Incidental Mutation 'R8919:Pex5l'
ID |
679101 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pex5l
|
Ensembl Gene |
ENSMUSG00000027674 |
Gene Name |
peroxisomal biogenesis factor 5-like |
Synonyms |
PXR2, TRIP8b, Pex2, 1700016J08Rik |
MMRRC Submission |
068706-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.604)
|
Stock # |
R8919 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
33003557-33197396 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 33007333 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Alanine
at position 481
(V481A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000142008
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000078226]
[ENSMUST00000108221]
[ENSMUST00000108224]
[ENSMUST00000108225]
[ENSMUST00000108226]
[ENSMUST00000192093]
[ENSMUST00000193289]
[ENSMUST00000193681]
[ENSMUST00000194016]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000078226
AA Change: V446A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000077353 Gene: ENSMUSG00000027674 AA Change: V446A
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 damaging
Transcript: ENSMUST00000108221
AA Change: V175A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000103856 Gene: ENSMUSG00000027674 AA Change: V175A
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 damaging
Transcript: ENSMUST00000108224
AA Change: V422A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000103859 Gene: ENSMUSG00000027674 AA Change: V422A
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 damaging
Transcript: ENSMUST00000108225
AA Change: V446A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000103860 Gene: ENSMUSG00000027674 AA Change: V446A
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 |
possibly damaging
Transcript: ENSMUST00000108226
AA Change: V398A
PolyPhen 2
Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000103861 Gene: ENSMUSG00000027674 AA Change: V398A
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 damaging
Transcript: ENSMUST00000192093
AA Change: V446A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000141387 Gene: ENSMUSG00000027674 AA Change: V446A
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 damaging
Transcript: ENSMUST00000193289
AA Change: V481A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000142008 Gene: ENSMUSG00000027674 AA Change: V481A
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 damaging
Transcript: ENSMUST00000193681
AA Change: V481A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000141454 Gene: ENSMUSG00000027674 AA Change: V481A
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 damaging
Transcript: ENSMUST00000194016
AA Change: V481A
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000142196 Gene: ENSMUSG00000027674 AA Change: V481A
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 |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
99% (81/82) |
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: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
C |
T |
8: 60,993,158 (GRCm39) |
T373I |
possibly damaging |
Het |
Abca13 |
T |
C |
11: 9,241,653 (GRCm39) |
L1172P |
possibly damaging |
