Incidental Mutation 'IGL03261:2310022A10Rik'
ID 414821
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2310022A10Rik
Ensembl Gene ENSMUSG00000049643
Gene Name RIKEN cDNA 2310022A10 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.178) question?
Stock # IGL03261
Quality Score
Status
Chromosome 7
Chromosomal Location 27252658-27281524 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to G at 27279863 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 281 (Y281*)
Ref Sequence ENSEMBL: ENSMUSP00000140651 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000067386] [ENSMUST00000187032] [ENSMUST00000187960]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000067386
AA Change: Y281*
SMART Domains Protein: ENSMUSP00000066803
Gene: ENSMUSG00000049643
AA Change: Y281*

DomainStartEndE-ValueType
Blast:SAM 34 100 5e-20 BLAST
SCOP:d1b4fa_ 54 100 7e-5 SMART
low complexity region 164 176 N/A INTRINSIC
low complexity region 268 277 N/A INTRINSIC
low complexity region 300 325 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000186501
Predicted Effect probably null
Transcript: ENSMUST00000187032
AA Change: Y275*
SMART Domains Protein: ENSMUSP00000139423
Gene: ENSMUSG00000049643
AA Change: Y275*

DomainStartEndE-ValueType
Blast:SAM 28 92 4e-20 BLAST
SCOP:d1b4fa_ 48 94 6e-5 SMART
low complexity region 158 170 N/A INTRINSIC
low complexity region 262 271 N/A INTRINSIC
low complexity region 294 319 N/A INTRINSIC
low complexity region 378 386 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000187960
AA Change: Y281*
SMART Domains Protein: ENSMUSP00000140651
Gene: ENSMUSG00000049643
AA Change: Y281*

DomainStartEndE-ValueType
Blast:SAM 34 98 4e-20 BLAST
SCOP:d1b4fa_ 54 100 6e-5 SMART
low complexity region 164 176 N/A INTRINSIC
low complexity region 268 277 N/A INTRINSIC
low complexity region 300 325 N/A INTRINSIC
low complexity region 384 392 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000190656
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts3 T C 5: 90,030,756 (GRCm39) probably benign Het
Afp T C 5: 90,639,610 (GRCm39) probably null Het
Ap1g2 T C 14: 55,337,987 (GRCm39) T634A probably benign Het
Cidec A G 6: 113,410,133 (GRCm39) V32A probably benign Het
Dip2a G A 10: 76,140,982 (GRCm39) P315S possibly damaging Het
Hoxc11 T C 15: 102,863,178 (GRCm39) V73A probably benign Het
Jmjd1c A G 10: 67,067,849 (GRCm39) Y1784C probably damaging Het
Mmp21 A G 7: 133,276,403 (GRCm39) V480A probably benign Het
Nek4 C T 14: 30,697,247 (GRCm39) T471I probably benign Het
Nr4a2 A G 2: 57,000,199 (GRCm39) V299A probably benign Het
Or14j8 A T 17: 38,263,697 (GRCm39) S73T possibly damaging Het
Or6c5 A G 10: 129,074,272 (GRCm39) T85A possibly damaging Het
Ptprg A G 14: 12,225,552 (GRCm38) D505G probably damaging Het
Rag2 A G 2: 101,460,608 (GRCm39) D306G probably damaging Het
Rpap2 T A 5: 107,746,426 (GRCm39) S38T possibly damaging Het
Scart2 A G 7: 139,874,746 (GRCm39) H408R probably benign Het
Scgb2b7 A T 7: 31,404,506 (GRCm39) C65S probably damaging Het
Slx4ip A T 2: 136,888,659 (GRCm39) R113S probably benign Het
Smyd5 T A 6: 85,409,000 (GRCm39) M5K probably benign Het
Stkld1 A T 2: 26,842,789 (GRCm39) H587L probably benign Het
Taf4b A G 18: 14,954,585 (GRCm39) T554A probably benign Het
Tex16 C A X: 111,028,552 (GRCm39) D350E possibly damaging Het
Tex38 T C 4: 115,637,723 (GRCm39) K27E possibly damaging Het
Trdv4 T C 14: 54,312,875 (GRCm39) L83P possibly damaging Het
Ugt2a3 G A 5: 87,484,439 (GRCm39) P195L probably damaging Het
Vmn1r120 A G 7: 20,787,450 (GRCm39) L87P probably damaging Het
Zfp236 T C 18: 82,648,733 (GRCm39) D916G possibly damaging Het
Other mutations in 2310022A10Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02292:2310022A10Rik APN 7 27,263,982 (GRCm39) missense probably benign 0.05
R0305:2310022A10Rik UTSW 7 27,274,061 (GRCm39) missense probably damaging 1.00
R1080:2310022A10Rik UTSW 7 27,265,109 (GRCm39) missense probably benign
R1696:2310022A10Rik UTSW 7 27,260,022 (GRCm39) missense possibly damaging 0.94
R1773:2310022A10Rik UTSW 7 27,280,020 (GRCm39) missense probably damaging 0.98
R4171:2310022A10Rik UTSW 7 27,265,109 (GRCm39) missense probably benign
R4583:2310022A10Rik UTSW 7 27,274,017 (GRCm39) missense unknown
R4781:2310022A10Rik UTSW 7 27,271,076 (GRCm39) missense probably damaging 1.00
R4806:2310022A10Rik UTSW 7 27,265,070 (GRCm39) critical splice acceptor site probably null
R4998:2310022A10Rik UTSW 7 27,271,088 (GRCm39) missense probably damaging 1.00
R5000:2310022A10Rik UTSW 7 27,255,946 (GRCm39) missense probably benign 0.04
R5007:2310022A10Rik UTSW 7 27,278,192 (GRCm39) missense probably damaging 1.00
R5008:2310022A10Rik UTSW 7 27,278,192 (GRCm39) missense probably damaging 1.00
R5364:2310022A10Rik UTSW 7 27,278,192 (GRCm39) missense probably damaging 1.00
R6119:2310022A10Rik UTSW 7 27,265,138 (GRCm39) nonsense probably null
R6991:2310022A10Rik UTSW 7 27,279,871 (GRCm39) missense probably damaging 1.00
R7014:2310022A10Rik UTSW 7 27,278,198 (GRCm39) nonsense probably null
R7519:2310022A10Rik UTSW 7 27,274,155 (GRCm39) missense
R7787:2310022A10Rik UTSW 7 27,263,926 (GRCm39) missense probably damaging 1.00
R8244:2310022A10Rik UTSW 7 27,271,004 (GRCm39) missense probably damaging 1.00
R8525:2310022A10Rik UTSW 7 27,255,936 (GRCm39) missense possibly damaging 0.64
R9246:2310022A10Rik UTSW 7 27,279,961 (GRCm39) missense probably benign 0.06
R9500:2310022A10Rik UTSW 7 27,265,091 (GRCm39) missense possibly damaging 0.85
Posted On 2016-08-02