Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AL592187.3 |
A |
T |
15: 77,486,797 (GRCm39) |
Y58F |
probably benign |
Het |
Ano10 |
T |
C |
9: 122,082,190 (GRCm39) |
T494A |
probably damaging |
Het |
Asah2 |
A |
T |
19: 32,031,954 (GRCm39) |
F72I |
probably benign |
Het |
Atat1 |
T |
C |
17: 36,219,522 (GRCm39) |
D114G |
probably damaging |
Het |
Atp6v1e2 |
C |
T |
17: 87,251,773 (GRCm39) |
M208I |
probably benign |
Het |
Bicd1 |
A |
G |
6: 149,396,113 (GRCm39) |
Y161C |
probably damaging |
Het |
Camk2g |
T |
C |
14: 20,791,512 (GRCm39) |
S410G |
probably benign |
Het |
Car2 |
C |
T |
3: 14,965,113 (GRCm39) |
P249L |
possibly damaging |
Het |
Cdh23 |
T |
G |
10: 60,366,770 (GRCm39) |
I237L |
probably benign |
Het |
Dlat |
T |
A |
9: 50,569,274 (GRCm39) |
K176N |
probably damaging |
Het |
Dnajc12 |
T |
A |
10: 63,233,059 (GRCm39) |
C67S |
probably benign |
Het |
Fat1 |
G |
T |
8: 45,406,386 (GRCm39) |
E1046* |
probably null |
Het |
Gmip |
G |
A |
8: 70,264,050 (GRCm39) |
A137T |
probably damaging |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Grk6 |
A |
G |
13: 55,598,113 (GRCm39) |
I62V |
possibly damaging |
Het |
Hook1 |
G |
T |
4: 95,903,048 (GRCm39) |
L512F |
probably damaging |
Het |
Ighe |
T |
C |
12: 113,236,761 (GRCm39) |
T36A |
|
Het |
Il17rc |
A |
G |
6: 113,456,249 (GRCm39) |
N338S |
possibly damaging |
Het |
Itgb6 |
T |
C |
2: 60,480,322 (GRCm39) |
Y338C |
probably damaging |
Het |
Kcnd2 |
A |
G |
6: 21,216,707 (GRCm39) |
Y137C |
probably damaging |
Het |
L3mbtl3 |
T |
A |
10: 26,158,759 (GRCm39) |
|
probably null |
Het |
Map3k8 |
T |
C |
18: 4,334,060 (GRCm39) |
H344R |
probably damaging |
Het |
Marf1 |
A |
T |
16: 13,954,865 (GRCm39) |
I884N |
probably damaging |
Het |
Nalcn |
G |
A |
14: 123,530,877 (GRCm39) |
T1387I |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,962,398 (GRCm39) |
T540A |
probably damaging |
Het |
Or5p63 |
A |
T |
7: 107,811,349 (GRCm39) |
I129N |
probably damaging |
Het |
Pank2 |
T |
C |
2: 131,122,293 (GRCm39) |
Y273H |
probably benign |
Het |
Pgrmc2 |
A |
G |
3: 41,037,068 (GRCm39) |
V121A |
probably damaging |
Het |
Phldb2 |
C |
T |
16: 45,571,868 (GRCm39) |
V1175M |
probably damaging |
Het |
Prss3b |
A |
C |
6: 41,009,247 (GRCm39) |
S196A |
probably benign |
Het |
Ranbp2 |
A |
G |
10: 58,290,393 (GRCm39) |
|
probably null |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Syt7 |
A |
G |
19: 10,395,354 (GRCm39) |
T55A |
probably benign |
Het |
Tfcp2l1 |
T |
C |
1: 118,581,457 (GRCm39) |
S137P |
probably damaging |
Het |
Tom1 |
T |
A |
8: 75,778,603 (GRCm39) |
V140D |
probably damaging |
Het |
Ttc23l |
T |
G |
15: 10,515,224 (GRCm39) |
I385L |
probably damaging |
Het |
Vmn1r122 |
A |
G |
7: 20,867,896 (GRCm39) |
V53A |
probably damaging |
Het |
Vmn2r1 |
C |
T |
3: 64,012,146 (GRCm39) |
T669I |
probably benign |
Het |
Vmn2r86 |
A |
G |
10: 130,291,726 (GRCm39) |
L13P |
probably benign |
Het |
Zfp958 |
T |
C |
8: 4,678,377 (GRCm39) |
I134T |
probably benign |
Het |
|
Other mutations in Lcn3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02041:Lcn3
|
APN |
2 |
25,655,636 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02139:Lcn3
|
APN |
2 |
25,656,646 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02221:Lcn3
|
APN |
2 |
25,656,172 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02665:Lcn3
|
APN |
2 |
25,656,416 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03049:Lcn3
|
APN |
2 |
25,655,586 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R0552:Lcn3
|
UTSW |
2 |
25,656,421 (GRCm39) |
critical splice donor site |
probably null |
|
R3522:Lcn3
|
UTSW |
2 |
25,656,133 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4227:Lcn3
|
UTSW |
2 |
25,656,123 (GRCm39) |
missense |
probably benign |
0.00 |
R6684:Lcn3
|
UTSW |
2 |
25,656,170 (GRCm39) |
missense |
probably benign |
0.00 |
R6937:Lcn3
|
UTSW |
2 |
25,657,823 (GRCm39) |
nonsense |
probably null |
|
R7487:Lcn3
|
UTSW |
2 |
25,656,174 (GRCm39) |
critical splice donor site |
probably null |
|
R7966:Lcn3
|
UTSW |
2 |
25,656,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R8553:Lcn3
|
UTSW |
2 |
25,656,347 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9544:Lcn3
|
UTSW |
2 |
25,656,151 (GRCm39) |
missense |
probably benign |
|
R9609:Lcn3
|
UTSW |
2 |
25,657,596 (GRCm39) |
missense |
possibly damaging |
0.88 |
|