LRRTM1 (leucine rich repeat transmembrane neuronal 1) - Rat Genome Database

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Gene: LRRTM1 (leucine rich repeat transmembrane neuronal 1) Homo sapiens
Analyze
Symbol: LRRTM1
Name: leucine rich repeat transmembrane neuronal 1
RGD ID: 1351021
HGNC Page HGNC
Description: Predicted to be involved in several processes, including long-term synaptic potentiation; negative regulation of receptor internalization; and positive regulation of synapse assembly. Localizes to several cellular components, including GABA-ergic synapse; growth cone; and integral component of postsynaptic specialization membrane; INTERACTS WITH acrylamide; all-trans-retinoic acid; arsenite(3-).
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: FLJ32082; leucine-rich repeat transmembrane neuronal 1 protein; leucine-rich repeat transmembrane neuronal protein 1
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
GRCh38.p13 Ensembl280,288,351 - 80,304,752 (-)EnsemblGRCh38hg38GRCh38
GRCh38280,301,878 - 80,304,752 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37280,529,003 - 80,531,877 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36280,382,514 - 80,384,998 (-)NCBINCBI36hg18NCBI36
Build 34280,436,963 - 80,443,510NCBI
Celera280,357,641 - 80,360,125 (-)NCBI
Cytogenetic Map2p12NCBI
HuRef280,264,234 - 80,266,718 (-)NCBIHuRef
CHM1_1280,458,756 - 80,461,240 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

References

Additional References at PubMed
PMID:8125298   PMID:12477932   PMID:12676565   PMID:12975309   PMID:14702039   PMID:15489334   PMID:17667961   PMID:19125365   PMID:19125366   PMID:19125367   PMID:19626025   PMID:20678249  
PMID:21041608   PMID:21708131   PMID:21873635   PMID:24785688   PMID:25111784   PMID:26354767   PMID:27565350   PMID:28321770   PMID:28514442  


Genomics

Comparative Map Data
LRRTM1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl280,288,351 - 80,304,752 (-)EnsemblGRCh38hg38GRCh38
GRCh38280,301,878 - 80,304,752 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37280,529,003 - 80,531,877 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36280,382,514 - 80,384,998 (-)NCBINCBI36hg18NCBI36
Build 34280,436,963 - 80,443,510NCBI
Celera280,357,641 - 80,360,125 (-)NCBI
Cytogenetic Map2p12NCBI
HuRef280,264,234 - 80,266,718 (-)NCBIHuRef
CHM1_1280,458,756 - 80,461,240 (-)NCBICHM1_1
Lrrtm1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39677,192,762 - 77,236,898 (+)NCBIGRCm39mm39
GRCm39 Ensembl677,219,672 - 77,234,774 (+)Ensembl
GRCm38677,229,210 - 77,259,915 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl677,242,689 - 77,257,791 (+)EnsemblGRCm38mm10GRCm38
MGSCv37677,192,711 - 77,195,511 (+)NCBIGRCm37mm9NCBIm37
MGSCv36677,172,238 - 77,187,272 (+)NCBImm8
Celera679,273,556 - 79,276,356 (+)NCBICelera
Cytogenetic Map6C3NCBI
LRRTM1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.24109,701,815 - 109,718,924 (+)NCBI
Rnor_6.0 Ensembl4108,301,129 - 108,316,373 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.04108,300,927 - 108,316,373 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.04173,006,611 - 173,022,018 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44111,166,760 - 111,182,344 (+)NCBIRGSC3.4rn4RGSC3.4
Celera498,746,001 - 98,761,096 (+)NCBICelera
Cytogenetic Map4q33NCBI
Lrrtm1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554246,322,284 - 6,337,550 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554246,322,284 - 6,337,550 (+)NCBIChiLan1.0ChiLan1.0
LRRTM1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12A81,940,008 - 81,956,386 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A81,953,891 - 81,955,459 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v02A80,376,582 - 80,392,899 (-)NCBIMhudiblu_PPA_v0panPan3
LRRTM1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11743,833,906 - 43,842,911 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1743,834,562 - 43,836,130 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1743,529,484 - 43,532,366 (+)NCBI
ROS_Cfam_1.01744,646,891 - 44,649,819 (+)NCBI
UMICH_Zoey_3.11743,729,863 - 43,732,734 (+)NCBI
UNSW_CanFamBas_1.01743,765,294 - 43,768,169 (+)NCBI
UU_Cfam_GSD_1.01744,269,225 - 44,272,140 (+)NCBI
Lrrtm1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_0244062924,806,393 - 4,822,627 (+)NCBI
SpeTri2.0NW_0049365565,915,265 - 5,934,004 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LRRTM1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl363,587,499 - 63,590,407 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1363,585,784 - 63,590,368 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2366,675,615 - 66,678,394 (+)NCBISscrofa10.2Sscrofa10.2susScr3
LRRTM1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11426,926,681 - 26,929,347 (+)NCBI
ChlSab1.1 Ensembl1426,927,470 - 26,929,038 (+)Ensembl
Lrrtm1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474922,695,726 - 22,698,161 (+)NCBI

