TMEM238 (transmembrane protein 238) - Rat Genome Database

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Gene: TMEM238 (transmembrane protein 238) Homo sapiens
Analyze
Symbol: TMEM238
Name: transmembrane protein 238
RGD ID: 5488447
HGNC Page HGNC:40042
Description: Predicted to be located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: hypothetical protein LOC388564
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
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
GRCh381955,379,244 - 55,384,292 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1955,379,244 - 55,384,292 (-)EnsemblGRCh38hg38GRCh38
GRCh371955,890,612 - 55,895,660 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361960,582,425 - 60,589,054 (-)NCBINCBI36Build 36hg18NCBI36
Celera1952,931,435 - 52,936,450 (-)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1952,212,647 - 52,217,211 (-)NCBIHuRef
CHM1_11955,884,156 - 55,889,200 (-)NCBICHM1_1
T2T-CHM13v2.01958,474,730 - 58,479,780 (-)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
membrane  (IEA)

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:26760575  


Genomics

Comparative Map Data
TMEM238
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381955,379,244 - 55,384,292 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1955,379,244 - 55,384,292 (-)EnsemblGRCh38hg38GRCh38
GRCh371955,890,612 - 55,895,660 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361960,582,425 - 60,589,054 (-)NCBINCBI36Build 36hg18NCBI36
Celera1952,931,435 - 52,936,450 (-)NCBICelera
Cytogenetic Map19q13.42NCBI
HuRef1952,212,647 - 52,217,211 (-)NCBIHuRef
CHM1_11955,884,156 - 55,889,200 (-)NCBICHM1_1
T2T-CHM13v2.01958,474,730 - 58,479,780 (-)NCBIT2T-CHM13v2.0
Tmem238
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3974,787,784 - 4,792,559 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl74,787,556 - 4,792,655 (-)EnsemblGRCm39 Ensembl
GRCm3874,784,785 - 4,789,560 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl74,784,557 - 4,789,656 (-)EnsemblGRCm38mm10GRCm38
MGSCv3774,736,387 - 4,741,162 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3674,387,796 - 4,392,647 (-)NCBIMGSCv36mm8
Celera74,514,542 - 4,519,317 (-)NCBICelera
Cytogenetic Map7A1NCBI
cM Map72.77NCBI
Tmem238
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8178,085,880 - 78,091,272 (+)NCBIGRCr8
mRatBN7.2169,057,083 - 69,062,477 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl169,056,805 - 69,076,133 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx174,402,122 - 74,407,514 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0182,966,433 - 82,971,825 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0176,115,266 - 76,120,666 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0172,623,409 - 72,629,606 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0175,905,173 - 75,910,608 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4167,774,020 - 67,778,924 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera168,062,051 - 68,068,318 (-)NCBICelera
Cytogenetic Map1q12NCBI
Tmem238
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_004955442100,719 - 107,640 (+)NCBIChiLan1.0ChiLan1.0
TMEM238
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22061,517,658 - 61,522,858 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11963,246,282 - 63,253,167 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01952,422,284 - 52,428,838 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
TMEM238
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11102,306,235 - 102,309,572 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1102,306,775 - 102,307,302 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1102,363,243 - 102,366,280 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01102,959,735 - 102,962,772 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1102,959,975 - 102,960,502 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11102,597,020 - 102,600,057 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01102,309,036 - 102,312,073 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01103,072,285 - 103,075,322 (+)NCBIUU_Cfam_GSD_1.0
LOC101971213
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344114,772,601 - 114,784,385 (+)NCBIHiC_Itri_2
SpeTri2.0NW_0049365012,870,570 - 2,876,250 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TMEM238
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl659,554,323 - 59,554,859 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1659,551,569 - 59,556,013 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
TMEM238
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1647,980,897 - 47,987,078 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl647,985,126 - 47,985,653 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666045626,474 - 632,138 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in TMEM238
12 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3 copy number gain See cases [RCV000050883] Chr19:50191219..58535818 [GRCh38]
Chr19:50694476..59047185 [GRCh37]
Chr19:55386288..63738997 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3 copy number gain See cases [RCV000052915] Chr19:47929575..58572206 [GRCh38]
Chr19:48432832..59083573 [GRCh37]
Chr19:53124644..63775385 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3 copy number gain See cases [RCV000052925] Chr19:49907832..58557889 [GRCh38]
Chr19:50411089..59069256 [GRCh37]
Chr19:55102901..63761068 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3 copy number gain See cases [RCV000052926] Chr19:51141518..58539965 [GRCh38]
Chr19:51644775..59051332 [GRCh37]
Chr19:56336587..63743144 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3 copy number gain See cases [RCV000052914] Chr19:47908540..58539965 [GRCh38]
Chr19:48411797..59051332 [GRCh37]
Chr19:53103609..63743144 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3 copy number gain See cases [RCV000134139] Chr19:52955056..58581203 [GRCh38]
Chr19:53458309..59092570 [GRCh37]
