Incidental Mutation 'IGL01078:Gm773'
ID 53324
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm773
Ensembl Gene ENSMUSG00000073177
Gene Name predicted gene 773
Synonyms LOC331416
Accession Numbers
Essential gene? Probably non essential (E-score: 0.049) question?
Stock # IGL01078
Quality Score
Status
Chromosome X
Chromosomal Location 55235187-55258241 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 55242013 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 112 (E112G)
Ref Sequence ENSEMBL: ENSMUSP00000099097 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000101561]
AlphaFold Q3TML4
Predicted Effect probably damaging
Transcript: ENSMUST00000101561
AA Change: E112G

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000099097
Gene: ENSMUSG00000073177
AA Change: E112G

DomainStartEndE-ValueType
low complexity region 12 23 N/A INTRINSIC
Pfam:Cor1 71 199 1.1e-40 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126937
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 10 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cc2d1a C T 8: 84,866,894 (GRCm39) V393M possibly damaging Het
Dpep3 G A 8: 106,704,860 (GRCm39) A150V probably damaging Het
Etl4 C T 2: 20,811,342 (GRCm39) R1510* probably null Het
Hlcs A G 16: 93,934,019 (GRCm39) I760T probably damaging Het
Mllt3 A G 4: 87,798,297 (GRCm39) probably benign Het
Or5p56 T A 7: 107,590,150 (GRCm39) S193T probably benign Het
Plxna2 T A 1: 194,469,001 (GRCm39) probably benign Het
Trp53inp1 T A 4: 11,165,369 (GRCm39) V131D probably damaging Het
Vmn2r117 A G 17: 23,696,778 (GRCm39) W210R probably damaging Het
Zfyve19 T A 2: 119,046,981 (GRCm39) C350* probably null Het
Other mutations in Gm773
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00470:Gm773 APN X 55,247,373 (GRCm39) missense probably benign 0.02
R1432:Gm773 UTSW X 55,247,377 (GRCm39) missense probably benign
X0028:Gm773 UTSW X 55,247,434 (GRCm39) missense probably benign 0.02
Posted On 2013-06-21