CEMP1 (cementum protein 1) - Rat Genome Database

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Gene: CEMP1 (cementum protein 1) Homo sapiens
Analyze
Symbol: CEMP1
Name: cementum protein 1
RGD ID: 1605138
HGNC Page HGNC:32553
Description: Enables hydroxyapatite binding activity. Involved in several processes, including biomineral tissue development; cell population proliferation; and odontogenesis. Located in cytoplasm and nucleoplasm.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: cementoblastoma-derived protein 1; cementum protein 23; cementum protein-23; CP-23; CP23
RGD Orthologs
Bonobo
Green Monkey
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
GRCh38162,530,035 - 2,531,408 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl162,530,035 - 2,531,417 (-)EnsemblGRCh38hg38GRCh38
GRCh37162,580,036 - 2,581,409 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36162,520,037 - 2,521,410 (-)NCBINCBI36Build 36hg18NCBI36
Celera162,794,972 - 2,808,983 (-)NCBICelera
Cytogenetic Map16p13.3NCBI
HuRef162,506,108 - 2,507,481 (-)NCBIHuRef
CHM1_1162,579,985 - 2,581,358 (-)NCBICHM1_1
T2T-CHM13v2.0162,552,157 - 2,553,530 (-)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
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IDA,IEA)
nucleoplasm  (IDA)
nucleus  (IDA,IEA)

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
Additional References at PubMed
PMID:8889548   PMID:12477932   PMID:16263347   PMID:17509525   PMID:19393626   PMID:21465469   PMID:21929512   PMID:22349547   PMID:24117017   PMID:26011628   PMID:26652387   PMID:30113883  
PMID:30804111   PMID:31410920   PMID:31809792   PMID:32075221   PMID:32296183   PMID:33961781   PMID:35442377   PMID:37154214  


