Incidental Mutation 'R8111:Lrba'
ID 630855
Institutional Source Beutler Lab
Gene Symbol Lrba
Ensembl Gene ENSMUSG00000028080
Gene Name LPS-responsive beige-like anchor
Synonyms Lba, D3Ertd775e
MMRRC Submission 067540-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8111 (G1)
Quality Score 225.009
Status Not validated
Chromosome 3
Chromosomal Location 86131987-86689999 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 86235012 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 852 (N852K)
Ref Sequence ENSEMBL: ENSMUSP00000103261 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000107635] [ENSMUST00000192145] [ENSMUST00000194759] [ENSMUST00000212390]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000107635
AA Change: N852K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000103261
Gene: ENSMUSG00000028080
AA Change: N852K

DomainStartEndE-ValueType
low complexity region 12 31 N/A INTRINSIC
Pfam:Laminin_G_3 211 377 4.6e-13 PFAM
Pfam:DUF4704 446 717 2.5e-109 PFAM
coiled coil region 1019 1037 N/A INTRINSIC
low complexity region 1073 1089 N/A INTRINSIC
low complexity region 1100 1113 N/A INTRINSIC
low complexity region 1585 1600 N/A INTRINSIC
low complexity region 1614 1630 N/A INTRINSIC
low complexity region 1698 1713 N/A INTRINSIC
low complexity region 1738 1757 N/A INTRINSIC
low complexity region 1848 1861 N/A INTRINSIC
Pfam:DUF1088 1882 2049 7e-88 PFAM
Pfam:PH_BEACH 2075 2172 9.1e-31 PFAM
Beach 2203 2480 2.87e-207 SMART
WD40 2578 2615 7.4e0 SMART
WD40 2618 2661 1.72e0 SMART
WD40 2677 2716 3.99e-1 SMART
WD40 2760 2798 1.79e-1 SMART
WD40 2801 2840 4.28e0 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000192145
AA Change: N852K

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000142179
Gene: ENSMUSG00000028080
AA Change: N852K

DomainStartEndE-ValueType
low complexity region 12 31 N/A INTRINSIC
Pfam:Laminin_G_3 205 377 7.4e-18 PFAM
coiled coil region 1019 1037 N/A INTRINSIC
low complexity region 1073 1089 N/A INTRINSIC
low complexity region 1100 1113 N/A INTRINSIC
low complexity region 1585 1600 N/A INTRINSIC
low complexity region 1614 1630 N/A INTRINSIC
low complexity region 1698 1713 N/A INTRINSIC
low complexity region 1738 1757 N/A INTRINSIC
low complexity region 1848 1861 N/A INTRINSIC
Pfam:DUF1088 1882 2050 1.5e-92 PFAM
Pfam:PH_BEACH 2068 2172 7.5e-32 PFAM
Beach 2203 2480 2.87e-207 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000194759
AA Change: N852K

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000142043
Gene: ENSMUSG00000028080
AA Change: N852K

DomainStartEndE-ValueType
low complexity region 12 31 N/A INTRINSIC
Pfam:Laminin_G_3 205 377 8.1e-18 PFAM
coiled coil region 1019 1037 N/A INTRINSIC
low complexity region 1073 1089 N/A INTRINSIC
low complexity region 1100 1113 N/A INTRINSIC
low complexity region 1585 1600 N/A INTRINSIC
low complexity region 1614 1630 N/A INTRINSIC
low complexity region 1698 1713 N/A INTRINSIC
low complexity region 1738 1757 N/A INTRINSIC
low complexity region 1848 1861 N/A INTRINSIC
Pfam:DUF1088 1882 2050 1.6e-92 PFAM
Pfam:PH_BEACH 2068 2172 8.3e-32 PFAM
Beach 2203 2480 2.87e-207 SMART
WD40 2578 2615 7.4e0 SMART
