Other mutations in this stock |
Total: 14 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambra1 |
G |
A |
2: 91,599,381 (GRCm39) |
R167H |
possibly damaging |
Het |
Ankrd50 |
G |
A |
3: 38,509,836 (GRCm39) |
R844C |
probably damaging |
Het |
Arfgef1 |
T |
C |
1: 10,286,784 (GRCm39) |
E42G |
probably benign |
Het |
Arhgap42 |
T |
A |
9: 9,015,313 (GRCm39) |
I444F |
probably damaging |
Het |
Cspg4b |
G |
A |
13: 113,505,951 (GRCm39) |
|
probably benign |
Het |
Ift56 |
A |
G |
6: 38,387,728 (GRCm39) |
D393G |
probably damaging |
Het |
Ift70a2 |
A |
T |
2: 75,806,823 (GRCm39) |
I563N |
probably damaging |
Het |
Il25 |
G |
A |
14: 55,170,212 (GRCm39) |
|
probably benign |
Het |
Jak1 |
A |
G |
4: 101,046,291 (GRCm39) |
L105P |
probably damaging |
Het |
Or2ad1 |
C |
T |
13: 21,326,337 (GRCm39) |
V297I |
probably benign |
Het |
Ralgapa2 |
A |
G |
2: 146,199,902 (GRCm39) |
V1214A |
probably benign |
Het |
Supt16 |
G |
A |
14: 52,411,581 (GRCm39) |
R601* |
probably null |
Het |
Vmn1r113 |
A |
T |
7: 20,521,356 (GRCm39) |
R49S |
probably benign |
Het |
Vmn1r64 |
C |
T |
7: 5,887,210 (GRCm39) |
S111N |
probably damaging |
Het |
|
Other mutations in Shtn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00945:Shtn1
|
APN |
19 |
59,007,384 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01619:Shtn1
|
APN |
19 |
59,016,601 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01880:Shtn1
|
APN |
19 |
59,063,881 (GRCm39) |
splice site |
probably benign |
|
IGL02214:Shtn1
|
APN |
19 |
58,988,318 (GRCm39) |
splice site |
probably benign |
|
IGL03400:Shtn1
|
APN |
19 |
59,020,690 (GRCm39) |
splice site |
probably benign |
|
R0011:Shtn1
|
UTSW |
19 |
59,020,650 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0011:Shtn1
|
UTSW |
19 |
59,020,650 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0299:Shtn1
|
UTSW |
19 |
59,007,383 (GRCm39) |
missense |
probably benign |
0.00 |
R0606:Shtn1
|
UTSW |
19 |
58,988,372 (GRCm39) |
missense |
probably damaging |
0.99 |
R1081:Shtn1
|
UTSW |
19 |
58,963,447 (GRCm39) |
missense |
probably benign |
0.04 |
R1677:Shtn1
|
UTSW |
19 |
58,998,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Shtn1
|
UTSW |
19 |
59,020,632 (GRCm39) |
missense |
probably damaging |
0.99 |
R1966:Shtn1
|
UTSW |
19 |
58,963,470 (GRCm39) |
missense |
probably benign |
|
R3076:Shtn1
|
UTSW |
19 |
58,983,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R3552:Shtn1
|
UTSW |
19 |
58,963,470 (GRCm39) |
missense |
probably benign |
0.28 |
R3736:Shtn1
|
UTSW |
19 |
59,010,700 (GRCm39) |
missense |
probably benign |
|
R4615:Shtn1
|
UTSW |
19 |
59,010,648 (GRCm39) |
missense |
probably benign |
0.18 |
R4789:Shtn1
|
UTSW |
19 |
59,039,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R4791:Shtn1
|
UTSW |
19 |
59,039,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R4792:Shtn1
|
UTSW |
19 |
59,039,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R4939:Shtn1
|
UTSW |
19 |
59,010,633 (GRCm39) |
missense |
probably benign |
0.00 |
R5245:Shtn1
|
UTSW |
19 |
59,020,652 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5387:Shtn1
|
UTSW |
19 |
59,026,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Shtn1
|
UTSW |
19 |
59,020,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R6013:Shtn1
|
UTSW |
19 |
58,963,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6374:Shtn1
|
UTSW |
19 |
59,026,728 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7030:Shtn1
|
UTSW |
19 |
58,998,266 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7143:Shtn1
|
UTSW |
19 |
59,007,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R7487:Shtn1
|
UTSW |
19 |
58,992,292 (GRCm39) |
missense |
probably damaging |
0.99 |
R7496:Shtn1
|
UTSW |
19 |
59,016,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7889:Shtn1
|
UTSW |
19 |
58,992,328 (GRCm39) |
missense |
probably damaging |
0.99 |
R8209:Shtn1
|
UTSW |
19 |
58,992,328 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8226:Shtn1
|
UTSW |
19 |
58,992,328 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8290:Shtn1
|
UTSW |
19 |
58,988,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R8857:Shtn1
|
UTSW |
19 |
58,978,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R9289:Shtn1
|
UTSW |
19 |
58,998,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R9496:Shtn1
|
UTSW |
19 |
58,963,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R9598:Shtn1
|
UTSW |
19 |
59,026,735 (GRCm39) |
missense |
probably damaging |
0.99 |
|