 Gene-Chemical Interaction Annotations | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Gene Ontology Annotations |
Welcome {{ username}}
Message Center
{{ messageCount }} Messages
Watched Genes
{{$index + 1}}. {{ watchedObject.symbol }} (RGD ID:{{watchedObject.rgdId}})
Watched Ontology Terms
{{gene.symbol}}: {{ gene.description }}
Save List to My RGD
| Create Name: | |
| Description: |
|
| Save what matters to you |
| {{ loginError }} |
| Sign in with your RGD account |
| Create New Account | Recover Password |
{{ watchLinkText }}
Select categories you would like to watch. Updates to this gene will be send to {{ username }}
Analyze GeneStrainQTL List |
 Gene Annotator (Functional Annotation) unavailable |
 Gene Annotator (Annotation Distribution) unavailable |
 Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable |
Gene Annotator (Functional Annotation) |
Gene Annotator (Annotation Distribution) |
Variant Visualizer (Genomic Variants) |
 InterViewer (Protein-Protein Interactions) unavailable |
 Gviewer (Genome Viewer) unavailable |
 Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable |
InterViewer (Protein-Protein Interactions) |
GViewer (Genome Viewer) |
Variant Visualizer (Damaging Variants) |
 Gene Annotator (Annotation Comparison) unavailable |
 OLGA (Gene List Generator) unavailable |
 |
Gene Annotator (Annotation Comparison) |
OLGA (Gene List Generator) |
Excel (Download) |
 MOET (Multi-Ontology Enrichement) unavailable |
 GOLF (Gene-Ortholog Location Finder) unavailable |
|
MOET (Multi-Ontology Enrichement) |
GOLF (Gene-Ortholog Location Finder) |
Gene Ontology AnnotationsDisease AnnotationsGene-Chemical Interaction Annotations
|
|
|
Gene Ontology AnnotationsReferences - curatedReferences - uncuratedGenomics
Comparative Map Data| TMEM213 (Homo sapiens - human) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Tmem213 (Mus musculus - house mouse) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Tmem213 (Rattus norvegicus - Norway rat) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Tmem213 (Chinchilla lanigera - long-tailed chinchilla) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TMEM213 (Pan paniscus - bonobo/pygmy chimpanzee) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TMEM213 (Canis lupus familiaris - dog) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Tmem213 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| TMEM213 (Sus scrofa - pig) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Position Markers| D8S2279 |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| D11S3430 |
|
miRNA Target Status
Predicted Target Of
| 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
Sequence
Nucleotide Sequences| RefSeq Transcripts | NM_001085429 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
| XM_005250167 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| GenBank Nucleotide | AC018663 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
| AI672404 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK055760 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AK055841 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| AW771283 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BC058028 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| BC131697 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| CH236950 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| CH471070 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
| DA626421 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
Reference Sequences
| RefSeq Acc Id: | NM_001085429 ⟹ NP_001078898 | |||||||||||||||||||||||||||||||||||||||
| RefSeq Status: | VALIDATED | |||||||||||||||||||||||||||||||||||||||
| Type: | CODING | |||||||||||||||||||||||||||||||||||||||
| Position: |
|
|||||||||||||||||||||||||||||||||||||||
| Sequence: |
AGAGTTGCTTTCCAGCTCCTGCAGGTGGGAGTCGACTCACCTGCAGCAGGCACTCGGCACAACThide sequence |
| RefSeq Acc Id: | XM_005250167 ⟹ XP_005250224 | ||||||||||||||
| RefSeq Status: | |||||||||||||||
| Type: | CODING | ||||||||||||||
| Position: |
|
||||||||||||||
| Sequence: |
GGACTACAGGGTGAGCCCCCATGCCCAACCTCAAATGCCATTTTCTTCTTGAAGCATCCCATCAhide sequence |
