Incidental Mutation 'IGL01068:4931406B18Rik'
ID 51443
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4931406B18Rik
Ensembl Gene ENSMUSG00000013353
Gene Name RIKEN cDNA 4931406B18 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # IGL01068
Quality Score
Status
Chromosome 7
Chromosomal Location 43141468-43155364 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 43153599 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139468 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000013497] [ENSMUST00000163474] [ENSMUST00000163619] [ENSMUST00000168213] [ENSMUST00000168883] [ENSMUST00000171174] [ENSMUST00000191516]
AlphaFold A2RSL7
Predicted Effect probably benign
Transcript: ENSMUST00000013497
SMART Domains Protein: ENSMUSP00000013497
Gene: ENSMUSG00000013353

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
PDB:2ZG3|A 24 185 9e-7 PDB
Blast:IG_like 119 185 3e-19 BLAST
low complexity region 186 205 N/A INTRINSIC
SCOP:d1iray3 219 297 6e-3 SMART
transmembrane domain 311 333 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000163474
SMART Domains Protein: ENSMUSP00000126619
Gene: ENSMUSG00000013353

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Blast:IG_like 23 111 3e-12 BLAST
SCOP:d1he7a_ 111 203 1e-3 SMART
Blast:IG_like 125 194 1e-5 BLAST
transmembrane domain 217 239 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000163619
SMART Domains Protein: ENSMUSP00000131071
Gene: ENSMUSG00000013353

DomainStartEndE-ValueType
signal peptide 1 16 N/A INTRINSIC
PDB:2ZG3|A 17 88 1e-5 PDB
Blast:IG_like 22 88 2e-21 BLAST
low complexity region 89 104 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000168213
SMART Domains Protein: ENSMUSP00000129928
Gene: ENSMUSG00000013353

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Blast:IG_like 23 119 2e-13 BLAST
Predicted Effect noncoding transcript
Transcript: ENSMUST00000168636
Predicted Effect probably benign
Transcript: ENSMUST00000168883
Predicted Effect probably benign
Transcript: ENSMUST00000171174
SMART Domains Protein: ENSMUSP00000129888
Gene: ENSMUSG00000013353

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:Ig_2 113 216 5.6e-3 PFAM
Pfam:Ig_2 200 297 7.7e-3 PFAM
transmembrane domain 311 333 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000191516
SMART Domains Protein: ENSMUSP00000139468
Gene: ENSMUSG00000013353

