TMCO6 (transmembrane and coiled-coil domains 6) - Rat Genome Database

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Gene: TMCO6 (transmembrane and coiled-coil domains 6) Homo sapiens
Analyze
Symbol: TMCO6
Name: transmembrane and coiled-coil domains 6
RGD ID: 1605060
HGNC Page HGNC:28814
Description: Predicted to enable nuclear import signal receptor activity. Predicted to be involved in protein import into nucleus. Predicted to be located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ39769; PRO1580; transmembrane and coiled-coil domain-containing protein 6
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
GRCh385140,596,530 - 140,647,732 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl5140,639,435 - 140,645,408 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,019,036 - 140,024,989 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365139,999,196 - 140,005,173 (+)NCBINCBI36Build 36hg18NCBI36
Celera5136,095,757 - 136,101,734 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,164,249 - 135,170,226 (+)NCBIHuRef
CHM1_15139,452,252 - 139,458,225 (+)NCBICHM1_1
T2T-CHM13v2.05141,164,858 - 141,170,811 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
membrane  (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:12477932   PMID:14702039   PMID:16189514   PMID:16344560   PMID:19423540   PMID:19729601   PMID:20406964   PMID:20438785   PMID:21873635   PMID:25416956   PMID:26186194   PMID:28514442  
PMID:29845934   PMID:32296183   PMID:33961781   PMID:35559673  


Genomics

Comparative Map Data
TMCO6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385140,596,530 - 140,647,732 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl5140,639,435 - 140,645,408 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,019,036 - 140,024,989 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365139,999,196 - 140,005,173 (+)NCBINCBI36Build 36hg18NCBI36
Celera5136,095,757 - 136,101,734 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,164,249 - 135,170,226 (+)NCBIHuRef
CHM1_15139,452,252 - 139,458,225 (+)NCBICHM1_1
T2T-CHM13v2.05141,164,858 - 141,170,811 (+)NCBIT2T-CHM13v2.0
Tmco6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391836,868,072 - 36,875,453 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1836,868,092 - 36,875,450 (+)EnsemblGRCm39 Ensembl
GRCm381836,735,019 - 36,742,400 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1836,735,039 - 36,742,397 (+)EnsemblGRCm38mm10GRCm38
MGSCv371836,894,724 - 36,902,045 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361836,861,042 - 36,868,371 (+)NCBIMGSCv36mm8
Celera1837,187,143 - 37,194,456 (+)NCBICelera
Cytogenetic Map18B2NCBI
Tmco6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21828,349,248 - 28,355,843 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1828,349,248 - 28,355,843 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1828,476,398 - 28,482,993 (+)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.01829,238,478 - 29,245,067 (+)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.01828,573,700 - 28,580,295 (+)NCBIRnor_WKY
Rnor_6.01829,579,145 - 29,585,740 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1829,579,145 - 29,585,740 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01829,282,952 - 29,289,547 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41829,435,248 - 29,441,843 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11829,462,029 - 29,466,164 (+)NCBI
Celera1828,069,801 - 28,076,396 (+)NCBICelera
Cytogenetic Map18p11NCBI
Tmco6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541855,110 - 61,705 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541855,110 - 61,670 (-)NCBIChiLan1.0ChiLan1.0
TMCO6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.15142,120,756 - 142,126,727 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl5142,120,756 - 142,126,727 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v05136,003,993 - 136,009,960 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
