Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agap1 |
T |
C |
1: 89,558,141 (GRCm39) |
V143A |
probably damaging |
Het |
Agmo |
A |
G |
12: 37,292,044 (GRCm39) |
R2G |
probably benign |
Het |
Alms1 |
A |
T |
6: 85,598,479 (GRCm39) |
I1102L |
possibly damaging |
Het |
Ankrd13a |
T |
C |
5: 114,929,343 (GRCm39) |
I140T |
possibly damaging |
Het |
Arhgef10l |
T |
A |
4: 140,311,245 (GRCm39) |
|
probably null |
Het |
Atxn2l |
A |
T |
7: 126,092,345 (GRCm39) |
H967Q |
possibly damaging |
Het |
B3galnt2 |
A |
T |
13: 14,169,077 (GRCm39) |
N370I |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,080,477 (GRCm39) |
I325N |
|
Het |
Cacna1e |
C |
T |
1: 154,509,464 (GRCm39) |
D264N |
probably damaging |
Het |
Ccdc68 |
A |
C |
18: 70,080,246 (GRCm39) |
E197A |
probably damaging |
Het |
Cdr1 |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
AAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCAGAAGTCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCCGAAAATCCAAGTCTTCCC |
X: 60,228,130 (GRCm39) |
|
probably benign |
Het |
Cntn3 |
T |
C |
6: 102,242,392 (GRCm39) |
M418V |
probably benign |
Het |
Cpne4 |
T |
A |
9: 104,563,718 (GRCm39) |
C32S |
probably damaging |
Het |
Csf2rb2 |
A |
T |
15: 78,168,621 (GRCm39) |
S845T |
probably benign |
Het |
Ctnnd2 |
T |
G |
15: 31,027,733 (GRCm39) |
V1219G |
probably damaging |
Het |
Cyp4f14 |
G |
A |
17: 33,128,325 (GRCm39) |
A230V |
probably benign |
Het |
Cyth1 |
TGGGCAA |
T |
11: 118,074,749 (GRCm39) |
|
probably null |
Het |
Dmxl1 |
T |
A |
18: 50,094,214 (GRCm39) |
C2897S |
probably benign |
Het |
Elavl2 |
T |
A |
4: 91,260,280 (GRCm39) |
|
probably benign |
Het |
Elp1 |
A |
T |
4: 56,758,968 (GRCm39) |
S1191T |
possibly damaging |
Het |
Fam135a |
T |
C |
1: 24,083,331 (GRCm39) |
E298G |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,151,405 (GRCm39) |
I2534N |
probably damaging |
Het |
Fibin |
A |
G |
2: 110,192,825 (GRCm39) |
S106P |
probably damaging |
Het |
Fndc3a |
C |
T |
14: 72,802,100 (GRCm39) |
V568M |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,479,795 (GRCm39) |
F1966S |
probably damaging |
Het |
Gata4 |
T |
G |
14: 63,442,174 (GRCm39) |
E216A |
possibly damaging |
Het |
Gmps |
T |
A |
3: 63,922,984 (GRCm39) |
V649E |
probably benign |
Het |
Golga4 |
A |
T |
9: 118,388,379 (GRCm39) |
N1834Y |
possibly damaging |
Het |
Gpr89 |
A |
T |
3: 96,778,806 (GRCm39) |
Y422* |
probably null |
Het |
Gzmc |
A |
T |
14: 56,469,829 (GRCm39) |
F157Y |
probably benign |
Het |
Hdhd2 |
A |
G |
18: 77,052,962 (GRCm39) |
D204G |
probably damaging |
Het |
Hspa4 |
T |
G |
11: 53,171,530 (GRCm39) |
T225P |
possibly damaging |
Het |
Klhl30 |
T |
A |
1: 91,287,059 (GRCm39) |
D448E |
probably benign |
Het |
Kptn |
A |
G |
7: 15,853,966 (GRCm39) |
Y28C |
probably damaging |
Het |
Krt10 |
A |
T |
11: 99,278,432 (GRCm39) |
N242K |
probably damaging |
Het |
Krt6b |
A |
T |
15: 101,587,009 (GRCm39) |
N254K |
probably damaging |
Het |
Lama5 |
G |
T |
2: 179,843,605 (GRCm39) |
D447E |
probably damaging |
Het |
Lgr6 |
T |
C |
1: 134,915,419 (GRCm39) |
Y720C |
probably damaging |
Het |
Macf1 |
G |
C |
4: 123,301,392 (GRCm39) |
P1037A |
probably benign |
Het |
Map3k19 |
