Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca17 |
G |
C |
17: 24,508,481 (GRCm39) |
T1018R |
probably damaging |
Het |
Acte1 |
T |
A |
7: 143,447,800 (GRCm39) |
Y214* |
probably null |
Het |
Akap9 |
A |
G |
5: 4,026,353 (GRCm39) |
|
probably benign |
Het |
Ankrd29 |
G |
A |
18: 12,387,757 (GRCm39) |
A275V |
possibly damaging |
Het |
Ano6 |
T |
A |
15: 95,841,308 (GRCm39) |
C468* |
probably null |
Het |
Arhgef10l |
G |
T |
4: 140,242,598 (GRCm39) |
H890Q |
probably benign |
Het |
Ccnj |
T |
A |
19: 40,833,158 (GRCm39) |
L112Q |
probably damaging |
Het |
Chaf1a |
T |
C |
17: 56,351,114 (GRCm39) |
|
probably null |
Het |
Chchd4 |
A |
G |
6: 91,442,200 (GRCm39) |
S73P |
probably damaging |
Het |
Chd3 |
T |
C |
11: 69,254,924 (GRCm39) |
K139E |
possibly damaging |
Het |
Cyp2b13 |
T |
G |
7: 25,785,456 (GRCm39) |
|
probably null |
Het |
Dagla |
T |
C |
19: 10,248,448 (GRCm39) |
I71V |
possibly damaging |
Het |
Epor |
A |
T |
9: 21,870,936 (GRCm39) |
W315R |
probably damaging |
Het |
Etv1 |
T |
A |
12: 38,833,809 (GRCm39) |
|
probably null |
Het |
Fbn2 |
A |
T |
18: 58,202,314 (GRCm39) |
C1280S |
probably damaging |
Het |
Fbxo2 |
G |
C |
4: 148,250,468 (GRCm39) |
R269P |
probably damaging |
Het |
Ggnbp2 |
C |
T |
11: 84,723,797 (GRCm39) |
|
probably null |
Het |
Grm7 |
G |
T |
6: 110,623,309 (GRCm39) |
V161F |
probably damaging |
Het |
Ibsp |
G |
A |
5: 104,458,260 (GRCm39) |
E266K |
possibly damaging |
Het |
Lamb3 |
T |
A |
1: 193,013,092 (GRCm39) |
M439K |
possibly damaging |
Het |
Lnx1 |
C |
T |
5: 74,780,784 (GRCm39) |
V246M |
probably benign |
Het |
Lrrc32 |
A |
G |
7: 98,148,984 (GRCm39) |
Q588R |
probably benign |
Het |
Magi2 |
A |
AG |
5: 20,807,459 (GRCm39) |
|
probably null |
Het |
Med13 |
C |
T |
11: 86,189,988 (GRCm39) |
A974T |
possibly damaging |
Het |
Mogat2 |
A |
T |
7: 98,871,573 (GRCm39) |
I246N |
possibly damaging |
Het |
Myl2 |
T |
C |
5: 122,242,748 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Or1p1c |
T |
A |
11: 74,161,049 (GRCm39) |
V278D |
probably damaging |
Het |
Osbpl8 |
T |
A |
10: 111,105,297 (GRCm39) |
S251T |
probably benign |
Het |
Pik3r2 |
A |
G |
8: 71,225,029 (GRCm39) |
Y145H |
probably benign |
Het |
Plg |
A |
G |
17: 12,622,987 (GRCm39) |
E509G |
possibly damaging |
Het |
Pnkp |
T |
A |
7: 44,508,102 (GRCm39) |
S142T |
probably damaging |
Het |
Ros1 |
C |
T |
10: 52,048,936 (GRCm39) |
|
probably null |
Het |
Sbno1 |
A |
G |
5: 124,526,635 (GRCm39) |
M960T |
probably damaging |
Het |
Smad1 |
T |
C |
8: 80,080,084 (GRCm39) |
|
probably null |
Het |
Ssc5d |
G |
A |
7: 4,939,906 (GRCm39) |
|
probably null |
Het |
Tfcp2 |
C |
T |
15: 100,449,201 (GRCm39) |
|
probably null |
Het |
Tmem121 |
A |
G |
12: 113,152,028 (GRCm39) |
Y82C |
probably damaging |
Het |
Tmem131 |
T |
C |
1: 36,880,788 (GRCm39) |
I161V |
possibly damaging |
Het |
Tpp2 |
T |
A |
1: 44,010,783 (GRCm39) |
F523L |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,601,849 (GRCm39) |
|
silent |
Het |
Ttpal |
A |
G |
2: 163,457,503 (GRCm39) |
|
probably null |
Het |
Vdr |
T |
A |
15: 97,757,008 (GRCm39) |
Y288F |
probably benign |
Het |
Wipf2 |
C |
T |
11: 98,783,480 (GRCm39) |
A302V |
probably benign |
Het |
Zfp346 |
T |
G |
13: 55,253,163 (GRCm39) |
C3G |
possibly damaging |
Het |
|
Other mutations in Fer1l4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00417:Fer1l4
|
APN |
2 |
155,861,840 (GRCm39) |
nonsense |
probably null |
|
IGL01025:Fer1l4
|
APN |
2 |
155,894,105 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01103:Fer1l4
|
APN |
2 |
155,886,361 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01322:Fer1l4
|
APN |
2 |
155,862,259 (GRCm39) |
splice site |
probably null |
|
IGL01391:Fer1l4
|
APN |
2 |
155,878,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02176:Fer1l4
