CCL24 (C-C motif chemokine ligand 24) - Rat Genome Database

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Gene: CCL24 (C-C motif chemokine ligand 24) Homo sapiens
Analyze
Symbol: CCL24
Name: C-C motif chemokine ligand 24
RGD ID: 1321033
HGNC Page HGNC
Description: Enables CCR3 chemokine receptor binding activity and chemokine activity. Involved in several processes, including eosinophil chemotaxis; positive regulation of actin filament polymerization; and positive regulation of endothelial cell proliferation. Predicted to be active in extracellular space. Implicated in asthma and rhinitis. Biomarker of asthma; chronic fatigue syndrome; and rhinitis.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: C-C motif chemokine 24; chemokine (C-C motif) ligand 24; CK-beta-6; Ckb-6; eosinophil chemotactic protein 2; eotaxin-2; MPIF-2; MPIF2; myeloid progenitor inhibitory factor 2; SCYA24; small inducible cytokine subfamily A (Cys-Cys), member 24; small-inducible cytokine A24
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
GRCh38.p13 Ensembl775,810,825 - 75,823,356 (-)EnsemblGRCh38hg38GRCh38
GRCh38775,810,825 - 75,823,372 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37775,440,143 - 75,452,690 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36775,279,050 - 75,280,969 (-)NCBINCBI36hg18NCBI36
Build 34775,085,764 - 75,087,684NCBI
Celera770,308,880 - 70,310,799 (-)NCBI
Cytogenetic Map7q11.23NCBI
HuRef770,527,210 - 70,529,129 (-)NCBIHuRef
CHM1_1775,371,135 - 75,373,054 (-)NCBICHM1_1
CRA_TCAGchr7v2774,774,178 - 74,776,097 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

Additional References at PubMed
PMID:9104803   PMID:9365122   PMID:9598329   PMID:10072545   PMID:10713092   PMID:10913244   PMID:11141953   PMID:11286614   PMID:11425309   PMID:11467997   PMID:12034562   PMID:12192108  
PMID:12193745   PMID:12218106   PMID:12477932   PMID:12853948   PMID:14718574   PMID:15340161   PMID:15489334   PMID:15744457   PMID:16391516   PMID:17207965   PMID:17438849   PMID:17630924  
PMID:17703412   PMID:17908961   PMID:17917245   PMID:18055844   PMID:19247692   PMID:19258923   PMID:19264973   PMID:19423540   PMID:19522186   PMID:19525930   PMID:19828696   PMID:20056178  
PMID:20143648   PMID:20236835   PMID:20237496   PMID:20406964   PMID:20438785   PMID:20503287   PMID:20659406   PMID:21077277   PMID:21873635   PMID:22846146   PMID:22946025   PMID:23025269  
PMID:23477905   PMID:23696919   PMID:24600981   PMID:24989688   PMID:25377782   PMID:25774667   PMID:26861136   PMID:27664933   PMID:28042950   PMID:28381538   PMID:28587510   PMID:29766567  
PMID:30583236   PMID:32419252   PMID:32513696   PMID:32826979   PMID:33472578  


Genomics

Comparative Map Data
CCL24
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl775,810,825 - 75,823,356 (-)EnsemblGRCh38hg38GRCh38
GRCh38775,810,825 - 75,823,372 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37775,440,143 - 75,452,690 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36775,279,050 - 75,280,969 (-)NCBINCBI36hg18NCBI36
Build 34775,085,764 - 75,087,684NCBI
Celera770,308,880 - 70,310,799 (-)NCBI
Cytogenetic Map7q11.23NCBI
HuRef770,527,210 - 70,529,129 (-)NCBIHuRef
CHM1_1775,371,135 - 75,373,054 (-)NCBICHM1_1
CRA_TCAGchr7v2774,774,178 - 74,776,097 (-)NCBI
Ccl24
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395135,598,789 - 135,601,977 (-)NCBIGRCm39mm39
GRCm39 Ensembl5135,598,791 - 135,601,903 (-)Ensembl
GRCm385135,569,935 - 135,573,123 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5135,569,937 - 135,573,049 (-)EnsemblGRCm38mm10GRCm38
MGSCv375136,045,807 - 136,048,913 (-)NCBIGRCm37mm9NCBIm37
MGSCv365135,855,239 - 135,857,652 (-)NCBImm8
Celera5132,581,470 - 132,584,576 (-)NCBICelera
Cytogenetic Map5G2NCBI
Ccl24
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21221,100,835 - 21,104,832 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl1221,100,835 - 21,104,893 (+)Ensembl
Rnor_6.01224,131,529 - 24,152,626 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1224,148,567 - 24,152,625 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01226,128,835 - 26,149,929 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41222,255,293 - 22,259,290 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11222,252,921 - 22,256,286 (+)NCBI
Celera1222,863,236 - 22,867,233 (+)NCBICelera
Cytogenetic Map12q12NCBI
Ccl24
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545614,583,610 - 14,585,169 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495545614,582,812 - 14,588,574 (-)NCBIChiLan1.0ChiLan1.0
CCL24
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1782,263,310 - 82,265,480 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl782,263,310 - 82,265,480 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0768,206,688 - 68,210,343 (+)NCBIMhudiblu_PPA_v0panPan3
CCL24
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.167,166,165 - 7,179,606 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl67,166,479 - 7,180,051 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha68,864,028 - 8,865,941 (-)NCBI
ROS_Cfam_1.066,986,790 - 7,000,238 (-)NCBI
UMICH_Zoey_3.166,957,433 - 6,959,341 (-)NCBI
UNSW_CanFamBas_1.066,920,823 - 6,922,728 (-)NCBI
UU_Cfam_GSD_1.067,084,112 - 7,086,021 (-)NCBI
Ccl24
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344131,632,998 - 131,635,886 (-)NCBI
SpeTri2.0NW_0049365432,400,743 - 2,403,558 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CCL24
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1310,347,397 - 10,361,500 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
CCL24
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12810,067,482 - 10,069,992 (-)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl2810,066,664 - 10,069,695 (-)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660706,366,836 - 6,369,294 (+)NCBIVero_WHO_p1.0
Ccl24
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474014,640,486 - 14,652,414 (-)NCBIHetGla_female_1.0hetGla2

