Incidental Mutation 'PIT4354001:Gm1587'
ID554830
Institutional Source Beutler Lab
Gene Symbol Gm1587
Ensembl Gene ENSMUSG00000075512
Gene Namepredicted gene 1587
SynonymsLOC380920
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.087) question?
Stock #PIT4354001 (G1)
Quality Score225.009
Status Not validated
Chromosome14
Chromosomal Location77793945-77798968 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to A at 77797033 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Stop codon at position 32 (R32*)
Ref Sequence ENSEMBL: ENSMUSP00000097941 (fasta)
Predicted Effect probably null
Transcript: ENSMUST00000100372
AA Change: R32*
Coding Region Coverage
  • 1x: 92.5%
  • 3x: 90.1%
  • 10x: 83.2%
  • 20x: 69.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arap2 A T 5: 62,654,049 Y1140N probably damaging Het
Ccdc83 A T 7: 90,223,974 M391K probably benign Het
Cntnap1 A T 11: 101,181,297 I459F probably damaging Het
Cr2 T A 1: 195,166,309 Y302F probably damaging Het
Ctu2 A T 8: 122,478,975 D179V probably damaging Het
Cubn G A 2: 13,468,852 Q427* probably null Het
Depdc7 A G 2: 104,728,188 S163P probably benign Het
Eif2s3y C T Y: 1,020,126 R385C probably benign Het
Gigyf1 A G 5: 137,524,104 K728R unknown Het
Gm17689 T A 9: 36,581,301 S103C possibly damaging Het
Hfe2 T C 3: 96,528,445 C340R probably damaging Het
Isy1 A G 6: 87,833,671 I53T possibly damaging Het
Myh8 A T 11: 67,289,630 N564I probably benign Het
Neb A T 2: 52,245,318 I3260N probably damaging Het
Npc1 C T 18: 12,211,535 G426E probably benign Het
Nrd1 G A 4: 109,054,025 probably null Het
Olfr1221 C A 2: 89,112,486 E9* probably null Het
Olfr1257 T A 2: 89,881,508 S227R probably benign Het
Olfr56 G A 11: 49,134,305 V38M probably damaging Het
Prss51 T A 14: 64,097,097 V91D probably damaging Het
Qpct A C 17: 79,081,759 Y280S probably benign Het
Rbpms A G 8: 33,806,838 V137A possibly damaging Het
Rgl2 T A 17: 33,933,940 M441K possibly damaging Het
Sdhaf3 A T 6: 6,956,072 I16F possibly damaging Het
Slc38a3 T G 9: 107,657,649 N176H probably benign Het
Sos1 T C 17: 80,449,356 S256G possibly damaging Het
Spg11 A T 2: 122,088,185 C988S probably damaging Het
Sync A T 4: 129,306,654 Q451L possibly damaging Het
Tbc1d31 A G 15: 57,967,933 Y929C probably benign Het
Thbs2 G A 17: 14,689,968 T123I probably damaging Het
Thsd7a A C 6: 12,331,927 probably null Het
Tnfrsf11a T C 1: 105,821,517 L220P probably damaging Het
Trbv13-2 G A 6: 41,121,818 C109Y probably damaging Het
Ugt3a1 G A 15: 9,306,360 W198* probably null Het
Usp14 G A 18: 9,996,189 R464W probably damaging Het
Vmn1r2 C T 4: 3,172,162 S27L probably benign Het
Vmn1r68 T A 7: 10,528,031 N47Y probably benign Het
Zfc3h1 T A 10: 115,427,039 Y1719* probably null Het
Other mutations in Gm1587
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02158:Gm1587 APN 14 77798842 missense unknown
R1928:Gm1587 UTSW 14 77798848 missense unknown
R2133:Gm1587 UTSW 14 77794856 nonsense probably null
R3114:Gm1587 UTSW 14 77798832 missense unknown
R3983:Gm1587 UTSW 14 77794843 missense unknown
R7509:Gm1587 UTSW 14 77797024 missense unknown
Predicted Primers PCR Primer
(F):5'- CTGTGGTGGGGCTATACAAG -3'
(R):5'- TGGGTTTCAGTAAACGGTCG -3'

Sequencing Primer
(F):5'- cctctcgatgaaccttga -3'
(R):5'- GATCTCTGTGAGTTCCAGTAAAGCC -3'
Posted On2019-06-07