Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
T |
A |
10: 10,274,708 (GRCm39) |
M750L |
probably benign |
Het |
Ahnak2 |
T |
A |
12: 112,745,428 (GRCm39) |
H673L |
|
Het |
Alg1 |
T |
C |
16: 5,059,201 (GRCm39) |
L338P |
probably damaging |
Het |
Anapc1 |
A |
C |
2: 128,459,642 (GRCm39) |
S1806A |
probably benign |
Het |
Anks1 |
C |
T |
17: 28,272,880 (GRCm39) |
T925I |
probably benign |
Het |
Aoc1l1 |
A |
G |
6: 48,952,324 (GRCm39) |
N83S |
probably benign |
Het |
Apob |
G |
A |
12: 8,056,629 (GRCm39) |
A1704T |
probably damaging |
Het |
Arnt |
G |
A |
3: 95,395,687 (GRCm39) |
V422M |
possibly damaging |
Het |
Cblb |
C |
A |
16: 51,986,701 (GRCm39) |
S648* |
probably null |
Het |
Cdk18 |
A |
G |
1: 132,044,183 (GRCm39) |
|
probably null |
Het |
Celsr1 |
T |
C |
15: 85,863,231 (GRCm39) |
D1267G |
probably damaging |
Het |
Chtf18 |
C |
T |
17: 25,942,732 (GRCm39) |
R399H |
probably damaging |
Het |
Cntnap1 |
T |
A |
11: 101,076,052 (GRCm39) |
Y979N |
probably damaging |
Het |
Col22a1 |
T |
C |
15: 71,853,794 (GRCm39) |
D256G |
probably damaging |
Het |
Dbn1 |
C |
T |
13: 55,629,760 (GRCm39) |
R174Q |
probably damaging |
Het |
Dnah10 |
G |
A |
5: 124,871,507 (GRCm39) |
|
probably null |
Het |
Dnah9 |
T |
A |
11: 65,838,368 (GRCm39) |
D3143V |
probably damaging |
Het |
Dnajc6 |
G |
A |
4: 101,494,098 (GRCm39) |
|
probably null |
Het |
Dsg1b |
A |
G |
18: 20,525,071 (GRCm39) |
N169S |
possibly damaging |
Het |
Eloa |
A |
G |
4: 135,737,847 (GRCm39) |
V371A |
probably benign |
Het |
Epb41l4b |
A |
T |
4: 57,076,553 (GRCm39) |
V327E |
probably damaging |
Het |
Fbxo15 |
A |
T |
18: 84,977,372 (GRCm39) |
T140S |
probably benign |
Het |
Fryl |
A |
T |
5: 73,349,152 (GRCm39) |
F3L |
unknown |
Het |
Galnt16 |
T |
C |
12: 80,644,880 (GRCm39) |
V501A |
probably damaging |
Het |
Haus6 |
A |
G |
4: 86,502,101 (GRCm39) |
I590T |
probably benign |
Het |
Hcfc2 |
T |
A |
10: 82,574,937 (GRCm39) |
F199I |
probably damaging |
Het |
Hoxd13 |
A |
G |
2: 74,499,327 (GRCm39) |
Y225C |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,314,362 (GRCm39) |
L4282P |
probably benign |
Het |
Ing2 |
T |
C |
8: 48,127,561 (GRCm39) |
E52G |
probably benign |
Het |
Itsn2 |
T |
C |
12: 4,679,730 (GRCm39) |
S180P |
unknown |
Het |
Kansl1l |
T |
C |
1: 66,765,129 (GRCm39) |
E727G |
probably damaging |
Het |
Klhl26 |
A |
G |
8: 70,904,156 (GRCm39) |
F585L |
probably benign |
Het |
Lce1a1 |
T |
G |
3: 92,554,190 (GRCm39) |
S95R |
unknown |
Het |
Lrp1b |
A |
T |
2: 41,013,640 (GRCm39) |
V1955E |
|
Het |
Megf6 |
G |
A |
4: 154,340,534 (GRCm39) |
G583E |
probably damaging |
Het |
Mex3a |
A |
G |
3: 88,443,505 (GRCm39) |
I194V |
possibly damaging |
Het |
Muc2 |
A |
T |
7: 141,279,389 (GRCm39) |
D155V |
probably damaging |
Het |
Ncam2 |
T |
C |
16: 81,252,252 (GRCm39) |
C232R |
probably damaging |
Het |
Nopchap1 |
T |
C |
10: 83,196,129 (GRCm39) |
F3L |
probably benign |
Het |
Or13n4 |
T |
C |
7: 106,423,707 (GRCm39) |
I9V |
probably benign |
Het |
Pdgfd |
C |
A |
9: 6,293,903 (GRCm39) |
A159E |
possibly damaging |
Het |
Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,341,589 (GRCm39) |
|
probably null |
Het |
Plekha8 |
C |
A |
6: 54,605,846 (GRCm39) |
T307K |
probably damaging |
Het |
Pnpla6 |
T |
C |
8: 3,571,417 (GRCm39) |
|
probably null |
Het |
Prkdc |
T |
G |
16: 15,496,136 (GRCm39) |
S776A |
probably damaging |
Het |
Prrc2b |
T |
C |
2: 32,104,125 (GRCm39) |
I1201T |
probably benign |
Het |
Pxmp4 |
C |
A |
2: 154,430,004 (GRCm39) |
M128I |
probably benign |
Het |
Siglech |
T |
C |
7: 55,422,312 (GRCm39) |
S306P |
probably benign |
Het |
Strc |
C |
T |
2: 121,198,211 (GRCm39) |
E1449K |
probably damaging |
Het |
Tchh |
A |
T |
3: 93,354,346 (GRCm39) |
