MIEN1 (migration and invasion enhancer 1) - Rat Genome Database

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Gene: MIEN1 (migration and invasion enhancer 1) Homo sapiens
Analyze
Symbol: MIEN1
Name: migration and invasion enhancer 1
RGD ID: 1315438
HGNC Page HGNC:28230
Description: Involved in negative regulation of apoptotic process; positive regulation of cell migration; and positive regulation of filopodium assembly. Located in cytoplasmic side of plasma membrane and cytosol.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C17orf37; C35; HBV X-transactivated gene 4 protein; HBV XAg-transactivated protein 4; hypothetical protein LOC84299; MGC14832; ORB3; RDX12; XTP4
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
GRCh381739,728,510 - 39,730,532 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1739,728,496 - 39,730,532 (-)EnsemblGRCh38hg38GRCh38
GRCh371737,884,763 - 37,886,785 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361735,138,935 - 35,140,314 (-)NCBINCBI36Build 36hg18NCBI36
Build 341735,138,936 - 35,140,314NCBI
Celera1734,545,142 - 34,546,521 (-)NCBICelera
Cytogenetic Map17q12NCBI
HuRef1733,679,153 - 33,680,533 (-)NCBIHuRef
CHM1_11738,121,161 - 38,122,540 (-)NCBICHM1_1
T2T-CHM13v2.01740,592,070 - 40,594,092 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
2. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:12739007   PMID:15010812   PMID:15489334   PMID:17117180   PMID:17121940   PMID:17207965   PMID:17503775   PMID:19124506   PMID:19503095   PMID:20628393   PMID:21068479   PMID:21347235  
PMID:21483102   PMID:21628459   PMID:21873635   PMID:22658674   PMID:23284973   PMID:23376485   PMID:23880825   PMID:25406943   PMID:25416956   PMID:25464930   PMID:25996585   PMID:26173296  
PMID:26186194   PMID:26272794   PMID:26827826   PMID:27462783   PMID:27589566   PMID:28198505   PMID:28859163   PMID:29721183   PMID:31694235   PMID:32296183   PMID:32305633   PMID:32867128  
PMID:33349155   PMID:33961781   PMID:38272230  


Genomics

Comparative Map Data
MIEN1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381739,728,510 - 39,730,532 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1739,728,496 - 39,730,532 (-)EnsemblGRCh38hg38GRCh38
GRCh371737,884,763 - 37,886,785 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361735,138,935 - 35,140,314 (-)NCBINCBI36Build 36hg18NCBI36
Build 341735,138,936 - 35,140,314NCBI
Celera1734,545,142 - 34,546,521 (-)NCBICelera
Cytogenetic Map17q12NCBI
HuRef1733,679,153 - 33,680,533 (-)NCBIHuRef
CHM1_11738,121,161 - 38,122,540 (-)NCBICHM1_1
T2T-CHM13v2.01740,592,070 - 40,594,092 (-)NCBIT2T-CHM13v2.0
Mien1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391198,328,534 - 98,349,056 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1198,328,534 - 98,329,817 (-)EnsemblGRCm39 Ensembl
GRCm381198,437,708 - 98,458,230 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1198,437,708 - 98,438,991 (-)EnsemblGRCm38mm10GRCm38
MGSCv371198,299,022 - 98,300,302 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361198,253,815 - 98,255,060 (-)NCBIMGSCv36mm8
Celera11108,091,912 - 108,093,192 (-)NCBICelera
Cytogenetic Map11DNCBI
cM Map1161.75NCBI
Mien1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81083,931,485 - 83,932,778 (-)NCBIGRCr8
mRatBN7.21083,435,198 - 83,436,491 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1083,434,710 - 83,436,488 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1088,379,613 - 88,380,906 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01087,877,698 - 87,878,991 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01083,270,350 - 83,271,643 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01086,391,848 - 86,393,141 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1086,391,848 - 86,393,141 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01086,187,783 - 86,189,076 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41087,243,039 - 87,244,331 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11087,257,383 - 87,258,699 (-)NCBI
Celera1082,182,638 - 82,183,897 (-)NCBICelera
Cytogenetic Map10q31NCBI
Mien1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545114,456,484 - 14,462,082 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495545114,456,484 - 14,462,082 (-)NCBIChiLan1.0ChiLan1.0
MIEN1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21925,224,970 - 25,226,391 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11727,119,785 - 27,121,206 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01717,558,422 - 17,559,849 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11717,775,355 - 17,777,558 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1717,775,355 - 17,776,941 (+)Ensemblpanpan1.1panPan2
MIEN1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1922,758,493 - 22,759,935 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl922,758,538 - 22,759,886 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha922,230,962 - 22,232,404 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0923,552,029 - 23,553,471 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl923,552,074 - 23,553,422 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1922,324,830 - 22,326,273 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0922,585,827 - 22,587,269 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0922,710,944 - 22,712,386 (+)NCBIUU_Cfam_GSD_1.0
Mien1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560222,163,236 - 22,164,662 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649014,908,449 - 14,912,369 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649014,910,477 - 14,911,899 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MIEN1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1222,587,919 - 22,590,251 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11222,588,194 - 22,589,912 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21223,045,691 - 23,047,404 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MIEN1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11666,433,591 - 66,434,989 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1666,433,628 - 66,435,243 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607737,335,845 - 37,344,475 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Mien1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247953,371,384 - 3,372,812 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247953,371,383 - 3,372,819 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MIEN1
7 total Variants

