Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930556J24Rik |
TAA |
TAAA |
11: 3,887,945 (GRCm39) |
|
probably null |
Het |
4930556J24Rik |
C |
T |
11: 3,926,324 (GRCm39) |
A27T |
unknown |
Het |
Ago3 |
C |
T |
4: 126,298,056 (GRCm39) |
V155I |
probably benign |
Het |
Ago3 |
G |
A |
4: 126,298,103 (GRCm39) |
A139V |
probably benign |
Het |
Ago3 |
C |
T |
4: 126,298,098 (GRCm39) |
A141T |
probably benign |
Het |
Ahdc1 |
ACCTCCT |
ACCTCCTCCT |
4: 132,790,065 (GRCm39) |
|
probably benign |
Het |
Azin2 |
A |
G |
4: 128,839,927 (GRCm39) |
Y222H |
probably benign |
Het |
Bpifb5 |
C |
A |
2: 154,071,384 (GRCm39) |
|
probably null |
Het |
Castor1 |
G |
C |
11: 4,170,445 (GRCm39) |
G147A |
probably benign |
Het |
Ccdc157 |
C |
T |
11: 4,096,246 (GRCm39) |
A455T |
probably damaging |
Het |
Ccng1 |
A |
C |
11: 40,644,871 (GRCm39) |
S9A |
probably benign |
Het |
Cfh |
T |
C |
1: 140,082,336 (GRCm39) |
T164A |
probably benign |
Het |
Cherp |
TTGGACCTGGACCTGGACCTGGACCTGGA |
TTGGACCTGGACCTGGACCTGGA |
8: 73,215,878 (GRCm39) |
|
probably benign |
Het |
Chrng |
T |
C |
1: 87,138,348 (GRCm39) |
S380P |
probably benign |
Het |
Clspn |
ACGGCGGCGGCGGCG |
ACGGCGGCGGCGGCGGCGGCG |
4: 126,460,230 (GRCm39) |
|
probably benign |
Het |
Ctrc |
T |
TA |
4: 141,572,507 (GRCm39) |
|
probably null |
Het |
Cxxc1 |
C |
T |
18: 74,353,992 (GRCm39) |
R593C |
probably damaging |
Het |
Dlgap1 |
T |
C |
17: 70,823,950 (GRCm39) |
S312P |
possibly damaging |
Het |
Dnah10 |
A |
G |
5: 124,840,130 (GRCm39) |
S1255G |
probably benign |
Het |
Dpep1 |
A |
T |
8: 123,927,727 (GRCm39) |
S388C |
probably damaging |
Het |
Emid1 |
T |
C |
11: 5,094,386 (GRCm39) |
T42A |
probably damaging |
Het |
Emid1 |
A |
C |
11: 5,078,884 (GRCm39) |
L353V |
probably benign |
Het |
Epn3 |
A |
G |
11: 94,382,733 (GRCm39) |
|
probably null |
Het |
Fam124b |
T |
C |
1: 80,190,843 (GRCm39) |
E180G |
probably benign |
Het |
Fam135b |
T |
G |
15: 71,335,734 (GRCm39) |
T487P |
probably damaging |
Het |
Gja4 |
G |
C |
4: 127,206,024 (GRCm39) |
H246Q |
probably benign |
Het |
Gm9972 |
GA |
GAA |
11: 42,927,597 (GRCm39) |
|
probably null |
Het |
Hmmr |
G |
C |
11: 40,614,243 (GRCm39) |
N148K |
probably damaging |
Het |
Homez |
C |
T |
14: 55,094,796 (GRCm39) |
R304K |
possibly damaging |
Het |
Inpp5j |
G |
T |
11: 3,452,527 (GRCm39) |
T241N |
possibly damaging |
Het |
Kif12 |
GGGGC |
GGGGCCTCCACCCGGCGGGC |
4: 63,089,660 (GRCm39) |
|
probably benign |
Het |
Kremen1 |
C |
T |
11: 5,145,105 (GRCm39) |
A424T |
probably benign |
Het |
Mat2b |
G |
A |
11: 40,570,918 (GRCm39) |
T302I |
probably benign |
Het |
Mtmr3 |
C |
T |
11: 4,438,441 (GRCm39) |
R671K |
probably benign |
Het |
Nacad |
A |
G |
11: 6,551,632 (GRCm39) |
C520R |
probably benign |
Het |
Nacad |
GCAGGGTCAGGGTC |
GCAGGGTCAGGGTCAGGGTC |
11: 6,549,750 (GRCm39) |
|
probably benign |
Het |
Nacad |
T |
C |
11: 6,551,622 (GRCm39) |
N523S |
probably benign |
Het |
Nefh |
G |
A |
11: 4,890,151 (GRCm39) |
P823S |
probably benign |
Het |
Nfrkb |
G |
C |
9: 31,308,379 (GRCm39) |
A230P |
probably benign |
Het |
Nlrp4a |
A |
G |
7: 26,149,062 (GRCm39) |
E223G |
probably damaging |
Het |
Notch3 |
T |
A |
17: 32,365,391 (GRCm39) |
Y1107F |
probably damaging |
Het |
Or10ak9 |
G |
T |
4: 118,726,500 (GRCm39) |
R174M |
probably benign |
Het |
Or13g1 |
A |
T |
7: 85,955,492 (GRCm39) |
Y276* |
probably null |
Het |
Or6c35 |
A |
G |
10: 129,169,314 (GRCm39) |
D188G |
probably benign |
Het |
Osm |
A |
G |
11: 4,189,588 (GRCm39) |
D124G |
probably benign |
Het |
Plekhm2 |
TTCCTCCTCCT |
TTCCTCCT |
4: 141,359,292 (GRCm39) |
|
probably benign |
Het |
Pomgnt1 |
C |
T |
4: 115,994,624 (GRCm39) |
|
probably benign |
Het |
Spen |
A |
G |
4: 141,201,664 (GRCm39) |
V2321A |
probably benign |
Het |
Sytl1 |
TCTGC |
TC |
4: 132,984,305 (GRCm39) |
|
probably benign |
Het |
Tcn2 |
G |
C |
11: 3,873,487 (GRCm39) |
F286L |
possibly damaging |
Het |
Tg |
T |
C |
15: 66,560,712 (GRCm39) |
S10P |
probably benign |
Het |
Tmprss7 |
C |
T |
16: 45,501,096 (GRCm39) |
