Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl2 |
T |
C |
3: 148,565,122 (GRCm39) |
I153V |
probably benign |
Het |
Arhgap21 |
A |
C |
2: 20,886,116 (GRCm39) |
S354A |
probably benign |
Het |
Bcan |
T |
C |
3: 87,896,516 (GRCm39) |
T727A |
probably damaging |
Het |
Catsperd |
A |
G |
17: 56,970,419 (GRCm39) |
Y697C |
probably damaging |
Het |
Ccdc39 |
T |
A |
3: 33,886,808 (GRCm39) |
K267* |
probably null |
Het |
Ccdc47 |
C |
A |
11: 106,092,971 (GRCm39) |
V92L |
possibly damaging |
Het |
Cyp2c54 |
A |
T |
19: 40,059,990 (GRCm39) |
I181N |
probably damaging |
Het |
Ddx60 |
A |
T |
8: 62,427,184 (GRCm39) |
D753V |
probably damaging |
Het |
Dlg2 |
A |
T |
7: 91,935,796 (GRCm39) |
K641N |
probably damaging |
Het |
Eloa |
G |
A |
4: 135,736,668 (GRCm39) |
R527C |
probably benign |
Het |
Fancd2 |
C |
T |
6: 113,545,187 (GRCm39) |
P835L |
probably damaging |
Het |
Fbln2 |
C |
G |
6: 91,227,846 (GRCm39) |
T428S |
probably damaging |
Het |
Fbn2 |
G |
A |
18: 58,153,462 (GRCm39) |
A2600V |
possibly damaging |
Het |
Gbe1 |
A |
G |
16: 70,233,876 (GRCm39) |
Y251C |
probably damaging |
Het |
Gnptab |
T |
A |
10: 88,268,508 (GRCm39) |
|
probably null |
Het |
Hspa1a |
T |
A |
17: 35,191,033 (GRCm39) |
|
probably benign |
Het |
Ifi204 |
G |
A |
1: 173,587,839 (GRCm39) |
P107S |
probably damaging |
Het |
Kif6 |
A |
G |
17: 49,978,164 (GRCm39) |
I119V |
probably damaging |
Het |
Lmntd2 |
G |
A |
7: 140,790,427 (GRCm39) |
H554Y |
probably benign |
Het |
Lrrc8e |
C |
A |
8: 4,284,218 (GRCm39) |
H148N |
probably damaging |
Het |
Lrriq1 |
T |
C |
10: 103,050,914 (GRCm39) |
N613D |
probably damaging |
Het |
Map4k4 |
C |
T |
1: 40,028,136 (GRCm39) |
T319M |
probably damaging |
Het |
Mbtps1 |
C |
T |
8: 120,268,413 (GRCm39) |
V253I |
probably damaging |
Het |
Mcm4 |
C |
A |
16: 15,450,042 (GRCm39) |
C330F |
probably damaging |
Het |
Mok |
A |
G |
12: 110,776,341 (GRCm39) |
|
probably null |
Het |
Nedd4 |
T |
C |
9: 72,577,321 (GRCm39) |
C49R |
probably damaging |
Het |
Nlrp4e |
T |
C |
7: 23,020,983 (GRCm39) |
V490A |
probably benign |
Het |
Nsf |
A |
T |
11: 103,819,584 (GRCm39) |
F27I |
probably damaging |
Het |
Or10g3b |
A |
T |
14: 52,586,696 (GRCm39) |
L269Q |
probably damaging |
Het |
Or14c44 |
A |
G |
7: 86,061,647 (GRCm39) |
S26G |
probably benign |
Het |
Or4a47 |
T |
C |
2: 89,665,609 (GRCm39) |
N227D |
probably benign |
Het |
Or5p73 |
G |
T |
7: 108,064,784 (GRCm39) |
M84I |
possibly damaging |
Het |
Or6c66 |
A |
G |
10: 129,461,114 (GRCm39) |
I272T |
possibly damaging |
Het |
Pax1 |
A |
G |
2: 147,206,968 (GRCm39) |
M1V |
probably null |
Het |
Pcdhga12 |
A |
G |
18: 37,900,631 (GRCm39) |
T488A |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,864,909 (GRCm39) |
D99G |
possibly damaging |
Het |
Polr3h |
T |
C |
15: 81,800,824 (GRCm39) |
T173A |
probably benign |
Het |
Pramel6 |
C |
T |
2: 87,339,045 (GRCm39) |
L82F |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,230,463 (GRCm39) |
I1034N |
probably damaging |
Het |
Rbfox1 |
G |
A |
16: 7,042,319 (GRCm39) |
V58I |
probably damaging |
Het |
Reln |
T |
A |
5: 22,104,027 (GRCm39) |
I3315L |
probably benign |
Het |
Rev3l |
T |
A |
10: 39,682,844 (GRCm39) |
S321T |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,740,292 (GRCm39) |
T3908A |
probably damaging |
Het |
Secisbp2l |
G |
T |
2: 125,617,502 (GRCm39) |
Y58* |
probably null |
Het |
Sgms1 |
C |
A |
19: 32,102,697 (GRCm39) |
V337L |
probably benign |
Het |
Slc38a2 |
G |
A |
15: 96,593,172 (GRCm39) |
Q136* |
probably null |
Het |
Smarcd1 |
T |
A |
15: 99,605,657 (GRCm39) |
V296D |
probably damaging |
Het |
Smcr8 |
A |
C |
11: 60,674,822 (GRCm39) |
H866P |
probably damaging |
Het |
Spcs1 |
T |
A |
14: 30,722,721 (GRCm39) |
I33L |
probably benign |
Het |
Stxbp5 |
T |
C |
10: 9,688,033 (GRCm39) |
