Incidental Mutation 'IGL01448:Stra6l'
ID 84542
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Stra6l
Ensembl Gene ENSMUSG00000028327
Gene Name STRA6-like
Synonyms 1300002K09Rik, Rbpr2
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01448
Quality Score
Status
Chromosome 4
Chromosomal Location 45848664-45887008 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 45864864 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000103412 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000030011] [ENSMUST00000030011] [ENSMUST00000107782] [ENSMUST00000107783]
AlphaFold Q9DBN1
Predicted Effect probably null
Transcript: ENSMUST00000030011
SMART Domains Protein: ENSMUSP00000030011
Gene: ENSMUSG00000028327

DomainStartEndE-ValueType
Pfam:RBP_receptor 13 602 8.7e-228 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000030011
SMART Domains Protein: ENSMUSP00000030011
Gene: ENSMUSG00000028327

DomainStartEndE-ValueType
Pfam:RBP_receptor 13 602 8.7e-228 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000107782
SMART Domains Protein: ENSMUSP00000103411
Gene: ENSMUSG00000028327

DomainStartEndE-ValueType
Pfam:RBP_receptor 1 512 2.8e-221 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000107783
SMART Domains Protein: ENSMUSP00000103412
Gene: ENSMUSG00000028327

DomainStartEndE-ValueType
Pfam:RBP_receptor 12 603 1e-254 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000128947
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700020A23Rik A T 2: 130,247,767 (GRCm39) E75D possibly damaging Het
1700084J12Rik A G 15: 33,405,779 (GRCm39) probably benign Het
2610303G11Rik T A 9: 98,068,762 (GRCm39) noncoding transcript Het
4931414P19Rik T C 14: 54,823,417 (GRCm39) D320G possibly damaging Het
Adamts6 G A 13: 104,433,672 (GRCm39) E34K probably damaging Het
Alms1 T A 6: 85,654,881 (GRCm39) N3142K possibly damaging Het
Anapc7 G A 5: 122,566,276 (GRCm39) A62T probably damaging Het
Atp8b3 G A 10: 80,356,256 (GRCm39) P1152L probably benign Het
Cc2d2a C T 5: 43,841,527 (GRCm39) T181I possibly damaging Het
Celsr2 A G 3: 108,300,555 (GRCm39) L2835P probably damaging Het
Ctns A T 11: 73,079,548 (GRCm39) V99D possibly damaging Het
Dchs1 T C 7: 105,421,134 (GRCm39) R429G probably damaging Het
Ddx11 T C 17: 66,441,132 (GRCm39) V218A probably damaging Het
Eftud2 G A 11: 102,756,389 (GRCm39) probably benign Het
Erich1 G T 8: 14,128,853 (GRCm39) T29N possibly damaging Het
Exosc8 T C 3: 54,636,686 (GRCm39) E215G probably damaging Het
Fam184a G T 10: 53,575,045 (GRCm39) A188E probably benign Het
Fign A G 2: 63,810,032 (GRCm39) S413P probably damaging Het
Fkbp6 A G 5: 135,378,550 (GRCm39) S33P probably damaging Het
Glb1 A G 9: 114,279,745 (GRCm39) probably benign Het
H2-Q1 T C 17: 35,542,437 (GRCm39) probably benign Het
Helz2 T C 2: 180,875,770 (GRCm39) T1575A probably damaging Het
Il18r1 A G 1: 40,513,890 (GRCm39) E32G probably damaging Het
Ints5 C T 19: 8,872,851 (GRCm39) P270L possibly damaging Het
Itga7 G T 10: 128,785,337 (GRCm39) E847* probably null Het
Kcns3 A C 12: 11,141,644 (GRCm39) S352A possibly damaging Het
Kiz A G 2: 146,705,721 (GRCm39) K94E probably benign Het
Lin7b C T 7: 45,018,624 (GRCm39) V12M probably damaging Het
Myo18b A T 5: 112,959,570 (GRCm39) I1409N probably damaging Het
Myo5b A G 18: 74,777,161 (GRCm39) H407R probably damaging Het
Nelfa T C 5: 34,056,146 (GRCm39) T506A probably damaging Het
