TMEM207 (transmembrane protein 207) - Rat Genome Database

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Gene: TMEM207 (transmembrane protein 207) Homo sapiens
Analyze
Symbol: TMEM207
Name: transmembrane protein 207
RGD ID: 1602436
HGNC Page HGNC:33705
Description: Predicted to be located in membrane. Predicted to be integral component of membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: SRSR846; UNQ846
RGD Orthologs
Mouse
Rat
Bonobo
Dog
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
GRCh383190,428,655 - 190,449,901 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl3190,428,655 - 190,449,901 (-)EnsemblGRCh38hg38GRCh38
GRCh373190,146,444 - 190,167,690 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 363191,629,138 - 191,650,359 (-)NCBINCBI36hg18NCBI36
Celera3188,576,940 - 188,598,162 (-)NCBI
Cytogenetic Map3q28NCBI
HuRef3187,546,181 - 187,567,403 (-)NCBIHuRef
CHM1_13190,109,629 - 190,130,847 (-)NCBICHM1_1
T2T-CHM13v2.03193,244,971 - 193,266,217 (-)NCBI
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
atrazine  (EXP)
CGP 52608  (EXP)
gentamycin  (ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Schizophrenia  (IAGP)
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:12975309   PMID:17207965   PMID:19322201   PMID:22226915   PMID:23824909   PMID:26819645   PMID:29164763   PMID:32296183  


Genomics

Comparative Map Data
TMEM207
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh383190,428,655 - 190,449,901 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl3190,428,655 - 190,449,901 (-)EnsemblGRCh38hg38GRCh38
GRCh373190,146,444 - 190,167,690 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 363191,629,138 - 191,650,359 (-)NCBINCBI36hg18NCBI36
Celera3188,576,940 - 188,598,162 (-)NCBI
Cytogenetic Map3q28NCBI
HuRef3187,546,181 - 187,567,403 (-)NCBIHuRef
CHM1_13190,109,629 - 190,130,847 (-)NCBICHM1_1
T2T-CHM13v2.03193,244,971 - 193,266,217 (-)NCBI
Tmem207
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391626,322,543 - 26,345,521 (-)NCBIGRCm39mm39
GRCm39 Ensembl1626,322,406 - 26,345,519 (-)Ensembl
GRCm381626,503,793 - 26,526,771 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1626,503,656 - 26,526,769 (-)EnsemblGRCm38mm10GRCm38
MGSCv371626,503,879 - 26,526,857 (-)NCBIGRCm37mm9NCBIm37
MGSCv361626,504,594 - 26,526,809 (-)NCBImm8
Celera1627,047,228 - 27,070,206 (-)NCBICelera
Cytogenetic Map16B2NCBI
Tmem207
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21174,251,042 - 74,270,180 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl1174,250,815 - 74,270,680 (+)Ensembl
Rnor_6.01177,644,539 - 77,664,616 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1177,644,541 - 77,668,754 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01183,052,504 - 83,072,489 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41176,274,664 - 76,293,867 (+)NCBIRGSC3.4rn4RGSC3.4
Celera1173,168,575 - 73,188,717 (+)NCBICelera
Cytogenetic Map11q22NCBI
TMEM207
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.13196,007,786 - 196,027,636 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl3196,007,786 - 196,027,609 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v03187,453,327 - 187,474,174 (-)NCBIMhudiblu_PPA_v0panPan3
TMEM207
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.13422,423,847 - 22,442,627 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl3422,393,266 - 22,442,497 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha3426,514,767 - 26,535,677 (-)NCBI
