Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
C |
T |
7: 41,275,829 (GRCm39) |
R511* |
probably null |
Het |
Add1 |
C |
A |
5: 34,788,058 (GRCm39) |
D702E |
probably benign |
Het |
Aff3 |
A |
G |
1: 38,248,791 (GRCm39) |
I772T |
probably damaging |
Het |
Ankar |
T |
C |
1: 72,714,979 (GRCm39) |
I382V |
probably benign |
Het |
Anks1 |
A |
G |
17: 28,272,879 (GRCm39) |
T925A |
probably benign |
Het |
Asprv1 |
T |
A |
6: 86,605,348 (GRCm39) |
C65S |
probably damaging |
Het |
Atp8a1 |
T |
C |
5: 67,805,049 (GRCm39) |
D1022G |
probably benign |
Het |
Cep250 |
A |
G |
2: 155,836,798 (GRCm39) |
K2256E |
probably benign |
Het |
Chsy1 |
G |
A |
7: 65,821,912 (GRCm39) |
G716R |
probably damaging |
Het |
Cntln |
T |
C |
4: 84,892,264 (GRCm39) |
|
probably null |
Het |
Col13a1 |
G |
A |
10: 61,797,110 (GRCm39) |
R106W |
probably damaging |
Het |
Col2a1 |
A |
G |
15: 97,873,976 (GRCm39) |
I1402T |
unknown |
Het |
Col4a3 |
T |
C |
1: 82,626,321 (GRCm39) |
L86P |
unknown |
Het |
Cul9 |
A |
G |
17: 46,813,154 (GRCm39) |
V2355A |
probably damaging |
Het |
Ddx43 |
C |
A |
9: 78,313,661 (GRCm39) |
Y197* |
probably null |
Het |
Dnah7b |
T |
A |
1: 46,246,732 (GRCm39) |
I1636N |
probably damaging |
Het |
Dpysl5 |
G |
A |
5: 30,948,941 (GRCm39) |
D399N |
probably damaging |
Het |
Dyrk2 |
T |
A |
10: 118,696,242 (GRCm39) |
K339* |
probably null |
Het |
Fam187b |
A |
C |
7: 30,677,154 (GRCm39) |
D221A |
probably benign |
Het |
Fbxw21 |
A |
G |
9: 108,974,578 (GRCm39) |
I314T |
probably benign |
Het |
Fgd6 |
T |
A |
10: 93,880,056 (GRCm39) |
F303L |
probably benign |
Het |
Fstl3 |
T |
C |
10: 79,617,057 (GRCm39) |
V200A |
probably benign |
Het |
Gm10784 |
A |
T |
13: 50,099,233 (GRCm39) |
|
noncoding transcript |
Het |
Gpr45 |
G |
A |
1: 43,071,668 (GRCm39) |
D104N |
possibly damaging |
Het |
Gria1 |
C |
T |
11: 57,076,627 (GRCm39) |
Q8* |
probably null |
Het |
H2-T22 |
A |
G |
17: 36,351,537 (GRCm39) |
L231S |
probably damaging |
Het |
Ice1 |
A |
T |
13: 70,750,697 (GRCm39) |
D1796E |
probably benign |
Het |
Ing1 |
T |
A |
8: 11,611,641 (GRCm39) |
S26R |
probably benign |
Het |
Klhl2 |
C |
T |
8: 65,205,794 (GRCm39) |
V376M |
probably benign |
Het |
Lrriq1 |
A |
G |
10: 103,050,761 (GRCm39) |
S664P |
probably benign |
Het |
Ltf |
G |
T |
9: 110,857,540 (GRCm39) |
C443F |
possibly damaging |
Het |
Mgam |
T |
C |
6: 40,745,154 (GRCm39) |
V1807A |
possibly damaging |
Het |
Mnd1 |
C |
A |
3: 84,041,416 (GRCm39) |
C62F |
probably benign |
Het |
Mycbp2 |
A |
G |
14: 103,534,794 (GRCm39) |
V304A |
probably benign |
Het |
Nek10 |
T |
C |
14: 14,836,202 (GRCm38) |
L141P |
probably damaging |
Het |
Noa1 |
T |
C |
5: 77,454,191 (GRCm39) |
E483G |
possibly damaging |
Het |
Or5b101 |
C |
T |
19: 13,005,412 (GRCm39) |
A94T |
probably benign |
Het |
Pkd1l1 |
T |
A |
11: 8,824,236 (GRCm39) |
S1110C |
probably damaging |
Het |
Potefam1 |
A |
T |
2: 111,034,364 (GRCm39) |
S359T |
possibly damaging |
Het |
Ppp4r4 |
T |
C |
12: 103,579,080 (GRCm39) |
S873P |
probably damaging |
Het |
Pth |
T |
C |
7: 112,985,136 (GRCm39) |
H79R |
probably benign |
Het |
Rab21 |
T |
C |
