Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AB041806 |
G |
T |
4: 138,123,312 (GRCm39) |
P3T |
probably damaging |
Het |
Abl1 |
C |
T |
2: 31,691,682 (GRCm39) |
A1048V |
probably benign |
Het |
Acap2 |
A |
G |
16: 30,923,726 (GRCm39) |
V659A |
probably damaging |
Het |
Acox1 |
A |
G |
11: 116,080,317 (GRCm39) |
S29P |
possibly damaging |
Het |
Adamts1 |
A |
G |
16: 85,594,634 (GRCm39) |
I405T |
probably benign |
Het |
Afm |
A |
T |
5: 90,679,511 (GRCm39) |
E335V |
probably null |
Het |
Akap6 |
C |
T |
12: 52,842,747 (GRCm39) |
P32S |
probably damaging |
Het |
Alk |
T |
C |
17: 72,182,028 (GRCm39) |
M1332V |
possibly damaging |
Het |
Ankrd39 |
C |
T |
1: 36,581,062 (GRCm39) |
G96R |
probably damaging |
Het |
Atp2c1 |
C |
A |
9: 105,336,936 (GRCm39) |
A16S |
probably damaging |
Het |
Ccdc141 |
T |
C |
2: 76,844,753 (GRCm39) |
E1438G |
probably damaging |
Het |
Csmd2 |
T |
C |
4: 128,404,741 (GRCm39) |
Y2376H |
possibly damaging |
Het |
Csmd3 |
T |
C |
15: 48,177,492 (GRCm39) |
T349A |
probably benign |
Het |
Dot1l |
CCAGCCCCACCCTCAGCC |
CCAGCC |
10: 80,619,462 (GRCm39) |
|
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,031,718 (GRCm39) |
S3516P |
possibly damaging |
Het |
Ehd4 |
A |
G |
2: 119,958,100 (GRCm39) |
S162P |
possibly damaging |
Het |
Ets2 |
T |
C |
16: 95,513,165 (GRCm39) |
W114R |
probably damaging |
Het |
Fignl1 |
A |
T |
11: 11,751,603 (GRCm39) |
V484E |
probably damaging |
Het |
Golph3 |
C |
A |
15: 12,321,922 (GRCm39) |
S35R |
probably benign |
Het |
Gzf1 |
T |
C |
2: 148,526,248 (GRCm39) |
Y240H |
probably damaging |
Het |
Hook3 |
A |
G |
8: 26,558,639 (GRCm39) |
F75S |
possibly damaging |
Het |
Ifi209 |
T |
A |
1: 173,468,763 (GRCm39) |
S198T |
probably benign |
Het |
Iqch |
A |
T |
9: 63,403,535 (GRCm39) |
|
probably null |
Het |
Katnip |
T |
C |
7: 125,419,249 (GRCm39) |
F472S |
probably damaging |
Het |
Lrrk2 |
C |
T |
15: 91,696,553 (GRCm39) |
T2447I |
probably benign |
Het |
Mesp2 |
T |
C |
7: 79,461,367 (GRCm39) |
S231P |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,422,240 (GRCm39) |
C4459R |
possibly damaging |
Het |
Myh10 |
A |
G |
11: 68,659,113 (GRCm39) |
E497G |
possibly damaging |
Het |
Nalcn |
A |
T |
14: 123,515,698 (GRCm39) |
V1701E |
possibly damaging |
Het |
Nat8f1 |
T |
C |
6: 85,887,891 (GRCm39) |
D23G |
probably damaging |
Het |
Nfia |
G |
A |
4: 97,902,497 (GRCm39) |
E250K |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,177,817 (GRCm39) |
M1067V |
probably benign |
Het |
Or4k36 |
T |
C |
2: 111,145,916 (GRCm39) |
F31L |
possibly damaging |
Het |
Pde4d |
T |
A |
13: 110,084,930 (GRCm39) |
|
probably null |
Het |
Rtn4 |
G |
A |
11: 29,691,011 (GRCm39) |
V1101I |
probably damaging |
Het |
Sema4c |
A |
G |
1: 36,591,398 (GRCm39) |
Y348H |
probably damaging |
Het |
Sema6a |
A |
G |
18: 47,381,595 (GRCm39) |
V958A |
possibly damaging |
Het |
Sez6l2 |
A |
G |
7: 126,566,002 (GRCm39) |
Y677C |
probably damaging |
Het |
Smad5 |
T |
C |
13: 56,883,654 (GRCm39) |
C347R |
probably damaging |
Het |
Smim19 |
A |
G |
8: 22,953,383 (GRCm39) |
Y95H |
probably benign |
Het |
Srrm2 |
C |
A |
17: 24,037,450 (GRCm39) |
|
probably benign |
Het |
Ssb |
A |
G |
2: 69,701,474 (GRCm39) |
