Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
A |
G |
7: 78,743,951 (GRCm39) |
T661A |
probably damaging |
Het |
Actrt2 |
T |
C |
4: 154,751,383 (GRCm39) |
Y251C |
probably benign |
Het |
Adat3 |
T |
A |
10: 80,442,255 (GRCm39) |
V31D |
probably damaging |
Het |
Adgrf4 |
T |
C |
17: 42,980,548 (GRCm39) |
H179R |
possibly damaging |
Het |
Ahcyl1 |
A |
T |
3: 107,578,513 (GRCm39) |
Y241* |
probably null |
Het |
Anks1 |
C |
A |
17: 28,227,114 (GRCm39) |
T589K |
possibly damaging |
Het |
Arhgap15 |
A |
G |
2: 43,670,630 (GRCm39) |
T5A |
probably benign |
Het |
Cacna1e |
A |
T |
1: 154,344,734 (GRCm39) |
M1130K |
probably null |
Het |
Ccdc121rt1 |
G |
A |
1: 181,338,443 (GRCm39) |
Q170* |
probably null |
Het |
Ceacam18 |
A |
T |
7: 43,286,298 (GRCm39) |
D57V |
probably damaging |
Het |
Celf1 |
C |
T |
2: 90,835,100 (GRCm39) |
Q194* |
probably null |
Het |
Celsr2 |
T |
A |
3: 108,306,218 (GRCm39) |
T2029S |
probably benign |
Het |
Cep170 |
T |
C |
1: 176,583,595 (GRCm39) |
D163G |
probably damaging |
Het |
Cfap210 |
A |
T |
2: 69,606,488 (GRCm39) |
D309E |
probably benign |
Het |
Cftr |
T |
C |
6: 18,214,295 (GRCm39) |
F157S |
probably damaging |
Het |
Chchd3 |
T |
C |
6: 32,945,164 (GRCm39) |
E114G |
probably damaging |
Het |
Cntnap2 |
T |
A |
6: 46,460,963 (GRCm39) |
S666R |
possibly damaging |
Het |
Col6a5 |
C |
T |
9: 105,753,075 (GRCm39) |
V2266I |
probably benign |
Het |
Ctr9 |
A |
G |
7: 110,633,133 (GRCm39) |
D127G |
probably benign |
Het |
Ctsl |
A |
T |
13: 64,514,882 (GRCm39) |
F141I |
probably damaging |
Het |
Dcpp1 |
T |
A |
17: 24,101,615 (GRCm39) |
Y121* |
probably null |
Het |
Ddx42 |
T |
C |
11: 106,138,565 (GRCm39) |
V788A |
probably benign |
Het |
Ehd4 |
T |
C |
2: 119,921,874 (GRCm39) |
I461V |
probably benign |
Het |
Elp6 |
C |
A |
9: 110,134,376 (GRCm39) |
L5I |
possibly damaging |
Het |
Faap20 |
T |
C |
4: 155,334,793 (GRCm39) |
S2P |
|
Het |
Fam98b |
A |
C |
2: 117,094,344 (GRCm39) |
Y218S |
probably damaging |
Het |
Fbxl4 |
T |
A |
4: 22,376,655 (GRCm39) |
D30E |
probably benign |
Het |
Fcrlb |
T |
C |
1: 170,736,210 (GRCm39) |
T189A |
probably damaging |
Het |
Gfpt1 |
A |
G |
6: 87,043,671 (GRCm39) |
D302G |
probably benign |
Het |
Gzmg |
T |
G |
14: 56,394,284 (GRCm39) |
E203D |
not run |
Het |
Hsph1 |
A |
C |
5: 149,553,838 (GRCm39) |
V210G |
probably damaging |
Het |
Il20rb |
A |
T |
9: 100,350,479 (GRCm39) |
M138K |
probably damaging |
Het |
Itpr1 |
A |
T |
6: 108,360,639 (GRCm39) |
E688D |
probably benign |
Het |
Jmjd1c |
T |
G |
10: 67,067,794 (GRCm39) |
S1585A |
probably damaging |
Het |
Kcnk3 |
A |
T |
5: 30,780,062 (GRCm39) |
T371S |
possibly damaging |
Het |
Kif11 |
T |
A |
19: 37,398,255 (GRCm39) |
S694T |
possibly damaging |
Het |
Kpna7 |
T |
A |
5: 144,942,731 (GRCm39) |
H85L |
probably benign |
Het |
Lipf |
A |
T |
19: 33,954,006 (GRCm39) |
I366F |
probably damaging |
Het |
Lrrc27 |
A |
G |
7: 138,794,748 (GRCm39) |
H37R |
probably benign |
Het |
Mki67 |
T |
C |
7: 135,302,512 (GRCm39) |
T841A |
possibly damaging |
Het |
Mtss1 |
A |
G |
15: 58,820,210 (GRCm39) |
S120P |
probably damaging |
Het |
Nav1 |
A |
G |
1: 135,397,404 (GRCm39) |
W922R |
probably damaging |
Het |
Nwd1 |
A |
G |
8: 73,434,021 (GRCm39) |
E1206G |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,885,635 (GRCm39) |
S7933G |
unknown |
Het |
Or13j1 |
T |
C |
4: 43,706,316 (GRCm39) |
H84R |
probably damaging |
Het |
Or1p4-ps1 |
T |
C |
11: 74,208,010 (GRCm39) |
V53A |
probably benign |
Het |
Or2g25 |
T |
A |
17: 37,971,122 (GRCm39) |
Y34F |
probably damaging |
Het |
Or2k2 |
T |
C |
4: 58,785,648 (GRCm39) |
I25V |
probably benign |
Het |
Or4c52 |
T |
C |
