Incidental Mutation 'IGL01570:Gm7676'
ID 91115
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7676
Ensembl Gene ENSMUSG00000068631
Gene Name predicted gene 7676
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.176) question?
Stock # IGL01570
Quality Score
Status
Chromosome 8
Chromosomal Location 13946311-13946629 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 13946311 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: ENSMUST00000084055
SMART Domains Protein: ENSMUSP00000111801
Gene: ENSMUSG00000068631

DomainStartEndE-ValueType
Pfam:CD225 49 124 1.3e-30 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf3 T C 16: 20,378,748 (GRCm39) S54P probably damaging Het
Adam5 A G 8: 25,300,839 (GRCm39) V230A probably damaging Het
Arid4b T A 13: 14,361,394 (GRCm39) probably benign Het
Cep250 T G 2: 155,809,583 (GRCm39) probably benign Het
Col28a1 T A 6: 8,014,540 (GRCm39) D955V probably damaging Het
Hao1 A G 2: 134,396,120 (GRCm39) S45P probably damaging Het
Hars2 A T 18: 36,920,645 (GRCm39) I163L probably benign Het
Iqgap1 T C 7: 80,372,809 (GRCm39) Y1510C possibly damaging Het
Itga4 G A 2: 79,152,978 (GRCm39) probably null Het
Kif18b G A 11: 102,803,217 (GRCm39) H498Y probably benign Het
Kin C T 2: 10,096,763 (GRCm39) T204M probably benign Het
Lmo7 T C 14: 102,139,807 (GRCm39) probably null Het
Ltbp2 G A 12: 84,840,807 (GRCm39) T1009I probably benign Het
Mad1l1 A G 5: 140,103,032 (GRCm39) S489P probably benign Het
Memo1 A G 17: 74,524,103 (GRCm39) probably benign Het
Myocd T A 11: 65,091,633 (GRCm39) H103L probably benign Het
Nhlrc2 T A 19: 56,563,219 (GRCm39) F273I possibly damaging Het
Or10g7 T C 9: 39,905,625 (GRCm39) I173T probably damaging Het
Or1e26 C A 11: 73,480,209 (GRCm39) M118I probably benign Het
Or5p4 A T 7: 107,680,480 (GRCm39) T160S probably benign Het
Pappa2 A C 1: 158,642,110 (GRCm39) Y1315* probably null Het
Pdzk1ip1 C T 4: 114,946,214 (GRCm39) P25S possibly damaging Het
Ppp2r5d A T 17: 46,998,843 (GRCm39) V73D possibly damaging Het
Psmg2 G A 18: 67,786,293 (GRCm39) V218I probably benign Het
Qars1 C T 9: 108,388,738 (GRCm39) T266M probably damaging Het
Slc26a2 A C 18: 61,331,332 (GRCm39) C700G possibly damaging Het
Zfp638 C A 6: 83,924,829 (GRCm39) A724E probably damaging Het
Other mutations in Gm7676
AlleleSourceChrCoordTypePredicted EffectPPH Score
R5089:Gm7676 UTSW 8 13,946,401 (GRCm39) exon noncoding transcript
Posted On 2013-12-09