Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb9 |
T |
G |
5: 124,227,984 (GRCm39) |
I86L |
probably benign |
Het |
Ankfn1 |
A |
G |
11: 89,282,960 (GRCm39) |
L229P |
probably damaging |
Het |
Aoc1 |
T |
C |
6: 48,882,549 (GRCm39) |
S164P |
probably benign |
Het |
Arhgef28 |
C |
T |
13: 98,066,000 (GRCm39) |
V1618I |
probably benign |
Het |
Arpc3 |
T |
C |
5: 122,542,242 (GRCm39) |
F88S |
probably damaging |
Het |
Asgr2 |
G |
T |
11: 69,987,676 (GRCm39) |
R58L |
possibly damaging |
Het |
Bach2 |
T |
C |
4: 32,563,198 (GRCm39) |
F432S |
probably damaging |
Het |
Brms1l |
C |
A |
12: 55,891,293 (GRCm39) |
R116S |
probably damaging |
Het |
Casp2 |
T |
A |
6: 42,245,879 (GRCm39) |
C179S |
probably damaging |
Het |
Ccdc73 |
A |
T |
2: 104,821,906 (GRCm39) |
E618D |
probably benign |
Het |
Cdh6 |
T |
A |
15: 13,057,541 (GRCm39) |
D260V |
possibly damaging |
Het |
Cenpc1 |
G |
T |
5: 86,183,369 (GRCm39) |
N473K |
probably benign |
Het |
Chst2 |
T |
C |
9: 95,287,536 (GRCm39) |
E270G |
possibly damaging |
Het |
Chst9 |
C |
T |
18: 15,586,231 (GRCm39) |
E111K |
probably benign |
Het |
Cyp3a44 |
T |
G |
5: 145,711,250 (GRCm39) |
I474L |
probably benign |
Het |
Dbr1 |
G |
T |
9: 99,466,073 (GRCm39) |
E550D |
probably benign |
Het |
Dph6 |
T |
C |
2: 114,475,199 (GRCm39) |
|
probably null |
Het |
Fam227b |
T |
A |
2: 125,966,505 (GRCm39) |
I136L |
possibly damaging |
Het |
Fcgbp |
A |
G |
7: 27,819,950 (GRCm39) |
N2559S |
probably damaging |
Het |
Fh1 |
A |
T |
1: 175,431,581 (GRCm39) |
I435N |
probably damaging |
Het |
Gab1 |
A |
C |
8: 81,515,159 (GRCm39) |
S386R |
probably damaging |
Het |
Gkn1 |
T |
A |
6: 87,326,098 (GRCm39) |
N31Y |
probably damaging |
Het |
Grk2 |
A |
G |
19: 4,340,707 (GRCm39) |
C251R |
probably damaging |
Het |
H2-DMa |
G |
T |
17: 34,357,380 (GRCm39) |
|
probably null |
Het |
Hp1bp3 |
T |
C |
4: 137,957,009 (GRCm39) |
S63P |
probably damaging |
Het |
Ift74 |
A |
G |
4: 94,581,174 (GRCm39) |
|
probably null |
Het |
Inf2 |
G |
A |
12: 112,577,210 (GRCm39) |
R1018Q |
unknown |
Het |
Kat2b |
A |
G |
17: 53,931,425 (GRCm39) |
D141G |
probably benign |
Het |
Klhl30 |
T |
C |
1: 91,288,737 (GRCm39) |
S499P |
probably benign |
Het |
Lama2 |
A |
C |
10: 26,917,120 (GRCm39) |
D2268E |
probably damaging |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Marf1 |
T |
C |
16: 13,964,626 (GRCm39) |
N258S |
possibly damaging |
Het |
Mc1r |
T |
A |
8: 124,134,999 (GRCm39) |
C251S |
probably damaging |
Het |
Myo15b |
C |
A |
11: 115,771,327 (GRCm39) |
Q257K |
possibly damaging |
Het |
Nbeal2 |
A |
G |
9: 110,456,176 (GRCm39) |
F2431S |
probably damaging |
Het |
Neb |
T |
A |
2: 52,186,321 (GRCm39) |
H917L |
possibly damaging |
Het |
Nlrp1a |
A |
G |
11: 71,004,292 (GRCm39) |
|
probably null |
Het |
Nr1d2 |
A |
T |
14: 18,211,891 (GRCm38) |
M404K |
probably benign |
Het |
Or4b1d |
T |
G |
2: 89,969,157 (GRCm39) |
I109L |
possibly damaging |
Het |
Or8u8 |
T |
G |
2: 86,012,453 (GRCm39) |
M1L |
possibly damaging |
Het |
Otoa |
T |
C |
7: 120,755,713 (GRCm39) |
S1040P |
probably benign |
Het |
Pctp |
T |
C |
11: 89,893,640 (GRCm39) |
D10G |
probably benign |
Het |
Pja2 |
G |
T |
17: 64,616,613 (GRCm39) |
T94K |
probably benign |
Het |
Plxna1 |
C |
T |
6: 89,298,032 (GRCm39) |
V1749M |
probably damaging |
Het |
Prdm15 |
C |
T |
16: 97,638,800 (GRCm39) |
E87K |
probably damaging |
Het |
Rgsl1 |
A |
G |
1: 153,660,937 (GRCm39) |
F1028L |
probably benign |
Het |
Sepsecs |
