Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
G |
5: 88,120,451 (GRCm39) |
T403A |
probably benign |
Het |
Aco1 |
T |
C |
4: 40,184,983 (GRCm39) |
L551S |
probably damaging |
Het |
Acvr1 |
C |
T |
2: 58,364,230 (GRCm39) |
V200I |
probably damaging |
Het |
Adam26b |
T |
A |
8: 43,973,245 (GRCm39) |
T586S |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,580,656 (GRCm39) |
R1849G |
probably benign |
Het |
Alox5 |
T |
A |
6: 116,389,497 (GRCm39) |
D590V |
probably benign |
Het |
Anapc5 |
A |
G |
5: 122,931,498 (GRCm39) |
|
probably null |
Het |
Anln |
T |
C |
9: 22,269,965 (GRCm39) |
E743G |
possibly damaging |
Het |
Anpep |
T |
C |
7: 79,488,174 (GRCm39) |
K496R |
probably benign |
Het |
Aox3 |
T |
A |
1: 58,181,855 (GRCm39) |
S281T |
probably benign |
Het |
Arhgef11 |
C |
A |
3: 87,640,529 (GRCm39) |
P1258T |
probably damaging |
Het |
Atp2c2 |
A |
T |
8: 120,456,917 (GRCm39) |
D173V |
possibly damaging |
Het |
Aurka |
T |
G |
2: 172,210,949 (GRCm39) |
D22A |
probably benign |
Het |
B3gat1 |
A |
T |
9: 26,666,882 (GRCm39) |
D51V |
probably benign |
Het |
BC028528 |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT |
3: 95,795,448 (GRCm39) |
|
probably benign |
Het |
BC028528 |
TGGTTCTGTGGTCAC |
TGGTTCTGTGGTCACGGGTTCTGTGGTCAC |
3: 95,795,483 (GRCm39) |
|
probably benign |
Het |
BC028528 |
ACTGGTTCTGTGGTCACTGGTTCTGTGGTC |
ACTGGTTCTGTGGTCGCTGGTTCTGTGGTCACTGGTTCTGTGGTC |
3: 95,795,466 (GRCm39) |
|
probably benign |
Het |
BC028528 |
TTC |
TTCGGTGGTCACTGGCTC |
3: 95,795,456 (GRCm39) |
|
probably benign |
Het |
BC028528 |
GGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACT |
GGTTCTGTGGTCACTTGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACT |
3: 95,795,454 (GRCm39) |
|
probably benign |
Het |
BC028528 |
CTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCA |
CTGGTTCTGTGGTCAATGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCA |
3: 95,795,452 (GRCm39) |
|
probably benign |
Het |
BC028528 |
CACTG |
CACTGATTCTGTGGTGACTG |
3: 95,795,450 (GRCm39) |
|
probably benign |
Het |
Bcas3 |
G |
A |
11: 85,261,954 (GRCm39) |
G96S |
probably damaging |
Het |
Bltp1 |
C |
T |
3: 37,061,218 (GRCm39) |
A3309V |
probably damaging |
Het |
C2cd4d |
T |
A |
3: 94,270,860 (GRCm39) |
V42D |
probably damaging |
Het |
Ccdc127 |
T |
C |
13: 74,505,151 (GRCm39) |
L233P |
probably damaging |
Het |
Cdc42bpa |
A |
G |
1: 179,921,578 (GRCm39) |
K573E |
probably damaging |
Het |
Cend1 |
T |
C |
7: 141,007,544 (GRCm39) |
D92G |
probably damaging |
Het |
Crb1 |
T |
C |
1: 139,170,909 (GRCm39) |
D827G |
probably damaging |
Het |
Cyld |
G |
T |
8: 89,461,525 (GRCm39) |
C654F |
probably damaging |
Het |
Fastkd5 |
C |
T |
2: 130,458,557 (GRCm39) |
G11D |
probably damaging |
Het |
Foxj3 |
A |
T |
4: 119,477,252 (GRCm39) |
N354I |
possibly damaging |
Het |
Gimap8 |
G |
T |
6: 48,627,999 (GRCm39) |
C252F |
probably benign |
Het |
Glra1 |
T |
C |
11: 55,411,821 (GRCm39) |
Y329C |
probably damaging |
Het |
Gm10330 |
G |
A |
12: 23,829,980 (GRCm39) |
P67L |
probably benign |
Het |
Gpm6a |
T |
C |
8: 55,508,469 (GRCm39) |
I226T |
possibly damaging |
Het |
Gstt2 |
A |
G |
10: 75,668,418 (GRCm39) |
F121S |
probably benign |
Het |
Hjurp |
TCTGGGAGGGCTTGCTCCGGGGGCAGTGTGTCCTGTTCTTGTGCAGCCCCTGCT |
TCT |
1: 88,194,000 (GRCm39) |
|
probably benign |
Het |
Hmcn2 |
T |
C |
2: 31,310,311 (GRCm39) |
F3302L |
probably benign |
Het |
Hormad2 |