TMCO6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1235,797,298 - 35,803,491 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl235,797,464 - 35,803,199 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha232,836,310 - 32,842,502 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0236,252,697 - 36,259,144 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl236,252,863 - 36,258,852 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1233,305,443 - 33,311,513 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0234,173,074 - 34,179,277 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0234,925,782 - 34,931,978 (+)NCBIUU_Cfam_GSD_1.0
Tmco6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213152,024,429 - 152,032,212 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365319,579,316 - 9,587,009 (+)EnsemblSpeTri2.0
SpeTri2.0NW_0049365319,579,316 - 9,587,057 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TMCO6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl2142,352,030 - 142,359,036 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.12142,352,006 - 142,359,040 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.22148,295,948 - 148,302,984 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TMCO6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12343,272,568 - 43,278,525 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2343,272,662 - 43,278,223 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603434,605,998 - 34,611,962 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tmco6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474333,382,973 - 33,401,509 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474333,383,047 - 33,398,774 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in TMCO6
45 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3952
Count of miRNA genes:932
Interacting mature miRNAs:1144
Transcripts:ENST00000252100, ENST00000394669, ENST00000394671, ENST00000504069, ENST00000505086, ENST00000509217, ENST00000509269, ENST00000509605, ENST00000510336, ENST00000511410, ENST00000513002, ENST00000514449, ENST00000515265, ENST00000515653, ENST00000537378
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
RH78253  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,024,784 - 140,024,942UniSTSGRCh37
Build 365140,004,968 - 140,005,126RGDNCBI36
Celera5136,101,529 - 136,101,687RGD
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map5q31.3UniSTS
HuRef5135,170,021 - 135,170,179UniSTS
GeneMap99-GB4 RH Map5529.31UniSTS
NCBI RH Map5889.1UniSTS
A010A06  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,024,984 - 140,025,127UniSTSGRCh37
Build 365140,005,168 - 140,005,311RGDNCBI36
Celera5136,101,729 - 136,101,872RGD
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map5q31.3UniSTS
HuRef5135,170,221 - 135,170,364UniSTS
GeneMap99-GB4 RH Map5527.24UniSTS
NCBI RH Map5889.1UniSTS
G33038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,024,984 - 140,025,127UniSTSGRCh37
Celera5136,101,729 - 136,101,872UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map5q31.3UniSTS
HuRef5135,170,221 - 135,170,364UniSTS


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 1437 803 1460 463 1360 328 2452 592 1383 162 1325 1257 142 1020 1249 4 1
Low 1002 2187 266 161 590 137 1905 1605 2350 257 135 356 33 1 184 1539 2 1
Below cutoff 1 1 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001300980 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001300982 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_018502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005268477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537665 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011537668 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009617 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009619 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017009620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024446126 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417354 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417357 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047417358 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA398902 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC116353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK289495 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK301502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308722 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009618 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ066786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA035906 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB196005 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA988463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000252100   ⟹   ENSP00000252100
