Incidental Mutation 'R0025:Scn10a'
ID 40795
Institutional Source Beutler Lab
Gene Symbol Scn10a
Ensembl Gene ENSMUSG00000034533
Gene Name sodium channel, voltage-gated, type X, alpha
Synonyms Nav1.8
MMRRC Submission 038320-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.182) question?
Stock # R0025 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 119437522-119548388 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 119499550 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Tyrosine at position 248 (D248Y)
Ref Sequence ENSEMBL: ENSMUSP00000150830 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084787] [ENSMUST00000213392] [ENSMUST00000214408]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000084787
AA Change: D248Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000081845
Gene: ENSMUSG00000034533
AA Change: D248Y

DomainStartEndE-ValueType
Pfam:Ion_trans 129 406 7.9e-77 PFAM
low complexity region 557 572 N/A INTRINSIC
Pfam:Ion_trans 663 898 6.8e-53 PFAM
Pfam:Na_trans_assoc 903 1148 2.7e-57 PFAM
Pfam:Ion_trans 1152 1429 8.1e-66 PFAM
Pfam:Ion_trans 1476 1734 1.9e-55 PFAM
Pfam:PKD_channel 1561 1729 3.4e-8 PFAM
IQ 1851 1873 7.57e0 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000213392
AA Change: D248Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000214408
AA Change: D248Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216583
Meta Mutation Damage Score 0.8225 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.7%
  • 20x: 90.3%
Validation Efficiency 98% (115/117)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a tetrodotoxin-resistant voltage-gated sodium channel alpha subunit. The properties of the channel formed by the encoded transmembrane protein can be altered by interaction with different beta subunits. This protein may be involved in the onset of pain associated with peripheral neuropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit impaired perception of pain. Mice homozygous or heterozygous for an ENU-induced allele exhibit a catalepsy phenotype following scruffing and increased sensitivity to cold pain. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 106 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsm1 A T 7: 119,257,538 (GRCm39) T435S probably damaging Het
Agtpbp1 G A 13: 59,648,014 (GRCm39) T602I probably benign Het
Ahnak2 T A 12: 112,749,154 (GRCm39) D231V probably damaging Het
Ampd3 G A 7: 110,392,876 (GRCm39) D215N probably benign Het
Ankrd17 T C 5: 90,398,264 (GRCm39) D1762G probably damaging Het
Asb8 C T 15: 98,040,552 (GRCm39) V37I possibly damaging Het
Bicra T C 7: 15,721,436 (GRCm39) T694A possibly damaging Het
Btnl6 A T 17: 34,733,273 (GRCm39) M234K probably benign Het
Ccnb1 A T 13: 100,916,289 (GRCm39) V336D probably damaging Het
Cdca8 A T 4: 124,815,047 (GRCm39) L190Q possibly damaging Het
Cep290 A T 10: 100,373,693 (GRCm39) L1324F probably damaging Het
Ces1f T C 8: 93,998,513 (GRCm39) E161G probably benign Het
Ces2g A G 8: 105,692,628 (GRCm39) probably benign Het
