Incidental Mutation 'IGL01751:Gm6605'
ID153125
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6605
Ensembl Gene ENSMUSG00000094920
Gene Namepredicted gene 6605
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.209) question?
Stock #IGL01751
Quality Score
Status
Chromosome7
Chromosomal Location38446621-38450424 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 38448206 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000031488
SMART Domains Protein: ENSMUSP00000031488
Gene: ENSMUSG00000094920

DomainStartEndE-ValueType
Pfam:DUF4629 426 526 7.6e-31 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185975
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600015I10Rik A T 6: 48,930,588 H174L possibly damaging Het
1700018F24Rik A G 5: 145,043,171 probably null Het
Auts2 G T 5: 131,472,360 Q72K probably damaging Het
Btbd11 C A 10: 85,654,502 Q1011K probably damaging Het
Ccdc7b A T 8: 129,136,568 probably benign Het
Frem3 A G 8: 80,615,743 E1555G probably benign Het
Gm1966 T A 7: 106,602,309 N576I possibly damaging Het
Gm5263 T G 1: 146,420,564 noncoding transcript Het
Gm5828 A G 1: 16,769,984 noncoding transcript Het
Hps3 T C 3: 20,010,966 D638G probably damaging Het
Igdcc4 A T 9: 65,131,732 N887I probably damaging Het
Itpkc G A 7: 27,213,066 probably benign Het
Mfge8 A G 7: 79,136,655 probably null Het
Mrc2 G T 11: 105,325,734 L116F probably benign Het
Necab1 T C 4: 14,978,171 D226G probably damaging Het
Neurod2 T C 11: 98,327,375 E321G possibly damaging Het
Obp2b G T 2: 25,737,748 V59L possibly damaging Het
Olfr1173 A T 2: 88,274,633 C139S possibly damaging Het
Olfr134 G T 17: 38,175,686 V201L probably benign Het
Olfr292 A T 7: 86,694,789 Q111L probably benign Het
Olfr912 C T 9: 38,581,513 P79S probably damaging Het
Olr1 T C 6: 129,488,848 N65S possibly damaging Het
Rock1 A G 18: 10,079,113 probably null Het
Scn3a T A 2: 65,461,252 M1717L possibly damaging Het
Smg7 T C 1: 152,844,061 D903G possibly damaging Het
Tlr1 A T 5: 64,925,947 L429* probably null Het
Ttll9 A T 2: 152,983,105 N68I probably damaging Het
Ttn A G 2: 76,737,599 V25904A possibly damaging Het
Uaca G A 9: 60,869,857 V507M probably damaging Het
Vmn1r195 G T 13: 22,279,251 C297F probably benign Het
Zdhhc2 G A 8: 40,473,001 A346T probably benign Het
Other mutations in Gm6605
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0578:Gm6605 UTSW 7 38448275 exon noncoding transcript
R0579:Gm6605 UTSW 7 38448275 exon noncoding transcript
R0580:Gm6605 UTSW 7 38448275 exon noncoding transcript
R0581:Gm6605 UTSW 7 38448275 exon noncoding transcript
R0615:Gm6605 UTSW 7 38448275 exon noncoding transcript
R0675:Gm6605 UTSW 7 38448275 exon noncoding transcript
R2061:Gm6605 UTSW 7 38448282 exon noncoding transcript
R5027:Gm6605 UTSW 7 38450259 exon noncoding transcript
Posted On2014-02-04