Incidental Mutation 'IGL01071:Gm26938'
ID 51045
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 # IGL01071
Quality Score
Status
Chromosome 5
Chromosomal Location 139793733-139812162 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 139794228 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 117 (V117G)
Ref Sequence ENSEMBL: ENSMUSP00000035399 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000044002] [ENSMUST00000110832] [ENSMUST00000146780] [ENSMUST00000147328] [ENSMUST00000182839]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000044002
AA Change: V117G

PolyPhen 2 Score 0.774 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000035399
Gene: ENSMUSG00000036687
AA Change: V117G

DomainStartEndE-ValueType
low complexity region 5 15 N/A INTRINSIC
low complexity region 46 54 N/A INTRINSIC
Pfam:Solute_trans_a 82 356 2.2e-93 PFAM
low complexity region 408 435 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000110832
AA Change: V93G

PolyPhen 2 Score 0.354 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000106456
Gene: ENSMUSG00000036687
AA Change: V93G

DomainStartEndE-ValueType
low complexity region 22 30 N/A INTRINSIC
Pfam:Solute_trans_a 55 332 6.7e-101 PFAM
low complexity region 384 411 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000132677
Predicted Effect probably benign
Transcript: ENSMUST00000146780
SMART Domains Protein: ENSMUSP00000117714
Gene: ENSMUSG00000036687

DomainStartEndE-ValueType
low complexity region 22 30 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000147328
SMART Domains Protein: ENSMUSP00000119412
Gene: ENSMUSG00000036687

DomainStartEndE-ValueType
low complexity region 22 30 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000182839
AA Change: V165G

PolyPhen 2 Score 0.387 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000138120
Gene: ENSMUSG00000098140
AA Change: V165G

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: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930544G11Rik A C 6: 65,930,137 (GRCm39) D124A probably damaging Het
Arhgef17 C A 7: 100,534,907 (GRCm39) V1137L probably damaging Het
Birc6 A G 17: 74,873,127 (GRCm39) D462G possibly damaging Het
Birc6 A T 17: 74,938,696 (GRCm39) N2701Y probably damaging Het
Cadps C T 14: 12,509,091 (GRCm38) probably null Het
Camk2a T C 18: 61,113,228 (GRCm39) probably null Het
Capn10 T A 1: 92,872,797 (GRCm39) W508R probably damaging Het
Cntn3 A T 6: 102,397,212 (GRCm39) probably null Het
Crisp4 A G 1: 18,207,231 (GRCm39) V19A probably benign Het
Depdc1b A T 13: 108,493,975 (GRCm39) Y121F probably benign Het
Dsg1b T A 18: 20,542,272 (GRCm39) S926R probably damaging Het
Eml6 A G 11: 29,800,816 (GRCm39) probably null Het
Keg1 T A 19: 12,696,364 (GRCm39) Y183N probably damaging Het
Mpi A T 9: 57,457,875 (GRCm39) I109N probably damaging Het
Or12j3 C T 7: 139,953,098 (GRCm39) A142T probably benign Het
Or13a20 C T 7: 140,232,827 (GRCm39) H312Y possibly damaging Het
Or14a259 T C 7: 86,012,768 (GRCm39) K259R possibly damaging Het
Or4c112 A G 2: 88,853,519 (GRCm39) V276A probably benign Het
Pcdhb20 A G 18: 37,637,738 (GRCm39) E88G possibly damaging Het
Pde6b G A 5: 108,567,581 (GRCm39) W290* probably null Het
Phf20 T A 2: 156,136,008 (GRCm39) probably null Het
Pkd1l1 A T 11: 8,798,921 (GRCm39) H1830Q probably benign Het
Proc T C 18: 32,256,770 (GRCm39) D299G probably damaging Het
Psmd14 A G 2: 61,630,407 (GRCm39) T306A probably benign Het
Rab32 G A 10: 10,433,591 (GRCm39) A81V probably damaging Het
Samd14 G A 11: 94,912,294 (GRCm39) probably benign Het
Sh3rf1 T A 8: 61,678,993 (GRCm39) C12S probably damaging Het
Sipa1l3 C T 7: 29,023,645 (GRCm39) V663M possibly damaging Het
Slc2a5 A G 4: 150,205,190 (GRCm39) probably benign Het
Tasor T A 14: 27,164,579 (GRCm39) probably null Het
Tbkbp1 T C 11: 97,040,388 (GRCm39) I9V probably damaging Het
Trip10 C A 17: 57,561,332 (GRCm39) R196S possibly damaging Het
Vav1 T C 17: 57,606,176 (GRCm39) Y267H probably benign Het
Wdr1 T C 5: 38,687,410 (GRCm39) K207R probably benign Het
Other mutations in Gm26938
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00886:Gm26938 APN 5 139,812,091 (GRCm39) missense probably damaging 0.97
Posted On 2013-06-21