Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
C |
A |
6: 92,871,247 (GRCm39) |
A30S |
probably benign |
Het |
Aspg |
A |
G |
12: 112,089,387 (GRCm39) |
T392A |
probably benign |
Het |
Atp8b5 |
C |
A |
4: 43,368,010 (GRCm39) |
Q878K |
possibly damaging |
Het |
Ccdc85a |
G |
T |
11: 28,526,506 (GRCm39) |
H339Q |
probably damaging |
Het |
Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
Cog4 |
C |
T |
8: 111,592,717 (GRCm39) |
T430M |
probably benign |
Het |
Col6a5 |
A |
G |
9: 105,823,274 (GRCm39) |
Y28H |
unknown |
Het |
Cth |
A |
T |
3: 157,610,804 (GRCm39) |
Y343N |
probably damaging |
Het |
Dctn3 |
A |
T |
4: 41,719,854 (GRCm39) |
L84* |
probably null |
Het |
Epha5 |
A |
T |
5: 84,219,092 (GRCm39) |
I868N |
probably damaging |
Het |
Ephb2 |
T |
C |
4: 136,498,681 (GRCm39) |
N133D |
possibly damaging |
Het |
Epor |
G |
A |
9: 21,870,752 (GRCm39) |
P376L |
probably damaging |
Het |
Gsdme |
A |
G |
6: 50,204,354 (GRCm39) |
V201A |
possibly damaging |
Het |
Hdgf |
G |
A |
3: 87,821,831 (GRCm39) |
E149K |
possibly damaging |
Het |
Lrrfip2 |
T |
C |
9: 111,034,917 (GRCm39) |
|
probably null |
Het |
Ly6g6d |
T |
C |
17: 35,293,226 (GRCm39) |
I40V |
probably benign |
Het |
Mmp19 |
C |
T |
10: 128,634,011 (GRCm39) |
T304I |
probably damaging |
Het |
Mmp28 |
T |
C |
11: 83,334,602 (GRCm39) |
D384G |
possibly damaging |
Het |
Moxd1 |
T |
C |
10: 24,120,286 (GRCm39) |
|
probably null |
Het |
Mtcl3 |
T |
G |
10: 29,024,254 (GRCm39) |
L390R |
probably damaging |
Het |
Ncapg |
T |
C |
5: 45,828,477 (GRCm39) |
V76A |
probably benign |
Het |
Nos1 |
C |
T |
5: 118,005,774 (GRCm39) |
R165C |
probably benign |
Het |
Or1e1c |
T |
C |
11: 73,265,578 (GRCm39) |
M1T |
probably null |
Het |
Or2a57 |
A |
G |
6: 43,212,559 (GRCm39) |
T6A |
possibly damaging |
Het |
Pik3c2a |
T |
A |
7: 115,975,485 (GRCm39) |
H694L |
possibly damaging |
Het |
Psme2 |
A |
G |
14: 55,827,128 (GRCm39) |
L60P |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,237,175 (GRCm39) |
V4A |
probably benign |
Het |
Rgr |
G |
T |
14: 36,766,566 (GRCm39) |
T160K |
probably damaging |
Het |
Serpind1 |
A |
G |
16: 17,154,787 (GRCm39) |
I205V |
probably benign |
Het |
Skap2 |
T |
C |
6: 51,898,280 (GRCm39) |
Y150C |
probably damaging |
Het |
Srsf9 |
T |
C |
5: 115,470,187 (GRCm39) |
S122P |
probably damaging |
Het |
Stox1 |
T |
G |
10: 62,500,461 (GRCm39) |
I700L |
probably benign |
Het |
Tada1 |
A |
G |
1: 166,216,294 (GRCm39) |
D165G |
probably damaging |
Het |
Traf5 |
A |
G |
1: 191,731,828 (GRCm39) |
S338P |
probably benign |
Het |
Trim39 |
G |
A |
17: 36,574,617 (GRCm39) |
|
probably benign |
Het |
Wbp2 |
G |
A |
11: 115,972,066 (GRCm39) |
A130V |
possibly damaging |
Het |
Zcchc17 |
T |
C |
4: 130,230,902 (GRCm39) |
K96E |
probably benign |
Het |
Zfp800 |
G |
A |
6: 28,242,983 (GRCm39) |
L661F |
possibly damaging |
Het |
|
Other mutations in Mlh3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01402:Mlh3
|
APN |
12 |
85,314,703 (GRCm39) |
missense |
probably benign |
|
IGL01961:Mlh3
|
APN |
12 |
85,313,118 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02596:Mlh3
|
APN |
12 |
85,287,732 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03008:Mlh3
|
APN |
12 |
85,287,625 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03142:Mlh3
|
APN |
12 |
85,297,075 (GRCm39) |
critical splice donor site |
probably null |
|
R0032:Mlh3
|
UTSW |
12 |
85,292,523 (GRCm39) |
intron |
probably benign |
|
R0032:Mlh3
|
UTSW |
12 |
85,292,523 (GRCm39) |
intron |
probably benign |
|
R0078:Mlh3
|
UTSW |
12 |
85,315,592 (GRCm39) |
missense |
probably damaging |
0.98 |
R0129:Mlh3
|
UTSW |
12 |
85,312,914 (GRCm39) |
splice site |
probably benign |
|
R0269:Mlh3
|
UTSW |
12 |
85,315,179 (GRCm39) |
missense |
probably benign |
0.00 |
R0393:Mlh3
|
UTSW |
12 |
85,314,361 (GRCm39) |
nonsense |
probably null |
|
R0403:Mlh3
|
UTSW |
12 |
85,315,742 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0409:Mlh3
|
UTSW |
12 |
85,287,628 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0587:Mlh3
|
UTSW |
12 |
85,313,193 (GRCm39) |
missense |
probably benign |
0.00 |
R0701:Mlh3
|
UTSW |
12 |
85,314,677 (GRCm39) |
missense |
probably benign |
0.00 |
R0718:Mlh3
|
UTSW |
12 |
