Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5830454E08Rik |
T |
A |
9: 120,406,693 (GRCm39) |
|
probably benign |
Het |
Ada |
G |
A |
2: 163,572,406 (GRCm39) |
R225C |
probably benign |
Het |
Adamts9 |
T |
C |
6: 92,867,254 (GRCm39) |
K625R |
probably benign |
Het |
Ano1 |
T |
C |
7: 144,210,820 (GRCm39) |
I182V |
possibly damaging |
Het |
Aoc1l2 |
A |
T |
6: 48,908,292 (GRCm39) |
M431L |
probably benign |
Het |
Aox4 |
T |
C |
1: 58,285,445 (GRCm39) |
V643A |
possibly damaging |
Het |
Arcn1 |
T |
C |
9: 44,671,441 (GRCm39) |
I29V |
probably benign |
Het |
Arhgap15 |
A |
G |
2: 43,670,630 (GRCm39) |
T5A |
probably benign |
Het |
Asb10 |
A |
T |
5: 24,745,740 (GRCm39) |
L62Q |
probably damaging |
Het |
Atp23 |
T |
A |
10: 126,723,403 (GRCm39) |
H233L |
possibly damaging |
Het |
Bglap2 |
C |
T |
3: 88,289,432 (GRCm39) |
|
probably benign |
Het |
Carnmt1 |
T |
C |
19: 18,655,098 (GRCm39) |
S84P |
probably damaging |
Het |
Ccdc152 |
A |
G |
15: 3,312,319 (GRCm39) |
I180T |
probably damaging |
Het |
Cdr2l |
T |
C |
11: 115,284,186 (GRCm39) |
F174S |
probably damaging |
Het |
Celsr2 |
C |
T |
3: 108,301,312 (GRCm39) |
V2695I |
probably benign |
Het |
Chd1 |
C |
A |
17: 15,948,460 (GRCm39) |
S127R |
probably benign |
Het |
Chmp4c |
T |
A |
3: 10,450,646 (GRCm39) |
F75L |
probably benign |
Het |
Col13a1 |
A |
C |
10: 61,725,880 (GRCm39) |
V260G |
possibly damaging |
Het |
Col5a1 |
A |
G |
2: 27,915,664 (GRCm39) |
N183D |
probably damaging |
Het |
Cpn1 |
C |
T |
19: 43,974,634 (GRCm39) |
V32M |
probably damaging |
Het |
Cxcl1 |
A |
G |
5: 91,039,373 (GRCm39) |
M39V |
probably benign |
Het |
Dpep2 |
T |
A |
8: 106,712,825 (GRCm39) |
D455V |
probably damaging |
Het |
Dpp7 |
G |
A |
2: 25,242,749 (GRCm39) |
T441I |
possibly damaging |
Het |
Dst |
C |
A |
1: 34,241,640 (GRCm39) |
H4001N |
probably damaging |
Het |
Epg5 |
G |
A |
18: 78,038,828 (GRCm39) |
A1519T |
probably benign |
Het |
Esrp2 |
C |
T |
8: 106,858,820 (GRCm39) |
V606I |
probably benign |
Het |
Fbxo40 |
T |
C |
16: 36,789,236 (GRCm39) |
K625E |
probably damaging |
Het |
Gbp2b |
A |
T |
3: 142,303,946 (GRCm39) |
I14F |
probably damaging |
Het |
Gpr37l1 |
G |
T |
1: 135,094,676 (GRCm39) |
F189L |
probably damaging |
Het |
Heatr5a |
G |
A |
12: 52,003,020 (GRCm39) |
Q161* |
probably null |
Het |
Hspa4l |
T |
C |
3: 40,700,197 (GRCm39) |
Y30H |
possibly damaging |
Het |
Hspg2 |
G |
A |
4: 137,239,237 (GRCm39) |
C388Y |
probably damaging |
Het |
Kcna1 |
A |
G |
6: 126,619,330 (GRCm39) |
I330T |
probably damaging |
Het |
Klhl3 |
T |
A |
13: 58,166,781 (GRCm39) |
Y350F |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,919,118 (GRCm39) |
|
probably null |
Het |
Krtap10-4 |
A |
T |
10: 77,662,520 (GRCm39) |
C109* |
probably null |
Het |
Lrch4 |
T |
C |
5: 137,636,179 (GRCm39) |
S377P |
probably benign |
Het |
Lrrc8c |
C |
A |
5: 105,755,349 (GRCm39) |
H375N |
probably damaging |
Het |
Lsg1 |
T |
C |
16: 30,380,538 (GRCm39) |
E633G |
probably damaging |
Het |
