Incidental Mutation 'IGL01800:Gm5611'
ID 155472
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5611
Ensembl Gene ENSMUSG00000090602
Gene Name predicted gene 5611
Synonyms
Accession Numbers
Essential gene? Probably essential (E-score: 0.964) question?
Stock # IGL01800
Quality Score
Status
Chromosome 9
Chromosomal Location 16941341-16942192 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to G at 16941767 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: ENSMUST00000164523
SMART Domains Protein: ENSMUSP00000130546
Gene: ENSMUSG00000090602

DomainStartEndE-ValueType
Pfam:Nucleoplasmin 12 173 7.7e-64 PFAM
low complexity region 207 219 N/A INTRINSIC
Pfam:NPM1-C 223 271 8.1e-38 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc2 A G 19: 43,772,734 (GRCm39) Y48C possibly damaging Het
Acsm3 T C 7: 119,373,866 (GRCm39) S251P possibly damaging Het
Ano5 G A 7: 51,222,823 (GRCm39) probably null Het
Ccdc65 C T 15: 98,606,946 (GRCm39) A51V probably benign Het
Cspg5 A G 9: 110,080,218 (GRCm39) probably benign Het
Dhx30 A G 9: 109,914,581 (GRCm39) V935A possibly damaging Het
Disp3 T A 4: 148,334,258 (GRCm39) K1012* probably null Het
Dock2 T C 11: 34,647,100 (GRCm39) N18S probably damaging Het
Dst A T 1: 34,301,173 (GRCm39) I1180F probably damaging Het
Elp2 A G 18: 24,750,548 (GRCm39) Y295C probably benign Het
Eml2 A G 7: 18,935,122 (GRCm39) probably benign Het
Fat4 A G 3: 39,035,878 (GRCm39) T3177A probably damaging Het
Flrt2 A T 12: 95,746,462 (GRCm39) I267F probably damaging Het
Gstcd A G 3: 132,790,335 (GRCm39) probably null Het
Gucy1b2 T C 14: 62,649,104 (GRCm39) M476V probably benign Het
Jak2 A G 19: 29,263,693 (GRCm39) probably benign Het
Kcnt1 T C 2: 25,778,137 (GRCm39) F85S probably damaging Het
Kcnu1 G A 8: 26,427,528 (GRCm39) V282M probably damaging Het
Lancl1 T G 1: 67,060,029 (GRCm39) E132A probably benign Het
Or4g7 T C 2: 111,309,209 (GRCm39) F27L probably benign Het
Or5b106 A G 19: 13,123,993 (GRCm39) F10S probably damaging Het
Pigm G A 1: 172,204,770 (GRCm39) A169T probably damaging Het
Ppargc1a A G 5: 51,652,063 (GRCm39) Y212H probably damaging Het
Ppp1r13l A T 7: 19,111,936 (GRCm39) probably benign Het
Pramel12 T C 4: 143,145,650 (GRCm39) L373P probably damaging Het
Rictor T C 15: 6,804,182 (GRCm39) I554T probably damaging Het
Sbno1 G A 5: 124,519,568 (GRCm39) probably benign Het
Sesn2 G T 4: 132,226,418 (GRCm39) L194I probably damaging Het
Slc26a2 A T 18: 61,334,801 (GRCm39) Y217* probably null Het
Sptbn5 G T 2: 119,886,908 (GRCm39) probably benign Het
Tmem184a A T 5: 139,798,899 (GRCm39) S17T possibly damaging Het
Trhr T C 15: 44,092,603 (GRCm39) M280T possibly damaging Het
Ube2j1 A T 4: 33,045,115 (GRCm39) E129D probably benign Het
Ube4b A T 4: 149,415,951 (GRCm39) S3T probably damaging Het
Vmn2r49 A T 7: 9,710,601 (GRCm39) C710* probably null Het
Vmn2r82 C T 10: 79,192,581 (GRCm39) R53C probably benign Het
Zdhhc2 T C 8: 40,917,284 (GRCm39) L227P probably damaging Het
Zfp995 A C 17: 22,099,972 (GRCm39) H87Q possibly damaging Het
Other mutations in Gm5611
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01615:Gm5611 APN 9 16,941,647 (GRCm39) exon noncoding transcript
IGL01763:Gm5611 APN 9 16,941,699 (GRCm39) exon noncoding transcript
R1536:Gm5611 UTSW 9 16,941,903 (GRCm39) exon noncoding transcript
R1830:Gm5611 UTSW 9 16,942,073 (GRCm39) exon noncoding transcript
R4111:Gm5611 UTSW 9 16,941,989 (GRCm39) exon noncoding transcript
R4113:Gm5611 UTSW 9 16,941,989 (GRCm39) exon noncoding transcript
Posted On 2014-02-04