TMEM100 (transmembrane protein 100) - Rat Genome Database

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Gene: TMEM100 (transmembrane protein 100) Homo sapiens
Analyze
Symbol: TMEM100
Name: transmembrane protein 100
RGD ID: 1602475
HGNC Page HGNC:25607
Description: Involved in BMP signaling pathway. Located in several cellular components, including endoplasmic reticulum; perikaryon; and perinuclear region of cytoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ10970; FLJ37856
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
GRCh381755,719,627 - 55,732,081 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1755,719,627 - 55,732,121 (-)EnsemblGRCh38hg38GRCh38
GRCh371753,796,988 - 53,809,442 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361751,151,987 - 51,164,481 (-)NCBINCBI36hg18NCBI36
Celera1750,258,761 - 50,271,259 (-)NCBI
Cytogenetic Map17q22NCBI
HuRef1749,156,642 - 49,169,090 (-)NCBIHuRef
CHM1_11753,861,907 - 53,874,407 (-)NCBICHM1_1
T2T-CHM13v2.01756,595,735 - 56,608,191 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14702039   PMID:15489334   PMID:16344560   PMID:16712791   PMID:19058789   PMID:21516116   PMID:21873635   PMID:22021425   PMID:22223368   PMID:22783020   PMID:23485812  
PMID:25416956   PMID:25640077   PMID:25978032   PMID:29690857   PMID:30639579   PMID:31188741   PMID:32296183   PMID:32393512   PMID:34184748   PMID:34278505   PMID:34514518   PMID:34687431  


Genomics

Comparative Map Data
TMEM100
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381755,719,627 - 55,732,081 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1755,719,627 - 55,732,121 (-)EnsemblGRCh38hg38GRCh38
GRCh371753,796,988 - 53,809,442 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361751,151,987 - 51,164,481 (-)NCBINCBI36hg18NCBI36
Celera1750,258,761 - 50,271,259 (-)NCBI
Cytogenetic Map17q22NCBI
HuRef1749,156,642 - 49,169,090 (-)NCBIHuRef
CHM1_11753,861,907 - 53,874,407 (-)NCBICHM1_1
T2T-CHM13v2.01756,595,735 - 56,608,191 (-)NCBI
Tmem100
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391189,921,174 - 89,927,334 (+)NCBIGRCm39mm39
GRCm39 Ensembl1189,921,174 - 89,927,334 (+)Ensembl
GRCm381190,030,348 - 90,036,508 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1190,030,348 - 90,036,508 (+)EnsemblGRCm38mm10GRCm38
MGSCv371189,891,662 - 89,897,819 (+)NCBIGRCm37mm9NCBIm37
MGSCv361189,846,438 - 89,852,595 (+)NCBImm8
Celera1199,643,766 - 99,649,947 (+)NCBICelera
Cytogenetic Map11CNCBI
Tmem100
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21074,854,779 - 74,861,147 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl1074,854,468 - 74,862,941 (+)Ensembl
Rnor_6.01077,537,340 - 77,543,710 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1077,537,340 - 77,543,192 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01077,399,488 - 77,405,343 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41078,446,217 - 78,452,072 (+)NCBIRGSC3.4rn4RGSC3.4
Celera1073,746,435 - 73,752,274 (+)NCBICelera
Cytogenetic Map10q26NCBI
Tmem100
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554516,985,277 - 6,988,345 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554516,982,094 - 6,988,345 (+)NCBIChiLan1.0ChiLan1.0
TMEM100
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11754,665,406 - 54,677,888 (-)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v01749,802,649 - 49,808,568 (-)NCBIMhudiblu_PPA_v0panPan3
TMEM100
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1930,695,711 - 30,701,730 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl930,696,765 - 30,697,169 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha930,037,634 - 30,043,339 (-)NCBI
ROS_Cfam_1.0931,495,784 - 31,501,493 (-)NCBI
ROS_Cfam_1.0 Ensembl931,495,503 - 31,501,398 (-)Ensembl
UMICH_Zoey_3.1930,286,123 - 30,291,825 (-)NCBI
UNSW_CanFamBas_1.0930,520,731 - 30,526,437 (-)NCBI
UU_Cfam_GSD_1.0930,653,622 - 30,659,327 (-)NCBI
Tmem100
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560230,110,529 - 30,117,067 (-)NCBI
SpeTri2.0NW_0049364906,958,064 - 6,963,888 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TMEM100
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1232,008,012 - 32,014,009 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11232,008,007 - 32,014,094 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21232,675,132 - 32,681,152 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TMEM100
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11637,663,294 - 37,669,233 (+)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl1637,667,781 - 37,668,185 (+)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660778,500,710 - 8,506,629 (+)NCBIVero_WHO_p1.0
Tmem100
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462479510,938,366 - 10,945,021 (-)EnsemblHetGla_female_1.0hetGla2
HetGla 1.0NW_00462479510,938,521 - 10,944,919 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
D17S1607  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371753,809,816 - 53,809,932UniSTSGRCh37
Build 361751,164,815 - 51,164,931RGDNCBI36
Celera1750,271,593 - 50,271,708RGD
Cytogenetic Map17q22UniSTS
HuRef1749,169,424 - 49,169,542UniSTS
Marshfield Genetic Map1776.18RGD
Marshfield Genetic Map1776.18UniSTS
Genethon Genetic Map1776.4UniSTS
TNG Radiation Hybrid Map1724790.0UniSTS
GeneMap99-GB4 RH Map17364.94UniSTS
RH47271  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371753,797,443 - 53,797,608UniSTSGRCh37
Build 361751,152,442 - 51,152,607RGDNCBI36
Celera1750,259,216 - 50,259,381RGD
Cytogenetic Map17q22UniSTS
HuRef1749,157,097 - 49,157,262UniSTS
GeneMap99-GB4 RH Map17365.8UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1214
Count of miRNA genes:619
Interacting mature miRNAs:682
Transcripts:ENST00000424486, ENST00000570586, ENST00000571679, ENST00000575685, ENST00000575734, ENST00000575806
Prediction methods:Microtar, Miranda, Pita, 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.