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,504 - 140,645,408 (+)Ensembl
RefSeq Acc Id: ENST00000394669   ⟹   ENSP00000445469
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,463 - 140,641,780 (+)Ensembl
RefSeq Acc Id: ENST00000394671   ⟹   ENSP00000378166
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,451 - 140,645,404 (+)Ensembl
RefSeq Acc Id: ENST00000504069   ⟹   ENSP00000443223
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,469 - 140,643,012 (+)Ensembl
RefSeq Acc Id: ENST00000505086   ⟹   ENSP00000426221
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,495 - 140,642,337 (+)Ensembl
RefSeq Acc Id: ENST00000509217   ⟹   ENSP00000424937
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,448 - 140,641,727 (+)Ensembl
RefSeq Acc Id: ENST00000509269
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,643,363 - 140,643,912 (+)Ensembl
RefSeq Acc Id: ENST00000509605
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,641,898 - 140,644,183 (+)Ensembl
RefSeq Acc Id: ENST00000510336
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,641,306 - 140,645,408 (+)Ensembl
RefSeq Acc Id: ENST00000511410
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,453 - 140,642,385 (+)Ensembl
RefSeq Acc Id: ENST00000513002   ⟹   ENSP00000421613
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,435 - 140,642,053 (+)Ensembl
RefSeq Acc Id: ENST00000514449
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,491 - 140,642,413 (+)Ensembl
RefSeq Acc Id: ENST00000515265
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,642,572 - 140,645,311 (+)Ensembl
RefSeq Acc Id: ENST00000515653   ⟹   ENSP00000423297
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl5140,639,490 - 140,642,989 (+)Ensembl
RefSeq Acc Id: NM_001300980   ⟹   NP_001287909
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,645,404 (+)NCBI
CHM1_15139,452,252 - 139,458,229 (+)NCBI
T2T-CHM13v2.05141,164,858 - 141,170,811 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001300982   ⟹   NP_001287911
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,645,404 (+)NCBI
CHM1_15139,452,252 - 139,458,229 (+)NCBI
T2T-CHM13v2.05141,164,858 - 141,170,811 (+)NCBI
Sequence:
RefSeq Acc Id: NM_018502   ⟹   NP_060972
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,645,404 (+)NCBI
GRCh375140,019,012 - 140,024,989 (+)RGD
Build 365139,999,196 - 140,005,173 (+)NCBI Archive
Celera5136,095,757 - 136,101,734 (+)RGD
HuRef5135,164,249 - 135,170,226 (+)ENTREZGENE
CHM1_15139,452,252 - 139,458,229 (+)NCBI
T2T-CHM13v2.05141,164,858 - 141,170,811 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005268477   ⟹   XP_005268534
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,645,404 (+)NCBI
GRCh375140,019,012 - 140,024,989 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537663   ⟹   XP_011535965
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,647,257 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011537665   ⟹   XP_011535967
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,596,530 - 140,645,404 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017009618   ⟹   XP_016865107
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,645,404 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024446124   ⟹   XP_024301892
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,645,404 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024446125   ⟹   XP_024301893
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,596,530 - 140,645,404 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047417353   ⟹   XP_047273309
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,645,404 (+)NCBI
RefSeq Acc Id: XM_047417354   ⟹   XP_047273310
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,451 - 140,647,732 (+)NCBI
