Incidental Mutation 'IGL02006:Slc7a15'
ID 183213
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc7a15
Ensembl Gene ENSMUSG00000020600
Gene Name solute carrier family 7 (cationic amino acid transporter, y+ system), member 15
Synonyms Arpat, 9030221C07Rik, 2010001P20Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.151) question?
Stock # IGL02006
Quality Score
Status
Chromosome 12
Chromosomal Location 8578483-8649066 bp(-) (GRCm39)
Type of Mutation critical splice acceptor site
DNA Base Change (assembly) T to C at 8585508 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000129806 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036938] [ENSMUST00000036938] [ENSMUST00000095863] [ENSMUST00000165657]
AlphaFold Q50E62
Predicted Effect probably null
Transcript: ENSMUST00000036938
SMART Domains Protein: ENSMUSP00000047873
Gene: ENSMUSG00000020600

DomainStartEndE-ValueType
Pfam:AA_permease_2 1 197 2.6e-20 PFAM
Pfam:AA_permease 1 221 1.5e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000036938
SMART Domains Protein: ENSMUSP00000047873
Gene: ENSMUSG00000020600

DomainStartEndE-ValueType
Pfam:AA_permease_2 1 197 2.6e-20 PFAM
Pfam:AA_permease 1 221 1.5e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000095863
SMART Domains Protein: ENSMUSP00000093548
Gene: ENSMUSG00000020600

DomainStartEndE-ValueType
Pfam:AA_permease_2 31 453 2.6e-57 PFAM
Pfam:AA_permease 35 480 2.2e-21 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129465
Predicted Effect probably null
Transcript: ENSMUST00000165657
SMART Domains Protein: ENSMUSP00000129806
Gene: ENSMUSG00000020600

DomainStartEndE-ValueType
Pfam:AA_permease_2 1 197 2.6e-20 PFAM
Pfam:AA_permease 1 221 1.5e-9 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219595
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl1 G A 4: 86,117,582 (GRCm39) G182S probably damaging Het
Akr1b7 A T 6: 34,392,385 (GRCm39) N66I probably benign Het
Arrdc3 T A 13: 81,031,893 (GRCm39) I42N probably damaging Het
Atp6v0d2 G T 4: 19,878,325 (GRCm39) A316E probably damaging Het
Atp8a2 A G 14: 60,094,497 (GRCm39) V847A possibly damaging Het
Ccdc171 A G 4: 83,713,479 (GRCm39) N1173D possibly damaging Het
Crb2 A C 2: 37,676,475 (GRCm39) D152A probably damaging Het
Ecm1 T C 3: 95,641,557 (GRCm39) E559G probably damaging Het
Ephb1 A G 9: 102,071,971 (GRCm39) probably null Het
Fndc11 C A 2: 180,863,884 (GRCm39) R230S probably damaging Het
Frem1 A G 4: 82,911,037 (GRCm39) probably null Het
Fyco1 G A 9: 123,658,896 (GRCm39) Q427* probably null Het
Gm17541 A G 12: 4,739,619 (GRCm39) probably benign Het
Gm5431 C T 11: 48,779,330 (GRCm39) V809M probably damaging Het
Gm7293 A G 9: 51,534,043 (GRCm39) noncoding transcript Het
Ift52 T C 2: 162,865,289 (GRCm39) S47P probably benign Het
Iqcf6 A G 9: 106,504,510 (GRCm39) D58G probably benign Het
Itm2b T C 14: 73,600,488 (GRCm39) probably benign Het
Jakmip1 T C 5: 37,278,331 (GRCm39) I536T probably damaging Het
Kcnh1 T G 1: 191,873,323 (GRCm39) M3R possibly damaging Het
Kcnh5 G T 12: 74,944,322 (GRCm39) P976T probably damaging Het
Layn G A 9: 50,968,591 (GRCm39) probably benign Het
Lrrc37a T A 11: 103,347,317 (GRCm39) Q3126L probably damaging Het
Meioc A T 11: 102,565,092 (GRCm39) D180V probably damaging Het
Myo15a T A 11: 60,401,954 (GRCm39) C3066S probably damaging Het
Nbeal1 T C 1: 60,311,418 (GRCm39) probably null Het
Negr1 T C 3: 156,721,810 (GRCm39) probably benign Het
Nek1 T A 8: 61,557,226 (GRCm39) N940K probably benign Het
Nfkbib A T 7: 28,465,667 (GRCm39) probably null Het
Nol4 T A 18: 23,054,975 (GRCm39) T152S probably damaging Het
Oas3 G T 5: 120,907,300 (GRCm39) R446S probably benign Het
Oosp3 C T 19: 11,676,784 (GRCm39) L48F probably damaging Het
Or2r3 A G 6: 42,449,025 (GRCm39) V29A probably benign Het
Or2w25 T C 11: 59,503,985 (GRCm39) L65P probably damaging Het
Pik3ap1 C A 19: 41,291,032 (GRCm39) W500L probably benign Het
Ppih A G 4: 119,168,779 (GRCm39) probably benign Het
Ro60 G T 1: 143,636,084 (GRCm39) probably benign Het
Srl T C 16: 4,315,150 (GRCm39) E164G probably benign Het
Tbx10 C A 19: 4,048,186 (GRCm39) T237K probably damaging Het
Vwa5b2 T C 16: 20,415,843 (GRCm39) V392A probably damaging Het
Wfdc5 A T 2: 164,024,483 (GRCm39) probably benign Het
Xirp2 T C 2: 67,342,306 (GRCm39) F1516L possibly damaging Het
Znfx1 A G 2: 166,897,683 (GRCm39) C414R probably damaging Het
Other mutations in Slc7a15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00310:Slc7a15 APN 12 8,589,121 (GRCm39) missense probably damaging 1.00
IGL00507:Slc7a15 APN 12 8,585,474 (GRCm39) missense probably damaging 1.00
IGL01839:Slc7a15 APN 12 8,589,365 (GRCm39) missense probably damaging 1.00
IGL02201:Slc7a15 APN 12 8,589,023 (GRCm39) missense possibly damaging 0.93
R0422:Slc7a15 UTSW 12 8,584,400 (GRCm39) missense probably benign 0.17
R0794:Slc7a15 UTSW 12 8,589,278 (GRCm39) missense probably benign 0.19
R1194:Slc7a15 UTSW 12 8,585,772 (GRCm39) missense probably damaging 1.00
R1420:Slc7a15 UTSW 12 8,584,442 (GRCm39) missense probably benign 0.01
R2696:Slc7a15 UTSW 12 8,579,345 (GRCm39) makesense probably null
R4809:Slc7a15 UTSW 12 8,589,002 (GRCm39) missense probably benign 0.10
R5236:Slc7a15 UTSW 12 8,589,005 (GRCm39) missense probably benign 0.38
R5579:Slc7a15 UTSW 12 8,589,344 (GRCm39) missense probably benign 0.00
R6453:Slc7a15 UTSW 12 8,584,490 (GRCm39) missense possibly damaging 0.77
R7136:Slc7a15 UTSW 12 8,588,895 (GRCm39) missense probably damaging 0.98
R8005:Slc7a15 UTSW 12 8,589,395 (GRCm39) missense probably damaging 0.97
R8910:Slc7a15 UTSW 12 8,589,117 (GRCm39) start gained probably benign
R9474:Slc7a15 UTSW 12 8,588,794 (GRCm39) missense probably damaging 0.99
R9786:Slc7a15 UTSW 12 8,580,280 (GRCm39) missense probably benign 0.31
X0027:Slc7a15 UTSW 12 8,589,350 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07