2: 89,845,355 (GRCm39) |
L27S |
probably benign |
Het |
Otog |
A |
T |
7: 45,948,039 (GRCm39) |
I162F |
probably damaging |
Het |
Paf1 |
G |
A |
7: 28,095,293 (GRCm39) |
V153I |
possibly damaging |
Het |
Pcdhga11 |
T |
A |
18: 37,889,554 (GRCm39) |
D187E |
probably benign |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
G |
T |
13: 6,610,658 (GRCm39) |
R424L |
probably damaging |
Het |
Pla2g4e |
T |
A |
2: 120,004,819 (GRCm39) |
|
probably null |
Het |
Plaat1 |
T |
C |
16: 29,046,919 (GRCm39) |
V146A |
probably benign |
Het |
Prorp |
T |
C |
12: 55,351,206 (GRCm39) |
Y172H |
probably damaging |
Het |
Prrc2a |
T |
C |
17: 35,381,286 (GRCm39) |
N61S |
unknown |
Het |
Ror1 |
T |
A |
4: 100,190,827 (GRCm39) |
D61E |
probably benign |
Het |
Ryr3 |
G |
A |
2: 112,542,706 (GRCm39) |
P3168S |
probably benign |
Het |
Serinc4 |
T |
A |
2: 121,284,250 (GRCm39) |
I289F |
probably damaging |
Het |
Sez6l |
A |
T |
5: 112,623,347 (GRCm39) |
L68H |
possibly damaging |
Het |
Sez6l2 |
A |
G |
7: 126,560,915 (GRCm39) |
E460G |
probably benign |
Het |
Sh3tc1 |
C |
T |
5: 35,863,406 (GRCm39) |
G927D |
probably damaging |
Het |
Slc38a8 |
C |
A |
8: 120,227,820 (GRCm39) |
A37S |
possibly damaging |
Het |
Slc40a1 |
T |
C |
1: 45,958,134 (GRCm39) |
N100D |
probably damaging |
Het |
Slc49a3 |
G |
A |
5: 108,591,646 (GRCm39) |
|
probably null |
Het |
Snx30 |
T |
C |
4: 59,894,567 (GRCm39) |
F382L |
possibly damaging |
Het |
Sox1 |
A |
G |
8: 12,446,913 (GRCm39) |
N185D |
possibly damaging |
Het |
Spsb1 |
C |
T |
4: 149,991,385 (GRCm39) |
R61H |
possibly damaging |
Het |
Sptbn2 |
T |
C |
19: 4,798,110 (GRCm39) |
V1945A |
probably benign |
Het |
St18 |
T |
A |
1: 6,898,194 (GRCm39) |
N665K |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,283,446 (GRCm39) |
S1540P |
probably damaging |
Het |
Syne2 |
G |
A |
12: 76,141,100 (GRCm39) |
V1331M |
probably damaging |
Het |
Tfap2c |
T |
C |
2: 172,393,639 (GRCm39) |
S185P |
probably benign |
Het |
Tnfsf8 |
T |
A |
4: 63,769,398 (GRCm39) |
D71V |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,937,929 (GRCm39) |
D1196G |
probably benign |
Het |
Ttll8 |
A |
G |
15: 88,817,639 (GRCm39) |
|
probably null |
Het |
Tubgcp3 |
A |
G |
8: 12,691,207 (GRCm39) |
F444L |
probably damaging |
Het |
Txndc11 |
G |
A |
16: 10,905,742 (GRCm39) |
P596L |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,139,983 (GRCm39) |
P1189S |
possibly damaging |
Het |
Usp32 |
T |
C |
11: 84,913,724 (GRCm39) |
D869G |
possibly damaging |
Het |
Vmn1r202 |
G |
T |
13: 22,686,188 (GRCm39) |
N76K |
probably damaging |
Het |
Wfdc6a |
C |
T |
2: 164,421,761 (GRCm39) |
M132I |
probably benign |
Het |
Wnk2 |
A |
T |
13: 49,300,720 (GRCm39) |
|
probably null |
Het |
Xbp1 |
A |
G |
11: 5,474,683 (GRCm39) |
|
probably null |
Het |
Zfp551 |
A |
T |
7: 12,149,725 (GRCm39) |
Y561* |
probably null |
Het |
|
Other mutations in Slc22a27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01994:Slc22a27
|
APN |
19 |
7,887,108 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02516:Slc22a27
|
APN |
19 |
7,842,176 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02961:Slc22a27
|
APN |
19 |
7,903,886 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03008:Slc22a27
|
APN |
19 |
7,887,067 (GRCm39) |
missense |
possibly damaging |
0.92 |
PIT4544001:Slc22a27
|
UTSW |
19 |
7,887,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R0172:Slc22a27
|
UTSW |
19 |
7,843,201 (GRCm39) |
nonsense |
probably null |
|
R0234:Slc22a27
|
UTSW |
19 |
7,904,156 (GRCm39) |
start gained |
probably benign |
|
R0234:Slc22a27
|
UTSW |
19 |
7,904,156 (GRCm39) |
start gained |
probably benign |
|
R0280:Slc22a27
|
UTSW |