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 17q12-21.31(chr17:39199873-45629579)x3 copy number gain See cases [RCV000052479] Chr17:39199873..45629579 [GRCh38]
Chr17:37356126..43706945 [GRCh37]
Chr17:34609652..41062728 [NCBI36]
Chr17:17q12-21.31		 pathogenic
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 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 17q12(chr17:36972794-38033708)x4 copy number gain not provided [RCV000683933] Chr17:36972794..38033708 [GRCh37]
Chr17:17q12		 uncertain significance
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
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 17p11.2-q21.2(chr17:21690653-38772647)x3 copy number gain not provided [RCV000846852] Chr17:21690653..38772647 [GRCh37]
Chr17:17p11.2-q21.2		 pathogenic
NC_000017.10:g.(?_37821613)_(38458253_?)dup duplication Hypertrophic cardiomyopathy 25 [RCV003113302] Chr17:37821613..38458253 [GRCh37]
Chr17:17q12-21.2		 uncertain significance
NM_032339.5(MIEN1):c.337G>A (p.Val113Ile) single nucleotide variant Inborn genetic diseases [RCV003260543] Chr17:39729533 [GRCh38]
Chr17:37885786 [GRCh37]
Chr17:17q12		 likely benign
NM_032339.5(MIEN1):c.67G>A (p.Val23Ile) single nucleotide variant Inborn genetic diseases [RCV002870236] Chr17:39730429 [GRCh38]
Chr17:37886682 [GRCh37]
Chr17:17q12		 uncertain significance
NM_032339.5(MIEN1):c.317C>T (p.Thr106Ile) single nucleotide variant Inborn genetic diseases [RCV002939689] Chr17:39729553 [GRCh38]
Chr17:37885806 [GRCh37]
Chr17:17q12		 uncertain significance
NM_032339.5(MIEN1):c.131G>C (p.Ser44Thr) single nucleotide variant Inborn genetic diseases [RCV002649239] Chr17:39730250 [GRCh38]
Chr17:37886503 [GRCh37]
Chr17:17q12		 uncertain significance
NM_032339.5(MIEN1):c.23C>T (p.Thr8Met) single nucleotide variant Inborn genetic diseases [RCV002656219] Chr17:39730473 [GRCh38]
Chr17:37886726 [GRCh37]
Chr17:17q12		 uncertain significance
NM_032339.5(MIEN1):c.168G>C (p.Glu56Asp) single nucleotide variant Inborn genetic diseases [RCV003203056] Chr17:39730213 [GRCh38]
Chr17:37886466 [GRCh37]
Chr17:17q12		 uncertain significance
NM_032339.5(MIEN1):c.286G>T (p.Ala96Ser) single nucleotide variant Inborn genetic diseases [RCV003369229] Chr17:39729584 [GRCh38]
Chr17:37885837 [GRCh37]
Chr17:17q12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2014
Count of miRNA genes:634
Interacting mature miRNAs:713
Transcripts:ENST00000394231, ENST00000469568, ENST00000474210, ENST00000498164, ENST00000577810, ENST00000582963
Prediction methods:Microtar, Miranda, 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.