ROS_Cfam_1.03422,355,803 - 22,376,233 (-)NCBI
ROS_Cfam_1.0 Ensembl3422,358,809 - 22,376,144 (-)Ensembl
UMICH_Zoey_3.13422,377,094 - 22,398,043 (-)NCBI
UNSW_CanFamBas_1.03422,363,997 - 22,384,856 (-)NCBI
UU_Cfam_GSD_1.03422,605,893 - 22,627,030 (-)NCBI
TMEM207
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl13127,849,883 - 127,871,468 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.113127,849,072 - 127,871,404 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.213137,107,478 - 137,122,525 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TMEM207
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11584,635,774 - 84,657,241 (-)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl1584,636,714 - 84,656,355 (-)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366604158,226,884 - 58,247,895 (-)NCBIVero_WHO_p1.0
Tmem207
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473066,704,180 - 66,722,917 (+)NCBIHetGla_female_1.0hetGla2

Position Markers
UNQ846__5021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh373190,146,399 - 190,147,297UniSTSGRCh37
Build 363191,629,093 - 191,629,991RGDNCBI36
Celera3188,576,895 - 188,577,793RGD
HuRef3187,546,136 - 187,547,034UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:338
Count of miRNA genes:237
Interacting mature miRNAs:243
Transcripts:ENST00000354905
Prediction methods:Microtar, Miranda, Rnahybrid
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 adipose tissue appendage entire extraembryonic component
High
Medium 2 62 2 1
Low 7 6 6 6 6 8 2 1 89 74 12
Below cutoff 78 107 68 42 74 33 436 83 249 39 381 181 10 30 259 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000354905   ⟹   ENSP00000346981
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl3190,428,655 - 190,449,901 (-)Ensembl
RefSeq Acc Id: NM_207316   ⟹   NP_997199
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh383190,428,655 - 190,449,901 (-)NCBI
GRCh373190,146,444 - 190,167,665 (-)RGD
Build 363191,629,138 - 191,650,359 (-)NCBI Archive
Celera3188,576,940 - 188,598,162 (-)RGD
HuRef3187,546,181 - 187,567,403 (-)ENTREZGENE
CHM1_13190,109,629 - 190,130,847 (-)NCBI
T2T-CHM13v2.03193,244,971 - 193,266,217 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_997199 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH71780 (Get FASTA)   NCBI Sequence Viewer  
  AAQ88970 (Get FASTA)   NCBI Sequence Viewer  
  EAW78105 (Get FASTA)   NCBI Sequence Viewer  
  Q6UWW9 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_997199   ⟸   NM_207316
- Peptide Label: precursor
- UniProtKB: Q6UWW9 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000346981   ⟸   ENST00000354905

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q6UWW9-F1-model_v2 AlphaFold Q6UWW9 1-146 view protein structure


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 3q28(chr3:190233992-190498928)x3 copy number gain See cases [RCV000051562] Chr3:190233992..190498928 [GRCh38]
Chr3:189951781..190216717 [GRCh37]
Chr3:191434475..191699411 [NCBI36]
Chr3:3q28
uncertain significance
GRCh38/hg38 3q27.2-29(chr3:185485849-198110178)x1 copy number loss See cases [RCV000051608] Chr3:185485849..198110178 [GRCh38]
Chr3:185203637..197837049 [GRCh37]
Chr3:186686331..199321446 [NCBI36]
Chr3:3q27.2-29
pathogenic
