Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A030005L19Rik |
GTGGTGGCTG |
GTGGTGGCTGTGGTGGCTG |
1: 82,891,290 (GRCm39) |
|
probably benign |
Het |
A030005L19Rik |
TGCTG |
TGCTGTGGCGGCTG |
1: 82,891,307 (GRCm39) |
|
probably benign |
Het |
A030005L19Rik |
TGGCTGCTG |
TGGCTGCTGGGGCTGCTG |
1: 82,891,294 (GRCm39) |
|
probably benign |
Het |
AI837181 |
GCG |
GCGTCG |
19: 5,475,264 (GRCm39) |
|
probably benign |
Het |
Ankrd24 |
C |
CGGAGGCAGAGGA |
10: 81,479,405 (GRCm39) |
|
probably benign |
Het |
Aqp2 |
T |
C |
15: 99,481,753 (GRCm39) |
S216P |
probably damaging |
Het |
Brd10 |
T |
C |
19: 29,721,009 (GRCm39) |
K672R |
possibly damaging |
Het |
Cacna1f |
GGA |
GGAAGA |
X: 7,486,295 (GRCm39) |
|
probably benign |
Het |
Ccdc170 |
CCA |
CCAGCA |
10: 4,511,018 (GRCm39) |
|
probably benign |
Het |
Cela2a |
T |
C |
4: 141,549,026 (GRCm39) |
N117D |
probably benign |
Het |
Cul9 |
CTTC |
CTTCTTC |
17: 46,811,774 (GRCm39) |
|
probably benign |
Het |
Cyb5r2 |
A |
T |
7: 107,350,375 (GRCm39) |
S235R |
probably benign |
Het |
Dnmt1 |
CACAGTTCCTACCTCGTT |
CACAGTTCCTACCTCGTTTTGGGGGCGGAGAACAGTTCCTACCTCGTT |
9: 20,821,424 (GRCm39) |
|
probably null |
Het |
Dnmt1 |
TT |
TTTTGGGGGCGGAGCACAGTTCCTACCTCGAT |
9: 20,821,440 (GRCm39) |
|
probably null |
Het |
E4f1 |
CCG |
CCGTCG |
17: 24,674,160 (GRCm39) |
|
probably benign |
Het |
Fam171b |
TCCAGCA |
TCCAGCACCAGCA |
2: 83,643,217 (GRCm39) |
|
probably benign |
Het |
Fam171b |
GC |
GCAGCATC |
2: 83,643,239 (GRCm39) |
|
probably benign |
Het |
Fam81b |
CTGTT |
CTGTTGTT |
13: 76,419,435 (GRCm39) |
|
probably benign |
Het |
Fkbp1a |
GCCGCCGCCA |
G |
2: 151,384,619 (GRCm39) |
|
probably null |
Het |
Flii |
G |
A |
11: 60,607,069 (GRCm39) |
A969V |
probably benign |
Het |
Fscb |
AGTGGAACTTCTGCAGGCCCCTCTTCAGTTAGTGTAGGTGGAACTTCTGCAGGCCCCTCTTCAGTTAGTGGAGGTGGAACTTCTGCAGG |
AGTGGAACTTCTGCAGGCCCCTCTTCAGTTAGTGGAGGTGGAACTTCTGCAGG |
12: 64,519,768 (GRCm39) |
|
probably benign |
Het |
Gas1 |
G |
GAAA |
13: 60,324,345 (GRCm39) |
|
probably benign |
Het |
Grip1 |
A |
G |
10: 119,767,220 (GRCm39) |
D115G |
probably null |
Het |
Guca2b |
G |
T |
4: 119,514,044 (GRCm39) |
T89N |
possibly damaging |
Het |
Hcn4 |
T |
A |
9: 58,767,198 (GRCm39) |
S920T |
unknown |
Het |
Heatr1 |
A |
G |
13: 12,422,425 (GRCm39) |
M484V |
probably benign |
Het |
Iba57 |
G |
T |
11: 59,054,438 (GRCm39) |
A27E |
probably benign |
Het |
Ifi207 |
G |
C |
1: 173,556,687 (GRCm39) |
L684V |
not run |
Het |
Ints13 |
T |
C |
6: 146,457,738 (GRCm39) |
H380R |
probably damaging |
Het |
Jmjd1c |
C |
T |
10: 67,055,978 (GRCm39) |
T466I |
possibly damaging |
Het |
Kcnh8 |
G |
A |
17: 53,285,267 (GRCm39) |
R1079H |
probably benign |
Het |
Kif12 |
C |
CCTCCACCCGGCGGGG |
4: 63,089,664 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,543,457 (GRCm39) |
D1399E |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,367,648 (GRCm39) |
L2371Q |
probably damaging |
Het |
Mbd1 |
GTCTTCGTCTGCATCTGCATCTGCATCT |
GTCT |
18: 74,406,681 (GRCm39) |
|
probably benign |
Het |
Med12l |
GCA |
GCATCA |
3: 59,183,401 (GRCm39) |
|
probably benign |
Het |
Mgam |
C |
A |
6: 40,734,370 (GRCm39) |
Q1472K |
probably damaging |
Het |
Mup21 |
TATACTT |
TATACTTTTTAGATACTT |
4: 62,067,582 (GRCm39) |
|
probably benign |
Het |
Nalf2 |
CGCCGC |
CGCCGCAGCCGC |
X: 98,864,967 (GRCm39) |
|
probably benign |
Het |
Nipal1 |
A |
G |
5: 72,824,156 (GRCm39) |
N167D |
probably damaging |
Het |
Or4d10c |
C |
T |
19: 12,065,611 (GRCm39) |
V182I |
probably benign |
Het |
Or5be3 |
T |
A |
2: 86,864,385 (GRCm39) |
Y60F |
probably damaging |
Het |
Osbpl3 |
CCTGCA |
C |
6: 50,325,118 (GRCm39) |
