COX4I1 (cytochrome c oxidase subunit 4I1) - Rat Genome Database

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Gene: COX4I1 (cytochrome c oxidase subunit 4I1) Homo sapiens
Analyze
Symbol: COX4I1
Name: cytochrome c oxidase subunit 4I1
RGD ID: 68539
HGNC Page HGNC:2265
Description: Predicted to enable cytochrome-c oxidase activity. Predicted to be involved in mitochondrial electron transport, cytochrome c to oxygen. Located in mitochondrion and nucleoplasm. Part of mitochondrial membrane and respiratory chain complex IV. Implicated in mitochondrial complex IV deficiency nuclear type 16.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: COX IV-1; COX4; COX4-1; COXIV; COXIV-1; cytochrome c oxidase polypeptide IV; cytochrome c oxidase subunit 4 isoform 1, mitochondrial; cytochrome c oxidase subunit IV; cytochrome c oxidase, subunit 4a; FLJ23483; MC4DN16; MGC72016
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Related Pseudogenes: COX4I1P1   COX4I1P2  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381685,799,695 - 85,807,068 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1685,798,633 - 85,807,068 (+)EnsemblGRCh38hg38GRCh38
GRCh371685,833,301 - 85,840,674 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361684,390,697 - 84,398,109 (+)NCBINCBI36Build 36hg18NCBI36
Build 341684,390,696 - 84,398,109NCBI
Celera1670,136,278 - 70,143,686 (+)NCBICelera
Cytogenetic Map16q24.1NCBI
HuRef1671,574,688 - 71,582,119 (+)NCBIHuRef
CHM1_11687,244,717 - 87,252,148 (+)NCBICHM1_1
T2T-CHM13v2.01691,865,215 - 91,872,584 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-catechin  (EXP)
(+)-dexrazoxane  (ISO)
(1->4)-beta-D-glucan  (ISO)
(R)-lipoic acid  (ISO)
1,2-dimethylhydrazine  (ISO)
1-chloro-2,4-dinitrobenzene  (EXP)
1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one  (EXP)
2,2',4,4',5,5'-hexachlorobiphenyl  (ISO)
2,2',5,5'-tetrachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4-dinitrophenol  (ISO)
2-amino-14,16-dimethyloctadecan-3-ol  (EXP)
3,3',5-triiodo-L-thyronine  (ISO)
3-methylcholanthrene  (EXP,ISO)
3-nitropropanoic acid  (ISO)
4,4'-sulfonyldiphenol  (EXP)
4-phenylbutyric acid  (EXP)
5-methoxy-2-\{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl\}-1H-benzimidazole  (ISO)
6-propyl-2-thiouracil  (ISO)
8-bromo-3',5'-cyclic GMP  (EXP)
acetamiprid  (ISO)
acrolein  (ISO)
aflatoxin B1  (EXP)
aldehydo-D-glucose  (EXP)
all-trans-retinoic acid  (EXP)
alloxan  (ISO)
alpha-Zearalanol  (ISO)
AM-251  (ISO)
amiodarone  (ISO)
ammonium chloride  (ISO)
Aroclor 1254  (ISO)
arsenite(3-)  (EXP)
arsenous acid  (EXP)
atrazine  (EXP)
benzbromarone  (ISO)
berberine  (ISO)
beta-lapachone  (EXP)
bisphenol A  (EXP,ISO)
Bisphenol B  (EXP)
bisphenol F  (EXP)
cadmium atom  (EXP,ISO)
cadmium dichloride  (EXP,ISO)
calcitriol  (ISO)
capsaicin  (ISO)
CCCP  (EXP)
chloropicrin  (EXP)
chloroquine  (ISO)
clofibrate  (ISO)
cobalt dichloride  (EXP,ISO)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
copper(II) sulfate  (ISO)
corosolic acid  (EXP)
cyclosporin A  (EXP)
D-glucose  (EXP)
desferrioxamine B  (EXP)
diarsenic trioxide  (EXP)
dibutyl phthalate  (ISO)
dimethyl sulfoxide  (EXP)
dioxygen  (ISO)
diquat  (ISO)
disodium selenite  (EXP)
doxorubicin  (EXP,ISO)
ebselen  (EXP)
Erythropoietin  (EXP)
ethanol  (ISO)
etomoxir  (ISO)
flutamide  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
FR900359  (EXP)
glucose  (EXP)
hexadecanoic acid  (EXP)
hydrogen peroxide  (EXP)
hydroxytyrosol  (ISO)
imisopasem manganese  (ISO)
ivermectin  (EXP)
L-ethionine  (ISO)
limonene  (ISO)
lipoic acid  (ISO)
lipopolysaccharide  (EXP)
LY294002  (EXP)
melatonin  (ISO)
methidathion  (ISO)
methotrexate  (EXP)
Mitotane  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
monocrotophos  (ISO)
N-acetyl-L-cysteine  (ISO)
N-methyl-4-phenylpyridinium  (EXP,ISO)
nitric oxide  (ISO)
omeprazole  (ISO)
ozone  (ISO)
paracetamol  (EXP)
paraquat  (ISO)
PCB138  (ISO)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
phenylephrine  (ISO)
pirinixic acid  (ISO)
potassium dichromate  (EXP)
progesterone  (ISO)
pyrogallol  (ISO)
quercetin  (ISO)
resveratrol  (EXP,ISO)
rotenone  (EXP,ISO)
S-butyl-DL-homocysteine (S,R)-sulfoximine  (ISO)
SB 431542  (EXP)
silicon atom  (ISO)
sodium arsenite  (ISO)
sodium dichromate  (EXP)
sodium fluoride  (ISO)
sodium hydrogensulfite  (ISO)
sodium nitrate  (ISO)
sulfur dioxide  (ISO)
T-2 toxin  (ISO)
temozolomide  (EXP)
tetrachloromethane  (ISO)
thapsigargin  (ISO)
thimerosal  (EXP)
thioacetamide  (ISO)
toluene  (ISO)
triphenyl phosphate  (EXP)
triptonide  (ISO)
tungsten  (ISO)
tunicamycin  (EXP)
valproic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. KEGG: Kyoto Encyclopedia of Genes and Genomes KEGG
3. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
4. Undernutrition during suckling in rats elevates plasma adiponectin and its receptor in skeletal muscle regardless of diet composition: a protective effect? Prior LJ, etal., Int J Obes (Lond). 2008 Aug 26.
