Incidental Mutation 'R4810:Epha5'
ID |
370983 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Epha5
|
Ensembl Gene |
ENSMUSG00000029245 |
Gene Name |
Eph receptor A5 |
Synonyms |
Rek7, Cek7, Els1, Ehk1, Hek7, bsk |
MMRRC Submission |
042429-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R4810 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
5 |
Chromosomal Location |
84202620-84565241 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 84253750 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Asparagine
at position 548
(D548N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000109028
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053733]
[ENSMUST00000113398]
[ENSMUST00000113399]
[ENSMUST00000113401]
[ENSMUST00000113403]
[ENSMUST00000113406]
|
AlphaFold |
Q60629 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000053733
AA Change: D571N
PolyPhen 2
Score 0.227 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000060646 Gene: ENSMUSG00000029245 AA Change: D571N
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
20 |
N/A |
INTRINSIC |
low complexity region
|
42 |
57 |
N/A |
INTRINSIC |
EPH_lbd
|
62 |
235 |
7e-122 |
SMART |
FN3
|
307 |
387 |
1.92e-12 |
SMART |
Pfam:EphA2_TM
|
413 |
511 |
2.1e-22 |
PFAM |
TyrKc
|
514 |
771 |
9.33e-138 |
SMART |
SAM
|
801 |
868 |
6.65e-23 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113398
AA Change: D623N
PolyPhen 2
Score 0.142 (Sensitivity: 0.92; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000109025 Gene: ENSMUSG00000029245 AA Change: D623N
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
20 |
N/A |
INTRINSIC |
low complexity region
|
42 |
57 |
N/A |
INTRINSIC |
EPH_lbd
|
62 |
235 |
7e-122 |
SMART |
FN3
|
359 |
439 |
1.92e-12 |
SMART |
Pfam:EphA2_TM
|
465 |
563 |
8.4e-23 |
PFAM |
TyrKc
|
566 |
823 |
9.33e-138 |
SMART |
Pfam:SAM_1
|
854 |
894 |
7.2e-11 |
PFAM |
Pfam:SAM_2
|
856 |
894 |
1.6e-9 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113399
AA Change: D735N
PolyPhen 2
Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
|
SMART Domains |
Protein: ENSMUSP00000109026 Gene: ENSMUSG00000029245 AA Change: D735N
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
20 |
N/A |
INTRINSIC |
low complexity region
|
42 |
57 |
N/A |
INTRINSIC |
EPH_lbd
|
62 |
235 |
7e-122 |
SMART |
FN3
|
360 |
450 |
1.53e-6 |
SMART |
FN3
|
471 |
551 |
1.92e-12 |
SMART |
Pfam:EphA2_TM
|
577 |
675 |
3.4e-22 |
PFAM |
TyrKc
|
678 |
935 |
9.33e-138 |
SMART |
Pfam:SAM_1
|
966 |
1006 |
2.9e-10 |
PFAM |
Pfam:SAM_2
|
968 |
1006 |
5.9e-9 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000113401
AA Change: D548N
PolyPhen 2
Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000109028 Gene: ENSMUSG00000029245 AA Change: D548N
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
20 |
N/A |
INTRINSIC |
low complexity region
|
42 |
57 |
N/A |
INTRINSIC |
EPH_lbd
|
62 |
235 |
7e-122 |
SMART |
FN3
|
307 |
387 |
1.92e-12 |
SMART |
Pfam:EphA2_TM
|
411 |
488 |
3.1e-30 |
PFAM |
TyrKc
|
491 |
748 |
9.33e-138 |
SMART |
Pfam:SAM_1
|
779 |
819 |
1.7e-10 |
PFAM |
Pfam:SAM_2
|
781 |
819 |
3.5e-9 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113403
