Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,328,504 (GRCm39) |
C3526S |
probably damaging |
Het |
Adgrf2 |
T |
C |
17: 43,021,774 (GRCm39) |
N350S |
probably benign |
Het |
Atp12a |
G |
A |
14: 56,624,439 (GRCm39) |
|
probably null |
Het |
AW551984 |
T |
G |
9: 39,511,955 (GRCm39) |
S19R |
probably damaging |
Het |
Bet1l |
A |
G |
7: 140,434,418 (GRCm39) |
I77T |
possibly damaging |
Het |
Cfap206 |
T |
C |
4: 34,711,414 (GRCm39) |
I494M |
possibly damaging |
Het |
Cog3 |
A |
G |
14: 75,968,118 (GRCm39) |
I415T |
probably damaging |
Het |
Col15a1 |
C |
T |
4: 47,300,518 (GRCm39) |
P1060S |
probably damaging |
Het |
Ctrb1 |
A |
G |
8: 112,415,981 (GRCm39) |
V71A |
possibly damaging |
Het |
Ddhd2 |
T |
C |
8: 26,242,242 (GRCm39) |
Y211C |
probably benign |
Het |
Fbxl20 |
T |
C |
11: 98,000,336 (GRCm39) |
T128A |
probably benign |
Het |
Fdps |
A |
G |
3: 89,002,659 (GRCm39) |
|
probably null |
Het |
Gm4302 |
TGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA |
TGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA |
10: 100,177,361 (GRCm39) |
|
probably benign |
Het |
Gm8369 |
T |
A |
19: 11,489,200 (GRCm39) |
|
probably benign |
Het |
Grm6 |
T |
C |
11: 50,750,601 (GRCm39) |
V588A |
possibly damaging |
Het |
Heatr6 |
T |
C |
11: 83,649,167 (GRCm39) |
L174S |
probably benign |
Het |
Kif1a |
G |
A |
1: 92,993,859 (GRCm39) |
P364S |
probably damaging |
Het |
Klk7 |
A |
G |
7: 43,462,684 (GRCm39) |
D163G |
probably benign |
Het |
Kmt2e |
TGCCGCCGCCGCCGCCACCGCCGCCGCCGC |
TGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGC |
5: 23,704,474 (GRCm39) |
|
probably benign |
Het |
Lamb3 |
T |
C |
1: 193,017,169 (GRCm39) |
S787P |
possibly damaging |
Het |
Lrp5 |
C |
T |
19: 3,650,753 (GRCm39) |
C1227Y |
probably damaging |
Het |
Mgst1 |
G |
A |
6: 138,118,805 (GRCm39) |
|
probably benign |
Het |
Mllt6 |
T |
C |
11: 97,571,428 (GRCm39) |
S1022P |
probably damaging |
Het |
Mtmr2 |
T |
C |
9: 13,716,678 (GRCm39) |
I521T |
probably benign |
Het |
Naalad2 |
T |
C |
9: 18,296,426 (GRCm39) |
T75A |
possibly damaging |
Het |
Nadsyn1 |
A |
T |
7: 143,372,845 (GRCm39) |
I83N |
probably damaging |
Het |
Naip2 |
T |
C |
13: 100,291,468 (GRCm39) |
S1157G |
probably benign |
Het |
Neurl4 |
T |
A |
11: 69,799,336 (GRCm39) |
L904Q |
probably damaging |
Het |
Ngp |
A |
C |
9: 110,249,017 (GRCm39) |
I30L |
probably benign |
Het |
Or5af1 |
T |
C |
11: 58,722,903 (GRCm39) |
Y308H |
probably benign |
Het |
Or6c5c |
G |
A |
10: 129,299,023 (GRCm39) |
M159I |
probably benign |
Het |
Orm2 |
A |
T |
4: 63,282,196 (GRCm39) |
M125L |
probably benign |
Het |
Pax2 |
A |
T |
19: 44,777,260 (GRCm39) |
D151V |
possibly damaging |
Het |
Polg |
A |
G |
7: 79,109,857 (GRCm39) |
V382A |
probably benign |
Het |
Ppargc1b |
C |
A |
18: 61,440,747 (GRCm39) |
G724W |
probably damaging |
Het |
Pramel11 |
T |
A |
4: 143,622,252 (GRCm39) |
I368F |
probably benign |
Het |
Prss16 |
A |
T |
13: 22,190,237 (GRCm39) |