RefSeq Acc Id: XM_047417355   ⟹   XP_047273311
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,596,530 - 140,645,404 (+)NCBI
RefSeq Acc Id: XM_047417356   ⟹   XP_047273312
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,596,530 - 140,645,404 (+)NCBI
RefSeq Acc Id: XM_047417357   ⟹   XP_047273313
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,596,530 - 140,645,404 (+)NCBI
RefSeq Acc Id: XM_047417358   ⟹   XP_047273314
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,596,530 - 140,645,404 (+)NCBI
Reference Sequences
RefSeq Acc Id: NP_060972   ⟸   NM_018502
- Peptide Label: isoform 2
- UniProtKB: Q9P198 (UniProtKB/Swiss-Prot),   Q96DC7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005268534   ⟸   XM_005268477
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001287909   ⟸   NM_001300980
- Peptide Label: isoform 1
- UniProtKB: Q96DC7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001287911   ⟸   NM_001300982
- Peptide Label: isoform 3
- UniProtKB: Q96DC7 (UniProtKB/Swiss-Prot),   A8K0D0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011535967   ⟸   XM_011537665
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_011535965   ⟸   XM_011537663
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016865107   ⟸   XM_017009618
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_024301892   ⟸   XM_024446124
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_024301893   ⟸   XM_024446125
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: ENSP00000252100   ⟸   ENST00000252100
RefSeq Acc Id: ENSP00000443223   ⟸   ENST00000504069
RefSeq Acc Id: ENSP00000426221   ⟸   ENST00000505086
RefSeq Acc Id: ENSP00000424937   ⟸   ENST00000509217
RefSeq Acc Id: ENSP00000445469   ⟸   ENST00000394669
RefSeq Acc Id: ENSP00000378166   ⟸   ENST00000394671
RefSeq Acc Id: ENSP00000421613   ⟸   ENST00000513002
RefSeq Acc Id: ENSP00000423297   ⟸   ENST00000515653
RefSeq Acc Id: XP_047273312   ⟸   XM_047417356
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047273313   ⟸   XM_047417357
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047273314   ⟸   XM_047417358
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047273311   ⟸   XM_047417355
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047273310   ⟸   XM_047417354
- Peptide Label: isoform X5
RefSeq Acc Id: XP_047273309   ⟸   XM_047417353
- Peptide Label: isoform X3
Protein Domains
IBB

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96DC7-F1-model_v2 AlphaFold Q96DC7 1-493 view protein structure

Promoters
RGD ID:6803605
Promoter ID:HG_KWN:51288
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_018502,   UC003LGM.1,   UC010JFT.1
Position:
Human AssemblyChrPosition (strand)Source
Build 365139,998,996 - 139,999,496 (+)MPROMDB
RGD ID:6803606
Promoter ID:HG_KWN:51289
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3,   Lymphoblastoid
Transcripts:UC003LGN.1
Position:
Human AssemblyChrPosition (strand)Source
Build 365140,000,821 - 140,001,522 (+)MPROMDB
RGD ID:6803608
Promoter ID:HG_KWN:51290
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid
Transcripts:UC003LGO.1
Position:
Human AssemblyChrPosition (strand)Source
Build 365140,001,651 - 140,002,652 (+)MPROMDB
RGD ID:6870828
Promoter ID:EPDNEW_H8579
Type:initiation region
Name:TMCO6_2
Description:transmembrane and coiled-coil domains 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8582  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,596,530 - 140,596,590EPDNEW
RGD ID:6870834
Promoter ID:EPDNEW_H8582
Type:initiation region
Name:TMCO6_1
Description:transmembrane and coiled-coil domains 6
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8579  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh385140,639,463 - 140,639,523EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 copy number gain See cases [RCV000051193] Chr5:130860928..155321811 [GRCh38]
Chr5:130196621..154701371 [GRCh37]
Chr5:130224520..154681564 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-32(chr5:138871137-145812309)x1 copy number loss See cases [RCV000052142] Chr5:138871137..145812309 [GRCh38]
Chr5:138206826..145191872 [GRCh37]
Chr5:138234725..145172065 [NCBI36]
Chr5:5q31.2-32
