LRRC55 (leucine rich repeat containing 55) - Rat Genome Database

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Gene: LRRC55 (leucine rich repeat containing 55) Homo sapiens
Analyze
Symbol: LRRC55
Name: leucine rich repeat containing 55
RGD ID: 1603880
HGNC Page HGNC:32324
Description: Enables potassium channel activator activity; transmembrane transporter binding activity; and voltage-gated potassium channel activity. Involved in potassium ion transmembrane transport. Part of voltage-gated potassium channel complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: BK channel auxiliary gamma subunit LRRC55; BK channel auxilliary gamma snit LRRC55; DKFZp667D0425; FLJ13339; FLJ45686; leucine-rich repeat-containing protein 55
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381157,181,953 - 57,191,717 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1157,181,747 - 57,191,717 (+)EnsemblGRCh38hg38GRCh38
GRCh371156,949,427 - 56,959,191 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361156,705,797 - 56,714,154 (+)NCBINCBI36Build 36hg18NCBI36
Celera1154,308,169 - 54,318,131 (+)NCBICelera
Cytogenetic Map11q12.1NCBI
HuRef1153,298,067 - 53,308,021 (+)NCBIHuRef
CHM1_11156,815,331 - 56,825,298 (+)NCBICHM1_1
T2T-CHM13v2.01157,131,394 - 57,141,139 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14702039   PMID:15340161   PMID:20379614   PMID:21873635   PMID:22547800   PMID:26009545   PMID:31213650   PMID:33346797   PMID:33961781   PMID:36724073  


Genomics

Comparative Map Data
LRRC55
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381157,181,953 - 57,191,717 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1157,181,747 - 57,191,717 (+)EnsemblGRCh38hg38GRCh38
GRCh371156,949,427 - 56,959,191 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361156,705,797 - 56,714,154 (+)NCBINCBI36Build 36hg18NCBI36
Celera1154,308,169 - 54,318,131 (+)NCBICelera
Cytogenetic Map11q12.1NCBI
HuRef1153,298,067 - 53,308,021 (+)NCBIHuRef
CHM1_11156,815,331 - 56,825,298 (+)NCBICHM1_1
T2T-CHM13v2.01157,131,394 - 57,141,139 (+)NCBIT2T-CHM13v2.0
Lrrc55
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39285,018,411 - 85,029,110 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl284,992,678 - 85,027,541 (-)EnsemblGRCm39 Ensembl
GRCm38285,188,067 - 85,198,750 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl285,162,334 - 85,197,197 (-)EnsemblGRCm38mm10GRCm38
MGSCv37285,028,228 - 85,036,856 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36284,963,173 - 84,997,538 (-)NCBIMGSCv36mm8
Celera286,776,703 - 86,785,331 (-)NCBICelera
Cytogenetic Map2DNCBI
cM Map249.53NCBI
Lrrc55
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8390,676,547 - 90,687,392 (-)NCBIGRCr8
mRatBN7.2370,269,908 - 70,280,651 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl370,265,936 - 70,278,639 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx373,651,410 - 73,662,173 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0382,250,100 - 82,260,863 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0380,016,622 - 80,027,400 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0372,589,840 - 72,605,089 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl372,589,842 - 72,602,548 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0379,101,422 - 79,116,188 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4368,414,797 - 68,427,502 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera369,617,028 - 69,629,720 (-)NCBICelera
Cytogenetic Map3q24NCBI
Lrrc55
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555112,278,638 - 2,287,435 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555112,278,638 - 2,287,435 (+)NCBIChiLan1.0ChiLan1.0
LRRC55
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2958,337,227 - 58,348,948 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11159,352,894 - 59,364,616 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01152,420,379 - 52,432,103 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.13159,911,746 - 159,923,361 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl3159,911,746 - 159,923,361 (+)Ensemblpanpan1.1panPan2
LRRC55
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11838,921,576 - 38,932,838 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1838,925,660 - 38,931,357 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1838,466,624 - 38,477,701 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01839,603,555 - 39,614,636 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1839,605,471 - 39,614,453 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11839,185,373 - 39,196,448 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01838,758,857 - 38,769,935 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01839,389,295 - 39,400,373 (-)NCBIUU_Cfam_GSD_1.0
Lrrc55
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494715,162,913 - 15,172,522 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365815,275,363 - 5,284,959 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365815,275,407 - 5,286,319 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LRRC55
(Sus scrofa - pig)		 No map positions available.
