Incidental Mutation 'IGL01625:2210010C04Rik'
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ID92735
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2210010C04Rik
Ensembl Gene ENSMUSG00000029882
Gene NameRIKEN cDNA 2210010C04 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.085) question?
Stock #IGL01625
Quality Score
Status
Chromosome6
Chromosomal Location41030268-41035509 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to C at 41032948 bp
ZygosityHeterozygous
Amino Acid Change Serine to Alanine at position 151 (S151A)
Ref Sequence ENSEMBL: ENSMUSP00000031931 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031931]
Predicted Effect probably benign
Transcript: ENSMUST00000031931
AA Change: S151A

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000031931
Gene: ENSMUSG00000029882
AA Change: S151A

DomainStartEndE-ValueType
Tryp_SPc 24 240 3.52e-102 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700018F24Rik T A 5: 145,043,147 H37Q possibly damaging Het
Akr1c19 T A 13: 4,233,817 I16N probably damaging Het
Arpc1b T C 5: 145,121,745 probably null Het
Bzw1 A G 1: 58,401,440 T191A probably benign Het
Cacna1h T C 17: 25,383,485 D1523G probably damaging Het
Cacna1h G A 17: 25,385,712 T1209I possibly damaging Het
Cdc20b T C 13: 113,059,785 L148P possibly damaging Het
Cubn A G 2: 13,306,274 F3147L possibly damaging Het
Dagla A G 19: 10,251,202 probably benign Het
Dnah9 T C 11: 66,044,645 N1983D probably damaging Het
Fbxw10 G A 11: 62,860,027 D479N probably damaging Het
Fer A T 17: 64,037,626 Q630L probably damaging Het
Gbp5 A G 3: 142,503,028 N111D probably damaging Het
Gm8127 T G 14: 43,291,063 probably benign Het
Heatr1 T A 13: 12,413,528 N814K probably damaging Het
Iba57 G A 11: 59,158,949 R191W probably damaging Het
Itgae C A 11: 73,119,437 F584L probably benign Het
Kdm5b A G 1: 134,617,968 K956E possibly damaging Het
Muc4 C T 16: 32,755,544 probably benign Het
Mybpc2 T C 7: 44,516,913 K218E possibly damaging Het
Pcdh10 T C 3: 45,379,397 S49P probably damaging Het
Rai14 T C 15: 10,572,374 D889G probably benign Het
Rbpjl A G 2: 164,407,785 K102R possibly damaging Het
Retreg2 A G 1: 75,144,715 probably benign Het
Rfc4 A T 16: 23,115,823 L149Q probably damaging Het
Rft1 T A 14: 30,676,896 D274E possibly damaging Het
Rlf A T 4: 121,188,260 S143R possibly damaging Het
Rptn T A 3: 93,397,894 S845T probably benign Het
Slamf8 C A 1: 172,582,482 D267Y probably damaging Het
Smoc2 C T 17: 14,325,614 S55L probably damaging Het
Sptan1 C T 2: 30,026,114 A2038V probably damaging Het
Stx17 C A 4: 48,181,526 P210T probably damaging Het
Tbc1d5 A G 17: 50,917,573 Y317H probably benign Het
Tenm4 C A 7: 96,885,358 T1737N probably damaging Het
Tesk2 T C 4: 116,771,801 F116L possibly damaging Het
Tln2 T C 9: 67,370,623 S370G probably damaging Het
Tm6sf2 G T 8: 70,076,083 G162C probably null Het
Togaram2 A C 17: 71,714,698 E718D probably benign Het
Ttn A C 2: 76,747,983 F15862V probably damaging Het
Uba6 T A 5: 86,120,529 R916* probably null Het
Umodl1 A G 17: 30,996,255 M1018V probably benign Het
Wdr26 G A 1: 181,191,816 T332I possibly damaging Het
Xdh A T 17: 73,916,786 probably null Het
Other mutations in 2210010C04Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01120:2210010C04Rik APN 6 41031673 missense probably damaging 1.00
IGL02159:2210010C04Rik APN 6 41032957 missense probably benign 0.34
IGL03161:2210010C04Rik APN 6 41034306 missense probably damaging 0.96
R0419:2210010C04Rik UTSW 6 41034347 missense probably benign 0.05
R1715:2210010C04Rik UTSW 6 41032936 splice site probably null
R2057:2210010C04Rik UTSW 6 41032381 missense probably benign 0.06
R2059:2210010C04Rik UTSW 6 41032381 missense probably benign 0.06
R2136:2210010C04Rik UTSW 6 41035462 missense probably benign 0.28
R2446:2210010C04Rik UTSW 6 41031648 missense probably benign 0.15
R4862:2210010C04Rik UTSW 6 41032411 missense possibly damaging 0.74
R5068:2210010C04Rik UTSW 6 41032436 missense probably benign 0.35
R5369:2210010C04Rik UTSW 6 41033006 missense probably benign 0.00
R6392:2210010C04Rik UTSW 6 41032372 missense probably damaging 1.00
Posted On2013-12-09