Incidental Mutation 'IGL03138:Gm4876'
ID 453073
Institutional Source Beutler Lab
Gene Symbol Gm4876
Ensembl Gene ENSMUSG00000054556
Gene Name predicted gene 4876
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.253) question?
Stock # IGL03138 (G1)
Quality Score 52
Status Validated
Chromosome 6
Chromosomal Location 17076260-17171832 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to G at 17171736 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136503
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138170
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139701
Predicted Effect noncoding transcript
Transcript: ENSMUST00000140709
Predicted Effect noncoding transcript
Transcript: ENSMUST00000150251
Predicted Effect noncoding transcript
Transcript: ENSMUST00000166070
Coding Region Coverage
  • 1x: 0.0%
  • 3x: 0.0%
  • 10x: 0.0%
  • 20x: 0.0%
Validation Efficiency 95% (40/42)
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933416I08Rik TCC TCCC X: 52,692,862 (GRCm39) noncoding transcript Het
Casd1 A G 6: 4,613,236 (GRCm39) H118R probably damaging Het
Cilp TGGG TGG 9: 65,187,412 (GRCm39) probably null Het
Cmya5 T C 13: 93,201,850 (GRCm39) K3371E probably damaging Het
Crb1 CG C 1: 139,164,824 (GRCm39) probably null Het
Dpysl3 T C 18: 43,458,859 (GRCm39) T632A probably benign Het
Elapor1 T A 3: 108,379,309 (GRCm39) N392Y probably benign Het
Fbh1 T C 2: 11,754,320 (GRCm39) probably benign Het
Fcna G C 2: 25,520,693 (GRCm39) probably benign Het
Gbe1 T A 16: 70,325,951 (GRCm39) probably benign Het
Gvin-ps6 G T 7: 106,023,650 (GRCm39) noncoding transcript Het
Hsd17b7 C T 1: 169,780,649 (GRCm39) E320K probably damaging Het
Inhba T A 13: 16,192,099 (GRCm39) D73E probably benign Het
Kndc1 A G 7: 139,519,791 (GRCm39) N1717D possibly damaging Het
Knl1 G T 2: 118,902,840 (GRCm39) V1514F probably damaging Het
Map1b C T 13: 99,562,334 (GRCm39) A2459T unknown Het
Mmp1a TG TGG 9: 7,465,083 (GRCm38) probably null Het
Pias2 T C 18: 77,237,796 (GRCm39) probably null Het
Polr1b T C 2: 128,944,908 (GRCm39) F68S probably benign Het
Skic8 T C 9: 54,635,447 (GRCm39) probably benign Het
Slamf1 C A 1: 171,604,652 (GRCm39) Q141K possibly damaging Het
Speer4c1 A C 5: 15,919,214 (GRCm39) probably benign Het
Tpo T C 12: 30,124,170 (GRCm39) T877A probably benign Het
Ugt1a1 AT A 1: 88,140,093 (GRCm39) probably null Het
Vmn1r37 A G 6: 66,709,172 (GRCm39) K229R possibly damaging Het
Wdr17 T C 8: 55,102,178 (GRCm39) D947G probably damaging Het
Wiz G T 17: 32,578,093 (GRCm39) T473K probably damaging Het
Zmynd12 A G 4: 119,280,186 (GRCm39) Y35C probably damaging Het
Predicted Primers PCR Primer
(F):5'- GTTTACGATTGGAGAAAGCCCTC -3'
(R):5'- GGACATTCAGTACCAGGGACAC -3'

Sequencing Primer
(F):5'- ATTGGAGAAAGCCCTCTCTGG -3'
(R):5'- ACACAAGCCCGCTGTTGTAG -3'
Posted On 2017-01-27