Incidental Mutation 'IGL03126:Rinl'
ID 410177
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Rinl
Ensembl Gene ENSMUSG00000051735
Gene Name Ras and Rab interactor-like
Synonyms 9930116N10Rik, 5830482F20Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL03126
Quality Score
Status
Chromosome 7
Chromosomal Location 28488394-28498388 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 28495075 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000146576 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059857] [ENSMUST00000209035]
AlphaFold Q80UW3
Predicted Effect probably benign
Transcript: ENSMUST00000059857
SMART Domains Protein: ENSMUSP00000058447
Gene: ENSMUSG00000051735

DomainStartEndE-ValueType
Blast:SH2 50 132 2e-38 BLAST
SCOP:d1lkka_ 69 143 3e-3 SMART
low complexity region 183 196 N/A INTRINSIC
low complexity region 376 395 N/A INTRINSIC
Pfam:VPS9 410 514 2.5e-21 PFAM
low complexity region 542 553 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207345
Predicted Effect probably benign
Transcript: ENSMUST00000207462
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208149
Predicted Effect probably benign
Transcript: ENSMUST00000209035
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4833420G17Rik A G 13: 119,617,563 (GRCm39) N562S probably benign Het
Abi1 A G 2: 22,843,479 (GRCm39) V316A probably benign Het
Acsm1 A T 7: 119,232,403 (GRCm39) Q100L possibly damaging Het
Akr1c21 T C 13: 4,627,457 (GRCm39) Y184H possibly damaging Het
Anks3 T C 16: 4,775,891 (GRCm39) T104A probably damaging Het
Bcl2l2 A G 14: 55,122,224 (GRCm39) Y129C probably damaging Het
Cenpf T A 1: 189,391,207 (GRCm39) K875I probably damaging Het
Cntnap1 T C 11: 101,067,127 (GRCm39) V15A probably benign Het
Dnaaf9 A T 2: 130,633,915 (GRCm39) probably null Het
Elmo3 C A 8: 106,033,013 (GRCm39) R66S probably damaging Het
Elp1 A G 4: 56,779,717 (GRCm39) S565P probably benign Het
Epn1 C A 7: 5,098,684 (GRCm39) A370E probably benign Het
Esrrg T C 1: 187,730,184 (GRCm39) probably benign Het
Fgd5 T G 6: 92,042,145 (GRCm39) L1034R probably damaging Het
Fpgs A G 2: 32,573,135 (GRCm39) V567A possibly damaging Het
Fut2 C T 7: 45,300,193 (GRCm39) G193E possibly damaging Het
H3c3 T C 13: 23,929,425 (GRCm39) K19R possibly damaging Het
Hsd17b14 T C 7: 45,205,503 (GRCm39) F38S possibly damaging Het
Larp1 T C 11: 57,941,703 (GRCm39) V712A possibly damaging Het
Mep1b T C 18: 21,221,617 (GRCm39) F189S probably damaging Het
Mill1 T C 7: 17,989,832 (GRCm39) V38A probably benign Het
Niban2 C T 2: 32,766,398 (GRCm39) R13W possibly damaging Het
Npy4r T C 14: 33,868,290 (GRCm39) I333V probably benign Het
Numa1 G T 7: 101,649,874 (GRCm39) E1202* probably null Het
Or3a1b C T 11: 74,012,610 (GRCm39) A165V probably benign Het
Or6k6 A G 1: 173,945,276 (GRCm39) I102T probably benign Het
Oxr1 A T 15: 41,683,645 (GRCm39) Q356L possibly damaging Het
Prdx2 T C 8: 85,698,198 (GRCm39) F130L probably damaging Het
Rasa1 A T 13: 85,404,515 (GRCm39) S248R possibly damaging Het
Rgs19 A G 2: 181,333,114 (GRCm39) S49P probably benign Het
Serpinb11 T C 1: 107,307,654 (GRCm39) F362L probably damaging Het
Slamf8 T C 1: 172,411,736 (GRCm39) H253R possibly damaging Het
Tet3 C A 6: 83,353,769 (GRCm39) R829L probably damaging Het
Trappc8 A G 18: 20,996,652 (GRCm39) L420P probably damaging Het
Ube2u A T 4: 100,407,199 (GRCm39) *353Y probably null Het
Wbp1l A C 19: 46,632,838 (GRCm39) D46A probably damaging Het
Zbtb21 A G 16: 97,752,945 (GRCm39) V474A probably damaging Het
Other mutations in Rinl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02370:Rinl APN 7 28,494,397 (GRCm39) splice site probably null
IGL03345:Rinl APN 7 28,496,222 (GRCm39) missense possibly damaging 0.55
R1453:Rinl UTSW 7 28,496,329 (GRCm39) missense probably damaging 1.00
R1648:Rinl UTSW 7 28,497,057 (GRCm39) missense probably damaging 1.00
R1722:Rinl UTSW 7 28,491,669 (GRCm39) missense probably damaging 1.00
R2127:Rinl UTSW 7 28,496,168 (GRCm39) missense probably damaging 1.00
R2290:Rinl UTSW 7 28,491,696 (GRCm39) missense probably benign 0.00
R2472:Rinl UTSW 7 28,489,803 (GRCm39) missense possibly damaging 0.83
R2883:Rinl UTSW 7 28,497,083 (GRCm39) frame shift probably null
R4062:Rinl UTSW 7 28,490,140 (GRCm39) missense probably benign
R6180:Rinl UTSW 7 28,496,365 (GRCm39) missense probably benign 0.02
R7080:Rinl UTSW 7 28,496,101 (GRCm39) missense probably damaging 0.99
R8112:Rinl UTSW 7 28,490,014 (GRCm39) critical splice acceptor site probably null
R8893:Rinl UTSW 7 28,491,747 (GRCm39) missense probably damaging 1.00
R9145:Rinl UTSW 7 28,495,089 (GRCm39) missense
R9168:Rinl UTSW 7 28,490,084 (GRCm39) missense possibly damaging 0.82
RF044:Rinl UTSW 7 28,496,988 (GRCm39) missense probably damaging 1.00
X0023:Rinl UTSW 7 28,489,830 (GRCm39) missense probably benign
X0066:Rinl UTSW 7 28,491,768 (GRCm39) splice site probably null
Posted On 2016-08-02