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1311608   PMID:1319058   PMID:2157630   PMID:2162812   PMID:2444497   PMID:8223633   PMID:8619474   PMID:10337626   PMID:10878243   PMID:11311561   PMID:12477932   PMID:12766061  
PMID:14607829   PMID:15146197   PMID:15342556   PMID:15489334   PMID:15565177   PMID:16341674   PMID:16344560   PMID:17353931   PMID:17418790   PMID:18029348   PMID:19393246   PMID:19726511  
PMID:19843159   PMID:19946888   PMID:20186120   PMID:20307258   PMID:20413852   PMID:20833797   PMID:20877624   PMID:21771582   PMID:21802404   PMID:21832049   PMID:21841246   PMID:21873635  
PMID:21939634   PMID:21978537   PMID:22079200   PMID:22119785   PMID:22190034   PMID:22252130   PMID:22419111   PMID:23260140   PMID:23285255   PMID:23362268   PMID:23376485   PMID:23400010  
PMID:25416956   PMID:25544563   PMID:25642632   PMID:25726526   PMID:25959673   PMID:26186194   PMID:26321642   PMID:26344197   PMID:26496610   PMID:26746385   PMID:26759378   PMID:27342126  
PMID:27432908   PMID:27880917   PMID:28302793   PMID:28514442   PMID:28515276   PMID:28766551   PMID:28916538   PMID:29128334   PMID:29180619   PMID:29507755   PMID:29509190   PMID:29509794  
PMID:29540532   PMID:29568061   PMID:29937147   PMID:30021884   PMID:30030519   PMID:30097533   PMID:30223867   PMID:30833792   PMID:30884312   PMID:30948266   PMID:31056398   PMID:31180492  
PMID:31391242   PMID:31515488   PMID:31527615   PMID:31536960   PMID:31586073   PMID:31616248   PMID:31617661   PMID:31980649   PMID:32513696   PMID:32628020   PMID:32707033   PMID:32814053  
PMID:32838362   PMID:32877691   PMID:32913203   PMID:33672589   PMID:33957083   PMID:33961781   PMID:34079125   PMID:34349018   PMID:34373451   PMID:34800366   PMID:34901782   PMID:35140242  
PMID:35213938   PMID:35271311   PMID:35456968   PMID:35563538   PMID:35833506   PMID:35918402   PMID:35944360   PMID:36215168   PMID:36217030   PMID:36225252   PMID:36369321   PMID:36373674  
PMID:37071682   PMID:37164154   PMID:37616343   PMID:37827155   PMID:38113892   PMID:38149324   PMID:38334954   PMID:38718733   PMID:39147351  


Genomics

Comparative Map Data
COX4I1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381685,799,695 - 85,807,068 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1685,798,633 - 85,807,068 (+)EnsemblGRCh38hg38GRCh38
GRCh371685,833,301 - 85,840,674 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361684,390,697 - 84,398,109 (+)NCBINCBI36Build 36hg18NCBI36
Build 341684,390,696 - 84,398,109NCBI
Celera1670,136,278 - 70,143,686 (+)NCBICelera
Cytogenetic Map16q24.1NCBI
HuRef1671,574,688 - 71,582,119 (+)NCBIHuRef
CHM1_11687,244,717 - 87,252,148 (+)NCBICHM1_1
T2T-CHM13v2.01691,865,215 - 91,872,584 (+)NCBIT2T-CHM13v2.0
Cox4i1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398121,394,964 - 121,400,948 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl8121,394,961 - 121,400,946 (+)EnsemblGRCm39 Ensembl
GRCm388120,668,225 - 120,674,209 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8120,668,222 - 120,674,207 (+)EnsemblGRCm38mm10GRCm38
MGSCv378123,192,190 - 123,198,109 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv368123,554,281 - 123,572,260 (+)NCBIMGSCv36mm8
Celera8124,884,148 - 124,890,066 (+)NCBICelera
Cytogenetic Map8E1NCBI
cM Map869.99NCBI
Cox4i1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81965,630,383 - 65,636,623 (+)NCBIGRCr8
mRatBN7.21948,721,680 - 48,727,920 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1948,721,199 - 48,727,921 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1955,516,046 - 55,522,295 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01956,196,685 - 56,202,925 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01958,411,393 - 58,417,603 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01954,245,958 - 54,252,198 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1954,245,950 - 54,252,225 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01964,965,282 - 64,971,577 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41951,023,960 - 51,030,200 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11951,028,840 - 51,035,081 (+)NCBI
Celera1947,973,554 - 47,979,795 (+)NCBICelera
Cytogenetic Map19q12NCBI
LOC102020379
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955541884,988 - 890,890 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955541885,824 - 890,824 (+)NCBIChiLan1.0ChiLan1.0
LOC100969890
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21895,550,632 - 95,557,952 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan116101,467,899 - 101,475,288 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01666,467,259 - 66,474,652 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11685,805,595 - 85,812,851 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1685,805,611 - 85,812,851 (+)Ensemblpanpan1.1panPan2
COX4I1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1566,883,730 - 66,891,734 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl566,883,732 - 66,891,500 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha566,899,917 - 66,907,747 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0567,112,369 - 67,120,207 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl567,112,369 - 67,148,247 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1567,133,830 - 67,141,650 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0566,967,910 - 66,975,726 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0567,382,851 - 67,390,678 (-)NCBIUU_Cfam_GSD_1.0
