Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd8 |
A |
G |
8: 71,914,121 (GRCm39) |
V169A |
probably benign |
Het |
Aopep |
A |
G |
13: 63,357,939 (GRCm39) |
N648D |
probably benign |
Het |
BC024139 |
C |
A |
15: 76,005,343 (GRCm39) |
L506F |
probably benign |
Het |
Bltp3a |
T |
C |
17: 28,112,474 (GRCm39) |
L1221P |
probably damaging |
Het |
Cfap65 |
A |
T |
1: 74,967,507 (GRCm39) |
C190* |
probably null |
Het |
Cib2 |
A |
T |
9: 54,457,170 (GRCm39) |
H31Q |
probably damaging |
Het |
Emb |
A |
G |
13: 117,386,007 (GRCm39) |
|
probably benign |
Het |
Eml6 |
T |
C |
11: 29,755,175 (GRCm39) |
M867V |
probably benign |
Het |
Flnc |
A |
T |
6: 29,438,492 (GRCm39) |
K129* |
probably null |
Het |
Gckr |
C |
A |
5: 31,465,134 (GRCm39) |
H368N |
possibly damaging |
Het |
Gmds |
A |
T |
13: 32,409,145 (GRCm39) |
Y106* |
probably null |
Het |
Homez |
T |
C |
14: 55,095,355 (GRCm39) |
T118A |
probably damaging |
Het |
Kcnh7 |
G |
A |
2: 62,667,507 (GRCm39) |
T344I |
probably benign |
Het |
Kcnt2 |
A |
G |
1: 140,279,007 (GRCm39) |
I53V |
probably benign |
Het |
Krt13 |
A |
T |
11: 100,010,539 (GRCm39) |
L207Q |
probably damaging |
Het |
Lipo2 |
A |
G |
19: 33,708,348 (GRCm39) |
L222P |
possibly damaging |
Het |
Lrp2 |
A |
C |
2: 69,316,528 (GRCm39) |
V2151G |
possibly damaging |
Het |
Mrc2 |
A |
G |
11: 105,216,547 (GRCm39) |
D112G |
probably damaging |
Het |
Mrgpra6 |
T |
C |
7: 46,838,497 (GRCm39) |
T234A |
probably damaging |
Het |
Mroh2b |
A |
G |
15: 4,941,482 (GRCm39) |
N338S |
probably benign |
Het |
Mrpl23 |
T |
A |
7: 142,089,802 (GRCm39) |
|
probably benign |
Het |
Myo18a |
A |
G |
11: 77,741,073 (GRCm39) |
N1442S |
probably benign |
Het |
Nxn |
A |
G |
11: 76,165,480 (GRCm39) |
|
probably benign |
Het |
Or8w1 |
T |
C |
2: 87,465,424 (GRCm39) |
I222M |
possibly damaging |
Het |
Osmr |
A |
T |
15: 6,858,144 (GRCm39) |
N441K |
probably benign |
Het |
Patl2 |
A |
C |
2: 121,952,327 (GRCm39) |
S468R |
probably damaging |
Het |
Pcdhb1 |
T |
C |
18: 37,399,575 (GRCm39) |
S509P |
probably damaging |
Het |
Pmp22 |
G |
T |
11: 63,049,134 (GRCm39) |
V126F |
probably benign |
Het |
Prom1 |
A |
G |
5: 44,186,946 (GRCm39) |
|
probably benign |
Het |
Psd3 |
G |
T |
8: 68,416,521 (GRCm39) |
H459N |
probably benign |
Het |
Rasgrp1 |
A |
G |
2: 117,115,359 (GRCm39) |
L743P |
probably benign |
Het |
Rpusd4 |
G |
A |
9: 35,179,720 (GRCm39) |
R71Q |
probably damaging |
Het |
Rsf1 |
C |
T |
7: 97,313,977 (GRCm39) |
|
probably benign |
Het |
Scaf11 |
T |
C |
15: 96,318,725 (GRCm39) |
T280A |
possibly damaging |
Het |
Slc16a4 |
A |
G |
3: 107,210,415 (GRCm39) |
I362V |
probably benign |
Het |
Syt16 |
T |
C |
12: 74,313,616 (GRCm39) |
V514A |
probably benign |
Het |
Tdpoz2 |
A |
G |
3: 93,559,735 (GRCm39) |
V79A |
possibly damaging |
Het |
Tenm2 |
A |
G |
11: 35,937,768 (GRCm39) |
M1635T |
probably benign |
Het |
Vmn1r195 |
A |
G |
13: 22,463,255 (GRCm39) |
T242A |
probably benign |
Het |
Zfp423 |
A |
G |
8: 88,508,136 (GRCm39) |
V736A |
probably damaging |
Het |
|
Other mutations in Prss1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00577:Prss1
|
APN |
6 |
41,439,645 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL00661:Prss1
|
APN |
6 |
41,439,553 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02350:Prss1
|
APN |
6 |
41,440,139 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02357:Prss1
|
APN |
6 |
41,440,139 (GRCm39) |
missense |
probably damaging |
0.96 |
R0090:Prss1
|
UTSW |
6 |
41,438,166 (GRCm39) |
missense |
probably benign |
0.00 |
R0137:Prss1
|
UTSW |
6 |
41,439,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R0143:Prss1
|
UTSW |
6 |
41,440,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R0422:Prss1
|
UTSW |
6 |
41,440,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R0792:Prss1
|
UTSW |
6 |
41,435,878 (GRCm39) |
start codon destroyed |
probably null |
|
R0939:Prss1
|
UTSW |
6 |
41,440,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R2762:Prss1
|
UTSW |
6 |
41,440,215 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2896:Prss1
|
UTSW |
6 |
41,440,639 (GRCm39) |
nonsense |
probably null |
|
R2915:Prss1
|
UTSW |
6 |
41,439,545 (GRCm39) |
missense |
probably benign |
0.11 |
R2959:Prss1
|
UTSW |
6 |
41,440,172 (GRCm39) |
missense |
probably damaging |
0.99 |
R5123:Prss1
|
UTSW |
6 |
41,440,131 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5587:Prss1
|
UTSW |
6 |
41,440,199 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5610:Prss1
|
UTSW |
6 |
41,438,147 (GRCm39) |
missense |
probably benign |
0.07 |
R6521:Prss1
|
UTSW |
6 |
41,440,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Prss1
|
UTSW |
6 |
41,440,654 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7199:Prss1
|
UTSW |
6 |
41,439,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R7552:Prss1
|
UTSW |
6 |
41,439,507 (GRCm39) |
missense |
probably benign |
0.05 |
R8812:Prss1
|
UTSW |
6 |
41,439,520 (GRCm39) |
missense |
probably benign |
0.01 |
R9136:Prss1
|
UTSW |
6 |
41,438,280 (GRCm39) |
splice site |
probably benign |
|
R9255:Prss1
|
UTSW |
6 |
41,438,183 (GRCm39) |
missense |
probably damaging |
1.00 |
|