Cfap74 C T 4: 155,510,572 (GRCm39) R386C probably benign Het
Clec3b A G 9: 122,986,090 (GRCm39) T163A probably benign Het
Cntnap4 T G 8: 113,529,796 (GRCm39) L668R probably damaging Het
Col27a1 A G 4: 63,194,214 (GRCm39) D857G probably damaging Het
Csf1 A G 3: 107,655,960 (GRCm39) V245A probably benign Het
Ctss A G 3: 95,457,448 (GRCm39) Y302C probably damaging Het
Cyb5d1 A G 11: 69,285,792 (GRCm39) probably null Het
Cyp1a2 A G 9: 57,589,344 (GRCm39) S157P probably damaging Het
Cyp2b9 A T 7: 25,900,238 (GRCm39) T349S probably benign Het
Dennd6b T C 15: 89,070,386 (GRCm39) I428V probably benign Het
Denr A G 5: 124,065,298 (GRCm39) probably benign Het
Dnah9 G A 11: 65,860,781 (GRCm39) probably benign Het
Dock3 G T 9: 106,790,467 (GRCm39) Q1419K possibly damaging Het
Dph3b-ps A T 13: 106,683,375 (GRCm39) noncoding transcript Het
Emc7 G T 2: 112,289,830 (GRCm39) D87Y probably damaging Het
Enah T C 1: 181,740,938 (GRCm39) E462G possibly damaging Het
Eno1b T C 18: 48,180,806 (GRCm39) I328T probably benign Het
Enpp6 A G 8: 47,519,035 (GRCm39) K268E probably damaging Het
Eps15l1 T G 8: 73,135,341 (GRCm39) probably benign Het
Fam151a T C 4: 106,605,371 (GRCm39) Y578H probably benign Het
Fmn2 T C 1: 174,618,880 (GRCm39) V1512A probably damaging Het
Focad C A 4: 88,327,196 (GRCm39) N168K probably benign Het
Fyco1 A G 9: 123,658,074 (GRCm39) C701R probably damaging Het
Gabbr1 G T 17: 37,378,102 (GRCm39) probably benign Het
Golga7b A T 19: 42,255,278 (GRCm39) E76V probably damaging Het
Gucy2d A G 7: 98,116,959 (GRCm39) D924G probably benign Het
H2-M9 A G 17: 36,952,647 (GRCm39) F133S probably damaging Het
Hc A G 2: 34,876,304 (GRCm39) Y1581H probably damaging Het
Herc3 C T 6: 58,851,293 (GRCm39) P514L probably damaging Het
Hormad1 T C 3: 95,492,436 (GRCm39) probably benign Het
Iigp1 T A 18: 60,523,859 (GRCm39) S326T possibly damaging Het
Itga2 G A 13: 115,007,032 (GRCm39) S432L possibly damaging Het
Kcnk7 T G 19: 5,757,042 (GRCm39) *344G probably null Het
Kif13a A G 13: 46,939,987 (GRCm39) probably null Het
Kif1a A C 1: 92,970,080 (GRCm39) I1027S probably damaging Het
Kif2c G T 4: 117,022,714 (GRCm39) H416Q probably damaging Het
Liat1 AGAGGAGGAGGAGGAGG AGAGGAGGAGGAGG 11: 75,890,941 (GRCm39) probably benign Het
Map3k1 A G 13: 111,892,663 (GRCm39) V864A probably benign Het
Mark2 T C 19: 7,263,287 (GRCm39) D160G probably damaging Het
Mbd4 A G 6: 115,821,529 (GRCm39) probably null Het
Micu1 A G 10: 59,624,699 (GRCm39) probably null Het
Mink1 T C 11: 70,503,868 (GRCm39) W1263R probably damaging Het
Mov10 A C 3: 104,711,919 (GRCm39) L224R probably damaging Het
Ndel1 T C 11: 68,726,999 (GRCm39) E226G probably damaging Het
Neb A T 2: 52,112,786 (GRCm39) V4336E probably damaging Het
Nln T A 13: 104,173,399 (GRCm39) K602N probably damaging Het
Nlrp14 A T 7: 106,780,465 (GRCm39) probably benign Het
Nmd3 A T 3: 69,655,654 (GRCm39) D445V probably damaging Het
Nop14 T C 5: 34,801,297 (GRCm39) I625V probably benign Het
Notch1 T C 2: 26,360,943 (GRCm39) Q1134R probably damaging Het
