Incidental Mutation 'R6015:Syne1'
ID 478570
Institutional Source Beutler Lab
Gene Symbol Syne1
Ensembl Gene ENSMUSG00000096054
Gene Name spectrin repeat containing, nuclear envelope 1
Synonyms C130039F11Rik, enaptin165, SYNE-1, nesprin-1, A330049M09Rik
MMRRC Submission 043254-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6015 (G1)
Quality Score 225.009
Status Not validated
Chromosome 10
Chromosomal Location 4970917-5501482 bp(-) (GRCm39)
Type of Mutation critical splice donor site (2 bp from exon)
DNA Base Change (assembly) A to G at 5296819 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150262 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041639] [ENSMUST00000215295]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000041639
SMART Domains Protein: ENSMUSP00000039440
Gene: ENSMUSG00000096054

DomainStartEndE-ValueType
CH 29 139 4.55e-14 SMART
low complexity region 145 167 N/A INTRINSIC
CH 187 285 9.67e-18 SMART
coiled coil region 425 452 N/A INTRINSIC
Blast:SPEC 493 599 2e-28 BLAST
Blast:SPEC 606 695 7e-40 BLAST
Blast:SPEC 701 815 1e-32 BLAST
Blast:SPEC 815 913 4e-41 BLAST
Blast:SPEC 920 1013 9e-53 BLAST
Blast:SPEC 1117 1219 2e-60 BLAST
coiled coil region 1267 1329 N/A INTRINSIC
low complexity region 1349 1368 N/A INTRINSIC
coiled coil region 1399 1427 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000215295
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215887
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.3%
  • 20x: 95.1%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for an allele lacking the KASH domain exhibit neonatal and postnatal lethality, progressive muscular dystrophy, and limb weakness. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ano5 A C 7: 51,224,525 (GRCm39) S480R probably benign Het
Aqr A G 2: 114,005,646 (GRCm39) M1T probably null Het
Arhgef28 A G 13: 98,211,530 (GRCm39) V151A possibly damaging Het
Atp6v1b2 T A 8: 69,555,148 (GRCm39) I170N probably damaging Het
Atxn2 T A 5: 121,949,055 (GRCm39) V817D probably damaging Het
Cdh23 A C 10: 60,143,761 (GRCm39) I2950S probably damaging Het
Ces1h A G 8: 94,083,691 (GRCm39) L417P unknown Het
Cimap3 T C 3: 105,906,937 (GRCm39) D154G possibly damaging Het
Csf1r A G 18: 61,242,784 (GRCm39) E49G possibly damaging Het
Eml2 G A 7: 18,935,088 (GRCm39) V432I probably damaging Het
Fat3 A G 9: 16,287,346 (GRCm39) S726P possibly damaging Het
Grik2 A T 10: 49,399,959 (GRCm39) probably null Het
Il9r A G 11: 32,142,674 (GRCm39) V287A probably benign Het
Inpp5b T C 4: 124,692,143 (GRCm39) C909R possibly damaging Het
Kat7 G A 11: 95,174,860 (GRCm39) H384Y probably damaging Het
Lama5 A G 2: 179,827,185 (GRCm39) S2272P probably benign Het
Megf10 A G 18: 57,386,100 (GRCm39) H371R probably benign Het
Moxd2 A T 6: 40,860,688 (GRCm39) Y310N probably damaging Het
Ntrk2 A T 13: 59,208,209 (GRCm39) E685V probably damaging Het
Ogfr G T 2: 180,236,467 (GRCm39) G351W probably damaging Het
