Incidental Mutation 'IGL03388:6030468B19Rik'
ID420971
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 6030468B19Rik
Ensembl Gene ENSMUSG00000025573
Gene NameRIKEN cDNA 6030468B19 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.069) question?
Stock #IGL03388
Quality Score
Status
Chromosome11
Chromosomal Location117797660-117807301 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 117802770 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000101938 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106331]
Predicted Effect probably benign
Transcript: ENSMUST00000106331
SMART Domains Protein: ENSMUSP00000101938
Gene: ENSMUSG00000025573

DomainStartEndE-ValueType
signal peptide 1 18 N/A INTRINSIC
Pfam:Ig_3 31 100 6.1e-5 PFAM
Pfam:Ig_3 120 195 1.2e-6 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: No notable phenotype was detected in a high-throughput screen of homozygous null mice. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
B3gnt5 A G 16: 19,770,051 K340R possibly damaging Het
Ccr3 A G 9: 124,028,621 probably benign Het
Cdan1 A G 2: 120,730,511 probably benign Het
Clasp1 T A 1: 118,505,503 D237E possibly damaging Het
Ddx18 T C 1: 121,565,923 K111E possibly damaging Het
Defa21 T C 8: 21,025,748 L54P probably damaging Het
Dennd3 T C 15: 73,544,359 V486A probably damaging Het
Dnah9 T A 11: 65,947,542 D3143V probably damaging Het
Dnm1l A G 16: 16,314,052 probably benign Het
Epb41 T C 4: 131,974,794 Y510C probably damaging Het
Fat4 T C 3: 38,957,227 Y2159H probably damaging Het
Fmo1 A G 1: 162,836,147 V271A probably benign Het
Gm11492 T A 11: 87,568,216 L472* probably null Het
Gm12185 A G 11: 48,908,286 V460A probably benign Het
Hspa8 T C 9: 40,804,928 probably benign Het
Hspb7 A G 4: 141,424,045 E166G probably damaging Het
Il31ra C A 13: 112,546,212 S120I probably damaging Het
Kdm5b A G 1: 134,627,322 T1323A probably benign Het
Lgals9 T A 11: 78,963,421 I346F probably damaging Het
Lgi2 T C 5: 52,538,477 D372G probably damaging Het
Magi3 A C 3: 104,015,841 S1187A probably benign Het
Nr1d2 A G 14: 18,215,403 F203S probably benign Het
Nup210l G A 3: 90,170,044 V896I probably damaging Het
Nxf7 T C X: 135,584,740 K440E probably damaging Het
Olfr1505 T A 19: 13,919,620 V200D probably damaging Het
Olfr776 A T 10: 129,261,443 I161F probably benign Het
Pcdhb6 T C 18: 37,336,137 S20P probably damaging Het
Per2 G T 1: 91,444,789 probably benign Het
Pi15 G A 1: 17,602,777 A67T probably benign Het
Pnp2 A T 14: 50,963,538 N160I probably damaging Het
Ppp1r12c A G 7: 4,482,070 probably benign Het
Rabgap1l A T 1: 160,733,523 probably null Het
Rnf115 G A 3: 96,788,668 V257M probably damaging Het
Rtkn T A 6: 83,150,090 V346D probably benign Het
Rubcn A T 16: 32,841,568 N427K probably benign Het
Scgb2b7 A T 7: 31,705,081 C65S probably damaging Het
Sel1l2 A C 2: 140,263,364 probably benign Het
Slc5a5 A G 8: 70,890,328 V196A probably benign Het
Sox13 A T 1: 133,388,948 L207H probably damaging Het
Tmtc2 A G 10: 105,321,483 probably benign Het
Trip12 T C 1: 84,743,186 K1409R probably damaging Het
Ttn C T 2: 76,967,137 A528T probably benign Het
Ubr4 T C 4: 139,415,032 I1310T probably damaging Het
Ypel5 T C 17: 72,846,405 F35L probably damaging Het
Zfp13 G T 17: 23,576,914 R228S probably benign Het
Other mutations in 6030468B19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02168:6030468B19Rik APN 11 117798418 splice site probably benign
PIT4434001:6030468B19Rik UTSW 11 117806043 missense probably benign 0.01
R0477:6030468B19Rik UTSW 11 117802961 missense probably benign 0.00
R3824:6030468B19Rik UTSW 11 117802913 missense probably damaging 0.99
R3825:6030468B19Rik UTSW 11 117802913 missense probably damaging 0.99
R4114:6030468B19Rik UTSW 11 117802967 missense probably damaging 1.00
R4283:6030468B19Rik UTSW 11 117806261 missense probably benign 0.01
R4779:6030468B19Rik UTSW 11 117806008 missense probably benign 0.14
R4916:6030468B19Rik UTSW 11 117806266 nonsense probably null
R5068:6030468B19Rik UTSW 11 117802875 missense possibly damaging 0.85
R5725:6030468B19Rik UTSW 11 117806057 missense probably damaging 0.98
R6139:6030468B19Rik UTSW 11 117806324 missense probably damaging 0.98
R6992:6030468B19Rik UTSW 11 117797768 start codon destroyed probably null
R7157:6030468B19Rik UTSW 11 117802954 missense probably damaging 0.98
Posted On2016-08-02