Incidental Mutation 'IGL01567:Gm5129'
ID91021
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5129
Ensembl Gene ENSMUSG00000053121
Gene Namepredicted gene 5129
SynonymsENSMUSG00000053121
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01567
Quality Score
Status
Chromosome5
Chromosomal Location29735637-29735936 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 29735864 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142783 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000008733] [ENSMUST00000012734] [ENSMUST00000065372] [ENSMUST00000114839] [ENSMUST00000196528] [ENSMUST00000196785] [ENSMUST00000198694]
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: 76,421,880 S317G probably benign Het
Akna T C 4: 63,381,850 T652A probably benign Het
Anxa9 G A 3: 95,302,432 probably benign Het
Bpifb4 T A 2: 153,947,278 probably benign Het
Bptf A G 11: 107,058,774 S2125P probably damaging Het
Capns2 C A 8: 92,902,006 H174Q probably benign Het
Cd200 A C 16: 45,394,691 L199R probably damaging Het
Clasp2 T C 9: 113,880,096 V651A probably damaging Het
Cox18 G A 5: 90,217,588 Q251* probably null Het
Depdc1a T C 3: 159,526,546 S645P probably damaging Het
Dio3 T A 12: 110,279,427 C66S possibly damaging Het
Dock9 A T 14: 121,653,084 L258Q probably damaging Het
Ghrhr A G 6: 55,384,123 D274G probably damaging Het
Grb7 A G 11: 98,454,950 N518S probably damaging Het
Kdm5b G A 1: 134,602,540 A430T probably damaging Het
Map10 C A 8: 125,671,493 Q542K probably benign Het
Metap1 T C 3: 138,462,389 T325A probably damaging Het
Ncan A T 8: 70,108,334 M661K probably benign Het
Olfr38 T C 6: 42,762,727 I225T probably benign Het
Olfr572 A G 7: 102,928,416 I263V probably benign Het
Otog T C 7: 46,276,615 probably benign Het
Pip4k2b T C 11: 97,729,561 D116G probably damaging Het
Rps15 T A 10: 80,293,809 L86Q probably benign Het
Sfxn4 G T 19: 60,853,898 T122K probably damaging Het
Slc4a3 T C 1: 75,550,882 V165A probably damaging Het
Spata48 A G 11: 11,515,015 H122R possibly damaging Het
Synm A G 7: 67,735,232 V452A probably damaging Het
Tdpoz1 T C 3: 93,670,706 H257R possibly damaging Het
Tmem26 A G 10: 68,751,231 T170A probably damaging Het
Wdfy4 T G 14: 33,151,661 E230D probably benign Het
Other mutations in Gm5129
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02437:Gm5129 APN 5 29735863 unclassified probably benign
R1867:Gm5129 UTSW 5 29735656 unclassified probably benign
R2026:Gm5129 UTSW 5 29735734 unclassified probably benign
R6604:Gm5129 UTSW 5 29735767 unclassified probably benign
Posted On2013-12-09