SLITRK3 (SLIT and NTRK like family member 3) - Rat Genome Database

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Gene: SLITRK3 (SLIT and NTRK like family member 3) Homo sapiens
Analyze
Symbol: SLITRK3
Name: SLIT and NTRK like family member 3
RGD ID: 1321448
HGNC Page HGNC
Description: Involved in regulation of presynapse assembly and synaptic membrane adhesion. Is active in GABA-ergic synapse. Is integral component of postsynaptic specialization membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: KIAA0848; MGC138681; SLIT and NTRK-like family, member 3; SLIT and NTRK-like protein 3; slit and trk like gene 3
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 Ensembl3165,186,720 - 165,197,109 (-)EnsemblGRCh38hg38GRCh38
GRCh383165,186,720 - 165,197,109 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh373164,904,508 - 164,914,897 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 363166,387,202 - 166,397,163 (-)NCBINCBI36hg18NCBI36
Build 343166,387,211 - 166,397,171NCBI
Celera3163,303,200 - 163,313,157 (-)NCBI
Cytogenetic Map3q26.1NCBI
HuRef3162,274,102 - 162,284,057 (-)NCBIHuRef
CHM1_13164,867,392 - 164,877,350 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:10048485   PMID:12477932   PMID:14550773   PMID:14557068   PMID:16344560   PMID:19336002   PMID:20237496   PMID:21873635   PMID:23345436   PMID:26217092   PMID:27565350   PMID:28065597  
PMID:28611215   PMID:29987050   PMID:30021884   PMID:30639242   PMID:31391242   PMID:32814053  


Genomics

Comparative Map Data
SLITRK3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl3165,186,720 - 165,197,109 (-)EnsemblGRCh38hg38GRCh38
GRCh383165,186,720 - 165,197,109 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh373164,904,508 - 164,914,897 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 363166,387,202 - 166,397,163 (-)NCBINCBI36hg18NCBI36
Build 343166,387,211 - 166,397,171NCBI
Celera3163,303,200 - 163,313,157 (-)NCBI
Cytogenetic Map3q26.1NCBI
HuRef3162,274,102 - 162,284,057 (-)NCBIHuRef
CHM1_13164,867,392 - 164,877,350 (-)NCBICHM1_1
Slitrk3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39372,954,399 - 72,965,298 (-)NCBIGRCm39mm39
GRCm39 Ensembl372,954,598 - 72,965,136 (-)Ensembl
GRCm38373,047,066 - 73,057,953 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl373,047,265 - 73,057,803 (-)EnsemblGRCm38mm10GRCm38
MGSCv37372,852,047 - 72,860,865 (-)NCBIGRCm37mm9NCBIm37
MGSCv36373,134,051 - 73,142,869 (-)NCBImm8
Celera373,161,163 - 73,169,943 (-)NCBICelera
Cytogenetic Map3E3NCBI
Slitrk3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.22157,680,067 - 157,697,404 (-)NCBImRatBN7.2
mRatBN7.2 Ensembl2157,687,535 - 157,696,709 (-)Ensembl
Rnor_6.02170,446,582 - 170,461,513 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2170,452,702 - 170,460,754 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02189,791,839 - 189,803,411 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42163,703,843 - 163,711,895 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.12163,653,847 - 163,658,733 (-)NCBI
Celera2151,947,474 - 151,955,526 (-)NCBICelera
Cytogenetic Map2q32NCBI
Slitrk3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495544814,846,976 - 14,852,612 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495544814,846,976 - 14,852,612 (-)NCBIChiLan1.0ChiLan1.0
SLITRK3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.13170,263,109 - 170,274,217 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl3170,265,342 - 170,268,275 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v03162,207,530 - 162,223,830 (-)NCBIMhudiblu_PPA_v0panPan3
SLITRK3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13430,447,606 - 30,456,444 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3430,447,659 - 30,450,598 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3439,508,350 - 39,517,571 (-)NCBI