Or52ac1 G T 7: 104,245,915 (GRCm39) P158T probably damaging Het
Parp3 C T 9: 106,351,481 (GRCm39) V207M possibly damaging Het
Pfkfb3 T C 2: 11,486,146 (GRCm39) probably null Het
Pigr T C 1: 130,774,998 (GRCm39) V475A probably benign Het
Pik3ap1 T A 19: 41,316,640 (GRCm39) Y250F probably benign Het
Ppp1r3c A T 19: 36,711,206 (GRCm39) I188N probably damaging Het
Prmt7 T G 8: 106,961,640 (GRCm39) probably benign Het
Psapl1 T C 5: 36,361,594 (GRCm39) V62A probably benign Het
Relch T C 1: 105,619,683 (GRCm39) L280S probably damaging Het
Rpp14 G A 14: 8,090,462 (GRCm38) V129I probably benign Het
Sema4f A G 6: 82,916,553 (GRCm39) probably benign Het
Serpinb13 C A 1: 106,928,337 (GRCm39) A319E probably benign Het
Sez6l2 A T 7: 126,552,625 (GRCm39) S134C probably damaging Het
Slc4a10 T A 2: 62,059,046 (GRCm39) H184Q probably benign Het
Slc9a9 G T 9: 94,821,602 (GRCm39) A330S probably benign Het
Sord T C 2: 122,087,424 (GRCm39) V176A probably damaging Het
Ssbp2 G T 13: 91,817,862 (GRCm39) probably null Het
Stab2 G T 10: 86,773,906 (GRCm39) N808K probably damaging Het
Tpcn2 A G 7: 144,820,588 (GRCm39) V341A probably damaging Het
Unc13b C A 4: 43,177,995 (GRCm39) S2941* probably null Het
Utrn T A 10: 12,354,168 (GRCm39) H2806L possibly damaging Het
Vmn1r40 C A 6: 89,691,588 (GRCm39) A135D probably damaging Het
Vmn1r68 C T 7: 10,261,616 (GRCm39) V161M probably benign Het
Wiz T A 17: 32,606,574 (GRCm39) I54F probably damaging Het
Other mutations in Syne1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00684:Syne1 APN 10 5,342,167 (GRCm38) synonymous probably benign
IGL00725:Syne1 APN 10 5,344,922 (GRCm38) missense possibly damaging 0.48
IGL00799:Syne1 APN 10 5,347,878 (GRCm38) missense probably benign 0.00
IGL01087:Syne1 APN 10 5,375,708 (GRCm39) missense probably damaging 1.00
IGL01123:Syne1 APN 10 5,294,921 (GRCm39) nonsense probably null
IGL01147:Syne1 APN 10 5,002,691 (GRCm39) nonsense probably null
IGL01150:Syne1 APN 10 5,393,154 (GRCm39) missense probably damaging 1.00
IGL01154:Syne1 APN 10 5,310,848 (GRCm39) missense probably damaging 1.00
IGL01727:Syne1 APN 10 4,997,842 (GRCm39) missense probably damaging 0.99
IGL01761:Syne1 APN 10 5,355,456 (GRCm39) missense probably damaging 1.00
IGL01793:Syne1 APN 10 5,302,191 (GRCm39) missense possibly damaging 0.67
IGL01961:Syne1 APN 10 4,993,723 (GRCm39) missense possibly damaging 0.94
IGL01975:Syne1 APN 10 5,018,908 (GRCm39) intron probably benign
IGL02152:Syne1 APN 10 5,374,382 (GRCm39) missense probably damaging 1.00
IGL02423:Syne1 APN 10 5,318,295 (GRCm39) missense probably benign 0.00
IGL02457:Syne1 APN 10 5,292,167 (GRCm39) missense probably damaging 1.00
IGL02543:Syne1 APN 10 4,993,618 (GRCm39) missense probably damaging 0.97
IGL02836:Syne1 APN 10 5,359,875 (GRCm39) splice site probably benign
IGL03141:Syne1 APN 10 5,374,261 (GRCm39) missense probably damaging 1.00
FR4548:Syne1 UTSW 10 4,982,969 (GRCm39) missense probably benign 0.09
