Incidental Mutation 'IGL00327:Aup1'
ID 6350
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Aup1
Ensembl Gene ENSMUSG00000068328
Gene Name ancient ubiquitous protein 1
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.308) question?
Stock # IGL00327
Quality Score
Status
Chromosome 6
Chromosomal Location 83031483-83034663 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 83033390 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 267 (E267G)
Ref Sequence ENSEMBL: ENSMUSP00000090281 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000000707] [ENSMUST00000077502] [ENSMUST00000089645] [ENSMUST00000092618] [ENSMUST00000101257] [ENSMUST00000113962] [ENSMUST00000113963] [ENSMUST00000122955] [ENSMUST00000134606] [ENSMUST00000204803]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000000707
SMART Domains Protein: ENSMUSP00000000707
Gene: ENSMUSG00000000693

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
SR 45 146 2.1e-50 SMART
SR 170 283 1.09e-25 SMART
SR 308 408 3.72e-51 SMART
SR 418 526 8.5e-37 SMART
Pfam:Lysyl_oxidase 530 730 3.9e-103 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000077502
SMART Domains Protein: ENSMUSP00000076708
Gene: ENSMUSG00000009145

DomainStartEndE-ValueType
low complexity region 2 19 N/A INTRINSIC
DEXDc 30 236 5.01e-4 SMART
low complexity region 268 280 N/A INTRINSIC
low complexity region 288 301 N/A INTRINSIC
HA2 441 530 4e-19 SMART
Pfam:OB_NTP_bind 555 674 2.2e-11 PFAM
low complexity region 695 708 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000089645
SMART Domains Protein: ENSMUSP00000087073
Gene: ENSMUSG00000068329

DomainStartEndE-ValueType
low complexity region 28 39 N/A INTRINSIC
transmembrane domain 106 125 N/A INTRINSIC
low complexity region 128 143 N/A INTRINSIC
Pfam:Trypsin 170 341 1.1e-14 PFAM
Pfam:Trypsin_2 182 320 1.2e-34 PFAM
PDZ 371 445 2.86e-10 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000092618
AA Change: E267G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000090281
Gene: ENSMUSG00000068328
AA Change: E267G

DomainStartEndE-ValueType
low complexity region 10 40 N/A INTRINSIC
transmembrane domain 52 74 N/A INTRINSIC
PlsC 119 222 1.04e-1 SMART
low complexity region 307 322 N/A INTRINSIC
CUE 325 366 1.3e-9 SMART
low complexity region 378 392 N/A INTRINSIC
low complexity region 421 439 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000101257
SMART Domains Protein: ENSMUSP00000098815
Gene: ENSMUSG00000000693

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
SR 45 146 2.1e-50 SMART
SR 170 283 1.09e-25 SMART
SR 308 396 5.46e-17 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000113962
SMART Domains Protein: ENSMUSP00000109595
Gene: ENSMUSG00000068329

DomainStartEndE-ValueType
low complexity region 28 39 N/A INTRINSIC
transmembrane domain 106 125 N/A INTRINSIC
low complexity region 128 143 N/A INTRINSIC
Pfam:Trypsin_2 182 237 2.7e-12 PFAM
Pfam:Trypsin 212 277 4.5e-6 PFAM
PDZ 285 348 4.89e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000113963
SMART Domains Protein: ENSMUSP00000109596
Gene: ENSMUSG00000068329

DomainStartEndE-ValueType
low complexity region 28 39 N/A INTRINSIC
transmembrane domain 106 125 N/A INTRINSIC
low complexity region 128 143 N/A INTRINSIC
Pfam:Trypsin 170 342 6.8e-15 PFAM
Pfam:Trypsin_2 182 320 7.1e-24 PFAM
PDZ 350 413 4.89e-1 SMART
Predicted Effect unknown
Transcript: ENSMUST00000203915
AA Change: E255G
Predicted Effect noncoding transcript
Transcript: ENSMUST00000154829
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204209
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203749
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203180
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203339
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203331
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204281
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144058
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203123
Predicted Effect probably benign
Transcript: ENSMUST00000122955
SMART Domains Protein: ENSMUSP00000138153
Gene: ENSMUSG00000068329

DomainStartEndE-ValueType
low complexity region 28 39 N/A INTRINSIC
transmembrane domain 106 125 N/A INTRINSIC
low complexity region 128 143 N/A INTRINSIC
Pfam:Trypsin 170 321 2.1e-10 PFAM
Pfam:Trypsin_2 182 317 9.5e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000134606
SMART Domains Protein: ENSMUSP00000115547
Gene: ENSMUSG00000068329

DomainStartEndE-ValueType
Pfam:Trypsin 7 180 2.7e-15 PFAM
Pfam:Trypsin_2 20 158 3.1e-24 PFAM
PDZ 209 283 2.86e-10 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000150217
SMART Domains Protein: ENSMUSP00000118234
Gene: ENSMUSG00000068329

DomainStartEndE-ValueType
low complexity region 4 11 N/A INTRINSIC
Pfam:Trypsin 41 215 1.6e-11 PFAM
Pfam:Trypsin_2 53 190 1.8e-31 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000132099
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204752
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204385
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205042
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204383
Predicted Effect probably benign
Transcript: ENSMUST00000204719
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204510
Predicted Effect probably benign
Transcript: ENSMUST00000204803
SMART Domains Protein: ENSMUSP00000144697
Gene: ENSMUSG00000009145

