Incidental Mutation 'R4986:Gm9944'
Institutional Source Beutler Lab
Gene Symbol Gm9944
Ensembl Gene ENSMUSG00000095213
Gene Namepredicted gene 9944
MMRRC Submission 042580-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.055) question?
Stock #R4986 (G1)
Quality Score225
Status Validated
Chromosomal Location144453009-144453317 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 144453190 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101375 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105749] [ENSMUST00000177649]
Predicted Effect probably benign
Transcript: ENSMUST00000105749
SMART Domains Protein: ENSMUSP00000101375
Gene: ENSMUSG00000078507

transmembrane domain 2 24 N/A INTRINSIC
Pfam:Abhydrolase_3 116 263 1.8e-33 PFAM
Pfam:Abhydrolase_3 302 382 6.9e-12 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000177649
AA Change: N43S
Meta Mutation Damage Score 0.0576 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.5%
  • 20x: 89.2%
Validation Efficiency 95% (41/43)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3632451O06Rik A T 14: 49,751,654 D619E probably damaging Het
Abcc9 A T 6: 142,627,591 C1005S probably benign Het
Ccdc34 T C 2: 110,017,869 M1T probably null Het
Ceacam5 T A 7: 17,757,833 N709K possibly damaging Het
Ces2f G A 8: 104,952,025 S298N probably benign Het
Defa30 T A 8: 21,135,416 Y65* probably null Het
Dock3 A C 9: 106,931,983 C1314G probably damaging Het
Emc2 A G 15: 43,511,784 M226V probably benign Het
Fat3 T C 9: 15,998,340 Y2122C probably damaging Het
Gad1 A G 2: 70,600,693 D560G probably benign Het
Gpr137c A T 14: 45,246,286 probably null Het
Igf2bp2 C T 16: 22,070,306 probably null Het
Igsf10 T C 3: 59,328,606 T1385A probably benign Het
Itpr2 T A 6: 146,240,342 N1734I probably damaging Het
Kbtbd6 A G 14: 79,452,609 H248R probably damaging Het
Macf1 C T 4: 123,391,121 R5650Q probably damaging Het
Mdh1 A G 11: 21,558,545 F266L possibly damaging Het
Mecom G T 3: 29,980,699 P466Q probably damaging Het
Muc20 A G 16: 32,777,635 probably benign Het
Olfr1151 T A 2: 87,857,514 L113Q probably damaging Het
Olfr1265 A T 2: 90,037,428 N170Y probably damaging Het
Osmr A G 15: 6,816,580 probably null Het
Rrs1 G A 1: 9,545,767 E82K probably damaging Het
Sacs T A 14: 61,213,043 Y4179* probably null Het
Sept11 T C 5: 93,161,241 V203A probably damaging Het
Skint9 T A 4: 112,391,713 T173S probably benign Het
Slain1 A T 14: 103,688,105 R296S probably damaging Het
Slc36a3 T A 11: 55,146,766 *93C probably null Het
Sp110 G A 1: 85,591,760 P116S probably benign Het
Srl T C 16: 4,496,782 Y332C probably benign Het
Ubtf G A 11: 102,314,174 H95Y probably benign Het
Ugt1a1 CAGAGAGAGAGAGA CAGAGAGAGAGA 1: 88,211,984 probably benign Het
Wdfy3 C T 5: 101,943,119 D532N probably benign Het
Ybx1 C T 4: 119,282,430 V123I probably damaging Het
Zfp944 A T 17: 22,339,230 H345Q probably damaging Het
Zfp993 T A 4: 146,657,557 F113I probably benign Het
Other mutations in Gm9944
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02940:Gm9944 APN 4 144453139 unclassified probably benign
R1378:Gm9944 UTSW 4 144453203 unclassified probably benign
R1707:Gm9944 UTSW 4 144453263 unclassified probably benign
R3552:Gm9944 UTSW 4 144453043 unclassified probably benign
R5988:Gm9944 UTSW 4 144453205 unclassified probably benign
Predicted Primers PCR Primer

Sequencing Primer
Posted On2016-05-10