Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Abca14 |
T |
A |
7: 119,888,769 (GRCm39) |
Y1238* |
probably null |
Het |
Abcb5 |
A |
T |
12: 118,831,677 (GRCm39) |
V1225D |
probably damaging |
Het |
Arhgef15 |
A |
G |
11: 68,838,022 (GRCm39) |
|
probably benign |
Het |
As3mt |
A |
G |
19: 46,696,635 (GRCm39) |
R58G |
probably null |
Het |
Asap1 |
T |
G |
15: 63,999,263 (GRCm39) |
N525T |
possibly damaging |
Het |
Bhmt2 |
A |
G |
13: 93,807,938 (GRCm39) |
V50A |
probably benign |
Het |
Bpnt2 |
A |
C |
4: 4,767,963 (GRCm39) |
V271G |
possibly damaging |
Het |
Ccdc180 |
A |
T |
4: 45,890,935 (GRCm39) |
I36F |
possibly damaging |
Het |
Cd209c |
A |
G |
8: 3,994,976 (GRCm39) |
S63P |
probably damaging |
Het |
Cdc37 |
T |
C |
9: 21,054,457 (GRCm39) |
E56G |
possibly damaging |
Het |
Cdkal1 |
T |
C |
13: 29,510,135 (GRCm39) |
Y541C |
probably benign |
Het |
Cenph |
G |
T |
13: 100,898,280 (GRCm39) |
H208N |
probably benign |
Het |
Cfap65 |
A |
T |
1: 74,942,334 (GRCm39) |
L1740Q |
probably benign |
Het |
Cfap74 |
A |
G |
4: 155,521,197 (GRCm39) |
D623G |
probably damaging |
Het |
Ckap4 |
C |
A |
10: 84,363,474 (GRCm39) |
V530L |
probably damaging |
Het |
Cldn13 |
A |
T |
5: 134,943,869 (GRCm39) |
N105K |
probably benign |
Het |
Ddn |
T |
C |
15: 98,703,237 (GRCm39) |
D685G |
possibly damaging |
Het |
Fdxr |
T |
C |
11: 115,163,084 (GRCm39) |
I70V |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,663,339 (GRCm39) |
Y1050N |
probably damaging |
Het |
Iqcf3 |
A |
G |
9: 106,430,860 (GRCm39) |
I96T |
possibly damaging |
Het |
Itgax |
A |
G |
7: 127,741,455 (GRCm39) |
Y822C |
probably damaging |
Het |
Katnb1 |
A |
T |
8: 95,822,234 (GRCm39) |
I286L |
possibly damaging |
Het |
Lrp2 |
A |
C |
2: 69,355,572 (GRCm39) |
I424R |
probably benign |
Het |
Lrpprc |
C |
A |
17: 85,097,821 (GRCm39) |
A41S |
probably benign |
Het |
Mast3 |
A |
G |
8: 71,236,145 (GRCm39) |
L761P |
probably benign |
Het |
Mmp1b |
T |
C |
9: 7,384,897 (GRCm39) |
I251V |
possibly damaging |
Het |
Mpp4 |
C |
A |
1: 59,196,600 (GRCm39) |
R44L |
probably benign |
Het |
Nkain3 |
T |
A |
4: 20,484,889 (GRCm39) |
M63L |
probably benign |
Het |
Nup88 |
A |
C |
11: 70,835,842 (GRCm39) |
|
probably benign |
Het |
Obscn |
A |
T |
11: 58,953,518 (GRCm39) |
C3837S |
probably damaging |
Het |
Ogdh |
T |
G |
11: 6,302,126 (GRCm39) |
L850V |
probably damaging |
Het |
Or4f17-ps1 |
A |
G |
2: 111,358,048 (GRCm39) |
I148V |
probably benign |
Het |
Or5w11 |
A |
G |
2: 87,459,458 (GRCm39) |
Y217C |
probably damaging |
Het |
Panx2 |
T |
C |
15: 88,952,742 (GRCm39) |
I411T |
possibly damaging |
Het |
Papss1 |
T |
A |
3: 131,348,805 (GRCm39) |
M585K |
probably damaging |
Het |
Pcbp2 |