IGL02799:Syne1 UTSW 10 5,309,059 (GRCm39) missense probably damaging 1.00
PIT4305001:Syne1 UTSW 10 5,283,023 (GRCm39) missense probably damaging 1.00
PIT4687001:Syne1 UTSW 10 5,308,390 (GRCm39) missense possibly damaging 0.87
R0004:Syne1 UTSW 10 5,393,132 (GRCm39) splice site probably benign
R0110:Syne1 UTSW 10 5,317,600 (GRCm39) missense probably damaging 1.00
R0165:Syne1 UTSW 10 4,983,096 (GRCm39) missense probably benign 0.28
R0194:Syne1 UTSW 10 5,374,311 (GRCm39) missense probably benign
R0311:Syne1 UTSW 10 5,298,943 (GRCm39) missense possibly damaging 0.92
R0328:Syne1 UTSW 10 5,298,945 (GRCm39) missense possibly damaging 0.62
R0379:Syne1 UTSW 10 5,491,989 (GRCm39) missense probably damaging 1.00
R0387:Syne1 UTSW 10 5,301,029 (GRCm39) missense probably benign
R0452:Syne1 UTSW 10 5,355,435 (GRCm39) missense probably damaging 0.98
R0456:Syne1 UTSW 10 5,292,252 (GRCm39) missense probably benign 0.04
R0457:Syne1 UTSW 10 4,972,041 (GRCm39) missense probably damaging 1.00
R0469:Syne1 UTSW 10 5,317,600 (GRCm39) missense probably damaging 1.00
R0510:Syne1 UTSW 10 5,317,600 (GRCm39) missense probably damaging 1.00
R0533:Syne1 UTSW 10 5,308,438 (GRCm39) missense probably benign 0.00
R0617:Syne1 UTSW 10 5,300,933 (GRCm39) missense probably damaging 1.00
R0690:Syne1 UTSW 10 4,983,138 (GRCm39) splice site probably benign
R0964:Syne1 UTSW 10 4,993,652 (GRCm39) missense possibly damaging 0.95
R1133:Syne1 UTSW 10 5,299,044 (GRCm39) missense possibly damaging 0.77
R1327:Syne1 UTSW 10 4,998,925 (GRCm39) splice site probably benign
R1339:Syne1 UTSW 10 5,317,571 (GRCm39) missense probably damaging 1.00
R1531:Syne1 UTSW 10 5,297,875 (GRCm39) nonsense probably null
R1558:Syne1 UTSW 10 5,299,280 (GRCm39) nonsense probably null
R1633:Syne1 UTSW 10 5,299,388 (GRCm39) missense probably damaging 1.00
R1642:Syne1 UTSW 10 5,298,694 (GRCm39) missense possibly damaging 0.94
R1658:Syne1 UTSW 10 5,317,616 (GRCm39) missense probably benign 0.03
R1753:Syne1 UTSW 10 5,317,621 (GRCm39) missense probably benign 0.28
R1759:Syne1 UTSW 10 5,299,369 (GRCm39) missense probably damaging 1.00
R1792:Syne1 UTSW 10 4,990,975 (GRCm39) missense probably damaging 1.00
R2076:Syne1 UTSW 10 4,990,897 (GRCm39) missense probably damaging 0.99
R2079:Syne1 UTSW 10 5,311,502 (GRCm39) missense probably benign 0.01
R2102:Syne1 UTSW 10 5,006,514 (GRCm39) missense probably damaging 1.00
R2233:Syne1 UTSW 10 4,991,484 (GRCm39) missense probably benign 0.01
R2305:Syne1 UTSW 10 4,997,573 (GRCm39) missense probably damaging 0.97
R3435:Syne1 UTSW 10 5,298,565 (GRCm39) missense probably damaging 1.00
R3749:Syne1 UTSW 10 5,002,267 (GRCm39) splice site probably benign
R3876:Syne1 UTSW 10 5,002,345 (GRCm39) missense possibly damaging 0.57
R3895:Syne1 UTSW 10 5,355,456 (GRCm39) missense probably damaging 0.98
R3974:Syne1 UTSW 10 4,993,630 (GRCm39) missense probably benign 0.06
R4042:Syne1 UTSW 10 4,991,584 (GRCm39) missense probably benign 0.21
R4120:Syne1 UTSW 10 5,359,798 (GRCm39) missense probably damaging 1.00
