TMEM233 (transmembrane protein 233) - Rat Genome Database

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Gene: TMEM233 (transmembrane protein 233) Homo sapiens
Analyze
Symbol: TMEM233
Name: transmembrane protein 233
RGD ID: 2923596
HGNC Page HGNC:37219
Description: Located in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: dispanin subfamily B member 2; DSPB2; IFITMD2; interferon induced transmembrane protein domain containing 2; interferon-induced transmembrane domain-containing protein D2
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
GRCh3812119,593,774 - 119,654,295 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl12119,593,774 - 119,643,075 (+)EnsemblGRCh38hg38GRCh38
GRCh3712120,031,579 - 120,080,880 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3612118,515,647 - 118,563,001 (+)NCBINCBI36Build 36hg18NCBI36
Celera12119,664,354 - 119,712,412 (+)NCBICelera
Cytogenetic Map12q24.23NCBI
HuRef12117,039,657 - 117,087,590 (+)NCBIHuRef
CHM1_112119,998,984 - 120,047,050 (+)NCBICHM1_1
T2T-CHM13v2.012119,581,202 - 119,641,838 (+)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  (IBA,IEA)
plasma membrane  (IDA,IEA)

Molecular Function

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:20379614   PMID:21328370   PMID:21873635   PMID:22363774   PMID:29987050   PMID:37117223  