K390E |
probably damaging |
Het |
Tars1 |
G |
A |
15: 11,392,068 (GRCm39) |
T248M |
probably damaging |
Het |
Tcirg1 |
A |
T |
19: 3,948,858 (GRCm39) |
F442L |
probably damaging |
Het |
Tex55 |
A |
G |
16: 38,648,336 (GRCm39) |
Y258H |
probably benign |
Het |
Tlk2 |
A |
G |
11: 105,112,133 (GRCm39) |
E162G |
probably benign |
Het |
Tmc6 |
A |
G |
11: 117,660,271 (GRCm39) |
C656R |
probably damaging |
Het |
Ttn |
G |
T |
2: 76,719,406 (GRCm39) |
|
probably benign |
Het |
Uqcrc2 |
C |
T |
7: 120,244,461 (GRCm39) |
T201I |
probably damaging |
Het |
Zfp282 |
G |
T |
6: 47,867,579 (GRCm39) |
A252S |
possibly damaging |
Het |
Zfp473 |
G |
C |
7: 44,383,575 (GRCm39) |
P253A |
probably benign |
Het |
Zfp541 |
A |
G |
7: 15,824,786 (GRCm39) |
N1068D |
probably damaging |
Het |
Zfp946 |
A |
G |
17: 22,674,365 (GRCm39) |
Q373R |
probably damaging |
Het |
Zmat2 |
G |
A |
18: 36,927,010 (GRCm39) |
G6R |
probably benign |
Het |
|
Other mutations in Ctsr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00647:Ctsr
|
APN |
13 |
61,310,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01327:Ctsr
|
APN |
13 |
61,310,489 (GRCm39) |
splice site |
probably benign |
|
IGL02169:Ctsr
|
APN |
13 |
61,311,054 (GRCm39) |
splice site |
probably benign |
|
IGL02516:Ctsr
|
APN |
13 |
61,310,992 (GRCm39) |
missense |
probably benign |
|
IGL02739:Ctsr
|
APN |
13 |
61,309,658 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4687001:Ctsr
|
UTSW |
13 |
61,308,346 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0180:Ctsr
|
UTSW |
13 |
61,310,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Ctsr
|
UTSW |
13 |
61,310,259 (GRCm39) |
missense |
probably benign |
0.00 |
R2362:Ctsr
|
UTSW |
13 |
61,310,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R3856:Ctsr
|
UTSW |
13 |
61,309,750 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4125:Ctsr
|
UTSW |
13 |
61,309,659 (GRCm39) |
missense |
probably benign |
0.17 |
R4135:Ctsr
|
UTSW |
13 |
61,309,084 (GRCm39) |
missense |
probably benign |
0.15 |
R4903:Ctsr
|
UTSW |
13 |
61,310,945 (GRCm39) |
missense |
probably benign |
0.01 |
R5705:Ctsr
|
UTSW |
13 |
61,309,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5721:Ctsr
|
UTSW |
13 |
61,309,667 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6132:Ctsr
|
UTSW |
13 |
61,309,582 (GRCm39) |
critical splice donor site |
probably null |
|
R6196:Ctsr
|
UTSW |
13 |
61,308,345 (GRCm39) |
missense |
probably benign |
0.09 |
R6719:Ctsr
|
UTSW |
13 |
61,308,265 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7530:Ctsr
|
UTSW |
13 |
61,310,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R7698:Ctsr
|
UTSW |
13 |
61,310,381 (GRCm39) |
missense |
probably benign |
0.01 |
R7963:Ctsr
|
UTSW |
13 |
61,310,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Ctsr
|
UTSW |
13 |
61,310,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R8431:Ctsr
|
UTSW |
13 |
61,308,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Ctsr
|
UTSW |
13 |
61,309,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Ctsr
|
UTSW |
13 |
61,307,295 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9572:Ctsr
|
UTSW |
13 |
61,310,978 (GRCm39) |
missense |
probably benign |
|
|