V307E |
probably damaging |
Het |
Rspo1 |
A |
G |
4: 124,900,976 (GRCm39) |
H108R |
probably benign |
Het |
Sh3bp5l |
C |
A |
11: 58,237,098 (GRCm39) |
H352N |
probably damaging |
Het |
Skor1 |
T |
C |
9: 63,047,636 (GRCm39) |
|
probably null |
Het |
Smad6 |
A |
G |
9: 63,919,509 (GRCm39) |
Y289H |
probably benign |
Het |
Spart |
G |
A |
3: 55,034,982 (GRCm39) |
G456D |
probably damaging |
Het |
Spg11 |
T |
C |
2: 121,923,924 (GRCm39) |
E799G |
probably damaging |
Het |
Tbc1d4 |
T |
G |
14: 101,845,695 (GRCm39) |
K68Q |
probably damaging |
Het |
Treml2 |
A |
G |
17: 48,616,247 (GRCm39) |
M296V |
probably benign |
Het |
Ugt2b1 |
C |
A |
5: 87,067,116 (GRCm39) |
D436Y |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,325,042 (GRCm39) |
|
probably null |
Homo |
Vmn2r6 |
T |
C |
3: 64,445,580 (GRCm39) |
Y626C |
probably damaging |
Het |
Xpc |
G |
A |
6: 91,483,839 (GRCm39) |
A169V |
probably benign |
Het |
Zfp131 |
A |
G |
13: 120,228,129 (GRCm39) |
V506A |
probably damaging |
Het |
Zfp74 |
A |
G |
7: 29,633,860 (GRCm39) |
I616T |
probably benign |
Het |
|
Other mutations in Prss54 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02340:Prss54
|
APN |
8 |
96,292,237 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02598:Prss54
|
APN |
8 |
96,292,337 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03085:Prss54
|
APN |
8 |
96,292,258 (GRCm39) |
missense |
probably benign |
0.02 |
R0324:Prss54
|
UTSW |
8 |
96,292,295 (GRCm39) |
missense |
probably benign |
0.00 |
R0733:Prss54
|
UTSW |
8 |
96,286,368 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1487:Prss54
|
UTSW |
8 |
96,286,276 (GRCm39) |
missense |
probably benign |
0.01 |
R2272:Prss54
|
UTSW |
8 |
96,297,735 (GRCm39) |
nonsense |
probably null |
|
R4769:Prss54
|
UTSW |
8 |
96,286,003 (GRCm39) |
missense |
probably benign |
|
R5275:Prss54
|
UTSW |
8 |
96,291,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R5295:Prss54
|
UTSW |
8 |
96,291,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R6117:Prss54
|
UTSW |
8 |
96,292,086 (GRCm39) |
splice site |
probably null |
|
R6167:Prss54
|
UTSW |
8 |
96,286,173 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7179:Prss54
|
UTSW |
8 |
96,292,199 (GRCm39) |
missense |
probably benign |
0.03 |
R7261:Prss54
|
UTSW |
8 |
96,286,367 (GRCm39) |
missense |
probably benign |
0.02 |
R7864:Prss54
|
UTSW |
8 |
96,286,297 (GRCm39) |
missense |
probably benign |
0.22 |
R8284:Prss54
|
UTSW |
8 |
96,285,994 (GRCm39) |
nonsense |
probably null |
|
R8318:Prss54
|
UTSW |
8 |
96,291,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R8747:Prss54
|
UTSW |
8 |
96,286,351 (GRCm39) |
missense |
probably benign |
0.05 |
R8780:Prss54
|
UTSW |
8 |
96,286,057 (GRCm39) |
missense |
probably benign |
|
R9004:Prss54
|
UTSW |
8 |
96,292,137 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1177:Prss54
|
UTSW |
8 |
96,291,079 (GRCm39) |
missense |
probably damaging |
1.00 |
|