Incidental Mutation 'IGL01455:Stxbp3-ps'
ID 84733
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 # IGL01455
Quality Score
Status
Chromosome 19
Chromosomal Location 9535156-9536547 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 9535371 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: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsl6 A G 11: 54,214,131 (GRCm39) D87G possibly damaging Het
Adgra3 G A 5: 50,144,899 (GRCm39) R565* probably null Het
Akap12 C T 10: 4,306,886 (GRCm39) T1232I probably damaging Het
Arb2a A T 13: 78,050,766 (GRCm39) probably benign Het
B3gnt2 A T 11: 22,787,042 (GRCm39) W49R probably damaging Het
Ccdc112 T A 18: 46,426,511 (GRCm39) K137N possibly damaging Het
Ccdc117 G T 11: 5,484,297 (GRCm39) T181K possibly damaging Het
Cfh T C 1: 140,033,277 (GRCm39) K756E possibly damaging Het
Clca3a1 C T 3: 144,713,539 (GRCm39) M697I probably benign Het
Cyp2c29 T A 19: 39,317,561 (GRCm39) I349K possibly damaging Het
Dcaf15 T C 8: 84,825,219 (GRCm39) T434A probably benign Het
Entpd5 T C 12: 84,441,451 (GRCm39) I106V probably benign Het
Eps8l1 T A 7: 4,481,922 (GRCm39) probably benign Het
Erbin G T 13: 103,995,895 (GRCm39) P269Q probably damaging Het
Fbxw22 C T 9: 109,214,062 (GRCm39) M251I probably benign Het
Fgd4 T A 16: 16,308,354 (GRCm39) T9S probably benign Het
Haus8 T C 8: 71,705,875 (GRCm39) I270V probably benign Het
Herc4 T A 10: 63,121,922 (GRCm39) probably null Het
Hspg2 G A 4: 137,281,128 (GRCm39) V3367M probably damaging Het
Htr1f A T 16: 64,746,385 (GRCm39) F302L probably damaging Het
Inpp5f T C 7: 128,279,773 (GRCm39) C458R probably damaging Het
Klhl18 T C 9: 110,261,511 (GRCm39) E411G probably damaging Het
Krt20 A T 11: 99,322,769 (GRCm39) F289I probably benign Het
Mical1 T C 10: 41,355,065 (GRCm39) probably null Het
Nav1 T C 1: 135,397,373 (GRCm39) D932G probably benign Het
Nme4 A T 17: 26,311,036 (GRCm39) D176E probably benign Het
Nox4 C T 7: 87,025,424 (GRCm39) S517L possibly damaging Het
Or1j13 A T 2: 36,369,368 (GRCm39) L258H probably damaging Het
Pate8 T A 9: 36,492,659 (GRCm39) H82L probably benign Het
Pip5k1a T C 3: 94,975,471 (GRCm39) D333G probably benign Het
Polb T C 8: 23,143,088 (GRCm39) Y36C probably damaging Het
Spta1 T C 1: 174,030,877 (GRCm39) I953T possibly damaging Het
Sptb A T 12: 76,659,686 (GRCm39) D1071E probably damaging Het
Tmcc3 A T 10: 94,422,617 (GRCm39) I356F probably damaging Het
Tmem262 G T 19: 6,130,189 (GRCm39) R6L probably damaging Het
Tnks C A 8: 35,408,054 (GRCm39) V225L probably damaging 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
IGL02698:Stxbp3-ps APN 19 9,535,688 (GRCm39) exon noncoding transcript
IGL02756:Stxbp3-ps APN 19 9,535,193 (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 2013-11-11