Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
C |
10: 100,610,665 (GRCm38) |
L257S |
probably damaging |
Het |
2210010C04Rik |
T |
C |
6: 41,032,957 (GRCm38) |
T148A |
probably benign |
Het |
Abca13 |
A |
G |
11: 9,314,545 (GRCm38) |
S2976G |
probably benign |
Het |
Afmid |
T |
C |
11: 117,836,426 (GRCm38) |
W267R |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 21,058,177 (GRCm38) |
K969R |
probably benign |
Het |
Aldh1l1 |
A |
G |
6: 90,594,656 (GRCm38) |
|
probably benign |
Het |
Ank3 |
A |
G |
10: 69,808,892 (GRCm38) |
H62R |
probably damaging |
Het |
Arid2 |
T |
C |
15: 96,358,912 (GRCm38) |
|
probably benign |
Het |
BC030867 |
G |
A |
11: 102,260,165 (GRCm38) |
|
probably null |
Het |
Caps2 |
G |
A |
10: 112,204,023 (GRCm38) |
V457M |
probably benign |
Het |
Capza1 |
T |
C |
3: 104,864,371 (GRCm38) |
D3G |
possibly damaging |
Het |
Cav1 |
T |
A |
6: 17,307,972 (GRCm38) |
V41E |
possibly damaging |
Het |
Celf2 |
G |
T |
2: 6,604,177 (GRCm38) |
C264* |
probably null |
Het |
Clec4a2 |
C |
T |
6: 123,139,326 (GRCm38) |
S150L |
probably benign |
Het |
D7Ertd443e |
A |
T |
7: 134,349,400 (GRCm38) |
D181E |
possibly damaging |
Het |
Epyc |
A |
G |
10: 97,670,631 (GRCm38) |
E100G |
probably benign |
Het |
Hdac11 |
A |
G |
6: 91,173,102 (GRCm38) |
I294M |
probably damaging |
Het |
Hsdl1 |
A |
G |
8: 119,566,414 (GRCm38) |
V73A |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,311,343 (GRCm38) |
S2501T |
probably benign |
Het |
Map3k19 |
C |
A |
1: 127,823,170 (GRCm38) |
G815C |
probably benign |
Het |
Muc13 |
C |
A |
16: 33,799,479 (GRCm38) |
T199K |
unknown |
Het |
Nif3l1 |
G |
T |
1: 58,447,946 (GRCm38) |
|
probably null |
Het |
Nlrp12 |
A |
T |
7: 3,249,545 (GRCm38) |
|
probably benign |
Het |
Nup205 |
T |
C |
6: 35,189,178 (GRCm38) |
S244P |
probably damaging |
Het |
Olfr1353 |
A |
T |
10: 78,969,901 (GRCm38) |
N84I |
probably damaging |
Het |
Parl |
G |
A |
16: 20,280,088 (GRCm38) |
|
probably benign |
Het |
Pax8 |
A |
G |
2: 24,440,788 (GRCm38) |
I211T |
possibly damaging |
Het |
Pglyrp4 |
A |
G |
3: 90,730,853 (GRCm38) |
E158G |
possibly damaging |
Het |
Plekhm1 |
A |
G |
11: 103,380,231 (GRCm38) |
L478P |
probably benign |
Het |
Serpina1a |
C |
T |
12: 103,854,706 (GRCm38) |
G338R |
probably damaging |
Het |
Serpina5 |
T |
C |
12: 104,105,298 (GRCm38) |
L388P |
possibly damaging |
Het |
Sorbs1 |
A |
G |
19: 40,327,596 (GRCm38) |
V367A |
probably damaging |
Het |
Srgap2 |
A |
G |
1: 131,319,666 (GRCm38) |
|
probably benign |
Het |
Surf1 |
A |
G |
2: 26,915,651 (GRCm38) |
L26P |
probably damaging |
Het |
Taf4 |
A |
G |
2: 179,938,470 (GRCm38) |
S486P |
probably benign |
Het |
Tdrd6 |
A |
T |
17: 43,628,390 (GRCm38) |
V589E |
