Incidental Mutation 'IGL00714:2900092C05Rik'
List |< first << previous [record 58 of 10171] next >> last >|
ID8445
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2900092C05Rik
Ensembl Gene ENSMUSG00000030385
Gene NameRIKEN cDNA 2900092C05 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.019) question?
Stock #IGL00714
Quality Score
Status
Chromosome7
Chromosomal Location12512517-12556323 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to C at 12556004 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000032541 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032541]
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 Q1951R probably damaging Het
Cd22 T C 7: 30,876,147 M157V probably benign Het
Csta1 A G 16: 36,124,999 V48A probably damaging Het
Fxr1 T C 3: 34,047,627 probably benign Het
Pcdh1 G A 18: 38,198,729 T407I possibly damaging Het
Pcdha1 A T 18: 36,932,175 T631S probably damaging Het
Sec23b C T 2: 144,559,225 A2V probably benign Het
Tbc1d2 A G 4: 46,649,745 V97A probably benign Het
Ttll9 A C 2: 152,984,260 E130A probably damaging Het
Zfp160 A T 17: 21,026,702 T505S probably benign Het
Other mutations in 2900092C05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01744:2900092C05Rik APN 7 12550532 missense possibly damaging 0.92
IGL03047:2900092C05Rik UTSW 7 12512641 missense possibly damaging 0.92
R0001:2900092C05Rik UTSW 7 12554607 splice site probably benign
R0607:2900092C05Rik UTSW 7 12554698 missense probably benign 0.19
R0831:2900092C05Rik UTSW 7 12550596 splice site probably benign
R1468:2900092C05Rik UTSW 7 12512580 start codon destroyed probably null 0.83
R1468:2900092C05Rik UTSW 7 12512580 start codon destroyed probably null 0.83
R1846:2900092C05Rik UTSW 7 12512882 missense probably benign 0.38
R1852:2900092C05Rik UTSW 7 12512702 splice site probably null
R1912:2900092C05Rik UTSW 7 12554655 missense probably benign 0.01
R3442:2900092C05Rik UTSW 7 12512656 nonsense probably null
R3694:2900092C05Rik UTSW 7 12550516 missense possibly damaging 0.46
R3751:2900092C05Rik UTSW 7 12556046 missense probably benign 0.02
R5977:2900092C05Rik UTSW 7 12554737 missense probably benign 0.17
R6158:2900092C05Rik UTSW 7 12512672 missense probably benign 0.37
R6777:2900092C05Rik UTSW 7 12512829 missense probably benign 0.00
R6931:2900092C05Rik UTSW 7 12512596 missense unknown
Posted On2012-12-06