R423G |
possibly damaging |
Het |
Syt4 |
A |
T |
18: 31,576,790 (GRCm39) |
M188K |
possibly damaging |
Het |
Tchhl1 |
A |
G |
3: 93,376,869 (GRCm39) |
D22G |
probably damaging |
Het |
Tiparp |
T |
A |
3: 65,453,655 (GRCm39) |
N134K |
probably benign |
Het |
Topaz1 |
A |
G |
9: 122,579,001 (GRCm39) |
D637G |
possibly damaging |
Het |
Trav14d-3-dv8 |
A |
T |
14: 53,316,192 (GRCm39) |
|
probably benign |
Het |
Vmn1r19 |
A |
T |
6: 57,382,166 (GRCm39) |
M240L |
probably benign |
Het |
Vmn1r77 |
T |
A |
7: 11,775,514 (GRCm39) |
S29T |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,881,817 (GRCm39) |
F1253L |
probably benign |
Het |
Zfp407 |
G |
A |
18: 84,580,895 (GRCm39) |
R73* |
probably null |
Het |
Zfp446 |
T |
A |
7: 12,716,555 (GRCm39) |
F334I |
possibly damaging |
Het |
Zfp654 |
A |
T |
16: 64,606,011 (GRCm39) |
Y730* |
probably null |
Het |
|
Other mutations in Brinp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00818:Brinp1
|
APN |
4 |
68,681,084 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01024:Brinp1
|
APN |
4 |
68,680,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02048:Brinp1
|
APN |
4 |
68,681,379 (GRCm39) |
missense |
probably benign |
|
IGL02115:Brinp1
|
APN |
4 |
68,680,635 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02332:Brinp1
|
APN |
4 |
68,823,121 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03115:Brinp1
|
APN |
4 |
68,822,973 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02796:Brinp1
|
UTSW |
4 |
68,680,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R0382:Brinp1
|
UTSW |
4 |
68,680,545 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0468:Brinp1
|
UTSW |
4 |
68,681,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1141:Brinp1
|
UTSW |
4 |
68,711,215 (GRCm39) |
missense |
probably benign |
0.00 |
R1164:Brinp1
|
UTSW |
4 |
68,716,928 (GRCm39) |
missense |
probably benign |
|
R1178:Brinp1
|
UTSW |
4 |
68,680,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R1545:Brinp1
|
UTSW |
4 |
68,681,192 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1672:Brinp1
|
UTSW |
4 |
68,747,520 (GRCm39) |
splice site |
probably null |
|
R1998:Brinp1
|
UTSW |
4 |
68,680,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R2218:Brinp1
|
UTSW |
4 |
68,680,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R2262:Brinp1
|
UTSW |
4 |
68,747,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R2370:Brinp1
|
UTSW |
4 |
68,681,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R4542:Brinp1
|
UTSW |
4 |
68,680,329 (GRCm39) |
missense |
probably benign |
0.00 |
R4617:Brinp1
|
UTSW |
4 |
68,681,198 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4864:Brinp1
|
UTSW |
4 |
68,717,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R5287:Brinp1
|
UTSW |
4 |
68,711,201 (GRCm39) |
missense |
probably benign |
0.04 |
R5403:Brinp1
|
UTSW |
4 |
68,711,201 (GRCm39) |
missense |
probably benign |
0.04 |
R5932:Brinp1
|
UTSW |
4 |
68,711,178 (GRCm39) |
missense |
probably benign |
0.00 |
R7106:Brinp1
|
UTSW |
4 |
68,747,615 (GRCm39) |
missense |
probably benign |
0.36 |
R7127:Brinp1
|
UTSW |
4 |
68,711,260 (GRCm39) |
missense |
probably benign |
0.00 |
R7398:Brinp1
|
UTSW |
4 |
68,759,591 (GRCm39) |
missense |
probably benign |
|
R7917:Brinp1
|
UTSW |
4 |
68,823,190 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
R8164:Brinp1
|
UTSW |
4 |
68,681,158 (GRCm39) |
nonsense |
probably null |
|
R8369:Brinp1
|
UTSW |
4 |
68,716,936 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9124:Brinp1
|
UTSW |
4 |
68,747,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R9253:Brinp1
|
UTSW |
4 |
68,711,083 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Brinp1
|
UTSW |
4 |
68,716,988 (GRCm39) |
nonsense |
probably null |
|
|