably benign |
|
IGL02282:Ttc21b
|
APN |
2 |
66,022,081 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02431:Ttc21b
|
APN |
2 |
66,082,229 (GRCm39) |
splice site |
probably benign |
|
IGL02478:Ttc21b
|
APN |
2 |
66,018,624 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02487:Ttc21b
|
APN |
2 |
66,065,500 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03327:Ttc21b
|
APN |
2 |
66,068,192 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03346:Ttc21b
|
APN |
2 |
66,068,192 (GRCm39) |
missense |
possibly damaging |
0.92 |
plus-sized
|
UTSW |
2 |
66,073,023 (GRCm39) |
missense |
probably damaging |
1.00 |
puffer
|
UTSW |
2 |
66,057,244 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4696001:Ttc21b
|
UTSW |
2 |
66,061,563 (GRCm39) |
splice site |
probably null |
|
R0049:Ttc21b
|
UTSW |
2 |
66,053,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R0049:Ttc21b
|
UTSW |
2 |
66,053,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R0373:Ttc21b
|
UTSW |
2 |
66,018,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R0440:Ttc21b
|
UTSW |
2 |
66,066,726 (GRCm39) |
missense |
probably benign |
0.03 |
R0504:Ttc21b
|
UTSW |
2 |
66,053,142 (GRCm39) |
splice site |
probably benign |
|
R0600:Ttc21b
|
UTSW |
2 |
66,069,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R0621:Ttc21b
|
UTSW |
2 |
66,056,355 (GRCm39) |
missense |
probably benign |
0.07 |
R0633:Ttc21b
|
UTSW |
2 |
66,066,577 (GRCm39) |
missense |
probably benign |
|
R0863:Ttc21b
|
UTSW |
2 |
66,073,117 (GRCm39) |
missense |
probably benign |
|
R1617:Ttc21b
|
UTSW |
2 |
66,056,379 (GRCm39) |
missense |
probably benign |
0.22 |
R1837:Ttc21b
|
UTSW |
2 |
66,028,106 (GRCm39) |
missense |
probably benign |
0.01 |
R1844:Ttc21b
|
UTSW |
2 |
66,053,921 (GRCm39) |
nonsense |
probably null |
|
R2120:Ttc21b
|
UTSW |
2 |
66,057,098 (GRCm39) |
missense |
probably benign |
0.12 |
R2205:Ttc21b
|
UTSW |
2 |
66,065,467 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2392:Ttc21b
|
UTSW |
2 |
66,037,794 (GRCm39) |
critical splice donor site |
probably null |
|
R3689:Ttc21b
|
UTSW |
2 |
66,054,488 (GRCm39) |
missense |
probably benign |
0.22 |
R3810:Ttc21b
|
UTSW |
2 |
66,082,577 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3847:Ttc21b
|
UTSW |
2 |
66,073,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R3897:Ttc21b
|
UTSW |
2 |
66,065,413 (GRCm39) |
missense |
probably benign |
0.01 |
R4561:Ttc21b
|
UTSW |
2 |
66,016,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R4671:Ttc21b
|
UTSW |
2 |
66,057,257 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5161:Ttc21b
|
UTSW |
2 |
66,059,367 (GRCm39) |
missense |
probably damaging |
0.98 |
R5274:Ttc21b
|
UTSW |
2 |
66,066,627 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5594:Ttc21b
|
UTSW |
2 |
66,066,579 (GRCm39) |
missense |
probably benign |
0.39 |
R6210:Ttc21b
|
UTSW |
2 |
66,066,698 (GRCm39) |
missense |
probably benign |
0.00 |
R6305:Ttc21b
|
UTSW |
2 |
66,018,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R6456:Ttc21b
|
UTSW |
2 |
66,018,675 (GRCm39) |
missense |
probably damaging |
0.97 |
R6482:Ttc21b
|
UTSW |
2 |
66,057,244 (GRCm39) |
missense |
probably benign |
0.12 |
R6645:Ttc21b
|
UTSW |
2 |
66,066,721 (GRCm39) |
missense |
probably benign |
0.01 |
R6800:Ttc21b
|
UTSW |
2 |
66,038,994 (GRCm39) |
splice site |
probably null |
|
R6815:Ttc21b
|
UTSW |
2 |
66,057,134 (GRCm39) |
missense |
probably benign |
0.00 |
R6959:Ttc21b
|
UTSW |
2 |
66,061,656 (GRCm39) |
missense |
probably benign |
0.05 |
R7125:Ttc21b
|
UTSW |
2 |
66,066,670 (GRCm39) |
missense |
probably benign |
0.00 |
R7265:Ttc21b
|
UTSW |
2 |
66,040,517 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7283:Ttc21b
|
UTSW |
2 |
66,039,062 (GRCm39) |
missense |
probably damaging |
0.96 |
R7560:Ttc21b
|
UTSW |
2 |
66,047,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7561:Ttc21b
|
UTSW |
2 |
66,047,548 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7816:Ttc21b
|
UTSW |
2 |
66,077,705 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8172:Ttc21b
|
UTSW |
2 |
66,082,500 (GRCm39) |
missense |
probably benign |
0.01 |
R8179:Ttc21b
|
UTSW |
2 |
66,031,824 (GRCm39) |
missense |
probably benign |
|
R9047:Ttc21b
|
UTSW |
2 |
66,031,596 (GRCm39) |
missense |
|
|
R9282:Ttc21b
|
UTSW |
2 |
66,056,349 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9336:Ttc21b
|
UTSW |
2 |
66,057,287 (GRCm39) |
missense |
probably benign |
|
R9464:Ttc21b
|
UTSW |
2 |
66,053,866 (GRCm39) |
missense |
probably damaging |
1.00 |
X0013:Ttc21b
|
UTSW |
2 |
66,056,294 (GRCm39) |
nonsense |
probably null |
|
|