Incidental Mutation 'IGL03063:Gm17190'
ID 409546
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17190
Ensembl Gene ENSMUSG00000099115
Gene Name predicted gene 17190
Synonyms
Accession Numbers
Essential gene? Possibly essential (E-score: 0.552) question?
Stock # IGL03063
Quality Score
Status
Chromosome 13
Chromosomal Location 96218562-96219410 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to A at 96219270 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000152074 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000161263] [ENSMUST00000182289] [ENSMUST00000185178] [ENSMUST00000220449]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000161263
SMART Domains Protein: ENSMUSP00000124473
Gene: ENSMUSG00000051111

DomainStartEndE-ValueType
low complexity region 51 61 N/A INTRINSIC
Pfam:Sugar_tr 117 428 9.1e-31 PFAM
Pfam:MFS_1 154 470 5e-27 PFAM
Pfam:Pentapeptide_4 496 573 4.8e-12 PFAM
Pfam:MFS_1 564 725 1.5e-11 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000182289
SMART Domains Protein: ENSMUSP00000138317
Gene: ENSMUSG00000051111

DomainStartEndE-ValueType
low complexity region 51 61 N/A INTRINSIC
Pfam:Sugar_tr 119 427 2.2e-30 PFAM
Pfam:MFS_1 154 470 5e-27 PFAM
Pfam:Pentapeptide_4 496 571 6.2e-15 PFAM
transmembrane domain 581 603 N/A INTRINSIC
transmembrane domain 610 632 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000184369
Predicted Effect unknown
Transcript: ENSMUST00000185178
AA Change: G202D
SMART Domains Protein: ENSMUSP00000138965
Gene: ENSMUSG00000099115
AA Change: G202D

DomainStartEndE-ValueType
internal_repeat_1 32 57 4.12e-5 PROSPERO
RRM 72 144 5.93e-17 SMART
low complexity region 153 278 N/A INTRINSIC
low complexity region 286 311 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000220449
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc6 C T 7: 45,665,856 (GRCm39) V255I probably benign Het
Arfgef2 T C 2: 166,701,702 (GRCm39) probably benign Het
Bpifb2 A T 2: 153,731,044 (GRCm39) Q205L probably damaging Het
Ccdc30 C T 4: 119,206,964 (GRCm39) R386Q possibly damaging Het
Cdk5rap2 T A 4: 70,273,114 (GRCm39) probably null Het
Comtd1 A G 14: 21,897,735 (GRCm39) probably null Het
Dao T C 5: 114,159,076 (GRCm39) C261R probably damaging Het
Dner A G 1: 84,563,059 (GRCm39) V187A possibly damaging Het
Dsg3 T C 18: 20,666,425 (GRCm39) probably benign Het
Eif3j2 A G 18: 43,610,444 (GRCm39) L123P possibly damaging Het
Esf1 G A 2: 139,996,706 (GRCm39) probably benign Het
Exo5 G A 4: 120,778,830 (GRCm39) T345I possibly damaging Het
Fancl A T 11: 26,337,299 (GRCm39) I29F probably damaging Het
Gadl1 C T 9: 115,795,335 (GRCm39) H313Y probably damaging Het
Gtf3c1 G T 7: 125,245,675 (GRCm39) T1580N possibly damaging Het
Gtf3c6 T A 10: 40,127,155 (GRCm39) I66L probably benign Het
Hhla1 A G 15: 65,813,639 (GRCm39) I231T probably damaging Het
Hk2 A G 6: 82,716,630 (GRCm39) Y273H probably damaging Het
Hk2 A G 6: 82,726,213 (GRCm39) I83T probably benign Het
Ifit1 T C 19: 34,625,404 (GRCm39) V180A possibly damaging Het
Igkv9-129 A T 6: 67,817,172 (GRCm39) D92V probably damaging Het
Lrrc1 A G 9: 77,406,551 (GRCm39) F36S probably damaging Het
Man1b1 A G 2: 25,224,416 (GRCm39) E102G possibly damaging Het
Myh8 A G 11: 67,179,031 (GRCm39) S475G probably benign Het
Or52s1 T A 7: 102,861,841 (GRCm39) V247D probably damaging Het
Otud4 T A 8: 80,390,419 (GRCm39) M343K probably benign Het
Peg10 A T 6: 4,756,647 (GRCm39) probably benign Het
Plet1 T A 9: 50,415,722 (GRCm39) N197K probably benign Het
Ppp1r12a C T 10: 108,097,115 (GRCm39) R243C probably damaging Het
Serpinb10 A T 1: 107,469,957 (GRCm39) K146N possibly damaging Het
Sis A G 3: 72,835,630 (GRCm39) F911L probably benign Het
Spon1 G A 7: 113,632,260 (GRCm39) V528M possibly damaging Het
Tdrd9 T C 12: 112,010,733 (GRCm39) V1100A probably benign Het
Tmtc3 T C 10: 100,283,468 (GRCm39) M696V probably benign Het
Triobp A G 15: 78,875,084 (GRCm39) E122G probably damaging Het
Wt1 G A 2: 105,000,368 (GRCm39) probably null Het
Other mutations in Gm17190
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6603:Gm17190 UTSW 13 96,218,770 (GRCm39) missense possibly damaging 0.81
R7359:Gm17190 UTSW 13 96,218,970 (GRCm39) missense probably damaging 0.98
R7466:Gm17190 UTSW 13 96,219,287 (GRCm39) nonsense probably null
R8166:Gm17190 UTSW 13 96,219,142 (GRCm39) missense unknown
Posted On 2016-08-02