T |
C |
11: 4,358,841 (GRCm39) |
T189A |
probably damaging |
Het |
Hps5 |
A |
T |
7: 46,418,826 (GRCm39) |
S815T |
probably benign |
Het |
Hydin |
G |
T |
8: 111,282,239 (GRCm39) |
R3113L |
possibly damaging |
Het |
Inava |
A |
G |
1: 136,155,279 (GRCm39) |
S109P |
probably benign |
Het |
Inpp5f |
T |
A |
7: 128,294,037 (GRCm39) |
C698S |
probably benign |
Het |
Irs1 |
T |
G |
1: 82,267,605 (GRCm39) |
M204L |
probably benign |
Het |
Itfg1 |
T |
C |
8: 86,490,909 (GRCm39) |
D340G |
probably damaging |
Het |
Itm2c |
T |
A |
1: 85,833,032 (GRCm39) |
I122N |
probably damaging |
Het |
Lamp3 |
T |
A |
16: 19,474,247 (GRCm39) |
T376S |
probably damaging |
Het |
Lrba |
T |
A |
3: 86,622,872 (GRCm39) |
I2418N |
probably damaging |
Het |
Lrcol1 |
T |
A |
5: 110,502,715 (GRCm39) |
V161D |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,259,016 (GRCm39) |
Q4558L |
probably benign |
Het |
Lrrfip2 |
A |
T |
9: 111,034,836 (GRCm39) |
Q175L |
probably damaging |
Het |
Mib1 |
T |
G |
18: 10,778,187 (GRCm39) |
S572R |
probably damaging |
Het |
Mis18bp1 |
A |
T |
12: 65,199,532 (GRCm39) |
D456E |
possibly damaging |
Het |
Mlh1 |
T |
A |
9: 111,090,581 (GRCm39) |
T116S |
possibly damaging |
Het |
Mpp4 |
T |
C |
1: 59,160,521 (GRCm39) |
N594S |
probably damaging |
Het |
Nbas |
A |
G |
12: 13,455,458 (GRCm39) |
E1224G |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,110,997 (GRCm39) |
D163G |
possibly damaging |
Het |
Nectin4 |
T |
C |
1: 171,207,941 (GRCm39) |
V111A |
possibly damaging |
Het |
Nfatc2ip |
G |
A |
7: 125,989,617 (GRCm39) |
R256* |
probably null |
Het |
Nlgn2 |
G |
A |
11: 69,716,760 (GRCm39) |
R594C |
probably damaging |
Het |
Nufip1 |
A |
G |
14: 76,352,442 (GRCm39) |
S198G |
possibly damaging |
Het |
Or2n1 |
T |
C |
17: 38,486,158 (GRCm39) |
F61S |
probably damaging |
Het |
Or5ac23 |
C |
T |
16: 59,149,606 (GRCm39) |
D89N |
possibly damaging |
Het |
Or8s8 |
C |
T |
15: 98,354,574 (GRCm39) |
H128Y |
probably benign |
Het |
Pcdhga8 |
G |
A |
18: 37,859,896 (GRCm39) |
M317I |
probably benign |
Het |
Phactr1 |
A |
T |
13: 42,863,239 (GRCm39) |
I55L |
probably benign |
Het |
Prl3c1 |
G |
A |
13: 27,383,367 (GRCm39) |
R31Q |
probably benign |
Het |
Prss55 |
A |
T |
14: 64,319,180 (GRCm39) |
F59Y |
possibly damaging |
Het |
Ptprb |
T |
C |
10: 116,158,392 (GRCm39) |
W488R |
probably damaging |
Het |
Qrich2 |
GAAACCAGGCTGATCTGCCCCAGGCTGCAACAAACCAGGCTGATCTGCCCCAGGCTGCAACAAACCAGGCTGATCTGCCCCAGGCTGCAACAAACCAGGCTGATCTGTCCCAGGCTGCAACAAACCAGGCTGATC |
GAAACCAGGCTGATCTGCCCCAGGCTGCAACAAACCAGGCTGATCTGCCCCAGGCTGCAACAAACCAGGCTGATCTGTCCCAGGCTGCAACAAACCAGGCTGATC |
11: 116,346,608 (GRCm39) |
|
probably benign |
Het |
Ros1 |
G |
T |
10: 52,044,791 (GRCm39) |
T172K |
probably damaging |
Het |
Rtel1 |
C |
T |
2: 180,997,869 (GRCm39) |
R1206W |
possibly damaging |
Het |
Slf2 |
A |
T |
19: 44,930,682 (GRCm39) |
K586N |
probably damaging |
Het |
Smc2 |
T |
A |
4: 52,450,854 (GRCm39) |
M224K |
probably benign |
Het |
Spata31d1e |
A |
T |
13: 59,890,329 (GRCm39) |
I497K |
probably damaging |
Het |
Spinkl |
T |
C |
18: 44,299,716 (GRCm39) |
Y83C |
probably damaging |
Het |
Srgap1 |
CTACCTCCTCTTAGGGACCACGCCCACCCCCTCCCAGGGACCATGCTTACCTCCTCTTAGGGACCACGCCCACCCCCTCCCAGGGACCATGCTTACCTCCTC |
CTACCTCCTCTTAGGGACCACGCCCACCCCCTCCCAGGGACCATGCTTACCTCCTC |
10: 121,689,458 (GRCm39) |
|
probably benign |
Het |
St13 |
T |
C |
15: 81,283,719 (GRCm39) |
