Incidental Mutation 'PIT4354001:Gm1587'
ID 554830
Institutional Source Beutler Lab
Gene Symbol Gm1587
Ensembl Gene ENSMUSG00000075512
Gene Name predicted gene 1587
Synonyms LOC380920
Accession Numbers
Essential gene? Probably non essential (E-score: 0.120) question?
Stock # PIT4354001 (G1)
Quality Score 225.009
Status Not validated
Chromosome 14
Chromosomal Location 78031385-78036408 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 78034473 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 32 (R32*)
Ref Sequence ENSEMBL: ENSMUSP00000097941 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100372]
AlphaFold no structure available at present
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: 62,811,392 (GRCm39) Y1140N probably damaging Het
Ccdc83 A T 7: 89,873,182 (GRCm39) M391K probably benign Het
Cntnap1 A T 11: 101,072,123 (GRCm39) I459F probably damaging Het
Cr2 T A 1: 194,848,617 (GRCm39) Y302F probably damaging Het
Ctu2 A T 8: 123,205,714 (GRCm39) D179V probably damaging Het
Cubn G A 2: 13,473,663 (GRCm39) Q427* probably null Het
Depdc7 A G 2: 104,558,533 (GRCm39) S163P probably benign Het
Eif2s3y C T Y: 1,020,126 (GRCm39) R385C probably benign Het
Gigyf1 A G 5: 137,522,366 (GRCm39) K728R unknown Het
Hjv T C 3: 96,435,761 (GRCm39) C340R probably damaging Het
Isy1 A G 6: 87,810,653 (GRCm39) I53T possibly damaging Het
Myh8 A T 11: 67,180,456 (GRCm39) N564I probably benign Het
Neb A T 2: 52,135,330 (GRCm39) I3260N probably damaging Het
Npc1 C T 18: 12,344,592 (GRCm39) G426E probably benign Het
Nrdc G A 4: 108,911,222 (GRCm39) probably null Het
Or2v1 G A 11: 49,025,132 (GRCm39) V38M probably damaging Het
Or4c10b T A 2: 89,711,852 (GRCm39) S227R probably benign Het
Or4c116 C A 2: 88,942,830 (GRCm39) E9* probably null Het
Pate8 T A 9: 36,492,597 (GRCm39) S103C possibly damaging Het
Prss51 T A 14: 64,334,546 (GRCm39) V91D probably damaging Het
Qpct A C 17: 79,389,188 (GRCm39) Y280S probably benign Het
Rbpms A G 8: 34,296,866 (GRCm39) V137A possibly damaging Het
Rgl2 T A 17: 34,152,914 (GRCm39) M441K possibly damaging Het
Sdhaf3 A T 6: 6,956,072 (GRCm39) I16F possibly damaging Het
Slc38a3 T G 9: 107,534,848 (GRCm39) N176H probably benign Het
Sos1 T C 17: 80,756,785 (GRCm39) S256G possibly damaging Het
Spg11 A T 2: 121,918,666 (GRCm39) C988S probably damaging Het
Sync A T 4: 129,200,447 (GRCm39) Q451L possibly damaging Het
Tbc1d31 A G 15: 57,831,329 (GRCm39) Y929C probably benign Het
Thbs2 G A 17: 14,910,230 (GRCm39) T123I probably damaging Het
Thsd7a A C 6: 12,331,926 (GRCm39) probably null Het
Tnfrsf11a T C 1: 105,749,242 (GRCm39) L220P probably damaging Het
Trbv13-2 G A 6: 41,098,752 (GRCm39) C109Y probably damaging Het
Ugt3a1 G A 15: 9,306,446 (GRCm39) W198* probably null Het
Usp14 G A 18: 9,996,189 (GRCm39) R464W probably damaging Het
Vmn1r2 C T 4: 3,172,162 (GRCm39) S27L probably benign Het
Vmn1r68 T A 7: 10,261,958 (GRCm39) N47Y probably benign Het
Zfc3h1 T A 10: 115,262,944 (GRCm39) Y1719* probably null Het
Other mutations in Gm1587
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02158:Gm1587 APN 14 78,036,282 (GRCm39) missense unknown
R1928:Gm1587 UTSW 14 78,036,288 (GRCm39) missense unknown
R2133:Gm1587 UTSW 14 78,032,296 (GRCm39) nonsense probably null
R3114:Gm1587 UTSW 14 78,036,272 (GRCm39) missense unknown
R3983:Gm1587 UTSW 14 78,032,283 (GRCm39) missense unknown
R7509:Gm1587 UTSW 14 78,034,464 (GRCm39) 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 On 2019-06-07