Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb3 |
T |
C |
10: 85,223,947 (GRCm39) |
V252A |
unknown |
Het |
Actn4 |
T |
C |
7: 28,604,044 (GRCm39) |
I406V |
probably benign |
Het |
Acyp2 |
C |
T |
11: 30,456,354 (GRCm39) |
E98K |
possibly damaging |
Het |
Ank1 |
T |
A |
8: 23,606,114 (GRCm39) |
F1124I |
probably damaging |
Het |
Arhgap44 |
CTGCT |
CTGCTTGCT |
11: 64,922,910 (GRCm39) |
|
probably null |
Het |
Atp9a |
C |
A |
2: 168,476,790 (GRCm39) |
V1000L |
probably benign |
Het |
Bnip3 |
A |
G |
7: 138,511,033 (GRCm39) |
|
probably benign |
Het |
Btnl6 |
T |
A |
17: 34,727,371 (GRCm39) |
R386S |
probably damaging |
Het |
Calcrl |
A |
G |
2: 84,205,658 (GRCm39) |
V11A |
probably benign |
Het |
Cc2d1a |
G |
T |
8: 84,863,571 (GRCm39) |
A597D |
possibly damaging |
Het |
Celsr3 |
A |
G |
9: 108,714,350 (GRCm39) |
T1960A |
probably benign |
Het |
Cfb |
T |
A |
17: 35,081,078 (GRCm39) |
|
probably null |
Het |
Chd8 |
A |
G |
14: 52,458,528 (GRCm39) |
I860T |
possibly damaging |
Het |
Col28a1 |
A |
G |
6: 8,168,102 (GRCm39) |
|
probably null |
Het |
Crhr2 |
T |
A |
6: 55,068,277 (GRCm39) |
T428S |
probably damaging |
Het |
Crybg2 |
A |
T |
4: 133,819,388 (GRCm39) |
I1753F |
probably damaging |
Het |
Ctsq |
A |
T |
13: 61,186,955 (GRCm39) |
V46E |
probably benign |
Het |
Cxcr1 |
T |
C |
1: 74,231,440 (GRCm39) |
E194G |
probably damaging |
Het |
Dop1a |
A |
T |
9: 86,397,396 (GRCm39) |
H900L |
probably damaging |
Het |
Dpyd |
T |
A |
3: 119,225,224 (GRCm39) |
M999K |
probably benign |
Het |
Gbp3 |
A |
C |
3: 142,273,560 (GRCm39) |
D369A |
possibly damaging |
Het |
Glmp |
A |
G |
3: 88,232,495 (GRCm39) |
E36G |
probably damaging |
Het |
Gm10113 |
T |
C |
13: 46,330,919 (GRCm39) |
|
noncoding transcript |
Het |
Gm6486 |
T |
A |
5: 3,120,846 (GRCm39) |
|
noncoding transcript |
Het |
Gm973 |
T |
G |
1: 59,671,509 (GRCm39) |
L891R |
unknown |
Het |
Heatr3 |
C |
T |
8: 88,866,582 (GRCm39) |
T8M |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,352,831 (GRCm39) |
M2106V |
probably damaging |
Het |
Hfm1 |
A |
T |
5: 107,046,509 (GRCm39) |
|
probably null |
Het |
Hspa14 |
A |
G |
2: 3,490,801 (GRCm39) |
V462A |
possibly damaging |
Het |
Hspa5 |
C |
A |
2: 34,665,761 (GRCm39) |
T535K |
possibly damaging |
Het |
Ift140 |
A |
G |
17: 25,274,563 (GRCm39) |
D745G |
probably benign |
Het |
Ift27 |
A |
T |
15: 78,057,981 (GRCm39) |
C8S |
possibly damaging |
Het |
Irak1bp1 |
G |
A |
9: 82,728,616 (GRCm39) |
W182* |
probably null |
Het |
Itga3 |
A |
G |
11: 94,953,541 (GRCm39) |
I236T |
probably benign |
Het |
Kctd15 |
T |
A |
7: 34,349,547 (GRCm39) |
N26Y |
possibly damaging |
Het |
Kdm1b |
T |
C |
13: 47,232,729 (GRCm39) |
V733A |
possibly damaging |
Het |
Lhx8 |
A |
T |
3: 154,027,340 (GRCm39) |
L234H |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,337,098 (GRCm39) |
T1225S |
probably damaging |
Het |
Lrrn1 |
G |
A |
6: 107,545,488 (GRCm39) |
D429N |
probably benign |
Het |
Mettl3 |
A |
T |
14: 52,536,243 (GRCm39) |
N200K |
possibly damaging |
Het |
Mixl1 |
G |
T |
1: 180,524,336 (GRCm39) |
A81D |
possibly damaging |
Het |
Mroh2b |
T |
C |
15: 4,980,763 (GRCm39) |
I1444T |
probably benign |
Het |
Muc15 |
T |
A |
2: 110,561,786 (GRCm39) |
L74* |
probably null |
Het |
Olfm2 |
T |
A |
9: 20,579,824 (GRCm39) |
Y317F |
probably damaging |
Het |
Or52a33 |
C |
T |
7: 103,288,886 (GRCm39) |
V154M |
probably benign |
Het |
Or5b114-ps1 |
