ERG28 (ergosterol biosynthesis 28 homolog) - Rat Genome Database

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Gene: ERG28 (ergosterol biosynthesis 28 homolog) Homo sapiens
Analyze
Symbol: ERG28
Name: ergosterol biosynthesis 28 homolog
RGD ID: 1321865
HGNC Page HGNC:1187
Description: Enables identical protein binding activity. Predicted to be involved in sterol biosynthetic process. Located in transport vesicle.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C14orf1; chromosome 14 open reading frame 1; ergosterol biosynthetic protein 28 homolog; NET51; probable ergosterol biosynthetic protein 28
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
GRCh381475,649,791 - 75,660,876 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1475,649,791 - 75,660,876 (-)EnsemblGRCh38hg38GRCh38
GRCh371476,116,134 - 76,127,219 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361475,185,884 - 75,196,912 (-)NCBINCBI36Build 36hg18NCBI36
Build 341475,185,883 - 75,196,912NCBI
Celera1456,155,336 - 56,165,643 (-)NCBICelera
Cytogenetic Map14q24.3NCBI
HuRef1456,285,182 - 56,295,497 (-)NCBIHuRef
CHM1_11476,054,996 - 76,065,305 (-)NCBICHM1_1
T2T-CHM13v2.01469,858,902 - 69,869,980 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10449901   PMID:10931946   PMID:10967139   PMID:11042152   PMID:11076863   PMID:11160377   PMID:11230166   PMID:11256614   PMID:11910120   PMID:12477932   PMID:12508121   PMID:12958361  
PMID:15489334   PMID:15489336   PMID:16169070   PMID:16344560   PMID:16381901   PMID:21516116   PMID:21873635   PMID:21900206   PMID:21934552   PMID:22658674   PMID:23142642   PMID:24326590  
PMID:24623722   PMID:26514267   PMID:28298427   PMID:28931009   PMID:31536960   PMID:31980649   PMID:32296183   PMID:32687490   PMID:32694731   PMID:33961781   PMID:35271311   PMID:35696571  
PMID:36216146   PMID:36610398   PMID:36949045  


Genomics

Comparative Map Data
ERG28
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381475,649,791 - 75,660,876 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1475,649,791 - 75,660,876 (-)EnsemblGRCh38hg38GRCh38
GRCh371476,116,134 - 76,127,219 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361475,185,884 - 75,196,912 (-)NCBINCBI36Build 36hg18NCBI36
Build 341475,185,883 - 75,196,912NCBI
Celera1456,155,336 - 56,165,643 (-)NCBICelera
Cytogenetic Map14q24.3NCBI
HuRef1456,285,182 - 56,295,497 (-)NCBIHuRef
CHM1_11476,054,996 - 76,065,305 (-)NCBICHM1_1
T2T-CHM13v2.01469,858,902 - 69,869,980 (-)NCBIT2T-CHM13v2.0
Erg28
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391285,862,221 - 85,871,667 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1285,862,222 - 85,871,324 (-)EnsemblGRCm39 Ensembl
GRCm381285,815,447 - 85,824,893 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1285,815,448 - 85,824,550 (-)EnsemblGRCm38mm10GRCm38
MGSCv371287,156,405 - 87,165,495 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361286,704,558 - 86,713,648 (-)NCBIMGSCv36mm8
Celera1287,275,694 - 87,284,679 (-)NCBICelera
Cytogenetic Map12D2NCBI
cM Map1239.81NCBI
Erg28
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr86111,205,102 - 111,214,068 (-)NCBIGRCr8
mRatBN7.26105,474,112 - 105,483,078 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl6105,474,113 - 105,483,078 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx6105,643,750 - 105,652,716 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.06105,942,626 - 105,951,592 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.06105,312,269 - 105,321,237 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.06109,683,252 - 109,692,218 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl6109,683,253 - 109,692,218 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.06118,991,548 - 119,000,513 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46109,934,787 - 109,945,923 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.16109,938,317 - 109,949,121 (-)NCBI
