LY6G6F (lymphocyte antigen 6 family member G6F) - Rat Genome Database

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Gene: LY6G6F (lymphocyte antigen 6 family member G6F) Homo sapiens
Analyze
Symbol: LY6G6F
Name: lymphocyte antigen 6 family member G6F
RGD ID: 1342827
HGNC Page HGNC:13933
Description: Predicted to be located in plasma membrane and platelet alpha granule membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C6orf21; G6f; LY6G6; LY6G6D; lymphocyte antigen 6 complex locus protein G6f; lymphocyte antigen 6 complex, locus G6D; lymphocyte antigen 6 complex, locus G6F; NG32
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38631,706,866 - 31,710,679 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl631,706,866 - 31,710,679 (+)EnsemblGRCh38hg38GRCh38
GRCh37631,674,643 - 31,678,456 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36631,782,663 - 31,786,351 (+)NCBINCBI36Build 36hg18NCBI36
Build 34631,782,662 - 31,786,351NCBI
Celera633,272,902 - 33,276,590 (+)NCBICelera
Cytogenetic Map6p21.33NCBI
HuRef631,460,902 - 31,464,590 (+)NCBIHuRef
CHM1_1631,676,801 - 31,680,489 (+)NCBICHM1_1
T2T-CHM13v2.0631,559,901 - 31,563,714 (+)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:12852788   PMID:17192395   PMID:19851445   PMID:20587610   PMID:33961781  