LOC101971634
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934926,937,176 - 26,943,452 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366412,690,176 - 2,695,387 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366412,690,723 - 2,695,230 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
COX4I1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl63,131,019 - 3,137,530 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.163,131,017 - 3,137,619 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.263,453,560 - 3,458,877 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103233412
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1571,207,509 - 71,214,976 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl571,206,941 - 71,215,034 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660474,523,156 - 4,530,607 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
LOC101705610
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247462,187,492 - 2,194,040 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247462,187,443 - 2,193,874 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in COX4I1
21 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16q23.1-24.3(chr16:78816291-90081985)x3 copy number gain See cases [RCV000050840] Chr16:78816291..90081985 [GRCh38]
Chr16:78850188..90148393 [GRCh37]
Chr16:77407689..88675894 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q23.3-24.2(chr16:83878992-87223838)x1 copy number loss See cases [RCV000051122] Chr16:83878992..87223838 [GRCh38]
Chr16:83912597..87257444 [GRCh37]
Chr16:82470098..85814945 [NCBI36]
Chr16:16q23.3-24.2
pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3 copy number gain See cases [RCV000052421] Chr16:65313395..90081985 [GRCh38]
Chr16:65347298..90148393 [GRCh37]
Chr16:63904799..88675894 [NCBI36]
Chr16:16q21-24.3
pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70514631-90081985)x3 copy number gain See cases [RCV000052422] Chr16:70514631..90081985 [GRCh38]
Chr16:70548534..90148393 [GRCh37]
Chr16:69106035..88675894 [NCBI36]
Chr16:16q22.1-24.3
pathogenic
GRCh38/hg38 16q24.1(chr16:85568964-85843360)x1 copy number loss See cases [RCV000052020] Chr16:85568964..85843360 [GRCh38]
Chr16:85602570..85876966 [GRCh37]
Chr16:84160071..84434467 [NCBI36]
Chr16:16q24.1
uncertain significance
GRCh38/hg38 16q23.1-24.3(chr16:76873569-90081985)x3 copy number gain See cases [RCV000052423] Chr16:76873569..90081985 [GRCh38]
Chr16:76907466..90148393 [GRCh37]
Chr16:75464967..88675894 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:82173150-90081985)x3 copy number gain See cases [RCV000052424] Chr16:82173150..90081985 [GRCh38]
Chr16:82206755..90148393 [GRCh37]
Chr16:80764256..88675894 [NCBI36]
Chr16:16q23.3-24.3
pathogenic
GRCh38/hg38 16q24.1-24.3(chr16:84707538-90081985)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052425]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052425]|See cases [RCV000052425] Chr16:84707538..90081985 [GRCh38]
Chr16:84741144..90148393 [GRCh37]
Chr16:83298645..88675894 [NCBI36]
Chr16:16q24.1-24.3
pathogenic
GRCh38/hg38 16q23.1-24.2(chr16:78704275-87819342)x1 copy number loss See cases [RCV000053359] Chr16:78704275..87819342 [GRCh38]
Chr16:78738172..87852948 [GRCh37]
Chr16:77295673..86410449 [NCBI36]
Chr16:16q23.1-24.2
pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:83988570-90081985)x3 copy number gain See cases [RCV000135659] Chr16:83988570..90081985 [GRCh38]
Chr16:84022175..90148393 [GRCh37]
Chr16:82579676..88675894 [NCBI36]
Chr16:16q23.3-24.3
likely pathogenic
GRCh38/hg38 16q23.3-24.1(chr16:83687650-86073240)x1 copy number loss See cases [RCV000136504] Chr16:83687650..86073240 [GRCh38]
Chr16:83721255..86106846 [GRCh37]
Chr16:82278756..84664347 [NCBI36]
Chr16:16q23.3-24.1
pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80946659-90081985)x3 copy number gain See cases [RCV000136898] Chr16:80946659..90081985 [GRCh38]
Chr16:80980556..90148393 [GRCh37]
Chr16:79538057..88675894 [NCBI36]
Chr16:16q23.2-24.3
pathogenic|likely pathogenic
GRCh38/hg38 16q22.1-24.3(chr16:70749398-90096995)x3 copy number gain See cases [RCV000137495] Chr16:70749398..90096995 [GRCh38]
Chr16:70783301..90163403 [GRCh37]
Chr16:69340802..88690904 [NCBI36]
Chr16:16q22.1-24.3
pathogenic
GRCh38/hg38 16q23.3-24.3(chr16:83478453-89932910)x3 copy number gain See cases [RCV000137980] Chr16:83478453..89932910 [GRCh38]
Chr16:83512058..89999318 [GRCh37]
Chr16:82069559..88526819 [NCBI36]
Chr16:16q23.3-24.3
likely pathogenic
GRCh38/hg38 16q24.1(chr16:85026633-85843419)x3 copy number gain See cases [RCV000138715] Chr16:85026633..85843419 [GRCh38]
Chr16:85060239..85877025 [GRCh37]
Chr16:83617740..84434526 [NCBI36]
Chr16:16q24.1
likely benign
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3 copy number gain See cases [RCV000139426] Chr16:65511483..90096995 [GRCh38]
Chr16:65545386..90163403 [GRCh37]
Chr16:64102887..88690904 [NCBI36]
Chr16:16q21-24.3
pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:75377981-90081992)x3 copy number gain See cases [RCV000139302] Chr16:75377981..90081992 [GRCh38]
Chr16:75411879..90148400 [GRCh37]
Chr16:73969380..88675901 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q24.1-24.3(chr16:85552976-90096995)x3 copy number gain See cases [RCV000139658] Chr16:85552976..90096995 [GRCh38]
Chr16:85586582..90163403 [GRCh37]
Chr16:84144083..88690904 [NCBI36]
Chr16:16q24.1-24.3
pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80717291-90096662)x3 copy number gain See cases [RCV000141128] Chr16:80717291..90096662 [GRCh38]
Chr16:80751188..90163070 [GRCh37]
Chr16:79308689..88690571 [NCBI36]
Chr16:16q23.2-24.3
pathogenic
GRCh38/hg38 16q23.1-24.3(chr16:76336203-90088654)x3 copy number gain See cases [RCV000141700] Chr16:76336203..90088654 [GRCh38]
Chr16:76370100..90155062 [GRCh37]
Chr16:74927601..88682563 [NCBI36]
Chr16:16q23.1-24.3
pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3 copy number gain See cases [RCV000142578] Chr16:64389378..90081985 [GRCh38]
Chr16:64423281..90148393 [GRCh37]
Chr16:62980782..88675894 [NCBI36]
Chr16:16q21-24.3
pathogenic|likely pathogenic
GRCh38/hg38 16q23.2-24.3(chr16:80067315-90057871)x3 copy number gain See cases [RCV000142698] Chr16:80067315..90057871 [GRCh38]
Chr16:80101212..90124279 [GRCh37]
Chr16:78658713..88651780 [NCBI36]
Chr16:16q23.2-24.3
pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3 copy number gain See cases [RCV000143425] Chr16:52899183..90088654 [GRCh38]
Chr16:52933095..90155062 [GRCh37]
Chr16:51490596..88682563 [NCBI36]
Chr16:16q12.2-24.3
pathogenic
GRCh37/hg19 16q23.1-24.3(chr16:74872514-90274440)x3 copy number gain See cases [RCV000240108] Chr16:74872514..90274440 [GRCh37]
Chr16:16q23.1-24.3
pathogenic
t(5;16)(p15.31;q23.1) translocation not provided [RCV000203391] Chr5:1..8180513 [GRCh37]
Chr16:76935310..90354753 [GRCh37]
Chr5:5p15.33-15.31
Chr16:16q23.1-24.3
likely pathogenic
GRCh37/hg19 16q23.3-24.1(chr16:83553094-86098013)x1 copy number loss See cases [RCV000203439] Chr16:83553094..86098013 [GRCh37]
Chr16:16q23.3-24.1
likely pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1 copy number loss Breast ductal adenocarcinoma [RCV000207138] Chr16:46615804..90142285 [GRCh37]
Chr16:16q11.2-24.3
uncertain significance
GRCh37/hg19 16q22.2-24.3(chr16:72107834-90142285)x1 copy number loss Breast ductal adenocarcinoma [RCV000207182] Chr16:72107834..90142285 [GRCh37]
Chr16:16q22.2-24.3
uncertain significance
Single allele complex Breast ductal adenocarcinoma [RCV000207314] Chr16:56368689..90141355 [GRCh37]
Chr16:16q12.2-24.3
uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3 copy number gain See cases [RCV000446110] Chr16:46464488..90155062 [GRCh37]
Chr16:16q11.2-24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16q24.1-24.2(chr16:85491404-87883528)x1 copy number loss See cases [RCV000510624] Chr16:85491404..87883528 [GRCh37]
Chr16:16q24.1-24.2
pathogenic
GRCh37/hg19 16q24.1(chr16:85787339-86138570)x1 copy number loss See cases [RCV000511492] Chr16:85787339..86138570 [GRCh37]
Chr16:16q24.1
uncertain significance
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3
uncertain significance
GRCh37/hg19 16q24.1-24.3(chr16:84937273-89836905)x4 copy number gain See cases [RCV000511606] Chr16:84937273..89836905 [GRCh37]
Chr16:16q24.1-24.3
likely pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
NM_001861.6(COX4I1):c.124C>T (p.Arg42Cys) single nucleotide variant not specified [RCV004294006] Chr16:85804987 [GRCh38]
Chr16:85838593 [GRCh37]
Chr16:16q24.1
uncertain significance
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3 copy number gain See cases [RCV000512511] Chr16:57051473..89797669 [GRCh37]
Chr16:16q13-24.3
pathogenic
GRCh37/hg19 16q24.1-24.3(chr16:85838574-90155062)x3 copy number gain See cases [RCV000512440] Chr16:85838574..90155062 [GRCh37]
Chr16:16q24.1-24.3
pathogenic
GRCh37/hg19 16q23.3-24.3(chr16:83001540-90155062)x3 copy number gain See cases [RCV000512468] Chr16:83001540..90155062 [GRCh37]
Chr16:16q23.3-24.3
likely pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626435] Chr16:46455960..90354753 [GRCh37]
Chr16:16q11.2-24.3
drug response
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626429] Chr16:46497599..90354753 [GRCh37]
Chr16:16q11.2-24.3
drug response
GRCh37/hg19 16q23.2-24.3(chr16:79400436-90155062)x3 copy number gain not provided [RCV000683845] Chr16:79400436..90155062 [GRCh37]
Chr16:16q23.2-24.3
pathogenic
GRCh37/hg19 16q22.2-24.3(chr16:72515938-90155062)x3 copy number gain not provided [RCV000683831] Chr16:72515938..90155062 [GRCh37]
Chr16:16q22.2-24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16q23.3-24.3(chr16:82761333-90055381) copy number gain not provided [RCV000767619] Chr16:82761333..90055381 [GRCh37]
Chr16:16q23.3-24.3
pathogenic
GRCh37/hg19 16q24.1(chr16:85746644-85847401)x3 copy number gain not provided [RCV000847686] Chr16:85746644..85847401 [GRCh37]
Chr16:16q24.1
uncertain significance
GRCh37/hg19 16q24.1(chr16:84815936-86045285)x1 copy number loss not provided [RCV001006835] Chr16:84815936..86045285 [GRCh37]
Chr16:16q24.1
uncertain significance
GRCh37/hg19 16q24.1(chr16:85038804-85876297)x3 copy number gain not provided [RCV000847805] Chr16:85038804..85876297 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.228T>C (p.Asp76=) single nucleotide variant COX4I1-related disorder [RCV003970828]|Mitochondrial complex 4 deficiency, nuclear type 16 [RCV002488047]|not provided [RCV000961228] Chr16:85805091 [GRCh38]
Chr16:85838697 [GRCh37]
Chr16:16q24.1
benign|likely benign
NM_001861.6(COX4I1):c.159G>A (p.Lys53=) single nucleotide variant COX4I1-related disorder [RCV003975544]|not provided [RCV000882179] Chr16:85805022 [GRCh38]
Chr16:85838628 [GRCh37]
Chr16:16q24.1
benign
NM_001861.6(COX4I1):c.454C>A (p.Pro152Thr) single nucleotide variant Mitochondrial complex 4 deficiency, nuclear type 16 [RCV001034698] Chr16:85806818 [GRCh38]
Chr16:85840424 [GRCh37]
Chr16:16q24.1