Genomics

Comparative Map Data
CEMP1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38162,530,035 - 2,531,408 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl162,530,035 - 2,531,417 (-)EnsemblGRCh38hg38GRCh38
GRCh37162,580,036 - 2,581,409 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36162,520,037 - 2,521,410 (-)NCBINCBI36Build 36hg18NCBI36
Celera162,794,972 - 2,808,983 (-)NCBICelera
Cytogenetic Map16p13.3NCBI
HuRef162,506,108 - 2,507,481 (-)NCBIHuRef
CHM1_1162,579,985 - 2,581,358 (-)NCBICHM1_1
T2T-CHM13v2.0162,552,157 - 2,553,530 (-)NCBIT2T-CHM13v2.0
CEMP1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2183,031,779 - 3,032,648 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1166,812,899 - 6,813,642 (-)NCBINHGRI_mPanPan1
CEMP1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.152,404,443 - 2,405,733 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366606828,619,320 - 28,621,075 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in CEMP1
13 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16p13.3(chr16:2326840-3487106)x3 copy number gain See cases [RCV000052394] Chr16:2326840..3487106 [GRCh38]
Chr16:2376841..3537106 [GRCh37]
Chr16:2316842..3477107 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3 copy number gain See cases [RCV000052367] Chr16:23141..11296695 [GRCh38]
Chr16:73141..11390552 [GRCh37]
Chr16:13141..11298053 [NCBI36]
Chr16:16p13.3-13.13
pathogenic
GRCh38/hg38 16p13.3(chr16:29941-2560460)x3 copy number gain See cases [RCV000052368] Chr16:29941..2560460 [GRCh38]
Chr16:79941..2610461 [GRCh37]
Chr16:19941..2550462 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:46766-3214623)x3 copy number gain See cases [RCV000052370] Chr16:46766..3214623 [GRCh38]
Chr16:96766..3264623 [GRCh37]
Chr16:36766..3204624 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:2494804-3246579)x1 copy number loss See cases [RCV000053269] Chr16:2494804..3246579 [GRCh38]
Chr16:2544805..3296579 [GRCh37]
Chr16:2484806..3236580 [NCBI36]
Chr16:16p13.3
pathogenic
NM_001048212.3(CEMP1):c.193G>A (p.Gly65Ser) single nucleotide variant Malignant melanoma [RCV000063011] Chr16:2530881 [GRCh38]
Chr16:2580882 [GRCh37]
Chr16:2520883 [NCBI36]
Chr16:16p13.3
not provided
NM_001145815.1(AMDHD2):c.683C>T (p.Thr228Ile) single nucleotide variant Malignant melanoma [RCV000063009] Chr16:2528114 [GRCh38]
Chr16:2578115 [GRCh37]
Chr16:2518116 [NCBI36]
Chr16:16p13.3
not provided
NM_001145815.1(AMDHD2):c.684C>T (p.Thr228=) single nucleotide variant Malignant melanoma [RCV000063010] Chr16:2528115 [GRCh38]
Chr16:2578116 [GRCh37]
Chr16:2518117 [NCBI36]
Chr16:16p13.3
not provided
GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3 copy number gain See cases [RCV000133780] Chr16:46766..11525516 [GRCh38]
Chr16:96766..11619372 [GRCh37]
Chr16:36766..11526873 [NCBI36]
Chr16:16p13.3-13.13
pathogenic
GRCh38/hg38 16p13.3(chr16:46766-4247185)x3 copy number gain See cases [RCV000136687] Chr16:46766..4247185 [GRCh38]
Chr16:96766..4297186 [GRCh37]
Chr16:36766..4237187 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3 copy number gain See cases [RCV000139166] Chr16:43732..13326806 [GRCh38]
Chr16:93732..13420663 [GRCh37]
Chr16:33732..13328164 [NCBI36]
Chr16:16p13.3-13.12
pathogenic
GRCh38/hg38 16p13.3(chr16:2365461-2532960)x1 copy number loss See cases [RCV000138952] Chr16:2365461..2532960 [GRCh38]
Chr16:2415462..2582961 [GRCh37]
Chr16:2355463..2522962 [NCBI36]
Chr16:16p13.3
pathogenic|uncertain significance
GRCh38/hg38 16p13.3(chr16:2406643-2782411)x1 copy number loss See cases [RCV000141237] Chr16:2406643..2782411 [GRCh38]
Chr16:2456644..2832412 [GRCh37]
Chr16:2396645..2772413 [NCBI36]
Chr16:16p13.3
likely pathogenic
GRCh38/hg38 16p13.3(chr16:2365461-2764284)x1 copy number loss See cases [RCV000142469] Chr16:2365461..2764284 [GRCh38]
Chr16:2415462..2814285 [GRCh37]
Chr16:2355463..2754286 [NCBI36]
Chr16:16p13.3
uncertain significance
GRCh38/hg38 16p13.3(chr16:2304443-2676863)x1 copy number loss See cases [RCV000142177] Chr16:2304443..2676863 [GRCh38]
Chr16:2354444..2726864 [GRCh37]
Chr16:2294445..2666865 [NCBI36]
Chr16:16p13.3
uncertain significance
GRCh38/hg38 16p13.3-13.11(chr16:666662-15743104)x3 copy number gain See cases [RCV000143710] Chr16:666662..15743104 [GRCh38]
Chr16:716662..15836961 [GRCh37]
Chr16:656663..15744462 [NCBI36]
Chr16:16p13.3-13.11
pathogenic
GRCh37/hg19 16p13.3-11.2(chr16:102839-28327676)x3 copy number gain See cases [RCV000203445] Chr16:102839..28327676 [GRCh37]
Chr16:16p13.3-11.2
pathogenic
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3 copy number gain Ductal breast carcinoma [RCV000207053] Chr16:1279324..31926800 [GRCh37]
Chr16:16p13.3-11.2
uncertain significance
GRCh37/hg19 16p13.3-12.3(chr16:1274615-19073133)x3 copy number gain Ductal breast carcinoma [RCV000207326] Chr16:1274615..19073133 [GRCh37]
Chr16:16p13.3-12.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:2188712-2580690)x4 copy number gain See cases [RCV000240524] Chr16:2188712..2580690 [GRCh37]
Chr16:16p13.3
uncertain significance
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 16p13.3-13.2(chr16:78801-9169448) copy number gain See cases [RCV000446555] Chr16:78801..9169448 [GRCh37]
Chr16:16p13.3-13.2
pathogenic
GRCh37/hg19 16p13.3(chr16:97133-5122974)x3 copy number gain See cases [RCV000445663] Chr16:97133..5122974 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:643377-3125125)x3 copy number gain See cases [RCV000510815] Chr16:643377..3125125 [GRCh37]
Chr16:16p13.3
uncertain significance
maternal UPD(16p) complex Hemimegalencephaly [RCV000494707] Chr16:1280042..33710558 [GRCh37]
Chr16:16p13.3-11.2
pathogenic
GRCh37/hg19 16p13.3-13.2(chr16:85880-9883129)x3 copy number gain See cases [RCV000510698] Chr16:85880..9883129 [GRCh37]
Chr16:16p13.3-13.2
pathogenic
GRCh37/hg19 16p13.3-12.2(chr16:85880-22442007)x3 copy number gain See cases [RCV000511360] Chr16:85880..22442007 [GRCh37]
Chr16:16p13.3-12.2
pathogenic
GRCh37/hg19 16p13.3-12.3(chr16:85880-19806921)x3 copy number gain See cases [RCV000512194] Chr16:85880..19806921 [GRCh37]
Chr16:16p13.3-12.3
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
