Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
A |
6: 121,636,282 (GRCm39) |
M717K |
probably benign |
Het |
Acad12 |
C |
A |
5: 121,748,029 (GRCm39) |
V130L |
probably benign |
Het |
Cdca2 |
T |
C |
14: 67,937,471 (GRCm39) |
|
probably benign |
Het |
Cfap100 |
T |
A |
6: 90,389,332 (GRCm39) |
|
probably null |
Het |
Cfap43 |
T |
A |
19: 47,804,302 (GRCm39) |
E298V |
probably damaging |
Het |
Cic |
C |
T |
7: 24,990,500 (GRCm39) |
P1971S |
probably damaging |
Het |
Cnga1 |
T |
C |
5: 72,761,681 (GRCm39) |
D611G |
probably benign |
Het |
Daglb |
C |
T |
5: 143,486,948 (GRCm39) |
P522L |
probably damaging |
Het |
Dclre1b |
A |
T |
3: 103,710,597 (GRCm39) |
I438K |
probably benign |
Het |
Ddx5 |
C |
A |
11: 106,675,871 (GRCm39) |
R273M |
probably damaging |
Het |
Eepd1 |
C |
T |
9: 25,393,981 (GRCm39) |
L82F |
probably damaging |
Het |
Emilin3 |
G |
A |
2: 160,750,649 (GRCm39) |
Q320* |
probably null |
Het |
Exoc6 |
T |
C |
19: 37,582,217 (GRCm39) |
|
probably null |
Het |
Fcna |
G |
C |
2: 25,520,693 (GRCm39) |
|
probably benign |
Het |
Foxs1 |
T |
C |
2: 152,774,484 (GRCm39) |
T190A |
probably benign |
Het |
Gje1 |
A |
G |
10: 14,592,374 (GRCm39) |
L136P |
probably damaging |
Het |
Hdac11 |
A |
G |
6: 91,145,827 (GRCm39) |
T176A |
probably benign |
Het |
Hhip |
C |
A |
8: 80,698,967 (GRCm39) |
V700L |
probably damaging |
Het |
Hps5 |
T |
C |
7: 46,426,463 (GRCm39) |
|
probably benign |
Het |
Itgb1bp1 |
T |
C |
12: 21,329,436 (GRCm39) |
S13G |
unknown |
Het |
Kcna1 |
A |
T |
6: 126,619,148 (GRCm39) |
L391M |
possibly damaging |
Het |
Kif1a |
C |
T |
1: 93,010,128 (GRCm39) |
V6M |
probably damaging |
Het |
Klhl6 |
T |
C |
16: 19,801,639 (GRCm39) |
I39V |
probably benign |
Het |
Lpcat4 |
C |
A |
2: 112,072,334 (GRCm39) |
|
silent |
Het |
Ltn1 |
A |
T |
16: 87,202,509 (GRCm39) |
S1047R |
probably benign |
Het |
Mdn1 |
A |
G |
4: 32,694,495 (GRCm39) |
T1073A |
possibly damaging |
Het |
Megf10 |
G |
T |
18: 57,421,055 (GRCm39) |
A898S |
possibly damaging |
Het |
Mtmr6 |
T |
C |
14: 60,529,577 (GRCm39) |
|
probably null |
Het |
Mtnr1b |
T |
C |
9: 15,774,059 (GRCm39) |
I333M |
probably benign |
Het |
Muc5ac |
G |
T |
7: 141,348,950 (GRCm39) |
C463F |
probably benign |
Het |
Mycbpap |
G |
T |
11: 94,396,543 (GRCm39) |
T99N |
possibly damaging |
Het |
Myo7a |
C |
T |
7: 97,728,534 (GRCm39) |
C824Y |
probably damaging |
Het |
N4bp2 |
A |
G |
5: 65,948,303 (GRCm39) |
H311R |
probably damaging |
Het |
Nop56 |
A |
T |
2: 130,117,489 (GRCm39) |
|
probably benign |
Het |
Nup210 |
A |
G |
6: 90,995,978 (GRCm39) |
|
probably benign |
Het |
Or4d10c |
A |
G |
19: 12,065,391 (GRCm39) |
V255A |
probably damaging |
Het |
Or7g25 |
T |
A |
9: 19,160,441 (GRCm39) |
I85F |
probably damaging |
Het |
Pcna |
C |
T |
2: 132,093,673 (GRCm39) |
E109K |
probably benign |
Het |
Pgap6 |
A |
T |
17: 26,338,414 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
T |
G |
1: 20,607,589 (GRCm39) |
D1089A |
possibly damaging |
Het |
Plb1 |
A |
G |
5: 32,485,756 (GRCm39) |
R847G |
probably damaging |
Het |
Pou6f2 |
A |
G |
13: 18,303,612 (GRCm39) |
|
probably benign |
Het |
Prss43 |
C |
G |
9: 110,660,049 (GRCm39) |
S371C |
probably benign |
Het |
Ralgapa1 |