Chr19:58150121..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3 copy number gain See cases [RCV000135843] Chr19:50152520..58581203 [GRCh38]
Chr19:50655777..59092570 [GRCh37]
Chr19:55347589..63784382 [NCBI36]
Chr19:19q13.33-13.43		 pathogenic
GRCh38/hg38 19q13.42-13.43(chr19:55048514-56972458)x3 copy number gain See cases [RCV000138139] Chr19:55048514..56972458 [GRCh38]
Chr19:55595687..57483826 [GRCh37]
Chr19:60251694..62175638 [NCBI36]
Chr19:19q13.42-13.43		 likely pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3 copy number gain See cases [RCV000142008] Chr19:52143873..58445521 [GRCh38]
Chr19:52647126..58956888 [GRCh37]
Chr19:57338938..63648700 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.42-13.43(chr19:55037146-56982033)x3 copy number gain See cases [RCV000142245] Chr19:55037146..56982033 [GRCh38]
Chr19:55548514..57493401 [GRCh37]
Chr19:60240326..62185213 [NCBI36]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3 copy number gain See cases [RCV000445925] Chr19:50489390..59095359 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:55549385-57489784)x3 copy number gain See cases [RCV000510290] Chr19:55549385..57489784 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55844155-57408007)x3 copy number gain See cases [RCV000511123] Chr19:55844155..57408007 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55779884-56896574)x1 copy number loss not provided [RCV000684089] Chr19:55779884..56896574 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3 copy number gain not provided [RCV000684095] Chr19:54196216..58759679 [GRCh37]
Chr19:19q13.42-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3 copy number gain See cases [RCV000134174] Chr19:52612432..58581203 [GRCh38]
Chr19:53115685..59092570 [GRCh37]
Chr19:57807497..63784382 [NCBI36]
Chr19:19q13.41-13.43		 pathogenic
GRCh38/hg38 19q13.42(chr19:55066790-55789870)x3 copy number gain See cases [RCV000142067] Chr19:55066790..55789870 [GRCh38]
Chr19:55578158..56301236 [GRCh37]
Chr19:60269970..60993048 [NCBI36]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54344821-58956888)x3 copy number gain See cases [RCV000448186] Chr19:54344821..58956888 [GRCh37]
Chr19:19q13.42-13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
NM_001190764.2(TMEM238):c.40C>T (p.Pro14Ser) single nucleotide variant not provided [RCV000948490] Chr19:55384220 [GRCh38]
Chr19:55895588 [GRCh37]
Chr19:19q13.42		 benign
NM_001190764.2(TMEM238):c.397C>G (p.Pro133Ala) single nucleotide variant Inborn genetic diseases [RCV003276280] Chr19:55383863 [GRCh38]
Chr19:55895231 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42(chr19:55642778-55932200)x3 copy number gain not provided [RCV002473753] Chr19:55642778..55932200 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3 copy number gain not provided [RCV001259944] Chr19:48463931..57095254 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
GRCh37/hg19 19q13.42-13.43(chr19:55247893-56503347)x1 copy number loss not provided [RCV001834407] Chr19:55247893..56503347 [GRCh37]
Chr19:19q13.42-13.43		 likely pathogenic
NM_001190764.2(TMEM238):c.392A>G (p.Gln131Arg) single nucleotide variant Inborn genetic diseases [RCV003276279] Chr19:55383868 [GRCh38]
Chr19:55895236 [GRCh37]
Chr19:19q13.42		 uncertain significance
NM_001190764.2(TMEM238):c.436G>A (p.Ala146Thr) single nucleotide variant Inborn genetic diseases [RCV003276282] Chr19:55383824 [GRCh38]
Chr19:55895192 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:55434660-56463734)x1 copy number loss not provided [RCV002279751] Chr19:55434660..56463734 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
NM_001190764.2(TMEM238):c.44C>T (p.Pro15Leu) single nucleotide variant Inborn genetic diseases [RCV002689677] Chr19:55384216 [GRCh38]
Chr19:55895584 [GRCh37]
Chr19:19q13.42		 uncertain significance
NM_001190764.2(TMEM238):c.32A>G (p.Gln11Arg) single nucleotide variant Inborn genetic diseases [RCV002907402] Chr19:55384228 [GRCh38]
Chr19:55895596 [GRCh37]
Chr19:19q13.42		 uncertain significance
NM_001190764.2(TMEM238):c.430G>T (p.Ala144Ser) single nucleotide variant Inborn genetic diseases [RCV002666368] Chr19:55383830 [GRCh38]
Chr19:55895198 [GRCh37]
Chr19:19q13.42		 uncertain significance
NM_001190764.2(TMEM238):c.238T>C (p.Phe80Leu) single nucleotide variant Inborn genetic diseases [RCV003195795] Chr19:55384022 [GRCh38]
Chr19:55895390 [GRCh37]
Chr19:19q13.42		 uncertain significance
NM_001190764.2(TMEM238):c.302T>C (p.Leu101Pro) single nucleotide variant Inborn genetic diseases [RCV003174792] Chr19:55383958 [GRCh38]
Chr19:55895326 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3 copy number gain not provided [RCV003485200] Chr19:49625130..57647352 [GRCh37]
Chr19:19q13.33-13.43		 likely pathogenic
NM_001190764.2(TMEM238):c.59C>T (p.Ala20Val) single nucleotide variant Inborn genetic diseases [RCV003185817] Chr19:55384201 [GRCh38]
Chr19:55895569 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.33-13.43(chr19:50740074-59097160)x3 copy number gain not provided [RCV000740208] Chr19:50740074..59097160 [GRCh37]
Chr19:19q13.33-13.43		 pathogenic
NM_001190764.2(TMEM238):c.415A>G (p.Arg139Gly) single nucleotide variant Inborn genetic diseases [RCV003276281] Chr19:55383845 [GRCh38]
Chr19:55895213 [GRCh37]
Chr19:19q13.42		 uncertain significance
GRCh37/hg19 19q13.42-13.43(chr19:54334195-56434037)x3 copy number gain not provided [RCV001259948] Chr19:54334195..56434037 [GRCh37]
Chr19:19q13.42-13.43		 uncertain significance
NM_001190764.2(TMEM238):c.406G>A (p.Gly136Ser) single nucleotide variant Inborn genetic diseases [RCV003201258] Chr19:55383854 [GRCh38]
Chr19:55895222 [GRCh37]
Chr19:19q13.42		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:301
Count of miRNA genes:293
Interacting mature miRNAs:299
Transcripts:ENST00000444469
Prediction methods: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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 501 1 478 149 136 50 506 5 8 46 276 623 104 237 1 2
Low 1556 1817 1226 468 1695 407 3041 1151 2364 342 1024 970 70 1 1052 1885 2
Below cutoff 377 1120 22 7 103 8 794 1002 1346 28 156 20 149 654 3

