Incidental Mutation 'R1695:Pex5l'
ID |
192106 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pex5l
|
Ensembl Gene |
ENSMUSG00000027674 |
Gene Name |
peroxisomal biogenesis factor 5-like |
Synonyms |
PXR2, TRIP8b, Pex2, 1700016J08Rik |
MMRRC Submission |
039728-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.574)
|
Stock # |
R1695 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
3 |
Chromosomal Location |
33003557-33197396 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 33008531 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Isoleucine
at position 151
(N151I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000103856
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078226]
[ENSMUST00000108221]
[ENSMUST00000108224]
[ENSMUST00000108225]
[ENSMUST00000108226]
[ENSMUST00000194016]
[ENSMUST00000192093]
[ENSMUST00000193289]
[ENSMUST00000193681]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000078226
AA Change: N422I
PolyPhen 2
Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000077353 Gene: ENSMUSG00000027674 AA Change: N422I
Domain | Start | End | E-Value | Type |
low complexity region
|
113 |
129 |
N/A |
INTRINSIC |
low complexity region
|
214 |
228 |
N/A |
INTRINSIC |
TPR
|
349 |
382 |
6.95e-4 |
SMART |
Blast:TPR
|
383 |
416 |
4e-14 |
BLAST |
TPR
|
463 |
496 |
3.19e-3 |
SMART |
TPR
|
497 |
530 |
3.47e-4 |
SMART |
TPR
|
531 |
564 |
1.1e-1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000108219
|
SMART Domains |
Protein: ENSMUSP00000103854 Gene: ENSMUSG00000027674
Domain | Start | End | E-Value | Type |
low complexity region
|
124 |
140 |
N/A |
INTRINSIC |
low complexity region
|
226 |
240 |
N/A |
INTRINSIC |
PDB:4EQF|A
|
266 |
362 |
8e-64 |
PDB |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108221
AA Change: N151I
PolyPhen 2
Score 0.283 (Sensitivity: 0.91; Specificity: 0.88)
|
SMART Domains |
Protein: ENSMUSP00000103856 Gene: ENSMUSG00000027674 AA Change: N151I
Domain | Start | End | E-Value | Type |
TPR
|
78 |
111 |
6.95e-4 |
SMART |
Blast:TPR
|
112 |
145 |
2e-14 |
BLAST |
TPR
|
192 |
225 |
3.19e-3 |
SMART |
TPR
|
226 |
259 |
3.47e-4 |
SMART |
TPR
|
260 |
293 |
1.1e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108224
AA Change: N398I
PolyPhen 2
Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000103859 Gene: ENSMUSG00000027674 AA Change: N398I
Domain | Start | End | E-Value | Type |
low complexity region
|
88 |
104 |
N/A |
INTRINSIC |
low complexity region
|
190 |
204 |
N/A |
INTRINSIC |
TPR
|
325 |
358 |
6.95e-4 |
SMART |
Blast:TPR
|
359 |
392 |
2e-14 |
BLAST |
TPR
|
439 |
472 |
3.19e-3 |
SMART |
TPR
|
473 |
506 |
3.47e-4 |
SMART |
TPR
|
507 |
540 |
1.1e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108225
AA Change: N422I
PolyPhen 2
Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000103860 Gene: ENSMUSG00000027674 AA Change: N422I
Domain | Start | End | E-Value | Type |
low complexity region
|
113 |
129 |
N/A |
INTRINSIC |
low complexity region
|
214 |
228 |
N/A |
INTRINSIC |
TPR
|
349 |
382 |
6.95e-4 |
SMART |
Blast:TPR
|
383 |
416 |
4e-14 |
BLAST |
TPR
|
463 |
496 |
3.19e-3 |
SMART |
TPR
|
497 |
530 |
3.47e-4 |
SMART |
TPR
|
531 |
564 |
1.1e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000108226
AA Change: N374I
PolyPhen 2