Position Markers
SHGC-79114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37280,532,581 - 80,532,902UniSTSGRCh37
Build 36280,386,092 - 80,386,413RGDNCBI36
Celera280,361,219 - 80,361,540RGD
Cytogenetic Map2p12-p11.1UniSTS
Cytogenetic Map2p12UniSTS
HuRef280,267,812 - 80,268,133UniSTS
TNG Radiation Hybrid Map250954.0UniSTS
D2S1942E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37280,529,085 - 80,529,164UniSTSGRCh37
Build 36280,382,596 - 80,382,675RGDNCBI36
Celera280,357,723 - 80,357,802RGD
Cytogenetic Map2p12-p11.1UniSTS
Cytogenetic Map2p12UniSTS
HuRef280,264,316 - 80,264,395UniSTS
LRRTM1__7335  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37280,525,369 - 80,525,892UniSTSGRCh37
Build 36280,378,880 - 80,379,403RGDNCBI36
Celera280,354,009 - 80,354,532RGD
HuRef280,260,604 - 80,261,127UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2886
Count of miRNA genes:1021
Interacting mature miRNAs:1242
Transcripts:ENST00000295057, ENST00000409148, ENST00000415098, ENST00000416268, ENST00000417012, ENST00000433224, ENST00000452811
Prediction methods:Miranda, Rnahybrid, Targetscan
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.


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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1
Medium 28 21 2 63 3 736 42 113 25 60
Low 1662 316 713 54 94 20 726 861 2588 51 510 443 34 1 173 537 2
Below cutoff 607 1939 776 388 443 260 2903 956 373 140 723 757 130 952 1715 2

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000295057   ⟹   ENSP00000295057
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl280,301,878 - 80,304,752 (-)Ensembl
RefSeq Acc Id: ENST00000409148   ⟹   ENSP00000386646
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl280,301,880 - 80,304,274 (-)Ensembl
RefSeq Acc Id: ENST00000415098   ⟹   ENSP00000404557
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl280,303,493 - 80,304,321 (-)Ensembl
RefSeq Acc Id: ENST00000416268   ⟹   ENSP00000415368
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl280,303,151 - 80,304,595 (-)Ensembl
RefSeq Acc Id: ENST00000417012   ⟹   ENSP00000393562
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl280,288,351 - 80,304,393 (-)Ensembl
RefSeq Acc Id: ENST00000433224   ⟹   ENSP00000414523
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl280,298,181 - 80,304,730 (-)Ensembl
RefSeq Acc Id: ENST00000452811   ⟹   ENSP00000389473
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl280,303,269 - 80,304,440 (-)Ensembl
RefSeq Acc Id: NM_178839   ⟹   NP_849161
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38280,301,878 - 80,304,752 (-)NCBI
GRCh37280,515,481 - 80,531,718 (-)NCBI
Build 36280,382,514 - 80,384,998 (-)NCBI Archive
Celera280,357,641 - 80,360,125 (-)RGD
HuRef280,264,234 - 80,266,718 (-)RGD
CHM1_1280,458,756 - 80,461,240 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017003986   ⟹   XP_016859475
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38280,302,014 - 80,304,428 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017003987   ⟹   XP_016859476
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38280,302,014 - 80,304,394 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_849161   ⟸   NM_178839
- Peptide Label: precursor
- UniProtKB: Q86UE6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016859476   ⟸   XM_017003987
- Peptide Label: isoform X1
- UniProtKB: Q86UE6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016859475   ⟸   XM_017003986
- Peptide Label: isoform X1
- UniProtKB: Q86UE6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000389473   ⟸   ENST00000452811
RefSeq Acc Id: ENSP00000295057   ⟸   ENST00000295057
RefSeq Acc Id: ENSP00000404557   ⟸   ENST00000415098
RefSeq Acc Id: ENSP00000415368   ⟸   ENST00000416268
RefSeq Acc Id: ENSP00000393562   ⟸   ENST00000417012
RefSeq Acc Id: ENSP00000414523   ⟸   ENST00000433224
RefSeq Acc Id: ENSP00000386646   ⟸   ENST00000409148
Protein Domains
LRRCT   LRRNT

