Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
C |
A |
10: 78,903,565 (GRCm39) |
K250N |
probably damaging |
Het |
Adam5 |
A |
T |
8: 25,237,540 (GRCm39) |
D623E |
possibly damaging |
Het |
Akt3 |
T |
C |
1: 176,852,952 (GRCm39) |
Y473C |
probably damaging |
Het |
Ankib1 |
A |
G |
5: 3,805,617 (GRCm39) |
Y217H |
probably damaging |
Het |
Clca4b |
T |
A |
3: 144,616,927 (GRCm39) |
T908S |
probably benign |
Het |
Clec7a |
G |
A |
6: 129,440,126 (GRCm39) |
Q160* |
probably null |
Het |
Cntnap4 |
T |
A |
8: 113,460,103 (GRCm39) |
I152N |
probably damaging |
Het |
Ctdspl |
C |
T |
9: 118,866,445 (GRCm39) |
A179V |
probably damaging |
Het |
Ddx43 |
T |
C |
9: 78,313,668 (GRCm39) |
S200P |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,544,963 (GRCm39) |
D84G |
unknown |
Het |
Dmbt1 |
G |
A |
7: 130,675,987 (GRCm39) |
R625H |
unknown |
Het |
Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 72,684,217 (GRCm39) |
|
probably benign |
Het |
E2f7 |
C |
T |
10: 110,603,050 (GRCm39) |
T355I |
probably damaging |
Het |
E2f7 |
C |
A |
10: 110,614,918 (GRCm39) |
L541M |
probably damaging |
Het |
Elovl5 |
T |
A |
9: 77,890,007 (GRCm39) |
S273T |
possibly damaging |
Het |
Emc1 |
T |
A |
4: 139,093,705 (GRCm39) |
L605Q |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,887,124 (GRCm39) |
D2635E |
probably benign |
Het |
Gabrb1 |
G |
A |
5: 72,265,690 (GRCm39) |
G195E |
probably damaging |
Het |
Galm |
A |
G |
17: 80,457,561 (GRCm39) |
D199G |
possibly damaging |
Het |
Galntl6 |
T |
G |
8: 58,230,359 (GRCm39) |
S20R |
probably damaging |
Het |
Grb14 |
T |
G |
2: 64,768,744 (GRCm39) |
Y189S |
probably damaging |
Het |
Hk2 |
T |
A |
6: 82,705,895 (GRCm39) |
I803F |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,506,471 (GRCm39) |
R3779W |
probably damaging |
Het |
Hmgcr |
A |
C |
13: 96,796,403 (GRCm39) |
M260R |
probably damaging |
Het |
Hsbp1l1 |
T |
A |
18: 80,276,639 (GRCm39) |
K68N |
possibly damaging |
Het |
Inhba |
A |
C |
13: 16,192,263 (GRCm39) |
E128A |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Klhl3 |
G |
A |
13: 58,167,273 (GRCm39) |
P364S |
probably damaging |
Het |
Lhpp |
T |
C |
7: 132,243,312 (GRCm39) |
L176P |
probably damaging |
Het |
Lrp1b |
C |
A |
2: 40,491,599 (GRCm39) |
A223S |
probably damaging |
Het |
Lrp3 |
A |
G |
7: 34,903,489 (GRCm39) |
F286L |
probably damaging |
Het |
Lrrc7 |
T |
C |
3: 157,841,028 (GRCm39) |
T1337A |
probably benign |
Het |
Magi2 |
A |
G |
5: 20,400,019 (GRCm39) |
D17G |
probably benign |
Het |
Map3k21 |
T |
C |
8: 126,650,903 (GRCm39) |
S302P |
probably damaging |
Het |
Matcap2 |
T |
C |
9: 22,343,015 (GRCm39) |
M303T |
probably damaging |
Het |
Mbtd1 |
A |
G |
11: 93,816,511 (GRCm39) |
D386G |
probably benign |
Het |
Mfsd2b |
A |
T |
12: 4,916,820 (GRCm39) |
D306E |
possibly damaging |
Het |
Muc20 |
T |
C |
16: 32,614,453 (GRCm39) |
E308G |
probably damaging |
Het |
Myh13 |
G |
A |
11: 67,255,712 (GRCm39) |
S34N |
|
Het |
Nebl |
C |
A |
2: 17,374,421 (GRCm39) |
G894* |
probably null |
Het |
Nelfa |
A |
G |
5: 34,056,095 (GRCm39) |
Y523H |
probably damaging |
Het |
Ninj1 |
A |
G |
13: 49,341,076 (GRCm39) |
D13G |
probably benign |
Het |
Ninl |
A |
T |
2: 150,782,726 (GRCm39) |
S170T |
probably benign |
Het |
Nlrp4c |
G |
A |
7: 6,068,626 (GRCm39) |
V176M |
possibly damaging |
Het |
Nobox |
G |
A |
6: 43,284,115 (GRCm39) |
R144C |
probably damaging |
Het |
Oas1a |
G |
A |
5: 121,037,317 (GRCm39) |
L237F |
probably damaging |
Het |
Or4a81 |
A |
C |
2: 89,619,506 (GRCm39) |
Y63* |
probably null |
Het |
Or52z15 |
A |
T |
7: 103,332,477 (GRCm39) |
Y184F |
probably damaging |
Het |
Or5w20 |
T |
C |
2: 87,726,693 (GRCm39) |
M50T |
probably benign |
Het |
Or6z1 |
A |
G |
7: 6,505,150 (GRCm39) |
L25P |
probably benign |
Het |
Or7c70 |
T |
C |
10: 78,682,891 (GRCm39) |
N286S |
probably damaging |
Het |
Or8h9 |
A |
G |
2: 86,789,757 (GRCm39) |
M15T |
probably benign |
Het |
Orai1 |
A |
G |
5: 123,167,301 (GRCm39) |
N158S |
probably damaging |
Het |
Pa2g4 |
C |
A |
10: 128,398,967 (GRCm39) |
V121L |
probably benign |
Het |
Pclo |
T |
C |
5: 14,571,250 (GRCm39) |
S212P |
possibly damaging |
Het |
Plce1 |
G |
A |
19: 38,766,337 (GRCm39) |
E2121K |