Het |
Abcg2 |
A |
G |
6: 58,661,326 (GRCm39) |
Y459C |
probably benign |
Het |
AC125199.3 |
T |
C |
16: 88,609,061 (GRCm39) |
N4D |
possibly damaging |
Het |
Acad8 |
A |
G |
9: 26,910,785 (GRCm39) |
M3T |
probably benign |
Het |
Acsbg3 |
A |
C |
17: 57,189,218 (GRCm39) |
I209L |
probably benign |
Het |
Adcyap1r1 |
C |
T |
6: 55,474,080 (GRCm39) |
T472I |
probably damaging |
Het |
Ank3 |
A |
T |
10: 69,840,671 (GRCm39) |
K1890N |
possibly damaging |
Het |
Asic1 |
G |
A |
15: 99,569,826 (GRCm39) |
C49Y |
probably benign |
Het |
Atp1a1 |
T |
C |
3: 101,498,547 (GRCm39) |
N215S |
probably damaging |
Het |
C87436 |
A |
G |
6: 86,422,774 (GRCm39) |
Y116C |
probably damaging |
Het |
Car5a |
T |
C |
8: 122,671,519 (GRCm39) |
D5G |
probably benign |
Het |
Ccdc169 |
T |
C |
3: 55,058,368 (GRCm39) |
|
probably null |
Het |
Ccdc93 |
A |
G |
1: 121,426,970 (GRCm39) |
R586G |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,238,007 (GRCm39) |
V131A |
probably damaging |
Het |
Cox5a |
A |
G |
9: 57,436,329 (GRCm39) |
D60G |
possibly damaging |
Het |
Cpne6 |
A |
T |
14: 55,750,104 (GRCm39) |
E78D |
probably benign |
Het |
Cyp2u1 |
T |
C |
3: 131,089,114 (GRCm39) |
E390G |
probably damaging |
Het |
Dab2 |
C |
A |
15: 6,465,271 (GRCm39) |
N707K |
|
Het |
Dock10 |
A |
T |
1: 80,483,147 (GRCm39) |
D2101E |
probably benign |
Het |
Duoxa2 |
G |
A |
2: 122,132,357 (GRCm39) |
|
probably null |
Het |
Eif4a3 |
T |
C |
11: 119,190,758 (GRCm39) |
D22G |
probably benign |
Het |
Fhip1b |
T |
C |
7: 105,037,477 (GRCm39) |
T369A |
possibly damaging |
Het |
Fubp3 |
A |
G |
2: 31,482,476 (GRCm39) |
|
probably null |
Het |
Gm10330 |
A |
G |
12: 23,829,887 (GRCm39) |
L98P |
probably benign |
Het |
Gm5108 |
A |
G |
5: 68,134,299 (GRCm39) |
*102W |
probably null |
Het |
Gpr149 |
A |
C |
3: 62,438,478 (GRCm39) |
S560A |
probably damaging |
Het |
Haspin |
T |
C |
11: 73,027,430 (GRCm39) |
D553G |
probably benign |
Het |
Hsf1 |
C |
T |
15: 76,382,051 (GRCm39) |
H104Y |
probably benign |
Het |
Ifi203 |
T |
C |
1: 173,756,494 (GRCm39) |
T430A |
unknown |
Het |
Itih2 |
G |
A |
2: 10,102,822 (GRCm39) |
Q771* |
probably null |
Het |
Kazald1 |
T |
A |
19: 45,065,395 (GRCm39) |
L92Q |
probably damaging |
Het |
Krt19 |
T |
C |
11: 100,031,980 (GRCm39) |
E324G |
probably damaging |
Het |
Lrrc28 |
A |
T |
7: 67,268,833 (GRCm39) |
V79E |
possibly damaging |
Het |
Ltn1 |
T |
A |
16: 87,178,381 (GRCm39) |
Q1616L |
probably damaging |
Het |
Mdc1 |
A |
G |
17: 36,158,843 (GRCm39) |
K408E |
probably benign |
Het |
Nalcn |
A |
T |
14: 123,561,284 (GRCm39) |
M738K |
probably benign |
Het |
Ncoa4 |
T |
C |
14: 31,894,848 (GRCm39) |
L125P |
probably damaging |
Het |
Ncor2 |
G |
T |
5: 125,106,253 (GRCm39) |
R810S |
|
Het |
Neb |
C |
T |
2: 52,127,141 (GRCm39) |
G348D |
|
Het |
Nfat5 |
T |
A |
8: 108,095,228 (GRCm39) |
F1156L |
probably damaging |
Het |
Oit3 |
G |
A |
10: 59,277,468 (GRCm39) |
T13I |
unknown |
Het |
Opa1 |
A |
C |
16: 29,424,340 (GRCm39) |
Q230P |
probably damaging |
Het |
Or10j3b |
T |
C |
1: 173,044,064 (GRCm39) |
I282T |
probably damaging |
Het |
Or52k2 |
T |
A |
7: 102,253,711 (GRCm39) |
I50N |
probably damaging |
Het |
Or5p66 |
A |
G |