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 4 13
Medium 1099 387 409 38 136 10 1357 481 836 40 435 848 30 1094 717 1
Low 1182 1838 1220 518 593 383 2887 1670 2756 235 889 562 137 1 110 2055 3 2
Below cutoff 40 595 70 52 802 52 81 30 120 104 61 64 2 16

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001099640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017024816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436342 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047436343 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC009837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK001832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK095175 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX405901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC010128 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ027747 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB152959 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA579336 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA896013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000424486   ⟹   ENSP00000395328
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1755,719,627 - 55,722,864 (-)Ensembl
RefSeq Acc Id: ENST00000570586
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1755,721,501 - 55,722,864 (-)Ensembl
RefSeq Acc Id: ENST00000571679   ⟹   ENSP00000459290
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1755,720,683 - 55,721,798 (-)Ensembl
RefSeq Acc Id: ENST00000575685
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1755,721,463 - 55,723,024 (-)Ensembl
RefSeq Acc Id: ENST00000575734   ⟹   ENSP00000465638
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1755,719,918 - 55,732,121 (-)Ensembl
RefSeq Acc Id: ENST00000575806
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1755,722,556 - 55,731,884 (-)Ensembl
RefSeq Acc Id: NM_001099640   ⟹   NP_001093110
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381755,719,627 - 55,732,081 (-)NCBI
GRCh371753,796,988 - 53,809,482 (-)RGD
Build 361751,151,987 - 51,164,481 (-)NCBI Archive
Celera1750,258,761 - 50,271,259 (-)RGD
HuRef1749,156,642 - 49,169,090 (-)RGD
CHM1_11753,861,907 - 53,874,407 (-)NCBI
T2T-CHM13v2.01756,595,735 - 56,608,191 (-)NCBI
Sequence:
RefSeq Acc Id: NM_018286   ⟹   NP_060756
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381755,719,627 - 55,722,864 (-)NCBI
GRCh371753,796,988 - 53,809,482 (-)RGD
Build 361751,151,987 - 51,155,224 (-)NCBI Archive
Celera1750,258,761 - 50,271,259 (-)RGD
HuRef1749,156,642 - 49,169,090 (-)RGD
CHM1_11753,861,907 - 53,865,144 (-)NCBI
T2T-CHM13v2.01756,595,735 - 56,598,972 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024815   ⟹   XP_016880304
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381755,719,627 - 55,723,025 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017024816   ⟹   XP_016880305
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381755,719,627 - 55,722,864 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047436341   ⟹   XP_047292297
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381755,719,627 - 55,732,081 (-)NCBI
RefSeq Acc Id: XM_047436342   ⟹   XP_047292298
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381755,719,627 - 55,732,081 (-)NCBI
RefSeq Acc Id: XM_047436343   ⟹   XP_047292299
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381755,719,627 - 55,725,530 (-)NCBI
Reference Sequences
RefSeq Acc Id: NP_001093110   ⟸   NM_001099640
- UniProtKB: Q96FZ0 (UniProtKB/Swiss-Prot),   Q9NV29 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_060756   ⟸   NM_018286
- UniProtKB: Q96FZ0 (UniProtKB/Swiss-Prot),   Q9NV29 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016880304   ⟸   XM_017024815
- Peptide Label: isoform X1
- UniProtKB: Q96FZ0 (UniProtKB/Swiss-Prot),   Q9NV29 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016880305   ⟸   XM_017024816
- Peptide Label: isoform X1
- UniProtKB: Q96FZ0 (UniProtKB/Swiss-Prot),   Q9NV29 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000395328   ⟸   ENST00000424486
RefSeq Acc Id: ENSP00000459290   ⟸   ENST00000571679
RefSeq Acc Id: ENSP00000465638   ⟸   ENST00000575734
RefSeq Acc Id: XP_047292298   ⟸   XM_047436342
- Peptide Label: isoform X1
- UniProtKB: Q96FZ0 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047292297   ⟸   XM_047436341
- Peptide Label: isoform X1
- UniProtKB: Q96FZ0 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047292299   ⟸   XM_047436343
- Peptide Label: isoform X1
- UniProtKB: Q96FZ0 (UniProtKB/Swiss-Prot)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NV29-F1-model_v2 AlphaFold Q9NV29 1-134 view protein structure