|
APN |
2 |
155,890,371 (GRCm39) |
missense |
probably benign |
|
IGL02267:Fer1l4
|
APN |
2 |
155,873,172 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02291:Fer1l4
|
APN |
2 |
155,861,458 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02385:Fer1l4
|
APN |
2 |
155,887,348 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02423:Fer1l4
|
APN |
2 |
155,894,827 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02596:Fer1l4
|
APN |
2 |
155,881,052 (GRCm39) |
missense |
probably benign |
|
IGL02612:Fer1l4
|
APN |
2 |
155,889,848 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02716:Fer1l4
|
APN |
2 |
155,871,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Fer1l4
|
APN |
2 |
155,887,648 (GRCm39) |
missense |
probably benign |
|
IGL03035:Fer1l4
|
APN |
2 |
155,864,526 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03083:Fer1l4
|
APN |
2 |
155,881,286 (GRCm39) |
unclassified |
probably benign |
|
IGL03201:Fer1l4
|
APN |
2 |
155,886,650 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03349:Fer1l4
|
APN |
2 |
155,886,654 (GRCm39) |
nonsense |
probably null |
|
R0033:Fer1l4
|
UTSW |
2 |
155,866,026 (GRCm39) |
splice site |
probably benign |
|
R0356:Fer1l4
|
UTSW |
2 |
155,865,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Fer1l4
|
UTSW |
2 |
155,894,806 (GRCm39) |
missense |
probably benign |
0.43 |
R0504:Fer1l4
|
UTSW |
2 |
155,894,115 (GRCm39) |
missense |
probably benign |
0.36 |
R0731:Fer1l4
|
UTSW |
2 |
155,865,990 (GRCm39) |
missense |
probably benign |
0.17 |
R0800:Fer1l4
|
UTSW |
2 |
155,887,583 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0884:Fer1l4
|
UTSW |
2 |
155,861,233 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1017:Fer1l4
|
UTSW |
2 |
155,891,398 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1266:Fer1l4
|
UTSW |
2 |
155,888,169 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1544:Fer1l4
|
UTSW |
2 |
155,887,553 (GRCm39) |
missense |
probably benign |
0.00 |
R1657:Fer1l4
|
UTSW |
2 |
155,877,518 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1699:Fer1l4
|
UTSW |
2 |
155,871,605 (GRCm39) |
missense |
probably benign |
0.14 |
R1816:Fer1l4
|
UTSW |
2 |
155,877,119 (GRCm39) |
missense |
probably damaging |
0.98 |
R1950:Fer1l4
|
UTSW |
2 |
155,890,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Fer1l4
|
UTSW |
2 |
155,881,038 (GRCm39) |
missense |
probably benign |
0.00 |
R2219:Fer1l4
|
UTSW |
2 |
155,873,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R2220:Fer1l4
|
UTSW |
2 |
155,873,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Fer1l4
|
UTSW |
2 |
155,876,968 (GRCm39) |
missense |
probably benign |
0.01 |
R3806:Fer1l4
|
UTSW |
2 |
155,887,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Fer1l4
|
UTSW |
2 |
155,887,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R4224:Fer1l4
|
UTSW |
2 |
155,862,309 (GRCm39) |
missense |
probably benign |
0.37 |
R4274:Fer1l4
|
UTSW |
2 |
155,862,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4569:Fer1l4
|
UTSW |
2 |
155,878,559 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4619:Fer1l4
|
UTSW |
2 |
155,889,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Fer1l4
|
UTSW |
2 |
155,887,543 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4914:Fer1l4
|
UTSW |
2 |
155,873,220 (GRCm39) |
missense |
probably benign |
0.41 |
R4915:Fer1l4
|
UTSW |
2 |
155,873,220 (GRCm39) |
missense |
probably benign |
0.41 |
R4917:Fer1l4
|
UTSW |
2 |
155,873,220 (GRCm39) |
missense |
probably benign |
0.41 |
R4918:Fer1l4
|
UTSW |
2 |
155,873,220 (GRCm39) |
missense |
probably benign |
0.41 |
R4941:Fer1l4
|
UTSW |
2 |
155,887,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Fer1l4
|
UTSW |
2 |
155,873,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R5013:Fer1l4
