CUTA (cutA divalent cation tolerance homolog) - Rat Genome Database

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Gene: CUTA (cutA divalent cation tolerance homolog) Homo sapiens
Analyze
Symbol: CUTA
Name: cutA divalent cation tolerance homolog
RGD ID: 1346513
HGNC Page HGNC:21101
Description: Enables enzyme binding activity. Involved in protein localization. Located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: acetylcholinesterase-associated protein; ACHAP; brain acetylcholinesterase putative membrane anchor; C6orf82; chromosome 6 open reading frame 82; cutA divalent cation tolerance homolog (E. coli); divalent cation tolerant protein CUTA; MGC111154
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
GRCh38633,416,442 - 33,418,107 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl633,416,442 - 33,418,317 (-)EnsemblGRCh38hg38GRCh38
GRCh37633,384,219 - 33,385,884 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36633,492,297 - 33,494,043 (-)NCBINCBI36Build 36hg18NCBI36
Build 34633,492,296 - 33,493,669NCBI
Celera634,938,742 - 34,940,488 (-)NCBICelera
Cytogenetic Map6p21.32NCBI
HuRef633,126,468 - 33,128,214 (-)NCBIHuRef
CHM1_1633,386,214 - 33,387,959 (-)NCBICHM1_1
T2T-CHM13v2.0633,237,804 - 33,239,469 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


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
Additional References at PubMed
PMID:10800960   PMID:10954708   PMID:12477932   PMID:14574404   PMID:15146197   PMID:15231747   PMID:15489334   PMID:16712791   PMID:17924204   PMID:18624398   PMID:19056867   PMID:19851445  
PMID:20195357   PMID:21873635   PMID:22351782   PMID:22863883   PMID:22939629   PMID:23376485   PMID:23533145   PMID:25344844   PMID:25416956   PMID:25557959   PMID:26344197   PMID:26496610  
PMID:27609421   PMID:28514442   PMID:29128334   PMID:31343991   PMID:31515488   PMID:31536960   PMID:32296183   PMID:32513696   PMID:33961781   PMID:34428256   PMID:35253629   PMID:35696571  
PMID:36215168   PMID:36244648   PMID:36517590   PMID:36724073  


Genomics

Comparative Map Data
CUTA
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38633,416,442 - 33,418,107 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl633,416,442 - 33,418,317 (-)EnsemblGRCh38hg38GRCh38
GRCh37633,384,219 - 33,385,884 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36633,492,297 - 33,494,043 (-)NCBINCBI36Build 36hg18NCBI36
Build 34633,492,296 - 33,493,669NCBI
Celera634,938,742 - 34,940,488 (-)NCBICelera
Cytogenetic Map6p21.32NCBI
HuRef633,126,468 - 33,128,214 (-)NCBIHuRef
CHM1_1633,386,214 - 33,387,959 (-)NCBICHM1_1
T2T-CHM13v2.0633,237,804 - 33,239,469 (-)NCBIT2T-CHM13v2.0
Cuta
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391727,156,946 - 27,158,847 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1727,152,793 - 27,158,543 (-)EnsemblGRCm39 Ensembl
GRCm381726,937,972 - 26,939,884 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1726,933,819 - 26,939,569 (-)EnsemblGRCm38mm10GRCm38
MGSCv371727,074,917 - 27,076,423 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361726,665,561 - 26,667,067 (-)NCBIMGSCv36mm8
Celera1727,474,695 - 27,476,201 (-)NCBICelera
Cytogenetic Map17A3.3NCBI
cM Map1713.6NCBI
Cuta
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8205,024,816 - 5,026,446 (-)NCBIGRCr8
mRatBN7.2205,022,956 - 5,024,580 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl205,022,956 - 5,024,552 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx205,748,342 - 5,750,042 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0205,110,079 - 5,111,779 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0205,588,515 - 5,590,087 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0205,532,024 - 5,533,640 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl205,532,024 - 5,533,620 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0207,591,037 - 7,592,657 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4205,175,113 - 5,176,689 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1205,175,343 - 5,176,834 (-)NCBI