AA Change: D735N
PolyPhen 2
Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
|
SMART Domains |
Protein: ENSMUSP00000109030 Gene: ENSMUSG00000029245 AA Change: D735N
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
20 |
N/A |
INTRINSIC |
low complexity region
|
42 |
57 |
N/A |
INTRINSIC |
EPH_lbd
|
62 |
235 |
7e-122 |
SMART |
FN3
|
360 |
450 |
1.53e-6 |
SMART |
FN3
|
471 |
551 |
1.92e-12 |
SMART |
Pfam:EphA2_TM
|
577 |
675 |
1.2e-25 |
PFAM |
TyrKc
|
678 |
935 |
9.33e-138 |
SMART |
SAM
|
965 |
1032 |
6.65e-23 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000113406
AA Change: D712N
PolyPhen 2
Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
|
SMART Domains |
Protein: ENSMUSP00000109033 Gene: ENSMUSG00000029245 AA Change: D712N
Domain | Start | End | E-Value | Type |
low complexity region
|
7 |
20 |
N/A |
INTRINSIC |
low complexity region
|
42 |
57 |
N/A |
INTRINSIC |
EPH_lbd
|
62 |
235 |
7e-122 |
SMART |
FN3
|
360 |
450 |
1.53e-6 |
SMART |
FN3
|
471 |
551 |
1.92e-12 |
SMART |
Pfam:EphA2_TM
|
575 |
652 |
1.9e-30 |
PFAM |
TyrKc
|
655 |
912 |
9.33e-138 |
SMART |
SAM
|
942 |
1009 |
6.65e-23 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154804
|
Meta Mutation Damage Score |
0.0726 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.1%
|
Validation Efficiency |
99% (93/94) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the ephrin receptor subfamily of the protein-tyrosine kinase family. EPH and EPH-related receptors have been implicated in mediating developmental events, particularly in the nervous system. Receptors in the EPH subfamily typically have a single kinase domain and an extracellular region containing a Cys-rich domain and 2 fibronectin type III repeats. The ephrin receptors are divided into 2 groups based on the similarity of their extracellular domain sequences and their affinities for binding ephrin-A and ephrin-B ligands. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Aug 2013] PHENOTYPE: Homozygous mutant mice are overtly normal but show abnormal retinal axon mapping. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
C |
12: 71,236,216 (GRCm39) |
V1189A |
possibly damaging |
Het |
A3galt2 |
T |
C |
4: 128,649,356 (GRCm39) |
|
probably null |
Het |
Abca12 |
T |
C |
1: 71,342,771 (GRCm39) |
D903G |
probably benign |
Het |
Abcc12 |
T |
C |
8: 87,287,471 (GRCm39) |
M125V |
probably damaging |
Het |
Adad1 |
A |
G |
3: 37,146,183 (GRCm39) |
N517S |
probably damaging |
Het |
Ankrd44 |
A |
G |
1: 54,774,302 (GRCm39) |
|
probably benign |
Het |
Armc7 |
A |
G |
11: 115,379,787 (GRCm39) |
I162V |
probably benign |
Het |
Art3 |
T |
A |
5: 92,562,108 (GRCm39) |
V343D |
possibly damaging |
Het |
Bcl9l |
A |
G |
9: 44,419,650 (GRCm39) |
T1106A |
probably damaging |
Het |
Ccdc141 |
T |
C |
2: 76,876,099 (GRCm39) |
N644D |
possibly damaging |
Het |
Ccdc154 |
T |
C |
17: 25,382,472 (GRCm39) |
L98S |
probably damaging |
Het |
Ccne1 |
A |
G |
7: 37,799,018 (GRCm39) |
W237R |
probably damaging |
Het |
Cd33 |
T |
C |
7: 43,182,134 (GRCm39) |
I104V |
probably damaging |
Het |
Ceacam1 |
A |
T |
7: 25,173,945 (GRCm39) |