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:Ig_2 113 216 5.6e-3 PFAM
Pfam:Ig_2 200 297 7.7e-3 PFAM
transmembrane domain 311 333 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205508
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgra1 A G 7: 139,425,541 (GRCm39) E18G probably damaging Het
Aen G A 7: 78,557,050 (GRCm39) M299I probably damaging Het
Atg16l1 C T 1: 87,702,546 (GRCm39) S269L probably damaging Het
Atp8a1 A G 5: 67,824,680 (GRCm39) V853A probably benign Het
Bicral T C 17: 47,136,317 (GRCm39) I298V probably damaging Het
Cad A G 5: 31,219,114 (GRCm39) probably benign Het
Chd9 A T 8: 91,768,744 (GRCm39) Y2448F probably benign Het
Clstn3 A G 6: 124,439,098 (GRCm39) L16S probably damaging Het
Cmtr2 G A 8: 110,949,501 (GRCm39) V604M possibly damaging Het
Ctcf A T 8: 106,408,117 (GRCm39) probably benign Het
Eif2ak2 A G 17: 79,172,800 (GRCm39) I295T probably damaging Het
Foxm1 G A 6: 128,347,930 (GRCm39) R284H possibly damaging Het
Gabra2 T C 5: 71,119,415 (GRCm39) I362M probably benign Het
Hivep1 C A 13: 42,313,460 (GRCm39) P1900Q probably benign Het
Klhl25 G T 7: 75,515,897 (GRCm39) E268* probably null Het
Klk1b16 T C 7: 43,790,102 (GRCm39) L124P probably damaging Het
Ltf A T 9: 110,864,880 (GRCm39) probably null Het
Mpped2 T A 2: 106,695,091 (GRCm39) H248Q probably damaging Het
Mrpl1 T A 5: 96,371,895 (GRCm39) probably benign Het
Mthfd1l T A 10: 3,978,428 (GRCm39) S429R probably damaging Het
Myl2 G A 5: 122,244,767 (GRCm39) V146I probably benign Het
Myo10 T A 15: 25,739,395 (GRCm39) I527N possibly damaging Het
Ncoa3 T C 2: 165,894,715 (GRCm39) S333P probably damaging Het
Or1j4 T G 2: 36,740,282 (GRCm39) S75A probably damaging Het
Or4k47 T G 2: 111,451,685 (GRCm39) T245P probably damaging Het
Oxct1 T C 15: 4,083,246 (GRCm39) F155S probably damaging Het
P4ha1 T C 10: 59,175,157 (GRCm39) V39A probably damaging Het
Padi6 G T 4: 140,458,264 (GRCm39) T514N possibly damaging Het
Pgm2 G A 5: 64,265,139 (GRCm39) V387I probably damaging Het
Ppt1 G A 4: 122,737,800 (GRCm39) C46Y probably damaging Het
Rnf225 T C 7: 12,662,827 (GRCm39) probably benign Het
Rpl26 T C 11: 68,793,224 (GRCm39) Y42H probably benign Het
Rundc1 A G 11: 101,324,968 (GRCm39) N558S probably damaging Het
Sema3e T G 5: 14,283,732 (GRCm39) probably null Het
Slc8a1 T C 17: 81,696,371 (GRCm39) I888V probably benign Het
Thsd7b T C 1: 129,523,883 (GRCm39) C306R probably damaging Het
Tmem209 A C 6: 30,502,085 (GRCm39) L197R probably benign Het
Tmem38b T G 4: 53,849,024 (GRCm39) V119G probably damaging Het
Trpc1 T C 9: 95,608,547 (GRCm39) D82G probably damaging Het
Zfp292 A G 4: 34,806,763 (GRCm39) F2094L probably damaging Het
Zfp638 C T 6: 83,911,976 (GRCm39) R453W probably damaging Het
Other mutations in 4931406B18Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01902:4931406B18Rik APN 7 43,147,267 (GRCm39) missense probably damaging 0.96
IGL02616:4931406B18Rik APN 7 43,150,437 (GRCm39) splice site probably null
IGL02677:4931406B18Rik APN 7 43,150,519 (GRCm39) nonsense probably null
IGL03030:4931406B18Rik APN 7 43,145,057 (GRCm39) missense possibly damaging 0.62
R0007:4931406B18Rik UTSW 7 43,147,466 (GRCm39) splice site probably benign
R0788:4931406B18Rik UTSW 7 43,148,623 (GRCm39) missense probably damaging 0.98
R1544:4931406B18Rik UTSW 7 43,147,543 (GRCm39) missense possibly damaging 0.92
R2995:4931406B18Rik UTSW 7 43,148,792 (GRCm39) missense probably damaging 1.00
R4656:4931406B18Rik UTSW 7 43,150,565 (GRCm39) missense probably benign 0.20
R5595:4931406B18Rik UTSW 7 43,147,296 (GRCm39) missense possibly damaging 0.92
R6288:4931406B18Rik UTSW 7 43,147,549 (GRCm39) missense probably damaging 1.00
R6389:4931406B18Rik UTSW 7 43,147,254 (GRCm39) missense possibly damaging 0.94
R6651:4931406B18Rik UTSW 7 43,147,496 (GRCm39) missense possibly damaging 0.81
R6912:4931406B18Rik UTSW 7 43,150,571 (GRCm39) missense possibly damaging 0.95
R7254:4931406B18Rik UTSW 7 43,147,623 (GRCm39) missense probably damaging 0.99
R7615:4931406B18Rik UTSW 7 43,147,273 (GRCm39) missense possibly damaging 0.64
R8167:4931406B18Rik UTSW 7 43,147,288 (GRCm39) missense possibly damaging 0.79
R9052:4931406B18Rik UTSW 7 43,147,631 (GRCm39) nonsense probably null
R9109:4931406B18Rik UTSW 7 43,148,702 (GRCm39) missense
R9182:4931406B18Rik UTSW 7 43,153,640 (GRCm39) missense probably damaging 0.97
R9201:4931406B18Rik UTSW 7 43,150,709 (GRCm39) missense possibly damaging 0.46
R9787:4931406B18Rik UTSW 7 43,150,695 (GRCm39) missense probably benign 0.37
Posted On 2013-06-21