Celera206,605,378 - 6,606,954 (-)NCBICelera
Cytogenetic Map20p12NCBI
Cuta
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554371,947,093 - 1,948,541 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554371,947,139 - 1,948,657 (-)NCBIChiLan1.0ChiLan1.0
CUTA
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2547,901,557 - 47,904,152 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1643,768,742 - 43,771,338 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0632,995,889 - 32,997,581 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1634,107,227 - 34,109,009 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl634,107,228 - 34,108,958 (-)Ensemblpanpan1.1panPan2
CUTA
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1122,827,510 - 2,829,151 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl122,823,512 - 2,829,433 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha122,908,319 - 2,909,973 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0123,159,155 - 3,160,809 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl123,155,157 - 3,160,664 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1122,826,276 - 2,827,930 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0122,907,383 - 2,909,038 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0123,005,497 - 3,007,151 (-)NCBIUU_Cfam_GSD_1.0
Cuta
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494638,478,437 - 38,480,176 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647625,479,953 - 25,486,157 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647625,480,134 - 25,481,831 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CUTA
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl729,720,094 - 29,721,769 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1729,720,094 - 29,721,713 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2734,373,420 - 34,375,039 (+)NCBISscrofa10.2Sscrofa10.2susScr3
CUTA
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11738,648,181 - 38,649,906 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1738,648,140 - 38,649,810 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604433,265,237 - 33,267,013 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Cuta
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462475423,398,684 - 23,400,108 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462475423,398,591 - 23,400,111 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CUTA
10 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6p21.32(chr6:33415354-33432929)x3 copy number gain See cases [RCV000140862] Chr6:33415354..33432929 [GRCh38]
Chr6:33383131..33400706 [GRCh37]
Chr6:33491109..33508684 [NCBI36]
Chr6:6p21.32
uncertain significance
GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3 copy number gain See cases [RCV000143497] Chr6:156974..46789291 [GRCh38]
Chr6:156974..46757028 [GRCh37]
Chr6:101974..46864987 [NCBI36]
Chr6:6p25.3-12.3
pathogenic
GRCh37/hg19 6p21.32(chr6:33256191-33400523)x3 copy number gain Ductal breast carcinoma [RCV000207216] Chr6:33256191..33400523 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014840.2(CUTA):c.258G>A (p.Arg86=) single nucleotide variant Inborn genetic diseases [RCV003244480] Chr6:33417310 [GRCh38]
Chr6:33385087 [GRCh37]
Chr6:6p21.32
likely benign
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27
pathogenic
NM_001014840.2(CUTA):c.476C>T (p.Pro159Leu) single nucleotide variant Inborn genetic diseases [RCV003267760] Chr6:33416714 [GRCh38]
Chr6:33384491 [GRCh37]
Chr6:6p21.32
uncertain significance
GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367) copy number gain not provided [RCV000767714] Chr6:29455465..81447367 [GRCh37]
Chr6:6p22.1-q14.1
pathogenic
NC_000006.11:g.(?_33131435)_(33419703_?)dup duplication Intellectual disability, autosomal dominant 5 [RCV000817954] Chr6:33163658..33451926 [GRCh38]
