Incidental Mutation 'IGL01567:Gm5129'
ID 91021
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5129
Ensembl Gene ENSMUSG00000053121
Gene Name predicted gene 5129
Synonyms ENSMUSG00000053121
Accession Numbers
Essential gene? Not available question?
Stock # IGL01567
Quality Score
Status
Chromosome 5
Chromosomal Location 29940332-29940934 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to G at 29940862 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142783 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000008733] [ENSMUST00000012734] [ENSMUST00000065372] [ENSMUST00000114839] [ENSMUST00000196528] [ENSMUST00000196785] [ENSMUST00000198694]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000008733
SMART Domains Protein: ENSMUSP00000008733
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 4.64e-32 SMART
low complexity region 109 124 N/A INTRINSIC
low complexity region 125 158 N/A INTRINSIC
low complexity region 166 185 N/A INTRINSIC
low complexity region 249 261 N/A INTRINSIC
low complexity region 272 293 N/A INTRINSIC
low complexity region 339 363 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000012734
SMART Domains Protein: ENSMUSP00000012734
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 4.64e-32 SMART
low complexity region 111 124 N/A INTRINSIC
low complexity region 192 205 N/A INTRINSIC
coiled coil region 223 244 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000065372
AA Change: F25L
Predicted Effect probably benign
Transcript: ENSMUST00000114839
SMART Domains Protein: ENSMUSP00000110488
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 4.64e-32 SMART
low complexity region 109 124 N/A INTRINSIC
low complexity region 125 158 N/A INTRINSIC
low complexity region 166 185 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000127753
Predicted Effect probably benign
Transcript: ENSMUST00000196528
SMART Domains Protein: ENSMUSP00000142878
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 3e-34 SMART
low complexity region 109 124 N/A INTRINSIC
low complexity region 125 158 N/A INTRINSIC
low complexity region 166 185 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000196785
Predicted Effect probably benign
Transcript: ENSMUST00000198694
SMART Domains Protein: ENSMUSP00000142783
Gene: ENSMUSG00000029131

DomainStartEndE-ValueType
DnaJ 2 61 1.4e-23 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agbl1 A G 7: 76,071,628 (GRCm39) S317G probably benign Het
Akna T C 4: 63,300,087 (GRCm39) T652A probably benign Het
Anxa9 G A 3: 95,209,743 (GRCm39) probably benign Het
Bpifb4 T A 2: 153,789,198 (GRCm39) probably benign Het
Bptf A G 11: 106,949,600 (GRCm39) S2125P probably damaging Het
Capns2 C A 8: 93,628,634 (GRCm39) H174Q probably benign Het
Cd200 A C 16: 45,215,054 (GRCm39) L199R probably damaging Het
Clasp2 T C 9: 113,709,164 (GRCm39) V651A probably damaging Het
Cox18 G A 5: 90,365,447 (GRCm39) Q251* probably null Het
Depdc1a T C 3: 159,232,183 (GRCm39) S645P probably damaging Het
Dio3 T A 12: 110,245,861 (GRCm39) C66S possibly damaging Het
Dock9 A T 14: 121,890,496 (GRCm39) L258Q probably damaging Het
Ghrhr A G 6: 55,361,108 (GRCm39) D274G probably damaging Het
Grb7 A G 11: 98,345,776 (GRCm39) N518S probably damaging Het
Kdm5b G A 1: 134,530,278 (GRCm39) A430T probably damaging Het
Map10 C A 8: 126,398,232 (GRCm39) Q542K probably benign Het
Metap1 T C 3: 138,168,150 (GRCm39) T325A probably damaging Het
Ncan A T 8: 70,560,984 (GRCm39) M661K probably benign Het
Or2f1b T C 6: 42,739,661 (GRCm39) I225T probably benign Het
Or51h5 A G 7: 102,577,623 (GRCm39) I263V probably benign Het
Otog T C 7: 45,926,039 (GRCm39) probably benign Het
Pip4k2b T C 11: 97,620,387 (GRCm39) D116G probably damaging Het
Rps15 T A 10: 80,129,643 (GRCm39) L86Q probably benign Het
Sfxn4 G T 19: 60,842,336 (GRCm39) T122K probably damaging Het
Slc4a3 T C 1: 75,527,526 (GRCm39) V165A probably damaging Het
Spmip7 A G 11: 11,465,015 (GRCm39) H122R possibly damaging Het
Synm A G 7: 67,384,980 (GRCm39) V452A probably damaging Het
Tdpoz1 T C 3: 93,578,013 (GRCm39) H257R possibly damaging Het
Tmem26 A G 10: 68,587,061 (GRCm39) T170A probably damaging Het
Wdfy4 T G 14: 32,873,618 (GRCm39) E230D probably benign Het
Other mutations in Gm5129
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02437:Gm5129 APN 5 29,940,861 (GRCm39) unclassified probably benign
R1867:Gm5129 UTSW 5 29,940,654 (GRCm39) unclassified probably benign
R2026:Gm5129 UTSW 5 29,940,732 (GRCm39) unclassified probably benign
R6604:Gm5129 UTSW 5 29,940,765 (GRCm39) unclassified probably benign
Posted On 2013-12-09