R4201:Syne1 UTSW 10 5,297,870 (GRCm39) missense probably benign
R4364:Syne1 UTSW 10 5,303,987 (GRCm39) missense probably damaging 0.96
R4498:Syne1 UTSW 10 4,981,768 (GRCm39) missense probably benign 0.00
R4767:Syne1 UTSW 10 5,294,866 (GRCm39) nonsense probably null
R4804:Syne1 UTSW 10 5,299,310 (GRCm39) missense possibly damaging 0.95
R4917:Syne1 UTSW 10 5,007,909 (GRCm39) missense probably damaging 1.00
R4930:Syne1 UTSW 10 5,002,777 (GRCm39) missense probably damaging 0.99
R5081:Syne1 UTSW 10 4,997,767 (GRCm39) missense probably benign 0.04
R5089:Syne1 UTSW 10 5,355,444 (GRCm39) nonsense probably null
R5174:Syne1 UTSW 10 4,991,490 (GRCm39) missense probably damaging 0.99
R5205:Syne1 UTSW 10 5,002,295 (GRCm39) missense probably benign 0.05
R5303:Syne1 UTSW 10 5,370,464 (GRCm39) missense probably benign 0.00
R5384:Syne1 UTSW 10 4,991,494 (GRCm39) missense probably benign 0.00
R5385:Syne1 UTSW 10 4,991,494 (GRCm39) missense probably benign 0.00
R5392:Syne1 UTSW 10 5,298,661 (GRCm39) missense probably damaging 1.00
R5442:Syne1 UTSW 10 5,293,473 (GRCm39) missense probably benign 0.09
R5750:Syne1 UTSW 10 5,289,209 (GRCm39) missense probably benign 0.01
R5935:Syne1 UTSW 10 5,310,706 (GRCm39) splice site probably null
R6023:Syne1 UTSW 10 5,393,223 (GRCm39) missense probably benign 0.09
R6049:Syne1 UTSW 10 5,297,926 (GRCm39) missense possibly damaging 0.79
R6084:Syne1 UTSW 10 5,298,994 (GRCm39) missense probably damaging 1.00
R6145:Syne1 UTSW 10 5,002,750 (GRCm39) missense probably damaging 1.00
R6164:Syne1 UTSW 10 5,011,429 (GRCm39) missense probably damaging 1.00
R6165:Syne1 UTSW 10 5,375,678 (GRCm39) missense probably damaging 1.00
R6198:Syne1 UTSW 10 5,252,269 (GRCm39) missense probably damaging 0.99
R6217:Syne1 UTSW 10 5,243,761 (GRCm39) missense probably benign 0.00
R6247:Syne1 UTSW 10 5,299,071 (GRCm39) missense probably damaging 0.98
R6271:Syne1 UTSW 10 5,184,652 (GRCm39) missense probably damaging 1.00
R6338:Syne1 UTSW 10 5,205,475 (GRCm39) missense probably benign 0.00
R6344:Syne1 UTSW 10 4,972,212 (GRCm39) missense probably benign 0.08
R6434:Syne1 UTSW 10 5,268,422 (GRCm39) missense probably benign 0.01
R6476:Syne1 UTSW 10 5,104,531 (GRCm39) missense possibly damaging 0.88
R6479:Syne1 UTSW 10 5,406,826 (GRCm39) missense probably damaging 1.00
R6479:Syne1 UTSW 10 5,181,679 (GRCm39) nonsense probably null
R6546:Syne1 UTSW 10 5,168,645 (GRCm39) nonsense probably null
R6578:Syne1 UTSW 10 5,355,454 (GRCm39) nonsense probably null
R6611:Syne1 UTSW 10 4,995,273 (GRCm39) missense probably benign 0.01
R6615:Syne1 UTSW 10 5,251,340 (GRCm39) missense probably damaging 0.98
R6632:Syne1 UTSW 10 5,165,667 (GRCm39) critical splice donor site probably null
R6662:Syne1 UTSW 10 5,078,416 (GRCm39) missense probably damaging 1.00
R6677:Syne1 UTSW 10 4,990,942 (GRCm39) missense possibly damaging 0.82
R6764:Syne1 UTSW 10 5,179,011 (GRCm39) nonsense probably null