LRRC55
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1116,029,296 - 16,067,453 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666038113,390,456 - 113,403,769 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Lrrc55
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248643,338,012 - 3,347,670 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248643,339,041 - 3,348,432 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in LRRC55
15 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh38/hg38 11q12.1(chr11:57047366-57372313)x3 copy number gain See cases [RCV000138413] Chr11:57047366..57372313 [GRCh38]
Chr11:56814841..57139786 [GRCh37]
Chr11:56571417..56896362 [NCBI36]
Chr11:11q12.1		 likely benign
GRCh38/hg38 11q11-12.1(chr11:55316535-57539457)x3 copy number gain See cases [RCV000141200] Chr11:55316535..57539457 [GRCh38]
Chr11:55084011..57306930 [GRCh37]
Chr11:54840587..57063506 [NCBI36]
Chr11:11q11-12.1		 uncertain significance
GRCh38/hg38 11q11-12.1(chr11:55319519-58998777)x3 copy number gain See cases [RCV000142757] Chr11:55319519..58998777 [GRCh38]
Chr11:55086995..58766250 [GRCh37]
Chr11:54843571..58522826 [NCBI36]
Chr11:11q11-12.1		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p11.12-q12.1(chr11:51183548-56977098)x3 copy number gain See cases [RCV000512524] Chr11:51183548..56977098 [GRCh37]
Chr11:11p11.12-q12.1		 uncertain significance
GRCh37/hg19 11p11.12-q12.1(chr11:49313405-59008426)x3 copy number gain not provided [RCV000683370] Chr11:49313405..59008426 [GRCh37]
Chr11:11p11.12-q12.1		 uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11q12.1(chr11:56947528-56969455)x3 copy number gain not provided [RCV000750055] Chr11:56947528..56969455 [GRCh37]
Chr11:11q12.1		 benign
Single allele duplication not provided [RCV000844966] Chr11:55033164..57518726 [GRCh37]
Chr11:11q11-12.1		 not provided
GRCh37/hg19 11q12.1(chr11:56637024-57361915)x3 copy number gain not provided [RCV002473570] Chr11:56637024..57361915 [GRCh37]
Chr11:11q12.1		 uncertain significance
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
GRCh37/hg19 11p11.2-q12.2(chr11:51581311-54891247)x3 copy number gain See cases [RCV002286338] Chr11:51581311..54891247 [GRCh37]
Chr11:11p11.2-q12.2		 pathogenic
NM_001005210.4(LRRC55):c.316C>T (p.Arg106Trp) single nucleotide variant Inborn genetic diseases [RCV002751991] Chr11:57182338 [GRCh38]
Chr11:56949812 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.351C>G (p.His117Gln) single nucleotide variant Inborn genetic diseases [RCV002752666] Chr11:57182373 [GRCh38]
Chr11:56949847 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.133C>T (p.Arg45Cys) single nucleotide variant Inborn genetic diseases [RCV002660678] Chr11:57182155 [GRCh38]
Chr11:56949629 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.278T>G (p.Val93Gly) single nucleotide variant Inborn genetic diseases [RCV002691423] Chr11:57182300 [GRCh38]
Chr11:56949774 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.700G>A (p.Glu234Lys) single nucleotide variant Inborn genetic diseases [RCV002980104] Chr11:57187283 [GRCh38]
Chr11:56954757 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.171C>G (p.Phe57Leu) single nucleotide variant Inborn genetic diseases [RCV002763558] Chr11:57182193 [GRCh38]
Chr11:56949667 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.455G>C (p.Arg152Thr) single nucleotide variant Inborn genetic diseases [RCV002954733] Chr11:57182477 [GRCh38]
Chr11:56949951 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.-60G>A single nucleotide variant Inborn genetic diseases [RCV002644559] Chr11:57181963 [GRCh38]
Chr11:56949437 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.-36G>A single nucleotide variant Inborn genetic diseases [RCV002832301] Chr11:57181987 [GRCh38]
Chr11:56949461 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.227G>A (p.Arg76His) single nucleotide variant Inborn genetic diseases [RCV003183370] Chr11:57182249 [GRCh38]
Chr11:56949723 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.685G>A (p.Gly229Ser) single nucleotide variant Inborn genetic diseases [RCV003178722] Chr11:57187268 [GRCh38]
Chr11:56954742 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.889G>A (p.Glu297Lys) single nucleotide variant Inborn genetic diseases [RCV003196730] Chr11:57187472 [GRCh38]
Chr11:56954946 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.54G>A (p.Met18Ile) single nucleotide variant Inborn genetic diseases [RCV003207817] Chr11:57182076 [GRCh38]
Chr11:56949550 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.4(LRRC55):c.67C>T (p.Leu23Phe) single nucleotide variant Inborn genetic diseases [RCV003283310] Chr11:57182089 [GRCh38]
