Incidental Mutation 'R7622:Lrrc52'
ID589173
Institutional Source Beutler Lab
Gene Symbol Lrrc52
Ensembl Gene ENSMUSG00000040485
Gene Nameleucine rich repeat containing 52
Synonyms4930413P14Rik
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.083) question?
Stock #R7622 (G1)
Quality Score225.009
Status Not validated
Chromosome1
Chromosomal Location167445669-167466780 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 167466095 bp
ZygosityHeterozygous
Amino Acid Change Proline to Glutamine at position 207 (P207Q)
Ref Sequence ENSEMBL: ENSMUSP00000047213 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000036643]
Predicted Effect probably benign
Transcript: ENSMUST00000036643
AA Change: P207Q

PolyPhen 2 Score 0.160 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000047213
Gene: ENSMUSG00000040485
AA Change: P207Q

DomainStartEndE-ValueType
LRRNT 25 57 4.21e-3 SMART
LRR 56 73 2.03e2 SMART
LRR 76 99 3.09e1 SMART
LRR 100 123 1.37e1 SMART
LRR 124 148 5.89e1 SMART
LRR 149 172 1.06e2 SMART
Blast:LRRCT 184 237 3e-26 BLAST
transmembrane domain 246 268 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
MGI Phenotype PHENOTYPE: Male mice homozygous for a null allele display reduced fertility with impaired fertilization. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932438A13Rik C A 3: 36,948,413 C1502* probably null Het
Adgrd1 G A 5: 129,139,624 D384N probably benign Het
Aqp8 T C 7: 123,466,660 F226S possibly damaging Het
Arl6ip6 A G 2: 53,217,327 Y207C probably damaging Het
Cbfa2t2 A G 2: 154,500,445 E27G possibly damaging Het
Cdc42bpb T G 12: 111,294,772 E201A unknown Het
Cfap54 A C 10: 92,956,944 V1769G unknown Het
Dmxl2 C T 9: 54,472,218 G7S probably damaging Het
Dnah6 G T 6: 73,124,759 F1927L possibly damaging Het
Dnajc6 A G 4: 101,640,491 E942G probably damaging Het
Fam170a A G 18: 50,282,902 R324G probably benign Het
Gapdhs G A 7: 30,739,331 T9I unknown Het
Gm10320 T A 13: 98,489,724 R51* probably null Het
Gm19410 A T 8: 35,810,347 T1776S possibly damaging Het
Gm4846 A T 1: 166,495,872 M94K possibly damaging Het
Ighv2-5 G A 12: 113,685,738 Q32* probably null Het
Klc2 T C 19: 5,111,632 E310G probably damaging Het
Krt75 A G 15: 101,570,272 M309T probably damaging Het
Lrp11 G A 10: 7,590,172 G41R unknown Het
Lrrk2 A T 15: 91,812,323 D2438V probably damaging Het
Mycbp C T 4: 123,905,301 T28M probably damaging Het
Myh14 A G 7: 44,632,422 V804A probably benign Het
Myo16 A G 8: 10,376,238 I332V unknown Het
Ncor1 G T 11: 62,317,968 Q1359K probably benign Het
Olfr1055 A G 2: 86,347,662 Y35H possibly damaging Het
Olfr1112 A T 2: 87,192,250 I188L probably benign Het
Olfr50 A G 2: 36,793,931 K232E probably benign Het
Olfr548-ps1 A G 7: 102,542,623 H229R probably benign Het
Oog3 T C 4: 144,158,319 D349G probably benign Het
Pate4 A G 9: 35,608,299 S32P possibly damaging Het
Pcdhb7 A C 18: 37,342,461 S217R probably benign Het
Pde1c G A 6: 56,126,925 R580C probably damaging Het
Pi4ka C A 16: 17,293,977 A1545S Het
Pign G T 1: 105,648,117 T266K possibly damaging Het
Pitpnm2 A G 5: 124,122,027 I1134T probably benign Het
Ppfia2 G A 10: 106,830,659 V409I possibly damaging Het
Prr7 A G 13: 55,472,796 T206A probably benign Het
Rnf13 A T 3: 57,820,534 R212* probably null Het
Rwdd2b T C 16: 87,434,612 N218S probably benign Het
Serpina3m A G 12: 104,389,575 D167G possibly damaging Het
Slit2 A T 5: 47,985,205 N56Y probably damaging Het
Sprr3 G T 3: 92,457,285 T84K probably damaging Het
Stab2 A T 10: 86,873,902 H1626Q possibly damaging Het
Tex2 C A 11: 106,546,895 D650Y unknown Het
Tmprss6 A G 15: 78,446,726 S436P probably benign Het
Uba2 A C 7: 34,165,435 F63L probably damaging Het
Ubxn2b C T 4: 6,214,692 S242L probably damaging Het
Vmn1r86 T G 7: 13,102,758 I64L probably benign Het
Vmn2r67 A T 7: 85,136,454 V781E probably damaging Het
Vmn2r80 T A 10: 79,194,263 F641Y probably damaging Het
Wdfy4 A T 14: 33,078,274 I1965K Het
Wdr25 G A 12: 108,992,893 G344S possibly damaging Het
Wdr90 G T 17: 25,854,109 F837L probably benign Het
Xpo4 A G 14: 57,597,011 V704A possibly damaging Het
Zc3h12d A G 10: 7,867,269 K268E probably damaging Het
Other mutations in Lrrc52
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02126:Lrrc52 APN 1 167446006 missense probably damaging 1.00
IGL02232:Lrrc52 APN 1 167466380 missense probably damaging 0.99
R2030:Lrrc52 UTSW 1 167466459 missense probably benign 0.07
R2252:Lrrc52 UTSW 1 167466368 missense probably damaging 1.00
R4695:Lrrc52 UTSW 1 167466091 critical splice donor site probably null
R6155:Lrrc52 UTSW 1 167466727 start gained probably benign
R6248:Lrrc52 UTSW 1 167466395 missense probably damaging 1.00
R6661:Lrrc52 UTSW 1 167466353 missense probably damaging 1.00
R7135:Lrrc52 UTSW 1 167466450 missense probably damaging 1.00
R7622:Lrrc52 UTSW 1 167466096 missense probably benign 0.08
R8063:Lrrc52 UTSW 1 167466521 missense probably damaging 0.98
Z1088:Lrrc52 UTSW 1 167466494 missense possibly damaging 0.52
Predicted Primers PCR Primer
(F):5'- TTTCTAAAGGCACAGGAGTGG -3'
(R):5'- TTGAGGTACCTGGACCTCAG -3'

Sequencing Primer
(F):5'- TGACATGTTTGAGTTCTGAATTCTC -3'
(R):5'- TGGACCTCAGAAACACCGGATTG -3'
Posted On2019-10-24