T |
G |
15: 102,394,456 (GRCm39) |
L180R |
possibly damaging |
Het |
Pcdha7 |
A |
T |
18: 37,107,619 (GRCm39) |
T215S |
probably benign |
Het |
Pcdhga4 |
C |
T |
18: 37,818,477 (GRCm39) |
R9C |
probably benign |
Het |
Plin4 |
A |
G |
17: 56,411,970 (GRCm39) |
V687A |
probably benign |
Het |
Potefam1 |
A |
T |
2: 111,024,682 (GRCm39) |
Y61N |
possibly damaging |
Het |
Psma6 |
A |
G |
12: 55,454,213 (GRCm39) |
|
probably benign |
Het |
Rcn1 |
A |
T |
2: 105,219,471 (GRCm39) |
S241T |
probably benign |
Het |
Scgb2b18 |
A |
T |
7: 32,872,700 (GRCm39) |
L35H |
probably damaging |
Het |
Slc11a1 |
A |
C |
1: 74,423,304 (GRCm39) |
D385A |
probably damaging |
Het |
Stk31 |
T |
A |
6: 49,446,086 (GRCm39) |
C930S |
probably benign |
Het |
Syt10 |
T |
A |
15: 89,725,932 (GRCm39) |
Q14L |
probably benign |
Het |
Tnxb |
T |
G |
17: 34,909,205 (GRCm39) |
W1578G |
probably damaging |
Het |
Triml1 |
C |
T |
8: 43,583,327 (GRCm39) |
A425T |
possibly damaging |
Het |
Vil1 |
G |
A |
1: 74,471,549 (GRCm39) |
V777I |
probably benign |
Het |
Vmn1r175 |
T |
C |
7: 23,508,004 (GRCm39) |
I208V |
possibly damaging |
Het |
|
Other mutations in Nalf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01860:Nalf1
|
APN |
8 |
9,257,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02513:Nalf1
|
APN |
8 |
9,257,930 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02817:Nalf1
|
APN |
8 |
9,257,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03194:Nalf1
|
APN |
8 |
9,282,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R0842:Nalf1
|
UTSW |
8 |
9,820,114 (GRCm39) |
missense |
probably benign |
0.26 |
R1928:Nalf1
|
UTSW |
8 |
9,820,217 (GRCm39) |
missense |
probably benign |
|
R2004:Nalf1
|
UTSW |
8 |
9,820,607 (GRCm39) |
missense |
probably benign |
0.00 |
R4155:Nalf1
|
UTSW |
8 |
9,283,023 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4783:Nalf1
|
UTSW |
8 |
9,258,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5019:Nalf1
|
UTSW |
8 |
9,820,240 (GRCm39) |
missense |
probably benign |
0.13 |
R6798:Nalf1
|
UTSW |
8 |
9,820,205 (GRCm39) |
nonsense |
probably null |
|
R6956:Nalf1
|
UTSW |
8 |
9,820,744 (GRCm39) |
missense |
probably benign |
0.36 |
R7034:Nalf1
|
UTSW |
8 |
9,820,589 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8039:Nalf1
|
UTSW |
8 |
9,257,892 (GRCm39) |
missense |
probably benign |
0.03 |
R8382:Nalf1
|
UTSW |
8 |
9,257,972 (GRCm39) |
missense |
probably benign |
0.05 |
R9299:Nalf1
|
UTSW |
8 |
9,820,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R9342:Nalf1
|
UTSW |
8 |
9,821,006 (GRCm39) |
missense |
probably damaging |
0.99 |
R9658:Nalf1
|
UTSW |
8 |
9,820,114 (GRCm39) |
missense |
probably benign |
0.00 |
|