Chr6:33131435..33419703 [GRCh37]
Chr6:6p21.32
uncertain significance
NC_000006.12:g.(?_33173681)_(33451926_?)dup duplication Intellectual disability, autosomal dominant 5 [RCV001032258] Chr6:33141458..33419703 [GRCh37]
Chr6:6p21.32
uncertain significance
GRCh37/hg19 6p21.33-21.31(chr6:31036397-34088832)x3 copy number gain not provided [RCV001005791] Chr6:31036397..34088832 [GRCh37]
Chr6:6p21.33-21.31
likely pathogenic
NC_000006.12:g.(?_33391986)_(33672228_?)dup duplication Intellectual disability, autosomal dominant 5 [RCV001032764] Chr6:33359763..33640005 [GRCh37]
Chr6:6p21.32-21.31
uncertain significance
GRCh37/hg19 6p21.32-21.31(chr6:33069892-33751391) copy number gain not specified [RCV002053566] Chr6:33069892..33751391 [GRCh37]
Chr6:6p21.32-21.31
uncertain significance
NM_001014840.2(CUTA):c.202G>A (p.Val68Ile) single nucleotide variant not provided [RCV002227657] Chr6:33417536 [GRCh38]
Chr6:33385313 [GRCh37]
Chr6:6p21.32
uncertain significance
NC_000006.11:g.(?_30695893)_(36953949_?)dup duplication Proteasome-associated autoinflammatory syndrome 1 [RCV003113679] Chr6:30695893..36953949 [GRCh37]
Chr6:6p21.33-21.2
uncertain significance
NC_000006.11:g.(?_32148920)_(36953949_?)dup duplication not provided [RCV003154914] Chr6:32148920..36953949 [GRCh37]
Chr6:6p21.32-21.2
uncertain significance
NM_001014840.2(CUTA):c.293A>T (p.Asn98Ile) single nucleotide variant Inborn genetic diseases [RCV002749835] Chr6:33417275 [GRCh38]
Chr6:33385052 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014840.2(CUTA):c.217G>A (p.Val73Ile) single nucleotide variant Inborn genetic diseases [RCV002906368] Chr6:33417521 [GRCh38]
Chr6:33385298 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014840.2(CUTA):c.412C>T (p.Arg138Cys) single nucleotide variant Inborn genetic diseases [RCV002704480] Chr6:33416921 [GRCh38]
Chr6:33384698 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014840.2(CUTA):c.401C>G (p.Thr134Arg) single nucleotide variant Inborn genetic diseases [RCV002980938] Chr6:33416932 [GRCh38]
Chr6:33384709 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014433.2(CUTA):c.29G>A (p.Gly10Glu) single nucleotide variant Inborn genetic diseases [RCV002738923] Chr6:33418157 [GRCh38]
Chr6:33385934 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014840.2(CUTA):c.217G>C (p.Val73Leu) single nucleotide variant Inborn genetic diseases [RCV002987685] Chr6:33417521 [GRCh38]
Chr6:33385298 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014840.2(CUTA):c.161C>G (p.Ser54Trp) single nucleotide variant Inborn genetic diseases [RCV002648828] Chr6:33417577 [GRCh38]
Chr6:33385354 [GRCh37]
Chr6:6p21.32
uncertain significance
NM_001014840.2(CUTA):c.467G>A (p.Gly156Glu) single nucleotide variant Inborn genetic diseases [RCV002936180] Chr6:33416723 [GRCh38]
Chr6:33384500 [GRCh37]
Chr6:6p21.32
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3182
Count of miRNA genes:690
Interacting mature miRNAs:768
Transcripts:ENST00000374484, ENST00000374496, ENST00000374500, ENST00000440279, ENST00000462802, ENST00000465956, ENST00000479249, ENST00000482684, ENST00000487637, ENST00000488034, ENST00000488478, ENST00000492510, ENST00000494751, ENST00000607266
Prediction methods:Microtar, 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
G44723  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37633,383,937 - 33,384,062UniSTSGRCh37
GRCh37258,443,910 - 58,444,043UniSTSGRCh37
Build 36258,297,414 - 58,297,547RGDNCBI36
Celera634,938,360 - 34,938,485UniSTS
Celera258,287,087 - 58,287,220RGD
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2p16.1UniSTS
HuRef633,126,086 - 33,126,211UniSTS
HuRef258,185,200 - 58,185,333UniSTS
RH15807  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37633,384,004 - 33,384,166UniSTSGRCh37
Build 36633,491,982 - 33,492,144RGDNCBI36
Celera634,938,427 - 34,938,589RGD
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map6p21.3UniSTS
