Incidental Mutation 'IGL02216:5830473C10Rik'
ID284920
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 5830473C10Rik
Ensembl Gene ENSMUSG00000070690
Gene NameRIKEN cDNA 5830473C10 gene
SynonymsGm17754, ARG
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.222) question?
Stock #IGL02216
Quality Score
Status
Chromosome5
Chromosomal Location90561107-90597871 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) T to C at 90579579 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000144527 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094615] [ENSMUST00000200765]
Predicted Effect probably benign
Transcript: ENSMUST00000094615
SMART Domains Protein: ENSMUSP00000092198
Gene: ENSMUSG00000070690

DomainStartEndE-ValueType
ALBUMIN 17 207 8.87e-26 SMART
ALBUMIN 214 399 1.45e-53 SMART
ALBUMIN 406 598 7.07e-43 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000200765
SMART Domains Protein: ENSMUSP00000144527
Gene: ENSMUSG00000070690

DomainStartEndE-ValueType
ALBUMIN 17 207 4.3e-28 SMART
ALBUMIN 214 355 3.3e-15 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200783
Predicted Effect noncoding transcript
Transcript: ENSMUST00000200893
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610009O20Rik A T 18: 38,252,860 I102F probably damaging Het
4930544D05Rik T C 11: 70,616,179 F48L possibly damaging Het
Adamts12 A G 15: 11,241,485 N381S possibly damaging Het
Akp3 A T 1: 87,127,650 Q473L probably damaging Het
Ap5s1 T A 2: 131,212,967 probably benign Het
Atp10b T A 11: 43,259,789 L1438Q probably damaging Het
B3galt4 G A 17: 33,950,565 P233L probably damaging Het
Brd8 C T 18: 34,602,727 S899N probably damaging Het
Cc2d1a C A 8: 84,139,313 E393* probably null Het
Cd209a G T 8: 3,745,576 T165N probably damaging Het
Chid1 T C 7: 141,496,593 probably benign Het
Cln3 A T 7: 126,575,342 probably null Het
Cped1 A T 6: 22,059,945 R203S probably damaging Het
Dnttip2 G T 3: 122,276,261 W375L probably benign Het
Dync1h1 T C 12: 110,663,002 F4280S probably damaging Het
Ephb4 A G 5: 137,372,070 D844G possibly damaging Het
Fhl2 T A 1: 43,131,719 probably null Het
Gne T C 4: 44,044,761 K458E probably benign Het
Grid2 G T 6: 64,345,666 R550L probably damaging Het
Klhl1 T A 14: 96,123,222 T731S probably benign Het
Kng1 T A 16: 23,058,533 D30E probably damaging Het
Kyat1 A G 2: 30,187,252 V158A probably benign Het
Mcm8 G T 2: 132,839,529 V642F probably damaging Het
Mdn1 C T 4: 32,739,092 H3638Y probably benign Het
Neb T G 2: 52,226,490 probably null Het
Neo1 T C 9: 58,917,053 I697M probably damaging Het
Nfkb1 A T 3: 135,594,963 V614D probably damaging Het
Olfr860 G A 9: 19,846,565 S18L probably damaging Het
Otog T C 7: 46,301,468 S2555P probably damaging Het
Pkd1l1 T A 11: 8,834,897 R1962S probably damaging Het
Plxnb1 A G 9: 109,100,850 Y258C probably damaging Het
Pramef8 T A 4: 143,417,728 probably null Het
Prl3a1 A G 13: 27,270,144 D35G probably benign Het
Rag1 A T 2: 101,643,381 V472D possibly damaging Het
Rbpj-ps3 G A 6: 46,529,707 Het
Rnf112 C T 11: 61,449,978 V472M probably damaging Het
Rps18 A G 17: 33,952,041 probably benign Het
Rptn T C 3: 93,395,773 S138P possibly damaging Het
Sbpl A C 17: 23,953,716 N76K probably benign Het
Sh3bp1 A T 15: 78,905,164 M241L probably benign Het
Slc22a17 T C 14: 54,907,976 *198W probably null Het
Smc3 C T 19: 53,621,844 R221C probably damaging Het
Snai1 A G 2: 167,538,848 E87G probably benign Het
Snx22 C A 9: 66,069,188 A49S probably benign Het
Tas2r143 A T 6: 42,400,334 R33* probably null Het
Try4 A G 6: 41,305,031 I184V probably benign Het
Ttn T A 2: 76,754,552 K20355* probably null Het
Ttn A G 2: 76,791,725 V15491A probably benign Het
Vmn1r170 A G 7: 23,606,490 T106A probably damaging Het
Vmn2r59 A T 7: 42,012,393 V666E probably damaging Het
Vsx1 T C 2: 150,684,575 N221S possibly damaging Het
Zcchc6 T C 13: 59,800,423 T293A probably benign Het
Zfp846 A G 9: 20,588,609 E45G probably damaging Het
Other mutations in 5830473C10Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02343:5830473C10Rik APN 5 90579614 missense probably damaging 0.99
IGL02749:5830473C10Rik APN 5 90571765 missense possibly damaging 0.84
IGL02956:5830473C10Rik APN 5 90579638 missense possibly damaging 0.46
R0097:5830473C10Rik UTSW 5 90584936 missense probably benign 0.02
R0097:5830473C10Rik UTSW 5 90584936 missense probably benign 0.02
R0513:5830473C10Rik UTSW 5 90577927 missense probably benign 0.00
R0551:5830473C10Rik UTSW 5 90572719 missense probably damaging 1.00
R1508:5830473C10Rik UTSW 5 90581921 missense probably benign 0.00
R1797:5830473C10Rik UTSW 5 90579601 missense probably damaging 0.99
R2205:5830473C10Rik UTSW 5 90569562 missense possibly damaging 0.50
R2323:5830473C10Rik UTSW 5 90584852 nonsense probably null
R2440:5830473C10Rik UTSW 5 90572689 critical splice acceptor site probably null
R4074:5830473C10Rik UTSW 5 90592868 splice site probably null
R4211:5830473C10Rik UTSW 5 90564237 missense probably damaging 1.00
R4426:5830473C10Rik UTSW 5 90572783 missense probably damaging 1.00
R4625:5830473C10Rik UTSW 5 90571752 missense probably damaging 0.99
R4823:5830473C10Rik UTSW 5 90566503 missense probably benign 0.01
R4922:5830473C10Rik UTSW 5 90579711 missense possibly damaging 0.84
R4923:5830473C10Rik UTSW 5 90561299 missense probably benign 0.07
R5218:5830473C10Rik UTSW 5 90581918 missense probably benign 0.34
R5267:5830473C10Rik UTSW 5 90584857 missense probably damaging 0.99
R5447:5830473C10Rik UTSW 5 90584310 missense probably damaging 1.00
R5737:5830473C10Rik UTSW 5 90572783 missense probably damaging 1.00
R5966:5830473C10Rik UTSW 5 90571687 missense probably damaging 1.00
R6045:5830473C10Rik UTSW 5 90584989 missense possibly damaging 0.86
R6290:5830473C10Rik UTSW 5 90593005 critical splice donor site probably null
R6799:5830473C10Rik UTSW 5 90579615 missense probably damaging 0.99
R6923:5830473C10Rik UTSW 5 90577793 missense probably benign 0.32
Posted On2015-04-16