Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553M12Rik |
A |
T |
4: 88,786,496 (GRCm39) |
W41R |
unknown |
Het |
Aatf |
G |
A |
11: 84,402,335 (GRCm39) |
S117L |
possibly damaging |
Het |
Abca12 |
C |
A |
1: 71,342,046 (GRCm39) |
V972L |
probably benign |
Het |
Abcb11 |
T |
A |
2: 69,117,162 (GRCm39) |
R495S |
probably damaging |
Het |
Acss2 |
T |
A |
2: 155,403,086 (GRCm39) |
H621Q |
probably benign |
Het |
Akap9 |
T |
C |
5: 4,096,736 (GRCm39) |
L2537P |
probably benign |
Het |
Apbb1 |
C |
T |
7: 105,208,509 (GRCm39) |
A597T |
probably damaging |
Het |
Cacna1d |
A |
T |
14: 29,797,809 (GRCm39) |
I1448N |
probably damaging |
Het |
Cacna1e |
C |
T |
1: 154,288,863 (GRCm39) |
E1841K |
probably damaging |
Het |
Ccdc162 |
G |
T |
10: 41,463,371 (GRCm39) |
P1457Q |
probably damaging |
Het |
Cep70 |
A |
G |
9: 99,163,145 (GRCm39) |
K331E |
probably damaging |
Het |
Cplane1 |
C |
A |
15: 8,273,310 (GRCm39) |
Q2534K |
possibly damaging |
Het |
D430041D05Rik |
A |
T |
2: 104,087,504 (GRCm39) |
Y491N |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,002,703 (GRCm39) |
I3898V |
probably benign |
Het |
Drd2 |
A |
G |
9: 49,316,277 (GRCm39) |
T346A |
probably benign |
Het |
Efcab9 |
T |
C |
11: 32,472,941 (GRCm39) |
T169A |
possibly damaging |
Het |
Fam163a |
A |
T |
1: 155,955,729 (GRCm39) |
I21N |
probably damaging |
Het |
Fam171a2 |
C |
T |
11: 102,329,389 (GRCm39) |
D457N |
probably benign |
Het |
Fbn1 |
A |
T |
2: 125,321,200 (GRCm39) |
|
probably null |
Het |
Gpr37 |
A |
T |
6: 25,689,049 (GRCm39) |
L16H |
probably damaging |
Het |
Gtf3c2 |
T |
C |
5: 31,330,175 (GRCm39) |
D265G |
probably benign |
Het |
Idh1 |
G |
T |
1: 65,198,649 (GRCm39) |
A407D |
probably benign |
Het |
Ifna12 |
A |
G |
4: 88,521,415 (GRCm39) |
M44T |
probably damaging |
Het |
Il22ra1 |
A |
G |
4: 135,461,561 (GRCm39) |
M109V |
probably benign |
Het |
Jag2 |
A |
T |
12: 112,879,089 (GRCm39) |
|
probably null |
Het |
Lca5l |
T |
C |
16: 95,960,761 (GRCm39) |
D572G |
unknown |
Het |
Lcn11 |
G |
A |
2: 25,667,830 (GRCm39) |
V73I |
probably benign |
Het |
Lrba |
A |
G |
3: 86,352,704 (GRCm39) |
T1951A |
probably damaging |
Het |
Ltbp2 |
A |
G |
12: 84,860,012 (GRCm39) |
|
probably null |
Het |
Malrd1 |
G |
A |
2: 15,802,610 (GRCm39) |
|
probably null |
Het |
Morc2b |
C |
A |
17: 33,356,218 (GRCm39) |
G518V |
probably benign |
Het |
Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
Myo5b |
A |
T |
18: 74,767,630 (GRCm39) |
T313S |
probably benign |
Het |
Neto2 |
C |
A |
8: 86,396,329 (GRCm39) |
L140F |
probably damaging |
Het |
Nlgn1 |
C |
T |
3: 25,488,467 (GRCm39) |
V623I |
probably damaging |
Het |
Optc |
A |
G |
1: 133,834,730 (GRCm39) |
S15P |
possibly damaging |
Het |
Or1e25 |
C |
T |
11: 73,494,332 (GRCm39) |
Q309* |
probably null |
Het |
Or1l4b |
A |
G |
2: 37,036,858 (GRCm39) |
I211M |
possibly damaging |
Het |
Or52e19b |
C |
A |
7: 103,032,945 (GRCm39) |
W88L |
probably damaging |
Het |
Or7c19 |
T |
A |
8: 85,957,427 (GRCm39) |
M101K |
possibly damaging |
Het |
Or9k2 |
T |
G |
10: 129,998,698 (GRCm39) |
T166P |
probably damaging |
Het |
Otogl |
A |
G |
10: 107,705,407 (GRCm39) |
V640A |
probably damaging |
Het |
Pcdhgb2 |