HuRef633,126,153 - 33,126,315UniSTS
GeneMap99-GB4 RH Map6120.03UniSTS
NCBI RH Map6509.1UniSTS
STS-Z41506  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37633,384,330 - 33,384,391UniSTSGRCh37
Build 36633,492,308 - 33,492,369RGDNCBI36
Celera634,938,753 - 34,938,814RGD
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map6p21.3UniSTS
HuRef633,126,479 - 33,126,540UniSTS
GeneMap99-GB4 RH Map6120.15UniSTS
NCBI RH Map6509.1UniSTS
RH1523  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37633,384,353 - 33,384,524UniSTSGRCh37
Build 36633,492,331 - 33,492,502RGDNCBI36
Celera634,938,776 - 34,938,947RGD
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map6p21.3UniSTS
HuRef633,126,502 - 33,126,673UniSTS
GeneMap99-GB4 RH Map6145.45UniSTS
NCBI RH Map6509.1UniSTS
STS-Z40841  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37633,384,144 - 33,384,192UniSTSGRCh37
Build 36633,492,122 - 33,492,170RGDNCBI36
Celera634,938,567 - 34,938,615RGD
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map6p21.3UniSTS
HuRef633,126,293 - 33,126,341UniSTS
GeneMap99-GB4 RH Map6145.45UniSTS
NCBI RH Map6509.1UniSTS
D1S3689  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map6p21.32UniSTS


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 1 1 1 1 22
Medium 2439 2963 1725 623 1941 464 4356 2178 3733 418 1438 1613 175 1 1204 2788 6 2
Low 28 10 19 1 1
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_016137 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001014433 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001014837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001014838 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001014840 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_015921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF106943 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF230924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311556 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL021366 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL050332 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL533788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL662799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC005890 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC107751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG472577 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU540844 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX088650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX334868 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB106834 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN363642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HF583432 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000374484   ⟹   ENSP00000363608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,550 - 33,418,142 (-)Ensembl
RefSeq Acc Id: ENST00000374496   ⟹   ENSP00000363620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,619 - 33,418,070 (-)Ensembl
RefSeq Acc Id: ENST00000374500   ⟹   ENSP00000363624
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,442 - 33,418,317 (-)Ensembl
RefSeq Acc Id: ENST00000440279   ⟹   ENSP00000403268
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,552 - 33,417,921 (-)Ensembl
RefSeq Acc Id: ENST00000462802
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,442 - 33,418,043 (-)Ensembl
RefSeq Acc Id: ENST00000465956
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,551 - 33,417,889 (-)Ensembl
RefSeq Acc Id: ENST00000479249
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,542 - 33,417,543 (-)Ensembl
RefSeq Acc Id: ENST00000482684   ⟹   ENSP00000417823
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,550 - 33,418,107 (-)Ensembl
RefSeq Acc Id: ENST00000487637
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,561 - 33,418,108 (-)Ensembl
RefSeq Acc Id: ENST00000488034   ⟹   ENSP00000417544
