Incidental Mutation 'IGL00563:1500035N22Rik'
ID 332618
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1500035N22Rik
Ensembl Gene ENSMUSG00000059631
Gene Name RIKEN cDNA 1500035N22 gene
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00563
Quality Score
Status
Chromosome 5
Chromosomal Location 25190840-25203166 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 25202619 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000075651 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030784] [ENSMUST00000076306]
AlphaFold no structure available at present
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
Atp13a4 T C 16: 29,222,596 (GRCm39) probably benign Het
AU016765 C A 17: 64,826,877 (GRCm39) noncoding transcript Het
Clstn2 A G 9: 97,464,505 (GRCm39) probably benign Het
Crip1 T A 12: 113,117,232 (GRCm39) probably null Het
Dnah6 T C 6: 73,172,603 (GRCm39) N285S possibly damaging Het
Fktn A T 4: 53,747,007 (GRCm39) probably null Het
Fndc3a C A 14: 72,796,797 (GRCm39) probably benign Het
Focad T A 4: 88,267,046 (GRCm39) M1019K unknown Het
Fuca2 A T 10: 13,381,651 (GRCm39) D188V probably damaging Het
Gzmk C T 13: 113,309,658 (GRCm39) V92I probably benign Het
Mprip C T 11: 59,643,443 (GRCm39) R520W probably damaging Het
Mrpl19 A G 6: 81,942,853 (GRCm39) V19A probably benign Het
Ndufb3 T A 1: 58,634,958 (GRCm39) H103Q possibly damaging Het
Pkd1l3 T C 8: 110,382,779 (GRCm39) V1675A possibly damaging Het
Saxo1 C T 4: 86,363,809 (GRCm39) E225K probably damaging Het
Sbno1 A G 5: 124,540,268 (GRCm39) S383P probably damaging Het
Slc22a29 T A 19: 8,138,993 (GRCm39) T490S probably benign Het
Smc6 T A 12: 11,351,532 (GRCm39) S854T probably benign Het
Smim23 T C 11: 32,771,893 (GRCm39) T58A probably benign Het
Tas2r134 T C 2: 51,518,100 (GRCm39) I193T possibly damaging Het
Thsd7a G T 6: 12,379,658 (GRCm39) probably null Het
Trav13n-4 T G 14: 53,601,423 (GRCm39) V64G possibly damaging Het
Trmt10a G A 3: 137,853,177 (GRCm39) E13K probably damaging Het
Txndc11 T C 16: 10,922,496 (GRCm39) S239G probably damaging Het
Vmn2r96 T A 17: 18,804,077 (GRCm39) N442K probably benign Het
Vps13a C T 19: 16,712,078 (GRCm39) probably null Het
Wdr64 A G 1: 175,526,366 (GRCm39) D5G probably benign Het
Other mutations in 1500035N22Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00562:1500035N22Rik APN 5 25,202,619 (GRCm39) unclassified probably benign
IGL02311:1500035N22Rik APN 5 25,202,705 (GRCm39) unclassified probably benign
IGL03087:1500035N22Rik APN 5 25,202,630 (GRCm39) unclassified probably benign
IGL03365:1500035N22Rik APN 5 25,202,809 (GRCm39) unclassified probably benign
Posted On 2015-08-05