Genomics

Comparative Map Data
TMEM233
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3812119,593,774 - 119,654,295 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl12119,593,774 - 119,643,075 (+)EnsemblGRCh38hg38GRCh38
GRCh3712120,031,579 - 120,080,880 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 3612118,515,647 - 118,563,001 (+)NCBINCBI36Build 36hg18NCBI36
Celera12119,664,354 - 119,712,412 (+)NCBICelera
Cytogenetic Map12q24.23NCBI
HuRef12117,039,657 - 117,087,590 (+)NCBIHuRef
CHM1_112119,998,984 - 120,047,050 (+)NCBICHM1_1
T2T-CHM13v2.012119,581,202 - 119,641,838 (+)NCBIT2T-CHM13v2.0
Tmem233
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395116,176,807 - 116,221,326 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl5116,176,814 - 116,221,303 (-)EnsemblGRCm39 Ensembl
GRCm385116,038,755 - 116,083,267 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5116,038,755 - 116,083,244 (-)EnsemblGRCm38mm10GRCm38
GRCm38.p6 Ensembl5116,038,755 - 116,083,246 (-)EnsemblGRCm38mm10GRCm38
MGSCv375116,490,541 - 116,533,255 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv365116,301,573 - 116,344,243 (-)NCBIMGSCv36mm8
Celera5113,141,220 - 113,187,179 (-)NCBICelera
Cytogenetic Map5FNCBI
cM Map556.1NCBI
Tmem233
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81246,189,247 - 46,230,434 (+)NCBIGRCr8
mRatBN7.21240,528,515 - 40,569,611 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1240,528,499 - 40,578,608 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1241,701,253 - 41,742,485 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01242,314,963 - 42,356,209 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01241,375,437 - 41,416,673 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01246,287,405 - 46,297,570 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1246,257,343 - 46,287,546 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01248,098,446 - 48,099,228 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41241,775,433 - 41,775,876 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera1242,156,713 - 42,207,682 (+)NCBICelera
Cytogenetic Map12q16NCBI
Tmem233
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545511,903,329 - 11,942,229 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495545511,903,329 - 11,942,229 (-)NCBIChiLan1.0ChiLan1.0
TMEM233
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v210127,659,435 - 127,708,983 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan112127,655,822 - 127,705,362 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v012117,172,620 - 117,222,197 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.112120,550,547 - 120,599,347 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl12120,550,547 - 120,598,598 (+)Ensemblpanpan1.1panPan2
TMEM233
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12615,653,031 - 15,688,556 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2615,653,020 - 15,686,539 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2615,658,051 - 15,693,400 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02615,921,527 - 15,948,568 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2615,921,303 - 15,947,005 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12615,890,849 - 15,926,207 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02615,958,766 - 15,994,170 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02615,999,987 - 16,035,325 (+)NCBIUU_Cfam_GSD_1.0
Tmem233
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118146,690,544 - 146,715,002 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049366681,177,717 - 1,213,825 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CCDC60
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1433,224,397 - 33,276,683 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11433,223,574 - 33,315,609 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21435,169,961 - 35,373,884 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TMEM233
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.111114,941,751 - 114,987,042 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl11114,943,403 - 114,989,190 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_023666037130,117,937 - 130,164,044 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tmem233
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474713,948,577 - 13,992,445 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474713,948,951 - 13,992,751 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TMEM233
7 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 12q24.23-24.33(chr12:118165459-133182322)x3 copy number gain See cases [RCV000050866] Chr12:118165459..133182322 [GRCh38]
Chr12:118603264..133758908 [GRCh37]
Chr12:117087647..132268981 [NCBI36]
Chr12:12q24.23-24.33
pathogenic
GRCh38/hg38 12q24.23-24.31(chr12:119286893-122638552)x3 copy number gain See cases [RCV000051981] Chr12:119286893..122638552 [GRCh38]
Chr12:119724698..123123099 [GRCh37]
Chr12:118209081..121689052 [NCBI36]
Chr12:12q24.23-24.31
uncertain significance
GRCh38/hg38 12q24.21-24.33(chr12:115131583-133166920)x3 copy number gain See cases [RCV000053689] Chr12:115131583..133166920 [GRCh38]
Chr12:115569388..133743506 [GRCh37]
Chr12:114053771..132253579 [NCBI36]
Chr12:12q24.21-24.33
pathogenic
GRCh38/hg38 12q24.23-24.33(chr12:119417382-133191400)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053691]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053691]|See cases [RCV000053691] Chr12:119417382..133191400 [GRCh38]
Chr12:119855187..133767986 [GRCh37]
Chr12:118339570..132278059 [NCBI36]
Chr12:12q24.23-24.33
pathogenic
GRCh38/hg38 12q24.23(chr12:119364009-119606602)x3 copy number gain See cases [RCV000139277] Chr12:119364009..119606602 [GRCh38]
Chr12:119801814..120044407 [GRCh37]
Chr12:118286197..118528790 [NCBI36]
Chr12:12q24.23
likely benign
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33
pathogenic
GRCh38/hg38 12q24.21-24.33(chr12:114268403-133201316)x3 copy number gain See cases [RCV000143656] Chr12:114268403..133201316 [GRCh38]
Chr12:114706208..133777902 [GRCh37]
Chr12:113190591..132287975 [NCBI36]
Chr12:12q24.21-24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic|likely pathogenic
GRCh37/hg19 12q24.23-24.31(chr12:118486842-120995382)x3 copy number gain See cases [RCV000447605] Chr12:118486842..120995382 [GRCh37]
Chr12:12q24.23-24.31
likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
NM_001136534.3(TMEM233):c.98T>C (p.Met33Thr) single nucleotide variant Inborn genetic diseases [RCV003256584] Chr12:119593946 [GRCh38]
Chr12:120031751 [GRCh37]
Chr12:12q24.23
likely benign
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33
pathogenic
GRCh37/hg19 12q24.22-24.33(chr12:117461902-133841395)x3 copy number gain Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures [RCV001801213] Chr12:117461902..133841395 [GRCh37]
Chr12:12q24.22-24.33
likely pathogenic
GRCh37/hg19 12q24.23-24.31(chr12:118486842-120995382) copy number gain not specified [RCV002053027] Chr12:118486842..120995382 [GRCh37]
Chr12:12q24.23-24.31
likely pathogenic
NM_001136534.3(TMEM233):c.324T>A (p.Asn108Lys) single nucleotide variant Inborn genetic diseases [RCV002906236] Chr12:119640699 [GRCh38]
Chr12:120078504 [GRCh37]
Chr12:12q24.23
likely benign
NM_001136534.3(TMEM233):c.85G>A (p.Glu29Lys) single nucleotide variant Inborn genetic diseases [RCV002783699] Chr12:119593933 [GRCh38]
Chr12:120031738 [GRCh37]
Chr12:12q24.23
uncertain significance
NM_001136534.3(TMEM233):c.10T>C (p.Tyr4His) single nucleotide variant Inborn genetic diseases [RCV002920908] Chr12:119593858 [GRCh38]
Chr12:120031663 [GRCh37]
Chr12:12q24.23
uncertain significance
NM_001136534.3(TMEM233):c.127G>A (p.Val43Ile) single nucleotide variant Inborn genetic diseases [RCV002724716] Chr12:119593975 [GRCh38]
Chr12:120031780 [GRCh37]
Chr12:12q24.23
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:538
Count of miRNA genes:419
Interacting mature miRNAs:446
Transcripts:ENST00000426426, ENST00000453450
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.

