Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
T |
A |
8: 41,208,239 (GRCm39) |
Y502N |
probably damaging |
Het |
Adam6a |
T |
A |
12: 113,509,484 (GRCm39) |
L619* |
probably null |
Het |
Akap9 |
A |
T |
5: 4,011,587 (GRCm39) |
R763S |
probably benign |
Het |
Akt3 |
G |
A |
1: 176,958,639 (GRCm39) |
P24S |
probably damaging |
Het |
Ano2 |
A |
T |
6: 125,857,382 (GRCm39) |
|
probably null |
Het |
B4galnt4 |
G |
A |
7: 140,647,957 (GRCm39) |
R491Q |
possibly damaging |
Het |
Bahcc1 |
A |
G |
11: 120,163,286 (GRCm39) |
D528G |
possibly damaging |
Het |
Camk1g |
G |
T |
1: 193,030,483 (GRCm39) |
Q409K |
probably benign |
Het |
Cdh3 |
T |
A |
8: 107,274,396 (GRCm39) |
N638K |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,562,632 (GRCm39) |
E882D |
possibly damaging |
Het |
Cplane1 |
A |
G |
15: 8,231,785 (GRCm39) |
N1077S |
possibly damaging |
Het |
Cyp3a16 |
A |
G |
5: 145,389,690 (GRCm39) |
L225P |
probably damaging |
Het |
Dchs1 |
T |
C |
7: 105,411,625 (GRCm39) |
E1497G |
probably damaging |
Het |
Denr |
T |
A |
5: 124,065,117 (GRCm39) |
S157T |
possibly damaging |
Het |
Disp3 |
A |
G |
4: 148,356,101 (GRCm39) |
I253T |
probably damaging |
Het |
Dlgap2 |
C |
T |
8: 14,896,653 (GRCm39) |
T1043M |
probably damaging |
Het |
Epb41l5 |
T |
C |
1: 119,535,804 (GRCm39) |
T355A |
probably damaging |
Het |
Etv6 |
G |
A |
6: 134,013,062 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,310,484 (GRCm39) |
I141V |
probably benign |
Het |
Fsip2 |
T |
G |
2: 82,819,272 (GRCm39) |
S5002A |
probably benign |
Het |
Gbf1 |
T |
G |
19: 46,271,837 (GRCm39) |
V1576G |
probably damaging |
Het |
Gmfg |
T |
A |
7: 28,140,733 (GRCm39) |
|
probably null |
Het |
Gsdmc4 |
T |
C |
15: 63,774,706 (GRCm39) |
E25G |
possibly damaging |
Het |
Igkv6-23 |
A |
T |
6: 70,237,884 (GRCm39) |
L12M |
possibly damaging |
Het |
Kank1 |
G |
A |
19: 25,388,138 (GRCm39) |
V604M |
probably damaging |
Het |
Kctd1 |
A |
G |
18: 15,140,822 (GRCm39) |
V40A |
probably damaging |
Het |
Krt222 |
T |
C |
11: 99,127,065 (GRCm39) |
K185R |
possibly damaging |
Het |
Ldc1 |
A |
G |
4: 130,115,527 (GRCm39) |
V7A |
probably benign |
Het |
Lipm |
T |
C |
19: 34,089,494 (GRCm39) |
F151L |
probably damaging |
Het |
Lrrc2 |
A |
T |
9: 110,791,710 (GRCm39) |
N154I |
probably damaging |
Het |
Map1a |
T |
A |
2: 121,132,865 (GRCm39) |
M1227K |
probably damaging |
Het |
Med1 |
T |
C |
11: 98,071,114 (GRCm39) |
T78A |
probably damaging |
Het |
Mrm1 |
A |
G |
11: 84,710,144 (GRCm39) |
S19P |
possibly damaging |
Het |
Naf1 |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
8: 67,313,200 (GRCm39) |
|
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,330,657 (GRCm39) |
Y354C |
probably damaging |
Het |
Npr1 |
A |
G |
3: 90,368,448 (GRCm39) |
V474A |
probably benign |
Het |
Nyap1 |
A |
T |
5: 137,733,840 (GRCm39) |
S398T |
probably damaging |
Het |
Obox7 |
C |
T |
7: 14,398,067 (GRCm39) |
Q36* |
probably null |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Or6c8 |
A |
T |
10: 128,915,358 (GRCm39) |
I158N |
probably benign |
Het |
P3h1 |
T |
A |
4: 119,090,428 (GRCm39) |
L92H |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,609,818 (GRCm39) |
T1548A |
possibly damaging |
Het |
Pnisr |
A |
G |
4: 21,873,586 (GRCm39) |
E443G |
probably damaging |
Het |