pathogenic
GRCh37/hg19 16q24.1-24.2(chr16:84872102-87678641) copy number loss Alveolar capillary dysplasia with pulmonary venous misalignment [RCV001004081] Chr16:84872102..87678641 [GRCh37]
Chr16:16q24.1-24.2
pathogenic
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3 copy number gain not provided [RCV001249359] Chr16:61524229..90155062 [GRCh37]
Chr16:16q21-24.3
not provided
NM_001861.6(COX4I1):c.303_304delinsTT (p.Lys101_Thr102delinsAsnSer) indel Mitochondrial complex IV deficiency, nuclear type 1 [RCV001034697] Chr16:85805794..85805795 [GRCh38]
Chr16:85839400..85839401 [GRCh37]
Chr16:16q24.1
pathogenic
Single allele deletion Alveolar capillary dysplasia with pulmonary venous misalignment [RCV001251455] Chr16:83931797..86285776 [GRCh37]
Chr16:16q23.3-24.1
likely pathogenic
GRCh37/hg19 16q23.2-24.3(chr16:80386595-90163348)x3 copy number gain not provided [RCV001795551] Chr16:80386595..90163348 [GRCh37]
Chr16:16q23.2-24.3
pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46503968-90155062)x3 copy number gain not provided [RCV002221458] Chr16:46503968..90155062 [GRCh37]
Chr16:16q11.2-24.3
pathogenic
GRCh37/hg19 16q22.2-24.3(chr16:71641395-90161959)x3 copy number gain Syndromic anorectal malformation [RCV002286607] Chr16:71641395..90161959 [GRCh37]
Chr16:16q22.2-24.3
likely pathogenic
NM_001861.6(COX4I1):c.379G>A (p.Gly127Ser) single nucleotide variant not specified [RCV004188456] Chr16:85806743 [GRCh38]
Chr16:85840349 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.140C>T (p.Pro47Leu) single nucleotide variant not specified [RCV004127454] Chr16:85805003 [GRCh38]
Chr16:85838609 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.25C>G (p.Leu9Val) single nucleotide variant not specified [RCV004170002] Chr16:85801230 [GRCh38]
Chr16:85834836 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.178A>G (p.Lys60Glu) single nucleotide variant not specified [RCV004282897] Chr16:85805041 [GRCh38]
Chr16:85838647 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.428A>G (p.Lys143Arg) single nucleotide variant not specified [RCV004268074] Chr16:85806792 [GRCh38]
Chr16:85840398 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.65G>A (p.Arg22Gln) single nucleotide variant not specified [RCV004249634] Chr16:85801270 [GRCh38]
Chr16:85834876 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.496G>A (p.Glu166Lys) single nucleotide variant not specified [RCV004345224] Chr16:85806860 [GRCh38]
Chr16:85840466 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.231G>C (p.Glu77Asp) single nucleotide variant not specified [RCV004344263] Chr16:85805094 [GRCh38]
Chr16:85838700 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.487G>A (p.Glu163Lys) single nucleotide variant not specified [RCV004350276] Chr16:85806851 [GRCh38]
Chr16:85840457 [GRCh37]
Chr16:16q24.1
uncertain significance
GRCh37/hg19 16q24.1-24.2(chr16:84555718-87910245)x1 copy number loss not provided [RCV003483302] Chr16:84555718..87910245 [GRCh37]
Chr16:16q24.1-24.2
pathogenic
NM_001861.6(COX4I1):c.240G>C (p.Glu80Asp) single nucleotide variant not provided [RCV003413018] Chr16:85805103 [GRCh38]
Chr16:85838709 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.122G>A (p.Arg41Gln) single nucleotide variant not provided [RCV003413017] Chr16:85804985 [GRCh38]
Chr16:85838591 [GRCh37]
Chr16:16q24.1
likely benign
GRCh37/hg19 16q24.1(chr16:85491404-86524881)x3 copy number gain not specified [RCV003987164] Chr16:85491404..86524881 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.454C>T (p.Pro152Ser) single nucleotide variant not specified [RCV004372262] Chr16:85806818 [GRCh38]
Chr16:85840424 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.43A>G (p.Ile15Val) single nucleotide variant not specified [RCV004372261] Chr16:85801248 [GRCh38]
Chr16:85834854 [GRCh37]
Chr16:16q24.1
uncertain significance
NM_001861.6(COX4I1):c.7G>A (p.Ala3Thr) single nucleotide variant COX4I1-related disorder [RCV003982367] Chr16:85801212 [GRCh38]
Chr16:85834818 [GRCh37]
Chr16:16q24.1
benign
NM_001861.6(COX4I1):c.504G>A (p.Lys168=) single nucleotide variant COX4I1-related disorder [RCV003961395] Chr16:85806868 [GRCh38]
Chr16:85840474 [GRCh37]
Chr16:16q24.1
benign
NM_001861.6(COX4I1):c.243G>A (p.Leu81=) single nucleotide variant COX4I1-related disorder [RCV003896809] Chr16:85805734 [GRCh38]
Chr16:85839340 [GRCh37]
Chr16:16q24.1
likely benign
GRCh37/hg19 16q23.3-24.3(chr16:82865402-90163542)x3 copy number gain not provided [RCV004577473] Chr16:82865402..90163542 [GRCh37]
Chr16:16q23.3-24.3
pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:3139
Count of miRNA genes:888
Interacting mature miRNAs:1078
Transcripts:ENST00000253452, ENST00000561569, ENST00000562336, ENST00000562929, ENST00000563774, ENST00000564544, ENST00000564648, ENST00000564903, ENST00000565078, ENST00000566115, ENST00000566405, ENST00000566617, ENST00000567241, ENST00000567266, ENST00000568339, ENST00000568794, ENST00000569997, ENST00000570123
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407039189GWAS688165_Hleprosy QTL GWAS688165 (human)0.0000004leprosy168580265085802651Human

Markers in Region
RH41774  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371685,840,432 - 85,840,581UniSTSGRCh37
Build 361684,397,933 - 84,398,082RGDNCBI36
Celera1670,143,510 - 70,143,659RGD
Cytogenetic Map16q24.1UniSTS
HuRef1671,581,943 - 71,582,092UniSTS
PMC164701P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371685,838,672 - 85,839,372UniSTSGRCh37