R6765:Syne1 UTSW 10 5,093,285 (GRCm39) splice site probably null
R6778:Syne1 UTSW 10 5,052,406 (GRCm39) missense probably damaging 0.97
R6851:Syne1 UTSW 10 5,212,703 (GRCm39) nonsense probably null
R6878:Syne1 UTSW 10 5,370,388 (GRCm39) missense possibly damaging 0.78
R6883:Syne1 UTSW 10 5,181,704 (GRCm39) nonsense probably null
R6910:Syne1 UTSW 10 4,998,887 (GRCm39) missense probably benign 0.01
R6916:Syne1 UTSW 10 5,177,912 (GRCm39) missense probably benign 0.00
R6925:Syne1 UTSW 10 5,076,682 (GRCm39) missense probably benign 0.00
R6943:Syne1 UTSW 10 5,033,940 (GRCm39) missense probably benign
R6947:Syne1 UTSW 10 5,125,789 (GRCm39) missense probably damaging 1.00
R6965:Syne1 UTSW 10 5,179,120 (GRCm39) missense possibly damaging 0.66
R6968:Syne1 UTSW 10 5,067,041 (GRCm39) missense probably benign 0.09
R7043:Syne1 UTSW 10 5,022,193 (GRCm39) missense possibly damaging 0.77
R7059:Syne1 UTSW 10 5,296,859 (GRCm39) missense probably damaging 1.00
R7067:Syne1 UTSW 10 5,184,586 (GRCm39) missense probably damaging 1.00
R7087:Syne1 UTSW 10 5,492,024 (GRCm39) start gained probably benign
R7099:Syne1 UTSW 10 5,073,744 (GRCm39) missense probably benign 0.43
R7107:Syne1 UTSW 10 5,082,078 (GRCm39) missense probably damaging 1.00
R7120:Syne1 UTSW 10 5,243,971 (GRCm39) missense probably benign
R7127:Syne1 UTSW 10 5,193,180 (GRCm39) missense probably damaging 1.00
R7128:Syne1 UTSW 10 5,193,180 (GRCm39) missense probably damaging 1.00
R7131:Syne1 UTSW 10 5,178,221 (GRCm39) missense probably damaging 1.00
R7132:Syne1 UTSW 10 5,193,180 (GRCm39) missense probably damaging 1.00
R7133:Syne1 UTSW 10 5,181,592 (GRCm39) missense probably damaging 1.00
R7135:Syne1 UTSW 10 5,183,409 (GRCm39) missense probably benign 0.01
R7147:Syne1 UTSW 10 5,199,340 (GRCm39) missense probably damaging 1.00
R7158:Syne1 UTSW 10 5,007,931 (GRCm39) missense probably damaging 1.00
R7189:Syne1 UTSW 10 5,374,295 (GRCm39) missense probably benign 0.03
R7193:Syne1 UTSW 10 5,183,406 (GRCm39) missense probably damaging 1.00
R7194:Syne1 UTSW 10 5,060,859 (GRCm39) missense probably damaging 1.00
R7233:Syne1 UTSW 10 5,252,160 (GRCm39) missense probably damaging 1.00
R7255:Syne1 UTSW 10 5,283,446 (GRCm39) missense probably damaging 0.98
R7267:Syne1 UTSW 10 5,178,218 (GRCm39) missense probably damaging 1.00
R7294:Syne1 UTSW 10 5,047,483 (GRCm39) critical splice donor site probably null
R7303:Syne1 UTSW 10 5,206,805 (GRCm39) missense probably benign 0.04
R7313:Syne1 UTSW 10 4,997,635 (GRCm39) missense probably damaging 1.00
R7330:Syne1 UTSW 10 5,078,434 (GRCm39) missense probably benign 0.00
R7334:Syne1 UTSW 10 5,007,886 (GRCm39) missense probably damaging 1.00
R7363:Syne1 UTSW 10 5,090,970 (GRCm39) missense possibly damaging 0.45
R7400:Syne1 UTSW 10 5,168,580 (GRCm39) missense probably benign 0.12
R7425:Syne1 UTSW 10 5,375,760 (GRCm39) missense probably damaging 1.00
R7427:Syne1 UTSW 10 5,223,718 (GRCm39) missense probably damaging 0.98
R7446:Syne1 UTSW 10 5,172,266 (GRCm39) missense probably benign 0.00
