Incidental Mutation 'IGL01534:B230307C23Rik'
ID 89906
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol B230307C23Rik
Ensembl Gene ENSMUSG00000080717
Gene Name RIKEN cDNA B230307C23 gene
Synonyms EG245305
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL01534
Quality Score
Status
Chromosome 16
Chromosomal Location 97798278-97817956 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 97809961 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000156366 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113729] [ENSMUST00000122450] [ENSMUST00000231913] [ENSMUST00000231936] [ENSMUST00000232278] [ENSMUST00000232308] [ENSMUST00000232346] [ENSMUST00000232387]
AlphaFold A0A338P6F4
Predicted Effect probably benign
Transcript: ENSMUST00000113729
SMART Domains Protein: ENSMUSP00000109358
Gene: ENSMUSG00000080717

DomainStartEndE-ValueType
KRAB 3 56 6.22e-11 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000122450
SMART Domains Protein: ENSMUSP00000113241
Gene: ENSMUSG00000080717

DomainStartEndE-ValueType
KRAB 4 57 6.22e-11 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000231913
Predicted Effect probably benign
Transcript: ENSMUST00000231936
Predicted Effect probably benign
Transcript: ENSMUST00000232278
Predicted Effect probably benign
Transcript: ENSMUST00000232308
Predicted Effect probably benign
Transcript: ENSMUST00000232346
Predicted Effect probably benign
Transcript: ENSMUST00000232387
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd5 T C 9: 122,197,146 (GRCm39) L111P possibly damaging Het
Adck5 C A 15: 76,478,926 (GRCm39) H383Q probably damaging Het
Arb2a T A 13: 78,147,830 (GRCm39) probably benign Het
Asns T A 6: 7,675,397 (GRCm39) H535L probably benign Het
Atf5 A G 7: 44,462,462 (GRCm39) S221P probably damaging Het
Atr T C 9: 95,747,599 (GRCm39) Y294H probably damaging Het
C1qtnf6 C T 15: 78,409,416 (GRCm39) E144K probably benign Het
Casp8ap2 C T 4: 32,648,134 (GRCm39) probably benign Het
Cd48 C A 1: 171,523,307 (GRCm39) P50Q possibly damaging Het
Cnnm4 T C 1: 36,538,596 (GRCm39) Y593H probably benign Het
Col27a1 G A 4: 63,144,019 (GRCm39) R569Q probably benign Het
Cubn A T 2: 13,470,744 (GRCm39) C549* probably null Het
Dsg1a T A 18: 20,474,053 (GRCm39) M1042K probably benign Het
Dzip1 T A 14: 119,114,651 (GRCm39) T835S probably damaging Het
Eif3c T C 7: 126,156,867 (GRCm39) T389A probably benign Het
Erlin2 G T 8: 27,521,985 (GRCm39) E177* probably null Het
Gabrb1 T A 5: 72,026,772 (GRCm39) S91T possibly damaging Het
Grik3 T C 4: 125,579,983 (GRCm39) V576A probably damaging Het
Gtpbp2 T A 17: 46,474,430 (GRCm39) Y70N probably damaging Het
Idh3a T A 9: 54,508,506 (GRCm39) probably benign Het
Ift74 G A 4: 94,568,181 (GRCm39) R406H probably benign Het
Kcna7 C A 7: 45,055,935 (GRCm39) N50K probably damaging Het
Kcnd2 T C 6: 21,726,144 (GRCm39) S546P probably benign Het
Lrp4 G A 2: 91,303,986 (GRCm39) D134N probably damaging Het
Mcm2 A G 6: 88,864,700 (GRCm39) probably null Het
Nlrp12 T C 7: 3,288,463 (GRCm39) Y683C probably benign Het
Or14j3 A T 17: 37,900,963 (GRCm39) Y94N possibly damaging Het
Or2d4 T A 7: 106,543,546 (GRCm39) I221F probably damaging Het
Or8i2 A G 2: 86,852,228 (GRCm39) I220T probably damaging Het
Or9i1 A T 19: 13,839,283 (GRCm39) N42I probably damaging Het
Or9i14 T A 19: 13,792,666 (GRCm39) H96L probably benign Het
P2rx7 A C 5: 122,814,761 (GRCm39) I409L probably damaging Het
Pde10a A G 17: 9,163,802 (GRCm39) N191S probably damaging Het
Rabggtb A G 3: 153,615,896 (GRCm39) probably null Het
Rgs4 A T 1: 169,572,085 (GRCm39) C71* probably null Het
Rnase10 T C 14: 51,245,436 (GRCm39) F5L probably benign Het
Scn11a T A 9: 119,609,888 (GRCm39) T987S probably benign Het
Shox2 A C 3: 66,885,696 (GRCm39) D126E probably benign Het
Slc12a1 A G 2: 125,059,830 (GRCm39) D910G probably damaging Het
Slc15a1 C T 14: 121,702,364 (GRCm39) C594Y possibly damaging Het
Spock2 C T 10: 59,962,883 (GRCm39) probably benign Het
Togaram1 G T 12: 65,013,321 (GRCm39) D191Y probably damaging Het
Triml2 T C 8: 43,640,660 (GRCm39) V172A probably benign Het
Tubb3 C T 8: 124,147,705 (GRCm39) R213C probably benign Het
Vmn2r4 A T 3: 64,313,844 (GRCm39) V379E probably damaging Het
Zfp446 C T 7: 12,713,493 (GRCm39) P153L probably damaging Het
Zfp608 A T 18: 55,032,004 (GRCm39) N645K probably damaging Het
Other mutations in B230307C23Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02316:B230307C23Rik APN 16 97,809,850 (GRCm39) missense probably damaging 1.00
R3686:B230307C23Rik UTSW 16 97,810,199 (GRCm39) missense probably benign 0.14
R3687:B230307C23Rik UTSW 16 97,810,199 (GRCm39) missense probably benign 0.14
R5255:B230307C23Rik UTSW 16 97,809,891 (GRCm39) missense possibly damaging 0.89
R6880:B230307C23Rik UTSW 16 97,798,627 (GRCm39) start gained probably benign
R7060:B230307C23Rik UTSW 16 97,811,331 (GRCm39) missense probably benign 0.01
Posted On 2013-12-03