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,442 - 33,418,107 (-)Ensembl
RefSeq Acc Id: ENST00000488478   ⟹   ENSP00000418612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,550 - 33,418,086 (-)Ensembl
RefSeq Acc Id: ENST00000492510   ⟹   ENSP00000499470
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,417,984 - 33,418,187 (-)Ensembl
RefSeq Acc Id: ENST00000494751   ⟹   ENSP00000418659
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,550 - 33,418,058 (-)Ensembl
RefSeq Acc Id: ENST00000607266   ⟹   ENSP00000475963
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,550 - 33,417,931 (-)Ensembl
RefSeq Acc Id: ENST00000611509   ⟹   ENSP00000480360
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl633,416,542 - 33,418,288 (-)Ensembl
RefSeq Acc Id: NM_001014433   ⟹   NP_001014433
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38633,416,442 - 33,418,107 (-)NCBI
GRCh37633,384,319 - 33,386,111 (-)NCBI
Build 36633,492,297 - 33,494,043 (-)NCBI Archive
Celera634,938,742 - 34,940,488 (-)RGD
HuRef633,126,468 - 33,128,214 (-)RGD
CHM1_1633,386,214 - 33,387,959 (-)NCBI
T2T-CHM13v2.0633,237,804 - 33,239,469 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001014837   ⟹   NP_001014837
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38633,416,442 - 33,418,107 (-)NCBI
GRCh37633,384,319 - 33,386,111 (-)NCBI
Build 36633,492,297 - 33,494,043 (-)NCBI Archive
Celera634,938,742 - 34,940,488 (-)RGD
HuRef633,126,468 - 33,128,214 (-)RGD
CHM1_1633,386,214 - 33,387,959 (-)NCBI
T2T-CHM13v2.0633,237,804 - 33,239,469 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001014838   ⟹   NP_001014838
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38633,416,442 - 33,418,107 (-)NCBI
GRCh37633,384,319 - 33,386,111 (-)NCBI
Build 36633,492,297 - 33,494,043 (-)NCBI Archive
Celera634,938,742 - 34,940,488 (-)RGD
HuRef633,126,468 - 33,128,214 (-)RGD
CHM1_1633,386,214 - 33,387,959 (-)NCBI
T2T-CHM13v2.0633,237,804 - 33,239,469 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001014840   ⟹   NP_001014840
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38633,416,442 - 33,418,107 (-)NCBI
GRCh37633,384,319 - 33,386,111 (-)NCBI
Build 36633,492,297 - 33,494,043 (-)NCBI Archive
Celera634,938,742 - 34,940,488 (-)RGD
HuRef633,126,468 - 33,128,214 (-)RGD
CHM1_1633,386,214 - 33,387,959 (-)NCBI
T2T-CHM13v2.0633,237,804 - 33,239,469 (-)NCBI
Sequence:
RefSeq Acc Id: NM_015921   ⟹   NP_057005
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38633,416,442 - 33,418,107 (-)NCBI
GRCh37633,384,319 - 33,386,111 (-)NCBI
Build 36633,492,297 - 33,494,043 (-)NCBI Archive
Celera634,938,742 - 34,940,488 (-)RGD
HuRef633,126,468 - 33,128,214 (-)RGD
CHM1_1633,386,214 - 33,387,959 (-)NCBI
T2T-CHM13v2.0633,237,804 - 33,239,469 (-)NCBI
Sequence:
RefSeq Acc Id: NP_001014433   ⟸   NM_001014433
- Peptide Label: isoform 1 precursor
- Sequence:
RefSeq Acc Id: NP_057005   ⟸   NM_015921
- Peptide Label: isoform 1 precursor
- UniProtKB: O60888 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001014837   ⟸   NM_001014837
- Peptide Label: isoform 1 precursor
- UniProtKB: O60888 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001014838   ⟸   NM_001014838
- Peptide Label: isoform 1 precursor
- UniProtKB: O60888 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001014840   ⟸   NM_001014840
- Peptide Label: isoform 3 precursor
- UniProtKB: Q5SU05 (UniProtKB/Swiss-Prot),   Q5JXM9 (UniProtKB/Swiss-Prot),   Q3B784 (UniProtKB/Swiss-Prot),   A2BEL4 (UniProtKB/Swiss-Prot),   A2AB26 (UniProtKB/Swiss-Prot),   Q9NYQ9 (UniProtKB/Swiss-Prot),   O60888 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000363608   ⟸   ENST00000374484
RefSeq Acc Id: ENSP00000363620   ⟸   ENST00000374496
RefSeq Acc Id: ENSP00000363624   ⟸   ENST00000374500
RefSeq Acc Id: ENSP00000499470   ⟸   ENST00000492510
RefSeq Acc Id: ENSP00000480360   ⟸   ENST00000611509
RefSeq Acc Id: ENSP00000403268   ⟸   ENST00000440279