Score 0.124 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000103861 Gene: ENSMUSG00000027674 AA Change: N374I
Domain | Start | End | E-Value | Type |
low complexity region
|
65 |
81 |
N/A |
INTRINSIC |
low complexity region
|
166 |
180 |
N/A |
INTRINSIC |
TPR
|
301 |
334 |
6.95e-4 |
SMART |
Blast:TPR
|
335 |
368 |
2e-14 |
BLAST |
TPR
|
415 |
448 |
3.19e-3 |
SMART |
TPR
|
449 |
482 |
3.47e-4 |
SMART |
TPR
|
483 |
516 |
1.1e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000194016
AA Change: N457I
PolyPhen 2
Score 0.175 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000142196 Gene: ENSMUSG00000027674 AA Change: N457I
Domain | Start | End | E-Value | Type |
low complexity region
|
148 |
164 |
N/A |
INTRINSIC |
low complexity region
|
249 |
263 |
N/A |
INTRINSIC |
TPR
|
384 |
417 |
6.95e-4 |
SMART |
Blast:TPR
|
418 |
451 |
4e-14 |
BLAST |
TPR
|
498 |
531 |
3.19e-3 |
SMART |
TPR
|
532 |
565 |
3.47e-4 |
SMART |
TPR
|
566 |
599 |
1.1e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000192093
AA Change: N422I
PolyPhen 2
Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000141387 Gene: ENSMUSG00000027674 AA Change: N422I
Domain | Start | End | E-Value | Type |
low complexity region
|
113 |
129 |
N/A |
INTRINSIC |
low complexity region
|
214 |
228 |
N/A |
INTRINSIC |
TPR
|
349 |
382 |
6.95e-4 |
SMART |
Blast:TPR
|
383 |
416 |
4e-14 |
BLAST |
TPR
|
463 |
496 |
3.19e-3 |
SMART |
TPR
|
497 |
530 |
3.47e-4 |
SMART |
TPR
|
531 |
564 |
1.1e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000193289
AA Change: N457I
PolyPhen 2
Score 0.175 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000142008 Gene: ENSMUSG00000027674 AA Change: N457I
Domain | Start | End | E-Value | Type |
low complexity region
|
148 |
164 |
N/A |
INTRINSIC |
low complexity region
|
249 |
263 |
N/A |
INTRINSIC |
TPR
|
384 |
417 |
6.95e-4 |
SMART |
Blast:TPR
|
418 |
451 |
4e-14 |
BLAST |
TPR
|
498 |
531 |
3.19e-3 |
SMART |
TPR
|
532 |
565 |
3.47e-4 |
SMART |
TPR
|
566 |
599 |
1.1e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000193681
AA Change: N457I
PolyPhen 2
Score 0.175 (Sensitivity: 0.92; Specificity: 0.87)
|
SMART Domains |
Protein: ENSMUSP00000141454 Gene: ENSMUSG00000027674 AA Change: N457I
Domain | Start | End | E-Value | Type |
low complexity region
|
148 |
164 |
N/A |
INTRINSIC |
low complexity region
|
249 |
263 |
N/A |
INTRINSIC |
TPR
|
384 |
417 |
6.95e-4 |
SMART |
Blast:TPR
|
418 |
451 |
4e-14 |
BLAST |
TPR
|
498 |
531 |
3.19e-3 |
SMART |
TPR
|
532 |
565 |
3.47e-4 |
SMART |
TPR
|
566 |
599 |
1.1e-1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192259
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.2%
|
Validation Efficiency |
|
MGI Phenotype |
PHENOTYPE: Mice homozygous for a targeted mutation lacking isoform b exhibit exhibit reduced hyperpolarization-activated current in CA1 pyramidal neuron, impaired motor learning, impaired nest-building, decreased startle reflex, and decreased depression-related behaviors. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
T |
A |
5: 121,638,970 (GRCm39) |
T692S |
probably benign |
Het |
Adgrf3 |
T |
A |
5: 30,408,553 (GRCm39) |
N75I |
probably benign |
Het |
Adgrg5 |
A |
G |
8: 95,664,373 (GRCm39) |
M328V |
probably damaging |
Het |
Adk |
A |
G |
14: 21,431,668 (GRCm39) |
D286G |
probably benign |
