Incidental Mutation 'IGL01449:Slc31a2'
ID 84569
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc31a2
Ensembl Gene ENSMUSG00000066152
Gene Name solute carrier family 31, member 2
Synonyms Ctr2
Accession Numbers
Essential gene? Probably non essential (E-score: 0.162) question?
Stock # IGL01449
Quality Score
Status
Chromosome 4
Chromosomal Location 62198630-62216649 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 62210933 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 22 (T22I)
Ref Sequence ENSEMBL: ENSMUSP00000103092 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084530] [ENSMUST00000107467] [ENSMUST00000107468]
AlphaFold Q9CPU9
Predicted Effect probably benign
Transcript: ENSMUST00000084530
AA Change: T24I

PolyPhen 2 Score 0.156 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000081578
Gene: ENSMUSG00000066152
AA Change: T24I

DomainStartEndE-ValueType
Pfam:Ctr 1 136 1.1e-28 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000107467
AA Change: T22I

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000103091
Gene: ENSMUSG00000066152
AA Change: T22I

DomainStartEndE-ValueType
Pfam:Ctr 1 134 3.7e-28 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000107468
AA Change: T22I

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000103092
Gene: ENSMUSG00000066152
AA Change: T22I

DomainStartEndE-ValueType
Pfam:Ctr 1 134 3.7e-28 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700030K09Rik A T 8: 73,198,693 (GRCm39) L33F probably benign Het
Actr8 T C 14: 29,712,927 (GRCm39) probably null Het
Aldh16a1 C A 7: 44,791,391 (GRCm39) A105S probably damaging Het
Angpt2 T C 8: 18,760,641 (GRCm39) T154A probably benign Het
BC051665 A G 13: 60,930,518 (GRCm39) V278A probably damaging Het
Cap1 T C 4: 122,753,980 (GRCm39) T458A probably damaging Het
Clcn3 A T 8: 61,387,632 (GRCm39) S179T probably damaging Het
Cyp2a22 T C 7: 26,632,978 (GRCm39) D408G probably benign Het
Fam217b T A 2: 178,062,943 (GRCm39) S302R probably damaging Het
Fcho2 A T 13: 98,926,315 (GRCm39) D89E probably benign Het
Fnip1 C T 11: 54,390,334 (GRCm39) R434C probably damaging Het
Gga3 G A 11: 115,479,928 (GRCm39) T261M probably damaging Het
Gm21985 T C 2: 112,169,741 (GRCm39) F292L probably damaging Het
Gm43638 A T 5: 87,634,074 (GRCm39) S178T possibly damaging Het
Igkv10-95 G A 6: 68,657,748 (GRCm39) G68E probably damaging Het
Katnip T A 7: 125,469,857 (GRCm39) V1442D probably damaging Het
Lpcat2 G A 8: 93,597,775 (GRCm39) R180Q possibly damaging Het
Muc6 C T 7: 141,218,527 (GRCm39) A1984T possibly damaging Het
Npy4r T A 14: 33,868,322 (GRCm39) Y322F probably damaging Het
Nwd2 T A 5: 63,962,937 (GRCm39) H840Q probably damaging Het
Or7g26 G A 9: 19,230,529 (GRCm39) G233D probably damaging Het
Osbpl2 G T 2: 179,786,987 (GRCm39) probably benign Het
Pclo T A 5: 14,728,530 (GRCm39) probably benign Het
Pold4 T C 19: 4,282,921 (GRCm39) probably benign Het
Ppp1r16a A G 15: 76,578,494 (GRCm39) probably benign Het
Pprc1 C T 19: 46,053,671 (GRCm39) probably benign Het
Prkcg A G 7: 3,368,135 (GRCm39) D343G probably benign Het
Scaf11 A C 15: 96,317,007 (GRCm39) S852R probably benign Het
Sox30 T A 11: 45,872,169 (GRCm39) D341E probably damaging Het
Tle4 A G 19: 14,442,704 (GRCm39) S339P probably benign Het
Tsg101 A T 7: 46,558,673 (GRCm39) Y78N probably damaging Het
Ttc1 T A 11: 43,629,630 (GRCm39) S179C probably damaging Het
Txnrd3 T A 6: 89,631,129 (GRCm39) S142T probably benign Het
Ubr4 C A 4: 139,140,047 (GRCm39) A1210E probably damaging Het
Uroc1 C A 6: 90,315,635 (GRCm39) P172Q probably damaging Het
Usp12 T C 5: 146,691,250 (GRCm39) D168G probably benign Het
Vmn1r32 T A 6: 66,529,916 (GRCm39) M287L probably benign Het
Vwa8 C T 14: 79,420,428 (GRCm39) Q1710* probably null Het
Wdfy4 T A 14: 32,825,994 (GRCm39) Q1219L probably damaging Het
Zbtb17 A G 4: 141,190,616 (GRCm39) T145A probably benign Het
Zfp697 T C 3: 98,334,846 (GRCm39) C204R probably damaging Het
Other mutations in Slc31a2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01977:Slc31a2 APN 4 62,214,197 (GRCm39) missense probably damaging 1.00
IGL01990:Slc31a2 APN 4 62,214,207 (GRCm39) missense probably benign 0.20
IGL02396:Slc31a2 APN 4 62,215,310 (GRCm39) missense probably damaging 1.00
R0410:Slc31a2 UTSW 4 62,210,890 (GRCm39) missense probably benign
R2471:Slc31a2 UTSW 4 62,214,312 (GRCm39) missense probably null 1.00
R4801:Slc31a2 UTSW 4 62,210,869 (GRCm39) missense probably damaging 1.00
R4802:Slc31a2 UTSW 4 62,210,869 (GRCm39) missense probably damaging 1.00
R4916:Slc31a2 UTSW 4 62,215,325 (GRCm39) missense probably damaging 0.97
R5467:Slc31a2 UTSW 4 62,210,924 (GRCm39) missense probably damaging 1.00
R5795:Slc31a2 UTSW 4 62,215,289 (GRCm39) missense probably damaging 1.00
R8678:Slc31a2 UTSW 4 62,210,896 (GRCm39) missense probably benign 0.44
Posted On 2013-11-11