Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
G |
T |
11: 101,308,185 (GRCm39) |
Y10* |
probably null |
Het |
Aass |
C |
A |
6: 23,107,633 (GRCm39) |
Q383H |
probably damaging |
Het |
Bag1 |
T |
C |
4: 40,936,657 (GRCm39) |
D333G |
probably damaging |
Het |
Cap2 |
A |
G |
13: 46,793,425 (GRCm39) |
|
probably benign |
Het |
Col27a1 |
G |
T |
4: 63,143,868 (GRCm39) |
A519S |
probably benign |
Het |
Cr2 |
A |
G |
1: 194,841,903 (GRCm39) |
V726A |
possibly damaging |
Het |
Csmd2 |
A |
G |
4: 128,374,638 (GRCm39) |
|
probably benign |
Het |
Dennd4c |
A |
G |
4: 86,717,788 (GRCm39) |
D595G |
possibly damaging |
Het |
Ercc2 |
G |
T |
7: 19,127,374 (GRCm39) |
R340L |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,206,640 (GRCm39) |
T35A |
probably benign |
Het |
Fndc3a |
A |
G |
14: 72,803,581 (GRCm39) |
Y525H |
probably benign |
Het |
Gm4922 |
T |
C |
10: 18,659,795 (GRCm39) |
Q309R |
probably benign |
Het |
Gm5263 |
T |
C |
1: 146,296,292 (GRCm39) |
|
noncoding transcript |
Het |
Gm6563 |
A |
C |
19: 23,653,751 (GRCm39) |
R180S |
probably damaging |
Het |
Gpr182 |
C |
A |
10: 127,586,733 (GRCm39) |
V73F |
probably damaging |
Het |
Gramd1b |
C |
T |
9: 40,227,069 (GRCm39) |
R179H |
probably damaging |
Het |
Hk1 |
C |
T |
10: 62,188,884 (GRCm39) |
A10T |
probably benign |
Het |
Hmgn3 |
C |
A |
9: 82,992,437 (GRCm39) |
|
probably benign |
Het |
Il1b |
C |
T |
2: 129,211,649 (GRCm39) |
E24K |
probably damaging |
Het |
Itgb6 |
G |
T |
2: 60,458,329 (GRCm39) |
Q475K |
probably benign |
Het |
Mfsd2b |
T |
C |
12: 4,916,469 (GRCm39) |
T234A |
possibly damaging |
Het |
Muc6 |
A |
T |
7: 141,237,327 (GRCm39) |
Y270N |
probably damaging |
Het |
Naip6 |
A |
G |
13: 100,424,603 (GRCm39) |
|
probably benign |
Het |
Or4b13 |
A |
T |
2: 90,082,476 (GRCm39) |
Y285* |
probably null |
Het |
Pear1 |
G |
A |
3: 87,659,608 (GRCm39) |
T742I |
probably damaging |
Het |
Peli2 |
G |
A |
14: 48,493,491 (GRCm39) |
V238I |
probably benign |
Het |
Pira2 |
A |
G |
7: 3,847,611 (GRCm39) |
L26P |
probably damaging |
Het |
Pot1b |
A |
G |
17: 55,969,521 (GRCm39) |
V549A |
possibly damaging |
Het |
Prdm16 |
T |
C |
4: 154,432,384 (GRCm39) |
Y295C |
probably benign |
Het |
Ptprd |
A |
T |
4: 76,058,744 (GRCm39) |
|
probably benign |
Het |
Rap1gap |
A |
T |
4: 137,443,466 (GRCm39) |
M145L |
probably benign |
Het |
Setd7 |
A |
T |
3: 51,440,388 (GRCm39) |
|
probably benign |
Het |
Ssx2ip |
T |
C |
3: 146,133,765 (GRCm39) |
I258T |
probably benign |
Het |
Stard9 |
T |
C |
2: 120,529,565 (GRCm39) |
Y1941H |
possibly damaging |
Het |
Stxbp3 |
T |
C |
3: 108,707,468 (GRCm39) |
E420G |
probably benign |
Het |
Tpra1 |
T |
C |
6: 88,886,324 (GRCm39) |
V101A |
probably damaging |
Het |
Tpx2 |
G |
T |
2: 152,726,155 (GRCm39) |
Q373H |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,557,352 (GRCm39) |
R29914Q |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,833,809 (GRCm39) |
|
probably null |
Het |
Usp18 |
G |
A |
6: 121,230,730 (GRCm39) |
G53D |
probably damaging |
Het |
Vps13c |
A |
T |
9: 67,863,062 (GRCm39) |
H3026L |
probably benign |
Het |
Zan |
T |
C |
5: 137,461,888 (GRCm39) |
E1097G |
unknown |
Het |
|
Other mutations in Lrrc74b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02402:Lrrc74b
|
APN |
16 |
17,376,028 (GRCm39) |
splice site |
probably benign |
|
P0043:Lrrc74b
|
UTSW |
16 |
17,376,023 (GRCm39) |
splice site |
probably benign |
|
R0131:Lrrc74b
|
UTSW |
16 |
17,371,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Lrrc74b
|
UTSW |
16 |
17,371,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0132:Lrrc74b
|
UTSW |
16 |
17,371,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R0829:Lrrc74b
|
UTSW |
16 |
17,376,254 (GRCm39) |
splice site |
probably benign |
|
R1463:Lrrc74b
|
UTSW |
16 |
17,377,737 (GRCm39) |
missense |
probably benign |
0.00 |
R1681:Lrrc74b
|
UTSW |
16 |
17,377,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Lrrc74b
|
UTSW |
16 |
17,371,058 (GRCm39) |
missense |
probably benign |
0.41 |
R4790:Lrrc74b
|
UTSW |
16 |
17,367,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R5428:Lrrc74b
|
UTSW |
16 |
17,376,125 (GRCm39) |
missense |
probably damaging |
0.99 |
R6198:Lrrc74b
|
UTSW |
16 |
17,366,650 (GRCm39) |
missense |
probably damaging |
0.96 |
R7910:Lrrc74b
|
UTSW |
16 |
17,376,213 (GRCm39) |
nonsense |
probably null |
|
R8233:Lrrc74b
|
UTSW |
16 |
17,376,089 (GRCm39) |
missense |
probably benign |
0.00 |
R8957:Lrrc74b
|
UTSW |
16 |
17,378,976 (GRCm39) |
missense |
probably benign |
0.09 |
R9030:Lrrc74b
|
UTSW |
16 |
17,367,640 (GRCm39) |
critical splice donor site |
probably null |
|
X0063:Lrrc74b
|
UTSW |
16 |
17,371,072 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Lrrc74b
|
UTSW |
16 |
17,376,036 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lrrc74b
|
UTSW |
16 |
17,376,032 (GRCm39) |
critical splice donor site |
probably null |
|
|