Het |
Ankrd28 |
T |
A |
14: 31,429,201 (GRCm39) |
D917V |
probably damaging |
Het |
Appl2 |
C |
T |
10: 83,457,446 (GRCm39) |
D141N |
probably damaging |
Het |
Arfgef2 |
T |
C |
2: 166,706,632 (GRCm39) |
V952A |
probably damaging |
Het |
Arpc2 |
T |
A |
1: 74,287,391 (GRCm39) |
H70Q |
probably damaging |
Het |
Bpifa5 |
T |
C |
2: 154,009,580 (GRCm39) |
L261P |
probably damaging |
Het |
Brca1 |
G |
T |
11: 101,415,281 (GRCm39) |
T951K |
probably damaging |
Het |
Ccdc73 |
A |
T |
2: 104,822,450 (GRCm39) |
S800C |
probably damaging |
Het |
Cdh15 |
C |
G |
8: 123,588,755 (GRCm39) |
D276E |
probably benign |
Het |
Cfap119 |
A |
G |
7: 127,186,745 (GRCm39) |
|
probably null |
Het |
Cfap418 |
T |
A |
4: 10,874,644 (GRCm39) |
D10E |
probably damaging |
Het |
Cfh |
T |
C |
1: 140,030,575 (GRCm39) |
I551V |
probably damaging |
Het |
Chd7 |
T |
A |
4: 8,833,960 (GRCm39) |
L1238Q |
probably damaging |
Het |
Chd9 |
T |
G |
8: 91,728,410 (GRCm39) |
F1275L |
probably damaging |
Het |
Chrnb3 |
A |
G |
8: 27,883,728 (GRCm39) |
Y155C |
probably damaging |
Het |
Cltc |
C |
A |
11: 86,591,886 (GRCm39) |
|
probably null |
Het |
Ctsll3 |
T |
A |
13: 60,948,791 (GRCm39) |
N55Y |
probably damaging |
Het |
Cysltr2 |
T |
C |
14: 73,267,321 (GRCm39) |
M130V |
probably benign |
Het |
Daglb |
T |
C |
5: 143,480,361 (GRCm39) |
M455T |
probably benign |
Het |
Dbn1 |
A |
G |
13: 55,624,521 (GRCm39) |
S343P |
probably benign |
Het |
Dnah2 |
T |
A |
11: 69,405,517 (GRCm39) |
D665V |
possibly damaging |
Het |
Dusp6 |
T |
A |
10: 99,099,555 (GRCm39) |
M1K |
probably null |
Het |
Eif3m |
T |
C |
2: 104,847,298 (GRCm39) |
E12G |
probably damaging |
Het |
Epha2 |
T |
C |
4: 141,033,828 (GRCm39) |
V29A |
possibly damaging |
Het |
Farp2 |
T |
A |
1: 93,488,047 (GRCm39) |
N91K |
probably damaging |
Het |
Ferd3l |
C |
A |
12: 33,978,971 (GRCm39) |
S161R |
probably benign |
Het |
Fgd2 |
A |
T |
17: 29,587,219 (GRCm39) |
D315V |
possibly damaging |
Het |
Fhip2a |
T |
C |
19: 57,367,603 (GRCm39) |
W337R |
probably damaging |
Het |
Fstl4 |
T |
A |
11: 53,056,705 (GRCm39) |
|
probably null |
Het |
Grm5 |
A |
G |
7: 87,685,311 (GRCm39) |
D476G |
possibly damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hdlbp |
A |
G |
1: 93,364,922 (GRCm39) |
L115P |
probably damaging |
Het |
Hk2 |
T |
A |
6: 82,721,932 (GRCm39) |
N136Y |
probably damaging |
Het |
Hs2st1 |
G |
T |
3: 144,140,415 (GRCm39) |
A302E |
probably benign |
Het |
Htr7 |
T |
C |
19: 35,947,136 (GRCm39) |
N293D |
probably benign |
Het |
Ikbkb |
T |
A |
8: 23,163,496 (GRCm39) |
E271D |
probably benign |
Het |
Il5ra |
A |
T |
6: 106,715,335 (GRCm39) |
Y166* |
probably null |
Het |
Il9r |
T |
A |
11: 32,143,227 (GRCm39) |
H244L |
probably benign |
Het |
Itih4 |
T |
C |
14: 30,613,456 (GRCm39) |
|
probably null |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Large1 |
A |
T |
8: 73,544,710 (GRCm39) |
D689E |
probably damaging |
Het |
Limk2 |
A |
G |
11: 3,303,275 (GRCm39) |
|
probably null |
Het |
Med15 |
A |
G |
16: 17,540,644 (GRCm39) |
F34S |
probably damaging |
Het |
Mprip |
C |
T |
11: 59,643,357 (GRCm39) |
T505I |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,623,364 (GRCm39) |
N2071K |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,408,729 (GRCm39) |
L2522P |
probably damaging |
Het |
Myd88 |
A |
