Incidental Mutation 'IGL00886:Gm26938'
ID 27372
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm26938
Ensembl Gene ENSMUSG00000098140
Gene Name predicted gene, 26938
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00886
Quality Score
Status
Chromosome 5
Chromosomal Location 139793733-139812162 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 139812091 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Valine at position 3 (D3V)
Ref Sequence ENSEMBL: ENSMUSP00000138120 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031531] [ENSMUST00000182602] [ENSMUST00000182839]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000031531
AA Change: D3V

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000031531
Gene: ENSMUSG00000029551
AA Change: D3V

DomainStartEndE-ValueType
Pfam:PAC3 34 119 1.9e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000182602
AA Change: D3V

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000138161
Gene: ENSMUSG00000029551
AA Change: D3V

DomainStartEndE-ValueType
Pfam:DUF2372 34 121 2.5e-35 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182743
Predicted Effect probably damaging
Transcript: ENSMUST00000182839
AA Change: D3V

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000138120
Gene: ENSMUSG00000098140
AA Change: D3V

DomainStartEndE-ValueType
Pfam:DUF2372 34 82 2e-14 PFAM
low complexity region 94 102 N/A INTRINSIC
Pfam:Solute_trans_a 127 226 3.5e-36 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca9 C T 11: 110,054,101 (GRCm39) R67H possibly damaging Het
Ak4 G T 4: 101,304,386 (GRCm39) E59* probably null Het
Ano10 T C 9: 122,100,390 (GRCm39) N116S probably benign Het
Arid1b T A 17: 5,177,254 (GRCm39) H658Q probably damaging Het
Atf2 G A 2: 73,675,847 (GRCm39) T208I possibly damaging Het
Bco1 T C 8: 117,857,376 (GRCm39) W448R probably damaging Het
Cel A T 2: 28,449,397 (GRCm39) C277S probably damaging Het
Chd5 T A 4: 152,444,156 (GRCm39) D296E probably benign Het
Crygd C T 1: 65,101,250 (GRCm39) R115Q probably benign Het
Fmo9 T C 1: 166,507,714 (GRCm39) probably null Het
Gdpgp1 T G 7: 79,889,100 (GRCm39) L377R probably damaging Het
Gpld1 T A 13: 25,146,336 (GRCm39) Y193* probably null Het
Gtf2h4 T C 17: 35,980,874 (GRCm39) H265R probably damaging Het
Hadh G T 3: 131,043,465 (GRCm39) T83K probably benign Het
Hao1 T C 2: 134,365,079 (GRCm39) M183V probably benign Het
Hnrnpm C A 17: 33,868,876 (GRCm39) R517L probably damaging Het
Ift88 T C 14: 57,715,525 (GRCm39) Y523H probably damaging Het
Il23r G T 6: 67,450,874 (GRCm39) Q202K possibly damaging Het
Iyd T C 10: 3,540,444 (GRCm38) D50A probably benign Het
Katnal2 A T 18: 77,090,450 (GRCm39) L248Q probably damaging Het
Krtap26-1 A T 16: 88,444,267 (GRCm39) V118E possibly damaging Het
Lzic T C 4: 149,577,753 (GRCm39) probably null Het
Meak7 T C 8: 120,500,007 (GRCm39) probably benign Het
Mical2 T A 7: 111,914,279 (GRCm39) N316K probably benign Het
Ndufc2 T A 7: 97,049,397 (GRCm39) M1K probably null Het
Net1 A G 13: 3,943,391 (GRCm39) probably benign Het
Or13g1 G A 7: 85,956,259 (GRCm39) L21F probably damaging Het
Pde1c A G 6: 56,150,659 (GRCm39) Y287H probably damaging Het
Pitpnm1 T C 19: 4,160,665 (GRCm39) probably null Het
Pla2r1 T A 2: 60,254,668 (GRCm39) E1300V probably damaging Het
Polr3g T C 13: 81,842,796 (GRCm39) Y73C probably damaging Het
Ryr1 T A 7: 28,723,654 (GRCm39) E4137V probably damaging Het
Scrib T C 15: 75,920,643 (GRCm39) D1425G possibly damaging Het
Slc25a12 A G 2: 71,174,376 (GRCm39) Y23H possibly damaging Het
Spef2 C A 15: 9,663,181 (GRCm39) G867W probably damaging Het
Strn3 A T 12: 51,656,933 (GRCm39) Y698N probably damaging Het
Ube3a T A 7: 58,934,485 (GRCm39) F533I probably damaging Het
Other mutations in Gm26938
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01071:Gm26938 APN 5 139,794,228 (GRCm39) missense possibly damaging 0.77
Posted On 2013-04-17