WD40 2618 2661 1.72e0 SMART
WD40 2677 2716 3.99e-1 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000212390
AA Change: N852K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.7%
  • 20x: 93.2%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the WDL-BEACH-WD (WBW) gene family. Its expression is induced in B cells and macrophages by bacterial lipopolysaccharides (LPS). The encoded protein associates with protein kinase A and may be involved in leading intracellular vesicles to activated receptor complexes, which aids in the secretion and/or membrane deposition of immune effector molecules. Defects in this gene are associated with the disorder common variable immunodeficiency-8 with autoimmunity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased numbers of myeloid-derived suppressor cells and regulatory T cells, abnormal NK cell physiology, impaired rejection of allogeneic, xenogeneic and missing self bone-marrow grafts, and resistance to acute graft vs host disease. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3425401B19Rik C T 14: 32,382,266 (GRCm39) W1233* probably null Het
4930590J08Rik A G 6: 91,894,691 (GRCm39) I247V probably benign Het
8030423J24Rik T A 13: 71,032,077 (GRCm39) C50S unknown Het
Adam29 T G 8: 56,324,585 (GRCm39) H623P probably benign Het
Adamts5 A G 16: 85,696,203 (GRCm39) V318A probably damaging Het
Ano3 T C 2: 110,614,058 (GRCm39) D215G possibly damaging Het
Ap3b2 A G 7: 81,113,530 (GRCm39) I893T unknown Het
Apob G A 12: 8,058,801 (GRCm39) A2428T probably benign Het
Armc3 T C 2: 19,301,674 (GRCm39) V660A probably benign Het
Atf7 G T 15: 102,471,769 (GRCm39) T42K probably damaging Het
Atg9a A T 1: 75,164,366 (GRCm39) I160N probably damaging Het
Atp2b1 T C 10: 98,832,786 (GRCm39) V429A possibly damaging Het
Bpifb3 A C 2: 153,764,609 (GRCm39) H167P probably benign Het
Cacna1f G T X: 7,487,326 (GRCm39) E921D probably damaging Het
Ccdc57 T A 11: 120,769,713 (GRCm39) L713F probably damaging Het
Chd1l C T 3: 97,494,526 (GRCm39) E385K possibly damaging Het
Csmd1 C T 8: 15,967,306 (GRCm39) V3186I probably benign Het
Dclre1c T A 2: 3,448,185 (GRCm39) D349E probably benign Het
Dlg1 C T 16: 31,661,620 (GRCm39) T657M possibly damaging Het
Dync2h1 T C 9: 7,148,688 (GRCm39) I919V probably benign Het
Dync2i2 C A 2: 29,921,859 (GRCm39) A501S possibly damaging Het
Eml5 A G 12: 98,758,773 (GRCm39) probably null Het
Epas1 C A 17: 87,125,860 (GRCm39) S286* probably null Het
Fat1 G A 8: 45,479,095 (GRCm39) V2714I possibly damaging Het
Fuca2 T C 10: 13,390,545 (GRCm39) M447T probably benign Het
Gm10800 CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA CAAGAAAACTGAAAATCA 2: 98,497,361 (GRCm39) probably null Het
Gm11110 A C 17: 57,410,427 (GRCm39) C24G probably null Het
Gm6176 T A 7: 21,750,593 (GRCm39) I113F probably benign Het
Gmcl1 G T 6: 86,698,408 (GRCm39) A163E probably damaging Het
Gpat2 G T 2: 127,275,777 (GRCm39) L518F probably damaging Het
Gpr137b T C 13: 13,533,991 (GRCm39) Y355C Het
Hgsnat C T 8: 26,458,440 (GRCm39) V195I probably benign Het
Hivep3 T A 4: 119,955,583 (GRCm39) S1300T probably damaging Het
Hs3st2 A T 7: 120,992,362 (GRCm39) H137L probably damaging Het
