Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm2 |
T |
A |
7: 119,190,321 (GRCm39) |
D70E |
probably damaging |
Het |
Adamts14 |
C |
T |
10: 61,057,674 (GRCm39) |
G561R |
probably damaging |
Het |
Alpk3 |
A |
T |
7: 80,728,401 (GRCm39) |
K510N |
probably damaging |
Het |
Ap3b1 |
A |
G |
13: 94,576,781 (GRCm39) |
N269D |
probably benign |
Het |
Ap3b1 |
T |
C |
13: 94,619,773 (GRCm39) |
S144P |
probably damaging |
Het |
Apba2 |
C |
A |
7: 64,395,464 (GRCm39) |
Q635K |
probably benign |
Het |
Aspg |
C |
T |
12: 112,079,519 (GRCm39) |
T99I |
probably benign |
Het |
Atp7b |
A |
G |
8: 22,487,512 (GRCm39) |
V1179A |
probably damaging |
Het |
Bbs12 |
T |
C |
3: 37,374,197 (GRCm39) |
V215A |
probably damaging |
Het |
Bcl2l11 |
C |
A |
2: 127,969,703 (GRCm39) |
|
probably benign |
Het |
Bglap3 |
T |
G |
3: 88,283,653 (GRCm39) |
|
probably benign |
Het |
Cchcr1 |
G |
A |
17: 35,835,890 (GRCm39) |
R284Q |
probably damaging |
Het |
Cdh26 |
C |
T |
2: 178,123,443 (GRCm39) |
Q662* |
probably null |
Het |
Cftr |
T |
A |
6: 18,313,645 (GRCm39) |
F1290I |
probably damaging |
Het |
Clip3 |
G |
A |
7: 29,991,731 (GRCm39) |
E36K |
probably damaging |
Het |
Cog2 |
A |
G |
8: 125,272,825 (GRCm39) |
I541V |
probably benign |
Het |
Cpt1b |
A |
T |
15: 89,309,417 (GRCm39) |
W39R |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 15,982,471 (GRCm39) |
V2732A |
probably damaging |
Het |
Dlec1 |
A |
G |
9: 118,955,380 (GRCm39) |
D688G |
probably damaging |
Het |
Dnah12 |
A |
G |
14: 26,428,022 (GRCm39) |
E216G |
probably benign |
Het |
Dnah7b |
C |
A |
1: 46,226,450 (GRCm39) |
L1294I |
probably damaging |
Het |
Duox1 |
T |
A |
2: 122,174,637 (GRCm39) |
L1265Q |
probably damaging |
Het |
Fam91a1 |
T |
A |
15: 58,303,166 (GRCm39) |
D358E |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,910,797 (GRCm39) |
I1735S |
probably benign |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Gabrr1 |
T |
A |
4: 33,162,676 (GRCm39) |
M414K |
probably benign |
Het |
Gm21915 |
A |
C |
9: 40,581,995 (GRCm39) |
E29D |
possibly damaging |
Het |
Gm9955 |
G |
A |
18: 24,842,320 (GRCm39) |
|
probably benign |
Het |
Gpat2 |
C |
A |
2: 127,270,195 (GRCm39) |
D69E |
possibly damaging |
Het |
Grin2b |
T |
G |
6: 135,713,371 (GRCm39) |
I837L |
probably damaging |
Het |
Gucy2g |
T |
C |
19: 55,203,563 (GRCm39) |
D745G |
probably damaging |
Het |
H2-Q1 |
A |
G |
17: 35,540,332 (GRCm39) |
Y139C |
probably damaging |
Het |
Ints2 |
G |
C |
11: 86,141,798 (GRCm39) |
N216K |
probably benign |
Het |
Jmy |
G |
A |
13: 93,635,333 (GRCm39) |
P161L |
probably benign |
Het |
Kctd11 |
G |
A |
11: 69,770,799 (GRCm39) |
R80W |
possibly damaging |
Het |
Kif7 |
A |
G |
