Incidental Mutation 'IGL01975:Gm11559'
ID 182652
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11559
Ensembl Gene ENSMUSG00000090225
Gene Name predicted gene 11559
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.158) question?
Stock # IGL01975
Quality Score
Status
Chromosome 11
Chromosomal Location 99755302-99756397 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 99755682 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Histidine at position 110 (Q110H)
Ref Sequence ENSEMBL: ENSMUSP00000090367 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092694]
AlphaFold Q9D3H7
Predicted Effect unknown
Transcript: ENSMUST00000092694
AA Change: Q110H
SMART Domains Protein: ENSMUSP00000090367
Gene: ENSMUSG00000090225
AA Change: Q110H

DomainStartEndE-ValueType
Pfam:Keratin_B2_2 49 88 4.3e-6 PFAM
Pfam:Keratin_B2_2 84 127 9.9e-14 PFAM
Pfam:Keratin_B2_2 127 169 5.5e-11 PFAM
low complexity region 175 191 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam22 C T 5: 8,217,396 (GRCm39) C133Y probably damaging Het
Akap3 G T 6: 126,850,963 (GRCm39) S827I probably damaging Het
Arhgap20 C T 9: 51,761,097 (GRCm39) Q947* probably null Het
Csf2rb2 A G 15: 78,173,086 (GRCm39) I258T probably benign Het
Egln2 T C 7: 26,859,745 (GRCm39) I323V possibly damaging Het
Erlin1 C A 19: 44,025,370 (GRCm39) G348V probably damaging Het
Fbxo38 C T 18: 62,648,484 (GRCm39) A685T probably damaging Het
Gm10272 G A 10: 77,542,608 (GRCm39) C50Y probably damaging Het
Gpr75 T C 11: 30,841,835 (GRCm39) S247P probably benign Het
Grid1 A T 14: 35,045,383 (GRCm39) M409L probably benign Het
Herc3 A C 6: 58,893,561 (GRCm39) D941A possibly damaging Het
Ilf3 T A 9: 21,303,675 (GRCm39) S166T probably benign Het
Kcnu1 A C 8: 26,424,525 (GRCm39) E273D probably benign Het
Kdm8 A G 7: 125,051,529 (GRCm39) S41G probably benign Het
Ldlr G A 9: 21,644,993 (GRCm39) V174I probably benign Het
Lpar5 T C 6: 125,058,750 (GRCm39) L157P probably damaging Het
Mcrs1 A G 15: 99,141,559 (GRCm39) probably null Het
Ndst3 T A 3: 123,395,163 (GRCm39) Y489F possibly damaging Het
Or6c69c A G 10: 129,911,139 (GRCm39) I287V probably damaging Het
Palmd A T 3: 116,717,283 (GRCm39) S405T probably benign Het
Ptger1 T C 8: 84,396,149 (GRCm39) probably benign Het
Rbp3 A T 14: 33,680,602 (GRCm39) K1068M probably damaging Het
Rimbp2 T C 5: 128,874,712 (GRCm39) D293G probably benign Het
Rnf20 T A 4: 49,654,473 (GRCm39) D843E probably benign Het
Rxfp1 A G 3: 79,567,385 (GRCm39) S322P possibly damaging Het
Slc22a8 T A 19: 8,582,775 (GRCm39) I152N probably damaging Het
Slc6a21 T A 7: 44,937,275 (GRCm39) D268E probably benign Het
Sstr1 A G 12: 58,260,412 (GRCm39) N345S probably benign Het
Stx17 T C 4: 48,180,670 (GRCm39) S172P probably damaging Het
Syne1 A G 10: 5,018,908 (GRCm39) probably benign Het
Tpte A G 8: 22,839,353 (GRCm39) T467A probably damaging Het
Trappc12 A G 12: 28,742,491 (GRCm39) probably null Het
Trav13-2 A T 14: 53,872,823 (GRCm39) T100S possibly damaging Het
Trip12 A G 1: 84,792,534 (GRCm39) probably benign Het
Wdr36 A G 18: 32,985,541 (GRCm39) H486R probably damaging Het
Zswim5 T C 4: 116,822,889 (GRCm39) I453T probably benign Het
Other mutations in Gm11559
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1620:Gm11559 UTSW 11 99,755,882 (GRCm39) missense unknown
R1792:Gm11559 UTSW 11 99,755,755 (GRCm39) missense unknown
R4212:Gm11559 UTSW 11 99,755,726 (GRCm39) missense unknown
R5633:Gm11559 UTSW 11 99,755,412 (GRCm39) nonsense probably null
R6464:Gm11559 UTSW 11 99,755,542 (GRCm39) missense unknown
R7326:Gm11559 UTSW 11 99,755,707 (GRCm39) missense unknown
R8130:Gm11559 UTSW 11 99,755,416 (GRCm39) missense unknown
Z1088:Gm11559 UTSW 11 99,755,775 (GRCm39) nonsense probably null
Z1177:Gm11559 UTSW 11 99,755,589 (GRCm39) frame shift probably null
Posted On 2014-05-07