T |
9: 119,166,908 (GRCm39) |
|
probably null |
Het |
Myo7a |
A |
C |
7: 97,741,703 (GRCm39) |
F484V |
possibly damaging |
Het |
Nme1 |
A |
C |
11: 93,851,593 (GRCm39) |
L81R |
probably benign |
Het |
Ntn4 |
T |
A |
10: 93,569,464 (GRCm39) |
|
probably null |
Het |
Or2y13 |
T |
C |
11: 49,415,162 (GRCm39) |
V204A |
probably benign |
Het |
Or4p19 |
T |
C |
2: 88,242,444 (GRCm39) |
D186G |
probably damaging |
Het |
Or51l4 |
A |
T |
7: 103,404,131 (GRCm39) |
Y220* |
probably null |
Het |
Otogl |
T |
G |
10: 107,649,878 (GRCm39) |
N1159T |
probably damaging |
Het |
Pabpc6 |
G |
A |
17: 9,887,003 (GRCm39) |
T516I |
probably benign |
Het |
Pcdh1 |
C |
T |
18: 38,335,921 (GRCm39) |
R238H |
probably damaging |
Het |
Plekha7 |
T |
C |
7: 115,727,920 (GRCm39) |
N980S |
probably damaging |
Het |
Reg4 |
C |
T |
3: 98,143,677 (GRCm39) |
T157I |
probably benign |
Het |
Rev3l |
A |
T |
10: 39,700,612 (GRCm39) |
E1703V |
probably damaging |
Het |
Rev3l |
G |
T |
10: 39,700,611 (GRCm39) |
E1703* |
probably null |
Het |
Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Saal1 |
T |
C |
7: 46,342,340 (GRCm39) |
K368E |
probably damaging |
Het |
Scn9a |
C |
T |
2: 66,335,220 (GRCm39) |
W1245* |
probably null |
Het |
Slc38a11 |
T |
A |
2: 65,147,315 (GRCm39) |
L387F |
probably damaging |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Sptb |
C |
A |
12: 76,667,641 (GRCm39) |
V819L |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,086,124 (GRCm39) |
T1195A |
probably benign |
Het |
Ssna1 |
C |
A |
2: 25,162,024 (GRCm39) |
V57F |
possibly damaging |
Het |
Stk32a |
G |
T |
18: 43,446,485 (GRCm39) |
E312* |
probably null |
Het |
Synpo |
A |
G |
18: 60,736,459 (GRCm39) |
F496L |
probably benign |
Het |
Syt15 |
C |
T |
14: 33,944,858 (GRCm39) |
T135M |
probably benign |
Het |
Tm9sf4 |
A |
G |
2: 153,032,832 (GRCm39) |
E246G |
probably benign |
Het |
Trim44 |
T |
C |
2: 102,187,830 (GRCm39) |
M308V |
possibly damaging |
Het |
Unc119b |
T |
A |
5: 115,272,885 (GRCm39) |
K29* |
probably null |
Het |
Vim |
T |
A |
2: 13,584,921 (GRCm39) |
D367E |
probably benign |
Het |
Virma |
T |
A |
4: 11,494,814 (GRCm39) |
N38K |
probably damaging |
Het |
Vmn1r228 |
A |
T |
17: 20,996,560 (GRCm39) |
D319E |
possibly damaging |
Het |
Vmn2r32 |
T |
A |
7: 7,466,991 (GRCm39) |
I846F |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,576,667 (GRCm39) |
V1025A |
probably benign |
Het |
Vps13c |
G |
T |
9: 67,879,357 (GRCm39) |
E566* |
probably null |
Het |
|
Other mutations in Pex5l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01397:Pex5l
|
APN |
3 |
33,006,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01621:Pex5l
|
APN |
3 |
33,069,110 (GRCm39) |
splice site |
probably null |
|
IGL01813:Pex5l
|
APN |
3 |
33,136,204 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02313:Pex5l
|
APN |
3 |
33,047,141 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02508:Pex5l
|
APN |
3 |
33,047,051 (GRCm39) |
splice site |
probably benign |
|
IGL02997:Pex5l
|
APN |
3 |
33,009,991 (GRCm39) |
splice site |
probably benign |
|
R0195:Pex5l
|
UTSW |
3 |
33,047,102 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0674:Pex5l
|
UTSW |
3 |
33,006,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Pex5l
|
UTSW |
3 |
33,008,685 (GRCm39) |
splice site |
probably benign |