85,294,471 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0883:Mlh3
|
UTSW |
12 |
85,282,488 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0989:Mlh3
|
UTSW |
12 |
85,316,169 (GRCm39) |
missense |
probably benign |
0.22 |
R0990:Mlh3
|
UTSW |
12 |
85,314,539 (GRCm39) |
missense |
probably benign |
|
R1467:Mlh3
|
UTSW |
12 |
85,284,374 (GRCm39) |
nonsense |
probably null |
|
R1467:Mlh3
|
UTSW |
12 |
85,284,374 (GRCm39) |
nonsense |
probably null |
|
R1562:Mlh3
|
UTSW |
12 |
85,313,694 (GRCm39) |
missense |
probably benign |
0.14 |
R1599:Mlh3
|
UTSW |
12 |
85,315,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Mlh3
|
UTSW |
12 |
85,313,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Mlh3
|
UTSW |
12 |
85,315,528 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1822:Mlh3
|
UTSW |
12 |
85,312,919 (GRCm39) |
splice site |
probably benign |
|
R1874:Mlh3
|
UTSW |
12 |
85,284,287 (GRCm39) |
critical splice donor site |
probably null |
|
R1914:Mlh3
|
UTSW |
12 |
85,308,442 (GRCm39) |
missense |
probably benign |
0.08 |
R1915:Mlh3
|
UTSW |
12 |
85,308,442 (GRCm39) |
missense |
probably benign |
0.08 |
R2075:Mlh3
|
UTSW |
12 |
85,315,915 (GRCm39) |
nonsense |
probably null |
|
R2083:Mlh3
|
UTSW |
12 |
85,315,815 (GRCm39) |
missense |
probably benign |
0.16 |
R2267:Mlh3
|
UTSW |
12 |
85,307,585 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2334:Mlh3
|
UTSW |
12 |
85,314,851 (GRCm39) |
missense |
probably benign |
0.00 |
R2882:Mlh3
|
UTSW |
12 |
85,314,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Mlh3
|
UTSW |
12 |
85,315,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R3624:Mlh3
|
UTSW |
12 |
85,315,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R3963:Mlh3
|
UTSW |
12 |
85,315,454 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4376:Mlh3
|
UTSW |
12 |
85,305,972 (GRCm39) |
missense |
probably benign |
0.00 |
R5334:Mlh3
|
UTSW |
12 |
85,292,535 (GRCm39) |
critical splice donor site |
probably null |
|
R5526:Mlh3
|
UTSW |
12 |
85,316,147 (GRCm39) |
nonsense |
probably null |
|
R5556:Mlh3
|
UTSW |
12 |
85,315,267 (GRCm39) |
nonsense |
probably null |
|
R5611:Mlh3
|
UTSW |
12 |
85,314,219 (GRCm39) |
missense |
probably benign |
0.21 |
R5911:Mlh3
|
UTSW |
12 |
85,315,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R6050:Mlh3
|
UTSW |
12 |
85,287,620 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6221:Mlh3
|
UTSW |
12 |
85,315,192 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6377:Mlh3
|
UTSW |
12 |
85,315,271 (GRCm39) |
missense |
probably damaging |
0.97 |
R6820:Mlh3
|
UTSW |
12 |
85,294,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R6826:Mlh3
|
UTSW |
12 |
85,292,598 (GRCm39) |
missense |
probably benign |
0.38 |
R6992:Mlh3
|
UTSW |
12 |
85,282,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R7217:Mlh3
|
UTSW |
12 |
85,313,481 (GRCm39) |
missense |
probably benign |
|
R7228:Mlh3
|
UTSW |
12 |
85,282,430 (GRCm39) |
missense |
probably benign |
0.07 |
R7348:Mlh3
|
UTSW |
12 |
85,314,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R7599:Mlh3
|
UTSW |
12 |
85,314,973 (GRCm39) |
nonsense |
probably null |
|
R7722:Mlh3
|
UTSW |
12 |
85,314,266 (GRCm39) |
missense |
probably benign |
0.01 |
R7762:Mlh3
|
UTSW |
12 |
85,315,058 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7786:Mlh3
|
UTSW |
12 |
85,313,511 (GRCm39) |
missense |
probably benign |
0.00 |
R8231:Mlh3
|
UTSW |
12 |
85,307,572 (GRCm39) |
critical splice donor site |
probably null |
|
R8415:Mlh3
|
UTSW |
12 |
85,315,854 (GRCm39) |
missense |
probably benign |
0.35 |
R8750:Mlh3
|
UTSW |
12 |
85,308,488 (GRCm39) |
missense |
probably damaging |
0.99 |
R8794:Mlh3
|
UTSW |
12 |
85,282,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R9301:Mlh3
|
UTSW |
12 |
85,292,613 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9385:Mlh3
|
UTSW |
12 |
85,316,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9518:Mlh3
|
UTSW |
12 |
85,313,004 (GRCm39) |
missense |
probably benign |
0.00 |
R9549:Mlh3
|
UTSW |
12 |
85,313,249 (GRCm39) |
missense |
probably benign |
0.01 |
RF014:Mlh3
|
UTSW |
12 |
85,314,803 (GRCm39) |
missense |
probably benign |
|
X0024:Mlh3
|
UTSW |
12 |
85,294,443 (GRCm39) |
missense |
probably damaging |
1.00 |
|