Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
C |
T |
19: 3,767,364 (GRCm39) |
T317I |
possibly damaging |
Het |
Adamts7 |
T |
A |
9: 90,077,251 (GRCm39) |
V1306E |
probably damaging |
Het |
Adcy9 |
C |
T |
16: 4,106,547 (GRCm39) |
D1093N |
probably damaging |
Het |
Adgra3 |
A |
G |
5: 50,164,250 (GRCm39) |
V243A |
probably damaging |
Het |
Aqp4 |
C |
T |
18: 15,526,687 (GRCm39) |
A265T |
probably benign |
Het |
Atad2 |
A |
T |
15: 57,970,119 (GRCm39) |
|
probably null |
Het |
Atp13a4 |
A |
G |
16: 29,260,398 (GRCm39) |
V560A |
|
Het |
Best2 |
A |
C |
8: 85,740,051 (GRCm39) |
C38G |
|
Het |
Bicra |
A |
T |
7: 15,705,880 (GRCm39) |
S1520R |
probably damaging |
Het |
C1s2 |
A |
G |
6: 124,602,588 (GRCm39) |
L541P |
probably damaging |
Het |
Calcoco2 |
T |
A |
11: 95,991,185 (GRCm39) |
H184L |
probably benign |
Het |
Cav1 |
A |
T |
6: 17,339,403 (GRCm39) |
I163F |
probably benign |
Het |
Cep57l1 |
T |
C |
10: 41,597,563 (GRCm39) |
H356R |
probably damaging |
Het |
Clu |
A |
C |
14: 66,208,851 (GRCm39) |
H32P |
unknown |
Het |
Col5a1 |
T |
A |
2: 27,879,186 (GRCm39) |
D840E |
unknown |
Het |
Cramp1 |
C |
A |
17: 25,201,783 (GRCm39) |
K566N |
probably damaging |
Het |
Csmd1 |
C |
A |
8: 16,208,239 (GRCm39) |
V1239L |
probably benign |
Het |
Cubn |
T |
A |
2: 13,482,945 (GRCm39) |
Q267L |
probably benign |
Het |
Cul7 |
C |
T |
17: 46,975,212 (GRCm39) |
R1689W |
probably damaging |
Het |
Dao |
A |
T |
5: 114,152,060 (GRCm39) |
D126V |
probably benign |
Het |
Eif3l |
T |
C |
15: 78,978,423 (GRCm39) |
M560T |
probably benign |
Het |
F830016B08Rik |
T |
A |
18: 60,433,379 (GRCm39) |
I154N |
probably damaging |
Het |
Fam184a |
T |
C |
10: 53,517,144 (GRCm39) |
E980G |
probably damaging |
Het |
Fgf21 |
T |
C |
7: 45,264,703 (GRCm39) |
T10A |
probably benign |
Het |
Fhad1 |
A |
C |
4: 141,678,882 (GRCm39) |
V598G |
possibly damaging |
Het |
Foxc1 |
A |
T |
13: 31,991,863 (GRCm39) |
I225F |
possibly damaging |
Het |
Foxo3 |
C |
T |
10: 42,073,021 (GRCm39) |
V499M |
probably damaging |
Het |
Galnt9 |
G |
A |
5: 110,744,047 (GRCm39) |
G294S |
probably damaging |
Het |
Gp5 |
A |
C |
16: 30,128,393 (GRCm39) |
F94V |
probably damaging |
Het |
Idh2 |
A |
T |
7: 79,747,925 (GRCm39) |
Y258* |
probably null |
Het |
Immp2l |
T |
C |
12: 41,160,933 (GRCm39) |
V77A |
probably damaging |
Het |
Isl1 |
T |
C |
13: 116,441,924 (GRCm39) |
E103G |
|
Het |
Itgad |
A |
T |
7: 127,803,022 (GRCm39) |
T1059S |
probably damaging |
Het |
Kcnj6 |
G |
A |
16: 94,633,307 (GRCm39) |
T268I |
probably damaging |
Het |
Lgals3bp |
A |
G |
11: 118,284,037 (GRCm39) |
V514A |
probably benign |
Het |
Mcfd2 |
A |
T |
17: 87,565,421 (GRCm39) |
H27Q |
probably benign |
Het |
Mettl13 |
A |
G |
1: 162,364,769 (GRCm39) |
W537R |
probably damaging |
Het |
Mybl2 |
G |
T |
2: 162,906,225 (GRCm39) |
G102V |
probably damaging |
Het |
Nat8f3 |
A |
T |
6: 85,738,708 (GRCm39) |
V18E |
|
Het |
Npepps |
T |
C |
11: 97,149,177 (GRCm39) |
E115G |
probably benign |
Het |
Odad3 |
T |
C |
9: 21,904,310 (GRCm39) |
D322G |
probably benign |
Het |
Oog2 |
T |
A |
4: 143,922,707 (GRCm39) |
V324E |
probably damaging |
Het |
Or2y12 |
T |
A |
11: 49,426,071 (GRCm39) |
W20R |
probably damaging |
Het |
Or7g12 |
A |
T |
9: 18,899,526 (GRCm39) |
M81L |
possibly damaging |
Het |
Or8d2b |
G |
A |
9: 38,789,281 (GRCm39) |
V270M |
probably damaging |
Het |
Or8j3b |
A |
G |
2: 86,205,012 (GRCm39) |
V248A |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,375,486 (GRCm39) |
S1550P |
probably damaging |
Het |
Peg10 |
T |
TCCC |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Pms2 |
T |
C |
5: 143,854,420 (GRCm39) |
V243A |
probably benign |
Het |
