Incidental Mutation 'W0251:Gm4559'
ID 166607
Institutional Source Beutler Lab
Gene Symbol Gm4559
Ensembl Gene ENSMUSG00000056885
Gene Name predicted gene 4559
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.150) question?
Stock # W0251 (G3R) of strain daniel_gray
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 141827501-141828100 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to C at 141827535 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Glycine at position 189 (A189G)
Ref Sequence ENSEMBL: ENSMUSP00000079498 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080669]
AlphaFold A4IF42
Predicted Effect unknown
Transcript: ENSMUST00000080669
AA Change: A189G
SMART Domains Protein: ENSMUSP00000079498
Gene: ENSMUSG00000056885
AA Change: A189G

DomainStartEndE-ValueType
low complexity region 3 199 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.0%
  • 10x: 95.5%
  • 20x: 90.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 14 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bcl2a1b T A 9: 89,081,636 (GRCm39) M75K probably damaging Het
Btaf1 G A 19: 36,980,904 (GRCm39) R1575H probably damaging Het
Cfap46 T C 7: 139,183,862 (GRCm39) M2507V probably benign Het
Dcc T C 18: 71,959,154 (GRCm39) D206G probably damaging Het
Dnah6 T A 6: 73,155,501 (GRCm39) I705F possibly damaging Het
Entpd1 A T 19: 40,714,697 (GRCm39) I269F probably damaging Het
Ipo5 T A 14: 121,176,197 (GRCm39) M648K probably benign Het
Kdelr1 A G 7: 45,531,045 (GRCm39) Y96C probably damaging Het
Mmp17 C T 5: 129,672,591 (GRCm39) A181V probably benign Het
Muc20 T C 16: 32,614,223 (GRCm39) I385V possibly damaging Het
Or13c7 C T 4: 43,855,058 (GRCm39) L250F probably benign Het
Pik3r6 A G 11: 68,424,697 (GRCm39) Y434C probably benign Het
Pura T C 18: 36,420,843 (GRCm39) V210A probably benign Het
Spic C T 10: 88,515,766 (GRCm39) D19N probably damaging Het
Other mutations in Gm4559
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03184:Gm4559 APN 7 141,828,046 (GRCm39) missense unknown
R1493:Gm4559 UTSW 7 141,828,050 (GRCm39) nonsense probably null
R1879:Gm4559 UTSW 7 141,827,998 (GRCm39) missense unknown
R2299:Gm4559 UTSW 7 141,827,572 (GRCm39) missense unknown
R2330:Gm4559 UTSW 7 141,827,833 (GRCm39) missense unknown
R2495:Gm4559 UTSW 7 141,827,557 (GRCm39) missense unknown
R6475:Gm4559 UTSW 7 141,827,887 (GRCm39) missense unknown
R6785:Gm4559 UTSW 7 141,827,845 (GRCm39) missense unknown
R7576:Gm4559 UTSW 7 141,827,677 (GRCm39) missense unknown
R7651:Gm4559 UTSW 7 141,827,553 (GRCm39) missense unknown
R7837:Gm4559 UTSW 7 141,827,553 (GRCm39) missense unknown
R8077:Gm4559 UTSW 7 141,827,553 (GRCm39) missense unknown
R8080:Gm4559 UTSW 7 141,827,553 (GRCm39) missense unknown
R8317:Gm4559 UTSW 7 141,827,553 (GRCm39) small deletion probably benign
R8355:Gm4559 UTSW 7 141,827,694 (GRCm39) missense unknown
R8455:Gm4559 UTSW 7 141,827,694 (GRCm39) missense unknown
R8801:Gm4559 UTSW 7 141,827,553 (GRCm39) small deletion probably benign
Z1177:Gm4559 UTSW 7 141,827,771 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TGCAGAGGGGAATTTGTTAGCTCAC -3'
(R):5'- TGTCAATCTAGCTGCTGCAAGCC -3'

Sequencing Primer
(F):5'- CCAAATCTGAGTTGAAGCTGTG -3'
(R):5'- ccctgctgctgccagtc -3'
Posted On 2014-04-13