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(chr16:85880-3216551)x3 copy number gain not provided [RCV000683742] Chr16:85880..3216551 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1505184-4415346)x3 copy number gain not provided [RCV000683745] Chr16:1505184..4415346 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3-13.13(chr16:85880-11209288)x3 copy number gain not provided [RCV000683743] Chr16:85880..11209288 [GRCh37]
Chr16:16p13.3-13.13
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 16p13.3(chr16:2510603-2581022)x3 copy number gain not provided [RCV000751529] Chr16:2510603..2581022 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:2516738-2667855)x1 copy number loss not provided [RCV000751531] Chr16:2516738..2667855 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:109978-4316797) copy number gain Chromosome 16p13.3 duplication syndrome [RCV000767731] Chr16:109978..4316797 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:2070917-2592737)x3 copy number gain not provided [RCV000845878] Chr16:2070917..2592737 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:2527176-2581549)x1 copy number loss not provided [RCV000849402] Chr16:2527176..2581549 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.172G>A (p.Ala58Thr) single nucleotide variant Inborn genetic diseases [RCV003252637] Chr16:2530902 [GRCh38]
Chr16:2580903 [GRCh37]
Chr16:16p13.3
likely benign
GRCh37/hg19 16p13.3(chr16:85880-5249457)x3 copy number gain not provided [RCV001259749] Chr16:85880..5249457 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:84485-5251013)x3 copy number gain not provided [RCV001537890] Chr16:84485..5251013 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1830141-2592737)x3 copy number gain not provided [RCV001827737] Chr16:1830141..2592737 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:1847662-2653144) copy number gain not specified [RCV002052502] Chr16:1847662..2653144 [GRCh37]
Chr16:16p13.3
uncertain significance
NC_000016.9:g.(?_256302)_(5971108_?)dup duplication Familial Mediterranean fever [RCV001877532]|Fanconi anemia [RCV001877533]|not provided [RCV001877531] Chr16:256302..5971108 [GRCh37]
Chr16:16p13.3
uncertain significance
NC_000016.9:g.(?_256302)_(4852572_?)dup duplication Epilepsy [RCV003113403]|Idiopathic generalized epilepsy [RCV003109446]|Saldino-Mainzer syndrome [RCV003113404] Chr16:256302..4852572 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:111043-6627459)x3 copy number gain See cases [RCV002292215] Chr16:111043..6627459 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1942430-2653144)x3 copy number gain not provided [RCV002473837] Chr16:1942430..2653144 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001330449.2(AMDHD2):c.*967C>G single nucleotide variant Inborn genetic diseases [RCV003012655] Chr16:2530530 [GRCh38]
Chr16:2580531 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.173C>T (p.Ala58Val) single nucleotide variant Inborn genetic diseases [RCV002992094] Chr16:2530901 [GRCh38]
Chr16:2580902 [GRCh37]
Chr16:16p13.3
likely benign
NM_001330449.2(AMDHD2):c.*719C>G single nucleotide variant Inborn genetic diseases [RCV002762543] Chr16:2530282 [GRCh38]
Chr16:2580283 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.238C>T (p.Arg80Cys) single nucleotide variant Inborn genetic diseases [RCV002705171] Chr16:2530836 [GRCh38]
Chr16:2580837 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.365C>T (p.Pro122Leu) single nucleotide variant Inborn genetic diseases [RCV002873371] Chr16:2530709 [GRCh38]
Chr16:2580710 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.53C>T (p.Thr18Ile) single nucleotide variant Inborn genetic diseases [RCV002719941] Chr16:2531021 [GRCh38]
Chr16:2581022 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.263C>T (p.Pro88Leu) single nucleotide variant Inborn genetic diseases [RCV002940907] Chr16:2530811 [GRCh38]
Chr16:2580812 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.483G>T (p.Arg161Ser) single nucleotide variant Inborn genetic diseases [RCV002747671] Chr16:2530591 [GRCh38]
Chr16:2580592 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.458C>T (p.Ala153Val) single nucleotide variant Inborn genetic diseases [RCV002672410] Chr16:2530616 [GRCh38]
Chr16:2580617 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.104C>G (p.Pro35Arg) single nucleotide variant Inborn genetic diseases [RCV002897951] Chr16:2530970 [GRCh38]
Chr16:2580971 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.185C>T (p.Ala62Val) single nucleotide variant Inborn genetic diseases [RCV002809595] Chr16:2530889 [GRCh38]
Chr16:2580890 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:2564105-2647768)x1 copy number loss not provided [RCV003222892] Chr16:2564105..2647768 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.432G>C (p.Gln144His) single nucleotide variant Inborn genetic diseases [RCV003370569] Chr16:2530642 [GRCh38]
Chr16:2580643 [GRCh37]
Chr16:16p13.3
uncertain significance
NM_001048212.3(CEMP1):c.463C>A (p.Arg155Ser) single nucleotide variant Inborn genetic diseases [RCV003376501] Chr16:2530611 [GRCh38]
Chr16:2580612 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:2480793-2590012)x1 copy number loss not provided [RCV003483257] Chr16:2480793..2590012 [GRCh37]
Chr16:16p13.3
likely pathogenic
GRCh37/hg19 16p13.3(chr16:1054247-2592737)x3 copy number gain not provided [RCV003485080] Chr16:1054247..2592737 [GRCh37]
Chr16:16p13.3
likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1238
Count of miRNA genes:583
Interacting mature miRNAs:656
Transcripts:ENST00000382350, ENST00000565480, ENST00000567119
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
GDB:176413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37162,708,369 - 2,708,777UniSTSGRCh37
GRCh37162,592,589 - 2,592,997UniSTSGRCh37
Build 36162,532,590 - 2,532,998RGDNCBI36
Celera162,807,495 - 2,807,903RGD
Celera162,907,943 - 2,908,351UniSTS
Cytogenetic Map16p13.3UniSTS
HuRef162,667,087 - 2,667,495UniSTS
HuRef162,675,956 - 2,676,364UniSTS
SHGC-61364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37162,580,338 - 2,580,595UniSTSGRCh37
Build 36162,520,339 - 2,520,596RGDNCBI36
Celera162,795,274 - 2,795,531RGD
Cytogenetic Map16p13.3UniSTS
HuRef162,506,410 - 2,506,667UniSTS
GeneMap99-GB4 RH Map1662.83UniSTS