E26G |
possibly damaging |
Het |
Teddm3 |
T |
A |
16: 20,971,699 (GRCm39) |
Q290L |
probably benign |
Het |
Tfec |
C |
A |
6: 16,840,467 (GRCm39) |
|
probably null |
Het |
Trank1 |
C |
A |
9: 111,220,596 (GRCm39) |
D2444E |
probably benign |
Het |
Ttc17 |
T |
A |
2: 94,209,166 (GRCm39) |
N96I |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,560,130 (GRCm39) |
T29424A |
possibly damaging |
Het |
Tut7 |
C |
A |
13: 59,946,819 (GRCm39) |
Q1003H |
probably damaging |
Het |
Vmn1r68 |
G |
A |
7: 10,261,237 (GRCm39) |
T287I |
probably benign |
Het |
Vmn2r52 |
C |
A |
7: 9,896,877 (GRCm39) |
V532L |
probably benign |
Het |
Vmn2r92 |
A |
T |
17: 18,404,970 (GRCm39) |
T705S |
possibly damaging |
Het |
Vps13d |
T |
C |
4: 144,899,697 (GRCm39) |
D200G |
|
Het |
Wdr48 |
G |
A |
9: 119,733,405 (GRCm39) |
C84Y |
probably damaging |
Het |
Zscan25 |
T |
A |
5: 145,227,321 (GRCm39) |
H328Q |
probably benign |
Het |
|
Other mutations in Or8b49 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01092:Or8b49
|
APN |
9 |
38,506,201 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02028:Or8b49
|
APN |
9 |
38,505,715 (GRCm39) |
nonsense |
probably null |
|
IGL02256:Or8b49
|
APN |
9 |
38,505,840 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03103:Or8b49
|
APN |
9 |
38,505,823 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Or8b49
|
APN |
9 |
38,505,821 (GRCm39) |
missense |
probably benign |
0.01 |
R2152:Or8b49
|
UTSW |
9 |
38,505,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Or8b49
|
UTSW |
9 |
38,505,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Or8b49
|
UTSW |
9 |
38,505,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R3176:Or8b49
|
UTSW |
9 |
38,505,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Or8b49
|
UTSW |
9 |
38,505,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4985:Or8b49
|
UTSW |
9 |
38,505,658 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5043:Or8b49
|
UTSW |
9 |
38,506,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R5871:Or8b49
|
UTSW |
9 |
38,505,628 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6106:Or8b49
|
UTSW |
9 |
38,506,252 (GRCm39) |
missense |
probably benign |
0.11 |
R6583:Or8b49
|
UTSW |
9 |
38,506,260 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6823:Or8b49
|
UTSW |
9 |
38,506,201 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7472:Or8b49
|
UTSW |
9 |
38,506,200 (GRCm39) |
missense |
probably benign |
0.10 |
R8036:Or8b49
|
UTSW |
9 |
38,506,186 (GRCm39) |
missense |
probably benign |
0.00 |
R8182:Or8b49
|
UTSW |
9 |
38,505,840 (GRCm39) |
missense |
probably benign |
0.01 |
R8390:Or8b49
|
UTSW |
9 |
38,505,887 (GRCm39) |
nonsense |
probably null |
|
R8806:Or8b49
|
UTSW |
9 |
38,506,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R8886:Or8b49
|
UTSW |
9 |
38,506,446 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8928:Or8b49
|
UTSW |
9 |
38,505,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Or8b49
|
UTSW |
9 |
38,506,123 (GRCm39) |
missense |
probably damaging |
0.99 |
R9123:Or8b49
|
UTSW |
9 |
38,506,108 (GRCm39) |
missense |
probably damaging |
0.97 |
R9125:Or8b49
|
UTSW |
9 |
38,506,108 (GRCm39) |
missense |
probably damaging |
0.97 |
R9572:Or8b49
|
UTSW |
9 |
38,505,627 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Or8b49
|
UTSW |
9 |
38,505,585 (GRCm39) |
missense |
probably damaging |
1.00 |
|