Celera6103,300,790 - 103,309,751 (-)NCBICelera
Cytogenetic Map6q31NCBI
Erg28
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495561299,119 - 109,525 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495561299,107 - 109,679 (-)NCBIChiLan1.0ChiLan1.0
ERG28
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21576,736,592 - 76,746,575 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11475,953,089 - 75,963,080 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01456,205,947 - 56,216,227 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11475,048,692 - 75,058,970 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1475,048,692 - 75,058,970 (-)Ensemblpanpan1.1panPan2
ERG28
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1848,642,610 - 48,651,637 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl848,643,200 - 48,651,306 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha848,325,527 - 48,334,317 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0848,866,790 - 48,875,591 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.1848,539,642 - 48,548,424 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0848,561,072 - 48,569,861 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0848,957,300 - 48,966,096 (-)NCBIUU_Cfam_GSD_1.0
Erg28
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864027,345,935 - 27,354,631 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049364884,714,374 - 4,722,941 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049364884,714,337 - 4,722,928 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ERG28
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl798,811,716 - 98,821,930 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1798,811,710 - 98,822,641 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.27104,709,854 - 104,709,986 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ERG28
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12452,895,060 - 52,905,265 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2452,894,420 - 52,905,224 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605341,113,289 - 41,123,583 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Erg28
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462473426,021,880 - 26,030,440 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462473426,021,761 - 26,031,026 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q24.3(chr14:73877072-78042422)x1 copy number loss See cases [RCV000051548] Chr14:73877072..78042422 [GRCh38]
Chr14:74343775..78508765 [GRCh37]
Chr14:73413528..77578518 [NCBI36]
Chr14:14q24.3		 pathogenic
GRCh38/hg38 14q24.3-31.1(chr14:75489052-79610332)x1 copy number loss See cases [RCV000051549] Chr14:75489052..79610332 [GRCh38]
Chr14:75955395..80076675 [GRCh37]
Chr14:75025148..79146428 [NCBI36]
Chr14:14q24.3-31.1		 pathogenic
GRCh38/hg38 14q24.2-32.2(chr14:72787506-99596719)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052293]|See cases [RCV000052293] Chr14:72787506..99596719 [GRCh38]
Chr14:73254214..100063056 [GRCh37]
Chr14:72323967..99132809 [NCBI36]
Chr14:14q24.2-32.2		 pathogenic
GRCh38/hg38 14q24.3(chr14:75489052-75967965)x3 copy number gain See cases [RCV000052084] Chr14:75489052..75967965 [GRCh38]
Chr14:75955395..76434308 [GRCh37]
Chr14:75025148..75504061 [NCBI36]
Chr14:14q24.3		 uncertain significance
GRCh37/hg19 14q24.2-q24.3(chr14:73152115..77698582) deletion Intellectual disability, mild [RCV000190520] Chr14:73152115..77698582 [GRCh37]
Chr14:14q24.2-24.3		 pathogenic|likely pathogenic
GRCh38/hg38 14q24.1-31.1(chr14:69562099-81975384)x1 copy number loss See cases [RCV000134154] Chr14:69562099..81975384 [GRCh38]
Chr14:70028816..82441728 [GRCh37]
Chr14:69098569..81511481 [NCBI36]
Chr14:14q24.1-31.1		 pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:73655772-106879298)x3 copy number gain See cases [RCV000134000] Chr14:73655772..106879298 [GRCh38]