G |
A |
19: 13,352,698 (GRCm39) |
S124N |
probably benign |
Het |
Or5p54 |
T |
A |
7: 107,554,001 (GRCm39) |
I51N |
probably benign |
Het |
Pclo |
A |
T |
5: 14,763,302 (GRCm39) |
Y3925F |
unknown |
Het |
Pik3c2g |
A |
T |
6: 139,599,137 (GRCm39) |
R84S |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,842,518 (GRCm39) |
Q449R |
probably damaging |
Het |
Psg28 |
T |
C |
7: 18,160,305 (GRCm39) |
E297G |
probably damaging |
Het |
Qrich2 |
A |
T |
11: 116,337,832 (GRCm39) |
|
probably benign |
Het |
Rgs9 |
A |
G |
11: 109,130,386 (GRCm39) |
I363T |
probably damaging |
Het |
Rnpepl1 |
A |
G |
1: 92,844,543 (GRCm39) |
D345G |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,658,023 (GRCm39) |
F726I |
probably damaging |
Het |
Sart3 |
A |
T |
5: 113,893,507 (GRCm39) |
I330N |
probably damaging |
Het |
Scn5a |
T |
C |
9: 119,391,440 (GRCm39) |
D84G |
probably damaging |
Het |
Sema4a |
T |
C |
3: 88,348,008 (GRCm39) |
T438A |
probably damaging |
Het |
Sfxn1 |
A |
C |
13: 54,242,961 (GRCm39) |
Y73S |
probably benign |
Het |
Slc24a2 |
A |
G |
4: 86,914,882 (GRCm39) |
M585T |
probably damaging |
Het |
Smok2a |
T |
G |
17: 13,445,021 (GRCm39) |
D199E |
probably benign |
Het |
Tbc1d10c |
T |
C |
19: 4,235,030 (GRCm39) |
I344V |
probably benign |
Het |
Tll1 |
A |
T |
8: 64,506,925 (GRCm39) |
Y605* |
probably null |
Het |
Trim75 |
G |
A |
8: 65,435,535 (GRCm39) |
P305L |
probably damaging |
Het |
Unc13c |
T |
C |
9: 73,838,166 (GRCm39) |
N895S |
probably benign |
Het |
Vmn2r25 |
A |
T |
6: 123,799,876 (GRCm39) |
I822N |
probably damaging |
Het |
Wasf3 |
T |
G |
5: 146,407,166 (GRCm39) |
D495E |
unknown |
Het |
Wdhd1 |
T |
A |
14: 47,510,667 (GRCm39) |
K119* |
probably null |
Het |
Wnt2b |
T |
A |
3: 104,858,339 (GRCm39) |
D310V |
probably damaging |
Het |
Zfat |
G |
T |
15: 68,052,626 (GRCm39) |
D389E |
probably damaging |
Het |
Zfp282 |
G |
A |
6: 47,857,102 (GRCm39) |
V112M |
probably damaging |
Het |
Zfp617 |
A |
T |
8: 72,687,257 (GRCm39) |
K529I |
probably damaging |
Het |
Zfp866 |
A |
T |
8: 70,218,373 (GRCm39) |
C416S |
probably damaging |
Het |
Zfp991 |
G |
A |
4: 147,264,222 (GRCm39) |
G533D |
probably benign |
Het |
|
Other mutations in Slc26a7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00471:Slc26a7
|
APN |
4 |
14,548,403 (GRCm39) |
splice site |
probably benign |
|
IGL00943:Slc26a7
|
APN |
4 |
14,506,477 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01878:Slc26a7
|
APN |
4 |
14,519,388 (GRCm39) |
splice site |
probably null |
|
IGL02698:Slc26a7
|
APN |
4 |
14,593,867 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03133:Slc26a7
|
APN |
4 |
14,532,576 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0200:Slc26a7
|
UTSW |
4 |
14,621,317 (GRCm39) |
missense |
probably benign |
0.04 |
R0240:Slc26a7
|
UTSW |
4 |
14,532,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0240:Slc26a7
|
UTSW |
4 |
14,532,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Slc26a7
|
UTSW |
4 |
14,621,317 (GRCm39) |
missense |
probably benign |
0.04 |
R0833:Slc26a7
|
UTSW |
4 |
14,593,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Slc26a7
|
UTSW |
4 |
14,506,489 (GRCm39) |
missense |
probably benign |
0.01 |
R1592:Slc26a7
|
UTSW |
4 |
14,552,470 (GRCm39) |
missense |
probably benign |
0.09 |
R1656:Slc26a7
|
UTSW |
4 |
14,621,221 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1758:Slc26a7
|
UTSW |