probably damaging |
Het |
Tuba3b |
T |
G |
6: 145,619,666 (GRCm38) |
S287A |
probably benign |
Het |
Txnrd3 |
G |
A |
6: 89,669,324 (GRCm38) |
R295H |
probably damaging |
Het |
Ubr5 |
G |
T |
15: 37,991,379 (GRCm38) |
|
probably benign |
Het |
Unc45b |
C |
T |
11: 82,940,181 (GRCm38) |
|
probably benign |
Het |
Usp32 |
A |
G |
11: 85,005,802 (GRCm38) |
|
probably null |
Het |
Utp23 |
G |
A |
15: 51,882,365 (GRCm38) |
R87K |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,466,484 (GRCm38) |
I405T |
possibly damaging |
Het |
|
Other mutations in Lrrc41 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01309:Lrrc41
|
APN |
4 |
116,096,466 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01358:Lrrc41
|
APN |
4 |
116,075,587 (GRCm38) |
missense |
probably benign |
0.16 |
IGL01734:Lrrc41
|
APN |
4 |
116,093,134 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01986:Lrrc41
|
APN |
4 |
116,089,322 (GRCm38) |
missense |
probably benign |
0.27 |
IGL02892:Lrrc41
|
APN |
4 |
116,088,835 (GRCm38) |
missense |
possibly damaging |
0.68 |
IGL03135:Lrrc41
|
APN |
4 |
116,088,531 (GRCm38) |
missense |
probably benign |
|
R1478:Lrrc41
|
UTSW |
4 |
116,095,208 (GRCm38) |
nonsense |
probably null |
|
R1765:Lrrc41
|
UTSW |
4 |
116,089,051 (GRCm38) |
missense |
possibly damaging |
0.94 |
R2233:Lrrc41
|
UTSW |
4 |
116,096,385 (GRCm38) |
missense |
possibly damaging |
0.66 |
R4080:Lrrc41
|
UTSW |
4 |
116,080,546 (GRCm38) |
splice site |
probably null |
|
R4677:Lrrc41
|
UTSW |
4 |
116,095,135 (GRCm38) |
missense |
probably benign |
|
R4833:Lrrc41
|
UTSW |
4 |
116,093,177 (GRCm38) |
unclassified |
probably benign |
|
R4877:Lrrc41
|
UTSW |
4 |
116,079,405 (GRCm38) |
missense |
probably damaging |
0.99 |
R4926:Lrrc41
|
UTSW |
4 |
116,089,324 (GRCm38) |
missense |
possibly damaging |
0.46 |
R6459:Lrrc41
|
UTSW |
4 |
116,088,780 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6817:Lrrc41
|
UTSW |
4 |
116,089,305 (GRCm38) |
missense |
possibly damaging |
0.66 |
R6834:Lrrc41
|
UTSW |
4 |
116,096,529 (GRCm38) |
missense |
possibly damaging |
0.46 |
R7479:Lrrc41
|
UTSW |
4 |
116,089,041 (GRCm38) |
missense |
probably damaging |
0.96 |
R7512:Lrrc41
|
UTSW |
4 |
116,092,994 (GRCm38) |
missense |
possibly damaging |
0.66 |
R7593:Lrrc41
|
UTSW |
4 |
116,092,944 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8006:Lrrc41
|
UTSW |
4 |
116,094,888 (GRCm38) |
missense |
possibly damaging |
0.79 |
R8810:Lrrc41
|
UTSW |
4 |
116,075,291 (GRCm38) |
unclassified |
probably benign |
|
R9134:Lrrc41
|
UTSW |
4 |
116,088,585 (GRCm38) |
missense |
possibly damaging |
0.89 |
R9495:Lrrc41
|
UTSW |
4 |
116,075,609 (GRCm38) |
critical splice donor site |
probably null |
|
|