Chr14:74122475..107287505 [GRCh37]
Chr14:73192228..106358550 [NCBI36]
Chr14:14q24.3-32.33		 pathogenic
GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3 copy number gain See cases [RCV000135543] Chr14:20151149..106855263 [GRCh38]
Chr14:20619308..107263478 [GRCh37]
Chr14:19689148..106334523 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q24.3(chr14:74986195-76399258)x1 copy number loss See cases [RCV000137114] Chr14:74986195..76399258 [GRCh38]
Chr14:75452898..76865601 [GRCh37]
Chr14:74522651..75935354 [NCBI36]
Chr14:14q24.3		 uncertain significance
GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3 copy number gain See cases [RCV000143373] Chr14:20043514..106877229 [GRCh38]
Chr14:20511673..107285437 [GRCh37]
Chr14:19581513..106356482 [NCBI36]
Chr14:14q11.2-32.33		 pathogenic
GRCh38/hg38 14q24.3-31.1(chr14:73343213-78835059)x1 copy number loss See cases [RCV000143265] Chr14:73343213..78835059 [GRCh38]
Chr14:73809921..79301402 [GRCh37]
Chr14:72879674..78371155 [NCBI36]
Chr14:14q24.3-31.1		 pathogenic|likely pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3 copy number gain See cases [RCV000446256] Chr14:19794561..107234280 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q23.2-32.33(chr14:62493932-107285437)x3 copy number gain See cases [RCV000448557] Chr14:62493932..107285437 [GRCh37]
Chr14:14q23.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437) copy number gain See cases [RCV000512041] Chr14:20511673..107285437 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q24.3(chr14:76082940-78372356)x1 copy number loss See cases [RCV000511668] Chr14:76082940..78372356 [GRCh37]
Chr14:14q24.3		 uncertain significance
GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3 copy number gain See cases [RCV000512497] Chr14:73750741..107285437 [GRCh37]
Chr14:14q24.2-32.33		 pathogenic
GRCh37/hg19 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19280733-107287663)x3 copy number gain not provided [RCV000738413] Chr14:19280733..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q11.2-32.33(chr14:19327823-107287663)x3 copy number gain not provided [RCV000738414] Chr14:19327823..107287663 [GRCh37]
Chr14:14q11.2-32.33		 pathogenic
GRCh37/hg19 14q24.3(chr14:74040231-76368547) copy number loss not provided [RCV000767572] Chr14:74040231..76368547 [GRCh37]
Chr14:14q24.3		 likely pathogenic
GRCh37/hg19 14q24.3(chr14:76057971-76576494)x3 copy number gain not provided [RCV000846916] Chr14:76057971..76576494 [GRCh37]
Chr14:14q24.3		 uncertain significance
NC_000014.8:g.(?_76090935)_(76187066_?)dup duplication not provided [RCV001922979] Chr14:76090935..76187066 [GRCh37]
Chr14:14q24.3		 uncertain significance
NC_000014.8:g.(?_76088402)_(76174070_?)dup duplication not provided [RCV003119496] Chr14:76088402..76174070 [GRCh37]
Chr14:14q24.3		 uncertain significance
GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2 copy number gain See cases [RCV002286356] Chr14:37671058..106985955 [GRCh37]
Chr14:14q13.3-32.33		 pathogenic
GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3 copy number gain not provided [RCV003485036] Chr14:58894502..107227240 [GRCh37]
Chr14:14q23.1-32.33		 pathogenic
GRCh37/hg19 14q24.3(chr14:74883763-77219310)x1 copy number loss not provided [RCV003483211] Chr14:74883763..77219310 [GRCh37]
Chr14:14q24.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:785
Count of miRNA genes:574
Interacting mature miRNAs:622
Transcripts:ENST00000256319
Prediction methods: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
RH98534  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,117,282 - 76,117,447UniSTSGRCh37
Build 361475,187,035 - 75,187,200RGDNCBI36
Celera1456,155,385 - 56,155,550RGD
Cytogenetic Map14q24.3UniSTS
HuRef1456,285,231 - 56,285,396UniSTS
GeneMap99-GB4 RH Map14200.99UniSTS
D14S1268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,121,515 - 76,121,602UniSTSGRCh37
Build 361475,191,268 - 75,191,355RGDNCBI36
