Incidental Mutation 'IGL02145:Tspan15'
ID 281734
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tspan15
Ensembl Gene ENSMUSG00000037031
Gene Name tetraspanin 15
Synonyms Tm4sf15, 2700063A19Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # IGL02145
Quality Score
Status
Chromosome 10
Chromosomal Location 62021175-62067030 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 62029751 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000047029 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000047883]
AlphaFold F7BWT7
Predicted Effect probably benign
Transcript: ENSMUST00000047883
SMART Domains Protein: ENSMUSP00000047029
Gene: ENSMUSG00000037031

DomainStartEndE-ValueType
Pfam:Tetraspannin 18 259 1.1e-52 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184761
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218824
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219106
Predicted Effect noncoding transcript
Transcript: ENSMUST00000220143
Coding Region Coverage
Validation Efficiency
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 a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. The use of alternate polyadenylation sites has been found for this gene. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agt A G 8: 125,291,187 (GRCm39) L40P probably damaging Het
Ahnak T C 19: 8,980,219 (GRCm39) I501T probably benign Het
Aldh2 A G 5: 121,706,056 (GRCm39) *196Q probably null Het
Ankrd65 A G 4: 155,875,848 (GRCm39) D23G possibly damaging Het
Anln A T 9: 22,250,292 (GRCm39) probably null Het
Armc3 C T 2: 19,301,671 (GRCm39) S663L possibly damaging Het
Armc3 G A 2: 19,290,948 (GRCm39) probably null Het
Cul5 A T 9: 53,546,375 (GRCm39) probably benign Het
Cyba T C 8: 123,151,796 (GRCm39) I134V probably damaging Het
Cybb T A X: 9,323,257 (GRCm39) Q93H probably damaging Het
Cyp4f37 G T 17: 32,849,009 (GRCm39) K292N probably benign Het
Dmxl2 T C 9: 54,281,981 (GRCm39) I2850V probably benign Het
Ep300 T C 15: 81,485,367 (GRCm39) I118T unknown Het
Ercc6l G T X: 101,189,148 (GRCm39) P454T probably benign Het
Grxcr1 A G 5: 68,267,821 (GRCm39) E190G probably damaging Het
Heatr3 C T 8: 88,871,227 (GRCm39) R194C probably benign Het
Hspa12b C T 2: 130,985,655 (GRCm39) probably benign Het
Inpp5d T C 1: 87,642,777 (GRCm39) V644A probably damaging Het
Kif26a G A 12: 112,143,409 (GRCm39) R1221H probably benign Het
Klra8 T C 6: 130,102,199 (GRCm39) N79D probably benign Het
Kntc1 T C 5: 123,900,661 (GRCm39) I253T possibly damaging Het
Lamp5 T C 2: 135,901,509 (GRCm39) V111A possibly damaging Het
Lmo7 T C 14: 102,139,659 (GRCm39) S859P probably benign Het
Mgarp T C 3: 51,296,453 (GRCm39) Q205R possibly damaging Het
Morf4l1 A G 9: 89,975,848 (GRCm39) Y315H probably benign Het
Naip6 A T 13: 100,433,486 (GRCm39) V1117E possibly damaging Het
Nipal1 A G 5: 72,824,274 (GRCm39) D206G probably damaging Het
Notch3 A G 17: 32,373,715 (GRCm39) S498P probably benign Het
Npepps A G 11: 97,109,328 (GRCm39) probably null Het
Or14c46 C A 7: 85,918,466 (GRCm39) C177F probably damaging Het
Or2ak6 T C 11: 58,592,886 (GRCm39) Y120H probably damaging Het
Phlpp1 A G 1: 106,317,613 (GRCm39) H1278R probably damaging Het
Pprc1 C A 19: 46,053,329 (GRCm39) probably benign Het
Rab8b A T 9: 66,755,000 (GRCm39) probably benign Het
Ripor2 T A 13: 24,901,554 (GRCm39) I875N probably damaging Het
Samd9l T C 6: 3,374,105 (GRCm39) E1052G probably benign Het
Slit3 A T 11: 35,520,569 (GRCm39) I569F probably damaging Het
Spata2l C T 8: 123,960,770 (GRCm39) G173D possibly damaging Het
Stc2 T G 11: 31,317,875 (GRCm39) probably benign Het
Tm6sf1 C A 7: 81,513,000 (GRCm39) Y65* probably null Het
Vmn2r14 A T 5: 109,368,454 (GRCm39) Y179* probably null Het
Washc5 C A 15: 59,241,060 (GRCm39) V92L probably benign Het
Wiz A G 17: 32,575,893 (GRCm39) S838P probably benign Het
Zp2 T A 7: 119,739,074 (GRCm39) probably null Het
Other mutations in Tspan15
AlleleSourceChrCoordTypePredicted EffectPPH Score
PIT1430001:Tspan15 UTSW 10 62,023,899 (GRCm39) missense probably damaging 0.98
R0071:Tspan15 UTSW 10 62,038,849 (GRCm39) splice site probably benign
R0071:Tspan15 UTSW 10 62,038,849 (GRCm39) splice site probably benign
R0310:Tspan15 UTSW 10 62,023,872 (GRCm39) missense probably benign 0.01
R2415:Tspan15 UTSW 10 62,037,570 (GRCm39) missense probably benign 0.00
R4152:Tspan15 UTSW 10 62,025,621 (GRCm39) missense possibly damaging 0.87
R4766:Tspan15 UTSW 10 62,027,323 (GRCm39) missense probably benign 0.00
R7446:Tspan15 UTSW 10 62,029,734 (GRCm39) missense probably benign
R8814:Tspan15 UTSW 10 62,023,835 (GRCm39) missense probably benign
Posted On 2015-04-16