Build 361684,396,173 - 84,396,873RGDNCBI36
Celera1670,141,750 - 70,142,451RGD
Cytogenetic Map16q24.1UniSTS
HuRef1671,580,183 - 71,580,884UniSTS
D13S1553  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.2-q34.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map7q33UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3p21.1-p14.2UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map1p34UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map16p13.11UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6p25.1UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
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Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
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Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
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Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
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Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
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Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
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Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
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Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
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Cytogenetic Map1q25UniSTS
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Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
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Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
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Cytogenetic Map5p13UniSTS
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Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
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Cytogenetic Map12qUniSTS
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Cytogenetic Map10p14UniSTS
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Cytogenetic Map19q13UniSTS
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Cytogenetic Map2q13UniSTS
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Cytogenetic Map15q26.2UniSTS
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Cytogenetic Map12p11.21UniSTS
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Cytogenetic Map14q24.2UniSTS
RH66835  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map16q24.1UniSTS
GeneMap99-GB4 RH Map16478.05UniSTS
NCBI RH Map16666.5UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
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Cytogenetic Map3p22-p21.3UniSTS
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Cytogenetic Map1q21UniSTS
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Cytogenetic Map2q37.3UniSTS
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Cytogenetic Map11p13UniSTS
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Cytogenetic Map3q22-q24UniSTS
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Cytogenetic MapXp22.2UniSTS
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Cytogenetic Map5q31.1UniSTS
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Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2439 2788 2253 4974 1726 2351 6 624 1951 465 2270 7306 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_042280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318794 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318797 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001318802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001861 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433623 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC018695 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF005889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF017115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AH005828 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027136 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC021236 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC039013 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC062437 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE615615 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE728651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG614492 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM835194 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP343428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT019825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU599266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CD677397 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471114 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN406213 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA623889 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB502762 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M21575 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M34600 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U90915 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X54802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000253452   ⟹   ENSP00000253452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,695 - 85,807,068 (+)Ensembl
Ensembl Acc Id: ENST00000561569   ⟹   ENSP00000457015
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,697 - 85,807,002 (+)Ensembl
Ensembl Acc Id: ENST00000562336   ⟹   ENSP00000457513