Nr4a2 T C 2: 56,998,627 (GRCm39) I392M probably benign Het
Or13n4 A G 7: 106,422,963 (GRCm39) F257L possibly damaging Het
Or4f6 T A 2: 111,839,365 (GRCm39) L55F probably damaging Het
Or8b57 A G 9: 40,003,549 (GRCm39) S234P probably damaging Het
Osbp T C 19: 11,961,322 (GRCm39) Y454H probably damaging Het
Pak4 G A 7: 28,263,708 (GRCm39) R343C probably damaging Het
Pak5 T C 2: 135,942,704 (GRCm39) K479E possibly damaging Het
Pard3 C A 8: 127,888,058 (GRCm39) D73E probably damaging Het
Pcdh10 T C 3: 45,334,934 (GRCm39) V416A possibly damaging Het
Plek A C 11: 16,935,594 (GRCm39) W261G probably damaging Het
Pmp22 A T 11: 63,049,076 (GRCm39) probably null Het
Prph2 A C 17: 47,230,697 (GRCm39) K197Q probably benign Het
Prss45 T A 9: 110,669,962 (GRCm39) L257Q probably damaging Het
Psmb6 C A 11: 70,417,171 (GRCm39) H73Q probably benign Het
Rin2 T C 2: 145,720,752 (GRCm39) probably benign Het
Rps6kb1 A T 11: 86,402,413 (GRCm39) probably null Het
Scn4a C T 11: 106,215,386 (GRCm39) V1197I probably benign Het
Siglecf A T 7: 43,001,349 (GRCm39) I106F probably benign Het
Sik1 A G 17: 32,066,249 (GRCm39) probably benign Het
Slc22a21 T G 11: 53,870,514 (GRCm39) N57T probably damaging Het
Slc36a2 A G 11: 55,053,621 (GRCm39) L339P probably damaging Het
Slc4a9 G T 18: 36,664,719 (GRCm39) probably benign Het
Smg1 G A 7: 117,811,666 (GRCm39) T104I possibly damaging Het
Stc2 A T 11: 31,315,559 (GRCm39) probably null Het
Stx18 T A 5: 38,249,908 (GRCm39) Y74N probably damaging Het
Stxbp5 A T 10: 9,638,492 (GRCm39) H1102Q probably damaging Het
Tnfaip8l2 G A 3: 95,047,339 (GRCm39) L175F probably damaging Het
Tom1l2 T C 11: 60,120,960 (GRCm39) K450E probably damaging Het
Tpo T C 12: 30,150,389 (GRCm39) Q497R probably benign Het
Tprg1l G T 4: 154,244,802 (GRCm39) probably benign Het
Triml2 A G 8: 43,638,469 (GRCm39) M146V probably benign Het
Tsc2 A G 17: 24,849,978 (GRCm39) probably benign Het
Tut7 A T 13: 59,953,142 (GRCm39) D99E probably benign Het
Vit G A 17: 78,907,264 (GRCm39) G229R probably benign Het
Vmn2r19 C T 6: 123,308,506 (GRCm39) L528F probably benign Het
Vwf T A 6: 125,659,775 (GRCm39) I2658N probably benign Het
Wdfy3 T C 5: 101,992,912 (GRCm39) D3341G probably damaging Het
Wdr36 T A 18: 32,992,360 (GRCm39) D632E probably damaging Het
Wdr47 G T 3: 108,545,307 (GRCm39) A733S probably damaging Het
Zfp458 T A 13: 67,405,962 (GRCm39) H156L probably damaging Het
Zfp654 A G 16: 64,605,181 (GRCm39) V466A probably benign Het
Zfp804b T C 5: 6,821,665 (GRCm39) E466G probably damaging Het
Zfp941 T C 7: 140,393,185 (GRCm39) D58G probably benign Het
Other mutations in Scn10a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00088:Scn10a APN 9 119,501,292 (GRCm39) missense probably damaging 1.00
IGL01339:Scn10a APN 9 119,451,832 (GRCm39) missense probably damaging 1.00
IGL01467:Scn10a APN 9 119,487,478 (GRCm39) missense probably benign 0.33
IGL01472:Scn10a APN 9 119,446,829 (GRCm39) missense probably damaging 1.00
