Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
C |
10: 100,446,527 (GRCm39) |
L257S |
probably damaging |
Het |
Abca13 |
A |
G |
11: 9,264,545 (GRCm39) |
S2976G |
probably benign |
Het |
Afmid |
T |
C |
11: 117,727,252 (GRCm39) |
W267R |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,934,076 (GRCm39) |
K969R |
probably benign |
Het |
Aldh1l1 |
A |
G |
6: 90,571,638 (GRCm39) |
|
probably benign |
Het |
Ank3 |
A |
G |
10: 69,644,722 (GRCm39) |
H62R |
probably damaging |
Het |
Arid2 |
T |
C |
15: 96,256,793 (GRCm39) |
|
probably benign |
Het |
Caps2 |
G |
A |
10: 112,039,928 (GRCm39) |
V457M |
probably benign |
Het |
Capza1 |
T |
C |
3: 104,771,687 (GRCm39) |
D3G |
possibly damaging |
Het |
Cav1 |
T |
A |
6: 17,307,971 (GRCm39) |
V41E |
possibly damaging |
Het |
Celf2 |
G |
T |
2: 6,608,988 (GRCm39) |
C264* |
probably null |
Het |
Clec4a2 |
C |
T |
6: 123,116,285 (GRCm39) |
S150L |
probably benign |
Het |
D7Ertd443e |
A |
T |
7: 133,951,129 (GRCm39) |
D181E |
possibly damaging |
Het |
Epyc |
A |
G |
10: 97,506,493 (GRCm39) |
E100G |
probably benign |
Het |
Hdac11 |
A |
G |
6: 91,150,084 (GRCm39) |
I294M |
probably damaging |
Het |
Hrob |
G |
A |
11: 102,150,991 (GRCm39) |
|
probably null |
Het |
Hsdl1 |
A |
G |
8: 120,293,153 (GRCm39) |
V73A |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,516,341 (GRCm39) |
S2501T |
probably benign |
Het |
Map3k19 |
C |
A |
1: 127,750,907 (GRCm39) |
G815C |
probably benign |
Het |
Muc13 |
C |
A |
16: 33,619,849 (GRCm39) |
T199K |
unknown |
Het |
Nif3l1 |
G |
T |
1: 58,487,105 (GRCm39) |
|
probably null |
Het |
Nlrp12 |
A |
T |
7: 3,298,175 (GRCm39) |
|
probably benign |
Het |
Nup205 |
T |
C |
6: 35,166,113 (GRCm39) |
S244P |
probably damaging |
Het |
Or7a37 |
A |
T |
10: 78,805,735 (GRCm39) |
N84I |
probably damaging |
Het |
Parl |
G |
A |
16: 20,098,838 (GRCm39) |
|
probably benign |
Het |
Pax8 |
A |
G |
2: 24,330,800 (GRCm39) |
I211T |
possibly damaging |
Het |
Pglyrp4 |
A |
G |
3: 90,638,160 (GRCm39) |
E158G |
possibly damaging |
Het |
Plekhm1 |
A |
G |
11: 103,271,057 (GRCm39) |
L478P |
probably benign |
Het |
Prss3b |
T |
C |
6: 41,009,891 (GRCm39) |
T148A |
probably benign |
Het |
Serpina1a |
C |
T |
12: 103,820,965 (GRCm39) |
G338R |
probably damaging |
Het |
Serpina5 |
T |
C |
12: 104,071,557 (GRCm39) |
L388P |
possibly damaging |
Het |
Sorbs1 |
A |
G |
19: 40,316,040 (GRCm39) |
V367A |
probably damaging |
Het |
Srgap2 |
A |
G |
1: 131,247,404 (GRCm39) |
|
probably benign |
Het |
Surf1 |
A |
G |
2: 26,805,663 (GRCm39) |
L26P |
probably damaging |
Het |
Taf4 |
A |
G |
2: 179,580,263 (GRCm39) |
S486P |
probably benign |
Het |
Tdrd6 |
A |
T |
17: 43,939,281 (GRCm39) |
V589E |
probably damaging |
Het |
Tuba3b |
T |
G |
6: 145,565,392 (GRCm39) |
S287A |
probably benign |
Het |
Txnrd3 |
G |
A |
6: 89,646,306 (GRCm39) |
R295H |
probably damaging |
Het |
Ubr5 |
G |
T |
15: 37,991,623 (GRCm39) |
|
probably benign |
Het |
Unc45b |
C |
T |
11: 82,831,007 (GRCm39) |
|
probably benign |
Het |
Usp32 |
A |
G |
11: 84,896,628 (GRCm39) |
|
probably null |
Het |
Utp23 |
G |
A |
15: 51,745,761 (GRCm39) |
R87K |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,285,234 (GRCm39) |
I405T |
possibly damaging |
Het |
|
Other mutations in Lrrc41 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01309:Lrrc41
|
APN |
4 |
115,953,663 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01358:Lrrc41
|
APN |
4 |
115,932,784 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01734:Lrrc41
|
APN |
4 |
115,950,331 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01986:Lrrc41
|
APN |
4 |
115,946,519 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02892:Lrrc41
|
APN |
4 |
115,946,032 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03135:Lrrc41
|
APN |
4 |
115,945,728 (GRCm39) |
missense |
probably benign |
|
R1478:Lrrc41
|
UTSW |
4 |
115,952,405 (GRCm39) |
nonsense |
probably null |
|
R1765:Lrrc41
|
UTSW |
4 |
115,946,248 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2233:Lrrc41
|
UTSW |
4 |
115,953,582 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4080:Lrrc41
|
UTSW |
4 |
115,937,743 (GRCm39) |
splice site |
probably null |
|
R4677:Lrrc41
|
UTSW |
4 |
115,952,332 (GRCm39) |
missense |
probably benign |
|
R4833:Lrrc41
|
UTSW |
4 |
115,950,374 (GRCm39) |
unclassified |
probably benign |
|
R4877:Lrrc41
|
UTSW |
4 |
115,936,602 (GRCm39) |
missense |
probably damaging |
0.99 |
R4926:Lrrc41
|
UTSW |
4 |
115,946,521 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6459:Lrrc41
|
UTSW |
4 |
115,945,977 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6817:Lrrc41
|
UTSW |
4 |
115,946,502 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6834:Lrrc41
|
UTSW |
4 |
115,953,726 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7479:Lrrc41
|
UTSW |
4 |
115,946,238 (GRCm39) |
missense |
probably damaging |
0.96 |
R7512:Lrrc41
|
UTSW |
4 |
115,950,191 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7593:Lrrc41
|
UTSW |
4 |
115,950,141 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8006:Lrrc41
|
UTSW |
4 |
115,952,085 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8810:Lrrc41
|
UTSW |
4 |
115,932,488 (GRCm39) |
unclassified |
probably benign |
|
R9134:Lrrc41
|
UTSW |
4 |
115,945,782 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9495:Lrrc41
|
UTSW |
4 |
115,932,806 (GRCm39) |
critical splice donor site |
probably null |
|
|