Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110025L11Rik |
G |
T |
16: 88,860,618 (GRCm39) |
S72Y |
unknown |
Het |
Abca8b |
T |
A |
11: 109,826,543 (GRCm39) |
K1568N |
probably benign |
Het |
Adcy6 |
T |
A |
15: 98,493,948 (GRCm39) |
Y865F |
probably benign |
Het |
Adgrf3 |
A |
T |
5: 30,402,204 (GRCm39) |
V608D |
probably benign |
Het |
Agbl1 |
G |
T |
7: 76,416,117 (GRCm39) |
A965S |
unknown |
Het |
Agbl3 |
C |
T |
6: 34,809,443 (GRCm39) |
P690L |
probably benign |
Het |
Akap9 |
C |
G |
5: 4,018,745 (GRCm39) |
H1109D |
probably benign |
Het |
Ankrd11 |
T |
A |
8: 123,620,403 (GRCm39) |
T1150S |
probably benign |
Het |
Arhgap15 |
A |
C |
2: 44,032,280 (GRCm39) |
H288P |
probably benign |
Het |
Arhgap39 |
A |
T |
15: 76,621,617 (GRCm39) |
M328K |
probably benign |
Het |
Arhgef12 |
T |
C |
9: 42,903,832 (GRCm39) |
K743R |
probably damaging |
Het |
Atg2a |
T |
G |
19: 6,301,293 (GRCm39) |
V789G |
probably damaging |
Het |
Ccdc54 |
T |
C |
16: 50,410,844 (GRCm39) |
T141A |
probably benign |
Het |
Ccng2 |
C |
G |
5: 93,421,202 (GRCm39) |
S237R |
probably benign |
Het |
Cdh5 |
T |
C |
8: 104,856,033 (GRCm39) |
|
probably null |
Het |
Cdkl3 |
T |
C |
11: 51,918,009 (GRCm39) |
V404A |
not run |
Het |
Chrm2 |
A |
T |
6: 36,500,184 (GRCm39) |
I14F |
probably benign |
Het |
Cnbp |
T |
C |
6: 87,822,258 (GRCm39) |
K89E |
possibly damaging |
Het |
Cntn6 |
T |
A |
6: 104,627,444 (GRCm39) |
D92E |
probably benign |
Het |
Col15a1 |
T |
C |
4: 47,245,591 (GRCm39) |
F114S |
possibly damaging |
Het |
Csrnp1 |
A |
G |
9: 119,801,469 (GRCm39) |
F530S |
probably benign |
Het |
Dcun1d3 |
C |
T |
7: 119,456,891 (GRCm39) |
V274M |
probably damaging |
Het |
Dph2 |
T |
A |
4: 117,747,478 (GRCm39) |
H302L |
possibly damaging |
Het |
Fam162a |
A |
T |
16: 35,866,770 (GRCm39) |
Y118* |
probably null |
Het |
Fam186a |
A |
G |
15: 99,837,725 (GRCm39) |
Y2840H |
unknown |
Het |
Fto |
A |
G |
8: 92,392,950 (GRCm39) |
K466E |
probably benign |
Het |
Gal |
T |
A |
19: 3,463,309 (GRCm39) |
Y41F |
probably damaging |
Het |
Gigyf2 |
A |
T |
1: 87,346,860 (GRCm39) |
L620F |
unknown |
Het |
Git2 |
C |
T |
5: 114,904,550 (GRCm39) |
R123H |
probably damaging |
Het |
Glud1 |
A |
T |
14: 34,033,114 (GRCm39) |
E87V |
probably benign |
Het |
Gm21190 |
T |
G |
5: 15,732,923 (GRCm39) |
E94A |
possibly damaging |
Het |
Gm5592 |
T |
C |
7: 40,938,134 (GRCm39) |
V472A |
probably benign |
Het |
Gpc5 |
T |
A |
14: 115,665,620 (GRCm39) |
N481K |
possibly damaging |
Het |
Gpn2 |
A |
G |
4: 133,318,687 (GRCm39) |
E304G |
probably benign |
Het |
Gsdmc2 |
T |
C |
15: 63,696,903 (GRCm39) |
T423A |
probably damaging |
Het |
Gucy2e |
G |
A |
11: 69,117,055 (GRCm39) |
Q789* |
probably null |
Het |
Gxylt2 |
T |
A |
6: 100,760,104 (GRCm39) |
V213E |
probably damaging |
Het |
Ighv1-75 |
G |
A |
12: 115,797,731 (GRCm39) |
L64F |
possibly damaging |
Het |
Il17re |
T |
C |
6: 113,435,943 (GRCm39) |