IGL01481:Scn10a APN 9 119,438,260 (GRCm39) missense probably damaging 1.00
IGL01539:Scn10a APN 9 119,467,764 (GRCm39) missense probably damaging 0.99
IGL01580:Scn10a APN 9 119,456,225 (GRCm39) missense probably damaging 1.00
IGL01676:Scn10a APN 9 119,501,231 (GRCm39) nonsense probably null
IGL01681:Scn10a APN 9 119,523,143 (GRCm39) missense probably damaging 1.00
IGL01748:Scn10a APN 9 119,456,150 (GRCm39) missense probably damaging 1.00
IGL01866:Scn10a APN 9 119,464,568 (GRCm39) nonsense probably null
IGL01998:Scn10a APN 9 119,438,742 (GRCm39) missense probably damaging 1.00
IGL02015:Scn10a APN 9 119,494,017 (GRCm39) missense probably benign 0.09
IGL02098:Scn10a APN 9 119,520,544 (GRCm39) missense possibly damaging 0.90
IGL02113:Scn10a APN 9 119,438,956 (GRCm39) missense probably damaging 1.00
IGL02245:Scn10a APN 9 119,501,218 (GRCm39) missense probably damaging 1.00
IGL02262:Scn10a APN 9 119,487,499 (GRCm39) missense possibly damaging 0.92
IGL02317:Scn10a APN 9 119,467,621 (GRCm39) missense probably benign 0.00
IGL02428:Scn10a APN 9 119,520,628 (GRCm39) missense probably damaging 1.00
IGL02439:Scn10a APN 9 119,447,914 (GRCm39) missense probably benign 0.40
IGL02583:Scn10a APN 9 119,520,506 (GRCm39) splice site probably benign
IGL02597:Scn10a APN 9 119,439,189 (GRCm39) missense probably damaging 0.99
IGL02680:Scn10a APN 9 119,495,125 (GRCm39) missense probably damaging 1.00
IGL02733:Scn10a APN 9 119,445,771 (GRCm39) missense probably damaging 1.00
IGL02851:Scn10a APN 9 119,500,674 (GRCm39) missense probably damaging 1.00
IGL02992:Scn10a APN 9 119,438,626 (GRCm39) missense possibly damaging 0.90
IGL03040:Scn10a APN 9 119,452,051 (GRCm39) missense probably damaging 1.00
IGL03049:Scn10a APN 9 119,495,056 (GRCm39) missense probably damaging 1.00
IGL03407:Scn10a APN 9 119,477,237 (GRCm39) missense probably damaging 0.99
possum UTSW 9 119,467,771 (GRCm39) missense probably damaging 1.00
R0030:Scn10a UTSW 9 119,499,056 (GRCm39) missense probably benign 0.01
R0328:Scn10a UTSW 9 119,523,168 (GRCm39) missense possibly damaging 0.92
R0494:Scn10a UTSW 9 119,453,166 (GRCm39) missense probably damaging 1.00
R0511:Scn10a UTSW 9 119,442,766 (GRCm39) missense probably damaging 0.99
R0548:Scn10a UTSW 9 119,494,994 (GRCm39) missense probably benign 0.00
R0584:Scn10a UTSW 9 119,499,597 (GRCm39) missense probably damaging 1.00
R0595:Scn10a UTSW 9 119,495,129 (GRCm39) missense probably benign 0.01
R0894:Scn10a UTSW 9 119,459,213 (GRCm39) missense probably damaging 1.00
R1022:Scn10a UTSW 9 119,438,340 (GRCm39) missense probably damaging 1.00
R1024:Scn10a UTSW 9 119,438,340 (GRCm39) missense probably damaging 1.00
R1263:Scn10a UTSW 9 119,446,799 (GRCm39) missense probably damaging 1.00
R1456:Scn10a UTSW 9 119,520,544 (GRCm39) missense probably benign 0.01
R1466:Scn10a UTSW 9 119,495,556 (GRCm39) missense probably damaging 1.00
R1466:Scn10a UTSW 9 119,495,556 (GRCm39) missense probably damaging 1.00
R1573:Scn10a UTSW 9 119,442,692 (GRCm39) missense probably benign 0.04
