Incidental Mutation 'IGL01518:4930447F04Rik'
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ID89385
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930447F04Rik
Ensembl Gene ENSMUSG00000031182
Gene NameRIKEN cDNA 4930447F04 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01518
Quality Score
Status
ChromosomeX
Chromosomal Location66303361-66304224 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 66304054 bp
ZygosityHeterozygous
Amino Acid Change Valine to Glycine at position 16 (V16G)
Ref Sequence ENSEMBL: ENSMUSP00000033525 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033525]
Predicted Effect unknown
Transcript: ENSMUST00000033525
AA Change: V16G
SMART Domains Protein: ENSMUSP00000033525
Gene: ENSMUSG00000031182
AA Change: V16G

DomainStartEndE-ValueType
low complexity region 56 68 N/A INTRINSIC
low complexity region 86 101 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427I04Rik A T 4: 123,860,701 E136V probably benign Het
Aadac A G 3: 60,035,899 D75G probably damaging Het
Arfgap1 T A 2: 180,972,725 S125T probably benign Het
Atxn2 G T 5: 121,810,979 A813S probably damaging Het
Cadps C A 14: 12,522,352 S604I probably damaging Het
Ces1a G T 8: 93,045,098 P24T probably damaging Het
Col4a4 T A 1: 82,455,759 M1488L unknown Het
Fndc3c1 T C X: 106,431,423 N941S probably damaging Het
Fryl T C 5: 73,086,962 Y1172C possibly damaging Het
Gm1527 T C 3: 28,895,588 probably benign Het
Hsf2 T C 10: 57,512,134 L458P probably damaging Het
Il2 T C 3: 37,123,007 T127A possibly damaging Het
Inpp5e A G 2: 26,397,934 Y617H probably damaging Het
Isoc2b G A 7: 4,850,764 S137F probably damaging Het
Map2 C T 1: 66,425,331 P241S probably damaging Het
Mfsd6 C A 1: 52,709,322 R128L probably damaging Het
Mrnip A G 11: 50,197,635 T153A probably damaging Het
Olfr1269 A G 2: 90,118,971 F209S possibly damaging Het
Olfr26 A T 9: 38,855,799 M246L probably benign Het
Pi4ka T C 16: 17,280,735 N2022S probably benign Het
Scrt2 C A 2: 152,093,640 R238S probably damaging Het
St3gal6 T A 16: 58,484,775 D108V probably benign Het
Tmem132b C T 5: 125,778,791 T529M probably damaging Het
Trappc11 T C 8: 47,501,869 probably null Het
Tspyl1 T A 10: 34,283,199 S307T possibly damaging Het
Ush2a A G 1: 188,399,785 S735G probably benign Het
Wnk2 T C 13: 49,068,192 M1186V possibly damaging Het
Other mutations in 4930447F04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0454:4930447F04Rik UTSW X 66303668 missense unknown
Posted On2013-12-03