4 |
14,548,491 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1861:Slc26a7
|
UTSW |
4 |
14,522,873 (GRCm39) |
missense |
probably benign |
|
R2429:Slc26a7
|
UTSW |
4 |
14,506,399 (GRCm39) |
splice site |
probably benign |
|
R2850:Slc26a7
|
UTSW |
4 |
14,593,806 (GRCm39) |
splice site |
probably benign |
|
R3442:Slc26a7
|
UTSW |
4 |
14,565,511 (GRCm39) |
missense |
probably benign |
0.11 |
R4158:Slc26a7
|
UTSW |
4 |
14,544,197 (GRCm39) |
missense |
probably benign |
0.38 |
R4160:Slc26a7
|
UTSW |
4 |
14,544,197 (GRCm39) |
missense |
probably benign |
0.38 |
R4721:Slc26a7
|
UTSW |
4 |
14,510,261 (GRCm39) |
splice site |
probably null |
|
R4727:Slc26a7
|
UTSW |
4 |
14,590,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Slc26a7
|
UTSW |
4 |
14,546,309 (GRCm39) |
missense |
probably benign |
0.18 |
R4992:Slc26a7
|
UTSW |
4 |
14,565,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5024:Slc26a7
|
UTSW |
4 |
14,532,572 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5344:Slc26a7
|
UTSW |
4 |
14,519,402 (GRCm39) |
missense |
probably benign |
0.00 |
R5373:Slc26a7
|
UTSW |
4 |
14,546,447 (GRCm39) |
missense |
probably damaging |
0.99 |
R5540:Slc26a7
|
UTSW |
4 |
14,506,621 (GRCm39) |
missense |
probably benign |
|
R6320:Slc26a7
|
UTSW |
4 |
14,524,498 (GRCm39) |
missense |
probably benign |
0.01 |
R6685:Slc26a7
|
UTSW |
4 |
14,593,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R6685:Slc26a7
|
UTSW |
4 |
14,593,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R6880:Slc26a7
|
UTSW |
4 |
14,516,159 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6958:Slc26a7
|
UTSW |
4 |
14,506,442 (GRCm39) |
missense |
probably benign |
0.00 |
R7000:Slc26a7
|
UTSW |
4 |
14,552,476 (GRCm39) |
missense |
probably benign |
|
R7090:Slc26a7
|
UTSW |
4 |
14,565,460 (GRCm39) |
nonsense |
probably null |
|
R7122:Slc26a7
|
UTSW |
4 |
14,533,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Slc26a7
|
UTSW |
4 |
14,546,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R8035:Slc26a7
|
UTSW |
4 |
14,621,338 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8252:Slc26a7
|
UTSW |
4 |
14,621,415 (GRCm39) |
start gained |
probably benign |
|
R8262:Slc26a7
|
UTSW |
4 |
14,621,269 (GRCm39) |
missense |
probably benign |
0.01 |
R8989:Slc26a7
|
UTSW |
4 |
14,533,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R9013:Slc26a7
|
UTSW |
4 |
14,506,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Slc26a7
|
UTSW |
4 |
14,593,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R9184:Slc26a7
|
UTSW |
4 |
14,506,630 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9287:Slc26a7
|
UTSW |
4 |
14,516,165 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9377:Slc26a7
|
UTSW |
4 |
14,516,189 (GRCm39) |
missense |
probably benign |
0.04 |
R9563:Slc26a7
|
UTSW |
4 |
14,519,496 (GRCm39) |
missense |
probably benign |
0.03 |
R9565:Slc26a7
|
UTSW |
4 |
14,519,496 (GRCm39) |
missense |
probably benign |
0.03 |
R9609:Slc26a7
|
UTSW |
4 |
14,532,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R9633:Slc26a7
|
UTSW |
4 |
14,524,540 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9762:Slc26a7
|
UTSW |
4 |
14,546,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Slc26a7
|
UTSW |
4 |
14,522,862 (GRCm39) |
missense |
probably benign |
0.00 |
R9794:Slc26a7
|
UTSW |
4 |
14,590,416 (GRCm39) |
missense |
possibly damaging |
0.81 |
|