Protein Sequences| Protein RefSeqs | NP_001078898 | (Get FASTA) | NCBI Sequence Viewer |
| XP_005250224 | (Get FASTA) | NCBI Sequence Viewer | |
| GenBank Protein | A2RRL7 | (Get FASTA) | NCBI Sequence Viewer |
| AAI31698 | (Get FASTA) | NCBI Sequence Viewer | |
| EAL24042 | (Get FASTA) | NCBI Sequence Viewer | |
| EAW83898 | (Get FASTA) | NCBI Sequence Viewer |
Reference Sequences
| RefSeq Acc Id: | NP_001078898 ⟸ NM_001085429 |
| - Peptide Label: | precursor |
| - UniProtKB: | A2RRL7 (UniProtKB/Swiss-Prot) |
| - Sequence: |
MQRLPAATRATLILSLAFASLHSACSAEASSSNSSSLTAHHPDPGTLEQCLNVDFCPQAARCCRhide sequence |
| RefSeq Acc Id: | XP_005250224 ⟸ XM_005250167 |
| - Peptide Label: | isoform X1 |
| - UniProtKB: | A2RRL7 (UniProtKB/Swiss-Prot) |
| - Sequence: |
MVFPPNTQHKFTSGRVAFQLLQVGVDSPAAGTRHNSAGPAHLHRALSTASSMQRLPAATRATLIhide sequence |
Promoters| RGD ID: | 7212027 | |||||||||
| Promoter ID: | EPDNEW_H11759 | |||||||||
| Type: | initiation region | |||||||||
| Name: | TMEM213_1 | |||||||||
| Description: | transmembrane protein 213 | |||||||||
| SO ACC ID: | SO:0000170 | |||||||||
| Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
| Experiment Methods: | Single-end sequencing. | |||||||||
| Position: |
|
Clinical Variants| Name | Type | Condition(s) | Position(s) | Clinical significance |
| GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 | copy number gain | Cleft palate, isolated [RCV000050876]|See cases [RCV000050876] | Chr7:129310166..159282390 [GRCh38] Chr7:128950007..159075079 [GRCh37] Chr7:128737243..158767840 [NCBI36] Chr7:7q32.1-36.3 |
pathogenic |
| GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|See cases [RCV000051101] | Chr7:132850196..159325876 [GRCh38] Chr7:132534956..159118566 [GRCh37] Chr7:132185496..158811327 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
| GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 | copy number loss | Ambiguous genitalia [RCV000052250]|See cases [RCV000052250] | Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh38/hg38 7q34(chr7:138795539-140364913)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053550]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053550]|See cases [RCV000053550] | Chr7:138795539..140364913 [GRCh38] Chr7:138480284..140064713 [GRCh37] Chr7:138130824..139711182 [NCBI36] Chr7:7q34 |
uncertain significance |
| GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 | copy number gain | Global developmental delay [RCV000053576]|See cases [RCV000053576] | Chr7:136309982..159307523 [GRCh38] Chr7:135994730..159100212 [GRCh37] Chr7:135645270..158792973 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
| GRCh38/hg38 7q32.3-36.1(chr7:132023155-149309794)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|See cases [RCV000054172] | Chr7:132023155..149309794 [GRCh38] Chr7:131707914..149006885 [GRCh37] Chr7:131358454..148637818 [NCBI36] Chr7:7q32.3-36.1 |
pathogenic |
| GRCh38/hg38 7q33-35(chr7:135414108-144140219)x1 | copy number loss | Obesity [RCV000054173]|See cases [RCV000054173] | Chr7:135414108..144140219 [GRCh38] Chr7:135098857..143837312 [GRCh37] Chr7:134749397..143468245 [NCBI36] Chr7:7q33-35 |
pathogenic |
| GRCh38/hg38 7q33-34(chr7:137741740-139688885)x1 | copy number loss | Cleft uvula [RCV000054174]|See cases [RCV000054174] | Chr7:137741740..139688885 [GRCh38] Chr7:137426486..139373631 [GRCh37] Chr7:137077026..139024171 [NCBI36] Chr7:7q33-34 |
pathogenic |
| GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 | copy number loss | See cases [RCV000135401] | Chr7:54185..159282390 [GRCh38] Chr7:54185..159075079 [GRCh37] Chr7:149268..158767840 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh38/hg38 7q33-36.2(chr7:137751200-154815582)x3 | copy number gain | See cases [RCV000136592] | Chr7:137751200..154815582 [GRCh38] Chr7:137435946..154607292 [GRCh37] Chr7:137086486..154238225 [NCBI36] Chr7:7q33-36.2 |
pathogenic |
| GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 | copy number gain | See cases [RCV000136717] | Chr7:97419852..158923762 [GRCh38] Chr7:97049164..158716453 [GRCh37] Chr7:96887100..158409214 [NCBI36] Chr7:7q21.3-36.3 |
pathogenic |
| GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 | copy number loss | See cases [RCV000138120] | Chr7:134666829..158591882 [GRCh38] Chr7:134351581..158384574 [GRCh37] Chr7:134002121..158077335 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
| GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 | copy number gain | See cases [RCV000138847] | Chr7:121863759..159335865 [GRCh38] Chr7:121503813..159128555 [GRCh37] Chr7:121291049..158821316 [NCBI36] Chr7:7q31.32-36.3 |
pathogenic |
| GRCh38/hg38 7q33-36.1(chr7:135017687-148807400)x1 | copy number loss | See cases [RCV000138903] | Chr7:135017687..148807400 [GRCh38] Chr7:134702438..148504492 [GRCh37] Chr7:134352978..148135425 [NCBI36] Chr7:7q33-36.1 |
pathogenic |
| GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 | copy number gain | See cases [RCV000139654] | Chr7:132444095..159335866 [GRCh38] Chr7:132128854..159128556 [GRCh37] Chr7:131779394..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
| GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 | copy number gain | See cases [RCV000141413] | Chr7:115459015..159325817 [GRCh38] Chr7:115099069..159118507 [GRCh37] Chr7:114886305..158811268 [NCBI36] Chr7:7q31.2-36.3 |
pathogenic |
| GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 | copy number gain | See cases [RCV000142802] | Chr7:131228764..159335866 [GRCh38] Chr7:130913523..159128556 [GRCh37] Chr7:130564063..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
| GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 | copy number gain | See cases [RCV000143754] | Chr7:131171478..159327017 [GRCh38] Chr7:130856237..159119707 [GRCh37] Chr7:130506777..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
| GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 | copy number gain | See cases [RCV000143707] | Chr7:132438072..159327017 [GRCh38] Chr7:132122831..159119707 [GRCh37] Chr7:131773371..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
| NM_020632.3(ATP6V0A4):c.-137C>T | single nucleotide variant | Distal Renal Tubular Acidosis, Recessive [RCV000277686] | Chr7:138798050 [GRCh38] Chr7:138482795 [GRCh37] Chr7:7q34 |
likely benign |
| NM_020632.3(ATP6V0A4):c.-169C>T | single nucleotide variant | Distal Renal Tubular Acidosis, Recessive [RCV000332752] | Chr7:138798082 [GRCh38] Chr7:138482827 [GRCh37] Chr7:7q34 |
likely benign |
| NM_020632.3(ATP6V0A4):c.-248G>A | single nucleotide variant | Distal Renal Tubular Acidosis, Recessive [RCV000329140] | Chr7:138798161 [GRCh38] Chr7:138482906 [GRCh37] Chr7:7q34 |
uncertain significance |
| NM_020632.3(ATP6V0A4):c.-240C>G | single nucleotide variant | Distal Renal Tubular Acidosis, Recessive [RCV000274134] | Chr7:138798153 [GRCh38] Chr7:138482898 [GRCh37] Chr7:7q34 |
uncertain significance |
| NM_020632.3(ATP6V0A4):c.-136C>T | single nucleotide variant | Distal Renal Tubular Acidosis, Recessive [RCV000353643] | Chr7:138798049 [GRCh38] Chr7:138482794 [GRCh37] Chr7:7q34 |
uncertain significance |
| NM_020632.3(ATP6V0A4):c.-206G>A | single nucleotide variant | Distal Renal Tubular Acidosis, Recessive [RCV000387041] | Chr7:138798119 [GRCh38] Chr7:138482864 [GRCh37] Chr7:7q34 |
uncertain significance |
| GRCh37/hg19 7q33-36.3(chr7:137589621-159119707)x3 | copy number gain | See cases [RCV000449264] | Chr7:137589621..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
| TMEM106B-BRAF fusion | deletion | Pleomorphic xanthoastrocytoma [RCV000454357] | Chr7:12258147..140494267 [GRCh37] Chr7:7p21.3-q34 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 | copy number loss | See cases [RCV000446044] | Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7q32.3-34(chr7:131642114-139107211)x1 | copy number loss | See cases [RCV000448552] | Chr7:131642114..139107211 [GRCh37] Chr7:7q32.3-34 |
pathogenic |
| GRCh37/hg19 7q33-36.3(chr7:133799185-159119707)x1 | copy number loss | See cases [RCV000448836] | Chr7:133799185..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
| GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 | copy number gain | See cases [RCV000447709] | Chr7:98969247..159119707 [GRCh37] Chr7:7q22.1-36.3 |
pathogenic |