Iffo1 T C 6: 125,122,781 (GRCm39) S188P possibly damaging Het
Itih1 T C 14: 30,654,225 (GRCm39) D684G probably damaging Het
Lrriq4 T C 3: 30,709,930 (GRCm39) S425P possibly damaging Het
Mdn1 T A 4: 32,674,003 (GRCm39) S562T possibly damaging Het
Mex3a T C 3: 88,444,064 (GRCm39) V380A probably benign Het
Mgat4d A T 8: 84,094,776 (GRCm39) N271I probably damaging Het
Mmp24 T A 2: 155,649,345 (GRCm39) V254E possibly damaging Het
Muc16 T A 9: 18,503,925 (GRCm39) R6455S possibly damaging Het
Npffr1 T A 10: 61,459,128 (GRCm39) V127E probably damaging Het
Obox5 T A 7: 15,492,541 (GRCm39) N165K probably damaging Het
Or10g3b G A 14: 52,587,344 (GRCm39) T53M possibly damaging Het
Otulin A C 15: 27,606,381 (GRCm39) V344G probably damaging Het
Pappa A G 4: 65,180,229 (GRCm39) D1030G probably damaging Het
Pdzd2 G A 15: 12,373,592 (GRCm39) S2181L probably benign Het
Ppp2r3c C A 12: 55,344,634 (GRCm39) M111I probably benign Het
Prss37 T C 6: 40,494,747 (GRCm39) T13A probably benign Het
Sfi1 TCGC TC 11: 3,096,254 (GRCm39) probably null Het
Sgo2b T A 8: 64,396,138 (GRCm39) K39N probably damaging Het
Sike1 T C 3: 102,909,123 (GRCm39) *208Q probably null Het
Spire1 A G 18: 67,652,391 (GRCm39) S229P probably damaging Het
Tmem132b A G 5: 125,699,857 (GRCm39) I132V probably benign Het
Umodl1 T C 17: 31,190,792 (GRCm39) V213A probably damaging Het
Washc1 C G 17: 66,423,033 (GRCm39) Q116E probably benign Het
Zfp553 T A 7: 126,836,093 (GRCm39) C549* probably null Het
Zfp9 G A 6: 118,441,561 (GRCm39) P367L probably damaging Het
Other mutations in Lrba
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00420:Lrba APN 3 86,267,089 (GRCm39) missense probably benign 0.00
IGL00788:Lrba APN 3 86,234,992 (GRCm39) missense probably damaging 0.97
IGL01139:Lrba APN 3 86,549,969 (GRCm39) missense possibly damaging 0.88
IGL01302:Lrba APN 3 86,202,707 (GRCm39) missense probably damaging 1.00
IGL01612:Lrba APN 3 86,683,484 (GRCm39) missense possibly damaging 0.89
IGL01718:Lrba APN 3 86,258,555 (GRCm39) missense probably damaging 1.00
IGL01719:Lrba APN 3 86,234,903 (GRCm39) splice site probably benign
IGL01730:Lrba APN 3 86,648,731 (GRCm39) missense possibly damaging 0.89
IGL01735:Lrba APN 3 86,234,968 (GRCm39) missense probably benign 0.28
IGL01875:Lrba APN 3 86,217,354 (GRCm39) missense probably damaging 1.00
IGL01884:Lrba APN 3 86,217,719 (GRCm39) missense possibly damaging 0.86
IGL02264:Lrba APN 3 86,687,569 (GRCm39) missense probably damaging 0.99
IGL02638:Lrba APN 3 86,232,380 (GRCm39) missense probably damaging 0.97
IGL02647:Lrba APN 3 86,267,038 (GRCm39) missense probably benign 0.00
IGL02664:Lrba APN 3 86,233,038 (GRCm39) missense possibly damaging 0.84
IGL02728:Lrba APN 3 86,683,356 (GRCm39) missense probably damaging 0.99
IGL02730:Lrba APN 3 86,235,506 (GRCm39) missense probably damaging 1.00
IGL02883:Lrba APN 3 86,352,720 (GRCm39) missense probably damaging 0.99
IGL02883:Lrba APN 3 86,261,513 (GRCm39) missense probably damaging 1.00
IGL02948:Lrba APN 3 86,217,691 (GRCm39) splice site probably null
IGL03090:Lrba APN 3 86,680,448 (GRCm39) missense probably benign 0.01