R7462:Syne1 UTSW 10 5,002,793 (GRCm39) missense possibly damaging 0.87
R7502:Syne1 UTSW 10 5,283,446 (GRCm39) missense probably damaging 0.98
R7525:Syne1 UTSW 10 5,135,559 (GRCm39) critical splice acceptor site probably null
R7529:Syne1 UTSW 10 5,374,382 (GRCm39) missense probably damaging 1.00
R7577:Syne1 UTSW 10 5,074,820 (GRCm39) missense probably damaging 1.00
R7579:Syne1 UTSW 10 5,299,324 (GRCm39) missense probably damaging 1.00
R7594:Syne1 UTSW 10 5,165,190 (GRCm39) critical splice donor site probably null
R7646:Syne1 UTSW 10 5,122,949 (GRCm39) missense probably damaging 1.00
R7651:Syne1 UTSW 10 5,293,416 (GRCm39) missense probably damaging 1.00
R7651:Syne1 UTSW 10 5,155,074 (GRCm39) missense probably benign 0.38
R7669:Syne1 UTSW 10 5,011,531 (GRCm39) missense probably damaging 1.00
R7672:Syne1 UTSW 10 5,168,527 (GRCm39) missense probably benign 0.02
R7682:Syne1 UTSW 10 5,112,461 (GRCm39) missense probably benign
R7702:Syne1 UTSW 10 5,195,835 (GRCm39) missense probably damaging 1.00
R7767:Syne1 UTSW 10 5,283,632 (GRCm39) missense possibly damaging 0.49
R7767:Syne1 UTSW 10 5,283,560 (GRCm39) missense possibly damaging 0.60
R7829:Syne1 UTSW 10 5,292,293 (GRCm39) missense probably damaging 0.96
R7840:Syne1 UTSW 10 5,082,078 (GRCm39) missense probably damaging 1.00
R7859:Syne1 UTSW 10 5,107,683 (GRCm39) missense possibly damaging 0.80
R7899:Syne1 UTSW 10 5,177,956 (GRCm39) nonsense probably null
R7918:Syne1 UTSW 10 5,309,078 (GRCm39) missense possibly damaging 0.50
R7923:Syne1 UTSW 10 5,214,738 (GRCm39) missense probably damaging 1.00
R7946:Syne1 UTSW 10 5,200,919 (GRCm39) missense possibly damaging 0.92
R7966:Syne1 UTSW 10 5,066,965 (GRCm39) critical splice donor site probably null
R7975:Syne1 UTSW 10 4,981,786 (GRCm39) missense probably benign 0.00
R7981:Syne1 UTSW 10 5,179,248 (GRCm39) missense probably benign 0.04
R8053:Syne1 UTSW 10 5,002,658 (GRCm39) nonsense probably null
R8054:Syne1 UTSW 10 5,220,970 (GRCm39) missense probably benign 0.22
R8062:Syne1 UTSW 10 5,135,394 (GRCm39) critical splice donor site probably null
R8085:Syne1 UTSW 10 5,178,021 (GRCm39) missense possibly damaging 0.78
R8087:Syne1 UTSW 10 5,283,034 (GRCm39) missense probably benign
R8094:Syne1 UTSW 10 5,067,031 (GRCm39) missense probably damaging 0.98
R8310:Syne1 UTSW 10 5,297,829 (GRCm39) missense probably benign
R8325:Syne1 UTSW 10 5,096,257 (GRCm39) missense probably benign 0.15
R8342:Syne1 UTSW 10 5,058,622 (GRCm39) missense probably benign 0.18
R8353:Syne1 UTSW 10 5,300,983 (GRCm39) missense probably damaging 1.00
R8376:Syne1 UTSW 10 4,993,615 (GRCm39) missense probably benign 0.09
R8398:Syne1 UTSW 10 5,074,923 (GRCm39) missense probably damaging 1.00
R8434:Syne1 UTSW 10 5,073,057 (GRCm39) missense probably benign 0.00
R8436:Syne1 UTSW 10 5,178,659 (GRCm39) missense probably benign 0.26
R8459:Syne1 UTSW 10 5,374,277 (GRCm39) nonsense probably null
