Incidental Mutation 'IGL02744:Gm11110'
ID 306007
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11110
Ensembl Gene ENSMUSG00000079414
Gene Name predicted gene 11110
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL02744
Quality Score
Status
Chromosome 17
Chromosomal Location 57399023-57412942 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 57399693 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000071135 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071135] [ENSMUST00000112915]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000071135
SMART Domains Protein: ENSMUSP00000071135
Gene: ENSMUSG00000062591

DomainStartEndE-ValueType
Tubulin 47 244 4.45e-67 SMART
Tubulin_C 246 383 5.5e-49 SMART
low complexity region 428 444 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000112915
AA Change: D108V
SMART Domains Protein: ENSMUSP00000108537
Gene: ENSMUSG00000079414
AA Change: D108V

DomainStartEndE-ValueType
low complexity region 66 78 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930564D02Rik A G 3: 104,985,852 (GRCm39) M89V unknown Het
Actl11 C A 9: 107,807,061 (GRCm39) H461Q probably benign Het
Aoc1l1 A G 6: 48,952,249 (GRCm39) E58G probably benign Het
Aox4 A T 1: 58,294,711 (GRCm39) R973S possibly damaging Het
Arhgef10 C T 8: 14,980,198 (GRCm39) A146V probably benign Het
Cep350 A T 1: 155,807,279 (GRCm39) S713T probably damaging Het
Epha5 T C 5: 84,255,848 (GRCm39) I458V probably benign Het
Galnt17 A G 5: 131,140,613 (GRCm39) I168T probably damaging Het
Gli3 T C 13: 15,788,471 (GRCm39) probably null Het
Gm8206 T C 14: 6,022,488 (GRCm38) I4V possibly damaging Het
Golga1 A G 2: 38,908,486 (GRCm39) S713P probably damaging Het
Ing5 T C 1: 93,744,210 (GRCm39) M172T probably damaging Het
Lyn A G 4: 3,738,808 (GRCm39) T27A probably benign Het
Or2b28 A G 13: 21,531,164 (GRCm39) Y22C probably damaging Het
Pou5f1 T C 17: 35,820,311 (GRCm39) V40A probably damaging Het
Pramel13 A T 4: 144,119,493 (GRCm39) L358Q probably damaging Het
Prdm16 A G 4: 154,429,910 (GRCm39) L353P probably damaging Het
Psg18 T A 7: 18,083,327 (GRCm39) Q276L probably benign Het
Ralgapb A C 2: 158,288,071 (GRCm39) Q369H probably damaging Het
Slc44a4 A G 17: 35,146,776 (GRCm39) N300D probably damaging Het
Slc6a15 A T 10: 103,253,894 (GRCm39) E610V probably benign Het
Slc8a2 T C 7: 15,878,954 (GRCm39) V480A possibly damaging Het
Speer1j C T 5: 11,555,340 (GRCm39) T103I possibly damaging Het
Spg7 T C 8: 123,820,400 (GRCm39) F617S probably damaging Het
Srcap A G 7: 127,133,838 (GRCm39) D863G probably damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Suox T C 10: 128,507,086 (GRCm39) E314G probably benign Het
Tln2 T A 9: 67,136,658 (GRCm39) K1276* probably null Het
Tmem72 A G 6: 116,672,451 (GRCm39) L130P probably damaging Het
Ttll1 T C 15: 83,373,778 (GRCm39) Y345C probably benign Het
Ush2a A T 1: 188,090,914 (GRCm39) probably null Het
Xpo6 G A 7: 125,707,620 (GRCm39) probably benign Het
Zc3h14 A T 12: 98,751,234 (GRCm39) Y512F possibly damaging Het
Zfp438 A T 18: 5,214,760 (GRCm39) M66K probably benign Het
Other mutations in Gm11110
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01779:Gm11110 APN 17 57,409,087 (GRCm39) unclassified probably benign
IGL01874:Gm11110 APN 17 57,399,693 (GRCm39) unclassified probably benign
R3423:Gm11110 UTSW 17 57,410,435 (GRCm39) unclassified probably benign
R6888:Gm11110 UTSW 17 57,409,143 (GRCm39) unclassified probably benign
R8111:Gm11110 UTSW 17 57,410,427 (GRCm39) missense probably null
R8904:Gm11110 UTSW 17 57,410,439 (GRCm39) missense unknown
R9687:Gm11110 UTSW 17 57,410,439 (GRCm39) missense unknown
R9732:Gm11110 UTSW 17 57,410,382 (GRCm39) missense unknown
Posted On 2015-04-16