molasses UTSW 3 86,261,614 (GRCm39) critical splice donor site probably null
oscar UTSW 3 86,257,611 (GRCm39) nonsense probably null
oscar2 UTSW 3 86,571,765 (GRCm39) nonsense probably null
P0023:Lrba UTSW 3 86,325,242 (GRCm39) missense probably damaging 1.00
PIT4802001:Lrba UTSW 3 86,571,801 (GRCm39) nonsense probably null
R0077:Lrba UTSW 3 86,449,995 (GRCm39) missense probably damaging 0.99
R0189:Lrba UTSW 3 86,275,816 (GRCm39) missense probably damaging 1.00
R0217:Lrba UTSW 3 86,550,029 (GRCm39) missense probably damaging 1.00
R0349:Lrba UTSW 3 86,447,312 (GRCm39) missense probably damaging 1.00
R0396:Lrba UTSW 3 86,202,486 (GRCm39) missense probably damaging 1.00
R0417:Lrba UTSW 3 86,622,961 (GRCm39) missense probably damaging 1.00
R0536:Lrba UTSW 3 86,622,839 (GRCm39) missense probably damaging 1.00
R0712:Lrba UTSW 3 86,205,297 (GRCm39) nonsense probably null
R0722:Lrba UTSW 3 86,513,296 (GRCm39) critical splice donor site probably null
R0828:Lrba UTSW 3 86,515,677 (GRCm39) splice site probably null
R0927:Lrba UTSW 3 86,687,540 (GRCm39) missense probably damaging 1.00
R1120:Lrba UTSW 3 86,202,499 (GRCm39) missense probably damaging 1.00
R1141:Lrba UTSW 3 86,526,865 (GRCm39) missense probably damaging 1.00
R1276:Lrba UTSW 3 86,571,833 (GRCm39) missense probably damaging 1.00
R1449:Lrba UTSW 3 86,261,585 (GRCm39) missense probably damaging 1.00
R1470:Lrba UTSW 3 86,644,449 (GRCm39) missense probably damaging 1.00
R1470:Lrba UTSW 3 86,644,449 (GRCm39) missense probably damaging 1.00
R1474:Lrba UTSW 3 86,687,573 (GRCm39) splice site probably benign
R1558:Lrba UTSW 3 86,258,622 (GRCm39) missense probably damaging 1.00
R1596:Lrba UTSW 3 86,257,611 (GRCm39) nonsense probably null
R1652:Lrba UTSW 3 86,447,245 (GRCm39) missense probably damaging 1.00
R1800:Lrba UTSW 3 86,259,175 (GRCm39) missense probably benign 0.00
R1819:Lrba UTSW 3 86,449,941 (GRCm39) missense possibly damaging 0.80
R1862:Lrba UTSW 3 86,680,510 (GRCm39) critical splice donor site probably null
R1917:Lrba UTSW 3 86,571,808 (GRCm39) missense probably damaging 1.00
R1965:Lrba UTSW 3 86,513,175 (GRCm39) critical splice acceptor site probably null
R1966:Lrba UTSW 3 86,513,175 (GRCm39) critical splice acceptor site probably null
R1969:Lrba UTSW 3 86,515,696 (GRCm39) missense probably damaging 0.99
R2011:Lrba UTSW 3 86,217,324 (GRCm39) missense probably damaging 0.99
R2179:Lrba UTSW 3 86,261,588 (GRCm39) missense probably damaging 1.00
R2186:Lrba UTSW 3 86,211,643 (GRCm39) missense probably damaging 1.00
R2281:Lrba UTSW 3 86,683,410 (GRCm39) missense possibly damaging 0.46
R2359:Lrba UTSW 3 86,256,057 (GRCm39) missense probably benign 0.01
R2412:Lrba UTSW 3 86,235,007 (GRCm39) missense probably damaging 1.00
R2496:Lrba UTSW 3 86,439,394 (GRCm39) missense probably damaging 1.00
R3153:Lrba UTSW 3 86,192,526 (GRCm39) missense probably damaging 0.99
R3708:Lrba UTSW 3 86,192,331 (GRCm39) missense possibly damaging 0.80
R3746:Lrba UTSW 3 86,283,260 (GRCm39) missense probably damaging 1.00
R3747:Lrba UTSW 3 86,283,260 (GRCm39) missense probably damaging 1.00
R3748:Lrba UTSW 3 86,283,260 (GRCm39) missense probably damaging 1.00