T |
C |
18: 37,823,023 (GRCm39) |
S5P |
probably benign |
Het |
Pde3a |
A |
T |
6: 141,404,975 (GRCm39) |
E400V |
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,449,804 (GRCm39) |
I3856V |
possibly damaging |
Het |
Pld2 |
G |
A |
11: 70,443,695 (GRCm39) |
|
probably null |
Het |
Plxna4 |
G |
T |
6: 32,129,807 (GRCm39) |
H1839N |
probably damaging |
Het |
Ppp6r2 |
T |
C |
15: 89,140,904 (GRCm39) |
V89A |
probably benign |
Het |
Rapgef3 |
T |
C |
15: 97,655,627 (GRCm39) |
D420G |
probably damaging |
Het |
Rnf17 |
T |
A |
14: 56,699,529 (GRCm39) |
|
probably null |
Het |
Rps6ka2 |
T |
A |
17: 7,544,848 (GRCm39) |
|
probably null |
Het |
Rptn |
A |
T |
3: 93,303,228 (GRCm39) |
D187V |
probably damaging |
Het |
Rtn1 |
T |
C |
12: 72,355,203 (GRCm39) |
K248E |
probably damaging |
Het |
Rtn4rl1 |
A |
T |
11: 75,155,871 (GRCm39) |
H101L |
probably benign |
Het |
Septin3 |
A |
G |
15: 82,174,974 (GRCm39) |
N305S |
probably benign |
Het |
Serpina3f |
G |
T |
12: 104,183,565 (GRCm39) |
K142N |
possibly damaging |
Het |
Ssh1 |
C |
A |
5: 114,104,295 (GRCm39) |
R116L |
probably benign |
Het |
Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,111,693 (GRCm39) |
K405E |
possibly damaging |
Het |
Trbv13-2 |
G |
A |
6: 41,098,634 (GRCm39) |
A70T |
probably benign |
Het |
Ttn |
A |
T |
2: 76,618,540 (GRCm39) |
I16248N |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,655,849 (GRCm39) |
|
probably null |
Het |
Vldlr |
A |
T |
19: 27,195,015 (GRCm39) |
M1L |
probably benign |
Het |
Wscd1 |
A |
G |
11: 71,675,191 (GRCm39) |
H366R |
probably damaging |
Het |
Zbtb8a |
A |
G |
4: 129,251,496 (GRCm39) |
|
probably null |
Het |
Zfp827 |
T |
C |
8: 79,916,958 (GRCm39) |
V511A |
|
Het |
|
Other mutations in Cstpp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02737:Cstpp1
|
APN |
2 |
91,135,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R6768_1110051M20Rik_026
|
UTSW |
2 |
91,252,303 (GRCm39) |
missense |
probably damaging |
0.97 |
BB004:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
BB014:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Cstpp1
|
UTSW |
2 |
91,112,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Cstpp1
|
UTSW |
2 |
91,252,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R0446:Cstpp1
|
UTSW |
2 |
91,135,109 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0846:Cstpp1
|
UTSW |
2 |
91,214,182 (GRCm39) |
missense |
probably damaging |
0.98 |
R6768:Cstpp1
|
UTSW |
2 |
91,252,303 (GRCm39) |
missense |
probably damaging |
0.97 |
R6888:Cstpp1
|
UTSW |
2 |
91,252,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Cstpp1
|
UTSW |
2 |
91,214,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Cstpp1
|
UTSW |
2 |
91,274,939 (GRCm39) |
start gained |
probably benign |
|
R7927:Cstpp1
|
UTSW |
2 |
91,252,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Cstpp1
|
UTSW |
2 |
91,107,343 (GRCm39) |
missense |
probably benign |
0.39 |
R9610:Cstpp1
|
UTSW |
2 |
91,135,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Cstpp1
|
UTSW |
2 |
91,135,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R9709:Cstpp1
|
UTSW |
2 |
91,112,099 (GRCm39) |
missense |
probably benign |
0.00 |
|