Genomics

Comparative Map Data
LY6G6F
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38631,706,866 - 31,710,679 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl631,706,866 - 31,710,679 (+)EnsemblGRCh38hg38GRCh38
GRCh37631,674,643 - 31,678,456 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36631,782,663 - 31,786,351 (+)NCBINCBI36Build 36hg18NCBI36
Build 34631,782,662 - 31,786,351NCBI
Celera633,272,902 - 33,276,590 (+)NCBICelera
Cytogenetic Map6p21.33NCBI
HuRef631,460,902 - 31,464,590 (+)NCBIHuRef
CHM1_1631,676,801 - 31,680,489 (+)NCBICHM1_1
T2T-CHM13v2.0631,559,901 - 31,563,714 (+)NCBIT2T-CHM13v2.0
Ly6g6f
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391735,299,514 - 35,304,571 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1735,299,456 - 35,304,586 (-)EnsemblGRCm39 Ensembl
GRCm381735,080,538 - 35,085,595 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1735,080,480 - 35,085,610 (-)EnsemblGRCm38mm10GRCm38
MGSCv371735,217,483 - 35,222,540 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361734,688,536 - 34,693,666 (-)NCBIMGSCv36mm8
Celera1738,177,222 - 38,182,277 (-)NCBICelera
Cytogenetic Map17B1NCBI
cM Map1718.59NCBI
Ly6g6f
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8203,742,116 - 3,746,984 (+)NCBIGRCr8
mRatBN7.2203,737,459 - 3,742,327 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl203,737,459 - 3,752,248 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx204,436,626 - 4,441,648 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0203,798,679 - 3,803,701 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0204,336,523 - 4,341,546 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0205,071,041 - 5,076,627 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl205,071,062 - 5,076,586 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0207,143,971 - 7,149,557 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4203,801,118 - 3,805,986 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1203,801,344 - 3,806,213 (+)NCBI
Celera204,283,655 - 4,288,523 (-)NCBICelera
Cytogenetic Map20p12NCBI
Ly6g6f
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955437247,094 - 250,695 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955437247,408 - 250,877 (+)NCBIChiLan1.0ChiLan1.0
LOC100969283
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2546,183,226 - 46,195,191 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1642,144,718 - 42,156,680 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0631,367,840 - 31,372,220 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1632,257,047 - 32,267,942 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl632,257,047 - 32,267,909 (+)Ensemblpanpan1.1panPan2
LY6G6F
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1121,185,592 - 1,189,757 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha121,322,247 - 1,325,462 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0121,331,051 - 1,334,270 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl121,331,077 - 1,336,071 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1121,190,377 - 1,201,671 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0121,257,548 - 1,260,761 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0121,324,994 - 1,328,210 (+)NCBIUU_Cfam_GSD_1.0
LOC101960526
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494635,735,761 - 35,745,170 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367271,822,803 - 1,825,563 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0 EnsemblNW_0049367271,816,220 - 1,817,933 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367271,822,803 - 1,825,563 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LY6G6F
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl723,817,640 - 23,822,382 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1723,815,682 - 23,823,306 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
LOC103221756
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11740,313,045 - 40,340,331 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1740,305,738 - 40,316,963 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604431,618,212 - 31,630,506 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ly6g6f
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462475424,500,678 - 24,503,519 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462475424,499,550 - 24,504,048 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in LY6G6F
14 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3 copy number gain See cases [RCV000143497] Chr6:156974..46789291 [GRCh38]
Chr6:156974..46757028 [GRCh37]
Chr6:101974..46864987 [NCBI36]
Chr6:6p25.3-12.3
pathogenic
NM_001003693.3(LY6G6F):c.313T>G (p.Trp105Gly) single nucleotide variant not specified [RCV004266597] Chr6:31707718 [GRCh38]
Chr6:31675495 [GRCh37]
Chr6:6p21.33
uncertain significance
GRCh37/hg19 6p21.33(chr6:31384577-31902308)x3 copy number gain See cases [RCV000448679] Chr6:31384577..31902308 [GRCh37]
Chr6:6p21.33
uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
NM_001003693.3(LY6G6F):c.848A>G (p.Asn283Ser) single nucleotide variant not specified [RCV004297414] Chr6:31710397 [GRCh38]
Chr6:31678174 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.275G>C (p.Trp92Ser) single nucleotide variant not specified [RCV004289784] Chr6:31707680 [GRCh38]
Chr6:31675457 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.398C>T (p.Ala133Val) single nucleotide variant not specified [RCV004291485] Chr6:31707886 [GRCh38]
Chr6:31675663 [GRCh37]
Chr6:6p21.33
uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p22.1-21.32(chr6:28130359-32108367)x3 copy number gain not provided [RCV000745592] Chr6:28130359..32108367 [GRCh37]
Chr6:6p22.1-21.32
uncertain significance
GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367) copy number gain not provided [RCV000767714] Chr6:29455465..81447367 [GRCh37]
Chr6:6p22.1-q14.1
pathogenic
NM_001003693.3(LY6G6F):c.101C>A (p.Pro34Gln) single nucleotide variant not provided [RCV000962151] Chr6:31707506 [GRCh38]
Chr6:31675283 [GRCh37]
Chr6:6p21.33
benign
GRCh37/hg19 6p21.33-21.31(chr6:31036397-34088832)x3 copy number gain not provided [RCV001005791] Chr6:31036397..34088832 [GRCh37]
Chr6:6p21.33-21.31
likely pathogenic
NC_000006.11:g.(?_30695893)_(31937492_?)dup duplication not provided [RCV003107453] Chr6:30695893..31937492 [GRCh37]
Chr6:6p21.33
uncertain significance
NC_000006.11:g.28005012_31683185del deletion Megacolon [RCV001290055] Chr6:28005012..31683185 [GRCh37]
Chr6:6p22.1-21.33
likely pathogenic
GRCh37/hg19 6p21.33(chr6:31384577-31902308) copy number gain not specified [RCV002053564] Chr6:31384577..31902308 [GRCh37]
Chr6:6p21.33
uncertain significance
NC_000006.11:g.(?_30695893)_(36953949_?)dup duplication Proteasome-associated autoinflammatory syndrome 1 [RCV003113679] Chr6:30695893..36953949 [GRCh37]
Chr6:6p21.33-21.2
uncertain significance
NM_001003693.3(LY6G6F):c.112C>T (p.Pro38Ser) single nucleotide variant not specified [RCV004125974] Chr6:31707517 [GRCh38]
Chr6:31675294 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.862C>T (p.Arg288Cys) single nucleotide variant not specified [RCV004181402] Chr6:31710411 [GRCh38]
Chr6:31678188 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.515C>T (p.Ser172Phe) single nucleotide variant not specified [RCV004114456] Chr6:31708003 [GRCh38]
Chr6:31675780 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.850A>T (p.Ile284Phe) single nucleotide variant not specified [RCV004095323] Chr6:31710399 [GRCh38]
Chr6:31678176 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.505C>T (p.Arg169Cys) single nucleotide variant not specified [RCV004116020] Chr6:31707993 [GRCh38]
Chr6:31675770 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.226A>C (p.Lys76Gln) single nucleotide variant not specified [RCV004266141] Chr6:31707631 [GRCh38]
Chr6:31675408 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.497T>G (p.Val166Gly) single nucleotide variant not specified [RCV004252349] Chr6:31707985 [GRCh38]
Chr6:31675762 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.133G>A (p.Glu45Lys) single nucleotide variant not specified [RCV004337022] Chr6:31707538 [GRCh38]
Chr6:31675315 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.416C>A (p.Ser139Tyr) single nucleotide variant not specified [RCV004345388] Chr6:31707904 [GRCh38]
Chr6:31675681 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.118A>G (p.Thr40Ala) single nucleotide variant not specified [RCV004410957] Chr6:31707523 [GRCh38]
Chr6:31675300 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.709C>G (p.Leu237Val) single nucleotide variant not specified [RCV004410958] Chr6:31710088 [GRCh38]
Chr6:31677865 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.787G>T (p.Gly263Trp) single nucleotide variant not specified [RCV004410959] Chr6:31710166 [GRCh38]
Chr6:31677943 [GRCh37]
Chr6:6p21.33
uncertain significance
NM_001003693.3(LY6G6F):c.809C>T (p.Ser270Leu) single nucleotide variant not specified [RCV004410960] Chr6:31710358 [GRCh38]
Chr6:31678135 [GRCh37]
Chr6:6p21.33
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:355
Count of miRNA genes:319
Interacting mature miRNAs:340
Transcripts:ENST00000375832, ENST00000556581
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.

