Incidental Mutation 'R4767:Syne1'
ID 366226
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 042408-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R4767 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 4970917-5501482 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 5294866 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 1246 (K1246*)
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
AA Change: K1246*
SMART Domains Protein: ENSMUSP00000039440
Gene: ENSMUSG00000096054
AA Change: K1246*

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
AA Change: K1246*
Predicted Effect noncoding transcript
Transcript: ENSMUST00000215887
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 94.3%
Validation Efficiency 95% (62/65)
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: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam19 T C 11: 46,029,804 (GRCm39) probably null Het
Aig1 T C 10: 13,677,602 (GRCm39) N130S probably damaging Het
Alx1 A T 10: 102,861,047 (GRCm39) Y160* probably null Het
Ap4e1 T C 2: 126,902,358 (GRCm39) I755T probably benign Het
Apoc3 C A 9: 46,145,833 (GRCm39) E21* probably null Het
Atp9b G T 18: 80,796,285 (GRCm39) H919Q probably damaging Het
Cemip T G 7: 83,622,514 (GRCm39) Y555S probably damaging Het
Cic T C 7: 24,971,025 (GRCm39) V252A possibly damaging Het
Cracr2a A T 6: 127,588,470 (GRCm39) N210Y probably damaging Het
Crocc2 G A 1: 93,130,578 (GRCm39) R953Q possibly damaging Het
Csnk1d A G 11: 120,859,954 (GRCm39) S318P probably benign Het
Ddx21 A G 10: 62,427,751 (GRCm39) L384P probably damaging Het
Dnah5 C T 15: 28,270,620 (GRCm39) T974I probably benign Het
Duox1 A G 2: 122,163,922 (GRCm39) Y863C possibly damaging Het
Epg5 C A 18: 78,066,498 (GRCm39) P2133T possibly damaging Het
Ephb6 A T 6: 41,591,119 (GRCm39) Q92L possibly damaging Het
Ercc4 C A 16: 12,939,959 (GRCm39) A73D probably damaging Het
Eva1c A T 16: 90,701,235 (GRCm39) Y290F probably damaging Het
Galnt5 T A 2: 57,918,156 (GRCm39) V798E possibly damaging Het
Haus4 T C 14: 54,786,342 (GRCm39) E149G probably damaging Het
Ighv1-13 A G 12: 114,594,556 (GRCm39) Y86C unknown Het
Igkv9-120 G T 6: 68,027,351 (GRCm39) R88S possibly damaging Het
Lama3 T C 18: 12,633,620 (GRCm39) V1584A probably benign Het
Lamb1 A G 12: 31,358,010 (GRCm39) E1119G probably damaging Het
Lao1 T C 4: 118,825,185 (GRCm39) L335P probably damaging Het
Mindy4 A G 6: 55,237,550 (GRCm39) D375G probably damaging Het
Myo5a T C 9: 75,051,358 (GRCm39) I317T probably damaging Het
Nhlrc2 G A 19: 56,558,898 (GRCm39) V128I probably benign Het
Nlrp2 C T 7: 5,331,023 (GRCm39) D458N probably damaging Het
Or1j18 A T 2: 36,624,335 (GRCm39) M1L probably benign Het
Or1o1 T A 17: 37,717,091 (GRCm39) C217* probably null Het
Or5a1 G T 19: 12,097,300 (GRCm39) H247N probably damaging Het
Or8g24 T C 9: 38,989,988 (GRCm39) T18A possibly damaging Het
Or9q2 A T 19: 13,772,409 (GRCm39) C189S probably damaging Het
Parp8 T C 13: 117,005,072 (GRCm39) H663R probably damaging Het
Pax6 T C 2: 105,525,705 (GRCm39) S377P probably benign Het
Pi15 A G 1: 17,672,990 (GRCm39) D63G probably benign Het
Plaa A G 4: 94,474,495 (GRCm39) probably benign Het
Rbm5 C A 9: 107,622,412 (GRCm39) W546C probably damaging Het
Rnf123 C A 9: 107,929,288 (GRCm39) C1257F probably damaging Het
Rnf185 A G 11: 3,382,551 (GRCm39) S45P possibly damaging Het
Sh3bp1 T C 15: 78,788,697 (GRCm39) S241P possibly damaging Het
Slfn8 G A 11: 82,894,023 (GRCm39) A872V possibly damaging Het
Smoc1 G A 12: 81,151,547 (GRCm39) probably null Het
Sox14 A T 9: 99,757,686 (GRCm39) W18R probably damaging Het
Spata31d1a T C 13: 59,848,969 (GRCm39) E1053G probably benign Het
Tbrg4 A C 11: 6,570,909 (GRCm39) S188A probably benign Het
Thnsl2 A T 6: 71,111,279 (GRCm39) D196E probably damaging Het
Tmem266 C T 9: 55,288,025 (GRCm39) T34I probably damaging Het
Tmem59l C A 8: 70,938,748 (GRCm39) R111L probably benign Het
Tpr T C 1: 150,306,280 (GRCm39) probably benign Het
Trpc6 T C 9: 8,643,687 (GRCm39) S491P probably damaging Het
Tspan10 A T 11: 120,336,992 (GRCm39) N254I probably damaging Het
Ubox5 A T 2: 130,433,814 (GRCm39) L511Q probably damaging Het
Vmn1r183 TATCCATC TATC 7: 23,754,531 (GRCm39) probably null Het
Vmn2r4 C T 3: 64,298,397 (GRCm39) C577Y probably damaging Het
Vmn2r86 A T 10: 130,291,606 (GRCm39) M53K probably benign Het
Zfp948 T A 17: 21,808,569 (GRCm39) I587N possibly 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
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
R6015:Syne1 UTSW 10 5,296,819 (GRCm39) critical splice donor 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'- AGCACAGAACTGCAAAGTGC -3'
(R):5'- TATAGCTTAGCTGTAGGCAAGGTC -3'

Sequencing Primer
(F):5'- AAAGTGCTTTGAGCTATCAGCCC -3'
(R):5'- GGCAAGGTCAATTTGTCACC -3'
Posted On 2015-12-21