Incidental Mutation 'IGL00476:2610002M06Rik'
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Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2610002M06Rik
Ensembl Gene ENSMUSG00000031242
Gene NameRIKEN cDNA 2610002M06 gene
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00476
Quality Score
Chromosomal Location107782751-107816334 bp(-) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to C at 107816160 bp
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

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

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

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

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