Or10p21 A G 10: 128,847,729 (GRCm39) T192A probably damaging Het
Or4d5 A T 9: 40,012,378 (GRCm39) M136K probably damaging Het
Or5p72 T A 7: 108,022,235 (GRCm39) Y152* probably null Het
Or6c69 A G 10: 129,748,114 (GRCm39) I11T possibly damaging Het
Pclo A C 5: 14,726,408 (GRCm39) probably benign Het
Pes1 G A 11: 3,927,979 (GRCm39) E544K possibly damaging Het
Rabgap1l A G 1: 160,568,315 (GRCm39) probably benign Het
Rapgef2 T C 3: 78,976,244 (GRCm39) M1521V probably benign Het
Rapgef2 C T 3: 79,011,269 (GRCm39) probably null Het
Reln A G 5: 22,245,403 (GRCm39) V735A probably benign Het
Slc2a4 A G 11: 69,835,902 (GRCm39) S316P possibly damaging Het
Smarce1 C T 11: 99,101,013 (GRCm39) G373E possibly damaging Het
Spata31d1a T A 13: 59,849,373 (GRCm39) R918S probably benign Het
St3gal4 T C 9: 34,963,627 (GRCm39) K227R probably benign Het
Stxbp5l T C 16: 37,036,341 (GRCm39) I425V probably damaging Het
Tcaf2 T C 6: 42,607,262 (GRCm39) T231A probably benign Het
Tiparp G T 3: 65,460,030 (GRCm39) G442* probably null Het
Tnks A G 8: 35,307,136 (GRCm39) Y1138H probably damaging Het
Vezt T A 10: 93,832,719 (GRCm39) I231F probably damaging Het
Vmn2r4 A T 3: 64,313,816 (GRCm39) N388K probably damaging Het
Zbed3 A G 13: 95,473,142 (GRCm39) K189E possibly damaging Het
Zfp512b T C 2: 181,229,578 (GRCm39) T625A possibly damaging Het
Zfp827 A T 8: 79,787,362 (GRCm39) Q176L possibly damaging Het
Other mutations in Stra6l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02343:Stra6l APN 4 45,869,588 (GRCm39) missense probably damaging 0.99
IGL02710:Stra6l APN 4 45,882,728 (GRCm39) missense possibly damaging 0.72
IGL02880:Stra6l APN 4 45,885,278 (GRCm39) missense possibly damaging 0.70
IGL03034:Stra6l APN 4 45,885,392 (GRCm39) missense probably benign 0.41
IGL03163:Stra6l APN 4 45,881,455 (GRCm39) missense probably benign 0.03
IGL03355:Stra6l APN 4 45,873,689 (GRCm39) missense probably benign 0.16
K2124:Stra6l UTSW 4 45,870,770 (GRCm39) splice site probably benign
R0800:Stra6l UTSW 4 45,882,797 (GRCm39) missense probably benign 0.29
R1171:Stra6l UTSW 4 45,864,982 (GRCm39) missense probably benign
R1931:Stra6l UTSW 4 45,882,698 (GRCm39) nonsense probably null
R1982:Stra6l UTSW 4 45,867,237 (GRCm39) nonsense probably null
R2331:Stra6l UTSW 4 45,858,224 (GRCm39) critical splice donor site probably null
R4691:Stra6l UTSW 4 45,882,851 (GRCm39) missense probably benign 0.39
R4846:Stra6l UTSW 4 45,873,682 (GRCm39) missense possibly damaging 0.76
R5175:Stra6l UTSW 4 45,870,860 (GRCm39) missense probably benign 0.01
R5633:Stra6l UTSW 4 45,881,455 (GRCm39) missense probably benign 0.00
R6212:Stra6l UTSW 4 45,884,664 (GRCm39) missense probably benign
R6517:Stra6l UTSW 4 45,879,473 (GRCm39) missense probably benign
R6534:Stra6l UTSW 4 45,860,041 (GRCm39) splice site probably null
R6584:Stra6l UTSW 4 45,869,635 (GRCm39) splice site probably null
R7763:Stra6l UTSW 4 45,869,570 (GRCm39) nonsense probably null
R8400:Stra6l UTSW 4 45,864,905 (GRCm39) missense probably damaging 1.00
R8511:Stra6l UTSW 4 45,885,347 (GRCm39) missense probably benign 0.00
R9007:Stra6l UTSW 4 45,864,910 (GRCm39) missense possibly damaging 0.81
R9313:Stra6l UTSW 4 45,881,454 (GRCm39) missense probably benign
R9379:Stra6l UTSW 4 45,849,093 (GRCm39) missense probably benign
R9400:Stra6l UTSW 4 45,885,293 (GRCm39) missense probably damaging 1.00
R9764:Stra6l UTSW 4 45,884,602 (GRCm39) missense probably damaging 0.98
Posted On 2013-11-11