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:662
Count of miRNA genes:307
Interacting mature miRNAs:329
Transcripts:ENST00000222902, ENST00000416943
Prediction methods: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.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1
Medium 398 14 11 9 406 9 19 1 2 3 16 105 40 2
Low 801 888 538 275 597 211 1544 315 325 119 765 803 70 757 822
Below cutoff 863 1301 775 247 361 168 1638 1133 991 158 419 410 83 1 353 1126 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000222902   ⟹   ENSP00000222902
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl775,810,825 - 75,813,806 (-)Ensembl
RefSeq Acc Id: ENST00000416943   ⟹   ENSP00000400533
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl775,811,665 - 75,823,356 (-)Ensembl
RefSeq Acc Id: NM_001371193   ⟹   NP_001358122
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38775,810,825 - 75,823,372 (-)NCBI
RefSeq Acc Id: NM_002991   ⟹   NP_002982
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38775,810,825 - 75,813,806 (-)NCBI
GRCh37775,440,766 - 75,452,674 (-)NCBI
Build 36775,279,050 - 75,280,969 (-)NCBI Archive
HuRef770,527,210 - 70,529,129 (-)ENTREZGENE
CHM1_1775,371,135 - 75,373,054 (-)NCBI
CRA_TCAGchr7v2774,774,178 - 74,776,097 (-)ENTREZGENE
Sequence:
RefSeq Acc Id: XM_011516460   ⟹   XP_011514762
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38775,810,825 - 75,816,244 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_002982   ⟸   NM_002991
- Peptide Label: precursor
- UniProtKB: O00175 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011514762   ⟸   XM_011516460
- Peptide Label: isoform X1
- UniProtKB: O00175 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001358122   ⟸   NM_001371193
- Peptide Label: precursor
RefSeq Acc Id: ENSP00000400533   ⟸   ENST00000416943
RefSeq Acc Id: ENSP00000222902   ⟸   ENST00000222902