*237K |
probably null |
Het |
Ces1e |
T |
A |
8: 93,935,259 (GRCm39) |
I398F |
probably benign |
Het |
Cfap44 |
T |
C |
16: 44,271,898 (GRCm39) |
I1217T |
probably damaging |
Het |
Clns1a |
T |
C |
7: 97,363,224 (GRCm39) |
S199P |
probably benign |
Het |
Cntn4 |
C |
A |
6: 106,632,572 (GRCm39) |
T532K |
probably benign |
Het |
Col11a2 |
C |
T |
17: 34,276,086 (GRCm39) |
S470L |
probably damaging |
Het |
Cst5 |
A |
T |
2: 149,247,463 (GRCm39) |
R60* |
probably null |
Het |
Cxcr6 |
A |
T |
9: 123,639,227 (GRCm39) |
D83V |
probably damaging |
Het |
Dis3l2 |
T |
C |
1: 86,975,296 (GRCm39) |
V774A |
probably damaging |
Het |
Dusp15 |
A |
G |
2: 152,787,374 (GRCm39) |
L79P |
probably damaging |
Het |
Elapor1 |
T |
A |
3: 108,377,327 (GRCm39) |
|
probably benign |
Het |
Eml6 |
A |
T |
11: 29,705,011 (GRCm39) |
V1511E |
possibly damaging |
Het |
Fam227b |
A |
G |
2: 125,829,859 (GRCm39) |
F450L |
probably benign |
Het |
Fam91a1 |
T |
A |
15: 58,306,589 (GRCm39) |
L452Q |
probably damaging |
Het |
Fbxo44 |
T |
C |
4: 148,240,903 (GRCm39) |
Y199C |
probably damaging |
Het |
Fgd3 |
A |
G |
13: 49,443,126 (GRCm39) |
S149P |
probably benign |
Het |
Gabra4 |
T |
C |
5: 71,781,325 (GRCm39) |
E362G |
probably damaging |
Het |
Galnt14 |
T |
C |
17: 73,819,116 (GRCm39) |
I325V |
probably damaging |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gm10088 |
G |
T |
16: 18,847,081 (GRCm39) |
|
noncoding transcript |
Het |
Grik5 |
T |
C |
7: 24,714,922 (GRCm39) |
N691D |
probably damaging |
Het |
Grm1 |
C |
G |
10: 10,658,438 (GRCm39) |
D351H |
probably damaging |
Het |
Grm8 |
T |
C |
6: 27,761,295 (GRCm39) |
S310G |
possibly damaging |
Het |
Gtf2h2 |
A |
G |
13: 100,617,510 (GRCm39) |
|
probably null |
Het |
Hhex |
G |
T |
19: 37,428,103 (GRCm39) |
L49F |
probably damaging |
Het |
Hkdc1 |
T |
A |
10: 62,247,304 (GRCm39) |
R159S |
probably benign |
Het |
Iqcm |
A |
G |
8: 76,615,281 (GRCm39) |
Y454C |
probably damaging |
Het |
Kcnh8 |
G |
A |
17: 53,212,248 (GRCm39) |
|
probably null |
Het |
Larp4b |
A |
G |
13: 9,208,627 (GRCm39) |
T427A |
probably benign |
Het |
Mtmr3 |
A |
T |
11: 4,448,046 (GRCm39) |
N297K |
probably benign |
Het |
Nek8 |
G |
A |
11: 78,058,629 (GRCm39) |
T557I |
probably benign |
Het |
Nlrp9c |
A |
C |
7: 26,077,602 (GRCm39) |
|
probably null |
Het |
Nmrk1 |
T |
A |
19: 18,617,273 (GRCm39) |
D48E |
probably benign |
Het |
Npepps |
G |
A |
11: 97,131,759 (GRCm39) |
T365I |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,922,417 (GRCm39) |
T5921M |
possibly damaging |
Het |
Or8b44 |
C |
A |
9: 38,410,620 (GRCm39) |
Y218* |
probably null |
Het |
Or8c9 |
A |
G |
9: 38,241,690 (GRCm39) |
E269G |
probably benign |
Het |
Otud7b |
C |
T |
3: 96,043,918 (GRCm39) |
A23V |
probably damaging |
Het |
Pcdhga9 |
G |
A |
18: 37,871,601 (GRCm39) |
A477T |
possibly damaging |
Het |
Plekha7 |
A |
T |
7: 115,744,173 (GRCm39) |
I663N |
probably damaging |
Het |
Plscr1l1 |
A |
G |
9: 92,236,683 (GRCm39) |
D190G |
probably damaging |
Het |
Polk |
A |
T |
13: 96,620,003 (GRCm39) |
S732R |
possibly damaging |
Het |
Ppfia2 |
A |
G |
10: 106,751,551 (GRCm39) |
I1166V |
probably benign |
Het |
