Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp11a |
T |
C |
8: 12,909,481 (GRCm39) |
|
probably null |
Het |
Best3 |
G |
T |
10: 116,838,556 (GRCm39) |
V205F |
probably benign |
Het |
Camkv |
T |
C |
9: 107,823,894 (GRCm39) |
|
probably null |
Het |
Cdk5rap2 |
A |
C |
4: 70,184,849 (GRCm39) |
D1200E |
possibly damaging |
Het |
Cep192 |
T |
A |
18: 67,967,784 (GRCm39) |
I756N |
probably damaging |
Het |
Crocc2 |
A |
T |
1: 93,130,560 (GRCm39) |
Q947L |
probably benign |
Het |
Dcaf1 |
A |
G |
9: 106,715,845 (GRCm39) |
T321A |
possibly damaging |
Het |
Dgkz |
T |
C |
2: 91,774,724 (GRCm39) |
M87V |
probably benign |
Het |
Dmrt2 |
T |
A |
19: 25,650,935 (GRCm39) |
S40R |
possibly damaging |
Het |
Dpep1 |
T |
G |
8: 123,927,391 (GRCm39) |
L315R |
probably damaging |
Het |
Fam221b |
G |
T |
4: 43,665,942 (GRCm39) |
T223N |
possibly damaging |
Het |
Fasn |
A |
T |
11: 120,706,185 (GRCm39) |
V1053E |
probably damaging |
Het |
Galc |
T |
C |
12: 98,208,973 (GRCm39) |
D227G |
probably damaging |
Het |
Grik1 |
A |
G |
16: 87,744,794 (GRCm39) |
L486P |
probably damaging |
Het |
Grik5 |
A |
G |
7: 24,713,019 (GRCm39) |
S836P |
probably benign |
Het |
Grpel2 |
T |
C |
18: 61,852,792 (GRCm39) |
K70R |
possibly damaging |
Het |
Ipo7 |
A |
G |
7: 109,617,675 (GRCm39) |
D15G |
possibly damaging |
Het |
Iqgap1 |
A |
G |
7: 80,377,772 (GRCm39) |
Y1284H |
probably damaging |
Het |
Lmo7 |
T |
C |
14: 102,138,072 (GRCm39) |
S692P |
probably damaging |
Het |
Mecom |
A |
G |
3: 30,034,905 (GRCm39) |
L447P |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,550,384 (GRCm39) |
D680G |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,572,004 (GRCm39) |
I172F |
unknown |
Het |
Musk |
A |
G |
4: 58,366,811 (GRCm39) |
I476M |
probably benign |
Het |
Myef2 |
T |
C |
2: 124,951,632 (GRCm39) |
T268A |
probably damaging |
Het |
Naip1 |
A |
G |
13: 100,563,060 (GRCm39) |
S702P |
probably damaging |
Het |
Napa |
G |
T |
7: 15,849,562 (GRCm39) |
S258I |
probably benign |
Het |
Nfasc |
T |
A |
1: 132,504,132 (GRCm39) |
I1039F |
probably damaging |
Het |
Nlrc5 |
A |
G |
8: 95,228,902 (GRCm39) |
S1238G |
probably benign |
Het |
Or10q12 |
T |
C |
19: 13,746,144 (GRCm39) |
V146A |
probably benign |
Het |
Or1j12 |
A |
G |
2: 36,342,734 (GRCm39) |
I46V |
probably benign |
Het |
Or5w8 |
T |
A |
2: 87,687,811 (GRCm39) |
C97* |
probably null |
Het |
Pacs1 |
G |
T |
19: 5,210,005 (GRCm39) |
N215K |
probably damaging |
Het |
Parp10 |
A |
G |
15: 76,126,388 (GRCm39) |
S267P |
probably benign |
Het |
Pbrm1 |
G |
T |
14: 30,806,052 (GRCm39) |
C995F |
probably damaging |
Het |
Pcdh7 |
A |
T |
5: 58,099,607 (GRCm39) |
|
probably null |
Het |
Ppef2 |
T |
C |
5: 92,383,613 (GRCm39) |
Y499C |
probably damaging |
Het |
Pramel16 |
G |
T |
4: 143,675,602 (GRCm39) |
T408K |
probably benign |
Het |
Prex2 |
A |
C |
1: 11,180,544 (GRCm39) |
I370L |
probably benign |
Het |
Ptprd |
A |
G |
4: 75,872,420 (GRCm39) |
Y1350H |
probably damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,124,351 (GRCm39) |
K284E |
probably damaging |
Het |
Rexo1 |
A |
T |
10: 80,379,915 (GRCm39) |
Y23N |
probably damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Sash3 |
C |
T |
X: 47,248,398 (GRCm39) |
L307F |
probably damaging |
Homo |