Promoters
RGD ID:6860846
Promoter ID:EPDNEW_H3588
Type:initiation region
Name:LRRTM1_2
Description:leucine rich repeat transmembrane neuronal 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H3589  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38280,304,435 - 80,304,495EPDNEW
RGD ID:6860848
Promoter ID:EPDNEW_H3589
Type:initiation region
Name:LRRTM1_1
Description:leucine rich repeat transmembrane neuronal 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H3588  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38280,304,710 - 80,304,770EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_178839.4(LRRTM1):c.1526C>T (p.Ser509Leu) single nucleotide variant Malignant melanoma [RCV000060619] Chr2:80302294 [GRCh38]
Chr2:80529419 [GRCh37]
Chr2:80382930 [NCBI36]
Chr2:2p12
not provided
GRCh38/hg38 2p12-11.2(chr2:77025216-90282666)x3 copy number gain See cases [RCV000134786] Chr2:77025216..90282666 [GRCh38]
Chr2:77252342..91619262 [GRCh37]
Chr2:77105850..90982989 [NCBI36]
Chr2:2p12-11.2
pathogenic
GRCh38/hg38 2p12(chr2:79680727-80974466)x3 copy number gain See cases [RCV000135457] Chr2:79680727..80974466 [GRCh38]
Chr2:79907853..81201590 [GRCh37]
Chr2:79761361..81055101 [NCBI36]
Chr2:2p12
uncertain significance
GRCh38/hg38 2p16.1-11.2(chr2:58279519-83586962)x3 copy number gain See cases [RCV000136053] Chr2:58279519..83586962 [GRCh38]
Chr2:58506654..83814086 [GRCh37]
Chr2:58360158..83667597 [NCBI36]
Chr2:2p16.1-11.2
pathogenic
GRCh38/hg38 2p16.3-11.2(chr2:47620388-86702722)x3 copy number gain See cases [RCV000137586] Chr2:47620388..86702722 [GRCh38]
Chr2:47847527..86929845 [GRCh37]
Chr2:47701031..86783356 [NCBI36]
Chr2:2p16.3-11.2
uncertain significance
GRCh38/hg38 2p12(chr2:79983983-80544440)x3 copy number gain See cases [RCV000139428] Chr2:79983983..80544440 [GRCh38]
Chr2:80211109..80771565 [GRCh37]
Chr2:80064620..80625076 [NCBI36]
Chr2:2p12
pathogenic|uncertain significance
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3 copy number gain See cases [RCV000141494] Chr2:7495123..87705899 [GRCh38]
Chr2:7635254..88005418 [GRCh37]
Chr2:7552705..87786533 [NCBI36]
Chr2:2p25.1-11.2
benign
GRCh38/hg38 2p12(chr2:79252886-81305516)x1 copy number loss See cases [RCV000143017] Chr2:79252886..81305516 [GRCh38]
Chr2:79480012..81532640 [GRCh37]
Chr2:79333520..81386151 [NCBI36]
Chr2:2p12
uncertain significance
GRCh37/hg19 2p12(chr2:80247964-81740468)x1 copy number loss not provided [RCV000585262] Chr2:80247964..81740468 [GRCh37]
Chr2:2p12
uncertain significance
GRCh37/hg19 2p15-11.2(chr2:62245236-86978895)x3 copy number gain See cases [RCV000448688] Chr2:62245236..86978895 [GRCh37]
Chr2:2p15-11.2
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p13.1-11.2(chr2:74365484-89129064)x1 copy number loss See cases [RCV000510763] Chr2:74365484..89129064 [GRCh37]
Chr2:2p13.1-11.2
pathogenic
Single allele inversion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3
likely pathogenic