Q1262L |
unknown |
Het |
Tln2 |
A |
T |
9: 67,273,249 (GRCm39) |
D410E |
possibly damaging |
Het |
Tmem175 |
A |
T |
5: 108,787,339 (GRCm39) |
Q62L |
probably benign |
Het |
Tpm3-rs7 |
A |
C |
14: 113,552,597 (GRCm39) |
M164L |
probably benign |
Het |
Trav8d-2 |
G |
A |
14: 53,280,220 (GRCm39) |
R70H |
probably damaging |
Het |
Tsc1 |
T |
C |
2: 28,561,858 (GRCm39) |
S332P |
probably benign |
Het |
Ttc41 |
T |
G |
10: 86,548,890 (GRCm39) |
I28R |
probably damaging |
Het |
Unc93a2 |
C |
T |
17: 7,637,164 (GRCm39) |
W341* |
probably null |
Het |
Vsig10 |
A |
C |
5: 117,463,140 (GRCm39) |
Y122S |
probably damaging |
Het |
Wnk2 |
A |
G |
13: 49,220,822 (GRCm39) |
W1260R |
probably damaging |
Het |
|
Other mutations in Mmp10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01084:Mmp10
|
APN |
9 |
7,505,651 (GRCm39) |
missense |
possibly damaging |
0.77 |
Disco
|
UTSW |
9 |
7,504,170 (GRCm39) |
nonsense |
probably null |
|
steel
|
UTSW |
9 |
7,506,513 (GRCm39) |
missense |
probably benign |
0.01 |
Strobe
|
UTSW |
9 |
7,508,199 (GRCm39) |
missense |
probably benign |
|
R0240:Mmp10
|
UTSW |
9 |
7,506,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Mmp10
|
UTSW |
9 |
7,506,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R0503:Mmp10
|
UTSW |
9 |
7,507,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Mmp10
|
UTSW |
9 |
7,508,199 (GRCm39) |
missense |
probably benign |
|
R1222:Mmp10
|
UTSW |
9 |
7,505,682 (GRCm39) |
splice site |
probably benign |
|
R1487:Mmp10
|
UTSW |
9 |
7,509,978 (GRCm39) |
missense |
probably damaging |
0.98 |
R1622:Mmp10
|
UTSW |
9 |
7,504,996 (GRCm39) |
nonsense |
probably null |
|
R1669:Mmp10
|
UTSW |
9 |
7,505,526 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1806:Mmp10
|
UTSW |
9 |
7,506,502 (GRCm39) |
missense |
probably benign |
0.01 |
R1880:Mmp10
|
UTSW |
9 |
7,505,575 (GRCm39) |
missense |
probably benign |
0.00 |
R4749:Mmp10
|
UTSW |
9 |
7,508,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R4866:Mmp10
|
UTSW |
9 |
7,508,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R5231:Mmp10
|
UTSW |
9 |
7,502,501 (GRCm39) |
critical splice donor site |
probably null |
|
R5367:Mmp10
|
UTSW |
9 |
7,505,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R5814:Mmp10
|
UTSW |
9 |
7,503,621 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6131:Mmp10
|
UTSW |
9 |
7,503,633 (GRCm39) |
splice site |
probably null |
|
R6542:Mmp10
|
UTSW |
9 |
7,506,513 (GRCm39) |
missense |
probably benign |
0.01 |
R6997:Mmp10
|
UTSW |
9 |
7,503,531 (GRCm39) |
missense |
probably benign |
0.08 |
R7400:Mmp10
|
UTSW |
9 |
7,503,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Mmp10
|
UTSW |
9 |
7,508,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R7593:Mmp10
|
UTSW |
9 |
7,503,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R7676:Mmp10
|
UTSW |
9 |
7,503,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Mmp10
|
UTSW |
9 |
7,507,284 (GRCm39) |
missense |
probably benign |
0.00 |
R7967:Mmp10
|
UTSW |
9 |
7,504,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Mmp10
|
UTSW |
9 |
7,508,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:Mmp10
|
UTSW |
9 |
7,508,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R8728:Mmp10
|
UTSW |
9 |
7,502,480 (GRCm39) |
missense |
probably benign |
|
R8788:Mmp10
|
UTSW |
9 |
7,502,687 (GRCm39) |
intron |
probably benign |
|
R9023:Mmp10
|
UTSW |
9 |
7,504,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Mmp10
|
UTSW |
9 |
7,504,170 (GRCm39) |
nonsense |
probably null |
|
R9414:Mmp10
|
UTSW |
9 |
7,502,489 (GRCm39) |
missense |
probably benign |
0.16 |
Z1176:Mmp10
|
UTSW |
9 |
7,508,206 (GRCm39) |
critical splice donor site |
probably null |
|
|