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 |
Nepro |
T |
A |
16: 44,552,509 (GRCm39) |
|
probably benign |
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 |
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 Rtp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02276:Rtp1
|
APN |
16 |
23,250,063 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02329:Rtp1
|
APN |
16 |
23,249,943 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02432:Rtp1
|
APN |
16 |
23,250,154 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02690:Rtp1
|
APN |
16 |
23,250,132 (GRCm39) |
missense |
probably damaging |
1.00 |
P0028:Rtp1
|
UTSW |
16 |
23,248,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R0319:Rtp1
|
UTSW |
16 |
23,250,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R0377:Rtp1
|
UTSW |
16 |
23,250,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R0972:Rtp1
|
UTSW |
16 |
23,250,058 (GRCm39) |
missense |
probably damaging |
0.99 |
R1498:Rtp1
|
UTSW |
16 |
23,249,970 (GRCm39) |
missense |
probably benign |
0.00 |
R1751:Rtp1
|
UTSW |
16 |
23,250,124 (GRCm39) |
missense |
probably damaging |
0.98 |
R1767:Rtp1
|
UTSW |
16 |
23,250,124 (GRCm39) |
missense |
probably damaging |
0.98 |
R1900:Rtp1
|
UTSW |
16 |
23,248,049 (GRCm39) |
missense |
probably benign |
|
R1921:Rtp1
|
UTSW |
16 |
23,250,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1922:Rtp1
|
UTSW |
16 |
23,250,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Rtp1
|
UTSW |
16 |
23,249,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R2102:Rtp1
|
UTSW |
16 |
23,250,108 (GRCm39) |
missense |
probably benign |
0.04 |
R5118:Rtp1
|
UTSW |
16 |
23,250,285 (GRCm39) |
missense |
probably benign |
0.00 |
R5484:Rtp1
|
UTSW |
16 |
23,248,025 (GRCm39) |
missense |
probably benign |
|
R5614:Rtp1
|
UTSW |
16 |
23,249,940 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8509:Rtp1
|
UTSW |
16 |
23,248,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R8699:Rtp1
|
UTSW |
16 |
23,250,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R9573:Rtp1
|
UTSW |
16 |
23,250,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
|