Incidental Mutation 'R6595:Svopl'
ID 526391
Institutional Source Beutler Lab
Gene Symbol Svopl
Ensembl Gene ENSMUSG00000029830
Gene Name SV2 related protein homolog (rat)-like
Synonyms 9430071P14Rik
MMRRC Submission 044719-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R6595 (G1)
Quality Score 225.009
Status Not validated
Chromosome 6
Chromosomal Location 37960674-38023931 bp(-) (GRCm39)
Type of Mutation splice site (4 bp from exon)
DNA Base Change (assembly) T to C at 38018002 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000093743 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096040]
AlphaFold Q6PDF3
Predicted Effect noncoding transcript
Transcript: ENSMUST00000040486
Predicted Effect probably null
Transcript: ENSMUST00000096040
SMART Domains Protein: ENSMUSP00000093743
Gene: ENSMUSG00000029830

DomainStartEndE-ValueType
Pfam:Sugar_tr 17 297 5.5e-20 PFAM
Pfam:MFS_1 50 308 2.1e-20 PFAM
transmembrane domain 349 371 N/A INTRINSIC
transmembrane domain 384 406 N/A INTRINSIC
transmembrane domain 459 481 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.5%
Validation Efficiency 97% (37/38)
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 thought to be a member of solute carrier family 22, which includes transmembrane proteins that transport toxins and drugs from the body. This gene is a paralog of the SVOP gene that encodes synaptic vesicle 2-related protein. [provided by RefSeq, Sep 2016]
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 A T 7: 119,993,710 (GRCm39) Y1310F probably benign Het
Ankrd54 A G 15: 78,942,185 (GRCm39) F148L probably damaging Het
Bag4 C T 8: 26,259,528 (GRCm39) D224N probably damaging Het
Bhlhe40 TG TGG 6: 108,641,818 (GRCm39) 254 probably null Het
Camk2b A T 11: 5,942,856 (GRCm39) H126Q probably damaging Het
Camsap3 G T 8: 3,654,186 (GRCm39) V608L probably damaging Het
Camsap3 A T 8: 3,658,742 (GRCm39) M796L probably damaging Het
Cdh19 T C 1: 110,853,517 (GRCm39) D308G probably benign Het
Cfap299 A T 5: 98,949,717 (GRCm39) D217V possibly damaging Het
Cpsf1 T C 15: 76,486,710 (GRCm39) I275M probably damaging Het
Cuta A G 17: 27,157,856 (GRCm39) probably null Het
Dclk2 A G 3: 86,699,374 (GRCm39) probably benign Het
Dst T G 1: 34,289,761 (GRCm39) L784R probably damaging Het
Fbn1 T C 2: 125,184,750 (GRCm39) M1681V possibly damaging Het
Fbxo9 A T 9: 77,994,494 (GRCm39) D274E probably damaging Het
Frem2 T A 3: 53,457,205 (GRCm39) D2049V probably damaging Het
Fscn3 T C 6: 28,430,174 (GRCm39) Y115H probably damaging Het
Glp2r G T 11: 67,655,603 (GRCm39) D46E probably benign Het
Gpat2 G C 2: 127,273,838 (GRCm39) G294R possibly damaging Het
Irx5 A G 8: 93,086,247 (GRCm39) Y110C probably damaging Het
Kdm5d T C Y: 939,829 (GRCm39) S994P probably benign Homo
Klhl2 A T 8: 65,196,077 (GRCm39) C555* probably null Het
Krtap4-7 A T 11: 99,534,560 (GRCm39) I101N unknown Het
Or13a27 A G 7: 139,925,560 (GRCm39) L114P probably damaging Het
Or4f57 A T 2: 111,790,515 (GRCm39) V301E possibly damaging Het
Pcdhb21 T C 18: 37,648,961 (GRCm39) S697P probably damaging Het
Pramel27 T C 4: 143,579,326 (GRCm39) C304R probably damaging Het
Rasgrf2 A T 13: 92,167,361 (GRCm39) H237Q probably damaging Het
Rnf216 A T 5: 143,076,412 (GRCm39) D157E probably benign Het
Rxrg T A 1: 167,454,905 (GRCm39) F163I probably damaging Het
Soat2 T A 15: 102,069,028 (GRCm39) I351N probably damaging Het
Srp72 C T 5: 77,132,047 (GRCm39) T242I probably benign Het
Tbc1d2b G A 9: 90,108,145 (GRCm39) P469S probably benign Het
Tbkbp1 G A 11: 97,029,578 (GRCm39) probably benign Het
Tecta A G 9: 42,295,523 (GRCm39) V324A probably damaging Het
Twnk T C 19: 44,998,931 (GRCm39) V557A probably damaging Het
Vmn2r18 G A 5: 151,485,889 (GRCm39) T535I probably damaging Het
Zc3h14 T A 12: 98,723,285 (GRCm39) S85T probably damaging Het
Other mutations in Svopl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00742:Svopl APN 6 38,007,952 (GRCm39) critical splice donor site probably null
IGL01531:Svopl APN 6 38,003,876 (GRCm39) splice site probably benign
IGL02161:Svopl APN 6 38,013,750 (GRCm39) splice site probably benign
IGL02554:Svopl APN 6 37,993,978 (GRCm39) missense probably damaging 0.99
IGL03249:Svopl APN 6 37,993,988 (GRCm39) missense probably benign 0.05
PIT4434001:Svopl UTSW 6 37,991,801 (GRCm39) missense possibly damaging 0.85
R0285:Svopl UTSW 6 37,961,457 (GRCm39) missense probably benign 0.02
R0423:Svopl UTSW 6 38,013,642 (GRCm39) splice site probably benign
R0692:Svopl UTSW 6 37,994,131 (GRCm39) missense probably damaging 1.00
R0960:Svopl UTSW 6 37,993,992 (GRCm39) nonsense probably null
R1163:Svopl UTSW 6 38,006,635 (GRCm39) missense possibly damaging 0.89
R1526:Svopl UTSW 6 38,006,570 (GRCm39) missense probably benign 0.03
R2295:Svopl UTSW 6 37,996,668 (GRCm39) missense possibly damaging 0.52
R2302:Svopl UTSW 6 38,018,101 (GRCm39) splice site probably benign
R5933:Svopl UTSW 6 37,993,949 (GRCm39) splice site probably benign
R6367:Svopl UTSW 6 37,996,614 (GRCm39) missense possibly damaging 0.88
R6903:Svopl UTSW 6 37,998,543 (GRCm39) missense probably benign 0.00
R7980:Svopl UTSW 6 37,991,744 (GRCm39) missense probably damaging 0.98
R8167:Svopl UTSW 6 37,993,979 (GRCm39) missense probably damaging 1.00
R8218:Svopl UTSW 6 37,991,741 (GRCm39) missense probably benign
R9046:Svopl UTSW 6 37,998,531 (GRCm39) missense probably benign 0.02
Z1177:Svopl UTSW 6 38,006,646 (GRCm39) missense probably damaging 1.00
Predicted Primers
Posted On 2018-06-25