Incidental Mutation 'R6362:Fer1l4'
| ID |
512492 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Fer1l4
|
| Ensembl Gene |
ENSMUSG00000013338 |
| Gene Name |
fer-1 like family member 4 |
| Synonyms |
9130402C12Rik |
| MMRRC Submission |
044512-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R6362 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
2 |
| Chromosomal Location |
155861059-155894867 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 155890170 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Isoleucine
at position 252
(V252I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000105240
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000109611]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109611
AA Change: V252I
PolyPhen 2
Score 0.077 (Sensitivity: 0.93; Specificity: 0.85)
|
| SMART Domains |
Protein: ENSMUSP00000105240
Gene: ENSMUSG00000013338
AA Change: V252I
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:3L9B|A
|
1 |
122 |
1e-12 |
PDB |
|
Blast:C2
|
2 |
96 |
2e-51 |
BLAST |
|
low complexity region
|
159 |
172 |
N/A |
INTRINSIC |
|
low complexity region
|
178 |
197 |
N/A |
INTRINSIC |
|
C2
|
228 |
329 |
2.87e-7 |
SMART |
|
FerI
|
312 |
383 |
7.93e-29 |
SMART |
|
C2
|
391 |
501 |
3.64e-9 |
SMART |
|
low complexity region
|
574 |
581 |
N/A |
INTRINSIC |
|
low complexity region
|
611 |
622 |
N/A |
INTRINSIC |
|
low complexity region
|
829 |
837 |
N/A |
INTRINSIC |
|
low complexity region
|
844 |
855 |
N/A |
INTRINSIC |
|
FerB
|
861 |
932 |
7.27e-37 |
SMART |
|
C2
|
968 |
1076 |
3.73e-6 |
SMART |
|
low complexity region
|
1249 |
1257 |
N/A |
INTRINSIC |
|
low complexity region
|
1280 |
1310 |
N/A |
INTRINSIC |
|
low complexity region
|
1327 |
1340 |
N/A |
INTRINSIC |
|
low complexity region
|
1397 |
1407 |
N/A |
INTRINSIC |
|
C2
|
1449 |
1548 |
5.65e-15 |
SMART |
|
C2
|
1692 |
1822 |
4.22e-5 |
SMART |
|
Pfam:Ferlin_C
|
1834 |
1987 |
1.6e-74 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.5%
- 20x: 96.0%
|
| Validation Efficiency |
99% (78/79) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 80 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aldh5a1 |
T |
G |
13: 25,102,533 (GRCm39) |
D310A |
probably benign |
Het |
| Als2cl |
T |
A |
9: 110,724,514 (GRCm39) |
|
probably null |
Het |
| Amacr |
C |
A |
15: 10,984,891 (GRCm39) |
R170S |
probably damaging |
Het |
| Brwd1 |
C |
T |
16: 95,803,507 (GRCm39) |
R2221Q |
probably damaging |
Het |
| Cacna1g |
A |
T |
11: 94,330,533 (GRCm39) |
|
probably null |
Het |
| Cd3d |
G |
A |
9: 44,897,589 (GRCm39) |
D157N |
probably damaging |
Het |
| Cep131 |
T |
C |
11: 119,955,516 (GRCm39) |
D1043G |
probably damaging |
Het |
| Cimip1 |
T |
G |
2: 173,369,967 (GRCm39) |
|
probably null |
Het |
| Cit |
A |
G |
5: 116,024,735 (GRCm39) |
D326G |
probably benign |
Het |
| Col16a1 |
G |
C |
4: 129,959,983 (GRCm39) |
G370R |
unknown |
Het |
| Col6a3 |