Ptpn9 |
A |
G |
9: 56,944,005 (GRCm39) |
D293G |
probably benign |
Het |
Ptprb |
A |
G |
10: 116,203,441 (GRCm39) |
K1784R |
probably damaging |
Het |
Rab23 |
CAA |
CA |
1: 33,764,077 (GRCm39) |
|
probably null |
Het |
Raf1 |
T |
C |
6: 115,596,597 (GRCm39) |
N576D |
probably benign |
Het |
Rasa4 |
C |
A |
5: 136,140,343 (GRCm39) |
H782Q |
possibly damaging |
Het |
Rims1 |
C |
A |
1: 22,491,969 (GRCm39) |
E168* |
probably null |
Het |
Rpgrip1l |
A |
T |
8: 91,987,434 (GRCm39) |
N874K |
possibly damaging |
Het |
Rxfp4 |
C |
T |
3: 88,559,969 (GRCm39) |
V161I |
possibly damaging |
Het |
Scel |
G |
A |
14: 103,843,032 (GRCm39) |
G558D |
probably damaging |
Het |
Sipa1l2 |
T |
C |
8: 126,196,565 (GRCm39) |
K723R |
probably null |
Het |
Slc12a1 |
A |
T |
2: 125,002,445 (GRCm39) |
R142W |
probably damaging |
Het |
Slc27a2 |
T |
A |
2: 126,409,736 (GRCm39) |
V306D |
probably damaging |
Het |
Sox4 |
C |
T |
13: 29,136,079 (GRCm39) |
G309D |
probably damaging |
Het |
Terb1 |
T |
C |
8: 105,223,476 (GRCm39) |
T111A |
probably benign |
Het |
Tgfa |
G |
A |
6: 86,248,397 (GRCm39) |
R133H |
probably damaging |
Het |
Ticrr |
T |
C |
7: 79,345,754 (GRCm39) |
S1836P |
probably damaging |
Het |
Tlk2 |
A |
G |
11: 105,138,328 (GRCm39) |
D292G |
probably benign |
Het |
Tmc7 |
A |
G |
7: 118,141,160 (GRCm39) |
I657T |
probably benign |
Het |
Tmprss11c |
G |
A |
5: 86,383,379 (GRCm39) |
T349I |
probably benign |
Het |
Trhr |
A |
G |
15: 44,060,981 (GRCm39) |
N167S |
probably benign |
Het |
Tsc22d1 |
T |
G |
14: 76,653,983 (GRCm39) |
I154S |
probably damaging |
Het |
Vmn1r2 |
T |
C |
4: 3,172,587 (GRCm39) |
Y169H |
probably damaging |
Het |
Vmn1r77 |
G |
T |
7: 11,775,766 (GRCm39) |
V181L |
probably benign |
Het |
|
Other mutations in Nars2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00796:Nars2
|
APN |
7 |
96,680,787 (GRCm39) |
missense |
probably benign |
0.40 |
IGL00796:Nars2
|
APN |
7 |
96,680,786 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00990:Nars2
|
APN |
7 |
96,651,997 (GRCm39) |
splice site |
probably benign |
|
IGL02954:Nars2
|
APN |
7 |
96,689,100 (GRCm39) |
splice site |
probably null |
|
IGL03256:Nars2
|
APN |
7 |
96,689,117 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL03394:Nars2
|
APN |
7 |
96,689,220 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0600:Nars2
|
UTSW |
7 |
96,689,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0943:Nars2
|
UTSW |
7 |
96,605,138 (GRCm39) |
splice site |
probably benign |
|
R1389:Nars2
|
UTSW |
7 |
96,652,036 (GRCm39) |
missense |
probably benign |
|
R4076:Nars2
|
UTSW |
7 |
96,607,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R4397:Nars2
|
UTSW |
7 |
96,622,771 (GRCm39) |
critical splice donor site |
probably null |
|
R4758:Nars2
|
UTSW |
7 |
96,622,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Nars2
|
UTSW |
7 |
96,684,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Nars2
|
UTSW |
7 |
96,672,948 (GRCm39) |
missense |
probably benign |
0.07 |
R5162:Nars2
|
UTSW |
7 |
96,709,027 (GRCm39) |
utr 3 prime |
probably benign |
|
R6209:Nars2
|
UTSW |
7 |
96,706,728 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Nars2
|
UTSW |
7 |
96,689,137 (GRCm39) |
missense |
probably benign |
0.40 |
R7979:Nars2
|
UTSW |
7 |
96,711,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R8284:Nars2
|
UTSW |
7 |
96,600,845 (GRCm39) |
utr 5 prime |
probably benign |
|
R8885:Nars2
|
UTSW |
7 |
96,652,095 (GRCm39) |
missense |
probably damaging |
0.98 |
R9658:Nars2
|
UTSW |
7 |
96,689,178 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Nars2
|
UTSW |
7 |
96,601,104 (GRCm39) |
missense |
probably benign |
0.04 |
|