Mcoln1 |
T |
C |
8: 3,560,697 (GRCm39) |
|
probably benign |
Het |
Med12l |
C |
A |
3: 59,167,109 (GRCm39) |
T1523K |
possibly damaging |
Het |
Mrps27 |
A |
T |
13: 99,547,973 (GRCm39) |
|
probably benign |
Het |
Mzb1 |
T |
A |
18: 35,780,717 (GRCm39) |
Y158F |
probably benign |
Het |
Nat8l |
T |
A |
5: 34,155,823 (GRCm39) |
C160S |
probably damaging |
Het |
Ncf4 |
T |
C |
15: 78,146,593 (GRCm39) |
|
probably benign |
Het |
Or1b1 |
A |
T |
2: 36,994,814 (GRCm39) |
Y283N |
probably damaging |
Het |
Or1o3 |
T |
C |
17: 37,573,730 (GRCm39) |
Y275C |
probably damaging |
Het |
Pak2 |
T |
A |
16: 31,861,936 (GRCm39) |
|
probably benign |
Het |
Pcdhga12 |
T |
C |
18: 37,901,160 (GRCm39) |
I664T |
probably benign |
Het |
Pcnx2 |
A |
C |
8: 126,564,749 (GRCm39) |
L1048R |
possibly damaging |
Het |
Pcsk5 |
T |
C |
19: 17,652,949 (GRCm39) |
M246V |
probably damaging |
Het |
Pkd2l2 |
T |
A |
18: 34,566,355 (GRCm39) |
V522D |
probably benign |
Het |
Plekhh1 |
A |
T |
12: 79,115,880 (GRCm39) |
M808L |
probably benign |
Het |
Plpp2 |
C |
A |
10: 79,362,973 (GRCm39) |
R157L |
probably benign |
Het |
Plrg1 |
T |
A |
3: 82,978,558 (GRCm39) |
H441Q |
probably benign |
Het |
Pnpla6 |
T |
C |
8: 3,572,613 (GRCm39) |
V300A |
probably damaging |
Het |
Ptprb |
A |
T |
10: 116,184,088 (GRCm39) |
K1633N |
possibly damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,659,508 (GRCm39) |
V2004A |
possibly damaging |
Het |
Rasd1 |
G |
T |
11: 59,854,933 (GRCm39) |
S182R |
possibly damaging |
Het |
Rc3h2 |
A |
T |
2: 37,288,373 (GRCm39) |
|
probably null |
Het |
Rrp1b |
T |
A |
17: 32,255,445 (GRCm39) |
|
probably benign |
Het |
Ruvbl1 |
T |
C |
6: 88,474,272 (GRCm39) |
I425T |
probably benign |
Het |
Shisal1 |
T |
C |
15: 84,301,427 (GRCm39) |
D72G |
probably damaging |
Het |
Sipa1l1 |
C |
T |
12: 82,487,682 (GRCm39) |
A1652V |
probably benign |
Het |
Slc12a2 |
A |
G |
18: 58,032,344 (GRCm39) |
Y348C |
probably damaging |
Het |
Slc14a2 |
C |
A |
18: 78,238,963 (GRCm39) |
V219L |
possibly damaging |
Het |
Smc1b |
G |
T |
15: 84,949,185 (GRCm39) |
P1242Q |
probably damaging |
Het |
Smim33 |
A |
G |
18: 35,861,894 (GRCm39) |
Y126C |
probably damaging |
Het |
Snx27 |
T |
A |
3: 94,431,551 (GRCm39) |
D281V |
probably damaging |
Het |
Spem2 |
C |
T |
11: 69,707,973 (GRCm39) |
V331I |
probably benign |
Het |
Sptb |
C |
A |
12: 76,656,052 (GRCm39) |
K1343N |
probably damaging |
Het |
Sult2a8 |
T |
C |
7: 14,147,584 (GRCm39) |
I236V |
probably benign |
Het |
Syk |
A |
G |
13: 52,765,071 (GRCm39) |
E66G |
probably damaging |
Het |
Synm |
T |
A |
7: 67,385,406 (GRCm39) |
E310V |
probably damaging |
Het |
Tas2r118 |
G |
A |
6: 23,969,209 (GRCm39) |
A284V |
probably benign |
Het |
Thoc2l |
T |
A |
5: 104,667,742 (GRCm39) |
F755I |
probably damaging |
Het |
Tlr11 |
A |
G |
14: 50,600,578 (GRCm39) |
N855D |
possibly damaging |
Het |
Tmem230 |
G |
T |
2: 132,087,871 (GRCm39) |
|
probably benign |
Het |
Trappc8 |
G |
A |
18: 20,977,237 (GRCm39) |
T844I |
probably benign |
