Incidental Mutation 'IGL00572:Gm4540'
ID 332663
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm4540
Ensembl Gene ENSMUSG00000092072
Gene Name predicted gene 4540
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00572
Quality Score
Status
Chromosome 3
Chromosomal Location 105941980-105942381 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to T at 105942123 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142477 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000200146]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170669
Predicted Effect probably benign
Transcript: ENSMUST00000200146
SMART Domains Protein: ENSMUSP00000142477
Gene: ENSMUSG00000043873

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Glyco_18 22 365 2.1e-133 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre4 A G 17: 56,127,648 (GRCm39) I563V probably benign Het
Adgrl2 A G 3: 148,532,134 (GRCm39) L1033P probably damaging Het
Aqr A C 2: 113,956,423 (GRCm39) I840M possibly damaging Het
Bmper G A 9: 23,317,823 (GRCm39) V481M probably damaging Het
Chd8 T C 14: 52,463,595 (GRCm39) E683G probably damaging Het
Cpn1 A G 19: 43,952,268 (GRCm39) V338A probably damaging Het
Cs A G 10: 128,196,833 (GRCm39) probably benign Het
Hdc A G 2: 126,443,792 (GRCm39) F296L probably benign Het
Helt T C 8: 46,746,559 (GRCm39) E32G probably damaging Het
Hivep1 C T 13: 42,312,347 (GRCm39) A1529V probably benign Het
Klk1b4 A T 7: 43,860,198 (GRCm39) H104L possibly damaging Het
Lrrc37 A G 11: 103,506,236 (GRCm39) F1911L probably benign Het
Ncf2 C A 1: 152,683,925 (GRCm39) T48N possibly damaging Het
Phkg1 G A 5: 129,893,914 (GRCm39) Q274* probably null Het
Slc1a2 A G 2: 102,607,921 (GRCm39) D520G possibly damaging Het
Slc25a10 G T 11: 120,387,933 (GRCm39) probably null Het
Slc8a1 A T 17: 81,696,155 (GRCm39) S960T probably damaging Het
Sp140 G A 1: 85,549,393 (GRCm39) R208K probably benign Het
St7 A G 6: 17,855,005 (GRCm39) E245G probably damaging Het
Sypl1 T A 12: 33,004,293 (GRCm39) S2T probably damaging Het
Tbx20 T C 9: 24,636,984 (GRCm39) T368A probably benign Het
Tmem126a T C 7: 90,100,040 (GRCm39) T168A probably benign Het
Ttn T C 2: 76,576,934 (GRCm39) D24653G probably damaging Het
Ttn A G 2: 76,777,323 (GRCm39) S1360P probably damaging Het
Uggt2 A T 14: 119,280,203 (GRCm39) F282L probably benign Het
Usp36 A T 11: 118,155,646 (GRCm39) N875K possibly damaging Het
Usp9x C A X: 12,991,815 (GRCm39) H869N probably benign Het
Xpnpep1 T C 19: 52,998,579 (GRCm39) E223G probably benign Het
Zfp729a G A 13: 67,767,440 (GRCm39) P930S probably benign Het
Zscan10 G A 17: 23,828,435 (GRCm39) V216M probably damaging Het
Other mutations in Gm4540
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02056:Gm4540 APN 3 105,942,056 (GRCm39) unclassified probably benign
Posted On 2015-08-05