Ppp2r5a |
C |
T |
1: 191,088,589 (GRCm39) |
|
probably benign |
Het |
Prkaa2 |
T |
C |
4: 104,897,011 (GRCm39) |
K401E |
probably damaging |
Het |
Ptpn23 |
A |
G |
9: 110,218,204 (GRCm39) |
Y611H |
possibly damaging |
Het |
Rab31 |
C |
T |
17: 66,028,998 (GRCm39) |
|
probably null |
Het |
Rad51ap2 |
T |
A |
12: 11,507,406 (GRCm39) |
C443S |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,841,778 (GRCm39) |
|
probably null |
Het |
Rev3l |
T |
C |
10: 39,699,721 (GRCm39) |
L1406P |
probably benign |
Het |
Rnaset2b |
T |
A |
17: 7,259,167 (GRCm39) |
D48E |
probably benign |
Het |
Rnf13 |
G |
T |
3: 57,703,693 (GRCm39) |
M105I |
probably damaging |
Het |
Rnf150 |
T |
C |
8: 83,716,991 (GRCm39) |
V166A |
possibly damaging |
Het |
Rps6kc1 |
C |
A |
1: 190,541,160 (GRCm39) |
R381L |
probably damaging |
Het |
Rspo2 |
C |
T |
15: 43,033,216 (GRCm39) |
R2H |
probably benign |
Het |
Septin8 |
A |
G |
11: 53,425,416 (GRCm39) |
D103G |
probably damaging |
Het |
Sirt4 |
A |
G |
5: 115,618,508 (GRCm39) |
W189R |
probably damaging |
Het |
Slco6d1 |
T |
C |
1: 98,350,979 (GRCm39) |
V110A |
possibly damaging |
Het |
Sncaip |
C |
A |
18: 53,040,271 (GRCm39) |
Q822K |
possibly damaging |
Het |
Spg11 |
A |
C |
2: 121,890,277 (GRCm39) |
F2070V |
probably damaging |
Het |
Sptb |
A |
T |
12: 76,669,971 (GRCm39) |
Y452* |
probably null |
Het |
Srsf4 |
C |
T |
4: 131,627,413 (GRCm39) |
|
probably benign |
Het |
Tead1 |
C |
A |
7: 112,441,073 (GRCm39) |
|
probably null |
Het |
Tmem156 |
G |
T |
5: 65,248,790 (GRCm39) |
|
probably benign |
Het |
Tmem169 |
A |
G |
1: 72,337,311 (GRCm39) |
D82G |
probably benign |
Het |
Tmem260 |
A |
G |
14: 48,709,930 (GRCm39) |
E51G |
probably damaging |
Het |
Trim36 |
G |
T |
18: 46,305,536 (GRCm39) |
N470K |
probably benign |
Het |
Trps1 |
T |
A |
15: 50,685,692 (GRCm39) |
T158S |
probably benign |
Het |
Ube2c |
A |
G |
2: 164,614,482 (GRCm39) |
*180W |
probably null |
Het |
Ube2i |
T |
C |
17: 25,484,121 (GRCm39) |
D45G |
probably benign |
Het |
Uggt2 |
A |
C |
14: 119,250,933 (GRCm39) |
L1188R |
probably damaging |
Het |
Uroc1 |
T |
C |
6: 90,340,135 (GRCm39) |
I680T |
probably damaging |
Het |
Vmn2r2 |
T |
A |
3: 64,044,883 (GRCm39) |
M88L |
probably damaging |
Het |
Zfp248 |
G |
A |
6: 118,406,807 (GRCm39) |
R261C |
possibly damaging |
Het |
Zfp418 |
G |
T |
7: 7,185,846 (GRCm39) |
R603L |
possibly damaging |
Het |
Zmpste24 |
T |
A |
4: 120,918,251 (GRCm39) |
Y457F |
probably damaging |
Het |
|
Other mutations in Epha5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00808:Epha5
|
APN |
5 |
84,254,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Epha5
|
APN |
5 |
84,218,946 (GRCm39) |
nonsense |
probably null |
|
IGL01462:Epha5
|
APN |
5 |
84,219,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Epha5
|
APN |
5 |
84,534,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01998:Epha5
|
APN |
5 |
84,232,593 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02744:Epha5
|
APN |
5 |
84,255,848 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03076:Epha5
|
APN |
5 |
84,479,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03123:Epha5
|
APN |
5 |
