Incidental Mutation 'IGL01710:Slc25a17'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc25a17
Ensembl Gene ENSMUSG00000022404
Gene Namesolute carrier family 25 (mitochondrial carrier, peroxisomal membrane protein), member 17
Synonyms34kDa, PMP34
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.224) question?
Stock #IGL01710
Quality Score
Chromosomal Location81318911-81360812 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 81327326 bp
Amino Acid Change Leucine to Stop codon at position 163 (L163*)
Ref Sequence ENSEMBL: ENSMUSP00000023040 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023040] [ENSMUST00000231140]
Predicted Effect probably null
Transcript: ENSMUST00000023040
AA Change: L163*
SMART Domains Protein: ENSMUSP00000023040
Gene: ENSMUSG00000022404
AA Change: L163*

Pfam:Mito_carr 6 97 1e-17 PFAM
Pfam:Mito_carr 97 197 6.3e-24 PFAM
Pfam:Mito_carr 199 297 3.2e-16 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229564
Predicted Effect noncoding transcript
Transcript: ENSMUST00000229617
Predicted Effect probably benign
Transcript: ENSMUST00000231140
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers. It is expressed in the liver, and is likely involved in transport. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ablim3 G A 18: 61,871,574 T48I probably damaging Het
Ccpg1 T C 9: 72,997,441 probably benign Het
Chkb G A 15: 89,426,640 Q379* probably null Het
Chst15 T A 7: 132,270,507 D15V probably benign Het
Cntn4 G A 6: 106,550,431 V425I possibly damaging Het
Cpa6 T A 1: 10,325,272 N390I probably damaging Het
Efhd2 A G 4: 141,860,561 F193S probably damaging Het
Ell3 T C 2: 121,441,512 H128R probably damaging Het
Ercc5 T G 1: 44,164,075 L291V probably damaging Het
Eva1c A G 16: 90,904,347 Y302C probably damaging Het
Fmo3 A C 1: 162,983,043 L26R probably damaging Het
Galntl6 T A 8: 58,535,968 D17V probably damaging Het
Gm6483 C T 8: 19,691,613 P55S probably damaging Het
Gstt2 A G 10: 75,833,745 probably benign Het
Hmcn2 T A 2: 31,343,102 L221Q probably damaging Het
Hoxa3 T C 6: 52,170,574 probably benign Het
Kctd12b T C X: 153,689,483 D70G probably damaging Het
Kdm7a T A 6: 39,175,386 E125D probably benign Het
Klk1b21 T A 7: 44,106,495 F249L probably benign Het
Mrpl41 T C 2: 24,974,417 D81G possibly damaging Het
Nomo1 T A 7: 46,038,556 L82Q probably damaging Het
Olfr482 G T 7: 108,095,242 F109L probably benign Het
Papolg A T 11: 23,864,026 S718T probably damaging Het
Pex6 A G 17: 46,725,326 probably benign Het
Pi4k2a T A 19: 42,104,979 L253Q probably damaging Het
Prdx6b T A 2: 80,293,146 F100I probably damaging Het
Prr36 G A 8: 4,215,243 P169L probably damaging Het
Ptgfrn T C 3: 101,073,088 E312G probably damaging Het
Rasgrf1 A G 9: 89,991,692 I685V probably benign Het
Setdb1 T C 3: 95,338,853 E586G probably damaging Het
Sez6l2 C A 7: 126,968,216 T841K probably damaging Het
Slc35f3 A T 8: 126,389,161 I276F probably benign Het
Tcerg1l T A 7: 138,395,060 K149N possibly damaging Het
Tex28 T A X: 74,152,333 K278* probably null Het
Tmprss9 A G 10: 80,897,959 probably benign Het
Tnfaip8l1 A G 17: 56,171,782 K24R probably benign Het
Trim36 T C 18: 46,188,388 probably benign Het
Uba1 C T X: 20,671,365 T274I possibly damaging Het
Ubr2 T C 17: 46,943,409 T1439A probably benign Het
Ubr4 A G 4: 139,418,461 D1523G possibly damaging Het
Uchl4 A T 9: 64,235,506 T90S probably benign Het
Other mutations in Slc25a17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02655:Slc25a17 APN 15 81323643 missense probably benign 0.02
IGL03258:Slc25a17 APN 15 81329042 splice site probably benign
big_guy UTSW 15 81360774 utr 5 prime probably benign
R0114:Slc25a17 UTSW 15 81337959 missense probably damaging 1.00
R0763:Slc25a17 UTSW 15 81323706 splice site probably benign
R1628:Slc25a17 UTSW 15 81360724 missense possibly damaging 0.92
R2179:Slc25a17 UTSW 15 81337950 missense probably benign 0.02
R3420:Slc25a17 UTSW 15 81360700 missense probably benign 0.04
R3421:Slc25a17 UTSW 15 81360700 missense probably benign 0.04
R3687:Slc25a17 UTSW 15 81327284 missense probably benign 0.01
R3688:Slc25a17 UTSW 15 81327284 missense probably benign 0.01
R4707:Slc25a17 UTSW 15 81327326 missense probably damaging 0.97
R5617:Slc25a17 UTSW 15 81360774 utr 5 prime probably benign
R5650:Slc25a17 UTSW 15 81329176 splice site probably null
R5817:Slc25a17 UTSW 15 81327060 missense probably damaging 0.97
R6207:Slc25a17 UTSW 15 81329064 missense probably damaging 1.00
R6727:Slc25a17 UTSW 15 81337953 missense probably benign 0.05
Posted On2014-01-21