Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts18 |
A |
G |
8: 114,431,805 (GRCm39) |
|
probably benign |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Amt |
A |
G |
9: 108,178,296 (GRCm39) |
D301G |
probably benign |
Het |
Arhgef26 |
T |
C |
3: 62,247,744 (GRCm39) |
V276A |
probably benign |
Het |
Bid |
C |
T |
6: 120,874,216 (GRCm39) |
A110T |
possibly damaging |
Het |
Ccdc63 |
T |
C |
5: 122,246,224 (GRCm39) |
T566A |
probably benign |
Het |
Cdk5rap1 |
A |
G |
2: 154,202,574 (GRCm39) |
S219P |
probably damaging |
Het |
Col1a2 |
T |
A |
6: 4,515,684 (GRCm39) |
|
probably null |
Het |
Ctns |
G |
A |
11: 73,075,823 (GRCm39) |
T342I |
probably benign |
Het |
Dst |
G |
A |
1: 34,267,428 (GRCm39) |
E4957K |
probably damaging |
Het |
Elp1 |
C |
T |
4: 56,770,969 (GRCm39) |
|
probably benign |
Het |
Fam163b |
A |
G |
2: 27,003,659 (GRCm39) |
|
probably benign |
Het |
Frem2 |
T |
C |
3: 53,457,152 (GRCm39) |
T2067A |
probably benign |
Het |
Gm9791 |
T |
C |
3: 34,059,225 (GRCm39) |
|
noncoding transcript |
Het |
Grik2 |
G |
T |
10: 49,404,087 (GRCm39) |
T258N |
probably damaging |
Het |
Herc3 |
T |
C |
6: 58,864,478 (GRCm39) |
L704P |
probably damaging |
Het |
Hjurp |
A |
C |
1: 88,193,768 (GRCm39) |
V380G |
probably damaging |
Het |
Lrrc56 |
A |
G |
7: 140,778,177 (GRCm39) |
|
probably benign |
Het |
Mast3 |
G |
A |
8: 71,233,938 (GRCm39) |
P187S |
probably damaging |
Het |
Mier2 |
A |
G |
10: 79,380,991 (GRCm39) |
V231A |
probably benign |
Het |
Muc5b |
A |
G |
7: 141,422,144 (GRCm39) |
T4427A |
possibly damaging |
Het |
Nox4 |
A |
G |
7: 86,896,072 (GRCm39) |
S7G |
possibly damaging |
Het |
Obscn |
G |
C |
11: 58,971,143 (GRCm39) |
Q2457E |
probably damaging |
Het |
Sh3bgrl2 |
C |
T |
9: 83,459,684 (GRCm39) |
|
probably benign |
Het |
Slc1a1 |
A |
G |
19: 28,812,611 (GRCm39) |
|
probably benign |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Stard9 |
C |
A |
2: 120,504,117 (GRCm39) |
S221R |
probably damaging |
Het |
Stat6 |
G |
C |
10: 127,487,094 (GRCm39) |
R200S |
possibly damaging |
Het |
Stxbp5l |
C |
A |
16: 37,068,231 (GRCm39) |
|
probably null |
Het |
Tanc1 |
A |
G |
2: 59,673,835 (GRCm39) |
S1647G |
probably benign |
Het |
Tmem132d |
T |
A |
5: 127,861,923 (GRCm39) |
M733L |
probably benign |
Het |
Unc13d |
A |
G |
11: 115,964,381 (GRCm39) |
|
probably benign |
Het |
Usp24 |
T |
C |
4: 106,199,550 (GRCm39) |
S165P |
possibly damaging |
Het |
Vmn1r9 |
T |
C |
6: 57,048,615 (GRCm39) |
I230T |
probably damaging |
Het |
Zscan20 |
T |
C |
4: 128,481,889 (GRCm39) |
D591G |
possibly damaging |
Het |
|
Other mutations in Gm7353 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00401:Gm7353
|
APN |
7 |
3,160,630 (GRCm39) |
exon |
noncoding transcript |
|
R0894:Gm7353
|
UTSW |
7 |
3,160,570 (GRCm39) |
exon |
noncoding transcript |
|
R4780:Gm7353
|
UTSW |
7 |
3,160,725 (GRCm39) |
exon |
noncoding transcript |
|
R4978:Gm7353
|
UTSW |
7 |
3,160,038 (GRCm39) |
exon |
noncoding transcript |
|
R5141:Gm7353
|
UTSW |
7 |
3,161,001 (GRCm39) |
unclassified |
noncoding transcript |
|
R5800:Gm7353
|
UTSW |
7 |
3,160,168 (GRCm39) |
critical splice acceptor site |
noncoding transcript |
|
|