7: 107,886,289 (GRCm39) |
F15L |
probably damaging |
Het |
Or5w12 |
A |
C |
2: 87,502,567 (GRCm39) |
L48W |
probably damaging |
Het |
Or6c5b |
G |
T |
10: 129,246,082 (GRCm39) |
M282I |
probably benign |
Het |
Parpbp |
T |
C |
10: 87,946,189 (GRCm39) |
H410R |
probably null |
Het |
Plekhh3 |
C |
A |
11: 101,057,225 (GRCm39) |
R344L |
probably benign |
Het |
Prrc2b |
T |
C |
2: 32,104,953 (GRCm39) |
V1477A |
probably benign |
Het |
Ptp4a2 |
G |
A |
4: 129,738,945 (GRCm39) |
G94S |
possibly damaging |
Het |
Ptprk |
T |
A |
10: 28,359,203 (GRCm39) |
Y598* |
probably null |
Het |
Rfx5 |
C |
A |
3: 94,864,475 (GRCm39) |
T207N |
probably damaging |
Het |
Rnase2b |
A |
G |
14: 51,400,347 (GRCm39) |
T143A |
possibly damaging |
Het |
Scn1a |
A |
G |
2: 66,168,330 (GRCm39) |
V92A |
probably benign |
Het |
Shank2 |
C |
A |
7: 143,965,265 (GRCm39) |
P958T |
probably damaging |
Het |
Slc13a1 |
A |
G |
6: 24,108,194 (GRCm39) |
I294T |
probably damaging |
Het |
Slc4a8 |
A |
T |
15: 100,712,421 (GRCm39) |
E1084D |
probably benign |
Het |
Smurf1 |
T |
A |
5: 144,820,422 (GRCm39) |
R549* |
probably null |
Het |
Spmip10 |
T |
C |
18: 56,725,537 (GRCm39) |
F66L |
probably damaging |
Het |
Sprr2b |
T |
C |
3: 92,225,032 (GRCm39) |
C93R |
unknown |
Het |
Tcn2 |
G |
T |
11: 3,873,569 (GRCm39) |
S259Y |
probably damaging |
Het |
Tent4a |
G |
T |
13: 69,651,828 (GRCm39) |
T531N |
possibly damaging |
Het |
Tle1 |
A |
G |
4: 72,076,525 (GRCm39) |
S168P |
possibly damaging |
Het |
Tnfrsf1b |
C |
T |
4: 144,950,150 (GRCm39) |
G264D |
probably damaging |
Het |
Tnks2 |
T |
A |
19: 36,823,088 (GRCm39) |
N118K |
probably damaging |
Het |
Topaz1 |
G |
T |
9: 122,626,930 (GRCm39) |
|
probably benign |
Het |
Traf3ip1 |
A |
G |
1: 91,443,796 (GRCm39) |
|
probably benign |
Het |
Ttk |
A |
G |
9: 83,721,322 (GRCm39) |
E69G |
probably damaging |
Het |
Tulp3 |
T |
C |
6: 128,310,966 (GRCm39) |
D87G |
probably benign |
Het |
Usp38 |
C |
T |
8: 81,708,479 (GRCm39) |
G1033D |
probably damaging |
Het |
Usp44 |
T |
A |
10: 93,693,775 (GRCm39) |
N707K |
probably benign |
Het |
Vipas39 |
T |
A |
12: 87,305,858 (GRCm39) |
R112* |
probably null |
Het |
Vmn1r185 |
A |
C |
7: 26,311,206 (GRCm39) |
S100A |
probably damaging |
Het |
Vmn1r209 |
T |
C |
13: 22,990,223 (GRCm39) |
M156V |
probably benign |
Het |
Vmn1r3 |
G |
A |
4: 3,184,863 (GRCm39) |
T148I |
probably benign |
Het |
Wdr41 |
G |
A |
13: 95,151,620 (GRCm39) |
R260H |
probably benign |
Het |
Wdr90 |
G |
A |
17: 26,076,146 (GRCm39) |
R104C |
|
Het |
Wnk2 |
A |
T |
13: 49,221,711 (GRCm39) |
H1183Q |
possibly damaging |
Het |
Zfp667 |
A |
T |
7: 6,308,256 (GRCm39) |
H308L |
possibly damaging |
Het |
Zfp952 |
A |
G |
17: 33,220,628 (GRCm39) |
N18D |
possibly damaging |
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 |
|
R1695:Pex5l
|
UTSW |
3 |
33,008,531 (GRCm39) |
missense |
probably benign |
0.28 |
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 |
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'- GCTGTGCTGGAATTTCTTACC -3'
(R):5'- TGAGAACCTTAATGTGGCTTGTATG -3'
Sequencing Primer
(F):5'- TACCTCTGGCCGAACTGTTAAGG -3'
(R):5'- ATAGACCTGTGTACCCAGTGCATG -3'
|
Posted On |
2021-08-02 |