Scn9a |
T |
A |
2: 66,398,608 (GRCm39) |
M1L |
possibly damaging |
Het |
Serpinb6e |
C |
A |
13: 34,021,805 (GRCm39) |
L174F |
probably benign |
Het |
Siae |
C |
T |
9: 37,544,277 (GRCm39) |
T275I |
probably benign |
Het |
Sptbn5 |
C |
A |
2: 119,884,900 (GRCm39) |
|
probably benign |
Het |
Ss18l2 |
C |
T |
9: 121,541,672 (GRCm39) |
T55I |
probably damaging |
Het |
Taf1c |
A |
G |
8: 120,328,518 (GRCm39) |
C163R |
probably damaging |
Het |
Tanc2 |
C |
T |
11: 105,748,382 (GRCm39) |
R505W |
probably damaging |
Het |
Tango6 |
C |
A |
8: 107,419,308 (GRCm39) |
P285Q |
possibly damaging |
Het |
Tdrd9 |
G |
T |
12: 112,008,186 (GRCm39) |
|
probably null |
Het |
Tead3 |
A |
T |
17: 28,552,299 (GRCm39) |
L307H |
probably damaging |
Het |
Ticrr |
A |
C |
7: 79,344,031 (GRCm39) |
|
probably null |
Het |
Trpc4 |
T |
C |
3: 54,224,995 (GRCm39) |
|
probably null |
Het |
Upb1 |
A |
T |
10: 75,264,135 (GRCm39) |
T194S |
probably benign |
Het |
Vav3 |
A |
G |
3: 109,470,512 (GRCm39) |
N566S |
probably benign |
Het |
Vmn1r196 |
T |
A |
13: 22,477,887 (GRCm39) |
S175R |
probably benign |
Het |
Zscan29 |
T |
C |
2: 120,991,917 (GRCm39) |
N589D |
possibly damaging |
Het |
|
Other mutations in C1qtnf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01805:C1qtnf1
|
APN |
11 |
118,338,993 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02376:C1qtnf1
|
APN |
11 |
118,338,894 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02609:C1qtnf1
|
APN |
11 |
118,338,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:C1qtnf1
|
UTSW |
11 |
118,337,454 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1170:C1qtnf1
|
UTSW |
11 |
118,339,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R1442:C1qtnf1
|
UTSW |
11 |
118,339,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:C1qtnf1
|
UTSW |
11 |
118,334,616 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1540:C1qtnf1
|
UTSW |
11 |
118,338,749 (GRCm39) |
missense |
probably benign |
0.28 |
R1896:C1qtnf1
|
UTSW |
11 |
118,334,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R2011:C1qtnf1
|
UTSW |
11 |
118,339,110 (GRCm39) |
missense |
probably benign |
0.04 |
R2012:C1qtnf1
|
UTSW |
11 |
118,339,110 (GRCm39) |
missense |
probably benign |
0.04 |
R2901:C1qtnf1
|
UTSW |
11 |
118,338,930 (GRCm39) |
splice site |
probably null |
|
R2902:C1qtnf1
|
UTSW |
11 |
118,338,930 (GRCm39) |
splice site |
probably null |
|
R4011:C1qtnf1
|
UTSW |
11 |
118,337,365 (GRCm39) |
missense |
probably benign |
|
R4897:C1qtnf1
|
UTSW |
11 |
118,338,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:C1qtnf1
|
UTSW |
11 |
118,339,176 (GRCm39) |
makesense |
probably null |
|
R8322:C1qtnf1
|
UTSW |
11 |
118,338,683 (GRCm39) |
missense |
probably benign |
0.00 |
R8558:C1qtnf1
|
UTSW |
11 |
118,339,149 (GRCm39) |
missense |
probably damaging |
0.99 |
R8679:C1qtnf1
|
UTSW |
11 |
118,337,340 (GRCm39) |
nonsense |
probably null |
|
R8920:C1qtnf1
|
UTSW |
11 |
118,339,068 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9289:C1qtnf1
|
UTSW |
11 |
118,334,672 (GRCm39) |
missense |
probably benign |
0.00 |
X0021:C1qtnf1
|
UTSW |
11 |
118,334,606 (GRCm39) |
nonsense |
probably null |
|
Z1177:C1qtnf1
|
UTSW |
11 |
118,334,580 (GRCm39) |
missense |
probably benign |
0.00 |
|