Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
T |
C |
7: 78,749,452 (GRCm39) |
S1408P |
probably damaging |
Het |
Acap3 |
T |
C |
4: 155,990,169 (GRCm39) |
V783A |
probably damaging |
Het |
Akap8 |
T |
C |
17: 32,525,504 (GRCm39) |
N525S |
probably damaging |
Het |
Aqp1 |
C |
T |
6: 55,313,606 (GRCm39) |
T44M |
probably damaging |
Het |
Arap1 |
T |
C |
7: 101,053,585 (GRCm39) |
Y1305H |
probably damaging |
Het |
Atg2a |
T |
G |
19: 6,300,651 (GRCm39) |
S743A |
probably benign |
Het |
AW551984 |
G |
T |
9: 39,511,307 (GRCm39) |
L133I |
probably damaging |
Het |
Bahcc1 |
C |
A |
11: 120,164,587 (GRCm39) |
P802T |
possibly damaging |
Het |
Brd8 |
C |
A |
18: 34,743,002 (GRCm39) |
V288L |
probably benign |
Het |
Carmil2 |
T |
C |
8: 106,412,947 (GRCm39) |
|
probably null |
Het |
Catspere2 |
G |
A |
1: 177,905,048 (GRCm39) |
E153K |
possibly damaging |
Het |
Ccdc162 |
C |
T |
10: 41,542,737 (GRCm39) |
R379Q |
probably benign |
Het |
Cd200l1 |
T |
C |
16: 45,264,199 (GRCm39) |
T120A |
probably benign |
Het |
Cdh16 |
A |
G |
8: 105,341,136 (GRCm39) |
L116P |
probably damaging |
Het |
Cenpj |
A |
T |
14: 56,796,076 (GRCm39) |
H260Q |
possibly damaging |
Het |
Cenpq |
A |
G |
17: 41,244,027 (GRCm39) |
V17A |
possibly damaging |
Het |
Cep350 |
T |
C |
1: 155,803,862 (GRCm39) |
K1074E |
probably damaging |
Het |
Chil4 |
C |
A |
3: 106,109,121 (GRCm39) |
C394F |
probably damaging |
Het |
Chst9 |
T |
C |
18: 15,850,983 (GRCm39) |
I28V |
probably benign |
Het |
Clasp2 |
C |
A |
9: 113,728,649 (GRCm39) |
N873K |
probably damaging |
Het |
Clec4b2 |
T |
A |
6: 123,158,269 (GRCm39) |
M45K |
probably benign |
Het |
Cmya5 |
T |
A |
13: 93,200,048 (GRCm39) |
T3427S |
possibly damaging |
Het |
Cnih4 |
A |
G |
1: 180,989,777 (GRCm39) |
Y130C |
probably damaging |
Het |
Cpne9 |
T |
A |
6: 113,281,506 (GRCm39) |
M529K |
probably damaging |
Het |
Crppa |
A |
T |
12: 36,440,481 (GRCm39) |
N130Y |
probably damaging |
Het |
Cyp2j13 |
G |
A |
4: 95,945,153 (GRCm39) |
H351Y |
probably benign |
Het |
Dixdc1 |
T |
A |
9: 50,613,265 (GRCm39) |
Q230L |
probably damaging |
Het |
Dpep1 |
A |
T |
8: 123,926,764 (GRCm39) |
I226F |
probably benign |
Het |
Efcab3 |
A |
T |
11: 104,805,721 (GRCm39) |
N3076I |
unknown |
Het |
Ehd2 |
A |
G |
7: 15,691,603 (GRCm39) |
V243A |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,306,232 (GRCm39) |
Y353N |
probably benign |
Het |
Fgg |
G |
T |
3: 82,920,322 (GRCm39) |
G367V |
probably damaging |
Het |
Gm9772 |
T |
C |
17: 22,225,310 (GRCm39) |
*61Q |
probably null |
Het |
Grk5 |
T |
G |
19: 61,078,432 (GRCm39) |
D496E |
possibly damaging |
Het |
Hc |
T |
C |
2: 34,909,535 (GRCm39) |
N915S |
probably benign |
Het |
Iah1 |
G |
T |
12: 21,367,388 (GRCm39) |
Q31H |
probably benign |
Het |
Insr |
T |
C |
8: 3,219,714 (GRCm39) |
D936G |
probably benign |
Het |
Ints6 |
A |
C |
14: 62,939,902 (GRCm39) |
V596G |
probably benign |
Het |
Kcnj16 |
A |
G |
11: 110,915,677 (GRCm39) |
D113G |
possibly damaging |
Het |
Kdm4b |
A |
T |
17: 56,706,771 (GRCm39) |
I928F |
probably damaging |
Het |
Lrrc41 |
C |
T |
4: 115,932,488 (GRCm39) |
|
probably benign |
Het |
Lrrc8e |
G |
A |
8: 4,285,070 (GRCm39) |
V432I |
probably benign |
Het |
Mamdc4 |
T |
C |
2: 25,458,501 (GRCm39) |
E336G |
probably benign |
Het |
Maml2 |
C |
A |
9: 13,532,918 (GRCm39) |
Q711K |
|
Het |
Map3k14 |
T |
C |
11: 103,118,498 (GRCm39) |
T563A |
