Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl5 |
A |
G |
10: 80,180,681 (GRCm39) |
V127A |
probably damaging |
Het |
Alox12 |
T |
A |
11: 70,143,662 (GRCm39) |
D202V |
probably damaging |
Het |
Ankib1 |
A |
G |
5: 3,779,655 (GRCm39) |
Y405H |
probably damaging |
Het |
Apbb2 |
A |
T |
5: 66,609,593 (GRCm39) |
M18K |
probably damaging |
Het |
Atad2 |
C |
A |
15: 57,989,229 (GRCm39) |
|
probably benign |
Het |
Birc6 |
T |
A |
17: 74,932,238 (GRCm39) |
|
probably benign |
Het |
Ccdc126 |
T |
C |
6: 49,311,076 (GRCm39) |
M28T |
possibly damaging |
Het |
Cdc16 |
A |
T |
8: 13,831,618 (GRCm39) |
D617V |
probably damaging |
Het |
Cep135 |
G |
A |
5: 76,763,557 (GRCm39) |
E516K |
probably damaging |
Het |
Cep135 |
G |
T |
5: 76,786,796 (GRCm39) |
M1081I |
probably benign |
Het |
Col6a3 |
A |
C |
1: 90,735,456 (GRCm39) |
V731G |
probably damaging |
Het |
Cstdc6 |
A |
T |
16: 36,143,346 (GRCm39) |
Y34* |
probably null |
Het |
Cwc27 |
C |
A |
13: 104,797,865 (GRCm39) |
E365* |
probably null |
Het |
Dip2b |
C |
A |
15: 100,060,600 (GRCm39) |
Y258* |
probably null |
Het |
Dnah17 |
A |
G |
11: 117,973,807 (GRCm39) |
V1900A |
probably damaging |
Het |
Dpysl2 |
A |
T |
14: 67,042,895 (GRCm39) |
|
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,139,432 (GRCm39) |
L1401Q |
probably damaging |
Het |
Esf1 |
A |
T |
2: 140,000,506 (GRCm39) |
Y427N |
possibly damaging |
Het |
Fbln1 |
T |
A |
15: 85,111,308 (GRCm39) |
V154D |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,563,530 (GRCm39) |
F326L |
probably damaging |
Het |
Gm4922 |
T |
A |
10: 18,659,813 (GRCm39) |
N303I |
possibly damaging |
Het |
H1f6 |
G |
T |
13: 23,880,307 (GRCm39) |
K153N |
possibly damaging |
Het |
Iigp1 |
G |
A |
18: 60,523,523 (GRCm39) |
V214M |
probably damaging |
Het |
Mcc |
A |
G |
18: 44,601,574 (GRCm39) |
L410P |
probably damaging |
Het |
Mfn2 |
A |
G |
4: 147,967,712 (GRCm39) |
F452S |
probably damaging |
Het |
Mib2 |
C |
T |
4: 155,743,917 (GRCm39) |
G42S |
probably damaging |
Het |
Micu2 |
A |
G |
14: 58,156,831 (GRCm39) |
F335L |
possibly damaging |
Het |
Mpp3 |
T |
G |
11: 101,896,173 (GRCm39) |
K450T |
possibly damaging |
Het |
Mtmr4 |
T |
A |
11: 87,489,714 (GRCm39) |
V79E |
probably damaging |
Het |
Nlrp4b |
A |
G |
7: 10,448,585 (GRCm39) |
I263V |
probably benign |
Het |
Or52p2 |
T |
C |
7: 102,237,738 (GRCm39) |
I71V |
probably benign |
Het |
Or6c76 |
T |
G |
10: 129,612,005 (GRCm39) |
V74G |
probably damaging |
Het |
Pdk1 |
G |
A |
2: 71,710,383 (GRCm39) |
W113* |
probably null |
Het |
Phaf1 |
T |
A |
8: 105,966,603 (GRCm39) |
|
probably benign |
Het |
Phxr4 |
A |
T |
9: 13,342,993 (GRCm39) |
|
probably benign |
Het |
Rad51ap2 |
T |
A |
12: 11,507,897 (GRCm39) |
H606Q |
probably benign |
Het |
Ralgapa1 |
A |
T |
12: 55,829,670 (GRCm39) |
I187K |
possibly damaging |
Het |
Rps27 |
A |
G |
3: 90,120,230 (GRCm39) |
|
probably benign |
Het |
Sema3e |
T |
A |
5: 14,286,099 (GRCm39) |
|
probably null |
Het |
Sh2d3c |
G |
A |
2: 32,643,064 (GRCm39) |
C749Y |
probably damaging |
Het |
Siah2 |
T |
C |
3: 58,583,656 (GRCm39) |
D210G |
probably benign |
Het |
Smap2 |
G |
A |
4: 120,834,174 (GRCm39) |
P155S |
probably benign |
Het |
Snrk |
C |
T |
9: 121,995,610 (GRCm39) |
T463M |
possibly damaging |
Het |
Tm9sf3 |
A |
G |
19: 41,233,964 (GRCm39) |
|
probably benign |
Het |
Tmem132d |
C |
T |
