Incidental Mutation 'IGL03287:Slc25a29'
ID 415765
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc25a29
Ensembl Gene ENSMUSG00000021265
Gene Name solute carrier family 25 (mitochondrial carrier, palmitoylcarnitine transporter), member 29
Synonyms mCACL, CACL, C030003J19Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03287
Quality Score
Status
Chromosome 12
Chromosomal Location 108791804-108801802 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 108797135 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 22 (F22L)
Ref Sequence ENSEMBL: ENSMUSP00000021693 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021693]
AlphaFold Q8BL03
Predicted Effect possibly damaging
Transcript: ENSMUST00000021693
AA Change: F22L

PolyPhen 2 Score 0.493 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000021693
Gene: ENSMUSG00000021265
AA Change: F22L

DomainStartEndE-ValueType
Pfam:Mito_carr 1 91 1.5e-21 PFAM
Pfam:Mito_carr 88 182 4.6e-25 PFAM
Pfam:Mito_carr 185 279 1.8e-21 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000137023
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139714
Predicted Effect noncoding transcript
Transcript: ENSMUST00000221453
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223296
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 nuclear-encoded mitochondrial protein that is a member of the large family of solute carrier family 25 (SLC25) mitochondrial transporters. The members of this superfamily are involved in numerous metabolic pathways and cell functions. This gene product was previously reported to be a mitochondrial carnitine-acylcarnitine-like (CACL) translocase (PMID:128829710) or an ornithine transporter (designated ORNT3, PMID:19287344), however, a recent study characterized the main role of this protein as a mitochondrial transporter of basic amino acids, with a preference for arginine and lysine (PMID:24652292). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Apr 2014]
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930519G04Rik A T 5: 115,008,237 (GRCm39) D17V probably damaging Het
Cdh5 T A 8: 104,854,747 (GRCm39) V225E probably damaging Het
Cfap52 C T 11: 67,826,802 (GRCm39) probably benign Het
Cib4 A G 5: 30,645,887 (GRCm39) L127P probably benign Het
Fbln2 A G 6: 91,210,476 (GRCm39) H140R probably damaging Het
Grm8 A G 6: 27,760,254 (GRCm39) F359L possibly damaging Het
Kat7 A T 11: 95,190,935 (GRCm39) D150E probably damaging Het
Kif1b A G 4: 149,299,438 (GRCm39) I944T possibly damaging Het
Krt87 T C 15: 101,330,218 (GRCm39) probably benign Het
Mast1 T C 8: 85,639,982 (GRCm39) S1142G probably benign Het
Neb A G 2: 52,027,335 (GRCm39) Y6889H probably damaging Het
Or10ak13 A G 4: 118,639,551 (GRCm39) V77A possibly damaging Het
Or1e16 A T 11: 73,286,845 (GRCm39) M1K probably null Het
Plk4 A T 3: 40,759,553 (GRCm39) I150L probably benign Het
Scn5a T C 9: 119,318,844 (GRCm39) D1598G probably damaging Het
Skor2 A G 18: 76,963,830 (GRCm39) K925E probably damaging Het
Slc27a2 A G 2: 126,395,312 (GRCm39) T80A probably damaging Het
Tlr3 A G 8: 45,855,817 (GRCm39) V121A probably benign Het
Tubgcp3 A T 8: 12,689,630 (GRCm39) D545E possibly damaging Het
Zdhhc8 T C 16: 18,042,964 (GRCm39) Y412C probably benign Het
Zmynd12 A G 4: 119,310,776 (GRCm39) E328G probably damaging Het
Other mutations in Slc25a29
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0116:Slc25a29 UTSW 12 108,793,017 (GRCm39) missense possibly damaging 0.94
R1876:Slc25a29 UTSW 12 108,793,637 (GRCm39) missense probably damaging 0.98
R2094:Slc25a29 UTSW 12 108,793,358 (GRCm39) missense probably damaging 1.00
R2233:Slc25a29 UTSW 12 108,801,587 (GRCm39) missense possibly damaging 0.92
R2276:Slc25a29 UTSW 12 108,792,852 (GRCm39) missense probably benign 0.09
R2277:Slc25a29 UTSW 12 108,792,852 (GRCm39) missense probably benign 0.09
R2279:Slc25a29 UTSW 12 108,792,852 (GRCm39) missense probably benign 0.09
R2383:Slc25a29 UTSW 12 108,792,934 (GRCm39) missense probably damaging 1.00
R4366:Slc25a29 UTSW 12 108,797,097 (GRCm39) intron probably benign
R7859:Slc25a29 UTSW 12 108,792,756 (GRCm39) missense probably benign 0.01
R9776:Slc25a29 UTSW 12 108,793,017 (GRCm39) missense possibly damaging 0.88
Posted On 2016-08-02