Markers in Region
G15655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3712120,036,598 - 120,036,705UniSTSGRCh37
Build 3612118,520,981 - 118,521,088RGDNCBI36
Celera12119,669,690 - 119,669,797RGD
Cytogenetic Map12q24.23UniSTS
HuRef12117,044,995 - 117,045,102UniSTS


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 2 448 4 3 3 802 806 38 22 9 452 1 799
Low 1324 1441 831 178 293 109 1700 973 1851 291 946 905 71 1051 990
Below cutoff 1037 1278 408 405 915 317 1786 407 1528 86 448 186 97 153 990 4

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001136534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005253880 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005253881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538328 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538329 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011538331 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372036 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372037 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372038 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372039 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054372040 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA476740 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC002070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC002563 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC315309 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC358991 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GD264605 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000426426   ⟹   ENSP00000403130
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12119,593,774 - 119,643,075 (+)Ensembl
RefSeq Acc Id: ENST00000453450
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl12119,593,914 - 119,640,813 (+)Ensembl
RefSeq Acc Id: NM_001136534   ⟹   NP_001130006
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812119,593,774 - 119,643,075 (+)NCBI
GRCh3712120,031,264 - 120,079,861 (+)NCBI
Celera12119,664,354 - 119,712,412 (+)RGD
HuRef12117,039,657 - 117,087,590 (+)RGD
CHM1_112119,998,984 - 120,047,050 (+)NCBI
T2T-CHM13v2.012119,581,202 - 119,630,453 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005253880   ⟹   XP_005253937
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812119,593,774 - 119,633,062 (+)NCBI
GRCh3712120,031,264 - 120,079,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005253881   ⟹   XP_005253938
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812119,593,774 - 119,643,075 (+)NCBI
GRCh3712120,031,264 - 120,079,861 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011538328   ⟹   XP_011536630
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812119,593,774 - 119,642,056 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011538329   ⟹   XP_011536631
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812119,593,774 - 119,654,295 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011538330   ⟹   XP_011536632
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812119,593,774 - 119,654,295 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011538331   ⟹   XP_011536633
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3812119,593,774 - 119,642,056 (+)NCBI
Sequence:
RefSeq Acc Id: XM_054372035   ⟹   XP_054228010
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012119,581,202 - 119,620,706 (+)NCBI
RefSeq Acc Id: XM_054372036   ⟹   XP_054228011
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012119,581,202 - 119,630,453 (+)NCBI
RefSeq Acc Id: XM_054372037   ⟹   XP_054228012
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012119,581,202 - 119,629,435 (+)NCBI
RefSeq Acc Id: XM_054372038   ⟹   XP_054228013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012119,581,202 - 119,641,590 (+)NCBI
RefSeq Acc Id: XM_054372039   ⟹   XP_054228014
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012119,581,202 - 119,641,838 (+)NCBI
RefSeq Acc Id: XM_054372040   ⟹   XP_054228015
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.012119,581,202 - 119,629,435 (+)NCBI
RefSeq Acc Id: NP_001130006   ⟸   NM_001136534
- UniProtKB: B4DJY2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005253938   ⟸   XM_005253881
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_005253937   ⟸   XM_005253880
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011536632   ⟸   XM_011538330
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011536631   ⟸   XM_011538329
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011536630   ⟸   XM_011538328
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011536633   ⟸   XM_011538331
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: ENSP00000403130   ⟸   ENST00000426426
RefSeq Acc Id: XP_054228014   ⟸   XM_054372039
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054228013   ⟸   XM_054372038
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054228011   ⟸   XM_054372036
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054228012   ⟸   XM_054372037
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054228015   ⟸   XM_054372040
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054228010   ⟸   XM_054372035
- Peptide Label: isoform X1

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-B4DJY2-F1-model_v2 AlphaFold B4DJY2 1-109 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:37219 AgrOrtholog
COSMIC TMEM233 COSMIC
Ensembl Genes ENSG00000224982 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000426426 ENTREZGENE
  ENST00000426426.3 UniProtKB/Swiss-Prot
GTEx ENSG00000224982 GTEx
HGNC ID HGNC:37219 ENTREZGENE
Human Proteome Map TMEM233 Human Proteome Map
InterPro CD225/Dispanin_fam UniProtKB/Swiss-Prot
KEGG Report hsa:387890 UniProtKB/Swiss-Prot
NCBI Gene 387890 ENTREZGENE
OMIM 618296 OMIM
PANTHER NG5 UniProtKB/Swiss-Prot
  TRANSMEMBRANE PROTEIN 233 UniProtKB/Swiss-Prot
Pfam CD225 UniProtKB/Swiss-Prot
PharmGKB PA165513584 PharmGKB
UniProt B4DJY2 ENTREZGENE, UniProtKB/Swiss-Prot