Incidental Mutation 'IGL00646:Scara3'
ID 13920
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Scara3
Ensembl Gene ENSMUSG00000034463
Gene Name scavenger receptor class A, member 3
Synonyms C130058N24Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # IGL00646
Quality Score
Status
Chromosome 14
Chromosomal Location 66156843-66191384 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 66158605 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 468 (K468*)
Ref Sequence ENSEMBL: ENSMUSP00000046525 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042046]
AlphaFold Q8C850
Predicted Effect probably null
Transcript: ENSMUST00000042046
AA Change: K468*
SMART Domains Protein: ENSMUSP00000046525
Gene: ENSMUSG00000034463
AA Change: K468*

DomainStartEndE-ValueType
transmembrane domain 55 77 N/A INTRINSIC
coiled coil region 117 155 N/A INTRINSIC
low complexity region 300 311 N/A INTRINSIC
Pfam:Collagen 455 513 3.1e-12 PFAM
Pfam:Collagen 499 558 4.2e-11 PFAM
Pfam:Collagen 544 606 2.9e-12 PFAM
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a macrophage scavenger receptor-like protein. This protein has been shown to deplete reactive oxygen species, and thus play an important role in protecting cells from oxidative stress. The expression of this gene is induced by oxidative stress. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 8 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cep290 T C 10: 100,337,016 (GRCm39) V407A probably benign Het
Cyp2c39 T A 19: 39,501,935 (GRCm39) probably benign Het
Hsd17b4 T A 18: 50,297,912 (GRCm39) F400L probably benign Het
Nol11 C T 11: 107,064,286 (GRCm39) V509I probably benign Het
Pdcd11 A G 19: 47,105,767 (GRCm39) T1145A possibly damaging Het
Rsrc2 T C 5: 123,877,685 (GRCm39) probably benign Het
Sycp2 T C 2: 178,016,252 (GRCm39) I737V probably benign Het
Zfp109 T A 7: 23,928,237 (GRCm39) K399* probably null Het
Other mutations in Scara3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00229:Scara3 APN 14 66,170,570 (GRCm39) missense probably benign 0.01
IGL00718:Scara3 APN 14 66,168,876 (GRCm39) missense possibly damaging 0.67
IGL01948:Scara3 APN 14 66,168,261 (GRCm39) missense probably damaging 0.99
IGL01979:Scara3 APN 14 66,168,412 (GRCm39) missense probably benign 0.01
IGL02399:Scara3 APN 14 66,170,559 (GRCm39) nonsense probably null
IGL02939:Scara3 APN 14 66,169,105 (GRCm39) missense probably benign 0.00
IGL02945:Scara3 APN 14 66,168,660 (GRCm39) missense probably damaging 1.00
IGL03075:Scara3 APN 14 66,168,603 (GRCm39) missense probably damaging 1.00
IGL03100:Scara3 APN 14 66,168,722 (GRCm39) missense probably damaging 1.00
IGL03156:Scara3 APN 14 66,168,603 (GRCm39) missense probably damaging 1.00
IGL03179:Scara3 APN 14 66,168,603 (GRCm39) missense probably damaging 1.00
condor UTSW 14 66,168,651 (GRCm39) missense probably damaging 1.00
PIT4362001:Scara3 UTSW 14 66,173,851 (GRCm39) missense probably benign
R0062:Scara3 UTSW 14 66,168,417 (GRCm39) missense probably damaging 1.00
R0062:Scara3 UTSW 14 66,168,417 (GRCm39) missense probably damaging 1.00
R0124:Scara3 UTSW 14 66,168,670 (GRCm39) missense probably benign 0.01
R0349:Scara3 UTSW 14 66,169,230 (GRCm39) missense probably damaging 0.98
R1584:Scara3 UTSW 14 66,158,553 (GRCm39) missense probably damaging 1.00
R4785:Scara3 UTSW 14 66,190,950 (GRCm39) start codon destroyed probably null 0.06
R5336:Scara3 UTSW 14 66,168,487 (GRCm39) missense probably damaging 1.00
R6307:Scara3 UTSW 14 66,175,710 (GRCm39) missense probably benign 0.24
R6420:Scara3 UTSW 14 66,175,701 (GRCm39) missense possibly damaging 0.92
R6610:Scara3 UTSW 14 66,168,670 (GRCm39) missense probably damaging 0.97
R7159:Scara3 UTSW 14 66,158,229 (GRCm39) missense probably damaging 0.98
R7208:Scara3 UTSW 14 66,168,715 (GRCm39) missense possibly damaging 0.62
R7246:Scara3 UTSW 14 66,169,093 (GRCm39) missense probably damaging 0.97
R7315:Scara3 UTSW 14 66,168,889 (GRCm39) missense probably damaging 1.00
R7324:Scara3 UTSW 14 66,168,865 (GRCm39) missense probably benign 0.03
R7497:Scara3 UTSW 14 66,168,651 (GRCm39) missense probably damaging 1.00
R7504:Scara3 UTSW 14 66,168,780 (GRCm39) missense possibly damaging 0.82
R7554:Scara3 UTSW 14 66,158,299 (GRCm39) missense possibly damaging 0.69
R8143:Scara3 UTSW 14 66,169,269 (GRCm39) missense probably damaging 0.96
R9043:Scara3 UTSW 14 66,169,070 (GRCm39) missense probably damaging 1.00
R9226:Scara3 UTSW 14 66,169,233 (GRCm39) missense possibly damaging 0.69
R9363:Scara3 UTSW 14 66,168,720 (GRCm39) missense probably benign 0.01
R9730:Scara3 UTSW 14 66,168,261 (GRCm39) missense probably damaging 0.99
YA93:Scara3 UTSW 14 66,168,398 (GRCm39) missense probably damaging 0.98
Posted On 2012-12-06