Incidental Mutation 'IGL01643:Slc37a2'
ID 93610
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slc37a2
Ensembl Gene ENSMUSG00000032122
Gene Name solute carrier family 37 (glycerol-3-phosphate transporter), member 2
Synonyms ci2, Slc37a1, G3PP, cI-2
Accession Numbers
Essential gene? Probably non essential (E-score: 0.086) question?
Stock # IGL01643
Quality Score
Status
Chromosome 9
Chromosomal Location 37140445-37166709 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 37146849 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000124569 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115068] [ENSMUST00000161114]
AlphaFold Q9WU81
Predicted Effect probably benign
Transcript: ENSMUST00000115068
SMART Domains Protein: ENSMUSP00000110720
Gene: ENSMUSG00000032122

DomainStartEndE-ValueType
Pfam:MFS_1 23 424 1.2e-40 PFAM
transmembrane domain 431 453 N/A INTRINSIC
transmembrane domain 460 482 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000161114
SMART Domains Protein: ENSMUSP00000124569
Gene: ENSMUSG00000032122

DomainStartEndE-ValueType
Pfam:MFS_1 24 426 1.2e-40 PFAM
transmembrane domain 431 453 N/A INTRINSIC
transmembrane domain 460 482 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000162018
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427D14Rik C T 11: 72,082,414 (GRCm39) R304Q probably damaging Het
Afap1l1 T A 18: 61,884,897 (GRCm39) E196V probably damaging Het
Bmp5 A T 9: 75,746,895 (GRCm39) D251V probably damaging Het
Ccser1 A G 6: 61,288,839 (GRCm39) H334R probably benign Het
Crnkl1 A G 2: 145,773,268 (GRCm39) M126T probably damaging Het
Ddrgk1 T C 2: 130,500,214 (GRCm39) probably benign Het
Dpy19l4 T C 4: 11,290,184 (GRCm39) probably benign Het
Eral1 A G 11: 77,965,104 (GRCm39) probably null Het
Ereg T A 5: 91,234,637 (GRCm39) S17T probably benign Het
Fgfr1 T A 8: 26,056,751 (GRCm39) M280K probably benign Het
Gpr65 A G 12: 98,242,013 (GRCm39) E222G probably damaging Het
Grid1 G T 14: 35,045,392 (GRCm39) probably null Het
Hspa12b A G 2: 130,984,617 (GRCm39) T329A probably damaging Het
Inpp4b A G 8: 82,798,400 (GRCm39) I863V probably damaging Het
Kash5 A T 7: 44,849,710 (GRCm39) M71K probably damaging Het
Krt8 G T 15: 101,905,508 (GRCm39) S447Y possibly damaging Het
Lama2 T A 10: 26,946,368 (GRCm39) probably benign Het
Lama4 A C 10: 38,932,846 (GRCm39) N574T probably benign Het
Lig3 T C 11: 82,689,118 (GRCm39) S791P probably damaging Het
Oas2 A T 5: 120,874,252 (GRCm39) probably benign Het
Or4c12b A T 2: 89,647,017 (GRCm39) I116F probably damaging Het
Pdk1 A G 2: 71,728,049 (GRCm39) D370G probably damaging Het
Popdc3 T A 10: 45,190,976 (GRCm39) I29N probably damaging Het
Rbp3 A T 14: 33,678,793 (GRCm39) I914F probably benign Het
Rnf207 C T 4: 152,402,718 (GRCm39) probably benign Het
Ryr2 T A 13: 11,707,563 (GRCm39) I2825F possibly damaging Het
Vps8 T C 16: 21,336,972 (GRCm39) V791A possibly damaging Het
Wdr64 T C 1: 175,599,877 (GRCm39) L127P probably damaging Het
Whrn T C 4: 63,334,672 (GRCm39) T368A possibly damaging Het
Other mutations in Slc37a2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01719:Slc37a2 APN 9 37,145,474 (GRCm39) missense probably damaging 1.00
IGL02039:Slc37a2 APN 9 37,144,980 (GRCm39) missense probably damaging 0.98
IGL02286:Slc37a2 APN 9 37,146,455 (GRCm39) missense probably damaging 1.00
IGL02951:Slc37a2 APN 9 37,166,611 (GRCm39) missense probably benign 0.00
PIT4581001:Slc37a2 UTSW 9 37,148,701 (GRCm39) missense probably benign 0.00
R0547:Slc37a2 UTSW 9 37,144,418 (GRCm39) splice site probably null
R0689:Slc37a2 UTSW 9 37,146,846 (GRCm39) splice site probably benign
R1301:Slc37a2 UTSW 9 37,148,177 (GRCm39) missense probably benign 0.05
R3927:Slc37a2 UTSW 9 37,146,803 (GRCm39) missense probably damaging 1.00
R4834:Slc37a2 UTSW 9 37,146,404 (GRCm39) missense probably damaging 0.97
R5154:Slc37a2 UTSW 9 37,142,939 (GRCm39) makesense probably null
R5292:Slc37a2 UTSW 9 37,150,453 (GRCm39) nonsense probably null
R6150:Slc37a2 UTSW 9 37,149,643 (GRCm39) missense probably damaging 1.00
R6959:Slc37a2 UTSW 9 37,152,630 (GRCm39) missense probably benign
R7014:Slc37a2 UTSW 9 37,145,183 (GRCm39) missense probably damaging 1.00
R7605:Slc37a2 UTSW 9 37,148,624 (GRCm39) missense possibly damaging 0.71
R7974:Slc37a2 UTSW 9 37,150,421 (GRCm39) splice site probably null
R8342:Slc37a2 UTSW 9 37,149,510 (GRCm39) critical splice donor site probably null
R8419:Slc37a2 UTSW 9 37,148,726 (GRCm39) missense probably benign 0.00
R9039:Slc37a2 UTSW 9 37,148,658 (GRCm39) missense probably benign
R9314:Slc37a2 UTSW 9 37,150,482 (GRCm39) missense possibly damaging 0.49
Posted On 2013-12-09