Het |
Trmt44 |
T |
C |
5: 35,722,812 (GRCm39) |
S419G |
possibly damaging |
Het |
Trpv1 |
T |
A |
11: 73,132,574 (GRCm39) |
V396E |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Tubgcp2 |
A |
G |
7: 139,587,354 (GRCm39) |
I337T |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,137,934 (GRCm39) |
I1097T |
probably damaging |
Het |
Vmn2r61 |
T |
C |
7: 41,949,953 (GRCm39) |
F791S |
possibly damaging |
Het |
Zdhhc2 |
T |
A |
8: 40,898,825 (GRCm39) |
M45K |
probably benign |
Het |
Zfp383 |
T |
A |
7: 29,614,166 (GRCm39) |
D140E |
probably damaging |
Het |
Zfp712 |
C |
A |
13: 67,189,425 (GRCm39) |
K367N |
probably damaging |
Het |
|
Other mutations in Zfp763 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02638:Zfp763
|
APN |
17 |
33,238,908 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03291:Zfp763
|
APN |
17 |
33,238,860 (GRCm39) |
missense |
probably damaging |
0.96 |
R0346:Zfp763
|
UTSW |
17 |
33,238,721 (GRCm39) |
missense |
probably benign |
0.26 |
R0675:Zfp763
|
UTSW |
17 |
33,238,774 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0683:Zfp763
|
UTSW |
17 |
33,237,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Zfp763
|
UTSW |
17 |
33,240,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R1521:Zfp763
|
UTSW |
17 |
33,252,276 (GRCm39) |
start codon destroyed |
probably benign |
0.03 |
R1607:Zfp763
|
UTSW |
17 |
33,238,881 (GRCm39) |
missense |
probably benign |
0.08 |
R1627:Zfp763
|
UTSW |
17 |
33,240,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R1714:Zfp763
|
UTSW |
17 |
33,238,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R1993:Zfp763
|
UTSW |
17 |
33,237,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Zfp763
|
UTSW |
17 |
33,238,752 (GRCm39) |
missense |
probably benign |
|
R4420:Zfp763
|
UTSW |
17 |
33,237,455 (GRCm39) |
missense |
probably benign |
0.43 |
R4612:Zfp763
|
UTSW |
17 |
33,237,922 (GRCm39) |
missense |
probably benign |
0.05 |
R5426:Zfp763
|
UTSW |
17 |
33,238,569 (GRCm39) |
missense |
probably benign |
|
R5503:Zfp763
|
UTSW |
17 |
33,238,507 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5534:Zfp763
|
UTSW |
17 |
33,240,768 (GRCm39) |
missense |
probably damaging |
0.97 |
R6133:Zfp763
|
UTSW |
17 |
33,237,675 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7141:Zfp763
|
UTSW |
17 |
33,237,769 (GRCm39) |
missense |
probably damaging |
0.97 |
R7365:Zfp763
|
UTSW |
17 |
33,252,352 (GRCm39) |
start gained |
probably benign |
|
R7430:Zfp763
|
UTSW |
17 |
33,238,506 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7552:Zfp763
|
UTSW |
17 |
33,237,625 (GRCm39) |
missense |
probably benign |
|
R8277:Zfp763
|
UTSW |
17 |
33,252,294 (GRCm39) |
start gained |
probably benign |
|
R8446:Zfp763
|
UTSW |
17 |
33,238,473 (GRCm39) |
missense |
probably benign |
0.28 |
R8964:Zfp763
|
UTSW |
17 |
33,240,710 (GRCm39) |
missense |
probably benign |
0.25 |
R9662:Zfp763
|
UTSW |
17 |
33,240,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|