Incidental Mutation 'IGL01345:4930518I15Rik'
ID278296
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930518I15Rik
Ensembl Gene ENSMUSG00000074629
Gene NameRIKEN cDNA 4930518I15 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01345
Quality Score
Status
Chromosome2
Chromosomal Location156856616-156857946 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 156857100 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000096745 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073352] [ENSMUST00000081335] [ENSMUST00000099141]
Predicted Effect probably benign
Transcript: ENSMUST00000073352
SMART Domains Protein: ENSMUSP00000073074
Gene: ENSMUSG00000062175

DomainStartEndE-ValueType
HOX 18 83 1.51e-12 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000081335
SMART Domains Protein: ENSMUSP00000096745
Gene: ENSMUSG00000062175

DomainStartEndE-ValueType
HOX 18 83 1.51e-12 SMART
Predicted Effect unknown
Transcript: ENSMUST00000099141
AA Change: S39P
Predicted Effect noncoding transcript
Transcript: ENSMUST00000153616
Predicted Effect noncoding transcript
Transcript: ENSMUST00000175634
Predicted Effect noncoding transcript
Transcript: ENSMUST00000176134
Predicted Effect noncoding transcript
Transcript: ENSMUST00000176281
SMART Domains Protein: ENSMUSP00000135007
Gene: ENSMUSG00000062175

DomainStartEndE-ValueType
PDB:2LK2|A 1 23 2e-7 PDB
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183465
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185402
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187327
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Armc4 T C 18: 7,266,947 K385E probably benign Het
Atr G A 9: 95,940,949 C2323Y probably damaging Het
Ccdc107 T A 4: 43,493,453 L8* probably null Het
Erc1 T A 6: 119,761,263 K240* probably null Het
Gcat T C 15: 79,034,065 probably benign Het
Gm4847 A T 1: 166,634,972 D316E probably damaging Het
Gm8267 A G 14: 44,724,955 S3P probably damaging Het
Gpr26 T C 7: 131,967,432 F169L possibly damaging Het
Itgal T A 7: 127,300,956 F129I possibly damaging Het
Kcnk1 T A 8: 126,025,407 C251S possibly damaging Het
Nfkb1 T C 3: 135,594,981 D608G probably damaging Het
Nlrp2 T C 7: 5,317,492 E882G probably benign Het
Pik3r5 G A 11: 68,496,194 D854N possibly damaging Het
Rnf220 G A 4: 117,273,270 R253* probably null Het
Slc22a15 A C 3: 101,880,176 S259R probably benign Het
Tln1 G A 4: 43,536,281 L2004F probably damaging Het
Tlnrd1 A G 7: 83,882,846 S126P probably damaging Het
Ulk4 T C 9: 121,208,162 T587A possibly damaging Het
Vasn A G 16: 4,648,368 I60V probably benign Het
Vps33a G T 5: 123,572,943 N13K probably benign Het
Zmiz2 A G 11: 6,405,015 D862G possibly damaging Het
Zswim3 T A 2: 164,820,137 L179H probably damaging Het
Other mutations in 4930518I15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01344:4930518I15Rik APN 2 156857100 unclassified probably benign
R4604:4930518I15Rik UTSW 2 156857154 unclassified probably benign
Posted On2015-04-16