R8461:Syne1 UTSW 10 5,011,463 (GRCm39) missense probably benign 0.34
R8496:Syne1 UTSW 10 5,268,441 (GRCm39) missense probably damaging 0.99
R8496:Syne1 UTSW 10 5,178,896 (GRCm39) missense probably damaging 0.99
R8693:Syne1 UTSW 10 5,090,928 (GRCm39) missense possibly damaging 0.60
R8698:Syne1 UTSW 10 5,179,229 (GRCm39) missense probably damaging 1.00
R8701:Syne1 UTSW 10 5,155,026 (GRCm39) nonsense probably null
R8713:Syne1 UTSW 10 5,266,040 (GRCm39) missense probably damaging 1.00
R8724:Syne1 UTSW 10 5,033,861 (GRCm39) missense possibly damaging 0.77
R8729:Syne1 UTSW 10 5,179,275 (GRCm39) missense probably benign 0.00
R8742:Syne1 UTSW 10 5,058,661 (GRCm39) missense probably benign 0.09
R8757:Syne1 UTSW 10 5,144,618 (GRCm39) missense probably damaging 1.00
R8776:Syne1 UTSW 10 5,181,783 (GRCm39) missense possibly damaging 0.81
R8776-TAIL:Syne1 UTSW 10 5,181,783 (GRCm39) missense possibly damaging 0.81
R8778:Syne1 UTSW 10 5,309,066 (GRCm39) missense probably benign 0.00
R8801:Syne1 UTSW 10 5,308,335 (GRCm39) missense probably damaging 1.00
R8803:Syne1 UTSW 10 5,311,535 (GRCm39) missense probably damaging 1.00
R8808:Syne1 UTSW 10 5,309,074 (GRCm39) missense probably damaging 1.00
R8829:Syne1 UTSW 10 5,058,685 (GRCm39) missense probably benign
R8843:Syne1 UTSW 10 5,143,040 (GRCm39) missense possibly damaging 0.88
R8843:Syne1 UTSW 10 5,280,204 (GRCm39) missense probably benign 0.01
R8854:Syne1 UTSW 10 5,078,503 (GRCm39) missense probably benign 0.00
R8863:Syne1 UTSW 10 5,049,527 (GRCm39) missense probably damaging 1.00
R8864:Syne1 UTSW 10 5,370,473 (GRCm39) missense probably benign 0.01
R8881:Syne1 UTSW 10 5,223,639 (GRCm39) missense probably damaging 1.00
R8884:Syne1 UTSW 10 5,181,822 (GRCm39) missense possibly damaging 0.93
R8893:Syne1 UTSW 10 5,299,020 (GRCm39) nonsense probably null
R8958:Syne1 UTSW 10 5,181,768 (GRCm39) missense probably benign
R8964:Syne1 UTSW 10 5,060,872 (GRCm39) missense
R8975:Syne1 UTSW 10 5,161,945 (GRCm39) missense probably benign 0.04
R8987:Syne1 UTSW 10 5,177,579 (GRCm39) missense possibly damaging 0.92
R8992:Syne1 UTSW 10 5,135,508 (GRCm39) missense probably benign 0.01
R9005:Syne1 UTSW 10 5,155,406 (GRCm39) missense probably benign
R9084:Syne1 UTSW 10 5,289,240 (GRCm39) missense probably benign 0.01
R9117:Syne1 UTSW 10 5,053,667 (GRCm39) missense probably damaging 0.96
R9128:Syne1 UTSW 10 5,058,556 (GRCm39) missense probably benign 0.38
R9181:Syne1 UTSW 10 5,063,994 (GRCm39) missense probably damaging 0.99
R9189:Syne1 UTSW 10 5,172,289 (GRCm39) missense probably benign 0.00
R9189:Syne1 UTSW 10 5,123,008 (GRCm39) missense probably damaging 1.00
R9205:Syne1 UTSW 10 5,152,013 (GRCm39) nonsense probably null
R9217:Syne1 UTSW 10 5,299,324 (GRCm39) missense probably damaging 1.00
R9246:Syne1 UTSW 10 5,255,706 (GRCm39) missense probably benign 0.00
R9264:Syne1 UTSW 10 5,212,793 (GRCm39) missense probably damaging 1.00
R9273:Syne1 UTSW 10 4,990,901 (GRCm39) missense probably benign 0.16