R235Q |
probably benign |
Het |
Tns3 |
G |
A |
11: 8,499,100 (GRCm39) |
|
probably benign |
Het |
Tns3 |
G |
T |
11: 8,401,146 (GRCm39) |
L1051M |
probably benign |
Het |
Tns3 |
T |
G |
11: 8,429,518 (GRCm39) |
E806A |
probably benign |
Het |
Toe1 |
T |
C |
4: 116,663,290 (GRCm39) |
I62M |
probably benign |
Het |
Txnrd2 |
A |
G |
16: 18,294,315 (GRCm39) |
H436R |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,179,092 (GRCm39) |
P2001S |
probably damaging |
Het |
Vmn2r23 |
T |
A |
6: 123,690,120 (GRCm39) |
M332K |
probably benign |
Het |
Zbtb8a |
GG |
GGATG |
4: 129,253,812 (GRCm39) |
|
probably benign |
Het |
Zbtb8a |
T |
C |
4: 129,254,005 (GRCm39) |
H163R |
probably benign |
Het |
Zfyve21 |
A |
G |
12: 111,794,067 (GRCm39) |
D206G |
probably damaging |
Het |
Zkscan4 |
AGAGGAG |
AGAG |
13: 21,663,370 (GRCm39) |
|
probably benign |
Het |
Zmym1 |
A |
C |
4: 126,943,466 (GRCm39) |
H307Q |
probably benign |
Het |
Zmym1 |
C |
T |
4: 126,941,740 (GRCm39) |
D785N |
probably benign |
Het |
Zmym1 |
C |
T |
4: 126,942,043 (GRCm39) |
V684I |
probably benign |
Het |
Zpld2 |
GTG |
GTGCTG |
4: 133,929,940 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ifngr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01066:Ifngr1
|
APN |
10 |
19,484,946 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01125:Ifngr1
|
APN |
10 |
19,473,161 (GRCm39) |
splice site |
probably benign |
|
IGL01366:Ifngr1
|
APN |
10 |
19,485,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Ifngr1
|
APN |
10 |
19,485,202 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02037:Ifngr1
|
APN |
10 |
19,483,007 (GRCm39) |
missense |
probably benign |
0.26 |
Marigold
|
UTSW |
10 |
19,477,233 (GRCm39) |
critical splice donor site |
probably null |
|
BB007:Ifngr1
|
UTSW |
10 |
19,484,931 (GRCm39) |
missense |
probably damaging |
1.00 |
BB017:Ifngr1
|
UTSW |
10 |
19,484,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Ifngr1
|
UTSW |
10 |
19,485,197 (GRCm39) |
nonsense |
probably null |
|
R0325:Ifngr1
|
UTSW |
10 |
19,473,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R0590:Ifngr1
|
UTSW |
10 |
19,479,690 (GRCm39) |
splice site |
probably benign |
|
R1305:Ifngr1
|
UTSW |
10 |
19,482,001 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1496:Ifngr1
|
UTSW |
10 |
19,477,193 (GRCm39) |
missense |
probably benign |
0.04 |
R1597:Ifngr1
|
UTSW |
10 |
19,485,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R2019:Ifngr1
|
UTSW |
10 |
19,467,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R2302:Ifngr1
|
UTSW |
10 |
19,485,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R2484:Ifngr1
|
UTSW |
10 |
19,477,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R4089:Ifngr1
|
UTSW |
10 |
19,477,233 (GRCm39) |
critical splice donor site |
probably null |
|
R4464:Ifngr1
|
UTSW |
10 |
19,473,265 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4863:Ifngr1
|
UTSW |
10 |
19,485,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R6045:Ifngr1
|
UTSW |
10 |
19,484,909 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6047:Ifngr1
|
UTSW |
10 |
19,482,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6089:Ifngr1
|
UTSW |
10 |
19,482,048 (GRCm39) |
missense |
probably benign |
0.01 |
R6750:Ifngr1
|
UTSW |
10 |
19,485,099 (GRCm39) |
missense |
probably benign |
0.06 |
R6950:Ifngr1
|
UTSW |
10 |
19,483,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R7162:Ifngr1
|
UTSW |
10 |
19,485,101 (GRCm39) |
missense |
probably benign |
|
R7930:Ifngr1
|
UTSW |
10 |
19,484,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R8178:Ifngr1
|
UTSW |
10 |
19,485,241 (GRCm39) |
missense |
probably benign |
0.03 |
R8436:Ifngr1
|
UTSW |
10 |
19,479,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R8975:Ifngr1
|
UTSW |
10 |
19,485,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Ifngr1
|
UTSW |
10 |
19,483,041 (GRCm39) |
missense |
possibly damaging |
0.61 |
X0005:Ifngr1
|
UTSW |
10 |
19,485,221 (GRCm39) |
missense |
probably damaging |
0.98 |
|