ROS_Cfam_1.03430,508,728 - 30,517,972 (-)NCBI
UMICH_Zoey_3.13430,452,470 - 30,461,687 (-)NCBI
UNSW_CanFamBas_1.03430,403,986 - 30,413,213 (-)NCBI
UU_Cfam_GSD_1.03430,673,215 - 30,682,473 (-)NCBI
Slitrk3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560296,524,602 - 96,539,253 (-)NCBI
SpeTri2.0NW_0049367071,315,267 - 1,324,793 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SLITRK3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13104,449,973 - 104,461,119 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113104,443,610 - 104,461,850 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.213112,883,358 - 112,893,492 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SLITRK3
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11524,361,523 - 24,374,865 (+)NCBI
ChlSab1.1 Ensembl1524,367,287 - 24,370,226 (+)Ensembl
Vero_WHO_p1.0NW_02366606333,329,965 - 33,345,375 (+)NCBI
Slitrk3
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473043,175,690 - 43,191,689 (-)NCBI

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1620
Count of miRNA genes:607
Interacting mature miRNAs:711
Transcripts:ENST00000241274, ENST00000475390, ENST00000497724
Prediction methods:Microtar, 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
High
Medium 484 21 21 9 21 5 429 308 2 58 11
Low 1222 211 274 217 68 202 295 481 2438 26 667 244 17 8 68
Below cutoff 560 1690 1135 265 439 131 3039 782 792 116 513 1110 139 1 700 2156

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000241274   ⟹   ENSP00000241274
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl3165,186,722 - 165,196,852 (-)Ensembl
RefSeq Acc Id: ENST00000475390   ⟹   ENSP00000420091
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl3165,186,720 - 165,196,384 (-)Ensembl
RefSeq Acc Id: ENST00000497724   ⟹   ENSP00000419611
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl3165,190,343 - 165,197,109 (-)Ensembl
RefSeq Acc Id: NM_001318810   ⟹   NP_001305739
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383165,186,720 - 165,196,384 (-)NCBI
CHM1_13164,867,392 - 164,876,671 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001318811   ⟹   NP_001305740
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383165,186,720 - 165,197,109 (-)NCBI
CHM1_13164,867,392 - 164,877,778 (-)NCBI
Sequence:
RefSeq Acc Id: NM_014926   ⟹   NP_055741
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383165,186,720 - 165,196,871 (-)NCBI
GRCh373164,902,010 - 164,914,469 (-)NCBI
Build 363166,387,202 - 166,397,163 (-)NCBI Archive
Celera3163,303,200 - 163,313,157 (-)RGD
HuRef3162,274,102 - 162,284,057 (-)ENTREZGENE
CHM1_13164,867,392 - 164,877,521 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_055741   ⟸   NM_014926
- Peptide Label: precursor
- UniProtKB: O94933 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305740   ⟸   NM_001318811
- Peptide Label: precursor
- UniProtKB: O94933 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305739   ⟸   NM_001318810
- Peptide Label: precursor
- UniProtKB: O94933 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000241274   ⟸   ENST00000241274
RefSeq Acc Id: ENSP00000419611   ⟸   ENST00000497724
RefSeq Acc Id: ENSP00000420091   ⟸   ENST00000475390
Protein Domains
LRRCT   LRRNT

Promoters
RGD ID:6866196
Promoter ID:EPDNEW_H6263
Type:initiation region
Name:SLITRK3_2
Description:SLIT and NTRK like family member 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H6264  EPDNEW_H6265  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh383165,195,902 - 165,195,962EPDNEW
RGD ID:6866198
Promoter ID:EPDNEW_H6264
Type:initiation region
Name:SLITRK3_3