Promoters
RGD ID:6794624
Promoter ID:HG_KWN:26638
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:NM_001099640
Position:
Human AssemblyChrPosition (strand)Source
Build 361751,164,156 - 51,164,656 (-)MPROMDB
RGD ID:7235731
Promoter ID:EPDNEW_H23612
Type:multiple initiation site
Name:TMEM100_1
Description:transmembrane protein 100
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
GRCh381755,722,864 - 55,722,924EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q21.33-22(chr17:49974533-56807609)x1 copy number loss See cases [RCV000053433] Chr17:49974533..56807609 [GRCh38]
Chr17:48051897..54884970 [GRCh37]
Chr17:45406896..52239969 [NCBI36]
Chr17:17q21.33-22		 pathogenic
NM_001099640.1(TMEM100):c.176C>T (p.Pro59Leu) single nucleotide variant Malignant melanoma [RCV000071576] Chr17:55720895 [GRCh38]
Chr17:53798256 [GRCh37]
Chr17:51153255 [NCBI36]
Chr17:17q22		 not provided
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
GRCh37/hg19 17q22(chr17:52189051-57477162)x3 copy number gain See cases [RCV000448801] Chr17:52189051..57477162 [GRCh37]
Chr17:17q22		 pathogenic
GRCh37/hg19 17q21.33-23.2(chr17:49076980-58740945)x3 copy number gain See cases [RCV000448805] Chr17:49076980..58740945 [GRCh37]
Chr17:17q21.33-23.2		 pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q22(chr17:53309576-54333707)x1 copy number loss not provided [RCV000683943] Chr17:53309576..54333707 [GRCh37]
Chr17:17q22		 uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25607 AgrOrtholog
COSMIC TMEM100 COSMIC
Ensembl Genes ENSG00000166292 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000395328 ENTREZGENE
  ENSP00000395328.2 UniProtKB/Swiss-Prot
  ENSP00000459290.1 UniProtKB/TrEMBL
  ENSP00000465638 ENTREZGENE
  ENSP00000465638.1 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000424486 ENTREZGENE
  ENST00000424486.3 UniProtKB/Swiss-Prot
  ENST00000571679.1 UniProtKB/TrEMBL
  ENST00000575734 ENTREZGENE
  ENST00000575734.5 UniProtKB/Swiss-Prot
GTEx ENSG00000166292 GTEx
HGNC ID HGNC:25607 ENTREZGENE
Human Proteome Map TMEM100 Human Proteome Map
InterPro TMEM100 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55273 UniProtKB/Swiss-Prot
NCBI Gene 55273 ENTREZGENE
OMIM 616334 OMIM
PANTHER PTHR16100:SF5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam TMEM100 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142670749 PharmGKB
UniProt A0A0A0MTR3_HUMAN UniProtKB/TrEMBL
  Q96FZ0 ENTREZGENE
  Q9NV29 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary D3DTY7 UniProtKB/Swiss-Prot
  I3L214 UniProtKB/Swiss-Prot
  Q96FZ0 UniProtKB/Swiss-Prot