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 entire extraembryonic component
High
Medium
Low 24 9 5 2 25 4 15 9 3 9 11 16 2
Below cutoff 22 31 23 73 25 12 33 42 15 32 46

Sequence


RefSeq Acc Id: ENST00000565480   ⟹   ENSP00000455479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl162,530,316 - 2,531,417 (-)Ensembl
RefSeq Acc Id: ENST00000567119   ⟹   ENSP00000457380
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl162,530,035 - 2,531,408 (-)Ensembl
RefSeq Acc Id: NM_001048212   ⟹   NP_001041677
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38162,530,035 - 2,531,408 (-)NCBI
GRCh37162,580,036 - 2,581,409 (-)ENTREZGENE
Build 36162,520,037 - 2,521,410 (-)NCBI Archive
Celera162,794,972 - 2,808,983 (-)RGD
HuRef162,506,108 - 2,507,481 (-)ENTREZGENE
CHM1_1162,579,985 - 2,581,358 (-)NCBI
T2T-CHM13v2.0162,552,157 - 2,553,530 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001041677 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI46926 (Get FASTA)   NCBI Sequence Viewer  
  AAI46927 (Get FASTA)   NCBI Sequence Viewer  
  AAT01221 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000455479.1
  ENSP00000457380
  ENSP00000457380.1
GenBank Protein Q6PRD7 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001041677   ⟸   NM_001048212
- UniProtKB: B2RUY1 (UniProtKB/Swiss-Prot),   Q6PRD7 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000455479   ⟸   ENST00000565480
RefSeq Acc Id: ENSP00000457380   ⟸   ENST00000567119

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q6PRD7-F1-model_v2 AlphaFold Q6PRD7 1-247 view protein structure

Promoters
RGD ID:6792899
Promoter ID:HG_KWN:22805
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:ENST00000382350
Position:
Human AssemblyChrPosition (strand)Source
Build 36162,520,121 - 2,522,142 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
COSMIC CEMP1 COSMIC
Ensembl Genes ENSG00000205923 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000565480.1 UniProtKB/TrEMBL
  ENST00000567119 ENTREZGENE
  ENST00000567119.1 UniProtKB/Swiss-Prot
GTEx ENSG00000205923 GTEx
HGNC ID HGNC:32553 ENTREZGENE
Human Proteome Map CEMP1 Human Proteome Map
KEGG Report hsa:752014 UniProtKB/Swiss-Prot
NCBI Gene 752014 ENTREZGENE
OMIM 611113 OMIM
PharmGKB PA162382169 PharmGKB
UniProt B2RUY1 ENTREZGENE
  CEMP1_HUMAN UniProtKB/Swiss-Prot
  H3BPU9_HUMAN UniProtKB/TrEMBL
  Q6PRD7 ENTREZGENE
UniProt Secondary B2RUY1 UniProtKB/Swiss-Prot