GRCh38/hg38 3q27.2-28(chr3:186204253-192214251)x1 copy number loss See cases [RCV000051609] Chr3:186204253..192214251 [GRCh38]
Chr3:185922042..191932040 [GRCh37]
Chr3:187404736..193414734 [NCBI36]
Chr3:3q27.2-28
pathogenic
GRCh38/hg38 3q27.3-29(chr3:187446231-195029133)x1 copy number loss See cases [RCV000051610] Chr3:187446231..195029133 [GRCh38]
Chr3:187164019..194749862 [GRCh37]
Chr3:188646713..196231151 [NCBI36]
Chr3:3q27.3-29
pathogenic
GRCh38/hg38 3q27.3-28(chr3:187446231-190839052)x1 copy number loss See cases [RCV000051611] Chr3:187446231..190839052 [GRCh38]
Chr3:187164019..190556841 [GRCh37]
Chr3:188646713..192039535 [NCBI36]
Chr3:3q27.3-28
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 3q26.32-29(chr3:178411707-198110319)x3 copy number gain See cases [RCV000051736] Chr3:178411707..198110319 [GRCh38]
Chr3:178129495..197837190 [GRCh37]
Chr3:179612189..199321587 [NCBI36]
Chr3:3q26.32-29
pathogenic
GRCh38/hg38 3q27.2-29(chr3:185920880-198110319)x3 copy number gain See cases [RCV000051738] Chr3:185920880..198110319 [GRCh38]
Chr3:185638668..197837190 [GRCh37]
Chr3:187121362..199321587 [NCBI36]
Chr3:3q27.2-29
pathogenic
GRCh38/hg38 3q28-29(chr3:189265371-198110178)x3 copy number gain See cases [RCV000051739] Chr3:189265371..198110178 [GRCh38]
Chr3:188983160..197837049 [GRCh37]
Chr3:190465854..199321446 [NCBI36]
Chr3:3q28-29
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
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 3q26.2-29(chr3:168167568-198110178)x3 copy number gain See cases [RCV000137106] Chr3:168167568..198110178 [GRCh38]
Chr3:167885356..197837049 [GRCh37]
Chr3:169368050..199321446 [NCBI36]
Chr3:3q26.2-29
pathogenic
GRCh38/hg38 3q26.32-29(chr3:176439911-198118383)x3 copy number gain See cases [RCV000138009] Chr3:176439911..198118383 [GRCh38]
Chr3:176157699..197845254 [GRCh37]
Chr3:177640393..199329651 [NCBI36]
Chr3:3q26.32-29
pathogenic|likely benign
GRCh38/hg38 3q27.3-29(chr3:186765148-194409416)x1 copy number loss See cases [RCV000137962] Chr3:186765148..194409416 [GRCh38]
Chr3:186482937..194130145 [GRCh37]
Chr3:187965631..195611434 [NCBI36]
Chr3:3q27.3-29
pathogenic|likely benign
GRCh38/hg38 3q26.32-29(chr3:176168525-198118383)x3 copy number gain See cases [RCV000138662] Chr3:176168525..198118383 [GRCh38]
Chr3:175886313..197845254 [GRCh37]
Chr3:177369007..199329651 [NCBI36]
Chr3:3q26.32-29
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
GRCh38/hg38 3q26.33-28(chr3:181138664-192512023)x1 copy number loss See cases [RCV000142019] Chr3:181138664..192512023 [GRCh38]
Chr3:180856452..192229812 [GRCh37]
Chr3:182339146..193712506 [NCBI36]
Chr3:3q26.33-28
pathogenic
GRCh38/hg38 3q26.1-29(chr3:166137209-198125115)x3 copy number gain See cases [RCV000143694] Chr3:166137209..198125115 [GRCh38]
Chr3:165854997..197851986 [GRCh37]
Chr3:167337691..199336383 [NCBI36]
Chr3:3q26.1-29
pathogenic
GRCh38/hg38 3q27.3-28(chr3:187434386-192142942)x1 copy number loss See cases [RCV000143464] Chr3:187434386..192142942 [GRCh38]
Chr3:187152174..191860731 [GRCh37]
Chr3:188634868..193343425 [NCBI36]
Chr3:3q27.3-28
likely pathogenic
GRCh37/hg19 3q28-29(chr3:189608636-197532175)x1 copy number loss 3q28q29 deletion syndrome [RCV001786535] Chr3:189608636..197532175 [GRCh37]
Chr3:3q28-29
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 3q27.3-28(chr3:186291045-191037240)x1 copy number loss See cases [RCV000240447] Chr3:186291045..191037240 [GRCh37]
Chr3:3q27.3-28
