Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300002M23Rik |
GGGTTATGGTCAGTACCCCCCAGTAGGGACCTGGGGCGGTTATGGTCAGTACCCCCCAGTAGGGCCCTGGGGCGGTTATGGTCAGTACCCCCCAGTAGGGACCTGGGG |
GGGTTATGGTCAGTACCCCCCAGTAGGGCCCTGGGGCGGTTATGGTCAGTACCCCCCAGTAGGGACCTGGGG |
17: 35,879,473 (GRCm39) |
|
probably benign |
Het |
Acap3 |
CCTGGGCTGCTG |
CCTGGGCTGCTGCATACTGGGCTGCTG |
4: 155,989,553 (GRCm39) |
|
probably benign |
Het |
Ankrd28 |
A |
G |
14: 31,500,943 (GRCm39) |
I16T |
probably damaging |
Het |
AY761185 |
GCACTGTGGGC |
G |
8: 21,433,927 (GRCm39) |
|
probably null |
Het |
Bend3 |
T |
A |
10: 43,386,180 (GRCm39) |
F191Y |
possibly damaging |
Het |
Calhm1 |
GTGGC |
GTGGCTGTGGCTATGGC |
19: 47,129,712 (GRCm39) |
|
probably benign |
Het |
Camkv |
CGCTGCTGC |
CGC |
9: 107,825,059 (GRCm39) |
|
probably benign |
Het |
Cfap251 |
TCTCA |
T |
5: 123,412,224 (GRCm39) |
|
probably benign |
Het |
Chga |
GCA |
GCATCA |
12: 102,527,662 (GRCm39) |
|
probably benign |
Het |
Cngb1 |
CTCTGGCTCTGGCTCTGGCTCTG |
C |
8: 96,030,278 (GRCm39) |
|
probably null |
Het |
Cnot3 |
T |
C |
7: 3,659,068 (GRCm39) |
V438A |
probably benign |
Het |
Cntnap5c |
T |
A |
17: 58,593,790 (GRCm39) |
W710R |
probably damaging |
Het |
Dyrk1a |
A |
G |
16: 94,478,422 (GRCm39) |
S404G |
probably benign |
Het |
Efhd2 |
GCCGCC |
GCCGCCTCCGCC |
4: 141,602,075 (GRCm39) |
|
probably benign |
Het |
Flywch1 |
GTGT |
GTGTGGGGAGGCTACGTACTCACCCACACCTGTTGT |
17: 23,981,149 (GRCm39) |
|
probably null |
Het |
Fmn2 |
T |
A |
1: 174,409,581 (GRCm39) |
S605T |
unknown |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,617 (GRCm39) |
|
probably benign |
Het |
Gabre |
GCTC |
GCTCCGTCTC |
X: 71,313,666 (GRCm39) |
|
probably benign |
Het |
Gli3 |
A |
G |
13: 15,900,954 (GRCm39) |
Y1447C |
probably damaging |
Het |
Hibch |
T |
C |
1: 52,952,891 (GRCm39) |
V297A |
probably benign |
Het |
Kcnh8 |
G |
A |
17: 53,285,267 (GRCm39) |
R1079H |
probably benign |
Het |
Lce1m |
GCTGCTGCC |
GCTGCTGCCCCCACTGCTGCC |
3: 92,925,597 (GRCm39) |
|
probably benign |
Het |
Lpo |
A |
G |
11: 87,711,928 (GRCm39) |
V43A |
probably benign |
Het |
Map1a |
A |
AGCTCCAGCTCCAGCCCCACCTCCAGCTCCC |
2: 121,136,799 (GRCm39) |
|
probably benign |
Het |
Mapk9 |
A |
G |
11: 49,745,083 (GRCm39) |
|
probably benign |
Het |
Mep1a |
G |
A |
17: 43,797,126 (GRCm39) |
H314Y |
probably damaging |
Het |
Myh3 |
ATTAC |
ATTACTTAC |
11: 66,977,182 (GRCm39) |
|
probably null |
Het |
Myh3 |
AC |
ACTTCC |
11: 66,977,185 (GRCm39) |
|
probably null |
Het |
Nusap1 |
ACGTTAGCAGTGAGGAGCAA |
ACGTTAGCAGTGAGGAGCAAACTGAGATACTCGTTAGCAGTGAGGAGCAA |
2: 119,458,065 (GRCm39) |
|
probably benign |
Het |
Or10ag56 |
T |
A |
2: 87,139,184 (GRCm39) |
V37E |
possibly damaging |
Het |
Or14a259 |
T |
C |
7: 86,012,594 (GRCm39) |
Q317R |
probably benign |
Het |
Pdcd11 |
AGGAGG |
A |
19: 47,101,890 (GRCm39) |
|
probably null |
Het |
Pfkm |
T |
A |
15: 98,027,674 (GRCm39) |
I651N |
possibly damaging |
Het |
Phldb3 |
CCCCCGCCCC |
CCCCC |
7: 24,325,920 (GRCm39) |
|
probably null |
Het |
Polr1has |
CACCACCAC |