R1704:Scn10a UTSW 9 119,438,460 (GRCm39) missense probably damaging 1.00
R1933:Scn10a UTSW 9 119,439,064 (GRCm39) missense probably damaging 1.00
R1945:Scn10a UTSW 9 119,520,520 (GRCm39) missense possibly damaging 0.91
R2013:Scn10a UTSW 9 119,442,802 (GRCm39) missense probably damaging 0.99
R2155:Scn10a UTSW 9 119,438,514 (GRCm39) missense probably benign 0.02
R2196:Scn10a UTSW 9 119,438,070 (GRCm39) missense probably benign
R2231:Scn10a UTSW 9 119,462,916 (GRCm39) missense possibly damaging 0.73
R2353:Scn10a UTSW 9 119,467,753 (GRCm39) missense probably damaging 1.00
R2392:Scn10a UTSW 9 119,456,268 (GRCm39) missense possibly damaging 0.86
R2895:Scn10a UTSW 9 119,490,467 (GRCm39) missense probably benign 0.00
R2926:Scn10a UTSW 9 119,467,767 (GRCm39) missense possibly damaging 0.93
R3783:Scn10a UTSW 9 119,520,628 (GRCm39) missense probably damaging 1.00
R3821:Scn10a UTSW 9 119,467,699 (GRCm39) missense probably benign
R4003:Scn10a UTSW 9 119,438,034 (GRCm39) missense probably null 0.00
R4208:Scn10a UTSW 9 119,445,842 (GRCm39) missense probably damaging 0.99
R4231:Scn10a UTSW 9 119,460,610 (GRCm39) missense probably damaging 0.98
R4626:Scn10a UTSW 9 119,460,571 (GRCm39) missense possibly damaging 0.87
R4702:Scn10a UTSW 9 119,462,857 (GRCm39) missense possibly damaging 0.59
R4713:Scn10a UTSW 9 119,438,717 (GRCm39) missense probably damaging 1.00
R4729:Scn10a UTSW 9 119,500,592 (GRCm39) missense probably damaging 1.00
R4782:Scn10a UTSW 9 119,451,976 (GRCm39) missense possibly damaging 0.70
R4822:Scn10a UTSW 9 119,467,738 (GRCm39) missense probably damaging 1.00
R4856:Scn10a UTSW 9 119,523,376 (GRCm39) missense possibly damaging 0.63
R4856:Scn10a UTSW 9 119,523,375 (GRCm39) missense possibly damaging 0.46
R4932:Scn10a UTSW 9 119,516,940 (GRCm39) splice site probably null
R5015:Scn10a UTSW 9 119,451,987 (GRCm39) missense possibly damaging 0.93
R5193:Scn10a UTSW 9 119,438,721 (GRCm39) missense probably damaging 1.00
R5211:Scn10a UTSW 9 119,490,298 (GRCm39) missense possibly damaging 0.87
R5320:Scn10a UTSW 9 119,477,175 (GRCm39) missense probably damaging 1.00
R5400:Scn10a UTSW 9 119,438,100 (GRCm39) missense probably damaging 0.99
R5448:Scn10a UTSW 9 119,517,013 (GRCm39) missense probably benign 0.25
R5457:Scn10a UTSW 9 119,523,193 (GRCm39) missense probably damaging 1.00
R5554:Scn10a UTSW 9 119,523,196 (GRCm39) missense probably benign 0.01
R5680:Scn10a UTSW 9 119,453,202 (GRCm39) missense probably damaging 1.00
R5762:Scn10a UTSW 9 119,464,507 (GRCm39) critical splice donor site probably null
R5935:Scn10a UTSW 9 119,456,237 (GRCm39) missense probably damaging 0.99
R5956:Scn10a UTSW 9 119,460,626 (GRCm39) missense probably damaging 1.00
R6041:Scn10a UTSW 9 119,438,535 (GRCm39) missense probably damaging 1.00
R6047:Scn10a UTSW 9 119,451,897 (GRCm39) missense probably benign 0.20
R6132:Scn10a UTSW 9 119,442,761 (GRCm39) missense possibly damaging 0.94
R6156:Scn10a UTSW 9 119,464,649 (GRCm39) missense probably benign 0.00
R6309:Scn10a UTSW 9 119,453,181 (GRCm39) missense possibly damaging 0.95