A |
T |
12: 55,741,942 (GRCm39) |
V1322D |
probably damaging |
Het |
Rrp8 |
A |
G |
7: 105,384,109 (GRCm39) |
V131A |
probably benign |
Het |
Rtp1 |
A |
T |
16: 23,248,044 (GRCm39) |
K39M |
probably benign |
Het |
Sanbr |
A |
T |
11: 23,565,150 (GRCm39) |
L279Q |
possibly damaging |
Het |
Slc1a6 |
A |
G |
10: 78,636,008 (GRCm39) |
I358V |
probably benign |
Het |
Slc25a15 |
T |
C |
8: 22,885,726 (GRCm39) |
|
probably benign |
Het |
Slc43a1 |
G |
A |
2: 84,684,897 (GRCm39) |
|
probably benign |
Het |
Speer4c1 |
A |
C |
5: 15,919,214 (GRCm39) |
|
probably benign |
Het |
Spock3 |
T |
G |
8: 63,802,018 (GRCm39) |
|
probably null |
Het |
Tbc1d7 |
T |
C |
13: 43,308,162 (GRCm39) |
|
probably null |
Het |
Tmem184c |
C |
T |
8: 78,326,286 (GRCm39) |
W260* |
probably null |
Het |
Trnau1ap |
A |
G |
4: 132,039,252 (GRCm39) |
Y265H |
probably damaging |
Het |
Usp25 |
T |
C |
16: 76,871,754 (GRCm39) |
F363S |
probably damaging |
Het |
Vcl |
T |
C |
14: 21,072,085 (GRCm39) |
F817L |
possibly damaging |
Het |
Vmn1r13 |
T |
A |
6: 57,187,717 (GRCm39) |
M292K |
probably benign |
Het |
Xpc |
G |
T |
6: 91,487,463 (GRCm39) |
A89E |
probably damaging |
Het |
|
Other mutations in Nepro |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00766:Nepro
|
APN |
16 |
44,549,668 (GRCm39) |
nonsense |
probably null |
|
IGL01688:Nepro
|
APN |
16 |
44,556,369 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03149:Nepro
|
APN |
16 |
44,547,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R0839:Nepro
|
UTSW |
16 |
44,556,382 (GRCm39) |
missense |
probably benign |
0.27 |
R1619:Nepro
|
UTSW |
16 |
44,547,391 (GRCm39) |
missense |
probably benign |
0.01 |
R1777:Nepro
|
UTSW |
16 |
44,556,216 (GRCm39) |
missense |
probably damaging |
0.99 |
R4273:Nepro
|
UTSW |
16 |
44,556,192 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4487:Nepro
|
UTSW |
16 |
44,556,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Nepro
|
UTSW |
16 |
44,550,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R4841:Nepro
|
UTSW |
16 |
44,555,160 (GRCm39) |
missense |
probably null |
1.00 |
R4842:Nepro
|
UTSW |
16 |
44,555,160 (GRCm39) |
missense |
probably null |
1.00 |
R4869:Nepro
|
UTSW |
16 |
44,550,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Nepro
|
UTSW |
16 |
44,555,156 (GRCm39) |
missense |
probably benign |
0.16 |
R4988:Nepro
|
UTSW |
16 |
44,554,905 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6480:Nepro
|
UTSW |
16 |
44,547,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Nepro
|
UTSW |
16 |
44,551,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Nepro
|
UTSW |
16 |
44,550,078 (GRCm39) |
critical splice donor site |
probably null |
|
R8024:Nepro
|
UTSW |
16 |
44,551,778 (GRCm39) |
missense |
probably benign |
0.05 |
R9256:Nepro
|
UTSW |
16 |
44,544,790 (GRCm39) |
missense |
probably benign |
0.01 |
R9430:Nepro
|
UTSW |
16 |
44,552,460 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9607:Nepro
|
UTSW |
16 |
44,551,832 (GRCm39) |
missense |
probably damaging |
1.00 |
U24488:Nepro
|
UTSW |
16 |
44,554,949 (GRCm39) |
missense |
probably benign |
0.02 |
X0067:Nepro
|
UTSW |
16 |
44,555,066 (GRCm39) |
missense |
possibly damaging |
0.59 |
|