pathogenic
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 copy number loss See cases [RCV000053524] Chr5:106619588..156124387 [GRCh38]
Chr5:105955289..155551397 [GRCh37]
Chr5:105983188..155483975 [NCBI36]
Chr5:5q21.3-33.2
pathogenic
GRCh38/hg38 5q31.2-31.3(chr5:137836682-140696361)x3 copy number gain See cases [RCV000134725] Chr5:137836682..140696361 [GRCh38]
Chr5:137172371..140075946 [GRCh37]
Chr5:137200270..140056130 [NCBI36]
Chr5:5q31.2-31.3
pathogenic
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 copy number gain See cases [RCV000138808] Chr5:129847794..153353546 [GRCh38]
Chr5:129183487..152733106 [GRCh37]
Chr5:129211386..152713299 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-31.3(chr5:138942857-144605017)x3 copy number gain See cases [RCV000142806] Chr5:138942857..144605017 [GRCh38]
Chr5:138278546..143984580 [GRCh37]
Chr5:138306445..143964773 [NCBI36]
Chr5:5q31.2-31.3
uncertain significance
NM_002488.5(NDUFA2):c.231C>T (p.Val77=) single nucleotide variant not provided [RCV000902487]|not specified [RCV000127108] Chr5:140645656 [GRCh38]
Chr5:140025241 [GRCh37]
Chr5:5q31.3
benign
NM_002488.5(NDUFA2):c.177C>T (p.Ser59=) single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000259757] Chr5:140647287 [GRCh38]
Chr5:140026872 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.225del (p.Asn76fs) deletion Cystic Leukoencephalopathy [RCV000515932]|Mitochondrial complex 1 deficiency, nuclear type 13 [RCV001256007]|not provided [RCV000514072] Chr5:140645662 [GRCh38]
Chr5:140025247 [GRCh37]
Chr5:5q31.3
pathogenic|uncertain significance
NM_002488.5(NDUFA2):c.280G>A (p.Val94Ile) single nucleotide variant not provided [RCV000198730] Chr5:140645607 [GRCh38]
Chr5:140025192 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.129G>A (p.Glu43=) single nucleotide variant not provided [RCV000677060]|not specified [RCV000127110] Chr5:140647335 [GRCh38]
Chr5:140026920 [GRCh37]
Chr5:5q31.3
benign|likely benign
NM_002488.4(NDUFA2):c.206A>G (p.Tyr69Cys) single nucleotide variant not specified [RCV000197043] Chr5:140647258 [GRCh38]
Chr5:140026843 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.134A>C (p.Lys45Thr) single nucleotide variant Cystic Leukoencephalopathy [RCV000516026]|Mitochondrial complex 1 deficiency, nuclear type 13 [RCV001256006] Chr5:140647330 [GRCh38]
Chr5:140026915 [GRCh37]
Chr5:5q31.3
pathogenic
NM_002488.5(NDUFA2):c.135G>A (p.Lys45=) single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000298528] Chr5:140647329 [GRCh38]
Chr5:140026914 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.191A>G (p.Lys64Arg) single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000360340] Chr5:140647273 [GRCh38]
Chr5:140026858 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3
likely benign
NM_002488.5(NDUFA2):c.199del (p.Ala67fs) deletion not specified [RCV000414604] Chr5:140647265 [GRCh38]
Chr5:140026850 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
NM_002488.5(NDUFA2):c.102-11C>G single nucleotide variant not provided [RCV001720066] Chr5:140647373 [GRCh38]
Chr5:140026958 [GRCh37]
Chr5:5q31.3
likely benign
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3
pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NC_000005.9:g.(?_86400000)_(154000000_?)del deletion Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] Chr5:86400000..154000000 [GRCh37]
Chr5:5q14.3-33.2
pathogenic
NM_002488.5(NDUFA2):c.209-28T>C single nucleotide variant not specified [RCV000614927] Chr5:140645706 [GRCh38]
Chr5:140025291 [GRCh37]
Chr5:5q31.3
likely benign
GRCh37/hg19 5q31.2-31.3(chr5:139147238-141540491)x1 copy number loss not provided [RCV000682600] Chr5:139147238..141540491 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
NM_002488.5(NDUFA2):c.208+5G>A single nucleotide variant Mitochondrial complex 1 deficiency, nuclear type 13 [RCV000007945] Chr5:140647251 [GRCh38]
Chr5:140026836 [GRCh37]
Chr5:5q31.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NM_002488.5(NDUFA2):c.209-355G>A single nucleotide variant not provided [RCV001581751] Chr5:140646033 [GRCh38]
Chr5:140025618 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.5(NDUFA2):c.209-364C>T single nucleotide variant not provided [RCV001570337] Chr5:140646042 [GRCh38]