19 |
7,874,187 (GRCm39) |
nonsense |
probably null |
|
R0561:Slc22a27
|
UTSW |
19 |
7,857,527 (GRCm39) |
critical splice donor site |
probably null |
|
R0597:Slc22a27
|
UTSW |
19 |
7,843,249 (GRCm39) |
missense |
probably benign |
0.00 |
R1005:Slc22a27
|
UTSW |
19 |
7,904,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1165:Slc22a27
|
UTSW |
19 |
7,887,059 (GRCm39) |
splice site |
probably null |
|
R1217:Slc22a27
|
UTSW |
19 |
7,904,033 (GRCm39) |
missense |
probably benign |
0.01 |
R1533:Slc22a27
|
UTSW |
19 |
7,844,348 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1940:Slc22a27
|
UTSW |
19 |
7,887,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Slc22a27
|
UTSW |
19 |
7,903,815 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3959:Slc22a27
|
UTSW |
19 |
7,887,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R4059:Slc22a27
|
UTSW |
19 |
7,856,973 (GRCm39) |
splice site |
probably benign |
|
R4249:Slc22a27
|
UTSW |
19 |
7,903,244 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4748:Slc22a27
|
UTSW |
19 |
7,903,241 (GRCm39) |
missense |
probably benign |
|
R5220:Slc22a27
|
UTSW |
19 |
7,843,303 (GRCm39) |
missense |
probably damaging |
0.96 |
R5221:Slc22a27
|
UTSW |
19 |
7,843,303 (GRCm39) |
missense |
probably damaging |
0.96 |
R5232:Slc22a27
|
UTSW |
19 |
7,843,303 (GRCm39) |
missense |
probably damaging |
0.96 |
R5330:Slc22a27
|
UTSW |
19 |
7,856,820 (GRCm39) |
missense |
probably benign |
0.13 |
R5331:Slc22a27
|
UTSW |
19 |
7,856,820 (GRCm39) |
missense |
probably benign |
0.13 |
R5345:Slc22a27
|
UTSW |
19 |
7,843,303 (GRCm39) |
missense |
probably damaging |
0.96 |
R5427:Slc22a27
|
UTSW |
19 |
7,856,753 (GRCm39) |
critical splice donor site |
probably null |
|
R5534:Slc22a27
|
UTSW |
19 |
7,903,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R5691:Slc22a27
|
UTSW |
19 |
7,904,035 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5828:Slc22a27
|
UTSW |
19 |
7,903,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R5878:Slc22a27
|
UTSW |
19 |
7,904,122 (GRCm39) |
missense |
probably benign |
0.01 |
R5918:Slc22a27
|
UTSW |
19 |
7,887,411 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6185:Slc22a27
|
UTSW |
19 |
7,903,953 (GRCm39) |
missense |
probably benign |
0.14 |
R6901:Slc22a27
|
UTSW |
19 |
7,903,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7139:Slc22a27
|
UTSW |
19 |
7,903,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R7336:Slc22a27
|
UTSW |
19 |
7,904,054 (GRCm39) |
missense |
probably benign |
0.02 |
R7556:Slc22a27
|
UTSW |
19 |
7,843,119 (GRCm39) |
missense |
probably damaging |
0.98 |
R7737:Slc22a27
|
UTSW |
19 |
7,874,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R7860:Slc22a27
|
UTSW |
19 |
7,887,472 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8050:Slc22a27
|
UTSW |
19 |
7,857,532 (GRCm39) |
missense |
probably benign |
0.18 |
R8090:Slc22a27
|
UTSW |
19 |
7,843,101 (GRCm39) |
splice site |
probably null |
|
R8150:Slc22a27
|
UTSW |
19 |
7,887,390 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8974:Slc22a27
|
UTSW |
19 |
7,903,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R9246:Slc22a27
|
UTSW |
19 |
7,874,209 (GRCm39) |
missense |
probably benign |
0.36 |
R9425:Slc22a27
|
UTSW |
19 |
7,874,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Slc22a27
|
UTSW |
19 |
7,843,227 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9731:Slc22a27
|
UTSW |
19 |
7,904,126 (GRCm39) |
nonsense |
probably null |
|
RF012:Slc22a27
|
UTSW |
19 |
7,903,949 (GRCm39) |
missense |
probably benign |
0.07 |
Z1177:Slc22a27
|
UTSW |
19 |
7,887,095 (GRCm39) |
missense |
probably benign |
0.00 |
|