7: 79,360,880 (GRCm39) |
|
probably benign |
Het |
Kifc1 |
C |
T |
17: 34,102,059 (GRCm39) |
|
probably benign |
Het |
Lcor |
G |
A |
19: 41,574,839 (GRCm39) |
R1198Q |
probably damaging |
Het |
Mir412 |
C |
A |
12: 109,709,733 (GRCm39) |
|
noncoding transcript |
Het |
Mknk1 |
T |
A |
4: 115,733,834 (GRCm39) |
|
probably benign |
Het |
Mmp16 |
A |
G |
4: 18,054,354 (GRCm39) |
|
probably benign |
Het |
Myh4 |
A |
C |
11: 67,150,126 (GRCm39) |
D1861A |
probably damaging |
Het |
Nup205 |
T |
C |
6: 35,209,343 (GRCm39) |
L1550P |
probably damaging |
Het |
Or10g1 |
C |
T |
14: 52,647,525 (GRCm39) |
G268D |
probably benign |
Het |
Or2a56 |
G |
T |
6: 42,932,650 (GRCm39) |
A73S |
possibly damaging |
Het |
Or4c113 |
T |
A |
2: 88,884,963 (GRCm39) |
H269L |
probably benign |
Het |
Or4c58 |
T |
A |
2: 89,674,859 (GRCm39) |
I153F |
probably benign |
Het |
Or51af1 |
A |
G |
7: 103,141,927 (GRCm39) |
S53P |
possibly damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pafah1b2 |
A |
T |
9: 45,887,405 (GRCm39) |
C35* |
probably null |
Het |
Pappa |
T |
A |
4: 65,232,830 (GRCm39) |
F1323Y |
possibly damaging |
Het |
Phtf2 |
A |
T |
5: 20,979,071 (GRCm39) |
F519Y |
probably damaging |
Het |
Pigk |
T |
C |
3: 152,472,150 (GRCm39) |
I354T |
possibly damaging |
Het |
Plekha7 |
T |
C |
7: 115,724,040 (GRCm39) |
D1265G |
possibly damaging |
Het |
Prss12 |
A |
G |
3: 123,299,150 (GRCm39) |
R641G |
probably benign |
Het |
Prss28 |
A |
G |
17: 25,528,717 (GRCm39) |
Y53C |
probably damaging |
Het |
Rabgap1 |
G |
T |
2: 37,451,908 (GRCm39) |
C936F |
possibly damaging |
Het |
Rap1a |
T |
C |
3: 105,639,385 (GRCm39) |
I91M |
possibly damaging |
Het |
Rap1gap2 |
A |
T |
11: 74,283,063 (GRCm39) |
M679K |
probably damaging |
Het |
Rapgef5 |
T |
A |
12: 117,692,473 (GRCm39) |
L352I |
probably damaging |
Het |
Rhbdl3 |
G |
A |
11: 80,222,715 (GRCm39) |
V255M |
probably benign |
Het |
Rhot1 |
T |
C |
11: 80,141,996 (GRCm39) |
|
probably benign |
Het |
Rita1 |
A |
C |
5: 120,747,626 (GRCm39) |
V224G |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,702,788 (GRCm39) |
Y2900F |
probably damaging |
Het |
Scaf11 |
A |
C |
15: 96,318,189 (GRCm39) |
H458Q |
probably damaging |
Het |
Scamp4 |
T |
A |
10: 80,448,255 (GRCm39) |
S159T |
probably benign |
Het |
Setd5 |
T |
A |
6: 113,105,451 (GRCm39) |
Y828N |
probably damaging |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Sipa1l2 |
A |
G |
8: 126,200,275 (GRCm39) |
S684P |
probably damaging |
Het |
Stard9 |
A |
T |
2: 120,544,039 (GRCm39) |
I4446F |
probably damaging |
Het |
Sult1c2 |
T |
C |
17: 54,138,926 (GRCm39) |
D217G |
probably benign |
Het |
Supt16 |
C |
A |
14: 52,419,653 (GRCm39) |
K148N |
probably benign |