Markers in Region
RH79751  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371737,886,875 - 37,887,063UniSTSGRCh37
Build 361735,140,401 - 35,140,589RGDNCBI36
Celera1734,546,608 - 34,546,796RGD
Cytogenetic Map17q12UniSTS
HuRef1733,680,620 - 33,680,808UniSTS
D17S2147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371737,885,460 - 37,885,597UniSTSGRCh37
Build 361735,138,986 - 35,139,123RGDNCBI36
Celera1734,545,193 - 34,545,330RGD
Cytogenetic Map17q12UniSTS
HuRef1733,679,204 - 33,679,341UniSTS


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 5 1 4 2
Medium 2425 2913 1714 613 1920 455 4339 2127 3707 414 1444 1605 171 1204 2772 4
Low 9 78 12 11 31 10 17 70 27 4 11 6 4 1 16 2 2
Below cutoff 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_007503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001330206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_032339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA010615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC079199 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF490253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ308025 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ308026 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL554581 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY508814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC063395 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC106016 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX646129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR986467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS566126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JA284279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000394231   ⟹   ENSP00000377778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1739,728,510 - 39,730,532 (-)Ensembl
RefSeq Acc Id: ENST00000469568
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1739,729,156 - 39,730,491 (-)Ensembl
RefSeq Acc Id: ENST00000474210
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1739,729,156 - 39,730,532 (-)Ensembl
RefSeq Acc Id: ENST00000498164
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1739,729,160 - 39,730,516 (-)Ensembl
RefSeq Acc Id: ENST00000577810   ⟹   ENSP00000462998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1739,729,158 - 39,730,510 (-)Ensembl
RefSeq Acc Id: ENST00000582963
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1739,728,496 - 39,730,494 (-)Ensembl
RefSeq Acc Id: NM_001330206   ⟹   NP_001317135
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381739,728,510 - 39,730,532 (-)NCBI
T2T-CHM13v2.01740,592,070 - 40,594,092 (-)NCBI
Sequence:
RefSeq Acc Id: NM_032339   ⟹   NP_115715
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381739,728,510 - 39,730,532 (-)NCBI
GRCh371737,885,409 - 37,886,792 (-)NCBI
Build 361735,138,935 - 35,140,314 (-)NCBI Archive
Celera1734,545,142 - 34,546,521 (-)RGD
HuRef1733,679,153 - 33,680,533 (-)ENTREZGENE
CHM1_11738,120,505 - 38,122,568 (-)NCBI
T2T-CHM13v2.01740,592,070 - 40,594,092 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_115715   ⟸   NM_032339
- Peptide Label: isoform 1
- UniProtKB: Q9BRT3 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001317135   ⟸   NM_001330206
- Peptide Label: isoform 2
- UniProtKB: J3KTI2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000462998   ⟸   ENST00000577810
RefSeq Acc Id: ENSP00000377778   ⟸   ENST00000394231

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BRT3-F1-model_v2 AlphaFold Q9BRT3 1-115 view protein structure

Promoters
RGD ID:6793803
Promoter ID:HG_KWN:26004
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000257020,   OTTHUMT00000257021,   OTTHUMT00000257022,   OTTHUMT00000257023
Position:
Human AssemblyChrPosition (strand)Source
Build 361735,140,031 - 35,140,531 (-)MPROMDB
RGD ID:7234867
Promoter ID:EPDNEW_H23179
Type:initiation region
Name:MIEN1_1
Description:migration and invasion enhancer 1
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
GRCh381739,730,532 - 39,730,592EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28230 AgrOrtholog
COSMIC MIEN1 COSMIC
Ensembl Genes ENSG00000141741 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000394231 ENTREZGENE
  ENST00000394231.8 UniProtKB/Swiss-Prot
  ENST00000577810 ENTREZGENE
  ENST00000577810.1 UniProtKB/TrEMBL
Gene3D-CATH Glutaredoxin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000141741 GTEx
HGNC ID HGNC:28230 ENTREZGENE
Human Proteome Map MIEN1 Human Proteome Map
InterPro Selenoprotein_Rdx-typ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Thioredoxin-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:84299 UniProtKB/Swiss-Prot
NCBI Gene 84299 ENTREZGENE
OMIM 611802 OMIM
PANTHER MIGRATION AND INVASION ENHANCER 1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SELENOPROTEIN W UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Rdx UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134947080 PharmGKB
Superfamily-SCOP SSF52833 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt J3KTI2 ENTREZGENE, UniProtKB/TrEMBL
  MIEN1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2011-09-27 MIEN1  migration and invasion enhancer 1  C17orf37  chromosome 17 open reading frame 37  Symbol and/or name change 5135510 APPROVED