Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
G |
A |
4: 124,504,369 (GRCm39) |
T61M |
unknown |
Het |
Adam34l |
T |
A |
8: 44,078,615 (GRCm39) |
R536S |
probably benign |
Het |
Ambn |
T |
C |
5: 88,613,149 (GRCm39) |
F217L |
probably benign |
Het |
Cast |
T |
C |
13: 74,876,484 (GRCm39) |
D121G |
possibly damaging |
Het |
Clmn |
T |
C |
12: 104,747,358 (GRCm39) |
I730V |
probably benign |
Het |
Cryzl1 |
T |
C |
16: 91,509,139 (GRCm39) |
K54R |
possibly damaging |
Het |
Cyp3a16 |
A |
G |
5: 145,392,290 (GRCm39) |
S222P |
probably benign |
Het |
Dcstamp |
T |
C |
15: 39,617,854 (GRCm39) |
S88P |
probably damaging |
Het |
F5 |
A |
G |
1: 164,020,243 (GRCm39) |
D906G |
possibly damaging |
Het |
Fam193a |
A |
G |
5: 34,602,081 (GRCm39) |
T428A |
probably benign |
Het |
Fbxw16 |
T |
G |
9: 109,265,754 (GRCm39) |
D355A |
probably benign |
Het |
Focad |
T |
C |
4: 88,047,291 (GRCm39) |
|
probably null |
Het |
Ftsj3 |
G |
A |
11: 106,145,489 (GRCm39) |
P82S |
possibly damaging |
Het |
Grwd1 |
A |
T |
7: 45,476,667 (GRCm39) |
H307Q |
probably damaging |
Het |
Hip1r |
T |
C |
5: 124,134,307 (GRCm39) |
F289S |
probably damaging |
Het |
Igkc |
C |
T |
6: 70,703,559 (GRCm39) |
R47* |
probably null |
Het |
Lmnb1 |
T |
C |
18: 56,882,871 (GRCm39) |
F572S |
probably benign |
Het |
Mrps17 |
T |
A |
5: 129,793,860 (GRCm39) |
I18N |
probably damaging |
Het |
Myo9a |
G |
A |
9: 59,687,275 (GRCm39) |
V127I |
probably benign |
Het |
Or2l13b |
T |
C |
16: 19,349,640 (GRCm39) |
D10G |
probably benign |
Het |
Or4c35 |
T |
C |
2: 89,808,773 (GRCm39) |
V217A |
possibly damaging |
Het |
Or5g23 |
T |
A |
2: 85,438,574 (GRCm39) |
K227* |
probably null |
Het |
Pcdhb21 |
A |
G |
18: 37,648,299 (GRCm39) |
D476G |
probably damaging |
Het |
Pkd2l2 |
T |
A |
18: 34,545,768 (GRCm39) |
Y56* |
probably null |
Het |
Pld1 |
C |
A |
3: 28,174,961 (GRCm39) |
D86E |
probably damaging |
Het |
Plpp1 |
A |
G |
13: 112,993,433 (GRCm39) |
T122A |
probably benign |
Het |
Prkag3 |
A |
G |
1: 74,779,883 (GRCm39) |
I484T |
probably benign |
Het |
Prl7d1 |
T |
A |
13: 27,896,066 (GRCm39) |
I104F |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,984,876 (GRCm39) |
S1540P |
probably damaging |
Het |
Pyroxd1 |
T |
G |
6: 142,300,457 (GRCm39) |
S196A |
probably benign |
Het |
Rbm42 |
G |
A |
7: 30,345,130 (GRCm39) |
P185S |
unknown |
Het |
Ror2 |
T |
A |
13: 53,265,200 (GRCm39) |
I619F |
probably damaging |
Het |
Slitrk4 |
T |
G |
X: 63,314,555 (GRCm39) |
E704A |
probably benign |
Het |
Sycp1 |
A |
G |
3: 102,772,430 (GRCm39) |
V626A |
probably benign |
Het |
Trmt44 |
T |
A |
5: 35,726,143 (GRCm39) |
K345* |
probably null |
Het |
Ugt1a6b |
T |
A |
1: 88,035,527 (GRCm39) |
|
probably benign |
Het |
Ulk4 |
T |
A |
9: 120,970,897 (GRCm39) |
|
probably null |
Het |
Zfp618 |
G |
T |
4: 63,051,773 (GRCm39) |
K758N |
probably damaging |
Het |
Zfp819 |
G |
T |
7: 43,261,534 (GRCm39) |
|
probably null |
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 |
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 |
|
R7010:Lcn3
|
UTSW |
2 |
25,656,068 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|