possibly damaging |
Het |
Plg |
A |
G |
17: 12,622,024 (GRCm39) |
Y448C |
probably damaging |
Het |
Plppr4 |
A |
T |
3: 117,116,866 (GRCm39) |
N330K |
probably damaging |
Het |
Pou2f2 |
A |
G |
7: 24,794,247 (GRCm39) |
L373S |
probably benign |
Het |
Rp1 |
A |
G |
1: 4,162,838 (GRCm39) |
|
probably null |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Slc5a4a |
GCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGC |
GCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGCCTTGC |
10: 75,986,238 (GRCm39) |
|
probably benign |
Het |
Slc5a5 |
T |
C |
8: 71,337,596 (GRCm39) |
D574G |
probably benign |
Het |
Slc7a15 |
T |
A |
12: 8,588,794 (GRCm39) |
N251I |
probably damaging |
Het |
Speer4a3 |
A |
T |
5: 26,158,136 (GRCm39) |
I72N |
probably damaging |
Het |
Susd4 |
T |
C |
1: 182,719,665 (GRCm39) |
S427P |
probably benign |
Het |
Tarbp1 |
T |
A |
8: 127,155,779 (GRCm39) |
T1320S |
probably benign |
Het |
Tbpl2 |
C |
T |
2: 23,984,650 (GRCm39) |
V166I |
probably benign |
Het |
Thbs1 |
T |
C |
2: 117,950,518 (GRCm39) |
|
probably null |
Het |
Tnfsf13b |
A |
G |
8: 10,081,648 (GRCm39) |
Y270C |
probably damaging |
Het |
Vps11 |
G |
T |
9: 44,260,290 (GRCm39) |
C857* |
probably null |
Het |
Vsig10 |
G |
A |
5: 117,463,104 (GRCm39) |
R110H |
probably benign |
Het |
Wee2 |
T |
A |
6: 40,432,044 (GRCm39) |
Y204* |
probably null |
Het |
Zfpm2 |
T |
A |
15: 40,966,867 (GRCm39) |
S1117R |
probably damaging |
Het |
Zscan5b |
A |
G |
7: 6,234,472 (GRCm39) |
N166S |
probably benign |
Het |
|
Other mutations in Rnpep |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01789:Rnpep
|
APN |
1 |
135,195,833 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0001:Rnpep
|
UTSW |
1 |
135,200,223 (GRCm39) |
splice site |
probably benign |
|
R0498:Rnpep
|
UTSW |
1 |
135,193,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Rnpep
|
UTSW |
1 |
135,200,157 (GRCm39) |
missense |
probably damaging |
0.99 |
R1728:Rnpep
|
UTSW |
1 |
135,211,715 (GRCm39) |
missense |
probably benign |
|
R1728:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1729:Rnpep
|
UTSW |
1 |
135,211,715 (GRCm39) |
missense |
probably benign |
|
R1729:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1730:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1739:Rnpep
|
UTSW |
1 |
135,211,367 (GRCm39) |
missense |
probably benign |
|
R1739:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1762:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1783:Rnpep
|
UTSW |
1 |
135,211,715 (GRCm39) |
missense |
probably benign |
|
R1783:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1784:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1785:Rnpep
|
UTSW |
1 |
135,211,715 (GRCm39) |
missense |
probably benign |
|
R1785:Rnpep
|
UTSW |
1 |
135,190,834 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2101:Rnpep
|
UTSW |
1 |
135,199,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R4933:Rnpep
|
UTSW |
1 |
135,194,764 (GRCm39) |
intron |
probably benign |
|
R4993:Rnpep
|
UTSW |
1 |
135,190,770 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5642:Rnpep
|
UTSW |
1 |
135,205,259 (GRCm39) |
missense |
probably damaging |
0.99 |
R6965:Rnpep
|
UTSW |
1 |
135,190,858 (GRCm39) |
nonsense |
probably null |
|
R7143:Rnpep
|
UTSW |
1 |
135,211,487 (GRCm39) |
missense |
probably benign |
0.41 |
R7508:Rnpep
|
UTSW |
1 |
135,206,596 (GRCm39) |
missense |
probably benign |
0.33 |
R8060:Rnpep
|
UTSW |
1 |
135,194,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R8094:Rnpep
|
UTSW |
1 |
135,211,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8191:Rnpep
|
UTSW |
1 |
135,200,172 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8300:Rnpep
|
UTSW |
1 |
135,211,397 (GRCm39) |
missense |
probably benign |
0.00 |
R8355:Rnpep
|
UTSW |
1 |
135,195,005 (GRCm39) |
missense |
probably damaging |
0.98 |
R9098:Rnpep
|
UTSW |
1 |
135,206,559 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9333:Rnpep
|
UTSW |
1 |
135,191,862 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Rnpep
|
UTSW |
1 |
135,211,574 (GRCm39) |
missense |
probably benign |
0.16 |
Z1176:Rnpep
|
UTSW |
1 |
135,199,493 (GRCm39) |
missense |
probably benign |
0.19 |
|