T |
A |
1: 90,738,285 (GRCm39) |
Y1078F |
probably damaging |
Het |
| Colgalt2 |
A |
C |
1: 152,347,549 (GRCm39) |
Y161S |
probably damaging |
Het |
| Cyp2j13 |
A |
G |
4: 95,959,932 (GRCm39) |
Y75H |
probably damaging |
Het |
| Daxx |
G |
A |
17: 34,130,338 (GRCm39) |
V118I |
probably damaging |
Het |
| Dennd5a |
G |
T |
7: 109,533,472 (GRCm39) |
C75* |
probably null |
Het |
| Diaph3 |
A |
G |
14: 87,009,566 (GRCm39) |
L1071P |
probably damaging |
Het |
| Disp3 |
A |
G |
4: 148,338,765 (GRCm39) |
L802P |
possibly damaging |
Het |
| Dmc1 |
A |
G |
15: 79,473,024 (GRCm39) |
V141A |
probably benign |
Het |
| Dsc2 |
A |
T |
18: 20,168,520 (GRCm39) |
Y45* |
probably null |
Het |
| Dspp |
A |
G |
5: 104,323,900 (GRCm39) |
I348V |
probably benign |
Het |
| Epb42 |
C |
A |
2: 120,856,260 (GRCm39) |
C428F |
possibly damaging |
Het |
| Fam227a |
G |
T |
15: 79,527,551 (GRCm39) |
P100Q |
possibly damaging |
Het |
| Fhod1 |
C |
A |
8: 106,058,273 (GRCm39) |
|
probably null |
Het |
| Fhod3 |
G |
T |
18: 24,887,312 (GRCm39) |
A68S |
probably benign |
Het |
| Gatm |
T |
C |
2: 122,428,677 (GRCm39) |
D328G |
probably benign |
Het |
| Gm6401 |
G |
T |
14: 41,789,727 (GRCm39) |
H44N |
probably benign |
Het |
| Gpat2 |
G |
C |
2: 127,273,838 (GRCm39) |
G294R |
possibly damaging |
Het |
| Gpr84 |
G |
A |
15: 103,216,937 (GRCm39) |
A380V |
probably damaging |
Het |
| Herc1 |
G |
T |
9: 66,379,190 (GRCm39) |
W3492L |
probably damaging |
Het |
| Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
| Jag2 |
T |
A |
12: 112,883,742 (GRCm39) |
K246N |
probably damaging |
Het |
| Klhl32 |
T |
C |
4: 24,629,195 (GRCm39) |
D524G |
probably null |
Het |
| Lax1 |
A |
G |
1: 133,608,334 (GRCm39) |
S136P |
possibly damaging |
Het |
| Lefty1 |
A |
G |
1: 180,764,725 (GRCm39) |
K217E |
probably benign |
Het |
| Lgr5 |
A |
G |
10: 115,314,430 (GRCm39) |
L169P |
probably damaging |
Het |
| Lrrc37 |
G |
C |
11: 103,511,478 (GRCm39) |
N163K |
unknown |
Het |
| Mad1l1 |
A |
T |
5: 140,300,810 (GRCm39) |
S29T |
possibly damaging |
Het |
| Man1a |
T |
C |
10: 53,950,891 (GRCm39) |
H77R |
probably benign |
Het |
| Met |
C |
T |
6: 17,558,732 (GRCm39) |
S1120F |
probably damaging |
Het |
| Mfsd4b2 |
A |
T |
10: 39,797,605 (GRCm39) |
I250N |
probably damaging |
Het |
| Myod1 |
A |
G |
7: 46,026,305 (GRCm39) |
H70R |
possibly damaging |
Het |
| Neb |
T |
C |
2: 52,102,704 (GRCm39) |
N4280S |
probably benign |
Het |
| Nudt6 |
T |
C |
3: 37,473,638 (GRCm39) |
T28A |
possibly damaging |
Het |
| Nup85 |
A |
G |
11: 115,474,560 (GRCm39) |
E628G |
probably damaging |
Het |
| Oaz3 |
A |
T |
3: 94,342,295 (GRCm39) |
D120E |
probably damaging |
Het |
| Or2y3 |
A |
T |
17: 38,393,620 (GRCm39) |
M83K |
probably damaging |
Het |
| Or5b102 |
A |
T |
19: 13,040,709 (GRCm39) |
|
probably benign |
Het |
| Or5be3 |
C |
T |
2: 86,863,633 (GRCm39) |
A311T |
probably benign |
Het |
| Or5m8 |
C |
A |