C30R |
probably benign |
Het |
Il7 |
G |
T |
3: 7,669,142 (GRCm39) |
D31E |
probably benign |
Het |
Ints4 |
T |
C |
7: 97,178,460 (GRCm39) |
Y687H |
possibly damaging |
Het |
Kdelr1 |
T |
G |
7: 45,532,401 (GRCm39) |
V202G |
probably benign |
Het |
Khnyn |
C |
A |
14: 56,124,596 (GRCm39) |
Y283* |
probably null |
Het |
Klf11 |
T |
C |
12: 24,703,670 (GRCm39) |
V52A |
probably damaging |
Het |
Klhl7 |
A |
G |
5: 24,346,284 (GRCm39) |
N310S |
probably benign |
Het |
Krt27 |
A |
T |
11: 99,240,312 (GRCm39) |
L202Q |
possibly damaging |
Het |
Lce1d |
A |
G |
3: 92,593,354 (GRCm39) |
C20R |
unknown |
Het |
Lim2 |
A |
T |
7: 43,083,054 (GRCm39) |
I80F |
possibly damaging |
Het |
Lrrk2 |
T |
A |
15: 91,584,561 (GRCm39) |
F326Y |
possibly damaging |
Het |
Lyst |
A |
T |
13: 13,905,061 (GRCm39) |
Y3246F |
possibly damaging |
Het |
Mafb |
T |
A |
2: 160,208,355 (GRCm39) |
H81L |
possibly damaging |
Het |
Mfsd5 |
G |
A |
15: 102,189,312 (GRCm39) |
R228H |
probably benign |
Het |
Mmp1b |
A |
T |
9: 7,386,675 (GRCm39) |
F150I |
possibly damaging |
Het |
Mthfd1 |
T |
A |
12: 76,317,209 (GRCm39) |
L20Q |
probably damaging |
Het |
Mxra8 |
A |
G |
4: 155,927,420 (GRCm39) |
T402A |
probably benign |
Het |
Ndc80 |
A |
T |
17: 71,815,658 (GRCm39) |
L376M |
probably damaging |
Het |
Nsd1 |
A |
T |
13: 55,425,452 (GRCm39) |
R1536S |
probably damaging |
Het |
Nup210l |
C |
A |
3: 90,119,300 (GRCm39) |
H1874Q |
probably benign |
Het |
Nyap1 |
T |
C |
5: 137,731,236 (GRCm39) |
H776R |
probably benign |
Het |
Patj |
C |
A |
4: 98,576,416 (GRCm39) |
H1773Q |
probably damaging |
Het |
Pax8 |
T |
A |
2: 24,326,523 (GRCm39) |
T280S |
probably benign |
Het |
Pcdhb19 |
A |
G |
18: 37,632,034 (GRCm39) |
T610A |
probably damaging |
Het |
Pde2a |
A |
G |
7: 101,160,788 (GRCm39) |
D919G |
possibly damaging |
Het |
Pdk2 |
T |
A |
11: 94,919,791 (GRCm39) |
Y240F |
probably damaging |
Het |
Peg3 |
A |
T |
7: 6,712,609 (GRCm39) |
I871N |
probably damaging |
Het |
Pex1 |
A |
T |
5: 3,646,244 (GRCm39) |
|
probably benign |
Het |
Pgm2l1 |
C |
T |
7: 99,899,535 (GRCm39) |
R50W |
probably damaging |
Het |
Phkg1 |
T |
A |
5: 129,894,764 (GRCm39) |
K262N |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,521,710 (GRCm39) |
E92G |
probably damaging |
Het |
Prmt6 |
A |
T |
3: 110,157,701 (GRCm39) |
V196E |
possibly damaging |
Het |
Ptprn2 |
T |
G |
12: 116,685,739 (GRCm39) |
M66R |
probably benign |
Het |
Rai14 |
C |
T |
15: 10,593,189 (GRCm39) |
G152R |
probably damaging |
Het |
Recql5 |
A |
T |
11: 115,814,102 (GRCm39) |
S348T |
probably damaging |
Het |
Rfk |
T |
G |
19: 17,376,046 (GRCm39) |
|
probably null |
Het |
Ro60 |
T |
C |
1: 143,646,611 (GRCm39) |
T45A |
probably damaging |
Het |
Selenbp1 |
A |
T |
3: 94,851,413 (GRCm39) |
M389L |
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,219,029 (GRCm39) |
R103C |
probably benign |
Het |
Slc10a6 |
T |
A |
5: 103,777,056 (GRCm39) |
