Incidental Mutation 'IGL01779:Gm11110'
ID153880
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm11110
Ensembl Gene ENSMUSG00000079414
Gene Namepredicted gene 11110
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.063) question?
Stock #IGL01779
Quality Score
Status
Chromosome17
Chromosomal Location57092035-57105942 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) C to T at 57102087 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000040412 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039490] [ENSMUST00000112915]
Predicted Effect probably benign
Transcript: ENSMUST00000039490
SMART Domains Protein: ENSMUSP00000040412
Gene: ENSMUSG00000035678

DomainStartEndE-ValueType
transmembrane domain 83 105 N/A INTRINSIC
TNF 147 302 1.16e-46 SMART
Predicted Effect unknown
Transcript: ENSMUST00000112915
AA Change: V72M
SMART Domains Protein: ENSMUSP00000108537
Gene: ENSMUSG00000079414
AA Change: V72M

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: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl3 A T 5: 81,387,870 I119F probably damaging Het
Akt1 C T 12: 112,657,169 G286R probably damaging Het
Apof A G 10: 128,269,477 I167V probably benign Het
Arhgap15 A G 2: 44,065,045 E220G possibly damaging Het
Clca3a2 T A 3: 144,819,378 Y31F possibly damaging Het
Clmn T C 12: 104,782,140 I383V probably benign Het
Cntnap5b A G 1: 99,967,339 D112G probably damaging Het
Col8a1 A T 16: 57,628,363 H261Q unknown Het
Csmd3 A T 15: 47,857,894 V1551D probably benign Het
Ddx60 G A 8: 62,017,823 V1450M possibly damaging Het
Ethe1 A T 7: 24,595,009 H79L probably damaging Het
Fhdc1 G A 3: 84,444,735 A1061V possibly damaging Het
Hs1bp3 C T 12: 8,341,945 T349I probably benign Het
Ifna16 A T 4: 88,676,645 I71N probably damaging Het
Il18bp A G 7: 102,016,795 Y59H possibly damaging Het
Kcnt1 T A 2: 25,900,967 I511N probably damaging Het
Mlph A G 1: 90,942,950 M528V probably benign Het
Olfr646 A G 7: 104,106,633 D118G probably damaging Het
Pprc1 T A 19: 46,062,202 I52N probably damaging Het
Rfx1 T A 8: 84,092,662 probably benign Het
Rnf17 A T 14: 56,462,063 I553F probably benign Het
Scaper A T 9: 55,892,240 H180Q probably benign Het
Slc26a4 C T 12: 31,528,854 probably benign Het
Slc30a10 A T 1: 185,464,179 Q346L possibly damaging Het
Stambpl1 A T 19: 34,240,027 H422L possibly damaging Het
Trim67 G A 8: 124,828,121 G701R probably damaging Het
Vipr1 T C 9: 121,664,630 F249S probably damaging Het
Vmn2r117 G T 17: 23,477,241 D397E probably benign Het
Other mutations in Gm11110
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01874:Gm11110 APN 17 57092693 unclassified probably benign
IGL02744:Gm11110 APN 17 57092693 unclassified probably benign
R3423:Gm11110 UTSW 17 57103435 unclassified probably benign
R6888:Gm11110 UTSW 17 57102143 unclassified probably benign
R8111:Gm11110 UTSW 17 57103427 missense probably null
Posted On2014-02-04