Chr5:140025627 [GRCh37]
Chr5:5q31.3
likely benign
NM_000591.4(CD14):c.438C>T (p.Ser146=) single nucleotide variant not provided [RCV000960030] Chr5:140632546 [GRCh38]
Chr5:140012131 [GRCh37]
Chr5:5q31.3
benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32
uncertain significance
NM_002488.5(NDUFA2):c.168C>T (p.Arg56=) single nucleotide variant not provided [RCV000891939] Chr5:140647296 [GRCh38]
Chr5:140026881 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.5(NDUFA2):c.209-221C>T single nucleotide variant not provided [RCV000842831] Chr5:140645899 [GRCh38]
Chr5:140025484 [GRCh37]
Chr5:5q31.3
benign
NM_002488.5(NDUFA2):c.208+314T>A single nucleotide variant not provided [RCV000829012] Chr5:140646942 [GRCh38]
Chr5:140026527 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.2-31.3(chr5:139447779-140047037)x3 copy number gain not provided [RCV000846756] Chr5:139447779..140047037 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
NM_002488.5(NDUFA2):c.150C>T (p.Asp50=) single nucleotide variant not provided [RCV000916918] Chr5:140647314 [GRCh38]
Chr5:140026899 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.5(NDUFA2):c.209-4T>C single nucleotide variant not provided [RCV000930089] Chr5:140645682 [GRCh38]
Chr5:140025267 [GRCh37]
Chr5:5q31.3
likely benign
NM_000591.4(CD14):c.702G>A (p.Met234Ile) single nucleotide variant not provided [RCV000887782] Chr5:140632282 [GRCh38]
Chr5:140011867 [GRCh37]
Chr5:5q31.3
benign
NM_002488.5(NDUFA2):c.209-333_209-332del deletion not provided [RCV001530683] Chr5:140646010..140646011 [GRCh38]
Chr5:140025595..140025596 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.5(NDUFA2):c.170A>C (p.Glu57Ala) single nucleotide variant Mitochondrial complex 1 deficiency, nuclear type 13 [RCV001256008] Chr5:140647294 [GRCh38]
Chr5:140026879 [GRCh37]
Chr5:5q31.3
pathogenic
NC_000005.9:g.(?_136633338)_(140998481_?)dup duplication Autosomal dominant nonsyndromic hearing loss 1 [RCV001319817]|PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] Chr5:136633338..140998481 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
NM_002488.5(NDUFA2):c.208+18G>A single nucleotide variant not provided [RCV001713309] Chr5:140647238 [GRCh38]
Chr5:140026823 [GRCh37]
Chr5:5q31.3
benign
NM_002488.5(NDUFA2):c.209-332del deletion not provided [RCV001654904] Chr5:140646010 [GRCh38]
Chr5:140025595 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.2-31.3(chr5:139493717-140517454)x1 copy number loss PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001801202] Chr5:139493717..140517454 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) copy number gain not specified [RCV002053526] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
NM_002488.5(NDUFA2):c.294dup (p.Ala99fs) duplication not provided [RCV002010481] Chr5:140645592..140645593 [GRCh38]
Chr5:140025177..140025178 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.201C>T (p.Ala67=) single nucleotide variant not provided [RCV002076394] Chr5:140647263 [GRCh38]
Chr5:140026848 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.5(NDUFA2):c.26G>C (p.Gly9Ala) single nucleotide variant not provided [RCV002009320] Chr5:140647558 [GRCh38]
Chr5:140027143 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.4(NDUFA2):c.-136A>G single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000333463]|not provided [RCV001653684] Chr5:140647719 [GRCh38]
Chr5:140027304 [GRCh37]
Chr5:5q31.3
benign|likely benign
NM_002488.5(NDUFA2):c.28G>A (p.Val10Ile) single nucleotide variant not provided [RCV001569568] Chr5:140647556 [GRCh38]
Chr5:140027141 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.4(NDUFA2):c.-114T>A single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV001156939] Chr5:140647697 [GRCh38]
Chr5:140027282 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.26G>T (p.Gly9Val) single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV001155277] Chr5:140647558 [GRCh38]
Chr5:140027143 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.40C>G (p.Leu14Val) single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV001155276]|not provided [RCV000441489]|not specified [RCV000127109] Chr5:140647544 [GRCh38]
