Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss2 |
T |
A |
2: 155,403,931 (GRCm39) |
D692E |
probably damaging |
Het |
Adgrb3 |
T |
A |
1: 25,543,529 (GRCm39) |
R366S |
probably damaging |
Het |
Afg3l2 |
C |
A |
18: 67,547,139 (GRCm39) |
|
probably benign |
Het |
Cd5 |
T |
C |
19: 10,703,653 (GRCm39) |
|
probably benign |
Het |
Cnbd1 |
A |
G |
4: 18,862,111 (GRCm39) |
S360P |
probably damaging |
Het |
Col13a1 |
A |
T |
10: 61,721,490 (GRCm39) |
L305I |
possibly damaging |
Het |
Commd7 |
A |
T |
2: 153,464,684 (GRCm39) |
|
probably benign |
Het |
Cpsf6 |
A |
T |
10: 117,203,884 (GRCm39) |
Y23N |
probably damaging |
Het |
Cry1 |
A |
G |
10: 84,992,993 (GRCm39) |
V75A |
possibly damaging |
Het |
Cyp2c39 |
A |
G |
19: 39,501,767 (GRCm39) |
N107D |
probably benign |
Het |
Dcaf11 |
T |
A |
14: 55,798,878 (GRCm39) |
V45E |
probably damaging |
Het |
Dnm2 |
A |
G |
9: 21,385,907 (GRCm39) |
E310G |
probably damaging |
Het |
Fat3 |
T |
A |
9: 15,915,158 (GRCm39) |
I1597L |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,728,685 (GRCm39) |
|
probably benign |
Het |
Fer |
A |
G |
17: 64,298,637 (GRCm39) |
I529V |
probably damaging |
Het |
Fhdc1 |
T |
C |
3: 84,351,826 (GRCm39) |
K1133R |
possibly damaging |
Het |
Foxd3 |
A |
G |
4: 99,545,432 (GRCm39) |
K191E |
probably damaging |
Het |
Fut2 |
C |
T |
7: 45,300,193 (GRCm39) |
G193E |
possibly damaging |
Het |
Gbp8 |
A |
G |
5: 105,164,410 (GRCm39) |
|
probably null |
Het |
Glb1 |
T |
G |
9: 114,259,389 (GRCm39) |
N106K |
probably damaging |
Het |
Hpx |
A |
G |
7: 105,241,609 (GRCm39) |
I295T |
probably damaging |
Het |
Ipo5 |
T |
A |
14: 121,180,099 (GRCm39) |
D844E |
probably damaging |
Het |
Krt17 |
T |
C |
11: 100,150,561 (GRCm39) |
I159V |
possibly damaging |
Het |
Lgi4 |
G |
A |
7: 30,762,605 (GRCm39) |
|
probably null |
Het |
Lrrc49 |
T |
C |
9: 60,573,563 (GRCm39) |
|
probably benign |
Het |
Ltn1 |
T |
C |
16: 87,222,499 (GRCm39) |
K178R |
probably damaging |
Het |
Myh8 |
T |
A |
11: 67,185,244 (GRCm39) |
W832R |
probably damaging |
Het |
Nbn |
A |
G |
4: 15,962,362 (GRCm39) |
N30S |
probably damaging |
Het |
Or2j3 |
A |
G |
17: 38,615,786 (GRCm39) |
S189P |
probably benign |
Het |
Or4a72 |
A |
T |
2: 89,405,593 (GRCm39) |
V159D |
probably damaging |
Het |
Or4f59 |
T |
A |
2: 111,873,321 (GRCm39) |
N19Y |
probably benign |
Het |
Or51ai2 |
T |
C |
7: 103,587,232 (GRCm39) |
V215A |
probably benign |
Het |
Pcdh15 |
A |
T |
10: 74,460,104 (GRCm39) |
I1314F |
probably damaging |
Het |
Phf14 |
G |
A |
6: 11,962,658 (GRCm39) |
S435N |
probably damaging |
Het |
Prss45 |
T |
A |
9: 110,669,618 (GRCm39) |
Y231* |
probably null |
Het |
Pus7l |
T |
C |
15: 94,434,449 (GRCm39) |
D339G |
probably damaging |
Het |
Serpina1b |
T |
G |
12: 103,698,329 (GRCm39) |
K173N |
possibly damaging |
Het |
Slc13a5 |
G |
A |
11: 72,136,004 (GRCm39) |
T469I |
probably damaging |
Het |
Spon1 |
A |
G |
7: 113,633,522 (GRCm39) |
E655G |
probably damaging |
Het |
Sv2b |
T |
C |
7: 74,806,508 (GRCm39) |
|
probably null |
Het |
Treh |
A |
G |
9: 44,597,228 (GRCm39) |
D514G |
probably damaging |
Het |
Umodl1 |
T |
A |
17: 31,215,329 (GRCm39) |
L1051Q |
probably damaging |
Het |
Usp5 |
A |
G |
6: 124,803,350 (GRCm39) |
F4S |
probably damaging |
Het |
Vmn1r16 |
A |
G |
6: 57,299,879 (GRCm39) |
S248P |
probably damaging |
Het |
|
Other mutations in Sbk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01419:Sbk2
|
APN |
7 |
4,960,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01595:Sbk2
|
APN |
7 |
4,960,712 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01688:Sbk2
|
APN |
7 |
4,960,716 (GRCm39) |
intron |
probably benign |
|
IGL02901:Sbk2
|
APN |
7 |
4,960,289 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1714:Sbk2
|
UTSW |
7 |
4,966,121 (GRCm39) |
missense |
probably benign |
0.15 |
R2679:Sbk2
|
UTSW |
7 |
4,960,119 (GRCm39) |
splice site |
probably null |
|
R3158:Sbk2
|
UTSW |
7 |
4,960,526 (GRCm39) |
nonsense |
probably null |
|
R4088:Sbk2
|
UTSW |
7 |
4,960,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R4709:Sbk2
|
UTSW |
7 |
4,960,577 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5211:Sbk2
|
UTSW |
7 |
4,965,966 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5906:Sbk2
|
UTSW |
7 |
4,960,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R6393:Sbk2
|
UTSW |
7 |
4,960,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Sbk2
|
UTSW |
7 |
4,967,146 (GRCm39) |
critical splice donor site |
probably null |
|
R7045:Sbk2
|
UTSW |
7 |
4,961,905 (GRCm39) |
missense |
probably damaging |
0.99 |
R7537:Sbk2
|
UTSW |
7 |
4,966,148 (GRCm39) |
missense |
probably benign |
0.02 |
R7810:Sbk2
|
UTSW |
7 |
4,961,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R8058:Sbk2
|
UTSW |
7 |
4,960,289 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9304:Sbk2
|
UTSW |
7 |
4,960,507 (GRCm39) |
missense |
probably damaging |
0.96 |
R9507:Sbk2
|
UTSW |
7 |
4,960,277 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9749:Sbk2
|
UTSW |
7 |
4,960,333 (GRCm39) |
missense |
probably benign |
0.08 |
|