R3749:Lrba UTSW 3 86,283,260 (GRCm39) missense probably damaging 1.00
R3750:Lrba UTSW 3 86,283,260 (GRCm39) missense probably damaging 1.00
R3758:Lrba UTSW 3 86,683,356 (GRCm39) missense probably damaging 0.99
R3975:Lrba UTSW 3 86,258,562 (GRCm39) missense probably damaging 1.00
R4210:Lrba UTSW 3 86,267,433 (GRCm39) missense probably damaging 1.00
R4258:Lrba UTSW 3 86,352,656 (GRCm39) missense probably damaging 1.00
R4657:Lrba UTSW 3 86,644,471 (GRCm39) missense probably damaging 1.00
R4713:Lrba UTSW 3 86,267,175 (GRCm39) missense probably benign 0.13
R4716:Lrba UTSW 3 86,550,021 (GRCm39) missense probably damaging 0.99
R4811:Lrba UTSW 3 86,683,448 (GRCm39) missense probably damaging 1.00
R4827:Lrba UTSW 3 86,267,457 (GRCm39) missense possibly damaging 0.85
R4840:Lrba UTSW 3 86,526,816 (GRCm39) critical splice acceptor site probably null
R4920:Lrba UTSW 3 86,571,765 (GRCm39) nonsense probably null
R4948:Lrba UTSW 3 86,192,335 (GRCm39) missense probably damaging 1.00
R4970:Lrba UTSW 3 86,132,678 (GRCm39) missense probably benign 0.23
R4985:Lrba UTSW 3 86,234,743 (GRCm39) splice site probably null
R4993:Lrba UTSW 3 86,267,344 (GRCm39) missense probably damaging 1.00
R5107:Lrba UTSW 3 86,267,086 (GRCm39) missense possibly damaging 0.47
R5112:Lrba UTSW 3 86,132,678 (GRCm39) missense probably benign 0.23
R5122:Lrba UTSW 3 86,256,461 (GRCm39) nonsense probably null
R5155:Lrba UTSW 3 86,258,607 (GRCm39) missense probably benign 0.25
R5194:Lrba UTSW 3 86,235,526 (GRCm39) missense probably damaging 1.00
R5280:Lrba UTSW 3 86,232,329 (GRCm39) missense possibly damaging 0.94
R5445:Lrba UTSW 3 86,275,902 (GRCm39) missense probably benign
R5469:Lrba UTSW 3 86,449,948 (GRCm39) missense probably damaging 1.00
R5513:Lrba UTSW 3 86,449,948 (GRCm39) missense probably damaging 1.00
R5578:Lrba UTSW 3 86,664,814 (GRCm39) missense probably benign 0.27
R5740:Lrba UTSW 3 86,235,649 (GRCm39) missense probably damaging 1.00
R5868:Lrba UTSW 3 86,226,911 (GRCm39) missense probably damaging 1.00
R6104:Lrba UTSW 3 86,261,099 (GRCm39) missense probably damaging 1.00
R6166:Lrba UTSW 3 86,261,614 (GRCm39) critical splice donor site probably null
R6279:Lrba UTSW 3 86,256,171 (GRCm39) missense probably benign 0.26
R6330:Lrba UTSW 3 86,255,664 (GRCm39) missense probably benign 0.07
R6367:Lrba UTSW 3 86,275,869 (GRCm39) missense probably benign 0.42
R6571:Lrba UTSW 3 86,267,367 (GRCm39) missense probably damaging 1.00
R6584:Lrba UTSW 3 86,571,883 (GRCm39) missense probably damaging 1.00
R6698:Lrba UTSW 3 86,211,732 (GRCm39) missense probably damaging 0.99
R6763:Lrba UTSW 3 86,261,570 (GRCm39) missense probably damaging 1.00
R6834:Lrba UTSW 3 86,257,593 (GRCm39) missense probably benign 0.00
R6951:Lrba UTSW 3 86,653,180 (GRCm39) missense probably benign 0.01
R6969:Lrba UTSW 3 86,526,897 (GRCm39) missense probably benign 0.21
R7045:Lrba UTSW 3 86,192,398 (GRCm39) missense probably benign 0.03
R7133:Lrba UTSW 3 86,302,238 (GRCm39) splice site probably null
R7182:Lrba UTSW 3 86,648,765 (GRCm39) frame shift probably null
R7214:Lrba UTSW 3 86,235,633 (GRCm39) missense probably damaging 1.00
R7224:Lrba UTSW 3 86,302,553 (GRCm39) missense probably damaging 1.00