Description:SLIT and NTRK like family member 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H6263  EPDNEW_H6265  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh383165,196,384 - 165,196,444EPDNEW
RGD ID:6866200
Promoter ID:EPDNEW_H6265
Type:initiation region
Name:SLITRK3_1
Description:SLIT and NTRK like family member 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H6263  EPDNEW_H6264  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh383165,196,871 - 165,196,931EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3q24-26.32(chr3:147442566-178522531)x3 copy number gain See cases [RCV000051724] Chr3:147442566..178522531 [GRCh38]
Chr3:147160353..178240319 [GRCh37]
Chr3:148643043..179723013 [NCBI36]
Chr3:3q24-26.32
pathogenic
GRCh38/hg38 3q24-29(chr3:147521892-198096565)x3 copy number gain See cases [RCV000051725] Chr3:147521892..198096565 [GRCh38]
Chr3:147239679..197823436 [GRCh37]
Chr3:148722369..199307833 [NCBI36]
Chr3:3q24-29
pathogenic
GRCh38/hg38 3q25.31-29(chr3:157293378-198134727)x3 copy number gain See cases [RCV000051726] Chr3:157293378..198134727 [GRCh38]
Chr3:157011167..197861598 [GRCh37]
Chr3:158493861..199345995 [NCBI36]
Chr3:3q25.31-29
pathogenic
GRCh38/hg38 3q25.32-26.31(chr3:158141556-172788324)x3 copy number gain See cases [RCV000051735] Chr3:158141556..172788324 [GRCh38]
Chr3:157859345..172506114 [GRCh37]
Chr3:159342039..173988808 [NCBI36]
Chr3:3q25.32-26.31
pathogenic
GRCh38/hg38 3q22.3-29(chr3:137126982-198110178)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051723]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051723]|See cases [RCV000051723] Chr3:137126982..198110178 [GRCh38]
Chr3:136845824..197837049 [GRCh37]
Chr3:138328514..199321446 [NCBI36]
Chr3:3q22.3-29
pathogenic
NM_014926.2(SLITRK3):c.2659C>T (p.Arg887Ter) single nucleotide variant Malignant melanoma [RCV000065905] Chr3:165188172 [GRCh38]
Chr3:164905960 [GRCh37]
Chr3:166388654 [NCBI36]
Chr3:3q26.1
not provided
NM_014926.2(SLITRK3):c.460C>T (p.Leu154=) single nucleotide variant Malignant melanoma [RCV000065906] Chr3:165190371 [GRCh38]
Chr3:164908159 [GRCh37]
Chr3:166390853 [NCBI36]
Chr3:3q26.1
not provided
NM_014926.2(SLITRK3):c.2555G>A (p.Gly852Glu) single nucleotide variant Malignant melanoma [RCV000060754] Chr3:165188276 [GRCh38]
Chr3:164906064 [GRCh37]
Chr3:166388758 [NCBI36]
Chr3:3q26.1
not provided
NM_014926.2(SLITRK3):c.1100C>T (p.Pro367Leu) single nucleotide variant Malignant melanoma [RCV000060755] Chr3:165189731 [GRCh38]
Chr3:164907519 [GRCh37]
Chr3:166390213 [NCBI36]
Chr3:3q26.1
not provided
NM_014926.2(SLITRK3):c.527G>A (p.Arg176Lys) single nucleotide variant Malignant melanoma [RCV000060756] Chr3:165190304 [GRCh38]
Chr3:164908092 [GRCh37]
Chr3:166390786 [NCBI36]
Chr3:3q26.1
not provided
GRCh38/hg38 3q13.11-29(chr3:103426882-198110178)x3 copy number gain See cases [RCV000134948] Chr3:103426882..198110178 [GRCh38]
Chr3:103145726..197837049 [GRCh37]
Chr3:104628416..199321446 [NCBI36]
Chr3:3q13.11-29
pathogenic
GRCh38/hg38 3q26.1-26.33(chr3:165158611-180130168)x3 copy number gain See cases [RCV000139359] Chr3:165158611..180130168 [GRCh38]
Chr3:164876399..179847956 [GRCh37]
Chr3:166359093..181330650 [NCBI36]
Chr3:3q26.1-26.33
pathogenic
GRCh38/hg38 3q25.1-29(chr3:152100512-198118383)x3 copy number gain See cases [RCV000139435] Chr3:152100512..198118383 [GRCh38]
Chr3:151818301..197845254 [GRCh37]
Chr3:153300991..199329651 [NCBI36]
Chr3:3q25.1-29
pathogenic
GRCh38/hg38 3q25.31-29(chr3:156321878-198113452)x3 copy number gain See cases [RCV000140849] Chr3:156321878..198113452 [GRCh38]
Chr3:156039667..197840323 [GRCh37]
Chr3:157522361..199324720 [NCBI36]
Chr3:3q25.31-29
pathogenic
GRCh38/hg38 3q25.31-29(chr3:156118441-198125115)x3 copy number gain See cases [RCV000142310] Chr3:156118441..198125115 [GRCh38]
Chr3:155836230..197851986 [GRCh37]