C |
T |
1: 127,751,383 (GRCm39) |
G656D |
probably benign |
Het |
Mroh7 |
A |
C |
4: 106,578,287 (GRCm39) |
N130K |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,551,801 (GRCm39) |
T4831A |
probably benign |
Het |
Nfkb1 |
A |
T |
3: 135,291,173 (GRCm39) |
L533H |
|
Het |
Oaf |
G |
A |
9: 43,134,077 (GRCm39) |
R215C |
probably damaging |
Het |
Or4x11 |
A |
G |
2: 89,867,626 (GRCm39) |
Y121C |
probably damaging |
Het |
Or51k1 |
C |
A |
7: 103,661,510 (GRCm39) |
R133L |
possibly damaging |
Het |
Or5m3b |
G |
A |
2: 85,871,949 (GRCm39) |
V97I |
probably benign |
Het |
Or8a1 |
A |
G |
9: 37,642,003 (GRCm39) |
I92T |
probably damaging |
Het |
Or8g2b |
A |
G |
9: 39,751,618 (GRCm39) |
D296G |
possibly damaging |
Het |
Otub1 |
T |
C |
19: 7,177,425 (GRCm39) |
D74G |
probably damaging |
Het |
Oxct2b |
A |
G |
4: 123,010,680 (GRCm39) |
E200G |
probably damaging |
Het |
Pcdh1 |
T |
C |
18: 38,322,662 (GRCm39) |
D1057G |
probably benign |
Het |
Pkd1 |
T |
A |
17: 24,805,174 (GRCm39) |
V3242E |
probably damaging |
Het |
Pkd1l3 |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
CCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACACAGGTGACATCAGACACACCTGCATCCAATAGCCCACCACAGGGGACATCAGACACACCTGGATTCAGCAGCCCAACACAGGTGACAACAGCCACACTTGTATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGACACATCTGCATCCATCAGCCCACCACAGGTAATATCAGACACACCTGCATCCAGCAGCCCACCACAGGTGACATCAGAGACACCTGCATCCAGCAGCCCAACA |
8: 110,350,420 (GRCm39) |
|
probably benign |
Het |
Pla2g4e |
T |
A |
2: 120,015,803 (GRCm39) |
D247V |
probably benign |
Het |
Pole |
T |
A |
5: 110,480,414 (GRCm39) |
M1995K |
probably benign |
Het |
Ppargc1a |
T |
C |
5: 51,705,855 (GRCm39) |
E76G |
probably benign |
Het |
Pten |
G |
T |
19: 32,777,396 (GRCm39) |
R130L |
probably damaging |
Het |
Ptprj |
A |
T |
2: 90,274,804 (GRCm39) |
V1186D |
probably damaging |
Het |
Rab4a |
T |
A |
8: 124,532,876 (GRCm39) |
M1K |
probably null |
Het |
Rapgef3 |
C |
A |
15: 97,656,271 (GRCm39) |
|
probably null |
Het |
Rarb |
C |
A |
14: 16,548,473 (GRCm38) |
V83F |
probably damaging |
Het |
Rgs22 |
A |
T |
15: 36,099,858 (GRCm39) |
F410I |
probably damaging |
Het |
Rhpn2 |
A |
C |
7: 35,080,912 (GRCm39) |
E459A |
probably benign |
Het |
Rims4 |
A |
T |
2: 163,705,974 (GRCm39) |
L220Q |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,770,132 (GRCm39) |
T531A |
possibly damaging |
Het |
Sbf2 |
T |
C |
7: 109,971,717 (GRCm39) |
H839R |
probably damaging |
Het |
Setbp1 |
T |
C |
18: 78,900,068 (GRCm39) |
R1200G |
probably benign |
Het |
Slc12a8 |
C |
A |
16: 33,444,930 (GRCm39) |
P275T |
probably damaging |
Het |
Slc23a1 |
G |
T |
18: 35,757,554 (GRCm39) |
T239N |
probably benign |
Het |
Slc37a3 |
T |
A |
6: 39,341,517 (GRCm39) |
T40S |
possibly damaging |
Het |
Speer4c1 |
T |
C |
5: 15,915,925 (GRCm39) |
|
probably null |
Het |
Tet1 |
A |
T |
10: 62,655,252 (GRCm39) |
H1556Q |
possibly damaging |
Het |
Tfcp2l1 |
T |
A |
1: 118,603,325 (GRCm39) |
D454E |
probably damaging |
Het |
Timd6 |
T |
A |
11: 46,468,058 (GRCm39) |
I44K |
not run |
Het |
Tmem123 |
A |
T |
9: 7,790,890 (GRCm39) |
M64L |
probably benign |
Het |
Tmem62 |
A |
T |
2: 120,814,853 (GRCm39) |
H172L |
probably benign |
