Incidental Mutation 'IGL00569:Gm10610'
ID 332649
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm10610
Ensembl Gene ENSMUSG00000094841
Gene Name predicted gene 10610
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.264) question?
Stock # IGL00569
Quality Score
Status
Chromosome 7
Chromosomal Location 83186018-83199802 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 83198778 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: ENSMUST00000177929
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207184
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208877
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca6 T G 11: 110,077,875 (GRCm39) N1311H possibly damaging Het
Adrm1b T C 3: 92,335,707 (GRCm39) T332A probably benign Het
Apol8 C T 15: 77,634,255 (GRCm39) R107H probably benign Het
Cacna1a T A 8: 85,189,343 (GRCm39) I98N probably damaging Het
Clps T A 17: 28,779,636 (GRCm39) probably benign Het
Dcc T A 18: 71,517,296 (GRCm39) probably null Het
Dock10 A G 1: 80,562,729 (GRCm39) F544L probably damaging Het
Eif2ak2 A T 17: 79,176,912 (GRCm39) S218T probably benign Het
Faf1 T C 4: 109,819,077 (GRCm39) *650Q probably null Het
Fxn A T 19: 24,244,714 (GRCm39) I142N probably damaging Het
Hspa1l C T 17: 35,196,441 (GRCm39) T160I probably damaging Het
Kcng4 A G 8: 120,353,070 (GRCm39) V280A probably benign Het
Khsrp T C 17: 57,330,092 (GRCm39) T646A possibly damaging Het
Lilra6 A G 7: 3,917,588 (GRCm39) S136P probably damaging Het
Lmo7 T G 14: 102,124,487 (GRCm39) N315K probably damaging Het
Map3k5 A G 10: 19,810,790 (GRCm39) T147A possibly damaging Het
Mical3 T C 6: 120,938,585 (GRCm39) E1134G possibly damaging Het
Nek3 A G 8: 22,648,722 (GRCm39) L103P probably damaging Het
Nudt17 G T 3: 96,614,343 (GRCm39) P222Q probably damaging Het
Pla2r1 G T 2: 60,250,769 (GRCm39) T1386K probably benign Het
Ptpn13 A G 5: 103,738,872 (GRCm39) probably benign Het
Rgl1 A C 1: 152,447,368 (GRCm39) S134A probably benign Het
Rnls T A 19: 33,145,888 (GRCm39) E195V probably benign Het
Sall4 T C 2: 168,597,232 (GRCm39) N536S probably benign Het
Serinc3 G T 2: 163,469,921 (GRCm39) P309Q probably damaging Het
Smc5 G A 19: 23,213,329 (GRCm39) R528C probably damaging Het
Stxbp3-ps A T 19: 9,535,186 (GRCm39) noncoding transcript Het
Tmem67 T A 4: 12,061,826 (GRCm39) I549L probably damaging Het
Trank1 C A 9: 111,174,579 (GRCm39) H269N possibly damaging Het
Wdr87-ps A T 7: 29,233,565 (GRCm39) noncoding transcript Het
Other mutations in Gm10610
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02642:Gm10610 APN 7 83,198,813 (GRCm39) exon noncoding transcript
R5541:Gm10610 UTSW 7 83,198,614 (GRCm39) intron noncoding transcript
Posted On 2015-08-05