84,479,085 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03381:Epha5
|
APN |
5 |
84,479,191 (GRCm39) |
missense |
probably damaging |
0.98 |
BB001:Epha5
|
UTSW |
5 |
84,232,705 (GRCm39) |
missense |
possibly damaging |
0.71 |
BB011:Epha5
|
UTSW |
5 |
84,232,705 (GRCm39) |
missense |
possibly damaging |
0.71 |
PIT4544001:Epha5
|
UTSW |
5 |
84,479,471 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0004:Epha5
|
UTSW |
5 |
84,479,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0490:Epha5
|
UTSW |
5 |
84,255,833 (GRCm39) |
splice site |
probably benign |
|
R0545:Epha5
|
UTSW |
5 |
84,215,217 (GRCm39) |
critical splice donor site |
probably null |
|
R0835:Epha5
|
UTSW |
5 |
84,534,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1074:Epha5
|
UTSW |
5 |
84,298,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R1074:Epha5
|
UTSW |
5 |
84,298,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R1075:Epha5
|
UTSW |
5 |
84,298,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R1075:Epha5
|
UTSW |
5 |
84,298,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R1102:Epha5
|
UTSW |
5 |
84,381,434 (GRCm39) |
splice site |
probably benign |
|
R1184:Epha5
|
UTSW |
5 |
84,219,134 (GRCm39) |
splice site |
probably null |
|
R1255:Epha5
|
UTSW |
5 |
84,298,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R1255:Epha5
|
UTSW |
5 |
84,298,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R1327:Epha5
|
UTSW |
5 |
84,254,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Epha5
|
UTSW |
5 |
84,381,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R1804:Epha5
|
UTSW |
5 |
84,479,674 (GRCm39) |
missense |
probably benign |
0.21 |
R1967:Epha5
|
UTSW |
5 |
84,564,288 (GRCm39) |
missense |
probably benign |
0.23 |
R2187:Epha5
|
UTSW |
5 |
84,234,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2282:Epha5
|
UTSW |
5 |
84,298,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R2899:Epha5
|
UTSW |
5 |
84,381,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R3746:Epha5
|
UTSW |
5 |
84,206,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4454:Epha5
|
UTSW |
5 |
84,304,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R4771:Epha5
|
UTSW |
5 |
84,298,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R4809:Epha5
|
UTSW |
5 |
84,253,750 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4825:Epha5
|
UTSW |
5 |
84,381,699 (GRCm39) |
missense |
probably damaging |
0.97 |
R4833:Epha5
|
UTSW |
5 |
84,253,750 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4961:Epha5
|
UTSW |
5 |
84,381,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Epha5
|
UTSW |
5 |
84,232,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R4981:Epha5
|
UTSW |
5 |
84,298,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R5149:Epha5
|
UTSW |
5 |
84,298,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R5422:Epha5
|
UTSW |
5 |
84,479,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R5575:Epha5
|
UTSW |
5 |
84,564,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R5664:Epha5
|
UTSW |
5 |
84,479,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Epha5
|
UTSW |
5 |
