Incidental Mutation 'IGL00562:1500035N22Rik'
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ID332612
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1500035N22Rik
Ensembl Gene ENSMUSG00000059631
Gene NameRIKEN cDNA 1500035N22 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00562
Quality Score
Status
Chromosome5
Chromosomal Location24985842-24998168 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 24997621 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000075651 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030784] [ENSMUST00000076306]
Predicted Effect probably benign
Transcript: ENSMUST00000030784
SMART Domains Protein: ENSMUSP00000030784
Gene: ENSMUSG00000028944

DomainStartEndE-ValueType
low complexity region 9 29 N/A INTRINSIC
low complexity region 81 95 N/A INTRINSIC
low complexity region 113 122 N/A INTRINSIC
low complexity region 129 144 N/A INTRINSIC
low complexity region 151 172 N/A INTRINSIC
low complexity region 228 243 N/A INTRINSIC
CBS 276 325 7.01e-6 SMART
CBS 357 406 4.28e-10 SMART
CBS 432 480 8.11e-11 SMART
CBS 504 552 3.62e-8 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000075081
Predicted Effect probably benign
Transcript: ENSMUST00000076306
SMART Domains Protein: ENSMUSP00000075651
Gene: ENSMUSG00000028944

DomainStartEndE-ValueType
low complexity region 33 46 N/A INTRINSIC
low complexity region 104 119 N/A INTRINSIC
CBS 153 202 7.01e-6 SMART
CBS 234 283 4.28e-10 SMART
CBS 309 357 8.11e-11 SMART
CBS 381 429 3.62e-8 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
AU016765 C A 17: 64,519,882 noncoding transcript Het
Chaf1b T C 16: 93,900,191 probably benign Het
Clstn2 A G 9: 97,582,452 probably benign Het
Crip1 T A 12: 113,153,612 probably null Het
Cubn A G 2: 13,294,230 S3211P probably benign Het
Dlx6 C T 6: 6,865,143 R172W probably damaging Het
Fktn A T 4: 53,747,007 probably null Het
Focad T A 4: 88,348,809 M1019K unknown Het
Fuca2 A T 10: 13,505,907 D188V probably damaging Het
Kcna3 A G 3: 107,036,730 D103G probably damaging Het
Mrpl19 A G 6: 81,965,872 V19A probably benign Het
Ndufb3 T A 1: 58,595,799 H103Q possibly damaging Het
Pkd1l3 T C 8: 109,656,147 V1675A possibly damaging Het
Ptger4 A T 15: 5,243,133 S2T probably benign Het
Saxo1 C T 4: 86,445,572 E225K probably damaging Het
Sftpb G T 6: 72,309,862 A228S probably benign Het
Slc22a29 T A 19: 8,161,629 T490S probably benign Het
Slc29a1 T C 17: 45,589,992 N50S probably damaging Het
Smc6 T A 12: 11,301,531 S854T probably benign Het
Smim23 T C 11: 32,821,893 T58A probably benign Het
Tas2r134 T C 2: 51,628,088 I193T possibly damaging Het
Thsd7a G T 6: 12,379,659 probably null Het
Trav13n-4 T G 14: 53,363,966 V64G possibly damaging Het
Trmt10a G A 3: 138,147,416 E13K probably damaging Het
Txndc11 T C 16: 11,104,632 S239G probably damaging Het
Vmn2r96 T A 17: 18,583,815 N442K probably benign Het
Vps13a C T 19: 16,734,714 probably null Het
Other mutations in 1500035N22Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00563:1500035N22Rik APN 5 24997621 unclassified probably benign
IGL02311:1500035N22Rik APN 5 24997707 unclassified probably benign
IGL03087:1500035N22Rik APN 5 24997632 unclassified probably benign
IGL03365:1500035N22Rik APN 5 24997811 unclassified probably benign
Posted On2015-08-05