Incidental Mutation 'IGL02316:Gm6686'
ID 288041
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6686
Ensembl Gene ENSMUSG00000095920
Gene Name predicted pseudogene 6686
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02316
Quality Score
Status
Chromosome 17
Chromosomal Location 15786426-15786683 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 15786500 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000131871 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000147532] [ENSMUST00000167994]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132675
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139911
Predicted Effect probably benign
Transcript: ENSMUST00000147532
SMART Domains Protein: ENSMUSP00000118454
Gene: ENSMUSG00000051977

DomainStartEndE-ValueType
Pfam:SSXRD 49 81 1.8e-19 PFAM
SET 123 243 2.56e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000167994
SMART Domains Protein: ENSMUSP00000131871
Gene: ENSMUSG00000051977

DomainStartEndE-ValueType
KRAB 30 89 5.54e-8 SMART
Pfam:SSXRD 175 205 1.5e-20 PFAM
SET 248 368 2.56e-2 SMART
ZnF_C2H2 392 415 3.29e-1 SMART
ZnF_C2H2 516 535 4.74e1 SMART
ZnF_C2H2 541 563 9.73e-4 SMART
ZnF_C2H2 569 591 1.3e-4 SMART
ZnF_C2H2 597 619 1.3e-4 SMART
ZnF_C2H2 625 647 4.24e-4 SMART
ZnF_C2H2 653 675 4.24e-4 SMART
ZnF_C2H2 681 703 1.95e-3 SMART
ZnF_C2H2 709 731 5.99e-4 SMART
ZnF_C2H2 737 759 1.95e-3 SMART
ZnF_C2H2 765 787 1.95e-3 SMART
ZnF_C2H2 793 815 1.3e-4 SMART
ZnF_C2H2 821 843 1.6e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178455
SMART Domains Protein: ENSMUSP00000137164
Gene: ENSMUSG00000095920

DomainStartEndE-ValueType
Pfam:Ribosomal_S21 11 50 1.4e-13 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c13 G T 13: 4,253,458 (GRCm39) probably benign Het
Arhgap26 C T 18: 38,775,599 (GRCm39) noncoding transcript Het
Atp5f1b T C 10: 127,920,178 (GRCm39) V108A probably benign Het
B230307C23Rik G A 16: 97,809,850 (GRCm39) V9M probably damaging Het
Ccdc85c T A 12: 108,177,829 (GRCm39) H321L probably damaging Het
Diaph3 A T 14: 87,223,551 (GRCm39) M321K possibly damaging Het
Dicer1 G A 12: 104,668,812 (GRCm39) A1290V probably damaging Het
Dnah6 G A 6: 73,145,894 (GRCm39) T839M probably benign Het
Eif3a G A 19: 60,760,076 (GRCm39) probably benign Het
Eml1 T C 12: 108,501,018 (GRCm39) probably benign Het
Exoc4 A G 6: 33,887,519 (GRCm39) Q769R probably damaging Het
Fam184a T G 10: 53,514,335 (GRCm39) T426P probably damaging Het
Fsip2 C A 2: 82,809,137 (GRCm39) H1819N probably benign Het
Hadha T C 5: 30,331,565 (GRCm39) S464G probably benign Het
Ighv5-17 A T 12: 113,822,775 (GRCm39) C115* probably null Het
Jmjd6 T C 11: 116,733,928 (GRCm39) Y31C possibly damaging Het
Klrb1-ps1 G A 6: 129,093,532 (GRCm39) noncoding transcript Het
Mgat1 T C 11: 49,152,185 (GRCm39) Y223H probably damaging Het
Muc4 T C 16: 32,569,668 (GRCm39) S243P possibly damaging Het
Numa1 T C 7: 101,650,577 (GRCm39) L69P probably damaging Het
Or11h6 T C 14: 50,879,744 (GRCm39) I2T probably benign Het
Or1j21 A T 2: 36,683,632 (GRCm39) H128L probably damaging Het
Or1j4 C A 2: 36,740,294 (GRCm39) P79T probably damaging Het
Or4p23 A G 2: 88,577,187 (GRCm39) F15S probably damaging Het
Pde1c A T 6: 56,128,336 (GRCm39) D332E possibly damaging Het
Pitpnm1 A G 19: 4,162,835 (GRCm39) I1143V probably benign Het
Rsl1 T A 13: 67,325,120 (GRCm39) probably null Het
Scg2 A C 1: 79,413,398 (GRCm39) L442V probably damaging Het
Sez6l A T 5: 112,610,828 (GRCm39) V530E probably damaging Het
Ubr4 T C 4: 139,200,489 (GRCm39) I4655T possibly damaging Het
Zcwpw1 T C 5: 137,808,272 (GRCm39) probably benign Het
Other mutations in Gm6686
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01929:Gm6686 APN 17 15,786,577 (GRCm39) unclassified probably benign
Posted On 2015-04-16