Incidental Mutation 'IGL00714:2900092C05Rik'
ID 8445
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2900092C05Rik
Ensembl Gene ENSMUSG00000030385
Gene Name RIKEN cDNA 2900092C05 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # IGL00714
Quality Score
Status
Chromosome 7
Chromosomal Location 12246444-12290250 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to C at 12289931 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000032541 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032541]
AlphaFold Q5I0V9
Predicted Effect probably benign
Transcript: ENSMUST00000032541
SMART Domains Protein: ENSMUSP00000032541
Gene: ENSMUSG00000030385

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
transmembrane domain 96 118 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209381
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 10 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Casp8ap2 A G 4: 32,649,192 (GRCm39) Q1951R probably damaging Het
Cd22 T C 7: 30,575,572 (GRCm39) M157V probably benign Het
Csta1 A G 16: 35,945,369 (GRCm39) V48A probably damaging Het
Fxr1 T C 3: 34,101,776 (GRCm39) probably benign Het
Pcdh1 G A 18: 38,331,782 (GRCm39) T407I possibly damaging Het
Pcdha1 A T 18: 37,065,228 (GRCm39) T631S probably damaging Het
Sec23b C T 2: 144,401,145 (GRCm39) A2V probably benign Het
Tbc1d2 A G 4: 46,649,745 (GRCm39) V97A probably benign Het
Ttll9 A C 2: 152,826,180 (GRCm39) E130A probably damaging Het
Zfp160 A T 17: 21,246,964 (GRCm39) T505S probably benign Het
Other mutations in 2900092C05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01744:2900092C05Rik APN 7 12,284,459 (GRCm39) missense possibly damaging 0.92
IGL03047:2900092C05Rik UTSW 7 12,246,568 (GRCm39) missense possibly damaging 0.92
R0001:2900092C05Rik UTSW 7 12,288,534 (GRCm39) splice site probably benign
R0607:2900092C05Rik UTSW 7 12,288,625 (GRCm39) missense probably benign 0.19
R0831:2900092C05Rik UTSW 7 12,284,523 (GRCm39) splice site probably benign
R1468:2900092C05Rik UTSW 7 12,246,507 (GRCm39) start codon destroyed probably null 0.83
R1468:2900092C05Rik UTSW 7 12,246,507 (GRCm39) start codon destroyed probably null 0.83
R1846:2900092C05Rik UTSW 7 12,246,809 (GRCm39) missense probably benign 0.38
R1852:2900092C05Rik UTSW 7 12,246,629 (GRCm39) splice site probably null
R1912:2900092C05Rik UTSW 7 12,288,582 (GRCm39) missense probably benign 0.01
R3442:2900092C05Rik UTSW 7 12,246,583 (GRCm39) nonsense probably null
R3694:2900092C05Rik UTSW 7 12,284,443 (GRCm39) missense possibly damaging 0.46
R3751:2900092C05Rik UTSW 7 12,289,973 (GRCm39) missense probably benign 0.02
R5977:2900092C05Rik UTSW 7 12,288,664 (GRCm39) missense probably benign 0.17
R6158:2900092C05Rik UTSW 7 12,246,599 (GRCm39) missense probably benign 0.37
R6777:2900092C05Rik UTSW 7 12,246,756 (GRCm39) missense probably benign 0.00
R6931:2900092C05Rik UTSW 7 12,246,523 (GRCm39) missense unknown
R7284:2900092C05Rik UTSW 7 12,246,605 (GRCm39) nonsense probably null
R7406:2900092C05Rik UTSW 7 12,249,391 (GRCm39) missense possibly damaging 0.66
R8472:2900092C05Rik UTSW 7 12,246,568 (GRCm39) missense possibly damaging 0.92
R8802:2900092C05Rik UTSW 7 12,249,415 (GRCm39) missense possibly damaging 0.66
R8877:2900092C05Rik UTSW 7 12,288,704 (GRCm39) critical splice donor site probably null
R9175:2900092C05Rik UTSW 7 12,249,412 (GRCm39) missense probably benign 0.00
Posted On 2012-12-06