|
probably benign |
Het |
Phf20 |
CCCCCCCCC |
CCCCCCCCCCCCCCCC |
2: 156,146,540 (GRCm39) |
|
probably benign |
Het |
Phf20 |
CCCCCCCC |
CCCCCCCCCCCCCCC |
2: 156,146,541 (GRCm39) |
|
probably benign |
Het |
Pramel16 |
C |
G |
4: 143,675,478 (GRCm39) |
Q449H |
probably damaging |
Het |
Rassf6 |
TCCTGTAGAGCAATGGGGATTC |
TCCTGTAGAGCAATGGGGATTCTGCCTCACTCATGGGCCTGTAGAGCAATGGGGATTC |
5: 90,756,780 (GRCm39) |
|
probably benign |
Het |
Rbm33 |
CCAGCCGCAGC |
CCAGC |
5: 28,599,179 (GRCm39) |
|
probably benign |
Het |
Rubcnl |
T |
C |
14: 75,281,878 (GRCm39) |
F445S |
probably damaging |
Het |
S100a10 |
TTTTTTTA |
T |
3: 93,471,541 (GRCm39) |
|
probably benign |
Het |
Sbp |
AA |
AAAATGCTGACAACGGA |
17: 24,164,328 (GRCm39) |
|
probably benign |
Het |
Sec14l3 |
A |
C |
11: 4,017,963 (GRCm39) |
Q81P |
possibly damaging |
Het |
Setd1a |
TGGTGGTGG |
TGGTGGTGGGGGTGGTGG |
7: 127,384,515 (GRCm39) |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,928,796 (GRCm39) |
|
probably benign |
Het |
Snapc5 |
ATGGAAGAAGAGG |
A |
9: 64,089,493 (GRCm39) |
|
probably benign |
Het |
Tbc1d12 |
CGGAGGAGG |
CGG |
19: 38,825,401 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
AGC |
AGCCGC |
18: 60,968,811 (GRCm39) |
|
probably benign |
Het |
Tox2 |
A |
G |
2: 163,067,484 (GRCm39) |
I68V |
probably benign |
Het |
Triml2 |
G |
T |
8: 43,636,201 (GRCm39) |
|
probably benign |
Het |
Tspan33 |
A |
G |
6: 29,716,729 (GRCm39) |
Y162C |
probably damaging |
Het |
Zfp384 |
GGCCCAGGCCCA |
GGCCCAGGCCCAAGCCCAGGCCCA |
6: 125,013,439 (GRCm39) |
|
probably benign |
Het |
Zfp948 |
T |
C |
17: 21,808,574 (GRCm39) |
Y589H |
probably damaging |
Het |
Zic1 |
T |
C |
9: 91,246,383 (GRCm39) |
I230V |
probably benign |
Het |
|
Other mutations in Cd109 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Cd109
|
APN |
9 |
78,524,251 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00465:Cd109
|
APN |
9 |
78,568,216 (GRCm39) |
nonsense |
probably null |
|
IGL00667:Cd109
|
APN |
9 |
78,592,159 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01432:Cd109
|
APN |
9 |
78,605,405 (GRCm39) |
missense |
probably benign |
|
IGL01795:Cd109
|
APN |
9 |
78,569,047 (GRCm39) |
splice site |
probably benign |
|
IGL02343:Cd109
|
APN |
9 |
78,596,237 (GRCm39) |
splice site |
probably benign |
|
IGL02450:Cd109
|
APN |
9 |
78,603,132 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02699:Cd109
|
APN |
9 |
78,579,271 (GRCm39) |
splice site |
probably benign |
|
IGL02738:Cd109
|
APN |
9 |
78,598,581 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02797:Cd109
|
APN |
9 |
78,568,995 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03160:Cd109
|
APN |
9 |
78,568,338 (GRCm39) |
splice site |
probably null |
|
IGL03349:Cd109
|
APN |
9 |
78,543,767 (GRCm39) |
missense |
probably benign |
0.34 |
FR4589:Cd109
|
UTSW |
9 |
78,619,811 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R0048:Cd109
|
UTSW |
9 |
78,587,303 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0060:Cd109
|
UTSW |
9 |
78,610,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Cd109
|
UTSW |
9 |
78,610,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R0158:Cd109
|
UTSW |
9 |
78,596,214 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0415:Cd109
|
UTSW |
9 |
78,619,897 (GRCm39) |
missense |
probably benign |
0.13 |
R0659:Cd109
|
UTSW |
9 |
78,587,452 (GRCm39) |
splice site |
probably benign |
|
R0709:Cd109
|
UTSW |
9 |
78,579,260 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0840:Cd109
|
UTSW |
9 |
78,571,612 (GRCm39) |
missense |
probably benign |
0.04 |
R0909:Cd109
|
UTSW |
9 |
