Incidental Mutation 'IGL02056:Gm4540'
ID 185243
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 # IGL02056
Quality Score
Status
Chromosome 3
Chromosomal Location 105941980-105942381 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 105942056 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: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atg101 T C 15: 101,188,218 (GRCm39) S108P probably damaging Het
BB014433 A T 8: 15,092,435 (GRCm39) C139* probably null Het
Cacna1s A G 1: 136,046,738 (GRCm39) N1808S probably benign Het
Ccdc148 A G 2: 58,894,081 (GRCm39) probably benign Het
Dnah7a T G 1: 53,543,501 (GRCm39) N2223T probably benign Het
Fgl2 T A 5: 21,580,543 (GRCm39) I295K probably damaging Het
Foxj3 T C 4: 119,442,954 (GRCm39) I126T probably damaging Het
Hps5 T G 7: 46,437,606 (GRCm39) K156N probably damaging Het
Hsp90aa1 T C 12: 110,660,449 (GRCm39) probably benign Het
Il12rb1 C T 8: 71,263,831 (GRCm39) R131* probably null Het
Itgb2l T C 16: 96,228,889 (GRCm39) E438G probably damaging Het
Kplce T A 3: 92,776,200 (GRCm39) Q161L probably benign Het
Nbeal2 A T 9: 110,456,392 (GRCm39) L2379Q probably benign Het
Neurl4 T C 11: 69,796,616 (GRCm39) V481A probably damaging Het
Nos1ap A G 1: 170,146,192 (GRCm39) F454S possibly damaging Het
Pik3r5 G T 11: 68,381,681 (GRCm39) G242C possibly damaging Het
Pkd1l3 A G 8: 110,358,010 (GRCm39) N834S probably benign Het
Prkar2b A G 12: 32,025,909 (GRCm39) probably benign Het
Pusl1 T C 4: 155,975,029 (GRCm39) T191A probably benign Het
Rasal2 A G 1: 157,126,831 (GRCm39) V51A probably damaging Het
Rsc1a1 T A 4: 141,412,796 (GRCm39) I39F probably benign Het
Slc2a3 G A 6: 122,712,437 (GRCm39) P269L probably damaging Het
Sntb1 C T 15: 55,511,435 (GRCm39) G383D possibly damaging Het
Washc5 T C 15: 59,222,185 (GRCm39) T547A possibly damaging Het
Zfr T C 15: 12,154,533 (GRCm39) V572A probably damaging Het
Zmym6 T A 4: 126,997,207 (GRCm39) N275K probably damaging Het
Other mutations in Gm4540
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00572:Gm4540 APN 3 105,942,123 (GRCm39) unclassified probably benign
Posted On 2014-05-07