|
R1500:Pex5l
|
UTSW |
3 |
33,069,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Pex5l
|
UTSW |
3 |
33,069,162 (GRCm39) |
nonsense |
probably null |
|
R1850:Pex5l
|
UTSW |
3 |
33,005,025 (GRCm39) |
splice site |
probably null |
|
R2165:Pex5l
|
UTSW |
3 |
33,007,281 (GRCm39) |
splice site |
probably null |
|
R2679:Pex5l
|
UTSW |
3 |
33,136,201 (GRCm39) |
missense |
probably benign |
0.02 |
R2880:Pex5l
|
UTSW |
3 |
33,047,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2881:Pex5l
|
UTSW |
3 |
33,047,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3766:Pex5l
|
UTSW |
3 |
33,061,327 (GRCm39) |
missense |
probably benign |
0.01 |
R3780:Pex5l
|
UTSW |
3 |
33,004,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R3934:Pex5l
|
UTSW |
3 |
33,061,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R3975:Pex5l
|
UTSW |
3 |
33,069,164 (GRCm39) |
missense |
probably damaging |
0.99 |
R4285:Pex5l
|
UTSW |
3 |
33,061,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Pex5l
|
UTSW |
3 |
33,047,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R4855:Pex5l
|
UTSW |
3 |
33,196,989 (GRCm39) |
splice site |
probably benign |
|
R4868:Pex5l
|
UTSW |
3 |
33,006,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5135:Pex5l
|
UTSW |
3 |
33,009,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Pex5l
|
UTSW |
3 |
33,061,477 (GRCm39) |
splice site |
probably null |
|
R5223:Pex5l
|
UTSW |
3 |
33,012,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R5362:Pex5l
|
UTSW |
3 |
33,047,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R5398:Pex5l
|
UTSW |
3 |
33,006,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5829:Pex5l
|
UTSW |
3 |
33,060,139 (GRCm39) |
missense |
probably benign |
0.00 |
R6731:Pex5l
|
UTSW |
3 |
33,012,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Pex5l
|
UTSW |
3 |
33,078,840 (GRCm39) |
splice site |
probably null |
|
R7452:Pex5l
|
UTSW |
3 |
33,058,467 (GRCm39) |
missense |
probably benign |
0.02 |
R7549:Pex5l
|
UTSW |
3 |
33,136,184 (GRCm39) |
missense |
probably benign |
0.04 |
R7563:Pex5l
|
UTSW |
3 |
33,008,625 (GRCm39) |
missense |
probably damaging |
0.98 |
R7757:Pex5l
|
UTSW |
3 |
33,136,300 (GRCm39) |
start gained |
probably benign |
|
R8030:Pex5l
|
UTSW |
3 |
33,008,568 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8143:Pex5l
|
UTSW |
3 |
33,136,658 (GRCm39) |
start gained |
probably benign |
|
R8242:Pex5l
|
UTSW |
3 |
33,060,184 (GRCm39) |
missense |
probably benign |
0.01 |
R8919:Pex5l
|
UTSW |
3 |
33,007,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R9034:Pex5l
|
UTSW |
3 |
33,006,683 (GRCm39) |
missense |
probably damaging |
0.99 |
R9422:Pex5l
|
UTSW |
3 |
33,136,401 (GRCm39) |
start gained |
probably benign |
|
R9585:Pex5l
|
UTSW |
3 |
33,060,091 (GRCm39) |
missense |
probably benign |
|
R9654:Pex5l
|
UTSW |
3 |
33,010,827 (GRCm39) |
missense |
probably benign |
0.08 |
R9711:Pex5l
|
UTSW |
3 |
33,136,204 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Pex5l
|
UTSW |
3 |
33,061,308 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Predicted Primers |
PCR Primer
(F):5'- GGCCATCATGCTGGTTATGTTTAAAGGA -3'
(R):5'- CTGCTGTCATGAGGATGTTTTAACCTCT -3'
Sequencing Primer
(F):5'- gggaaggagaaaaggggaac -3'
(R):5'- CGAGGATGTATAAAGTACCTCTCTG -3'
|
Posted On |
2014-05-14 |