S15C |
probably damaging |
Het |
Slc12a2 |
G |
T |
18: 58,065,596 (GRCm39) |
V944L |
probably benign |
Het |
Slc16a11 |
T |
A |
11: 70,106,143 (GRCm39) |
L127Q |
possibly damaging |
Het |
Spef1l |
T |
C |
7: 139,556,531 (GRCm39) |
N152S |
probably benign |
Het |
St6gal1 |
A |
G |
16: 23,174,978 (GRCm39) |
Y272C |
probably damaging |
Het |
Stab2 |
C |
A |
10: 86,816,999 (GRCm39) |
V133F |
probably benign |
Het |
Stradb |
G |
A |
1: 59,031,885 (GRCm39) |
V266I |
probably damaging |
Het |
Tmem150b |
A |
G |
7: 4,723,758 (GRCm39) |
W140R |
probably benign |
Het |
Tnnt3 |
A |
T |
7: 142,065,833 (GRCm39) |
K157* |
probably null |
Het |
Ttn |
T |
G |
2: 76,554,113 (GRCm39) |
K30863N |
probably damaging |
Het |
Vldlr |
G |
A |
19: 27,220,536 (GRCm39) |
R592H |
probably benign |
Het |
Vmn1r12 |
A |
T |
6: 57,135,883 (GRCm39) |
|
probably benign |
Het |
Vmn2r63 |
A |
C |
7: 42,574,693 (GRCm39) |
S519R |
probably damaging |
Het |
Zbtb22 |
G |
C |
17: 34,137,471 (GRCm39) |
E539Q |
probably damaging |
Het |
Zbtb44 |
G |
A |
9: 30,965,375 (GRCm39) |
A262T |
probably benign |
Het |
Zfp280d |
A |
T |
9: 72,231,354 (GRCm39) |
N455I |
probably damaging |
Het |
Zfp287 |
T |
C |
11: 62,616,089 (GRCm39) |
N201D |
probably damaging |
Het |
Zfp988 |
T |
C |
4: 147,416,751 (GRCm39) |
L395P |
probably damaging |
Het |
|
Other mutations in Amt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02657:Amt
|
APN |
9 |
108,178,579 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Amt
|
APN |
9 |
108,178,418 (GRCm39) |
missense |
probably benign |
|
R1333:Amt
|
UTSW |
9 |
108,178,296 (GRCm39) |
missense |
probably benign |
0.04 |
R1856:Amt
|
UTSW |
9 |
108,174,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R3843:Amt
|
UTSW |
9 |
108,174,420 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3844:Amt
|
UTSW |
9 |
108,174,420 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3903:Amt
|
UTSW |
9 |
108,174,420 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3904:Amt
|
UTSW |
9 |
108,174,420 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4729:Amt
|
UTSW |
9 |
108,177,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R4814:Amt
|
UTSW |
9 |
108,176,979 (GRCm39) |
missense |
probably benign |
|
R5149:Amt
|
UTSW |
9 |
108,178,650 (GRCm39) |
missense |
possibly damaging |
0.59 |
R6000:Amt
|
UTSW |
9 |
108,178,684 (GRCm39) |
missense |
probably benign |
0.20 |
R6044:Amt
|
UTSW |
9 |
108,174,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R6911:Amt
|
UTSW |
9 |
108,178,428 (GRCm39) |
critical splice donor site |
probably null |
|
R6957:Amt
|
UTSW |
9 |
108,177,032 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7618:Amt
|
UTSW |
9 |
108,177,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R7783:Amt
|
UTSW |
9 |
108,174,414 (GRCm39) |
nonsense |
probably null |
|
R9276:Amt
|
UTSW |
9 |
108,178,410 (GRCm39) |
missense |
probably benign |
0.00 |
|