Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
T |
A |
1: 11,588,904 (GRCm39) |
I107N |
probably damaging |
Het |
Adh1 |
G |
A |
3: 137,994,555 (GRCm39) |
V292I |
probably benign |
Het |
Brd1 |
C |
T |
15: 88,573,821 (GRCm39) |
V1093I |
possibly damaging |
Het |
Cep170 |
A |
G |
1: 176,610,061 (GRCm39) |
|
probably benign |
Het |
Col4a4 |
G |
A |
1: 82,458,215 (GRCm39) |
P1120S |
probably damaging |
Het |
Cramp1 |
A |
T |
17: 25,190,532 (GRCm39) |
N1067K |
probably damaging |
Het |
E2f1 |
C |
G |
2: 154,405,942 (GRCm39) |
G144R |
probably damaging |
Het |
Eml6 |
C |
A |
11: 29,759,360 (GRCm39) |
V798F |
probably benign |
Het |
Ext1 |
A |
T |
15: 52,939,306 (GRCm39) |
V581E |
probably damaging |
Het |
Fbf1 |
C |
T |
11: 116,038,622 (GRCm39) |
R833Q |
probably benign |
Het |
Fbln1 |
T |
A |
15: 85,111,279 (GRCm39) |
C144* |
probably null |
Het |
Gm10521 |
A |
G |
1: 171,723,712 (GRCm39) |
T8A |
unknown |
Het |
Hapln4 |
A |
T |
8: 70,539,615 (GRCm39) |
L215F |
probably damaging |
Het |
Hmgcr |
T |
C |
13: 96,799,624 (GRCm39) |
I157V |
probably damaging |
Het |
Irak4 |
T |
C |
15: 94,459,476 (GRCm39) |
I364T |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,640,086 (GRCm39) |
C1700S |
probably damaging |
Het |
Lama5 |
C |
T |
2: 179,829,015 (GRCm39) |
C2042Y |
probably damaging |
Het |
Lrrc9 |
T |
G |
12: 72,507,580 (GRCm39) |
Y360* |
probably null |
Het |
Lrrd1 |
T |
A |
5: 3,900,282 (GRCm39) |
S196T |
probably benign |
Het |
Mdc1 |
C |
T |
17: 36,156,821 (GRCm39) |
A76V |
probably damaging |
Het |
Mei1 |
C |
T |
15: 81,970,383 (GRCm39) |
T428M |
probably damaging |
Het |
Mib2 |
A |
G |
4: 155,739,741 (GRCm39) |
F810S |
probably damaging |
Het |
Nobox |
T |
G |
6: 43,284,167 (GRCm39) |
K126N |
probably damaging |
Het |
Ogn |
C |
T |
13: 49,776,307 (GRCm39) |
L249F |
probably benign |
Het |
Or10ag59 |
A |
G |
2: 87,406,057 (GRCm39) |
I210V |
probably benign |
Het |
Or6a2 |
A |
T |
7: 106,600,682 (GRCm39) |
Y128* |
probably null |
Het |
Paqr8 |
A |
G |
1: 21,005,856 (GRCm39) |
T337A |
probably benign |
Het |
Pcdhb15 |
T |
A |
18: 37,606,810 (GRCm39) |
V14E |
probably damaging |
Het |
Perm1 |
A |
T |
4: 156,302,403 (GRCm39) |
I316L |
probably benign |
Het |
Plxnb2 |
G |
A |
15: 89,041,458 (GRCm39) |
|
probably benign |
Het |
Rab3il1 |
A |
T |
19: 10,007,841 (GRCm39) |
T227S |
probably benign |
Het |
Rag2 |
A |
T |
2: 101,461,121 (GRCm39) |
Y477F |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,263,551 (GRCm39) |
V722E |
possibly damaging |
Het |
Rbp3 |
A |
T |
14: 33,677,969 (GRCm39) |
E639V |
probably damaging |
Het |
Sh2b1 |
A |
G |
7: 126,067,959 (GRCm39) |
V565A |
probably damaging |
Het |
Skint6 |
T |
C |
4: 112,700,096 (GRCm39) |
|
probably benign |
Het |
Slc47a1 |
C |
T |
11: 61,235,207 (GRCm39) |
R542Q |
possibly damaging |
Het |
Slc6a5 |
T |
C |
7: 49,586,062 (GRCm39) |
|
probably null |
Het |
Slc9a8 |
C |
A |
2: 167,299,272 (GRCm39) |
H215N |
probably benign |
Het |
Slit1 |
C |
T |
19: 41,635,406 (GRCm39) |
|
probably null |
Het |
Snx1 |
A |
T |
9: 66,012,933 (GRCm39) |
|
probably null |
Het |
Tbc1d30 |
T |
A |
10: 121,108,073 (GRCm39) |
N443I |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,061,443 (GRCm39) |
M565K |
probably benign |
Het |
Traf3ip1 |
T |
C |
1: 91,428,639 (GRCm39) |
|
probably benign |
Het |
Traf3ip1 |
A |
G |
1: 91,446,019 (GRCm39) |
D384G |
probably damaging |
Het |
Vldlr |
G |
A |
19: 27,215,731 (GRCm39) |
E243K |
probably damaging |
Het |
Vps35 |
A |
G |
8: 86,001,460 (GRCm39) |
S453P |
probably benign |
Het |
Zfp644 |
A |
G |
5: 106,784,249 (GRCm39) |
V766A |
probably benign |
Het |
|
Other mutations in Dhrs7c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02031:Dhrs7c
|
APN |
11 |
67,706,715 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02168:Dhrs7c
|
APN |
11 |
67,706,693 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02198:Dhrs7c
|
APN |
11 |
67,706,628 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1403:Dhrs7c
|
UTSW |
11 |
67,702,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Dhrs7c
|
UTSW |
11 |
67,702,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R1617:Dhrs7c
|
UTSW |
11 |
67,705,903 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2380:Dhrs7c
|
UTSW |
11 |
67,706,690 (GRCm39) |
missense |
probably benign |
0.22 |
R2972:Dhrs7c
|
UTSW |
11 |
67,706,697 (GRCm39) |
missense |
possibly damaging |
0.67 |
R3432:Dhrs7c
|
UTSW |
11 |
67,700,699 (GRCm39) |
missense |
probably benign |
0.00 |
R4498:Dhrs7c
|
UTSW |
11 |
67,706,706 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4886:Dhrs7c
|
UTSW |
11 |
67,700,620 (GRCm39) |
missense |
probably damaging |
0.97 |
R5202:Dhrs7c
|
UTSW |
11 |
67,706,627 (GRCm39) |
missense |
probably benign |
0.03 |
R6140:Dhrs7c
|
UTSW |
11 |
67,705,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R7157:Dhrs7c
|
UTSW |
11 |
67,700,722 (GRCm39) |
critical splice donor site |
probably null |
|
R7598:Dhrs7c
|
UTSW |
11 |
67,702,279 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7774:Dhrs7c
|
UTSW |
11 |
67,700,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R9721:Dhrs7c
|
UTSW |
11 |
67,705,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R9749:Dhrs7c
|
UTSW |
11 |
67,702,479 (GRCm39) |
missense |
probably damaging |
0.97 |
|