Het |
Trim15 |
T |
G |
17: 37,177,764 (GRCm39) |
Y77S |
probably benign |
Het |
Trim37 |
T |
A |
11: 87,092,270 (GRCm39) |
V693E |
possibly damaging |
Het |
Trim65 |
A |
G |
11: 116,017,082 (GRCm39) |
L460S |
probably damaging |
Het |
Ttc39a |
T |
C |
4: 109,279,687 (GRCm39) |
V109A |
probably benign |
Het |
Ttc7 |
A |
G |
17: 87,600,374 (GRCm39) |
M163V |
probably null |
Het |
Vps13b |
T |
C |
15: 35,423,378 (GRCm39) |
S233P |
probably damaging |
Het |
Vwf |
T |
C |
6: 125,633,766 (GRCm39) |
L2084P |
|
Het |
Wasl |
A |
G |
6: 24,633,922 (GRCm39) |
V114A |
possibly damaging |
Het |
Wdr5 |
A |
G |
2: 27,409,463 (GRCm39) |
S62G |
probably damaging |
Het |
Wfdc11 |
G |
T |
2: 164,507,445 (GRCm39) |
S4* |
probably null |
Het |
Wfikkn2 |
C |
A |
11: 94,129,810 (GRCm39) |
M110I |
probably benign |
Het |
Wiz |
T |
G |
17: 32,576,760 (GRCm39) |
E588A |
probably benign |
Het |
Xylt1 |
A |
G |
7: 117,255,891 (GRCm39) |
H821R |
probably benign |
Het |
Zbtb7c |
A |
T |
18: 76,278,772 (GRCm39) |
H410L |
probably benign |
Het |
Zc3h18 |
T |
A |
8: 123,110,710 (GRCm39) |
D186E |
probably damaging |
Het |
Zfp687 |
G |
T |
3: 94,917,673 (GRCm39) |
L700I |
possibly damaging |
Het |
Zmym2 |
T |
A |
14: 57,184,020 (GRCm39) |
M994K |
probably benign |
Het |
|
Other mutations in Ccdc112 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01455:Ccdc112
|
APN |
18 |
46,426,511 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02860:Ccdc112
|
APN |
18 |
46,420,509 (GRCm39) |
missense |
probably benign |
0.00 |
R0546:Ccdc112
|
UTSW |
18 |
46,424,139 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0566:Ccdc112
|
UTSW |
18 |
46,423,877 (GRCm39) |
missense |
probably damaging |
0.97 |
R1815:Ccdc112
|
UTSW |
18 |
46,424,173 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1847:Ccdc112
|
UTSW |
18 |
46,420,821 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1853:Ccdc112
|
UTSW |
18 |
46,418,767 (GRCm39) |
missense |
probably benign |
0.07 |
R2011:Ccdc112
|
UTSW |
18 |
46,420,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Ccdc112
|
UTSW |
18 |
46,432,365 (GRCm39) |
missense |
probably benign |
0.03 |
R4519:Ccdc112
|
UTSW |
18 |
46,420,613 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4795:Ccdc112
|
UTSW |
18 |
46,420,739 (GRCm39) |
missense |
probably benign |
0.20 |
R4873:Ccdc112
|
UTSW |
18 |
46,429,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Ccdc112
|
UTSW |
18 |
46,429,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R7208:Ccdc112
|
UTSW |
18 |
46,420,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R7807:Ccdc112
|
UTSW |
18 |
46,423,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R8060:Ccdc112
|
UTSW |
18 |
46,426,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R8104:Ccdc112
|
UTSW |
18 |
46,420,720 (GRCm39) |
missense |
probably benign |
0.37 |
R8886:Ccdc112
|
UTSW |
18 |
46,444,826 (GRCm39) |
missense |
unknown |
|
R9005:Ccdc112
|
UTSW |
18 |
46,429,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R9433:Ccdc112
|
UTSW |
18 |
46,424,040 (GRCm39) |
missense |
probably benign |
0.44 |
R9708:Ccdc112
|
UTSW |
18 |
46,444,780 (GRCm39) |
missense |
probably benign |
0.00 |
|