Incidental Mutation 'R0037:Gm5800'
ID15489
Institutional Source Beutler Lab
Gene Symbol Gm5800
Ensembl Gene ENSMUSG00000068506
Gene Namepredicted gene 5800
Synonyms
MMRRC Submission 038331-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.066) question?
Stock #R0037 (G1)
Quality Score
Status Validated
Chromosome14
Chromosomal Location51711643-51717183 bp(-) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 51716148 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000093605 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095916]
Predicted Effect probably benign
Transcript: ENSMUST00000095916
SMART Domains Protein: ENSMUSP00000093605
Gene: ENSMUSG00000068506

DomainStartEndE-ValueType
Pfam:Takusan 10 90 4.7e-28 PFAM
Coding Region Coverage
  • 1x: 81.5%
  • 3x: 73.9%
  • 10x: 52.8%
  • 20x: 32.9%
Validation Efficiency 94% (83/88)
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars G A 8: 111,043,259 R330Q possibly damaging Het
Amph A T 13: 19,100,653 S250C possibly damaging Het
Ankrd61 T C 5: 143,894,977 N3S probably damaging Het
Camsap2 C T 1: 136,281,892 E621K probably damaging Het
Cpt2 A G 4: 107,907,974 S152P probably damaging Het
Csmd1 T A 8: 15,917,248 Q3205L probably damaging Het
Dag1 G T 9: 108,207,353 P863Q probably damaging Het
Dclk1 A G 3: 55,256,059 I191V probably benign Het
Ddhd1 A G 14: 45,610,510 L567P probably damaging Het
Enox1 T C 14: 77,699,310 probably benign Het
Exoc3 T C 13: 74,199,539 E104G probably damaging Het
Foxp1 T A 6: 99,162,969 Q17L probably damaging Het
Fscn1 A G 5: 142,970,694 probably benign Het
Fut8 T C 12: 77,365,037 V91A probably benign Het
Gm5475 T A 15: 100,424,202 Y77* probably null Het
Hs2st1 T A 3: 144,437,644 K213* probably null Het
Il5ra T A 6: 106,742,686 Y62F probably damaging Het
Inpp5d A G 1: 87,708,129 E734G probably damaging Het
Insig2 A T 1: 121,306,920 C194S probably damaging Het
Lemd3 A C 10: 120,925,456 H898Q possibly damaging Het
Lrp4 A G 2: 91,471,203 T43A probably benign Het
Mast3 C T 8: 70,783,699 probably null Het
Melk T C 4: 44,360,864 probably benign Het
Myo10 C T 15: 25,666,532 probably benign Het
Nlrc5 G A 8: 94,489,535 V967M probably benign Het
Nlrp9b T A 7: 20,023,722 F295I probably damaging Het
Phf3 A T 1: 30,804,918 D1653E probably benign Het
Ppfia4 A T 1: 134,324,089 L449Q probably damaging Het
Ppp1r16b T A 2: 158,757,209 I367N probably damaging Het
Ralgapb T C 2: 158,437,411 L139S probably damaging Het
Slc20a1 T C 2: 129,210,772 V658A probably damaging Het
Son C A 16: 91,664,728 A347E probably damaging Het
Tprgl C A 4: 154,160,137 V134L possibly damaging Het
Trim24 A T 6: 37,957,549 N733I probably damaging Het
Uggt1 A T 1: 36,185,932 D540E probably benign Het
Urb2 T A 8: 124,047,195 F1488L probably damaging Het
Utp20 T C 10: 88,798,404 D810G probably benign Het
Zfp473 T A 7: 44,733,900 K335N probably damaging Het
Other mutations in Gm5800
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00958:Gm5800 APN 14 51713812 missense possibly damaging 0.96
IGL03325:Gm5800 APN 14 51714526 missense probably benign
R0597:Gm5800 UTSW 14 51716004 missense probably benign
R1577:Gm5800 UTSW 14 51714559 missense probably benign 0.05
R1834:Gm5800 UTSW 14 51716092 missense possibly damaging 0.85
R1934:Gm5800 UTSW 14 51711939 missense possibly damaging 0.96
R2169:Gm5800 UTSW 14 51713678 missense possibly damaging 0.53
R2180:Gm5800 UTSW 14 51715994 nonsense probably null
R4861:Gm5800 UTSW 14 51716047 missense probably damaging 0.98
R4861:Gm5800 UTSW 14 51716047 missense probably damaging 0.98
R5267:Gm5800 UTSW 14 51713837 splice site probably null
R6545:Gm5800 UTSW 14 51711962 missense possibly damaging 0.73
R6634:Gm5800 UTSW 14 51716138 missense possibly damaging 0.73
R6925:Gm5800 UTSW 14 51713700 missense possibly damaging 0.76
Posted On2012-12-21