78,543,755 (GRCm39) |
missense |
probably benign |
0.01 |
R0945:Cd109
|
UTSW |
9 |
78,596,223 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1344:Cd109
|
UTSW |
9 |
78,579,832 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1471:Cd109
|
UTSW |
9 |
78,561,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R1484:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R1570:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R1688:Cd109
|
UTSW |
9 |
78,612,373 (GRCm39) |
missense |
probably benign |
0.17 |
R1773:Cd109
|
UTSW |
9 |
78,611,006 (GRCm39) |
missense |
probably benign |
0.21 |
R1813:Cd109
|
UTSW |
9 |
78,524,287 (GRCm39) |
missense |
probably benign |
0.04 |
R2004:Cd109
|
UTSW |
9 |
78,611,044 (GRCm39) |
missense |
probably benign |
0.00 |
R2083:Cd109
|
UTSW |
9 |
78,574,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Cd109
|
UTSW |
9 |
78,574,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R2857:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2858:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2859:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2911:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2912:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2914:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2927:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3623:Cd109
|
UTSW |
9 |
78,574,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R3713:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3760:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3762:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3771:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3772:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3773:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3916:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3917:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4117:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4260:Cd109
|
UTSW |
9 |
78,543,745 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4387:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4389:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4526:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4527:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4528:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4700:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4708:Cd109
|
UTSW |
9 |
78,579,871 (GRCm39) |
missense |
probably benign |
0.00 |
R4723:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4750:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4751:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4754:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4755:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4773:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4984:Cd109
|
UTSW |
9 |
78,541,959 (GRCm39) |
critical splice donor site |
probably null |
|
R5259:Cd109
|
UTSW |
9 |
78,617,434 (GRCm39) |
missense |
probably benign |
0.30 |
R5353:Cd109
|
UTSW |
9 |
78,617,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5440:Cd109
|
UTSW |
9 |
78,587,446 (GRCm39) |
critical splice donor site |
probably null |
|
R5559:Cd109
|
UTSW |
9 |
78,568,250 (GRCm39) |
missense |
probably benign |
0.01 |
R5701:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R5995:Cd109
|
UTSW |
9 |
78,607,561 (GRCm39) |
missense |
probably benign |
0.01 |
R5997:Cd109
|
UTSW |
9 |
78,612,344 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6103:Cd109
|
UTSW |
9 |
78,605,596 (GRCm39) |
splice site |
probably null |
|
R6174:Cd109
|
UTSW |
9 |