RefSeq Acc Id: ENSP00000418659   ⟸   ENST00000494751
RefSeq Acc Id: ENSP00000417823   ⟸   ENST00000482684
RefSeq Acc Id: ENSP00000418612   ⟸   ENST00000488478
RefSeq Acc Id: ENSP00000417544   ⟸   ENST00000488034
RefSeq Acc Id: ENSP00000475963   ⟸   ENST00000607266

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O60888-F1-model_v2 AlphaFold O60888 1-179 view protein structure

Promoters
RGD ID:6872892
Promoter ID:EPDNEW_H9611
Type:initiation region
Name:CUTA_2
Description:cutA divalent cation tolerance homolog
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H9612  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38633,417,934 - 33,417,994EPDNEW
RGD ID:6872894
Promoter ID:EPDNEW_H9612
Type:initiation region
Name:CUTA_1
Description:cutA divalent cation tolerance homolog
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H9611  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38633,418,107 - 33,418,167EPDNEW
RGD ID:6803915
Promoter ID:HG_KWN:53208
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:NM_001014837,   OTTHUMT00000076534,   OTTHUMT00000076535,   OTTHUMT00000076536,   OTTHUMT00000076537,   OTTHUMT00000076539,   OTTHUMT00000076540,   OTTHUMT00000076541,   OTTHUMT00000276529,   OTTHUMT00000276531,   OTTHUMT00000276532
Position:
Human AssemblyChrPosition (strand)Source
Build 36633,493,056 - 33,494,337 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:21101 AgrOrtholog
COSMIC CUTA COSMIC
Ensembl Genes ENSG00000112514 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000226492 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000374484.8 UniProtKB/TrEMBL
  ENST00000374496 ENTREZGENE
  ENST00000374496.3 UniProtKB/Swiss-Prot
  ENST00000374500 ENTREZGENE
  ENST00000374500.10 UniProtKB/Swiss-Prot
  ENST00000435267.6 UniProtKB/Swiss-Prot
  ENST00000440279 ENTREZGENE
  ENST00000440279.7 UniProtKB/Swiss-Prot
  ENST00000440930.6 UniProtKB/Swiss-Prot
  ENST00000461913.5 UniProtKB/TrEMBL
  ENST00000464657.5 UniProtKB/TrEMBL
  ENST00000482684.5 UniProtKB/TrEMBL
  ENST00000487148.5 UniProtKB/Swiss-Prot
  ENST00000488034 ENTREZGENE
  ENST00000488034.6 UniProtKB/Swiss-Prot
  ENST00000488478.5 UniProtKB/TrEMBL
  ENST00000494751.5 UniProtKB/TrEMBL
  ENST00000607266 ENTREZGENE
  ENST00000607266.5 UniProtKB/Swiss-Prot
Gene3D-CATH 3.30.70.120 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000112514 GTEx
  ENSG00000226492 GTEx
HGNC ID HGNC:21101 ENTREZGENE
Human Proteome Map CUTA Human Proteome Map
InterPro Ion_tolerance_CutA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  N-reg_PII-like_a/b UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  N-reg_PII/ATP_PRibTrfase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:51596 UniProtKB/Swiss-Prot
NCBI Gene 51596 ENTREZGENE
OMIM 616953 OMIM
PANTHER PROTEIN CUTA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR23419 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam CutA1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134928220 PharmGKB
Superfamily-SCOP SSF54913 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A2AB26 ENTREZGENE
  A2BEL4 ENTREZGENE
  C9IZG4_HUMAN UniProtKB/TrEMBL
  C9IZQ5_HUMAN UniProtKB/TrEMBL
  CUTA_HUMAN UniProtKB/Swiss-Prot
  F2Z2Q5_HUMAN UniProtKB/TrEMBL
  H0YDR4_HUMAN UniProtKB/TrEMBL
  L8E740_HUMAN UniProtKB/TrEMBL
  O60888 ENTREZGENE
  Q3B784 ENTREZGENE
  Q5JXM9 ENTREZGENE
  Q5SU05 ENTREZGENE
  Q9NYQ9 ENTREZGENE
UniProt Secondary A2AB26 UniProtKB/Swiss-Prot
  A2BEL4 UniProtKB/Swiss-Prot
  Q3B784 UniProtKB/Swiss-Prot
  Q5JXM9 UniProtKB/Swiss-Prot
  Q5SU05 UniProtKB/Swiss-Prot
  Q9NYQ9 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-07-26 CUTA  cutA divalent cation tolerance homolog    cutA divalent cation tolerance homolog (E. coli)  Symbol and/or name change 5135510 APPROVED
2016-04-05 CUTA  cutA divalent cation tolerance homolog (E. coli)  ACHAP  acetylcholinesterase-associated protein  Data merged from RGD:1353412 737654 PROVISIONAL