Markers in Region
D6S2760  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37631,673,921 - 31,674,190UniSTSGRCh37
Build 36631,781,900 - 31,782,169RGDNCBI36
Celera633,272,142 - 33,272,408RGD
Cytogenetic Map6p21UniSTS
HuRef631,460,152 - 31,460,408UniSTS


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 1 268 271 13 19
Low 40 488 502 16 727 15 551 4 17 5 413 890 2 12 311
Below cutoff 819 881 603 200 206 128 1764 648 1655 90 443 383 75 597 1080 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001003693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF129756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ496460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL662899 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL670886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL805934 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL844216 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BA000025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC137212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC137213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX248244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR354443 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR753842 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR759787 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KU253635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500429 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500430 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500431 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KY500433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000375832   ⟹   ENSP00000364992
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl631,706,866 - 31,710,679 (+)Ensembl
RefSeq Acc Id: NM_001003693   ⟹   NP_001003693
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38631,706,866 - 31,710,679 (+)NCBI
GRCh37631,674,625 - 31,678,372 (+)NCBI
Build 36631,782,663 - 31,786,351 (+)NCBI Archive
Celera633,272,902 - 33,276,590 (+)RGD
HuRef631,460,902 - 31,464,590 (+)RGD
CHM1_1631,676,801 - 31,680,489 (+)NCBI
T2T-CHM13v2.0631,559,901 - 31,563,714 (+)NCBI
Sequence:
RefSeq Acc Id: NP_001003693   ⟸   NM_001003693
- Peptide Label: precursor
- UniProtKB: Q96QC7 (UniProtKB/Swiss-Prot),   Q7Z5H2 (UniProtKB/Swiss-Prot),   O95869 (UniProtKB/Swiss-Prot),   B0UXB7 (UniProtKB/Swiss-Prot),   Q9NZJ1 (UniProtKB/Swiss-Prot),   Q5SQ64 (UniProtKB/Swiss-Prot),   A0A1L6Z9Z3 (UniProtKB/TrEMBL),   A0A1U9X800 (UniProtKB/TrEMBL),   A0A1U9X801 (UniProtKB/TrEMBL),   A0A1U9X808 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000364992   ⟸   ENST00000375832
Protein Domains
Ig-like   Ig-like V-type