Chr5:140027129 [GRCh37]
Chr5:5q31.3
benign|likely benign|uncertain significance
NM_002488.5(NDUFA2):c.30C>T (p.Val10=) single nucleotide variant not provided [RCV000909218]|not specified [RCV000443910] Chr5:140647554 [GRCh38]
Chr5:140027139 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.4(NDUFA2):c.-51C>A single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000329989] Chr5:140647634 [GRCh38]
Chr5:140027219 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.101+27G>A single nucleotide variant not provided [RCV001571903] Chr5:140647456 [GRCh38]
Chr5:140027041 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.5(NDUFA2):c.48G>A (p.Leu16=) single nucleotide variant not provided [RCV000935919] Chr5:140647536 [GRCh38]
Chr5:140027121 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.4(NDUFA2):c.-63G>A single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000276097] Chr5:140647646 [GRCh38]
Chr5:140027231 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.5(NDUFA2):c.31G>C (p.Gly11Arg) single nucleotide variant Leigh syndrome [RCV001335039]|not provided [RCV001337355] Chr5:140647553 [GRCh38]
Chr5:140027138 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.4(NDUFA2):c.-53A>G single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000386841] Chr5:140647636 [GRCh38]
Chr5:140027221 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.4(NDUFA2):c.-145T>A single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000380861] Chr5:140647728 [GRCh38]
Chr5:140027313 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_002488.4(NDUFA2):c.-50G>A single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000263224]|not specified [RCV000612041] Chr5:140647633 [GRCh38]
Chr5:140027218 [GRCh37]
Chr5:5q31.3
likely benign|uncertain significance
NM_002488.4(NDUFA2):c.-48A>G single nucleotide variant Mitochondrial complex I deficiency, nuclear type 1 [RCV000355665]|not provided [RCV001672651] Chr5:140647631 [GRCh38]
Chr5:140027216 [GRCh37]
Chr5:5q31.3
benign|likely benign
NM_002488.4(NDUFA2):c.-106delG deletion not provided [RCV000835232] Chr5:140647689 [GRCh38]
Chr5:140027274 [GRCh37]
Chr5:5q31.3
likely benign
NM_002488.5(NDUFA2):c.279C>T (p.Asn93=) single nucleotide variant not provided [RCV002176209] Chr5:140645608 [GRCh38]
Chr5:140025193 [GRCh37]
Chr5:5q31.3
likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:28814 AgrOrtholog
COSMIC TMCO6 COSMIC
Ensembl Genes ENSG00000113119 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000252100 ENTREZGENE
  ENSP00000252100.6 UniProtKB/Swiss-Prot
  ENSP00000378166 ENTREZGENE
  ENSP00000378166.3 UniProtKB/Swiss-Prot
  ENSP00000421613.2 UniProtKB/TrEMBL
  ENSP00000423297.1 UniProtKB/TrEMBL
  ENSP00000424937.2 UniProtKB/TrEMBL
  ENSP00000426221.2 UniProtKB/TrEMBL
  ENSP00000443223.1 UniProtKB/TrEMBL
  ENSP00000445469.1 UniProtKB/TrEMBL
Ensembl Transcript ENST00000252100 ENTREZGENE
  ENST00000252100.6 UniProtKB/Swiss-Prot
  ENST00000394669.8 UniProtKB/TrEMBL
  ENST00000394671 ENTREZGENE
  ENST00000394671.8 UniProtKB/Swiss-Prot
  ENST00000504069.6 UniProtKB/TrEMBL
  ENST00000505086.2 UniProtKB/TrEMBL
  ENST00000509217.6 UniProtKB/TrEMBL
  ENST00000513002.5 UniProtKB/TrEMBL
  ENST00000515653.1 UniProtKB/TrEMBL
Gene3D-CATH 1.25.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000113119 GTEx
HGNC ID HGNC:28814 ENTREZGENE
Human Proteome Map TMCO6 Human Proteome Map
InterPro ARM-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ARM-type_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Armadillo UniProtKB/Swiss-Prot
  Importin-a_IBB UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:55374 UniProtKB/Swiss-Prot
NCBI Gene 55374 ENTREZGENE
Pfam IBB UniProtKB/TrEMBL
PharmGKB PA162405810 PharmGKB
PROSITE IBB UniProtKB/TrEMBL
SMART ARM UniProtKB/Swiss-Prot
Superfamily-SCOP SSF48371 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K0D0 ENTREZGENE, UniProtKB/TrEMBL
  D6R986_HUMAN UniProtKB/TrEMBL
  D6REQ9_HUMAN UniProtKB/TrEMBL
  D6REY4_HUMAN UniProtKB/TrEMBL
  Q96DC7 ENTREZGENE
  Q9P198 ENTREZGENE
  TMCO6_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary D6RH04 UniProtKB/TrEMBL
  Q9BUU0 UniProtKB/Swiss-Prot
  Q9P198 UniProtKB/Swiss-Prot