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 3q26.33-29(chr3:181911498-197851986)x4 copy number gain See cases [RCV000446732] Chr3:181911498..197851986 [GRCh37]
Chr3:3q26.33-29
pathogenic
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) copy number gain See cases [RCV000512358] Chr3:61892..197851986 [GRCh37]
Chr3:3p26.3-q29
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 3q26.33-29(chr3:182539234-197851986)x3 copy number gain not provided [RCV000682336] Chr3:182539234..197851986 [GRCh37]
Chr3:3q26.33-29
pathogenic
GRCh37/hg19 3q26.33-28(chr3:182650681-191275809)x1 copy number loss not provided [RCV000682337] Chr3:182650681..191275809 [GRCh37]
Chr3:3q26.33-28
pathogenic
GRCh37/hg19 3q27.1-29(chr3:184003967-197851986)x3 copy number gain not provided [RCV000682339] Chr3:184003967..197851986 [GRCh37]
Chr3:3q27.1-29
pathogenic
GRCh37/hg19 3q28-29(chr3:187913567-197851986)x3 copy number gain not provided [RCV000682344] Chr3:187913567..197851986 [GRCh37]
Chr3:3q28-29
pathogenic
GRCh37/hg19 3q27.3-29(chr3:186374365-197851986)x3 copy number gain not provided [RCV000682341] Chr3:186374365..197851986 [GRCh37]
Chr3:3q27.3-29
pathogenic
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
NC_000003.12:g.(?_187222939)_(194312782_?)del deletion Schizophrenia [RCV000754274] Chr3:187222939..194312782 [GRCh38]
Chr3:3q27.3-29
likely pathogenic
GRCh37/hg19 3q26.31-29(chr3:173281266-197838262)x3 copy number gain not provided [RCV000742968] Chr3:173281266..197838262 [GRCh37]
Chr3:3q26.31-29
pathogenic
GRCh37/hg19 3q27.3-29(chr3:186374671-197838262)x3 copy number gain not provided [RCV000743037] Chr3:186374671..197838262 [GRCh37]
Chr3:3q27.3-29
pathogenic
GRCh37/hg19 3q28-29(chr3:189101446-197838262)x1 copy number loss not provided [RCV000743049] Chr3:189101446..197838262 [GRCh37]
Chr3:3q28-29
pathogenic
GRCh37/hg19 3q28-29(chr3:188386566-197838262)x3 copy number gain See cases [RCV000790566] Chr3:188386566..197838262 [GRCh37]
Chr3:3q28-29
pathogenic
GRCh37/hg19 3q28(chr3:190110813-190149597)x1 copy number loss not provided [RCV000848390] Chr3:190110813..190149597 [GRCh37]
Chr3:3q28
uncertain significance
GRCh37/hg19 3q28(chr3:190110813-190153916)x1 copy number loss not provided [RCV000849859] Chr3:190110813..190153916 [GRCh37]
Chr3:3q28
uncertain significance
GRCh37/hg19 3q26.2-28(chr3:169617690-190593854)x3 copy number gain not provided [RCV001005487] Chr3:169617690..190593854 [GRCh37]
Chr3:3q26.2-28
pathogenic
GRCh37/hg19 3q28(chr3:189906773-190473124)x3 copy number gain See cases [RCV001194521] Chr3:189906773..190473124 [GRCh37]
Chr3:3q28
uncertain significance
NC_000003.11:g.(?_189526041)_(192126012_?)dup duplication not provided [RCV001987827] Chr3:189526041..192126012 [GRCh37]
Chr3:3q28
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:33705 AgrOrtholog
COSMIC TMEM207 COSMIC
Ensembl Genes ENSG00000198398 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000346981 ENTREZGENE
  ENSP00000346981.2 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000354905 ENTREZGENE
  ENST00000354905.3 UniProtKB/Swiss-Prot
GTEx ENSG00000198398 GTEx
HGNC ID HGNC:33705 ENTREZGENE
Human Proteome Map TMEM207 Human Proteome Map
InterPro TMEM207 UniProtKB/Swiss-Prot
KEGG Report hsa:131920 UniProtKB/Swiss-Prot
NCBI Gene 131920 ENTREZGENE
OMIM 614786 OMIM
PANTHER PTHR36467 UniProtKB/Swiss-Prot
PharmGKB PA162406407 PharmGKB
UniProt Q6UWW9 ENTREZGENE, UniProtKB/Swiss-Prot