5: 127,861,842 (GRCm39) |
E760K |
probably damaging |
Het |
Tmem184c |
A |
T |
8: 78,332,789 (GRCm39) |
|
probably null |
Het |
Tmem235 |
A |
T |
11: 117,751,674 (GRCm39) |
I33F |
possibly damaging |
Het |
Tmem267 |
A |
T |
13: 119,629,175 (GRCm39) |
|
probably null |
Het |
Top1 |
G |
A |
2: 160,556,185 (GRCm39) |
R548Q |
probably damaging |
Het |
Trio |
T |
C |
15: 27,805,908 (GRCm39) |
N527D |
probably damaging |
Het |
Upf3a |
A |
G |
8: 13,845,656 (GRCm39) |
K252E |
probably benign |
Het |
|
Other mutations in Luzp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00974:Luzp2
|
APN |
7 |
54,724,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01793:Luzp2
|
APN |
7 |
54,821,997 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01908:Luzp2
|
APN |
7 |
54,821,944 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02538:Luzp2
|
APN |
7 |
54,861,546 (GRCm39) |
nonsense |
probably null |
|
IGL02727:Luzp2
|
APN |
7 |
54,821,939 (GRCm39) |
splice site |
probably benign |
|
R0257:Luzp2
|
UTSW |
7 |
54,899,194 (GRCm39) |
missense |
probably benign |
0.17 |
R1581:Luzp2
|
UTSW |
7 |
54,899,238 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1648:Luzp2
|
UTSW |
7 |
54,914,018 (GRCm39) |
splice site |
probably null |
|
R1752:Luzp2
|
UTSW |
7 |
54,914,088 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1943:Luzp2
|
UTSW |
7 |
54,914,050 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2294:Luzp2
|
UTSW |
7 |
54,821,938 (GRCm39) |
splice site |
probably benign |
|
R2295:Luzp2
|
UTSW |
7 |
54,821,938 (GRCm39) |
splice site |
probably benign |
|
R4539:Luzp2
|
UTSW |
7 |
54,713,037 (GRCm39) |
missense |
probably damaging |
0.99 |
R4611:Luzp2
|
UTSW |
7 |
54,713,104 (GRCm39) |
splice site |
probably null |
|
R4716:Luzp2
|
UTSW |
7 |
54,485,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Luzp2
|
UTSW |
7 |
54,816,996 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4875:Luzp2
|
UTSW |
7 |
54,816,996 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5108:Luzp2
|
UTSW |
7 |
54,915,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R6023:Luzp2
|
UTSW |
7 |
54,707,815 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6034:Luzp2
|
UTSW |
7 |
54,816,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Luzp2
|
UTSW |
7 |
54,816,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R6412:Luzp2
|
UTSW |
7 |
54,707,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Luzp2
|
UTSW |
7 |
54,915,078 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7186:Luzp2
|
UTSW |
7 |
54,485,577 (GRCm39) |
start gained |
probably benign |
|
R7270:Luzp2
|
UTSW |
7 |
54,724,774 (GRCm39) |
missense |
probably damaging |
0.99 |
R7588:Luzp2
|
UTSW |
7 |
54,724,838 (GRCm39) |
critical splice donor site |
probably null |
|
R8036:Luzp2
|
UTSW |
7 |
54,724,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R8078:Luzp2
|
UTSW |
7 |
54,702,510 (GRCm39) |
nonsense |
probably null |
|
R8729:Luzp2
|
UTSW |
7 |
54,816,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R9287:Luzp2
|
UTSW |
7 |
54,914,108 (GRCm39) |
splice site |
probably benign |
|
R9652:Luzp2
|
UTSW |
7 |
54,702,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R9653:Luzp2
|
UTSW |
7 |
54,702,580 (GRCm39) |
missense |
probably damaging |
1.00 |
RF014:Luzp2
|
UTSW |
7 |
54,821,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|