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000444469   ⟹   ENSP00000416154
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1955,379,244 - 55,384,292 (-)Ensembl
RefSeq Acc Id: NM_001190764   ⟹   NP_001177693
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381955,379,244 - 55,384,292 (-)NCBI
GRCh371955,890,612 - 55,895,627 (-)ENTREZGENE
CHM1_11955,884,156 - 55,889,200 (-)NCBI
T2T-CHM13v2.01958,474,730 - 58,479,780 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001177693 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein C9JI98 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000416154
  ENSP00000416154.2
Reference Protein Sequences
RefSeq Acc Id: NP_001177693   ⟸   NM_001190764
- UniProtKB: C9JI98 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000416154   ⟸   ENST00000444469

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-C9JI98-F1-model_v2 AlphaFold C9JI98 1-176 view protein structure

Promoters
RGD ID:13205737
Promoter ID:EPDNEW_H26450
Type:initiation region
Name:TMEM238_1
Description:transmembrane protein 238
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26451  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381955,384,292 - 55,384,352EPDNEW
RGD ID:13205741
Promoter ID:EPDNEW_H26451
Type:initiation region
Name:TMEM238_2
Description:transmembrane protein 238
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H26450  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381955,385,737 - 55,385,797EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:40042 AgrOrtholog
COSMIC TMEM238 COSMIC
Ensembl Genes ENSG00000233493 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000444469 ENTREZGENE
  ENST00000444469.4 UniProtKB/Swiss-Prot
GTEx ENSG00000233493 GTEx
HGNC ID HGNC:40042 ENTREZGENE
Human Proteome Map TMEM238 Human Proteome Map
InterPro TMEM238 UniProtKB/Swiss-Prot
KEGG Report hsa:388564 UniProtKB/Swiss-Prot
NCBI Gene 388564 ENTREZGENE
PANTHER PTHR28613 UniProtKB/Swiss-Prot
  TRANSMEMBRANE PROTEIN 238 UniProtKB/Swiss-Prot
Pfam TMEM238 UniProtKB/Swiss-Prot
PharmGKB PA166049062 PharmGKB
UniProt C9JI98 ENTREZGENE, UniProtKB/Swiss-Prot