Chr3:157318924..199336383 [NCBI36]
Chr3:3q25.31-29
pathogenic
GRCh37/hg19 3q24-29(chr3:142995020-192997215)x4 copy number gain See cases [RCV000240256] Chr3:142995020..192997215 [GRCh37]
Chr3:3q24-29
pathogenic
GRCh37/hg19 3q25.32-29(chr3:158980631-197766890)x3 copy number gain See cases [RCV000447464] Chr3:158980631..197766890 [GRCh37]
Chr3:3q25.32-29
pathogenic
GRCh37/hg19 3q25.32-26.33(chr3:157128738-181637333)x3 copy number gain See cases [RCV000446611] Chr3:157128738..181637333 [GRCh37]
Chr3:3q25.32-26.33
pathogenic
GRCh37/hg19 3q24-26.2(chr3:147180945-168415875)x1 copy number loss See cases [RCV000448130] Chr3:147180945..168415875 [GRCh37]
Chr3:3q24-26.2
pathogenic
GRCh37/hg19 3q26.1(chr3:163657369-167073454)x1 copy number loss See cases [RCV000448579] Chr3:163657369..167073454 [GRCh37]
Chr3:3q26.1
uncertain significance
GRCh37/hg19 3q26.1-26.2(chr3:163595552-168022596)x3 copy number gain See cases [RCV000448072] Chr3:163595552..168022596 [GRCh37]
Chr3:3q26.1-26.2
uncertain significance
GRCh37/hg19 3q25.2-29(chr3:152356847-197851986)x3 copy number gain See cases [RCV000448608] Chr3:152356847..197851986 [GRCh37]
Chr3:3q25.2-29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3 copy number gain See cases [RCV000511055] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:61892-197851986) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3q26.1(chr3:162823013-165005878)x3 copy number gain not provided [RCV000682325] Chr3:162823013..165005878 [GRCh37]
Chr3:3q26.1
uncertain significance
GRCh37/hg19 3p26.3-q29(chr3:61495-197838262)x3 copy number gain not provided [RCV000742138] Chr3:61495..197838262 [GRCh37]
Chr3:3p26.3-q29
pathogenic
GRCh37/hg19 3p26.3-q29(chr3:60174-197948027)x3 copy number gain not provided [RCV000742133] Chr3:60174..197948027 [GRCh37]
Chr3:3p26.3-q29
pathogenic
NM_001318810.2(SLITRK3):c.2676T>C (p.Pro892=) single nucleotide variant not provided [RCV000881127] Chr3:165188155 [GRCh38]
Chr3:164905943 [GRCh37]
Chr3:3q26.1
benign
NM_001318810.2(SLITRK3):c.1816G>T (p.Glu606Ter) single nucleotide variant Intellectual disability [RCV001195721] Chr3:165189015 [GRCh38]
Chr3:164906803 [GRCh37]
Chr3:3q26.1
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23501 AgrOrtholog
COSMIC SLITRK3 COSMIC
Ensembl Genes ENSG00000121871 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000241274 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000419611 UniProtKB/TrEMBL
  ENSP00000420091 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000241274 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000475390 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000497724 UniProtKB/TrEMBL
Gene3D-CATH 3.80.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000121871 GTEx
HGNC ID HGNC:23501 ENTREZGENE
Human Proteome Map SLITRK3 Human Proteome Map
InterPro Cys-rich_flank_reg_C UniProtKB/Swiss-Prot
  Leu-rich_rpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Leu-rich_rpt_typical-subtyp UniProtKB/Swiss-Prot
  LRR_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Slitrk UniProtKB/Swiss-Prot
KEGG Report hsa:22865 UniProtKB/Swiss-Prot
NCBI Gene 22865 ENTREZGENE
OMIM 609679 OMIM
PANTHER PTHR45773 UniProtKB/Swiss-Prot
Pfam LRR_8 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134958002 PharmGKB
SMART LRR_TYP UniProtKB/Swiss-Prot
  LRRCT UniProtKB/Swiss-Prot
UniProt C9K0R4_HUMAN UniProtKB/TrEMBL
  O94933 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q1RMY6 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 SLITRK3  SLIT and NTRK like family member 3    SLIT and NTRK-like family, member 3  Symbol and/or name change 5135510 APPROVED
2011-09-01 SLITRK3  SLIT and NTRK-like family, member 3  SLITRK3  SLIT and NTRK-like family, member 3  Symbol and/or name change 5135510 APPROVED