R9315:Syne1 UTSW 10 5,283,553 (GRCm39) missense possibly damaging 0.79
R9331:Syne1 UTSW 10 5,073,666 (GRCm39) missense probably benign 0.45
R9355:Syne1 UTSW 10 5,318,255 (GRCm39) missense probably damaging 1.00
R9378:Syne1 UTSW 10 5,200,954 (GRCm39) missense probably damaging 0.96
R9389:Syne1 UTSW 10 5,179,193 (GRCm39) missense possibly damaging 0.65
R9395:Syne1 UTSW 10 5,261,728 (GRCm39) missense probably damaging 1.00
R9405:Syne1 UTSW 10 5,152,030 (GRCm39) missense probably damaging 1.00
R9417:Syne1 UTSW 10 5,082,021 (GRCm39) missense probably benign
R9419:Syne1 UTSW 10 5,155,071 (GRCm39) missense probably benign 0.01
R9473:Syne1 UTSW 10 5,198,258 (GRCm39) missense probably benign 0.00
R9484:Syne1 UTSW 10 5,170,359 (GRCm39) missense probably damaging 1.00
R9505:Syne1 UTSW 10 4,980,394 (GRCm39) missense probably benign 0.00
R9509:Syne1 UTSW 10 5,298,927 (GRCm39) critical splice donor site probably null
R9546:Syne1 UTSW 10 5,193,123 (GRCm39) missense probably damaging 1.00
R9567:Syne1 UTSW 10 5,196,386 (GRCm39) missense possibly damaging 0.54
R9601:Syne1 UTSW 10 5,209,270 (GRCm39) missense probably benign 0.23
R9619:Syne1 UTSW 10 5,090,909 (GRCm39) missense probably benign 0.03
R9621:Syne1 UTSW 10 5,273,887 (GRCm39) missense probably benign 0.01
R9623:Syne1 UTSW 10 5,152,009 (GRCm39) missense probably damaging 1.00
R9646:Syne1 UTSW 10 5,179,187 (GRCm39) missense possibly damaging 0.95
R9666:Syne1 UTSW 10 4,984,937 (GRCm39) missense probably damaging 1.00
R9677:Syne1 UTSW 10 5,215,125 (GRCm39) missense probably damaging 1.00
R9695:Syne1 UTSW 10 5,268,461 (GRCm39) missense probably benign 0.03
R9696:Syne1 UTSW 10 5,297,847 (GRCm39) missense probably benign 0.00
R9719:Syne1 UTSW 10 5,276,601 (GRCm39) missense possibly damaging 0.47
R9744:Syne1 UTSW 10 5,274,184 (GRCm39) missense probably benign 0.01
R9761:Syne1 UTSW 10 5,318,190 (GRCm39) critical splice donor site probably null
R9763:Syne1 UTSW 10 5,007,858 (GRCm39) missense probably benign 0.31
RF010:Syne1 UTSW 10 5,196,386 (GRCm39) missense possibly damaging 0.89
RF015:Syne1 UTSW 10 5,252,248 (GRCm39) missense probably benign 0.01
RF023:Syne1 UTSW 10 5,205,482 (GRCm39) missense probably damaging 1.00
X0017:Syne1 UTSW 10 5,296,917 (GRCm39) missense probably damaging 1.00
X0025:Syne1 UTSW 10 5,308,973 (GRCm39) nonsense probably null
X0063:Syne1 UTSW 10 5,002,354 (GRCm39) missense probably damaging 1.00
Z1176:Syne1 UTSW 10 5,280,251 (GRCm39) missense probably benign 0.10
Z1176:Syne1 UTSW 10 5,209,280 (GRCm39) missense probably benign
Z1176:Syne1 UTSW 10 5,198,364 (GRCm39) missense probably damaging 0.96
Z1177:Syne1 UTSW 10 5,209,349 (GRCm39) missense probably damaging 1.00
Z1177:Syne1 UTSW 10 5,093,230 (GRCm39) missense possibly damaging 0.78
Predicted Primers PCR Primer
(F):5'- GCTGACCATCTTTGGACTTTAGAC -3'
(R):5'- AGTGTCCTTTCATTCCAGGAGATC -3'

Sequencing Primer
(F):5'- TTAACTTGAACTACCCAGGCAGTAG -3'
(R):5'- CCTTTCATTCCAGGAGATCAGAAATG -3'
Posted On 2017-06-26