Incidental Mutation 'IGL01380:C130079G13Rik'
ID78802
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol C130079G13Rik
Ensembl Gene ENSMUSG00000036951
Gene NameRIKEN cDNA C130079G13 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.114) question?
Stock #IGL01380
Quality Score
Status
Chromosome3
Chromosomal Location59925214-59937949 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 59932632 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Alanine at position 42 (T42A)
Ref Sequence ENSEMBL: ENSMUSP00000047032 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000049476]
Predicted Effect probably benign
Transcript: ENSMUST00000049476
AA Change: T42A

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000047032
Gene: ENSMUSG00000036951
AA Change: T42A

DomainStartEndE-ValueType
Pfam:Abhydrolase_3 1 166 2.3e-31 PFAM
Pfam:Abhydrolase_3 148 254 4e-12 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc10 C A 17: 46,324,022 V352L possibly damaging Het
Ankrd44 A T 1: 54,727,565 M488K probably benign Het
Ano8 A G 8: 71,480,809 probably benign Het
Atp2a1 T A 7: 126,448,770 M623L possibly damaging Het
Atxn10 G T 15: 85,376,695 E214* probably null Het
Btla A C 16: 45,250,353 D225A probably benign Het
C030048H21Rik G A 2: 26,256,647 Q1218* probably null Het
Cacna1a A G 8: 84,559,117 Y750C probably damaging Het
Ccdc15 A T 9: 37,276,557 probably benign Het
Ccdc18 T A 5: 108,180,887 I724N probably damaging Het
Cluh T A 11: 74,665,946 F937L probably benign Het
Clybl G T 14: 122,379,349 A259S probably benign Het
Cyp4f39 T G 17: 32,481,858 I167S probably damaging Het
Dchs1 T A 7: 105,762,211 D1566V probably damaging Het
Dnah3 C T 7: 119,926,564 A3867T probably damaging Het
Dtwd1 T A 2: 126,159,927 L189Q probably benign Het
Dusp10 T C 1: 184,069,014 I326T possibly damaging Het
Eaf1 T A 14: 31,497,810 probably benign Het
Eif3c C T 7: 126,564,413 probably benign Het
Fam169a C T 13: 97,091,951 T44M probably damaging Het
Fam184a T C 10: 53,694,686 probably benign Het
Fam25c C T 14: 34,353,698 A46T probably null Het
Gckr A G 5: 31,299,633 probably benign Het
Gfra2 G T 14: 70,967,146 probably benign Het
Gm8237 A T 14: 5,863,703 probably null Het
H2-Eb2 G T 17: 34,335,809 L228F probably benign Het
Igf2r T C 17: 12,695,374 N1736S probably benign Het
Izumo1 T G 7: 45,627,095 S361A probably benign Het
Klri1 T C 6: 129,698,798 I170V probably benign Het
L3mbtl2 C T 15: 81,671,125 A193V possibly damaging Het
Lats1 T A 10: 7,691,780 M105K possibly damaging Het
Lrpprc T C 17: 84,722,730 D1080G probably benign Het
Lrrc74a A T 12: 86,761,722 M425L possibly damaging Het
Mfsd13a G T 19: 46,367,908 D151Y probably damaging Het
Mst1 G A 9: 108,084,588 E640K probably damaging Het
Napsa T C 7: 44,586,674 V379A probably damaging Het
Olfr1 A T 11: 73,395,191 M277K probably damaging Het
Olfr371 A T 8: 85,231,329 Y278F possibly damaging Het
Olfr371 C A 8: 85,231,146 S217Y probably damaging Het
Olfr544 C T 7: 102,484,385 C245Y probably damaging Het
Otop3 T C 11: 115,346,411 V567A probably damaging Het
Oxsr1 A T 9: 119,260,101 probably benign Het
Pak2 A T 16: 32,041,544 V167E probably benign Het
Pcdhb16 A G 18: 37,479,445 H486R probably benign Het
Plekha5 C T 6: 140,570,316 probably benign Het
Rbm6 T C 9: 107,788,349 D616G probably damaging Het
Sf3b1 T C 1: 54,987,949 Y1249C probably damaging Het
Sipa1l3 T C 7: 29,331,372 H534R possibly damaging Het
Slco1c1 T C 6: 141,540,051 Y136H probably damaging Het
Smarca4 A G 9: 21,679,073 M1333V probably benign Het
Smc4 A G 3: 69,025,828 D54G probably damaging Het
Spag5 T A 11: 78,304,617 V250E possibly damaging Het
Stxbp4 A G 11: 90,621,649 probably benign Het
Suv39h2 T A 2: 3,464,259 probably benign Het
Taar8b T A 10: 24,092,107 H63L probably damaging Het
Tex2 G A 11: 106,544,315 Q264* probably null Het
Thnsl2 A C 6: 71,138,756 S156A probably benign Het
Tmtc4 G T 14: 122,925,954 probably benign Het
Usp25 T C 16: 77,093,678 L758P probably benign Het
Zfyve1 G A 12: 83,552,507 R144C probably damaging Het
Zpld1 A G 16: 55,251,770 V42A probably damaging Het
Other mutations in C130079G13Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02850:C130079G13Rik APN 3 59936572 missense probably damaging 1.00
R0099:C130079G13Rik UTSW 3 59936435 missense probably benign 0.00
R0206:C130079G13Rik UTSW 3 59932689 missense probably damaging 1.00
R0208:C130079G13Rik UTSW 3 59932689 missense probably damaging 1.00
R0457:C130079G13Rik UTSW 3 59936633 missense possibly damaging 0.78
R0511:C130079G13Rik UTSW 3 59936350 missense possibly damaging 0.79
R1824:C130079G13Rik UTSW 3 59932580 nonsense probably null
R2567:C130079G13Rik UTSW 3 59929054 splice site probably benign
R2844:C130079G13Rik UTSW 3 59936409 missense probably benign 0.05
R3826:C130079G13Rik UTSW 3 59936475 missense possibly damaging 0.89
R4356:C130079G13Rik UTSW 3 59936280 missense probably damaging 1.00
R4755:C130079G13Rik UTSW 3 59936314 missense probably benign
R4975:C130079G13Rik UTSW 3 59932740 missense probably damaging 0.98
R5199:C130079G13Rik UTSW 3 59936485 missense probably damaging 1.00
R7221:C130079G13Rik UTSW 3 59928933 start gained probably benign
R7336:C130079G13Rik UTSW 3 59932753 splice site probably null
R8150:C130079G13Rik UTSW 3 59936137 missense probably damaging 0.99
R8159:C130079G13Rik UTSW 3 59936422 missense probably damaging 1.00
Posted On2013-11-05