CACCACCACCACCACCACCACTACCACCAC |
17: 37,275,955 (GRCm39) |
|
probably benign |
Het |
Prkce |
T |
C |
17: 86,795,627 (GRCm39) |
V288A |
probably damaging |
Het |
Pxmp4 |
A |
G |
2: 154,434,183 (GRCm39) |
S93P |
probably damaging |
Het |
Rfc4 |
T |
C |
16: 22,946,232 (GRCm39) |
T17A |
probably benign |
Het |
Rfx4 |
CTCTCTCT |
CTCTCTCTCTCTCTCTATCTCTCT |
10: 84,694,351 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
G |
T |
2: 112,606,015 (GRCm39) |
A2415E |
probably damaging |
Het |
Sbp |
ACAAAGATGCTGACAACAAAGATGCTGACA |
ACAAAGATGCTGACACCAAAGATGCTGACAACAAAGATGCTGACA |
17: 24,164,325 (GRCm39) |
|
probably benign |
Het |
Sec24c |
T |
A |
14: 20,738,783 (GRCm39) |
|
probably null |
Het |
Sec63 |
C |
A |
10: 42,682,620 (GRCm39) |
A437E |
probably benign |
Het |
Six3 |
GCG |
GCGTCG |
17: 85,928,783 (GRCm39) |
|
probably benign |
Het |
Slco5a1 |
G |
A |
1: 12,942,171 (GRCm39) |
T825I |
probably damaging |
Het |
Spmap2l |
CAG |
CAGCGATCCTCCCCAGTCCCGCAAGGCGAG |
5: 77,164,274 (GRCm39) |
|
probably benign |
Het |
Stard8 |
GGA |
GGAAGA |
X: 98,110,123 (GRCm39) |
|
probably benign |
Het |
Stxbp1 |
A |
G |
2: 32,711,927 (GRCm39) |
V30A |
probably benign |
Het |
Supt20 |
AGCAGC |
AGCAGCGGCAGC |
3: 54,635,083 (GRCm39) |
|
probably benign |
Het |
Syne1 |
T |
A |
10: 5,196,386 (GRCm39) |
D3882V |
possibly damaging |
Het |
T |
A |
G |
17: 8,660,540 (GRCm39) |
T384A |
probably benign |
Het |
Tbc1d12 |
CGGGGCGG |
CG |
19: 38,825,384 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
CAG |
CAGAAG |
18: 60,968,816 (GRCm39) |
|
probably benign |
Het |
Tcstv5 |
A |
T |
13: 120,411,582 (GRCm39) |
V8E |
probably benign |
Het |
Tfeb |
GCA |
GCAACA |
17: 48,097,019 (GRCm39) |
|
probably benign |
Het |
Tfeb |
CAG |
CAGAAG |
17: 48,097,032 (GRCm39) |
|
probably benign |
Het |
Thumpd3 |
C |
T |
6: 113,033,006 (GRCm39) |
A248V |
probably damaging |
Het |
Tlcd4 |
T |
A |
3: 121,022,533 (GRCm39) |
I103L |
probably benign |
Het |
Tmem181a |
T |
C |
17: 6,330,978 (GRCm39) |
|
probably null |
Het |
Trim41 |
A |
T |
11: 48,698,165 (GRCm39) |
H600Q |
probably damaging |
Het |
Ttbk2 |
A |
T |
2: 120,620,820 (GRCm39) |
C147* |
probably null |
Het |
Ttll2 |
C |
T |
17: 7,618,737 (GRCm39) |
A397T |
probably benign |
Het |
Unc79 |
T |
A |
12: 103,079,046 (GRCm39) |
L1737Q |
probably benign |
Het |
Usp47 |
T |
A |
7: 111,692,145 (GRCm39) |
V869E |
probably damaging |
Het |
Vmn1r231 |
T |
A |
17: 21,110,255 (GRCm39) |
Q220L |
probably damaging |
Het |
Vmn2r26 |
C |
T |
6: 124,016,448 (GRCm39) |
T304I |
possibly damaging |
Het |
Wrn |
T |
C |
8: 33,778,793 (GRCm39) |
N839S |
probably benign |
Het |
Zfp384 |
GCCCAGGCCCAGGCCCAGGCCCAG |
GCCCAGGCCCAGTCCCAGGCCCAGGCCCAGGCCCAG |
6: 125,013,434 (GRCm39) |
|
probably benign |
Het |
Zfp384 |
GGCCCAGG |
GGCCCAGGAGCACGCCCAGG |
6: 125,013,451 (GRCm39) |
|
probably benign |
Het |
Zfyve26 |
C |
T |
12: 79,302,112 (GRCm39) |
C1828Y |
probably damaging |
Het |
|
Other mutations in Ifi213 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00678:Ifi213
|
APN |
1 |