84,479,085 (GRCm39) |
critical splice donor site |
probably null |
|
R5821:Epha5
|
UTSW |
5 |
84,232,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5924:Epha5
|
UTSW |
5 |
84,381,533 (GRCm39) |
nonsense |
probably null |
|
R5951:Epha5
|
UTSW |
5 |
84,479,051 (GRCm39) |
intron |
probably benign |
|
R5956:Epha5
|
UTSW |
5 |
84,298,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R6127:Epha5
|
UTSW |
5 |
84,218,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R6189:Epha5
|
UTSW |
5 |
84,385,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Epha5
|
UTSW |
5 |
84,265,438 (GRCm39) |
missense |
probably benign |
0.27 |
R6343:Epha5
|
UTSW |
5 |
84,254,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R6463:Epha5
|
UTSW |
5 |
84,254,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R6517:Epha5
|
UTSW |
5 |
84,304,360 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6622:Epha5
|
UTSW |
5 |
84,385,387 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6667:Epha5
|
UTSW |
5 |
84,219,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R6741:Epha5
|
UTSW |
5 |
84,254,557 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6757:Epha5
|
UTSW |
5 |
84,253,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Epha5
|
UTSW |
5 |
84,479,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R6819:Epha5
|
UTSW |
5 |
84,254,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Epha5
|
UTSW |
5 |
84,564,321 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7031:Epha5
|
UTSW |
5 |
84,290,159 (GRCm39) |
missense |
probably benign |
0.12 |
R7213:Epha5
|
UTSW |
5 |
84,381,782 (GRCm39) |
splice site |
probably null |
|
R7728:Epha5
|
UTSW |
5 |
84,215,267 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7924:Epha5
|
UTSW |
5 |
84,232,705 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7953:Epha5
|
UTSW |
5 |
84,381,513 (GRCm39) |
missense |
probably benign |
0.19 |
R8043:Epha5
|
UTSW |
5 |
84,381,513 (GRCm39) |
missense |
probably benign |
0.19 |
R8468:Epha5
|
UTSW |
5 |
84,290,275 (GRCm39) |
splice site |
probably null |
|
R8558:Epha5
|
UTSW |
5 |
84,206,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R8796:Epha5
|
UTSW |
5 |
84,255,850 (GRCm39) |
missense |
probably damaging |
0.97 |
R9035:Epha5
|
UTSW |
5 |
84,255,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R9060:Epha5
|
UTSW |
5 |
84,218,977 (GRCm39) |
missense |
probably benign |
0.01 |
R9244:Epha5
|
UTSW |
5 |
84,265,441 (GRCm39) |
missense |
probably benign |
0.28 |
R9347:Epha5
|
UTSW |
5 |
84,479,731 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9355:Epha5
|
UTSW |
5 |
84,253,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9434:Epha5
|
UTSW |
5 |
84,479,227 (GRCm39) |
missense |
possibly damaging |
0.72 |
Z1088:Epha5
|
UTSW |
5 |
84,385,381 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Epha5
|
UTSW |
5 |
84,218,979 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
Predicted Primers |
PCR Primer
(F):5'- AAGCCCTGATCATAATGGTGGG -3'
(R):5'- CTGTGGACGTTTGGTCTCAC -3'
Sequencing Primer
(F):5'- CCTGATCATAATGGTGGGCATTTAAG -3'
(R):5'- CTGAACCTTAATCCTTCAGAAGTTTG -3'
|
Posted On |
2016-02-04 |