Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,240,969 (GRCm39) |
L944P |
probably damaging |
Het |
Akap13 |
A |
G |
7: 75,373,643 (GRCm39) |
S1885G |
probably damaging |
Het |
Aqp3 |
A |
G |
4: 41,093,632 (GRCm39) |
Y261H |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,793,305 (GRCm39) |
N1380K |
probably damaging |
Het |
Barx2 |
T |
C |
9: 31,758,141 (GRCm39) |
I266V |
unknown |
Het |
BC034090 |
C |
T |
1: 155,108,267 (GRCm39) |
R360H |
probably benign |
Het |
Bmal2 |
T |
A |
6: 146,711,164 (GRCm39) |
M56K |
probably benign |
Het |
Ccnb2 |
T |
C |
9: 70,326,189 (GRCm39) |
K52E |
probably damaging |
Het |
Cfap300 |
T |
C |
9: 8,042,432 (GRCm39) |
Y57C |
probably damaging |
Het |
Cyld |
G |
T |
8: 89,433,918 (GRCm39) |
V236F |
probably damaging |
Het |
Dst |
T |
C |
1: 34,208,410 (GRCm39) |
|
probably benign |
Het |
Ehmt1 |
G |
T |
2: 24,728,830 (GRCm39) |
A637E |
possibly damaging |
Het |
Erlin1 |
G |
T |
19: 44,057,758 (GRCm39) |
Y22* |
probably null |
Het |
Ezh1 |
A |
T |
11: 101,090,128 (GRCm39) |
M539K |
possibly damaging |
Het |
Fancc |
A |
T |
13: 63,548,059 (GRCm39) |
I80N |
probably damaging |
Het |
Fat1 |
G |
A |
8: 45,503,977 (GRCm39) |
S4447N |
probably benign |
Het |
Fem1al |
A |
G |
11: 29,774,755 (GRCm39) |
L234P |
probably damaging |
Het |
Fhip2a |
A |
G |
19: 57,369,777 (GRCm39) |
E440G |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,395,439 (GRCm39) |
Q1822R |
possibly damaging |
Het |
Iqgap1 |
C |
T |
7: 80,409,592 (GRCm39) |
V248I |
probably benign |
Het |
Itch |
T |
C |
2: 155,054,943 (GRCm39) |
I749T |
probably damaging |
Het |
Kcna10 |
T |
A |
3: 107,102,830 (GRCm39) |
M487K |
probably benign |
Het |
Krt87 |
A |
T |
15: 101,386,092 (GRCm39) |
L223Q |
probably benign |
Het |
Mtmr2 |
T |
C |
9: 13,697,212 (GRCm39) |
I84T |
probably benign |
Het |
Myocd |
G |
A |
11: 65,077,980 (GRCm39) |
T477M |
probably damaging |
Het |
Nfic |
A |
T |
10: 81,244,054 (GRCm39) |
V240E |
possibly damaging |
Het |
Or4d2 |
A |
G |
11: 87,784,447 (GRCm39) |
I101T |
possibly damaging |
Het |
Prkdc |
A |
T |
16: 15,608,330 (GRCm39) |
Y3044F |
probably benign |
Het |
Prkg1 |
A |
G |
19: 30,549,022 (GRCm39) |
I636T |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,535,546 (GRCm39) |
V477A |
probably benign |
Het |
Rab7b |
T |
A |
1: 131,626,329 (GRCm39) |
M119K |
possibly damaging |
Het |
Sec61a1 |
T |
C |
6: 88,483,922 (GRCm39) |
|
probably benign |
Het |
Sectm1b |
A |
G |
11: 120,946,799 (GRCm39) |
V32A |
probably benign |
Het |
Shroom2 |
A |
G |
X: 151,406,219 (GRCm39) |
S1034P |
probably benign |
Het |
Sipa1l3 |
A |
T |
7: 29,085,533 (GRCm39) |
I688N |
probably damaging |
Het |
Slc24a1 |
T |
C |
9: 64,835,301 (GRCm39) |
Y942C |
probably damaging |
Het |
Smg1 |
C |
T |
7: 117,810,017 (GRCm39) |
R139K |
possibly damaging |
Het |
Stt3b |
G |
A |
9: 115,080,915 (GRCm39) |
T574I |
probably benign |
Het |
Thoc2 |
A |
G |
X: 40,968,768 (GRCm39) |
I76T |
possibly damaging |
Het |
Tpm3 |
C |
T |
3: 89,995,024 (GRCm39) |
T180M |
probably damaging |
Het |
Uqcrfs1 |
C |
A |
13: 30,724,908 (GRCm39) |