2: 85,822,285 (GRCm39) |
N41K |
probably damaging |
Het |
| Or6c1b |
A |
C |
10: 129,272,812 (GRCm39) |
I44L |
probably damaging |
Het |
| Osbpl8 |
A |
T |
10: 111,108,929 (GRCm39) |
K404* |
probably null |
Het |
| Pcdhga2 |
A |
G |
18: 37,803,958 (GRCm39) |
N601D |
probably damaging |
Het |
| Pld2 |
T |
C |
11: 70,445,501 (GRCm39) |
Y638H |
probably damaging |
Het |
| Pramel27 |
A |
G |
4: 143,579,435 (GRCm39) |
Y340C |
probably damaging |
Het |
| Prickle2 |
C |
G |
6: 92,435,596 (GRCm39) |
V2L |
possibly damaging |
Het |
| Psmd6 |
G |
A |
14: 14,116,949 (GRCm38) |
R125C |
probably benign |
Het |
| Rnaset2b |
G |
A |
17: 7,259,093 (GRCm39) |
V24I |
probably benign |
Het |
| Rusc2 |
A |
T |
4: 43,416,416 (GRCm39) |
D574V |
probably benign |
Het |
| Scn8a |
T |
A |
15: 100,837,996 (GRCm39) |
|
probably null |
Het |
| Sec11a |
T |
C |
7: 80,572,879 (GRCm39) |
E134G |
probably benign |
Het |
| Senp5 |
A |
G |
16: 31,808,702 (GRCm39) |
V157A |
probably damaging |
Het |
| Shkbp1 |
C |
T |
7: 27,051,120 (GRCm39) |
|
probably null |
Het |
| Slc43a1 |
T |
C |
2: 84,690,128 (GRCm39) |
L435P |
probably damaging |
Het |
| Spn |
G |
A |
7: 126,735,895 (GRCm39) |
P204L |
possibly damaging |
Het |
| Srr |
T |
A |
11: 74,801,028 (GRCm39) |
Q173L |
probably damaging |
Het |
| Star |
C |
G |
8: 26,301,835 (GRCm39) |
T222S |
probably benign |
Het |
| Timm22 |
T |
A |
11: 76,301,953 (GRCm39) |
Y93N |
probably damaging |
Het |
| Tmc4 |
G |
T |
7: 3,678,458 (GRCm39) |
Q58K |
probably benign |
Het |
| Tmem86b |
C |
T |
7: 4,632,835 (GRCm39) |
M1I |
probably null |
Het |
| Tmtc2 |
A |
T |
10: 105,205,831 (GRCm39) |
I488N |
probably damaging |
Het |
| Tnxb |
A |
T |
17: 34,913,362 (GRCm39) |
Y1792F |
probably damaging |
Het |
| Tph1 |
T |
A |
7: 46,296,867 (GRCm39) |
R443W |
possibly damaging |
Het |
| Ttyh1 |
T |
A |
7: 4,132,323 (GRCm39) |
V253E |
possibly damaging |
Het |
| Usf3 |
A |
G |
16: 44,038,940 (GRCm39) |
D1140G |
probably benign |
Het |
| Usp10 |
T |
C |
8: 120,668,055 (GRCm39) |
S118P |
probably benign |
Het |
| Vmn2r63 |
C |
T |
7: 42,552,721 (GRCm39) |
C845Y |
probably benign |
Het |
| Vmn2r72 |
G |
T |
7: 85,400,382 (GRCm39) |
F222L |
probably damaging |
Het |
| Zfp654 |
G |
A |
16: 64,606,457 (GRCm39) |
Q582* |
probably null |
Het |
| Zfp791 |
C |
T |
8: 85,846,279 (GRCm39) |
|
probably benign |
Het |
| Zfp879 |
T |
A |
11: 50,729,302 (GRCm39) |
D32V |
probably 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 |
|
R2879:Fer1l4
|
UTSW |
2 |
155,894,120 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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 |
|
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 |
|
| Predicted Primers |
PCR Primer
(F):5'- TAACCTGGCTCAAAACGCAG -3'
(R):5'- GGAGACCCCTTCAAGGTTTG -3'
Sequencing Primer
(F):5'- GAACCAGCGACTTTGCATCCTG -3'
(R):5'- AGGACTTCCAGGTATGACTCTCAG -3'
|
| Posted On |
2018-04-27 |
Incidental Mutation