Chr11:56949563 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001005210.2(LRRC55):c.13C>T (p.Pro5Ser) single nucleotide variant Inborn genetic diseases [RCV003361712] Chr11:57181906 [GRCh38]
Chr11:56949380 [GRCh37]
Chr11:11q12.1		 likely benign
NM_001005210.4(LRRC55):c.787T>A (p.Phe263Ile) single nucleotide variant Inborn genetic diseases [RCV003354026] Chr11:57187370 [GRCh38]
Chr11:56954844 [GRCh37]
Chr11:11q12.1		 uncertain significance
GRCh37/hg19 11p11.12-q13.1(chr11:50398499-63924462)x3 copy number gain not specified [RCV003986918] Chr11:50398499..63924462 [GRCh37]
Chr11:11p11.12-q13.1		 likely pathogenic
GRCh37/hg19 11q12.1-13.3(chr11:56895955-69295402)x3 copy number gain not specified [RCV003986944] Chr11:56895955..69295402 [GRCh37]
Chr11:11q12.1-13.3		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1972
Count of miRNA genes:1033
Interacting mature miRNAs:1251
Transcripts:ENST00000497933
Prediction methods:Miranda
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
SHGC-142571  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371156,954,551 - 56,954,843UniSTSGRCh37
Build 361156,711,127 - 56,711,419RGDNCBI36
Celera1154,313,494 - 54,313,786RGD
Cytogenetic Map11q12.1UniSTS
HuRef1153,303,386 - 53,303,678UniSTS
TNG Radiation Hybrid Map1125097.0UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 4 2 1 100 7 51 6 1
Low 747 44 301 153 270 141 294 151 1833 68 203 140 12 155 28 1
Below cutoff 1494 1836 1254 387 480 247 3374 1816 1537 231 983 1179 142 979 2245 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000497933   ⟹   ENSP00000419542
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1157,181,953 - 57,191,717 (+)Ensembl
RefSeq Acc Id: ENST00000652194   ⟹   ENSP00000498533
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1157,181,747 - 57,191,714 (+)Ensembl
RefSeq Acc Id: NM_001005210   ⟹   NP_001005210
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381157,181,953 - 57,191,717 (+)NCBI
GRCh371156,949,221 - 56,959,188 (+)RGD
Build 361156,705,797 - 56,714,154 (+)NCBI Archive
Celera1154,308,169 - 54,318,131 (+)RGD
HuRef1153,298,067 - 53,308,021 (+)RGD
CHM1_11156,815,331 - 56,825,298 (+)NCBI
T2T-CHM13v2.01157,131,394 - 57,141,139 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001005210 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI36738 (Get FASTA)   NCBI Sequence Viewer  
  AAI36740 (Get FASTA)   NCBI Sequence Viewer  
  AAI50573 (Get FASTA)   NCBI Sequence Viewer  
  BAC87047 (Get FASTA)   NCBI Sequence Viewer  
  EAW73729 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000419542
  ENSP00000419542.2
  ENSP00000498533.1
GenBank Protein Q6ZSA7 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001005210   ⟸   NM_001005210
- Peptide Label: precursor
- UniProtKB: Q6ZSA7 (UniProtKB/Swiss-Prot),   A7E2U7 (UniProtKB/Swiss-Prot),   B2RN81 (UniProtKB/Swiss-Prot),   A0A494C0H1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000498533   ⟸   ENST00000652194
RefSeq Acc Id: ENSP00000419542   ⟸   ENST00000497933
Protein Domains
LRRCT   LRRNT

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q6ZSA7-F1-model_v2 AlphaFold Q6ZSA7 1-298 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:32324 AgrOrtholog
COSMIC LRRC55 COSMIC
Ensembl Genes ENSG00000183908 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000497933 ENTREZGENE
  ENST00000497933.3 UniProtKB/Swiss-Prot
  ENST00000652194.1 UniProtKB/TrEMBL
Gene3D-CATH 3.80.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000183908 GTEx
HGNC ID HGNC:32324 ENTREZGENE
Human Proteome Map LRRC55 Human Proteome Map
InterPro Cys-rich_flank_reg_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Leu-rich_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Leu-rich_rpt_typical-subtyp UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LRR_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LRRNT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:219527 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 219527 ENTREZGENE
OMIM 615213 OMIM
PANTHER GH08155P UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LEUCINE-RICH REPEAT-CONTAINING PROTEIN 55 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam LRR_8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142671514 PharmGKB
PROSITE LRR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART LRR_TYP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LRRCT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LRRNT UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP L domain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A494C0H1 ENTREZGENE, UniProtKB/TrEMBL
  A7E2U7 ENTREZGENE
  B2RN81 ENTREZGENE
  LRC55_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary A7E2U7 UniProtKB/Swiss-Prot
  B2RN81 UniProtKB/Swiss-Prot