Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
T |
2: 151,315,390 (GRCm39) |
L96Q |
probably damaging |
Het |
4931414P19Rik |
T |
C |
14: 54,822,533 (GRCm39) |
Y368C |
probably damaging |
Het |
Acin1 |
T |
C |
14: 54,924,215 (GRCm39) |
N8S |
probably benign |
Het |
Aspm |
T |
C |
1: 139,408,409 (GRCm39) |
V2432A |
probably benign |
Het |
Atf2 |
A |
T |
2: 73,659,025 (GRCm39) |
|
probably null |
Het |
B3gnt2 |
A |
G |
11: 22,787,105 (GRCm39) |
S28P |
probably damaging |
Het |
Crybg2 |
CTTCCAGAGCCATGGACCCATCTTTTCCA |
CTTCCA |
4: 133,800,029 (GRCm39) |
|
probably null |
Het |
Dennd3 |
A |
T |
15: 73,405,225 (GRCm39) |
H326L |
possibly damaging |
Het |
Dysf |
C |
A |
6: 84,074,697 (GRCm39) |
D499E |
probably damaging |
Het |
Eprs1 |
T |
C |
1: 185,118,475 (GRCm39) |
V461A |
possibly damaging |
Het |
Fhad1 |
G |
A |
4: 141,738,858 (GRCm39) |
Q31* |
probably null |
Het |
Gpr26 |
A |
G |
7: 131,576,082 (GRCm39) |
T249A |
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,386,735 (GRCm39) |
M958L |
probably damaging |
Het |
Kat2b-ps |
A |
G |
5: 93,539,299 (GRCm39) |
|
noncoding transcript |
Het |
Kdm2b |
A |
T |
5: 123,072,849 (GRCm39) |
V343E |
probably damaging |
Het |
Lipi |
A |
G |
16: 75,362,417 (GRCm39) |
|
probably null |
Het |
Ltb4r1 |
T |
C |
14: 56,004,925 (GRCm39) |
F76S |
probably damaging |
Het |
Msantd2 |
A |
G |
9: 37,434,387 (GRCm39) |
Y209C |
probably damaging |
Het |
Nid1 |
G |
A |
13: 13,647,437 (GRCm39) |
C401Y |
probably damaging |
Het |
Obox1 |
A |
T |
7: 15,290,089 (GRCm39) |
N144I |
probably damaging |
Het |
Or14j7 |
T |
C |
17: 38,234,813 (GRCm39) |
S119P |
probably damaging |
Het |
Or8h9 |
T |
C |
2: 86,789,665 (GRCm39) |
I46V |
possibly damaging |
Het |
Or8k20 |
T |
A |
2: 86,106,517 (GRCm39) |
I105F |
possibly damaging |
Het |
Plec |
T |
C |
15: 76,064,775 (GRCm39) |
E1630G |
unknown |
Het |
Ppp2r5e |
C |
T |
12: 75,516,533 (GRCm39) |
R218Q |
probably damaging |
Het |
Prkdc |
A |
G |
16: 15,589,894 (GRCm39) |
T2586A |
probably benign |
Het |
Ptprj |
T |
C |
2: 90,290,840 (GRCm39) |
N633S |
probably benign |
Het |
Rab11fip2 |
T |
C |
19: 59,924,452 (GRCm39) |
N284S |
probably benign |
Het |
Rlig1 |
T |
C |
10: 100,414,243 (GRCm39) |
I139V |
probably benign |
Het |
Ropn1 |
A |
G |
16: 34,497,675 (GRCm39) |
Q189R |
possibly damaging |
Het |
Rwdd2b |
A |
G |
16: 87,233,950 (GRCm39) |
|
probably null |
Het |
Ryr2 |
A |
T |
13: 11,610,119 (GRCm39) |
S4236T |
probably benign |
Het |
Sigmar1 |
A |
G |
4: 41,741,251 (GRCm39) |
M1T |
probably null |
Het |
Sncg |
T |
A |
14: 34,095,268 (GRCm39) |
N79I |
probably benign |
Het |
Traf3ip2 |
C |
T |
10: 39,515,256 (GRCm39) |
P345S |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,763,021 (GRCm39) |
G3213S |
probably damaging |
Het |
Uqcrc1 |
G |
A |
9: 108,776,929 (GRCm39) |
R77H |
probably damaging |
Het |
Vps13d |
A |
C |
4: 144,835,080 (GRCm39) |
L2756R |
possibly damaging |
Het |
|
Other mutations in Chil5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01812:Chil5
|
APN |
3 |
105,924,468 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02959:Chil5
|
APN |
3 |
105,926,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R0255:Chil5
|
UTSW |
3 |
105,926,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R0409:Chil5
|
UTSW |
3 |
105,942,282 (GRCm39) |
unclassified |
probably benign |
|
R0635:Chil5
|
UTSW |
3 |
105,924,519 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1403:Chil5
|
UTSW |
3 |
105,925,409 (GRCm39) |
missense |
probably benign |
0.06 |
R1403:Chil5
|
UTSW |
3 |
105,925,409 (GRCm39) |
missense |
probably benign |
0.06 |
R3500:Chil5
|
UTSW |
3 |
105,925,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R4426:Chil5
|
UTSW |
3 |
105,926,943 (GRCm39) |
missense |
probably damaging |
0.96 |
R4998:Chil5
|
UTSW |
3 |
105,927,248 (GRCm39) |
missense |
probably damaging |
0.99 |
R5045:Chil5
|
UTSW |
3 |
105,931,456 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5113:Chil5
|
UTSW |
3 |
105,925,294 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5274:Chil5
|
UTSW |
3 |
105,936,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R5627:Chil5
|
UTSW |
3 |
105,926,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6910:Chil5
|
UTSW |
3 |
105,926,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R7476:Chil5
|
UTSW |
3 |
105,927,323 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8772:Chil5
|
UTSW |
3 |
105,925,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R9730:Chil5
|
UTSW |
3 |
105,926,470 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1177:Chil5
|
UTSW |
3 |
105,936,134 (GRCm39) |
missense |
probably damaging |
1.00 |
|