Incidental Mutation 'IGL00476:2610002M06Rik'
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ID29562
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2610002M06Rik
Ensembl Gene ENSMUSG00000031242
Gene NameRIKEN cDNA 2610002M06 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00476
Quality Score
Status
ChromosomeX
Chromosomal Location107782751-107816334 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to C at 107816160 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000129483 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000101292] [ENSMUST00000120722] [ENSMUST00000143975] [ENSMUST00000144695] [ENSMUST00000167154]
Predicted Effect probably benign
Transcript: ENSMUST00000101292
SMART Domains Protein: ENSMUSP00000098850
Gene: ENSMUSG00000073007

DomainStartEndE-ValueType
DUF1693 9 328 6.24e-223 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000120722
SMART Domains Protein: ENSMUSP00000113588
Gene: ENSMUSG00000031242

DomainStartEndE-ValueType
Pfam:Snf7 7 176 5.7e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000143975
SMART Domains Protein: ENSMUSP00000122208
Gene: ENSMUSG00000073007

DomainStartEndE-ValueType
Pfam:DUF1693 9 82 5e-26 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000144695
Predicted Effect probably benign
Transcript: ENSMUST00000167154
SMART Domains Protein: ENSMUSP00000129483
Gene: ENSMUSG00000073007

DomainStartEndE-ValueType
DUF1693 9 328 6.24e-223 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931414P19Rik T C 14: 54,595,578 T47A possibly damaging Het
Adgrv1 A G 13: 81,489,074 F3416S probably damaging Het
Arhgap42 T C 9: 9,006,343 D684G probably damaging Het
Atp13a1 T C 8: 69,796,897 L270P probably damaging Het
Baz2b T C 2: 59,913,739 N1474S probably benign Het
Chrna6 A G 8: 27,406,532 I439T probably damaging Het
Cylc2 T C 4: 51,228,157 M76T probably damaging Het
Ddx19a T C 8: 110,976,470 K445R probably benign Het
Dennd4a A T 9: 64,911,762 Y1733F probably damaging Het
Dopey2 G A 16: 93,800,026 probably benign Het
Dpcr1 G T 17: 35,638,102 H202N possibly damaging Het
Ephb3 T A 16: 21,220,415 probably null Het
Gpc2 G A 5: 138,274,309 probably benign Het
Ift172 A G 5: 31,275,896 Y550H probably damaging Het
Kat2a G A 11: 100,705,384 R782W probably damaging Het
Ldhd G T 8: 111,628,638 R238S possibly damaging Het
Men1 G A 19: 6,337,207 probably null Het
Mipep T G 14: 60,827,361 L388R probably damaging Het
Naa35 A G 13: 59,630,055 D610G probably damaging Het
Nae1 A T 8: 104,526,381 L137Q possibly damaging Het
Nt5dc3 T C 10: 86,833,974 probably null Het
Nyx T C X: 13,487,025 F373L possibly damaging Het
Scaf11 A T 15: 96,418,580 D1034E possibly damaging Het
Sp2 C T 11: 96,954,561 R578H probably damaging Het
Taar7a A T 10: 23,992,396 probably benign Het
Tcf23 G T 5: 30,973,525 C169F probably benign Het
Trim7 A T 11: 48,848,078 N308I probably benign Het
Ubxn8 T C 8: 33,635,305 E89G probably benign Het
Other mutations in 2610002M06Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00595:2610002M06Rik APN X 107787844 missense probably damaging 0.97
IGL03355:2610002M06Rik APN X 107788283 missense possibly damaging 0.78
Posted On2013-04-17