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q5SQ64-F1-model_v2 AlphaFold Q5SQ64 1-297 view protein structure

Promoters
RGD ID:6872590
Promoter ID:EPDNEW_H9460
Type:initiation region
Name:LY6G6F_1
Description:lymphocyte antigen 6 family member G6F
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38631,706,883 - 31,706,943EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13933 AgrOrtholog
COSMIC LY6G6F COSMIC
Ensembl Genes ENSG00000204424 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000239741 UniProtKB/Swiss-Prot
  ENSG00000240008 UniProtKB/Swiss-Prot
  ENSG00000240957 UniProtKB/Swiss-Prot
  ENSG00000241822 UniProtKB/Swiss-Prot
  ENSG00000243003 UniProtKB/Swiss-Prot
  ENSG00000243804 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000375832 ENTREZGENE
  ENST00000375832.5 UniProtKB/Swiss-Prot
  ENST00000383420.4 UniProtKB/Swiss-Prot
  ENST00000442105.2 UniProtKB/Swiss-Prot
  ENST00000446062.2 UniProtKB/Swiss-Prot
  ENST00000447811.2 UniProtKB/Swiss-Prot
  ENST00000453044.2 UniProtKB/Swiss-Prot
  ENST00000455632.2 UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000204424 GTEx
  ENSG00000239741 GTEx
  ENSG00000240008 GTEx
  ENSG00000240957 GTEx
  ENSG00000241822 GTEx
  ENSG00000243003 GTEx
  ENSG00000243804 GTEx
HGNC ID HGNC:13933 ENTREZGENE
Human Proteome Map LY6G6F Human Proteome Map
InterPro Ig-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig-like_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_sub UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ig_V-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  LY6G6d/LY6G6f UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:259215 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 259215 ENTREZGENE
OMIM 611404 OMIM
PANTHER LYMPHOCYTE ANTIGEN 6 COMPLEX LOCUS PROTEIN G6F UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR32286 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam V-set UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA38371 PharmGKB
PROSITE IG_LIKE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SM00409 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF48726 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A1L6Z9Z3 ENTREZGENE, UniProtKB/TrEMBL
  A0A1U9X800 ENTREZGENE, UniProtKB/TrEMBL
  A0A1U9X801 ENTREZGENE, UniProtKB/TrEMBL
  A0A1U9X808 ENTREZGENE, UniProtKB/TrEMBL
  B0UXB7 ENTREZGENE
  LY66F_HUMAN UniProtKB/Swiss-Prot
  O95869 ENTREZGENE
  Q5SQ64 ENTREZGENE
  Q7Z5H2 ENTREZGENE
  Q96QC7 ENTREZGENE
  Q9NZJ1 ENTREZGENE
UniProt Secondary B0UXB7 UniProtKB/Swiss-Prot
  O95869 UniProtKB/Swiss-Prot
  Q7Z5H2 UniProtKB/Swiss-Prot
  Q96QC7 UniProtKB/Swiss-Prot
  Q9NZJ1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-01-31 LY6G6F  lymphocyte antigen 6 family member G6F  LY6G6F  lymphocyte antigen 6 complex, locus G6F  Symbol and/or name change 5135510 APPROVED