Celera1456,159,619 - 56,159,706RGD
Cytogenetic Map14q24.3UniSTS
HuRef1456,289,465 - 56,289,552UniSTS
A005P29  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,117,242 - 76,117,526UniSTSGRCh37
Build 361475,186,995 - 75,187,279RGDNCBI36
Celera1456,155,345 - 56,155,629RGD
Cytogenetic Map14q24.3UniSTS
HuRef1456,285,191 - 56,285,475UniSTS
GeneMap99-GB4 RH Map14202.99UniSTS
G32256  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371476,117,242 - 76,117,526UniSTSGRCh37
Celera1456,155,345 - 56,155,629UniSTS
Cytogenetic Map14q24.3UniSTS
HuRef1456,285,191 - 56,285,475UniSTS
SHGC-64295  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map14q24.3UniSTS
HuRef1456,285,307 - 56,285,447UniSTS
TNG Radiation Hybrid Map1427705.0UniSTS


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 2367 1647 1717 620 1190 463 3592 1040 3478 398 1446 1598 170 1125 2050 3
Low 70 1336 8 3 757 1 764 1156 249 20 9 13 5 1 79 738 2 1
Below cutoff 1 8 1 1 4 1 1 7 1 4 2 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000256319   ⟹   ENSP00000256319
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1475,649,791 - 75,660,876 (-)Ensembl
RefSeq Acc Id: NM_007176   ⟹   NP_009107
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,649,791 - 75,660,876 (-)NCBI
GRCh371476,117,233 - 76,127,538 (-)RGD
Build 361475,185,884 - 75,196,912 (-)NCBI Archive
Celera1456,155,336 - 56,165,643 (-)RGD
HuRef1456,285,182 - 56,295,497 (-)ENTREZGENE
CHM1_11476,054,996 - 76,065,305 (-)NCBI
T2T-CHM13v2.01469,858,902 - 69,869,980 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_009107   ⟸   NM_007176
- UniProtKB: Q9P093 (UniProtKB/Swiss-Prot),   Q9UPI2 (UniProtKB/Swiss-Prot),   Q9UKR5 (UniProtKB/Swiss-Prot),   Q6FII3 (UniProtKB/TrEMBL),   Q86TW5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000256319   ⟸   ENST00000256319

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9UKR5-F1-model_v2 AlphaFold Q9UKR5 1-140 view protein structure

Promoters
RGD ID:6791350
Promoter ID:HG_KWN:19824
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:ENST00000393826,   NM_015072,   UC001XRT.1,   UC001XRU.1,   UC001XRV.2,   UC001XRW.1,   UC010ASK.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361475,196,856 - 75,197,522 (-)MPROMDB
RGD ID:7228197
Promoter ID:EPDNEW_H19843
Type:initiation region
Name:C14orf1_1
Description:chromosome 14 open reading frame 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19845  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,660,876 - 75,660,936EPDNEW
RGD ID:7228199
Promoter ID:EPDNEW_H19845
Type:initiation region
Name:C14orf1_2
Description:chromosome 14 open reading frame 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H19843  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381475,661,116 - 75,661,176EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1187 AgrOrtholog
COSMIC ERG28 COSMIC
Ensembl Genes ENSG00000133935 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000256319 ENTREZGENE
  ENST00000256319.7 UniProtKB/Swiss-Prot
GTEx ENSG00000133935 GTEx
HGNC ID HGNC:1187 ENTREZGENE
Human Proteome Map ERG28 Human Proteome Map
InterPro Erg28 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:11161 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 11161 ENTREZGENE
OMIM 604576 OMIM
PANTHER ERGOSTEROL BIOSYNTHETIC PROTEIN 28 HOMOLOG UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR15451 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Erg28 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA25513 PharmGKB
UniProt ERG28_HUMAN UniProtKB/Swiss-Prot
  Q6FII3 ENTREZGENE, UniProtKB/TrEMBL
  Q86TW5 ENTREZGENE, UniProtKB/TrEMBL
  Q9P093 ENTREZGENE
  Q9UKR5 ENTREZGENE
  Q9UPI2 ENTREZGENE
UniProt Secondary Q9P093 UniProtKB/Swiss-Prot
  Q9UPI2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-05-30 ERG28  ergosterol biosynthesis 28 homolog  C14orf1  chromosome 14 open reading frame 1  Symbol and/or name change 5135510 APPROVED