78,572,828 (GRCm39) |
critical splice donor site |
probably null |
|
R6410:Cd109
|
UTSW |
9 |
78,564,798 (GRCm39) |
missense |
probably benign |
0.01 |
R6529:Cd109
|
UTSW |
9 |
78,619,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R6655:Cd109
|
UTSW |
9 |
78,592,220 (GRCm39) |
missense |
probably benign |
0.44 |
R6704:Cd109
|
UTSW |
9 |
78,587,357 (GRCm39) |
missense |
probably benign |
0.01 |
R6772:Cd109
|
UTSW |
9 |
78,588,092 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6817:Cd109
|
UTSW |
9 |
78,622,237 (GRCm39) |
missense |
probably benign |
0.01 |
R6903:Cd109
|
UTSW |
9 |
78,543,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R7294:Cd109
|
UTSW |
9 |
78,619,917 (GRCm39) |
missense |
probably damaging |
0.97 |
R7432:Cd109
|
UTSW |
9 |
78,622,225 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7566:Cd109
|
UTSW |
9 |
78,588,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R7767:Cd109
|
UTSW |
9 |
78,617,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Cd109
|
UTSW |
9 |
78,596,048 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8017:Cd109
|
UTSW |
9 |
78,614,828 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8019:Cd109
|
UTSW |
9 |
78,614,828 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8050:Cd109
|
UTSW |
9 |
78,571,633 (GRCm39) |
missense |
probably benign |
0.28 |
R8225:Cd109
|
UTSW |
9 |
78,568,972 (GRCm39) |
missense |
probably damaging |
0.99 |
R8269:Cd109
|
UTSW |
9 |
78,572,964 (GRCm39) |
missense |
probably benign |
0.06 |
R8479:Cd109
|
UTSW |
9 |
78,574,628 (GRCm39) |
nonsense |
probably null |
|
R8493:Cd109
|
UTSW |
9 |
78,564,801 (GRCm39) |
missense |
probably benign |
0.41 |
R8781:Cd109
|
UTSW |
9 |
78,543,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R8977:Cd109
|
UTSW |
9 |
78,614,810 (GRCm39) |
missense |
probably benign |
0.36 |
R9051:Cd109
|
UTSW |
9 |
78,619,813 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9051:Cd109
|
UTSW |
9 |
78,619,782 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9228:Cd109
|
UTSW |
9 |
78,577,042 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9366:Cd109
|
UTSW |
9 |
78,622,275 (GRCm39) |
missense |
probably benign |
0.11 |
R9430:Cd109
|
UTSW |
9 |
78,574,698 (GRCm39) |
critical splice donor site |
probably null |
|
R9572:Cd109
|
UTSW |
9 |
78,567,588 (GRCm39) |
missense |
probably benign |
0.16 |
R9691:Cd109
|
UTSW |
9 |
78,611,074 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9736:Cd109
|
UTSW |
9 |
78,619,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R9749:Cd109
|
UTSW |
9 |
78,592,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R9751:Cd109
|
UTSW |
9 |
78,605,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R9752:Cd109
|
UTSW |
9 |
78,614,834 (GRCm39) |
missense |
probably benign |
0.00 |
R9789:Cd109
|
UTSW |
9 |
78,541,944 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9797:Cd109
|
UTSW |
9 |
78,579,217 (GRCm39) |
missense |
probably benign |
0.04 |
RF002:Cd109
|
UTSW |
9 |
78,619,810 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF002:Cd109
|
UTSW |
9 |
78,619,805 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF003:Cd109
|
UTSW |
9 |
78,619,813 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF013:Cd109
|
UTSW |
9 |
78,619,813 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF047:Cd109
|
UTSW |
9 |
78,619,809 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF060:Cd109
|
UTSW |
9 |
78,619,807 (GRCm39) |
critical splice acceptor site |
probably benign |
|
Z1177:Cd109
|
UTSW |
9 |
78,598,595 (GRCm39) |
missense |
probably damaging |
0.96 |
|