possibly damaging |
Het |
Mcu |
T |
A |
10: 59,303,535 (GRCm39) |
K101* |
probably null |
Het |
Mettl22 |
T |
A |
16: 8,303,792 (GRCm39) |
V286E |
probably damaging |
Het |
Mon2 |
A |
T |
10: 122,845,516 (GRCm39) |
N1396K |
possibly damaging |
Het |
Mprip |
T |
C |
11: 59,587,851 (GRCm39) |
|
probably benign |
Het |
Mrpl51 |
C |
T |
6: 125,170,344 (GRCm39) |
L117F |
probably damaging |
Het |
Myo1d |
C |
A |
11: 80,565,758 (GRCm39) |
V356F |
probably damaging |
Het |
Myo1d |
T |
A |
11: 80,567,758 (GRCm39) |
I241F |
probably benign |
Het |
Naalad2 |
A |
T |
9: 18,297,230 (GRCm39) |
|
probably benign |
Het |
Nacad |
T |
C |
11: 6,552,853 (GRCm39) |
T113A |
probably benign |
Het |
Nrap |
T |
A |
19: 56,352,843 (GRCm39) |
|
probably benign |
Het |
Or10b1 |
G |
A |
10: 78,356,284 (GRCm39) |
V281M |
possibly damaging |
Het |
Or2z2 |
T |
C |
11: 58,345,936 (GRCm39) |
T280A |
possibly damaging |
Het |
Or56b2 |
T |
A |
7: 104,337,387 (GRCm39) |
I55N |
probably damaging |
Het |
Or5ae1 |
T |
A |
7: 84,565,626 (GRCm39) |
I213N |
possibly damaging |
Het |
Or5w1 |
T |
C |
2: 87,486,591 (GRCm39) |
I225V |
possibly damaging |
Het |
Or6z3 |
T |
C |
7: 6,463,763 (GRCm39) |
L85P |
probably damaging |
Het |
Osbpl3 |
T |
C |
6: 50,328,852 (GRCm39) |
D117G |
probably damaging |
Het |
Parp9 |
C |
T |
16: 35,773,981 (GRCm39) |
R318* |
probably null |
Het |
Pcdhb18 |
A |
G |
18: 37,623,374 (GRCm39) |
I235V |
probably benign |
Het |
Pex16 |
T |
G |
2: 92,209,366 (GRCm39) |
|
probably benign |
Het |
Piezo2 |
T |
A |
18: 63,248,034 (GRCm39) |
M489L |
probably benign |
Het |
Pmepa1 |
C |
A |
2: 173,069,628 (GRCm39) |
G271V |
probably damaging |
Het |
Safb |
A |
G |
17: 56,910,579 (GRCm39) |
E659G |
unknown |
Het |
Scn9a |
T |
C |
2: 66,332,010 (GRCm39) |
T1289A |
probably damaging |
Het |
Secisbp2l |
T |
C |
2: 125,617,596 (GRCm39) |
D27G |
possibly damaging |
Het |
Serpina1f |
A |
G |
12: 103,660,240 (GRCm39) |
V14A |
probably benign |
Het |
Serpinb9b |
C |
A |
13: 33,213,452 (GRCm39) |
T3N |
possibly damaging |
Het |
Sfxn5 |
C |
T |
6: 85,206,182 (GRCm39) |
M315I |
probably benign |
Het |
Slc9b2 |
A |
G |
3: 135,035,530 (GRCm39) |
D333G |
probably benign |
Het |
Sostdc1 |
A |
G |
12: 36,367,229 (GRCm39) |
N135S |
possibly damaging |
Het |
Spg11 |
T |
G |
2: 121,901,425 (GRCm39) |
D1505A |
probably damaging |
Het |
Spmip8 |
A |
T |
8: 96,047,883 (GRCm39) |
|
probably benign |
Het |
Taar7a |
T |
C |
10: 23,869,279 (GRCm39) |
N34S |
probably benign |
Het |
Tcerg1l |
C |
A |
7: 137,811,526 (GRCm39) |
R556L |
possibly damaging |
Het |
Tcp11l1 |
T |
C |
2: 104,518,763 (GRCm39) |
K311R |
probably benign |
Het |
Trbv16 |
T |
G |
6: 41,128,972 (GRCm39) |
F52C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,726,016 (GRCm39) |
R6073S |
unknown |
Het |
Uba1y |
T |
C |
Y: 828,818 (GRCm39) |
I542T |
possibly damaging |
Het |
Vmn1r214 |
T |
C |
13: 23,219,082 (GRCm39) |
I192T |
probably benign |
Het |
Vmn2r67 |
C |
T |
7: 84,786,346 (GRCm39) |
C553Y |
probably damaging |
Het |
Zdhhc17 |
G |
T |
10: 110,784,121 (GRCm39) |
H452N |
possibly damaging |
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 |
R5551:Ctsr
|
UTSW |
13 |
61,307,357 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
R9464:Ctsr
|
UTSW |
13 |
61,307,295 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9572:Ctsr
|
UTSW |
13 |
61,310,978 (GRCm39) |
missense |
probably benign |
|
|