R6318:Scn10a UTSW 9 119,456,181 (GRCm39) missense probably damaging 1.00
R6394:Scn10a UTSW 9 119,490,386 (GRCm39) missense probably benign 0.36
R6711:Scn10a UTSW 9 119,438,979 (GRCm39) missense probably damaging 1.00
R6751:Scn10a UTSW 9 119,500,617 (GRCm39) missense probably damaging 1.00
R6877:Scn10a UTSW 9 119,438,848 (GRCm39) missense probably damaging 0.96
R6909:Scn10a UTSW 9 119,438,856 (GRCm39) missense probably damaging 1.00
R7023:Scn10a UTSW 9 119,442,610 (GRCm39) missense probably damaging 0.99
R7205:Scn10a UTSW 9 119,442,616 (GRCm39) missense probably damaging 0.99
R7254:Scn10a UTSW 9 119,447,921 (GRCm39) missense probably damaging 0.99
R7261:Scn10a UTSW 9 119,438,790 (GRCm39) missense probably damaging 0.97
R7283:Scn10a UTSW 9 119,493,845 (GRCm39) critical splice donor site probably null
R7453:Scn10a UTSW 9 119,467,618 (GRCm39) missense probably benign
R7561:Scn10a UTSW 9 119,523,390 (GRCm39) start codon destroyed probably null 0.66
R7590:Scn10a UTSW 9 119,495,466 (GRCm39) missense probably damaging 1.00
R7759:Scn10a UTSW 9 119,477,198 (GRCm39) nonsense probably null
R7765:Scn10a UTSW 9 119,438,970 (GRCm39) missense possibly damaging 0.90
R7851:Scn10a UTSW 9 119,446,828 (GRCm39) missense probably damaging 0.99
R7875:Scn10a UTSW 9 119,464,508 (GRCm39) critical splice donor site probably null
R7975:Scn10a UTSW 9 119,501,286 (GRCm39) missense probably benign 0.31
R8010:Scn10a UTSW 9 119,490,233 (GRCm39) missense possibly damaging 0.56
R8027:Scn10a UTSW 9 119,462,856 (GRCm39) missense probably damaging 0.99
R8221:Scn10a UTSW 9 119,446,829 (GRCm39) missense probably damaging 1.00
R8249:Scn10a UTSW 9 119,446,840 (GRCm39) missense probably damaging 1.00
R8319:Scn10a UTSW 9 119,499,455 (GRCm39) missense probably benign 0.04
R8323:Scn10a UTSW 9 119,438,462 (GRCm39) missense possibly damaging 0.95
R8539:Scn10a UTSW 9 119,467,840 (GRCm39) nonsense probably null
R8679:Scn10a UTSW 9 119,501,194 (GRCm39) missense probably damaging 0.97
R8680:Scn10a UTSW 9 119,520,509 (GRCm39) critical splice donor site probably null
R8844:Scn10a UTSW 9 119,446,791 (GRCm39) missense probably damaging 0.98
R9011:Scn10a UTSW 9 119,459,160 (GRCm39) missense probably damaging 0.99
R9055:Scn10a UTSW 9 119,451,958 (GRCm39) missense probably damaging 0.98
R9206:Scn10a UTSW 9 119,445,827 (GRCm39) missense probably damaging 1.00
R9615:Scn10a UTSW 9 119,487,504 (GRCm39) missense possibly damaging 0.55
R9622:Scn10a UTSW 9 119,438,046 (GRCm39) missense probably benign 0.11
R9641:Scn10a UTSW 9 119,445,869 (GRCm39) missense possibly damaging 0.60
R9651:Scn10a UTSW 9 119,439,063 (GRCm39) missense probably benign 0.17
X0058:Scn10a UTSW 9 119,438,430 (GRCm39) nonsense probably null
Z1177:Scn10a UTSW 9 119,453,211 (GRCm39) critical splice acceptor site probably null
Predicted Primers PCR Primer
(F):5'- TCAGAGGATACCCTGGAATCCACAC -3'
(R):5'- CAGATGGAGAAGCCAGGTTTGACAC -3'

Sequencing Primer
(F):5'- AGCCAGAAGACCTTGCTTG -3'
(R):5'- ACACTGCCTGGGATGTGTAAG -3'
Posted On 2013-05-23