Het |
Syne3 |
G |
A |
12: 104,913,251 (GRCm39) |
S570L |
probably benign |
Het |
Tcf3 |
G |
T |
10: 80,248,878 (GRCm39) |
D534E |
probably benign |
Het |
Tmed6 |
G |
T |
8: 107,790,786 (GRCm39) |
T87K |
probably damaging |
Het |
Trbv3 |
T |
C |
6: 41,025,335 (GRCm39) |
I3T |
probably benign |
Het |
Trbv4 |
T |
A |
6: 41,036,563 (GRCm39) |
Y29* |
probably null |
Het |
Ttl |
A |
G |
2: 128,917,904 (GRCm39) |
N122S |
probably benign |
Het |
Txndc11 |
T |
C |
16: 10,892,935 (GRCm39) |
T932A |
probably benign |
Het |
Ube2e2 |
G |
A |
14: 18,586,910 (GRCm38) |
A150V |
probably damaging |
Het |
Ube2ql1 |
T |
C |
13: 69,887,459 (GRCm39) |
M1V |
probably null |
Het |
Uqcrc1 |
A |
G |
9: 108,776,554 (GRCm39) |
|
probably benign |
Het |
Utrn |
T |
C |
10: 12,362,227 (GRCm39) |
D2702G |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,840,810 (GRCm39) |
D618V |
probably damaging |
Het |
Vdac3-ps1 |
A |
G |
13: 18,205,787 (GRCm39) |
|
noncoding transcript |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Zap70 |
G |
A |
1: 36,810,030 (GRCm39) |
V47M |
probably damaging |
Het |
Zfp770 |
A |
G |
2: 114,028,027 (GRCm39) |
M14T |
possibly damaging |
Het |
Zup1 |
C |
T |
10: 33,825,458 (GRCm39) |
G8D |
probably damaging |
Het |
|
Other mutations in Mmp7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01349:Mmp7
|
APN |
9 |
7,699,335 (GRCm39) |
splice site |
probably benign |
|
IGL01522:Mmp7
|
APN |
9 |
7,692,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R1740:Mmp7
|
UTSW |
9 |
7,695,278 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3118:Mmp7
|
UTSW |
9 |
7,697,693 (GRCm39) |
missense |
probably benign |
|
R3195:Mmp7
|
UTSW |
9 |
7,692,219 (GRCm39) |
missense |
probably benign |
0.03 |
R3196:Mmp7
|
UTSW |
9 |
7,692,219 (GRCm39) |
missense |
probably benign |
0.03 |
R4595:Mmp7
|
UTSW |
9 |
7,697,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Mmp7
|
UTSW |
9 |
7,695,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R6564:Mmp7
|
UTSW |
9 |
7,695,185 (GRCm39) |
missense |
probably benign |
0.02 |
R6995:Mmp7
|
UTSW |
9 |
7,695,489 (GRCm39) |
missense |
probably damaging |
0.98 |
R7146:Mmp7
|
UTSW |
9 |
7,697,587 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7398:Mmp7
|
UTSW |
9 |
7,697,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Mmp7
|
UTSW |
9 |
7,697,749 (GRCm39) |
nonsense |
probably null |
|
R9104:Mmp7
|
UTSW |
9 |
7,697,947 (GRCm39) |
intron |
probably benign |
|
R9250:Mmp7
|
UTSW |
9 |
7,697,885 (GRCm39) |
intron |
probably benign |
|
Z1176:Mmp7
|
UTSW |
9 |
7,695,603 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mmp7
|
UTSW |
9 |
7,695,179 (GRCm39) |
missense |
probably benign |
0.03 |
|