Incidental Mutation 'IGL00731:Snx24'
ID14179
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: 0.074) question?
Stock #IGL00731
Quality Score
Status
Chromosome18
Chromosomal Location53245662-53390823 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) C to T at 53384609 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: 18 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars A G 8: 111,044,869 probably benign Het
Adcy10 T C 1: 165,572,614 F1531L probably benign Het
Dab2 T C 15: 6,435,710 S463P possibly damaging Het
Ehf C T 2: 103,266,840 probably null Het
Fnbp4 G T 2: 90,768,643 V704L probably benign Het
Gbp7 T C 3: 142,546,428 S591P probably benign Het
Gpr155 A G 2: 73,362,613 L498P probably damaging Het
Igll1 T C 16: 16,860,919 T176A probably benign Het
Klk1b21 A G 7: 44,105,923 E182G possibly damaging Het
Mb21d1 G A 9: 78,435,488 P344L probably damaging Het
Npat G A 9: 53,562,086 E393K probably damaging Het
Npnt C T 3: 132,904,657 probably null Het
Pde2a A G 7: 101,508,099 Y693C probably benign Het
Ralgapa1 A G 12: 55,702,452 S1269P possibly damaging Het
Rasal2 A C 1: 157,157,764 D804E probably benign Het
Rdh10 A G 1: 16,107,875 N124D probably benign Het
Slit3 G T 11: 35,622,154 D536Y probably damaging Het
Spink12 G A 18: 44,108,110 probably benign Het
Other mutations in Snx24
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02471:Snx24 APN 18 53385169 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 On2012-12-06