DomainStartEndE-ValueType
low complexity region 2 19 N/A INTRINSIC
DEXDc 30 236 2.1e-6 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204761
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205152
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204895
Predicted Effect probably benign
Transcript: ENSMUST00000204343
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: The protein encoded by this gene contains several conserved domains including a hydrophobic domain, an acetyltransferase domain, a ubiquitin binding domain, and a domain required for recruitment of ubiquitin-conjugating enzyme E2 G2 (Ube2g2). In humans, this protein localizes to the endoplasmic reticulum and to lipid droplets. This protein is thought to be involved both in the degradation of misfolded proteins from the endoplasmic reticulum and in the storage of neutral lipids. Reduced expression of the human ortholog of this gene strongly reduces lipid droplet clustering in the cell, and causes stabilization of misfolded proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atg16l2 A G 7: 100,949,367 (GRCm39) L60S probably damaging Het
Bpi T C 2: 158,116,764 (GRCm39) probably benign Het
Brinp2 A G 1: 158,074,670 (GRCm39) Y484H probably benign Het
Colq C T 14: 31,257,545 (GRCm39) probably null Het
Cubn T C 2: 13,431,867 (GRCm39) D1242G possibly damaging Het
Dclre1c T A 2: 3,434,821 (GRCm39) L95* probably null Het
Fry C T 5: 150,263,869 (GRCm39) R171* probably null Het
Krt23 T C 11: 99,383,610 (GRCm39) E94G probably damaging Het
Krt6b T G 15: 101,588,267 (GRCm39) Q131P probably benign Het
Lonp1 A G 17: 56,926,265 (GRCm39) L414P probably damaging Het
Lrit2 T A 14: 36,793,920 (GRCm39) M328K probably benign Het
Lysmd3 C T 13: 81,813,197 (GRCm39) L22F probably benign Het
Map3k20 A G 2: 72,242,514 (GRCm39) D388G probably damaging Het
Mrpl44 C T 1: 79,758,721 (GRCm39) L290F probably benign Het
Nell1 A G 7: 49,770,421 (GRCm39) H160R probably damaging Het
Nlrc3 T C 16: 3,773,030 (GRCm39) N109S probably damaging Het
Prpf40a T C 2: 53,040,700 (GRCm39) T553A probably benign Het
Ptpn23 G T 9: 110,217,174 (GRCm39) T894K probably benign Het
Scgb2b27 A G 7: 33,712,771 (GRCm39) C24R probably damaging Het
Sipa1l3 G T 7: 29,053,558 (GRCm39) H140N probably damaging Het
Slc22a23 T G 13: 34,489,228 (GRCm39) D219A probably damaging Het
Slc9a7 T C X: 20,005,158 (GRCm39) Y557C probably damaging Het
Slco1a1 A T 6: 141,854,851 (GRCm39) I600N probably damaging Het
Tmx2 T C 2: 84,503,643 (GRCm39) N190S probably benign Het
Tpr T G 1: 150,299,447 (GRCm39) probably benign Het
Yme1l1 T C 2: 23,082,512 (GRCm39) V501A probably benign Het
Other mutations in Aup1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02505:Aup1 APN 6 83,032,258 (GRCm39) missense probably benign 0.06
R0637:Aup1 UTSW 6 83,033,842 (GRCm39) missense probably damaging 1.00
R1544:Aup1 UTSW 6 83,032,187 (GRCm39) missense possibly damaging 0.84
R1686:Aup1 UTSW 6 83,032,226 (GRCm39) missense probably damaging 0.97
R4196:Aup1 UTSW 6 83,032,211 (GRCm39) missense probably damaging 1.00
R4512:Aup1 UTSW 6 83,033,368 (GRCm39) nonsense probably null
R5119:Aup1 UTSW 6 83,032,115 (GRCm39) missense probably damaging 0.96
R5387:Aup1 UTSW 6 83,032,005 (GRCm39) missense probably damaging 0.98
R6329:Aup1 UTSW 6 83,031,588 (GRCm39) unclassified probably benign
R6837:Aup1 UTSW 6 83,034,279 (GRCm39) missense possibly damaging 0.83
R7122:Aup1 UTSW 6 83,032,123 (GRCm39) missense probably benign 0.04
R7474:Aup1 UTSW 6 83,031,948 (GRCm39) missense probably benign 0.38
R7630:Aup1 UTSW 6 83,031,904 (GRCm39) missense unknown
R7701:Aup1 UTSW 6 83,032,908 (GRCm39) missense probably benign 0.21
R7747:Aup1 UTSW 6 83,031,776 (GRCm39) missense unknown
R8069:Aup1 UTSW 6 83,032,910 (GRCm39) nonsense probably null
R8213:Aup1 UTSW 6 83,031,588 (GRCm39) unclassified probably benign
R8732:Aup1 UTSW 6 83,033,602 (GRCm39) missense probably damaging 0.99
Z1176:Aup1 UTSW 6 83,033,614 (GRCm39) missense probably benign 0.00
Z1177:Aup1 UTSW 6 83,034,505 (GRCm39) missense unknown
Posted On 2012-04-20