10: 115,130,814 (GRCm39) |
N164S |
probably benign |
Het |
Rsf1 |
CG |
CGACGGCGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Slc4a5 |
C |
T |
6: 83,273,651 (GRCm39) |
T997I |
probably damaging |
Het |
Ssrp1 |
A |
G |
2: 84,871,930 (GRCm39) |
T385A |
possibly damaging |
Het |
Tcf15 |
T |
C |
2: 151,985,871 (GRCm39) |
I109T |
probably damaging |
Het |
Tcp11 |
C |
A |
17: 28,288,239 (GRCm39) |
D330Y |
probably benign |
Het |
Tktl2 |
T |
A |
8: 66,964,715 (GRCm39) |
V91E |
probably benign |
Het |
Usp48 |
G |
A |
4: 137,341,073 (GRCm39) |
V358M |
probably damaging |
Het |
Vmn1r228 |
A |
G |
17: 20,996,609 (GRCm39) |
I303T |
probably damaging |
Het |
Zfp229 |
T |
G |
17: 21,965,010 (GRCm39) |
H413Q |
probably damaging |
Het |
|
Other mutations in Prss35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01548:Prss35
|
APN |
9 |
86,637,327 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02749:Prss35
|
APN |
9 |
86,638,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R0346:Prss35
|
UTSW |
9 |
86,637,404 (GRCm39) |
missense |
probably benign |
0.04 |
R0403:Prss35
|
UTSW |
9 |
86,638,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R1664:Prss35
|
UTSW |
9 |
86,637,700 (GRCm39) |
missense |
probably benign |
0.29 |
R2016:Prss35
|
UTSW |
9 |
86,637,565 (GRCm39) |
missense |
probably benign |
0.37 |
R2017:Prss35
|
UTSW |
9 |
86,637,565 (GRCm39) |
missense |
probably benign |
0.37 |
R2325:Prss35
|
UTSW |
9 |
86,638,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R2429:Prss35
|
UTSW |
9 |
86,637,398 (GRCm39) |
missense |
probably benign |
|
R2966:Prss35
|
UTSW |
9 |
86,637,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R3961:Prss35
|
UTSW |
9 |
86,637,802 (GRCm39) |
missense |
probably benign |
0.02 |
R4792:Prss35
|
UTSW |
9 |
86,637,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Prss35
|
UTSW |
9 |
86,638,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R6169:Prss35
|
UTSW |
9 |
86,637,491 (GRCm39) |
missense |
probably benign |
0.00 |
R6446:Prss35
|
UTSW |
9 |
86,637,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R6753:Prss35
|
UTSW |
9 |
86,638,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7008:Prss35
|
UTSW |
9 |
86,638,361 (GRCm39) |
missense |
probably benign |
0.01 |
R7387:Prss35
|
UTSW |
9 |
86,637,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R7523:Prss35
|
UTSW |
9 |
86,637,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7587:Prss35
|
UTSW |
9 |
86,637,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7652:Prss35
|
UTSW |
9 |
86,638,023 (GRCm39) |
missense |
probably benign |
|
R8013:Prss35
|
UTSW |
9 |
86,637,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R8194:Prss35
|
UTSW |
9 |
86,637,666 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8871:Prss35
|
UTSW |
9 |
86,637,244 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9444:Prss35
|
UTSW |
9 |
86,638,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9462:Prss35
|
UTSW |
9 |
86,638,392 (GRCm39) |
missense |
|
|
R9695:Prss35
|
UTSW |
9 |
86,637,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|