Incidental Mutation 'IGL01578:Gm6489'
ID 91324
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6489
Ensembl Gene ENSMUSG00000094215
Gene Name predicted gene 6489
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.286) question?
Stock # IGL01578
Quality Score
Status
Chromosome 1
Chromosomal Location 31326026-31326787 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to T at 31326416 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178167
SMART Domains Protein: ENSMUSP00000136938
Gene: ENSMUSG00000094215

DomainStartEndE-ValueType
RRM 84 156 5.62e-18 SMART
FoP_duplication 165 253 2.91e-4 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap28 G A 17: 68,165,195 (GRCm39) T516I probably benign Het
Birc6 T C 17: 74,955,192 (GRCm39) C3486R probably benign Het
Camk2g G A 14: 20,797,922 (GRCm39) probably benign Het
Cplane1 A G 15: 8,300,194 (GRCm39) E3167G unknown Het
Dmxl1 T A 18: 50,095,272 (GRCm39) H2950Q probably damaging Het
Eml6 A T 11: 29,800,870 (GRCm39) S379T probably benign Het
Epb41l3 C T 17: 69,555,704 (GRCm39) H13Y probably damaging Het
Fam149a A T 8: 45,803,479 (GRCm39) D337E probably damaging Het
Galnt14 T A 17: 73,842,361 (GRCm39) probably benign Het
Hspg2 G A 4: 137,266,494 (GRCm39) R1885H probably damaging Het
Jag1 T A 2: 136,941,971 (GRCm39) probably benign Het
Nalcn A T 14: 123,809,503 (GRCm39) N216K probably benign Het
Ndst1 T C 18: 60,846,198 (GRCm39) Y37C probably damaging Het
Nr2c2 A G 6: 92,139,019 (GRCm39) N486S probably benign Het
Obscn A T 11: 58,890,506 (GRCm39) L7342Q unknown Het
Or13l2 A T 3: 97,318,036 (GRCm39) C154S probably damaging Het
Or56b2 A G 7: 104,338,052 (GRCm39) I277V probably benign Het
Or8k20 C A 2: 86,106,085 (GRCm39) V249F probably damaging Het
Pou4f2 A C 8: 79,162,284 (GRCm39) D106E probably damaging Het
Ppic G A 18: 53,551,001 (GRCm39) P10S unknown Het
Psd2 A G 18: 36,112,838 (GRCm39) T178A probably damaging Het
Ro60 A T 1: 143,637,038 (GRCm39) N391K probably damaging Het
Slc25a34 G T 4: 141,349,821 (GRCm39) probably null Het
Stap2 A G 17: 56,304,623 (GRCm39) S360P probably benign Het
Stx3 T C 19: 11,763,969 (GRCm39) E129G probably damaging Het
Sun3 T A 11: 8,979,436 (GRCm39) E28D probably damaging Het
Tmem126a C T 7: 90,100,750 (GRCm39) probably null Het
Trpc6 A T 9: 8,634,058 (GRCm39) H379L probably damaging Het
Ttf2 A G 3: 100,863,511 (GRCm39) S608P possibly damaging Het
Tubgcp3 T C 8: 12,711,297 (GRCm39) probably benign Het
Other mutations in Gm6489
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1957:Gm6489 UTSW 1 31,326,452 (GRCm39) exon noncoding transcript
R3740:Gm6489 UTSW 1 31,326,764 (GRCm39) unclassified noncoding transcript
R3741:Gm6489 UTSW 1 31,326,764 (GRCm39) unclassified noncoding transcript
R3742:Gm6489 UTSW 1 31,326,764 (GRCm39) unclassified noncoding transcript
R4489:Gm6489 UTSW 1 31,326,320 (GRCm39) exon noncoding transcript
R5239:Gm6489 UTSW 1 31,326,351 (GRCm39) exon noncoding transcript
Posted On 2013-12-09