T |
C |
5: 52,818,021 (GRCm39) |
N252S |
probably damaging |
Het |
Skint5 |
A |
T |
4: 113,574,304 (GRCm39) |
L749Q |
unknown |
Het |
Slc22a22 |
G |
A |
15: 57,114,268 (GRCm39) |
S353F |
probably benign |
Het |
Slc7a13 |
A |
T |
4: 19,819,212 (GRCm39) |
K137N |
probably damaging |
Het |
Snx13 |
G |
T |
12: 35,141,405 (GRCm39) |
V163L |
probably damaging |
Het |
Synrg |
A |
T |
11: 83,914,182 (GRCm39) |
T1115S |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,740,928 (GRCm39) |
V1185A |
possibly damaging |
Het |
Tent5b |
T |
C |
4: 133,213,815 (GRCm39) |
F229L |
probably benign |
Het |
Tg |
T |
A |
15: 66,700,397 (GRCm39) |
N118K |
probably benign |
Het |
Top1mt |
T |
C |
15: 75,541,916 (GRCm39) |
K153E |
probably damaging |
Het |
Trmt11 |
T |
C |
10: 30,466,821 (GRCm39) |
|
probably benign |
Het |
Unc80 |
A |
G |
1: 66,675,061 (GRCm39) |
D1953G |
possibly damaging |
Het |
Vmn2r25 |
T |
A |
6: 123,828,864 (GRCm39) |
S137C |
probably damaging |
Het |
Vwf |
C |
A |
6: 125,580,271 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Slc49a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02505:Slc49a4
|
APN |
16 |
35,555,928 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02990:Slc49a4
|
APN |
16 |
35,555,861 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0166:Slc49a4
|
UTSW |
16 |
35,539,684 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0319:Slc49a4
|
UTSW |
16 |
35,570,884 (GRCm39) |
missense |
probably benign |
0.01 |
R0323:Slc49a4
|
UTSW |
16 |
35,539,730 (GRCm39) |
frame shift |
probably null |
|
R0497:Slc49a4
|
UTSW |
16 |
35,555,974 (GRCm39) |
missense |
probably benign |
0.40 |
R1460:Slc49a4
|
UTSW |
16 |
35,539,736 (GRCm39) |
missense |
probably benign |
0.25 |
R2115:Slc49a4
|
UTSW |
16 |
35,518,309 (GRCm39) |
missense |
probably benign |
0.17 |
R4502:Slc49a4
|
UTSW |
16 |
35,539,787 (GRCm39) |
missense |
probably benign |
0.00 |
R4503:Slc49a4
|
UTSW |
16 |
35,539,787 (GRCm39) |
missense |
probably benign |
0.00 |
R4563:Slc49a4
|
UTSW |
16 |
35,518,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Slc49a4
|
UTSW |
16 |
35,555,945 (GRCm39) |
missense |
probably benign |
0.08 |
R5278:Slc49a4
|
UTSW |
16 |
35,518,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R5651:Slc49a4
|
UTSW |
16 |
35,555,986 (GRCm39) |
missense |
probably benign |
0.25 |
R5717:Slc49a4
|
UTSW |
16 |
35,539,799 (GRCm39) |
missense |
probably benign |
0.00 |
R5947:Slc49a4
|
UTSW |
16 |
35,550,676 (GRCm39) |
missense |
probably benign |
0.14 |
R6176:Slc49a4
|
UTSW |
16 |
35,525,167 (GRCm39) |
missense |
probably benign |
|
R7155:Slc49a4
|
UTSW |
16 |
35,555,947 (GRCm39) |
missense |
probably benign |
0.02 |
R7450:Slc49a4
|
UTSW |
16 |
35,589,344 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7645:Slc49a4
|
UTSW |
16 |
35,554,438 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7905:Slc49a4
|
UTSW |
16 |
35,589,320 (GRCm39) |
missense |
probably benign |
0.33 |
R8425:Slc49a4
|
UTSW |
16 |
35,555,967 (GRCm39) |
missense |
probably benign |
0.01 |
R8670:Slc49a4
|
UTSW |
16 |
35,556,005 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8827:Slc49a4
|
UTSW |
16 |
35,554,320 (GRCm39) |
missense |
probably benign |
0.01 |
R9022:Slc49a4
|
UTSW |
16 |
35,570,912 (GRCm39) |
missense |
probably benign |
0.00 |
R9421:Slc49a4
|
UTSW |
16 |
35,518,372 (GRCm39) |
missense |
|
|
R9779:Slc49a4
|
UTSW |
16 |
35,543,186 (GRCm39) |
missense |
probably benign |
0.30 |
|