Prdm2 |
A |
G |
4: 142,859,079 (GRCm39) |
S1404P |
possibly damaging |
Het |
Prom1 |
A |
T |
5: 44,190,284 (GRCm39) |
|
probably null |
Het |
Rbm27 |
A |
T |
18: 42,455,186 (GRCm39) |
Q646H |
probably damaging |
Het |
Scamp3 |
C |
T |
3: 89,087,561 (GRCm39) |
R134* |
probably null |
Het |
Scrt2 |
T |
C |
2: 151,924,018 (GRCm39) |
C17R |
probably benign |
Het |
Setbp1 |
A |
G |
18: 78,902,498 (GRCm39) |
S390P |
probably benign |
Het |
Shank2 |
A |
T |
7: 143,964,837 (GRCm39) |
D815V |
probably damaging |
Het |
Sirt7 |
G |
A |
11: 120,511,296 (GRCm39) |
T285M |
|
Het |
Sis |
T |
G |
3: 72,863,621 (GRCm39) |
S206R |
probably benign |
Het |
Slc24a4 |
T |
G |
12: 102,193,334 (GRCm39) |
D206E |
possibly damaging |
Het |
Slc26a4 |
C |
A |
12: 31,585,292 (GRCm39) |
G501C |
probably damaging |
Het |
Sptb |
T |
C |
12: 76,677,489 (GRCm39) |
N115S |
probably damaging |
Het |
Srprb |
T |
C |
9: 103,074,807 (GRCm39) |
T112A |
possibly damaging |
Het |
Tbk1 |
G |
T |
10: 121,389,841 (GRCm39) |
A537E |
probably benign |
Het |
Tbx19 |
T |
A |
1: 164,970,067 (GRCm39) |
H274L |
probably damaging |
Het |
Tmem130 |
A |
G |
5: 144,674,233 (GRCm39) |
S394P |
probably damaging |
Het |
Tmem40 |
A |
G |
6: 115,718,517 (GRCm39) |
S104P |
possibly damaging |
Het |
Tmprss2 |
T |
A |
16: 97,379,826 (GRCm39) |
Q158L |
probably damaging |
Het |
Tnip1 |
A |
T |
11: 54,828,876 (GRCm39) |
V97D |
possibly damaging |
Het |
Tpr |
T |
A |
1: 150,314,887 (GRCm39) |
S1985T |
probably benign |
Het |
Traf7 |
CA |
CAA |
17: 24,746,737 (GRCm39) |
|
probably benign |
Het |
Trio |
G |
T |
15: 27,744,158 (GRCm39) |
N2591K |
possibly damaging |
Het |
Ushbp1 |
A |
T |
8: 71,838,573 (GRCm39) |
C618S |
possibly damaging |
Het |
Usp34 |
A |
G |
11: 23,317,385 (GRCm39) |
S834G |
possibly damaging |
Het |
Vmn2r103 |
C |
A |
17: 20,019,525 (GRCm39) |
C536* |
probably null |
Het |
Vmn2r124 |
T |
A |
17: 18,293,758 (GRCm39) |
V615D |
probably damaging |
Het |
Zbtb38 |
G |
A |
9: 96,570,397 (GRCm39) |
T229I |
probably benign |
Het |
Zfhx4 |
T |
A |
3: 5,465,656 (GRCm39) |
V1963E |
probably damaging |
Het |
Zfp142 |
G |
A |
1: 74,610,933 (GRCm39) |
T954M |
probably benign |
Het |
Zgrf1 |
A |
G |
3: 127,409,216 (GRCm39) |
Y1730C |
probably benign |
Het |
|
Other mutations in Cpxm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01862:Cpxm2
|
APN |
7 |
131,661,540 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02039:Cpxm2
|
APN |
7 |
131,649,482 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03011:Cpxm2
|
APN |
7 |
131,650,807 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0033:Cpxm2
|
UTSW |
7 |
131,663,886 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0100:Cpxm2
|
UTSW |
7 |
131,656,600 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0100:Cpxm2
|
UTSW |
7 |
131,656,600 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0453:Cpxm2
|
UTSW |
7 |
131,730,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Cpxm2
|
UTSW |
7 |
131,645,772 (GRCm39) |
nonsense |
probably null |
|
R0655:Cpxm2
|
UTSW |
7 |
131,656,549 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0834:Cpxm2
|
UTSW |
7 |
131,756,342 (GRCm39) |
intron |
probably benign |
|
R1145:Cpxm2
|
UTSW |
7 |
131,659,377 (GRCm39) |
missense |
probably damaging |
0.99 |
R1145:Cpxm2
