Incidental Mutation 'IGL02471:Snx24'
ID294751
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Snx24
Ensembl Gene ENSMUSG00000024535
Gene Namesorting nexing 24
Synonyms2810011K15Rik, 5730433I16Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.084) question?
Stock #IGL02471
Quality Score
Status
Chromosome18
Chromosomal Location53245662-53390823 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) C to T at 53385169 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000131423 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025417] [ENSMUST00000165032]
Predicted Effect probably benign
Transcript: ENSMUST00000025417
SMART Domains Protein: ENSMUSP00000025417
Gene: ENSMUSG00000024535

DomainStartEndE-ValueType
PX 1 103 4.19e-10 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000165032
SMART Domains Protein: ENSMUSP00000131423
Gene: ENSMUSG00000024535

DomainStartEndE-ValueType
PX 1 103 4.19e-10 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 G T 1: 71,258,198 H2378N probably benign Het
Btaf1 C A 19: 37,000,192 A1470E probably damaging Het
Ccdc110 A G 8: 45,941,756 D228G probably benign Het
Cdc45 C T 16: 18,798,729 M200I probably benign Het
Cldn18 T C 9: 99,696,075 D205G probably benign Het
Clip2 T C 5: 134,518,022 T231A probably benign Het
Cltc A G 11: 86,718,034 V723A probably damaging Het
Cpa3 C T 3: 20,228,807 probably null Het
Cyfip2 T G 11: 46,200,803 T1097P possibly damaging Het
Dnah9 T A 11: 65,947,618 R667* probably null Het
Dock10 T C 1: 80,515,622 E1878G probably damaging Het
Ermap G A 4: 119,179,963 H353Y probably damaging Het
Etfa A T 9: 55,486,700 probably null Het
F5 C T 1: 164,174,291 P188S probably damaging Het
Foxq1 G A 13: 31,559,343 E143K possibly damaging Het
Gsr C T 8: 33,682,584 probably benign Het
Hebp1 T A 6: 135,155,276 Y31F probably benign Het
Ighv1-14 T C 12: 114,646,837 noncoding transcript Het
Lamb1 T A 12: 31,320,908 D1319E probably damaging Het
Lrp5 A T 19: 3,602,408 V1154E probably benign Het
Manba G A 3: 135,507,008 probably benign Het
Mknk2 A T 10: 80,668,121 F319I probably damaging Het
Mup6 A T 4: 60,003,971 probably benign Het
Nalcn T C 14: 123,323,314 T784A probably benign Het
Nt5dc1 T C 10: 34,403,725 E107G probably benign Het
Olfr1497 G A 19: 13,795,225 P129S probably damaging Het
Olfr688 T A 7: 105,289,045 F317L probably benign Het
Olfr745 A T 14: 50,642,757 I159F probably benign Het
Phldb1 T C 9: 44,711,233 E41G probably damaging Het
Ptk2 T C 15: 73,298,187 D309G probably benign Het
Rab11fip5 A G 6: 85,348,225 S367P probably damaging Het
Rb1cc1 T A 1: 6,240,051 N224K probably benign Het
Rchy1 A T 5: 91,957,546 C65* probably null Het
Rgs18 T C 1: 144,774,621 D56G probably benign Het
Rtraf A C 14: 19,812,228 L197R probably damaging Het
Slc44a5 G T 3: 154,256,576 W382L probably damaging Het
Sphkap T C 1: 83,276,176 D1284G probably damaging Het
Tmem54 A G 4: 129,108,318 M53V probably benign Het
Trip6 G A 5: 137,310,356 P414S probably benign Het
Vmn1r38 A G 6: 66,776,767 Y122H probably benign Het
Wapl T A 14: 34,691,920 N246K possibly damaging Het
Zfp12 G A 5: 143,244,796 G293R probably damaging Het
Zfp13 C T 17: 23,576,098 A493T probably benign Het
Zfp446 T G 7: 12,982,254 V209G probably benign Het
Zfp518a G A 19: 40,914,617 G997R probably damaging Het
Other mutations in Snx24
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00731:Snx24 APN 18 53384609 splice site probably benign
IGL02704:Snx24 APN 18 53327437 missense probably benign
R1645:Snx24 UTSW 18 53389562 missense probably benign
R4900:Snx24 UTSW 18 53385223 nonsense probably null
R5307:Snx24 UTSW 18 53340211 nonsense probably null
R7039:Snx24 UTSW 18 53340235 critical splice donor site probably null
R7299:Snx24 UTSW 18 53340172 missense probably damaging 1.00
R7301:Snx24 UTSW 18 53340172 missense probably damaging 1.00
R7805:Snx24 UTSW 18 53389551 missense probably benign 0.22
Posted On2015-04-16