Incidental Mutation 'IGL02756:Stxbp3-ps'
ID 306436
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Stxbp3-ps
Ensembl Gene ENSMUSG00000071640
Gene Name syntaxin-binding protein 3, pseudogene
Synonyms Stxbp3b, Munc18c(L)
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.301) question?
Stock # IGL02756
Quality Score
Status
Chromosome 19
Chromosomal Location 9535156-9536547 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) C to T at 9535193 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000090527
SMART Domains Protein: ENSMUSP00000088014
Gene: ENSMUSG00000071640

DomainStartEndE-ValueType
Pfam:Sec1 33 253 1.2e-48 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700113H08Rik A T 10: 87,000,970 (GRCm39) D54V probably damaging Het
Adamts18 C A 8: 114,440,976 (GRCm39) probably benign Het
Angptl3 T A 4: 98,919,399 (GRCm39) L53Q probably damaging Het
Apc A G 18: 34,447,588 (GRCm39) T1461A probably damaging Het
Arl11 T A 14: 61,548,535 (GRCm39) V115D probably damaging Het
Cabp4 C A 19: 4,188,560 (GRCm39) V173L possibly damaging Het
Casq1 T A 1: 172,042,672 (GRCm39) D230V probably damaging Het
Cdc42bpa A G 1: 179,936,824 (GRCm39) I821V possibly damaging Het
Cfap65 T C 1: 74,944,239 (GRCm39) Y1494C probably benign Het
Chd1 T A 17: 15,951,069 (GRCm39) S215T probably damaging Het
Csf2rb2 T C 15: 78,169,049 (GRCm39) E593G possibly damaging Het
Cstf1 A G 2: 172,217,795 (GRCm39) D136G probably damaging Het
Ddx19b T C 8: 111,737,910 (GRCm39) probably benign Het
Dido1 A T 2: 180,303,716 (GRCm39) L1396Q probably benign Het
Ermn A G 2: 57,937,824 (GRCm39) I263T probably damaging Het
F12 T A 13: 55,568,880 (GRCm39) Q294L possibly damaging Het
Far2 A T 6: 148,058,889 (GRCm39) I192F probably damaging Het
Fshb T A 2: 106,889,218 (GRCm39) I29F probably damaging Het
Gcgr T A 11: 120,427,811 (GRCm39) Y251N probably benign Het
Gpr158 A G 2: 21,831,890 (GRCm39) I997V possibly damaging Het
Gprc5d A G 6: 135,093,613 (GRCm39) V98A probably damaging Het
H2-T23 T C 17: 36,342,580 (GRCm39) E186G probably damaging Het
Khdrbs3 C T 15: 68,896,685 (GRCm39) T115I probably benign Het
Kifap3 C T 1: 163,689,597 (GRCm39) T527M probably damaging Het
Mfsd2a C T 4: 122,842,332 (GRCm39) A512T probably benign Het
Mmp9 A G 2: 164,791,235 (GRCm39) D135G probably benign Het
Mylk T C 16: 34,784,016 (GRCm39) V1394A probably benign Het
Nek9 A C 12: 85,358,110 (GRCm39) probably null Het
Or51q1c T C 7: 103,652,866 (GRCm39) I128T probably damaging Het
Or8k16 T C 2: 85,520,402 (GRCm39) S210P probably damaging Het
P2rx2 T A 5: 110,490,276 (GRCm39) probably benign Het
P4htm A G 9: 108,456,977 (GRCm39) L410P probably damaging Het
Pik3c2a A T 7: 115,963,748 (GRCm39) W921R probably benign Het
Pnisr T C 4: 21,862,175 (GRCm39) F288L probably benign Het
Ppp4r3a C T 12: 101,024,582 (GRCm39) probably null Het
Prss34 T C 17: 25,518,251 (GRCm39) S144P probably damaging Het
Qrsl1 T C 10: 43,758,110 (GRCm39) T328A probably benign Het
Rab33b A T 3: 51,391,945 (GRCm39) T65S probably damaging Het
Rdh8 A G 9: 20,736,637 (GRCm39) S235G possibly damaging Het
Rrp12 T C 19: 41,884,500 (GRCm39) K6R probably benign Het
Sec24a T C 11: 51,587,560 (GRCm39) D1025G probably benign Het
Sgo2a T G 1: 58,055,509 (GRCm39) N564K probably damaging Het
Slc43a3 A T 2: 84,774,612 (GRCm39) M130L probably benign Het
Soat1 T C 1: 156,274,145 (GRCm39) I89V probably benign Het
St3gal5 A G 6: 72,126,157 (GRCm39) D307G probably null Het
Tacr2 A G 10: 62,097,469 (GRCm39) probably benign Het
Tg C T 15: 66,606,435 (GRCm39) T193I probably benign Het
Tnik A G 3: 28,596,179 (GRCm39) T191A probably damaging Het
Trim27 T C 13: 21,374,256 (GRCm39) probably benign Het
Usf2 A T 7: 30,646,417 (GRCm39) C134* probably null Het
Usp14 A G 18: 10,001,769 (GRCm39) probably null Het
Usp47 T C 7: 111,692,270 (GRCm39) S911P possibly damaging Het
Vmn1r73 T A 7: 11,490,574 (GRCm39) S131T possibly damaging Het
Vmn2r80 T C 10: 79,030,145 (GRCm39) I657T probably damaging Het
Zfp935 A T 13: 62,602,701 (GRCm39) C166* probably null Het
Other mutations in Stxbp3-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00569:Stxbp3-ps APN 19 9,535,186 (GRCm39) exon noncoding transcript
IGL01296:Stxbp3-ps APN 19 9,535,256 (GRCm39) exon noncoding transcript
IGL01455:Stxbp3-ps APN 19 9,535,371 (GRCm39) exon noncoding transcript
IGL02698:Stxbp3-ps APN 19 9,535,688 (GRCm39) exon noncoding transcript
IGL03324:Stxbp3-ps APN 19 9,535,714 (GRCm39) exon noncoding transcript
R0217:Stxbp3-ps UTSW 19 9,536,496 (GRCm39) exon noncoding transcript
R4522:Stxbp3-ps UTSW 19 9,536,474 (GRCm39) critical splice donor site noncoding transcript
R5030:Stxbp3-ps UTSW 19 9,535,714 (GRCm39) exon noncoding transcript
R5541:Stxbp3-ps UTSW 19 9,535,334 (GRCm39) exon noncoding transcript
Posted On 2015-04-16