173,421,619 (GRCm39) |
splice site |
probably benign |
|
IGL00908:Ifi213
|
APN |
1 |
173,422,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00964:Ifi213
|
APN |
1 |
173,421,518 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02217:Ifi213
|
APN |
1 |
173,422,598 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0709:Ifi213
|
UTSW |
1 |
173,417,366 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1518:Ifi213
|
UTSW |
1 |
173,417,229 (GRCm39) |
missense |
probably damaging |
0.99 |
R1559:Ifi213
|
UTSW |
1 |
173,394,784 (GRCm39) |
missense |
probably benign |
0.18 |
R1822:Ifi213
|
UTSW |
1 |
173,417,408 (GRCm39) |
missense |
probably damaging |
0.99 |
R1839:Ifi213
|
UTSW |
1 |
173,417,166 (GRCm39) |
missense |
probably damaging |
0.98 |
R1989:Ifi213
|
UTSW |
1 |
173,396,374 (GRCm39) |
critical splice donor site |
probably null |
|
R2108:Ifi213
|
UTSW |
1 |
173,396,668 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2696:Ifi213
|
UTSW |
1 |
173,417,590 (GRCm39) |
missense |
probably benign |
|
R3890:Ifi213
|
UTSW |
1 |
173,394,822 (GRCm39) |
missense |
probably benign |
0.33 |
R4544:Ifi213
|
UTSW |
1 |
173,409,693 (GRCm39) |
splice site |
probably null |
|
R4611:Ifi213
|
UTSW |
1 |
173,417,480 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4689:Ifi213
|
UTSW |
1 |
173,417,986 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4710:Ifi213
|
UTSW |
1 |
173,394,738 (GRCm39) |
utr 3 prime |
probably benign |
|
R5126:Ifi213
|
UTSW |
1 |
173,417,581 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5472:Ifi213
|
UTSW |
1 |
173,394,838 (GRCm39) |
splice site |
probably null |
|
R5625:Ifi213
|
UTSW |
1 |
173,396,629 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5789:Ifi213
|
UTSW |
1 |
173,396,360 (GRCm39) |
splice site |
probably benign |
|
R5898:Ifi213
|
UTSW |
1 |
173,396,545 (GRCm39) |
missense |
probably benign |
0.01 |
R6025:Ifi213
|
UTSW |
1 |
173,422,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R6149:Ifi213
|
UTSW |
1 |
173,421,581 (GRCm39) |
missense |
probably benign |
0.18 |
R6348:Ifi213
|
UTSW |
1 |
173,417,848 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6564:Ifi213
|
UTSW |
1 |
173,422,862 (GRCm39) |
start codon destroyed |
probably null |
0.06 |
R7254:Ifi213
|
UTSW |
1 |
173,421,529 (GRCm39) |
missense |
probably damaging |
0.98 |
R7292:Ifi213
|
UTSW |
1 |
173,422,691 (GRCm39) |
missense |
probably damaging |
0.99 |
R7752:Ifi213
|
UTSW |
1 |
173,394,784 (GRCm39) |
missense |
probably benign |
0.18 |
R7901:Ifi213
|
UTSW |
1 |
173,394,784 (GRCm39) |
missense |
probably benign |
0.18 |
R8100:Ifi213
|
UTSW |
1 |
173,422,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R8352:Ifi213
|
UTSW |
1 |
173,422,835 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8425:Ifi213
|
UTSW |
1 |
173,417,426 (GRCm39) |
missense |
probably benign |
|
R8452:Ifi213
|
UTSW |
1 |
173,422,835 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9357:Ifi213
|
UTSW |
1 |
173,396,392 (GRCm39) |
missense |
probably benign |
0.01 |
|