V211F |
probably benign |
Het |
Usp47 |
A |
G |
7: 111,673,990 (GRCm39) |
S418G |
probably benign |
Het |
Usp5 |
T |
C |
6: 124,806,316 (GRCm39) |
T15A |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,768,147 (GRCm39) |
L122P |
probably damaging |
Het |
Zfp677 |
A |
T |
17: 21,617,930 (GRCm39) |
E329V |
probably benign |
Het |
Zfyve16 |
A |
T |
13: 92,653,046 (GRCm39) |
N846K |
possibly damaging |
Het |
Zp1 |
G |
T |
19: 10,896,141 (GRCm39) |
P195T |
probably damaging |
Het |
|
Other mutations in Ccp110 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Ccp110
|
APN |
7 |
118,321,647 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00725:Ccp110
|
APN |
7 |
118,329,946 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00899:Ccp110
|
APN |
7 |
118,321,907 (GRCm39) |
missense |
probably benign |
|
IGL01837:Ccp110
|
APN |
7 |
118,324,684 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4469001:Ccp110
|
UTSW |
7 |
118,321,600 (GRCm39) |
missense |
probably benign |
0.06 |
R1217:Ccp110
|
UTSW |
7 |
118,329,167 (GRCm39) |
splice site |
probably benign |
|
R1640:Ccp110
|
UTSW |
7 |
118,314,751 (GRCm39) |
splice site |
probably null |
|
R1700:Ccp110
|
UTSW |
7 |
118,334,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R1768:Ccp110
|
UTSW |
7 |
118,325,247 (GRCm39) |
splice site |
probably null |
|
R4737:Ccp110
|
UTSW |
7 |
118,323,771 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4859:Ccp110
|
UTSW |
7 |
118,324,653 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4933:Ccp110
|
UTSW |
7 |
118,324,542 (GRCm39) |
missense |
probably damaging |
0.96 |
R4970:Ccp110
|
UTSW |
7 |
118,321,614 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4999:Ccp110
|
UTSW |
7 |
118,329,235 (GRCm39) |
nonsense |
probably null |
|
R5212:Ccp110
|
UTSW |
7 |
118,328,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R5600:Ccp110
|
UTSW |
7 |
118,328,948 (GRCm39) |
critical splice donor site |
probably null |
|
R6953:Ccp110
|
UTSW |
7 |
118,321,644 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6998:Ccp110
|
UTSW |
7 |
118,332,120 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7076:Ccp110
|
UTSW |
7 |
118,331,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R7092:Ccp110
|
UTSW |
7 |
118,334,494 (GRCm39) |
missense |
probably benign |
0.26 |
R7336:Ccp110
|
UTSW |
7 |
118,321,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R7343:Ccp110
|
UTSW |
7 |
118,323,798 (GRCm39) |
missense |
probably benign |
0.03 |
R7866:Ccp110
|
UTSW |
7 |
118,322,241 (GRCm39) |
missense |
probably benign |
0.07 |
R8306:Ccp110
|
UTSW |
7 |
118,321,903 (GRCm39) |
missense |
probably benign |
0.12 |
R8951:Ccp110
|
UTSW |
7 |
118,321,015 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8961:Ccp110
|
UTSW |
7 |
118,322,110 (GRCm39) |
missense |
probably damaging |
0.96 |
R9036:Ccp110
|
UTSW |
7 |
118,324,680 (GRCm39) |
missense |
probably damaging |
0.98 |
R9252:Ccp110
|
UTSW |
7 |
118,321,673 (GRCm39) |
missense |
probably benign |
|
R9652:Ccp110
|
UTSW |
7 |
118,334,553 (GRCm39) |
missense |
|
|
|