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,693 - 85,807,044 (+)Ensembl
Ensembl Acc Id: ENST00000562929
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,805,069 - 85,807,031 (+)Ensembl
Ensembl Acc Id: ENST00000563774
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,696 - 85,805,350 (+)Ensembl
Ensembl Acc Id: ENST00000564544   ⟹   ENSP00000456452
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,708 - 85,806,975 (+)Ensembl
Ensembl Acc Id: ENST00000564648
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,801,202 - 85,806,967 (+)Ensembl
Ensembl Acc Id: ENST00000564903   ⟹   ENSP00000454714
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,801,202 - 85,806,968 (+)Ensembl
Ensembl Acc Id: ENST00000565078   ⟹   ENSP00000454869
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,798,633 - 85,804,992 (+)Ensembl
Ensembl Acc Id: ENST00000566115   ⟹   ENSP00000455437
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,638 - 85,805,096 (+)Ensembl
Ensembl Acc Id: ENST00000566405   ⟹   ENSP00000455301
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,698 - 85,806,802 (+)Ensembl
Ensembl Acc Id: ENST00000566617
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,760 - 85,805,309 (+)Ensembl
Ensembl Acc Id: ENST00000567241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,654 - 85,805,328 (+)Ensembl
Ensembl Acc Id: ENST00000567266
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,697 - 85,805,426 (+)Ensembl
Ensembl Acc Id: ENST00000568339
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,622 - 85,807,002 (+)Ensembl
Ensembl Acc Id: ENST00000568794   ⟹   ENSP00000455030
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,683 - 85,806,805 (+)Ensembl
Ensembl Acc Id: ENST00000569997
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,803,057 - 85,807,002 (+)Ensembl
Ensembl Acc Id: ENST00000570123
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1685,799,612 - 85,805,742 (+)Ensembl
RefSeq Acc Id: NM_001318786   ⟹   NP_001305715
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,807,068 (+)NCBI
CHM1_11687,244,717 - 87,252,149 (+)NCBI
T2T-CHM13v2.01691,865,215 - 91,872,584 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001318788   ⟹   NP_001305717
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,807,002 (+)NCBI
CHM1_11687,244,717 - 87,252,149 (+)NCBI
T2T-CHM13v2.01691,865,215 - 91,872,518 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001318794   ⟹   NP_001305723
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,807,002 (+)NCBI
CHM1_11687,244,717 - 87,252,149 (+)NCBI
T2T-CHM13v2.01691,865,215 - 91,872,518 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001318797   ⟹   NP_001305726
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,807,068 (+)NCBI
CHM1_11687,244,848 - 87,252,149 (+)NCBI
T2T-CHM13v2.01691,865,215 - 91,872,584 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001318802   ⟹   NP_001305731
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,807,002 (+)NCBI
CHM1_11687,244,717 - 87,252,149 (+)NCBI
T2T-CHM13v2.01691,865,215 - 91,872,518 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001861   ⟹   NP_001852
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,807,068 (+)NCBI
GRCh371685,833,173 - 85,840,608 (+)ENTREZGENE
Build 361684,390,697 - 84,398,109 (+)NCBI Archive
HuRef1671,574,688 - 71,582,119 (+)ENTREZGENE
CHM1_11687,244,717 - 87,252,149 (+)NCBI
T2T-CHM13v2.01691,865,215 - 91,872,584 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024450156   ⟹   XP_024305924
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,807,068 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047433623   ⟹   XP_047289579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,800,277 - 85,807,068 (+)NCBI
Protein Sequences
Protein RefSeqs NP_001305715 (Get FASTA)   NCBI Sequence Viewer  
  NP_001305717 (Get FASTA)   NCBI Sequence Viewer  
  NP_001305723 (Get FASTA)   NCBI Sequence Viewer  
  NP_001305726 (Get FASTA)   NCBI Sequence Viewer  
  NP_001305731 (Get FASTA)   NCBI Sequence Viewer  
  NP_001852 (Get FASTA)   NCBI Sequence Viewer  
  XP_024305924 (Get FASTA)   NCBI Sequence Viewer  
  XP_047289579 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA52059 (Get FASTA)   NCBI Sequence Viewer  
  AAA99312 (Get FASTA)   NCBI Sequence Viewer  
  AAB51058 (Get FASTA)   NCBI Sequence Viewer  
  AAB94819 (Get FASTA)   NCBI Sequence Viewer  
  AAB97750 (Get FASTA)   NCBI Sequence Viewer  
  AAC99578 (Get FASTA)   NCBI Sequence Viewer  
  AAH08704 (Get FASTA)   NCBI Sequence Viewer  
  AAH21236 (Get FASTA)   NCBI Sequence Viewer  
  AAH47869 (Get FASTA)   NCBI Sequence Viewer  
  AAH62437 (Get FASTA)   NCBI Sequence Viewer  
  AAV38628 (Get FASTA)   NCBI Sequence Viewer  
  BAG34789 (Get FASTA)   NCBI Sequence Viewer  
  CAA38573 (Get FASTA)   NCBI Sequence Viewer  
  EAW95436 (Get FASTA)   NCBI Sequence Viewer  
  EAW95437 (Get FASTA)   NCBI Sequence Viewer  
  EAW95438 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000253452
  ENSP00000253452.2
  ENSP00000454714.1
  ENSP00000454869.1
  ENSP00000455030
  ENSP00000455030.1
  ENSP00000455301
  ENSP00000455301.1
  ENSP00000455437.1
  ENSP00000456452.1
  ENSP00000457015
  ENSP00000457015.1
  ENSP00000457513.1
GenBank Protein P13073 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001852   ⟸   NM_001861
- Peptide Label: isoform 1 precursor
- UniProtKB: D3DUM7 (UniProtKB/Swiss-Prot),   B2R4J2 (UniProtKB/Swiss-Prot),   Q6P666 (UniProtKB/Swiss-Prot),   P13073 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305715   ⟸   NM_001318786