|
UTSW |
2 |
155,873,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R5130:Fer1l4
|
UTSW |
2 |
155,891,386 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5385:Fer1l4
|
UTSW |
2 |
155,879,286 (GRCm39) |
nonsense |
probably null |
|
R5441:Fer1l4
|
UTSW |
2 |
155,865,177 (GRCm39) |
missense |
probably benign |
0.00 |
R5555:Fer1l4
|
UTSW |
2 |
155,890,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R5838:Fer1l4
|
UTSW |
2 |
155,893,913 (GRCm39) |
missense |
probably benign |
0.01 |
R6125:Fer1l4
|
UTSW |
2 |
155,888,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R6184:Fer1l4
|
UTSW |
2 |
155,890,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6246:Fer1l4
|
UTSW |
2 |
155,866,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R6248:Fer1l4
|
UTSW |
2 |
155,888,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Fer1l4
|
UTSW |
2 |
155,871,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R6298:Fer1l4
|
UTSW |
2 |
155,866,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6362:Fer1l4
|
UTSW |
2 |
155,890,170 (GRCm39) |
missense |
probably benign |
0.08 |
R6490:Fer1l4
|
UTSW |
2 |
155,889,834 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6494:Fer1l4
|
UTSW |
2 |
155,887,390 (GRCm39) |
missense |
probably benign |
0.02 |
R6516:Fer1l4
|
UTSW |
2 |
155,877,119 (GRCm39) |
missense |
probably damaging |
0.98 |
R6530:Fer1l4
|
UTSW |
2 |
155,889,785 (GRCm39) |
critical splice donor site |
probably null |
|
R6740:Fer1l4
|
UTSW |
2 |
155,873,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Fer1l4
|
UTSW |
2 |
155,878,650 (GRCm39) |
missense |
probably benign |
0.05 |
R7121:Fer1l4
|
UTSW |
2 |
155,886,477 (GRCm39) |
missense |
probably benign |
0.13 |
R7132:Fer1l4
|
UTSW |
2 |
155,887,546 (GRCm39) |
missense |
probably damaging |
0.98 |
R7382:Fer1l4
|
UTSW |
2 |
155,862,669 (GRCm39) |
nonsense |
probably null |
|
R7631:Fer1l4
|
UTSW |
2 |
155,890,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R7693:Fer1l4
|
UTSW |
2 |
155,862,351 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7730:Fer1l4
|
UTSW |
2 |
155,890,854 (GRCm39) |
missense |
probably benign |
|
R8021:Fer1l4
|
UTSW |
2 |
155,864,511 (GRCm39) |
missense |
probably damaging |
0.98 |
R8161:Fer1l4
|
UTSW |
2 |
155,866,555 (GRCm39) |
missense |
probably benign |
0.03 |
R8171:Fer1l4
|
UTSW |
2 |
155,890,151 (GRCm39) |
missense |
probably benign |
0.29 |
R8241:Fer1l4
|
UTSW |
2 |
155,891,585 (GRCm39) |
missense |
probably benign |
|
R8245:Fer1l4
|
UTSW |
2 |
155,886,934 (GRCm39) |
critical splice donor site |
probably null |
|
R8280:Fer1l4
|
UTSW |
2 |
155,891,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R8369:Fer1l4
|
UTSW |
2 |
155,861,680 (GRCm39) |
missense |
probably benign |
0.17 |
R8403:Fer1l4
|
UTSW |
2 |
155,894,163 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8702:Fer1l4
|
UTSW |
2 |
155,861,310 (GRCm39) |
missense |
probably benign |
0.00 |
R8804:Fer1l4
|
UTSW |
2 |
155,893,914 (GRCm39) |
missense |
probably benign |
0.28 |
R8814:Fer1l4
|
UTSW |
2 |
155,894,163 (GRCm39) |
missense |
probably benign |
0.04 |
R8817:Fer1l4
|
UTSW |
2 |
155,890,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R9325:Fer1l4
|
UTSW |
2 |
155,877,934 (GRCm39) |
missense |
probably damaging |
1.00 |
R9342:Fer1l4
|
UTSW |
2 |
155,877,196 (GRCm39) |
missense |
probably benign |
0.08 |
R9527:Fer1l4
|
UTSW |
2 |
155,871,617 (GRCm39) |
missense |
probably damaging |
0.96 |
R9661:Fer1l4
|
UTSW |
2 |
155,862,336 (GRCm39) |
missense |
probably damaging |
0.98 |
RF030:Fer1l4
|
UTSW |
2 |
155,887,449 (GRCm39) |
small deletion |
probably benign |
|
X0063:Fer1l4
|
UTSW |
2 |
155,876,931 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fer1l4
|
UTSW |
2 |
155,890,349 (GRCm39) |
missense |
probably null |
1.00 |
|