R7243:Lrba UTSW 3 86,658,823 (GRCm39) splice site probably null
R7350:Lrba UTSW 3 86,259,209 (GRCm39) missense probably damaging 0.96
R7380:Lrba UTSW 3 86,232,381 (GRCm39) missense probably damaging 1.00
R7492:Lrba UTSW 3 86,571,835 (GRCm39) missense probably damaging 1.00
R7651:Lrba UTSW 3 86,648,773 (GRCm39) nonsense probably null
R7729:Lrba UTSW 3 86,225,474 (GRCm39) missense probably damaging 1.00
R7754:Lrba UTSW 3 86,352,704 (GRCm39) missense probably damaging 1.00
R7762:Lrba UTSW 3 86,439,508 (GRCm39) missense probably damaging 0.99
R7855:Lrba UTSW 3 86,222,737 (GRCm39) missense possibly damaging 0.94
R7867:Lrba UTSW 3 86,275,896 (GRCm39) missense probably damaging 1.00
R7912:Lrba UTSW 3 86,622,872 (GRCm39) missense probably damaging 1.00
R7995:Lrba UTSW 3 86,526,858 (GRCm39) missense probably damaging 1.00
R8013:Lrba UTSW 3 86,325,278 (GRCm39) missense probably damaging 1.00
R8014:Lrba UTSW 3 86,325,278 (GRCm39) missense probably damaging 1.00
R8024:Lrba UTSW 3 86,202,708 (GRCm39) nonsense probably null
R8027:Lrba UTSW 3 86,325,219 (GRCm39) missense probably benign 0.05
R8090:Lrba UTSW 3 86,255,796 (GRCm39) missense probably benign
R8118:Lrba UTSW 3 86,261,533 (GRCm39) missense probably benign
R8204:Lrba UTSW 3 86,222,710 (GRCm39) missense possibly damaging 0.95
R8239:Lrba UTSW 3 86,449,882 (GRCm39) missense probably damaging 1.00
R8509:Lrba UTSW 3 86,255,483 (GRCm39) missense probably benign 0.04
R8532:Lrba UTSW 3 86,664,790 (GRCm39) missense probably damaging 1.00
R8726:Lrba UTSW 3 86,261,062 (GRCm39) missense probably benign
R8744:Lrba UTSW 3 86,211,640 (GRCm39) missense probably benign 0.08
R8782:Lrba UTSW 3 86,549,976 (GRCm39) missense probably benign 0.00
R8784:Lrba UTSW 3 86,283,235 (GRCm39) missense probably damaging 1.00
R8922:Lrba UTSW 3 86,263,973 (GRCm39) missense probably damaging 1.00
R8964:Lrba UTSW 3 86,258,552 (GRCm39) missense probably benign 0.22
R8971:Lrba UTSW 3 86,522,388 (GRCm39) missense probably benign 0.00
R9046:Lrba UTSW 3 86,302,543 (GRCm39) missense possibly damaging 0.94
R9155:Lrba UTSW 3 86,202,508 (GRCm39) missense probably damaging 1.00
R9236:Lrba UTSW 3 86,261,066 (GRCm39) missense probably benign 0.05
R9266:Lrba UTSW 3 86,198,774 (GRCm39) missense probably benign 0.08
R9297:Lrba UTSW 3 86,280,873 (GRCm39) missense probably damaging 1.00
R9404:Lrba UTSW 3 86,205,224 (GRCm39) missense probably damaging 0.99
R9617:Lrba UTSW 3 86,267,169 (GRCm39) missense probably benign
R9640:Lrba UTSW 3 86,526,875 (GRCm39) nonsense probably null
R9779:Lrba UTSW 3 86,233,078 (GRCm39) missense probably damaging 1.00
X0065:Lrba UTSW 3 86,232,396 (GRCm39) missense possibly damaging 0.95
X0065:Lrba UTSW 3 86,205,206 (GRCm39) missense probably damaging 1.00
Z1176:Lrba UTSW 3 86,658,839 (GRCm39) missense possibly damaging 0.85
Z1176:Lrba UTSW 3 86,622,845 (GRCm39) missense probably benign 0.31
Z1177:Lrba UTSW 3 86,447,356 (GRCm39) missense probably null 1.00
Predicted Primers PCR Primer
(F):5'- AGCATGTTTCCCCAAGTTTTACAAG -3'
(R):5'- CTGGACCCAAGCCATAGTTATC -3'

Sequencing Primer
(F):5'- CCCCAAGTTTTACAAGATGTTTTTAG -3'
(R):5'- TCCTCACACTTATAAAGAGGA -3'
Posted On 2020-06-30