GRCh37/hg19 2p13.1-11.2(chr2:74527522-89125488)x1 copy number loss not provided [RCV000682167] Chr2:74527522..89125488 [GRCh37]
Chr2:2p13.1-11.2
pathogenic
Single allele duplication not provided [RCV000677942] Chr2:63671346..85698002 [GRCh37]
Chr2:2p15-11.2
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
NM_178839.5(LRRTM1):c.1012G>A (p.Gly338Ser) single nucleotide variant not provided [RCV000959536] Chr2:80302808 [GRCh38]
Chr2:80529933 [GRCh37]
Chr2:2p12
benign
GRCh37/hg19 2p12(chr2:76157543-82375906)x1 copy number loss not provided [RCV000847807] Chr2:76157543..82375906 [GRCh37]
Chr2:2p12
uncertain significance
GRCh37/hg19 2p12(chr2:78114851-82104559)x1 copy number loss not provided [RCV000849781] Chr2:78114851..82104559 [GRCh37]
Chr2:2p12
uncertain significance
GRCh37/hg19 2p13.1-12(chr2:74972080-83043893)x1 copy number loss not provided [RCV000846568] Chr2:74972080..83043893 [GRCh37]
Chr2:2p13.1-12
pathogenic
GRCh37/hg19 2p12-11.2(chr2:77907114-87330965)x1 copy number loss not provided [RCV000846587] Chr2:77907114..87330965 [GRCh37]
Chr2:2p12-11.2
pathogenic
GRCh37/hg19 2p12(chr2:79889710-81392136)x3 copy number gain not provided [RCV000846411] Chr2:79889710..81392136 [GRCh37]
Chr2:2p12
uncertain significance
GRCh37/hg19 2p12(chr2:76035305-81220405)x1 copy number loss not provided [RCV001260149] Chr2:76035305..81220405 [GRCh37]
Chr2:2p12
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:19408 AgrOrtholog
COSMIC LRRTM1 COSMIC
Ensembl Genes ENSG00000162951 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000295057 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000386646 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000389473 UniProtKB/TrEMBL
  ENSP00000393562 UniProtKB/Swiss-Prot
  ENSP00000404557 UniProtKB/TrEMBL
  ENSP00000414523 UniProtKB/Swiss-Prot
  ENSP00000415368 UniProtKB/TrEMBL
Ensembl Transcript ENST00000295057 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000409148 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000415098 UniProtKB/TrEMBL
  ENST00000416268 UniProtKB/TrEMBL
  ENST00000417012 UniProtKB/Swiss-Prot
  ENST00000433224 UniProtKB/Swiss-Prot
  ENST00000452811 UniProtKB/TrEMBL
Gene3D-CATH 3.80.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000162951 GTEx
HGNC ID HGNC:19408 ENTREZGENE
Human Proteome Map LRRTM1 Human Proteome Map
InterPro 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
KEGG Report hsa:347730 UniProtKB/Swiss-Prot
NCBI Gene 347730 ENTREZGENE
OMIM 610867 OMIM
Pfam LRR_8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134887293 PharmGKB
PROSITE LRR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART LRR_TYP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt C9JEE2_HUMAN UniProtKB/TrEMBL
  C9JF97_HUMAN UniProtKB/TrEMBL
  C9JPM9_HUMAN UniProtKB/TrEMBL
  LRRT1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary A8K397 UniProtKB/Swiss-Prot
  D6W5K1 UniProtKB/Swiss-Prot
  Q96DN1 UniProtKB/Swiss-Prot