- Peptide Label: isoform 1 precursor
- UniProtKB: D3DUM7 (UniProtKB/Swiss-Prot),   B2R4J2 (UniProtKB/Swiss-Prot),   Q6P666 (UniProtKB/Swiss-Prot),   P13073 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305731   ⟸   NM_001318802
- Peptide Label: isoform 5
- UniProtKB: P13073 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001305723   ⟸   NM_001318794
- Peptide Label: isoform 3 precursor
- UniProtKB: H3BNV9 (UniProtKB/TrEMBL),   H3BN72 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001305717   ⟸   NM_001318788
- Peptide Label: isoform 2 precursor
- UniProtKB: H3BN72 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001305726   ⟸   NM_001318797
- Peptide Label: isoform 4
- UniProtKB: H3BPG0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024305924   ⟸   XM_024450156
- Peptide Label: isoform X1
- Sequence:
Ensembl Acc Id: ENSP00000253452   ⟸   ENST00000253452
Ensembl Acc Id: ENSP00000457015   ⟸   ENST00000561569
Ensembl Acc Id: ENSP00000457513   ⟸   ENST00000562336
Ensembl Acc Id: ENSP00000454714   ⟸   ENST00000564903
Ensembl Acc Id: ENSP00000456452   ⟸   ENST00000564544
Ensembl Acc Id: ENSP00000454869   ⟸   ENST00000565078
Ensembl Acc Id: ENSP00000455301   ⟸   ENST00000566405
Ensembl Acc Id: ENSP00000455437   ⟸   ENST00000566115
Ensembl Acc Id: ENSP00000455030   ⟸   ENST00000568794
RefSeq Acc Id: XP_047289579   ⟸   XM_047433623
- Peptide Label: isoform X2
- UniProtKB: P13073 (UniProtKB/Swiss-Prot),   D3DUM7 (UniProtKB/Swiss-Prot),   B2R4J2 (UniProtKB/Swiss-Prot),   Q6P666 (UniProtKB/Swiss-Prot)

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P13073-F1-model_v2 AlphaFold P13073 1-169 view protein structure

Promoters
RGD ID:6792947
Promoter ID:HG_KWN:24406
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000253452,   NM_001142288,   OTTHUMT00000269099,   UC002FJF.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361684,390,606 - 84,391,227 (-)MPROMDB
RGD ID:6850928
Promoter ID:EP73260
Type:initiation region
Name:HS_COX4I1
Description:Cytochrome c oxidase subunit IV isoform 1 , nuclear gene encodingmitochondrial protein.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:NEDO full length human cDNA sequencing project.; Oligo-capping
Position:
Human AssemblyChrPosition (strand)Source
Build 361684,390,802 - 84,390,862EPD
RGD ID:6792931
Promoter ID:HG_KWN:24407
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   K562,   Lymphoblastoid
Transcripts:UC002FJG.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361684,391,199 - 84,391,699 (+)MPROMDB
RGD ID:6810912
Promoter ID:HG_ACW:32070
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:COX4I1.KAPR07-UNSPLICED
Position:
Human AssemblyChrPosition (strand)Source
Build 361684,396,841 - 84,397,341 (+)MPROMDB
RGD ID:7233051
Promoter ID:EPDNEW_H22272
Type:multiple initiation site
Name:COX4I1_2
Description:cytochrome c oxidase subunit 4I1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22274  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,798,528 - 85,798,588EPDNEW
RGD ID:7233055
Promoter ID:EPDNEW_H22274
Type:initiation region
Name:COX4I1_1
Description:cytochrome c oxidase subunit 4I1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22272  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381685,799,695 - 85,799,755EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:2265 AgrOrtholog
COSMIC COX4I1 COSMIC
Ensembl Genes ENSG00000131143 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000253452 ENTREZGENE
  ENST00000253452.8 UniProtKB/Swiss-Prot
  ENST00000561569 ENTREZGENE
  ENST00000561569.5 UniProtKB/Swiss-Prot
  ENST00000562336.5 UniProtKB/Swiss-Prot
  ENST00000564544.1 UniProtKB/TrEMBL
  ENST00000564903.1 UniProtKB/TrEMBL
  ENST00000565078.5 UniProtKB/TrEMBL
  ENST00000566115.5 UniProtKB/TrEMBL
  ENST00000566405 ENTREZGENE
  ENST00000566405.5 UniProtKB/TrEMBL
  ENST00000568794 ENTREZGENE
  ENST00000568794.5 UniProtKB/TrEMBL
Gene3D-CATH 1.10.442.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000131143 GTEx
HGNC ID HGNC:2265 ENTREZGENE
Human Proteome Map COX4I1 Human Proteome Map
InterPro Cyt_c_oxidase_su4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_c_oxidase_su4_fam UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cyt_c_oxidase_su4_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:1327 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 1327 ENTREZGENE
OMIM 123864 OMIM
PANTHER CYTOCHROME C OXIDASE SUBUNIT 4 ISOFORM 1, MITOCHONDRIAL UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10707 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam COX4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA26781 PharmGKB
PRINTS CYTCOXIDASE4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  F138DOMAIN UniProtKB/TrEMBL
Superfamily-SCOP SSF81406 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B2R4J2 ENTREZGENE
  COX41_HUMAN UniProtKB/Swiss-Prot
  D3DUM7 ENTREZGENE
  H3BN72 ENTREZGENE, UniProtKB/TrEMBL
  H3BNI5_HUMAN UniProtKB/TrEMBL
  H3BNV9 ENTREZGENE, UniProtKB/TrEMBL
  H3BPG0 ENTREZGENE, UniProtKB/TrEMBL
  H3BPR4_HUMAN UniProtKB/TrEMBL
  P13073 ENTREZGENE
  Q6P666 ENTREZGENE
  Q86WV2_HUMAN UniProtKB/TrEMBL
UniProt Secondary B2R4J2 UniProtKB/Swiss-Prot
  D3DUM7 UniProtKB/Swiss-Prot
  Q6P666 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-16 COX4I1  cytochrome c oxidase subunit 4I1  COX4I1  cytochrome c oxidase subunit IV isoform 1  Symbol and/or name change 5135510 APPROVED