|
UTSW |
7 |
131,659,377 (GRCm39) |
missense |
probably damaging |
0.99 |
R1249:Cpxm2
|
UTSW |
7 |
131,730,079 (GRCm39) |
critical splice donor site |
probably null |
|
R1563:Cpxm2
|
UTSW |
7 |
131,745,411 (GRCm39) |
missense |
probably benign |
0.00 |
R1565:Cpxm2
|
UTSW |
7 |
131,663,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Cpxm2
|
UTSW |
7 |
131,661,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R1863:Cpxm2
|
UTSW |
7 |
131,745,392 (GRCm39) |
splice site |
probably null |
|
R1874:Cpxm2
|
UTSW |
7 |
131,661,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R1958:Cpxm2
|
UTSW |
7 |
131,663,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Cpxm2
|
UTSW |
7 |
131,661,581 (GRCm39) |
intron |
probably benign |
|
R3806:Cpxm2
|
UTSW |
7 |
131,681,820 (GRCm39) |
missense |
probably benign |
0.12 |
R3861:Cpxm2
|
UTSW |
7 |
131,656,648 (GRCm39) |
missense |
probably benign |
0.00 |
R4570:Cpxm2
|
UTSW |
7 |
131,745,435 (GRCm39) |
missense |
probably benign |
0.11 |
R4642:Cpxm2
|
UTSW |
7 |
131,672,610 (GRCm39) |
missense |
probably benign |
0.11 |
R4684:Cpxm2
|
UTSW |
7 |
131,650,767 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4717:Cpxm2
|
UTSW |
7 |
131,656,574 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4863:Cpxm2
|
UTSW |
7 |
131,661,476 (GRCm39) |
missense |
probably benign |
0.13 |
R5079:Cpxm2
|
UTSW |
7 |
131,756,014 (GRCm39) |
critical splice donor site |
probably null |
|
R5341:Cpxm2
|
UTSW |
7 |
131,756,342 (GRCm39) |
intron |
probably benign |
|
R5626:Cpxm2
|
UTSW |
7 |
131,661,581 (GRCm39) |
intron |
probably benign |
|
R5666:Cpxm2
|
UTSW |
7 |
131,656,625 (GRCm39) |
missense |
probably benign |
0.44 |
R5815:Cpxm2
|
UTSW |
7 |
131,645,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Cpxm2
|
UTSW |
7 |
131,756,035 (GRCm39) |
missense |
probably benign |
|
R6133:Cpxm2
|
UTSW |
7 |
131,730,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R6224:Cpxm2
|
UTSW |
7 |
131,745,460 (GRCm39) |
missense |
probably benign |
|
R6468:Cpxm2
|
UTSW |
7 |
131,672,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Cpxm2
|
UTSW |
7 |
131,650,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Cpxm2
|
UTSW |
7 |
131,745,408 (GRCm39) |
missense |
probably benign |
0.32 |
R7100:Cpxm2
|
UTSW |
7 |
131,656,544 (GRCm39) |
missense |
probably benign |
0.06 |
R7198:Cpxm2
|
UTSW |
7 |
131,681,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Cpxm2
|
UTSW |
7 |
131,756,107 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7855:Cpxm2
|
UTSW |
7 |
131,659,424 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7867:Cpxm2
|
UTSW |
7 |
131,650,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R8513:Cpxm2
|
UTSW |
7 |
131,745,431 (GRCm39) |
missense |
probably benign |
0.01 |
R8694:Cpxm2
|
UTSW |
7 |
131,681,783 (GRCm39) |
missense |
probably benign |
0.03 |
R8874:Cpxm2
|
UTSW |
7 |
131,708,010 (GRCm39) |
critical splice donor site |
probably null |
|
R8967:Cpxm2
|
UTSW |
7 |
131,661,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R9759:Cpxm2
|
UTSW |
7 |
131,756,242 (GRCm39) |
missense |
probably benign |
0.03 |
RF014:Cpxm2
|
UTSW |
7 |
131,672,592 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Cpxm2
|
UTSW |
7 |
131,656,730 (GRCm39) |
missense |
probably benign |
0.01 |
|