Incidental Mutation 'IGL00926:Gm24124'
ID 29508
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm24124
Ensembl Gene ENSMUSG00000077291
Gene Name predicted gene, 24124
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00926
Quality Score
Status
Chromosome 19
Chromosomal Location 13612947-13613078 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) G to T at 13611421 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149711 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053113] [ENSMUST00000217182]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000053113
SMART Domains Protein: ENSMUSP00000062444
Gene: ENSMUSG00000045678

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 1.7e-53 PFAM
Pfam:7tm_1 39 289 1.2e-15 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104103
Predicted Effect probably benign
Transcript: ENSMUST00000217182
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agtr2 A T X: 21,352,524 (GRCm39) M53L probably benign Het
Apob T C 12: 8,065,421 (GRCm39) V4097A probably benign Het
Brip1 T C 11: 86,039,227 (GRCm39) K436E possibly damaging Het
Cadps C A 14: 12,491,795 (GRCm38) R785L probably damaging Het
Cavin2 A G 1: 51,340,036 (GRCm39) K238E probably damaging Het
Ccdc158 G A 5: 92,798,626 (GRCm39) T358I probably damaging Het
Cds1 A G 5: 101,957,767 (GRCm39) I246M probably damaging Het
Cep19 A G 16: 31,925,898 (GRCm39) E102G probably damaging Het
Clec4a1 T A 6: 122,899,014 (GRCm39) C28S possibly damaging Het
Csmd3 T A 15: 47,574,360 (GRCm39) Y2082F possibly damaging Het
Fbn1 T A 2: 125,160,962 (GRCm39) T2193S possibly damaging Het
Gpbp1l1 T A 4: 116,444,710 (GRCm39) probably null Het
Helq T C 5: 100,912,948 (GRCm39) probably benign Het
Hnrnpm C A 17: 33,868,876 (GRCm39) R517L probably damaging Het
Itga3 G A 11: 94,956,712 (GRCm39) H122Y probably damaging Het
Mettl18 T A 1: 163,823,795 (GRCm39) S39T possibly damaging Het
Ndst4 A T 3: 125,355,102 (GRCm39) T337S probably benign Het
Neb A G 2: 52,160,329 (GRCm39) probably benign Het
Nrbp1 T C 5: 31,401,141 (GRCm39) S6P probably benign Het
Oprk1 A G 1: 5,669,128 (GRCm39) I191M probably damaging Het
Or2a56 A T 6: 42,933,370 (GRCm39) probably benign Het
Or51k2 A G 7: 103,596,204 (GRCm39) T144A probably benign Het
Or52z13 A G 7: 103,247,369 (GRCm39) N282S possibly damaging Het
Psap T C 10: 60,128,316 (GRCm39) V69A probably damaging Het
Scn7a C T 2: 66,514,475 (GRCm39) E1100K probably benign Het
Tmem145 A G 7: 25,014,155 (GRCm39) N423S possibly damaging Het
Tpd52 A T 3: 9,012,692 (GRCm39) probably null Het
Trmt13 G A 3: 116,383,884 (GRCm39) Q58* probably null Het
Ttn T C 2: 76,589,125 (GRCm39) E21346G probably damaging Het
Posted On 2013-04-17