| GRCh37/hg19 7q32.1-34(chr7:127295698-139524358)x1 | copy number loss | See cases [RCV000447722] | Chr7:127295698..139524358 [GRCh37] Chr7:7q32.1-34 |
pathogenic |
| GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 | copy number gain | See cases [RCV000447956] | Chr7:128276078..159119707 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) | copy number gain | See cases [RCV000510686] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7q33-36.3(chr7:136758593-159119707)x3 | copy number gain | See cases [RCV000510490] | Chr7:136758593..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 | copy number gain | See cases [RCV000511549] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1 | copy number loss | See cases [RCV000511889] | Chr7:137917376..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
| GRCh37/hg19 7q33-34(chr7:137434852-140349546)x3 | copy number gain | See cases [RCV000512176] | Chr7:137434852..140349546 [GRCh37] Chr7:7q33-34 |
uncertain significance |
| GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 | copy number gain | not provided [RCV000682911] | Chr7:98693388..159119707 [GRCh37] Chr7:7q22.1-36.3 |
pathogenic |
| Single allele | complex | Renal transitional cell carcinoma [RCV000754611] | Chr7:129367205..140482957 [GRCh37] Chr7:7q32.2-34 |
likely pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 | copy number gain | not provided [RCV000746278] | Chr7:10704..159122532 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 | copy number gain | not provided [RCV000746280] | Chr7:44935..159126310 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7q34(chr7:138323516-138673567)x3 | copy number gain | not provided [RCV000747066] | Chr7:138323516..138673567 [GRCh37] Chr7:7q34 |
benign |
| GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 | copy number gain | not provided [RCV000848126] | Chr7:10365..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
| GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220) | copy number gain | not provided [RCV000767558] | Chr7:128312450..159119220 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
| GRCh37/hg19 7q33-34(chr7:137848980-138897699)x3 | copy number gain | not provided [RCV000846058] | Chr7:137848980..138897699 [GRCh37] Chr7:7q33-34 |
uncertain significance |
| GRCh37/hg19 7q33-34(chr7:137675423-139084024)x1 | copy number loss | not provided [RCV000846410] | Chr7:137675423..139084024 [GRCh37] Chr7:7q33-34 |
uncertain significance |
| GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3 | copy number gain | not provided [RCV000849569] | Chr7:130592554..159119707 [GRCh37] Chr7:7q32.3-36.3 |
pathogenic |
Additional Information
External Database Links| Database | Acc Id | Source(s) |
| AGR Gene | HGNC:27220 | AgrOrtholog |
| COSMIC | TMEM213 | COSMIC |
| Ensembl Genes | ENSG00000214128 | ENTREZGENE, UniProtKB/Swiss-Prot |
| Ensembl Protein | ENSP00000380727 | UniProtKB/Swiss-Prot |
| ENSP00000390407 | ENTREZGENE, UniProtKB/Swiss-Prot | |
| ENSP00000393891 | UniProtKB/Swiss-Prot | |
| ENSP00000401570 | UniProtKB/Swiss-Prot | |
| Ensembl Transcript | ENST00000397602 | UniProtKB/Swiss-Prot |
| ENST00000413208 | UniProtKB/Swiss-Prot | |
| ENST00000442682 | ENTREZGENE, UniProtKB/Swiss-Prot | |
| ENST00000458494 | UniProtKB/Swiss-Prot | |
| GTEx | ENSG00000214128 | GTEx |
| HGNC ID | HGNC:27220 | ENTREZGENE |
| Human Proteome Map | TMEM213 | Human Proteome Map |
| InterPro | TMEM213 | UniProtKB/Swiss-Prot |
| KEGG Report | hsa:155006 | UniProtKB/Swiss-Prot |
| NCBI Gene | 155006 | ENTREZGENE |
| PANTHER | PTHR36293 | UniProtKB/Swiss-Prot |
| Pfam | TMEM213 | UniProtKB/Swiss-Prot |
| PharmGKB | PA162406494 | PharmGKB |
| UniGene | Hs.567729 | ENTREZGENE |
| UniProt | A2RRL7 | ENTREZGENE, UniProtKB/Swiss-Prot |
| UniProt Secondary | A4D1R3 | UniProtKB/Swiss-Prot |
| C9JH49 | UniProtKB/Swiss-Prot | |
| C9JX41 | UniProtKB/Swiss-Prot | |
| C9K0P0 | UniProtKB/Swiss-Prot |
 |
| More on TMEM213 | |
|
Alliance Gene |
|
NCBI Gene |
|
Ensembl Gene |
|
|
JBrowse: hg19 hg38 |
|
HGNC Report |
|
NCBI Genome Data Viewer |
| CRRD Object Information | |
| CRRD ID: | 2293900 |
| Created: | 2008-06-20 |
| Species: | Homo sapiens |
| Last Modified: | 2019-11-26 |
| Status: | ACTIVE |