Promoters
RGD ID:6805368
Promoter ID:HG_KWN:58131
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:OTTHUMT00000344885
Position:
Human AssemblyChrPosition (strand)Source
Build 36775,280,781 - 75,281,281 (-)MPROMDB
RGD ID:7210845
Promoter ID:EPDNEW_H11168
Type:initiation region
Name:CCL24_1
Description:C-C motif chemokine ligand 24
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11169  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38775,813,806 - 75,813,866EPDNEW
RGD ID:7210847
Promoter ID:EPDNEW_H11169
Type:initiation region
Name:CCL24_2
Description:C-C motif chemokine ligand 24
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H11168  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38775,823,369 - 75,823,429EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 7q11.22-21.11(chr7:71225344-81735657)x1 copy number loss See cases [RCV000050709] Chr7:71225344..81735657 [GRCh38]
Chr7:70690330..81364973 [GRCh37]
Chr7:70328266..81202909 [NCBI36]
Chr7:7q11.22-21.11
pathogenic
GRCh38/hg38 7q11.23(chr7:75526437-76499472)x1 copy number loss See cases [RCV000051302] Chr7:75526437..76499472 [GRCh38]
Chr7:75155767..76128789 [GRCh37]
Chr7:74993703..75966725 [NCBI36]
Chr7:7q11.23
uncertain significance
GRCh38/hg38 7q11.23(chr7:75567961-76584901)x1 copy number loss See cases [RCV000051303] Chr7:75567961..76584901 [GRCh38]
Chr7:75197265..76214218 [GRCh37]
Chr7:75035201..76052154 [NCBI36]
Chr7:7q11.23
uncertain significance
GRCh38/hg38 7q11.21-21.11(chr7:64560824-79186156)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052318]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052318]|See cases [RCV000052318] Chr7:64560824..79186156 [GRCh38]
Chr7:64021202..78815472 [GRCh37]
Chr7:63658637..78653408 [NCBI36]
Chr7:7q11.21-21.11
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 copy number loss See cases [RCV000052250] Chr7:53985..159282531 [GRCh38]
Chr7:53985..159075220 [GRCh37]
Chr7:149068..158767981 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q11.23(chr7:75769688-76066509)x1 copy number loss See cases [RCV000052686] Chr7:75769688..76066509 [GRCh38]
Chr7:75236942..75533763 [NCBI36]
Chr7:7q11.23
uncertain significance
GRCh38/hg38 7q11.22-11.23(chr7:69382353-77823832)x1 copy number loss See cases [RCV000054111] Chr7:69382353..77823832 [GRCh38]
Chr7:68847339..77453149 [GRCh37]
Chr7:68485275..77291085 [NCBI36]
Chr7:7q11.22-11.23
pathogenic
GRCh38/hg38 7q11.23-21.11(chr7:73873420-83988860)x1 copy number loss See cases [RCV000054118] Chr7:73873420..83988860 [GRCh38]
Chr7:73992744..83618176 [GRCh37]
Chr7:72925686..83456112 [NCBI36]
Chr7:7q11.23-21.11
pathogenic
GRCh38/hg38 7q11.23-21.11(chr7:75496701-78375575)x1 copy number loss See cases [RCV000054153] Chr7:75496701..78375575 [GRCh38]
Chr7:75126024..78004892 [GRCh37]
Chr7:74963960..77842828 [NCBI36]
Chr7:7q11.23-21.11
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 copy number gain not provided [RCV000848126] Chr7:10365..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q11.23(chr7:73352304-76722261)x1 copy number loss See cases [RCV000133638] Chr7:73352304..76722261 [GRCh38]
Chr7:72766313..76351578 [GRCh37]
Chr7:72404249..76189514 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 copy number loss See cases [RCV000135401] Chr7:54185..159282390 [GRCh38]
Chr7:54185..159075079 [GRCh37]
Chr7:149268..158767840 [NCBI36]
Chr7:7p22.3-q36.3
pathogenic
GRCh38/hg38 7q11.23(chr7:75432651-76418304)x1 copy number loss See cases [RCV000135520] Chr7:75432651..76418304 [GRCh38]
Chr7:75061927..76047621 [GRCh37]
Chr7:74899863..75885557 [NCBI36]
Chr7:7q11.23
likely pathogenic
GRCh38/hg38 7q11.23(chr7:75529854-76611483)x1 copy number loss See cases [RCV000136113] Chr7:75529854..76611483 [GRCh38]
Chr7:75159180..76240800 [GRCh37]
Chr7:74997116..76078736 [NCBI36]
Chr7:7q11.23
pathogenic
GRCh38/hg38 7q11.23(chr7:75568161-76584760)x1 copy number loss See cases [RCV000136550] Chr7:75568161..76584760 [GRCh38]
Chr7:75197465..76214077 [GRCh37]
Chr7:75035401..76052013 [NCBI36]
Chr7:7q11.23
uncertain significance
GRCh38/hg38 7q11.23(chr7:75529854-76626561)x3 copy number gain See cases [RCV000135929] Chr7:75529854..76626561 [GRCh38]
Chr7:75159180..76255878 [GRCh37]
Chr7:74997116..76093814 [NCBI36]
Chr7:7q11.23
uncertain significance
GRCh38/hg38 7q11.23-21.11(chr7:74377395-82031742)x1 copy number loss See cases [RCV000142381] Chr7:74377395..82031742 [GRCh38]
Chr7:73992744..81661058 [GRCh37]
Chr7:73429661..81498994 [NCBI36]
Chr7:7q11.23-21.11
pathogenic
GRCh38/hg38 7q11.22-21.11(chr7:72179092-79164071) copy number gain See cases [RCV000143454] Chr7:72179092..79164071 [GRCh38]
Chr7:71644077..78793387 [GRCh37]
Chr7:71282013..78631323 [NCBI36]
Chr7:7q11.22-21.11
likely pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 copy number loss See cases [RCV000446044] Chr7:43360..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:73591993-75914797)x1 copy number loss See cases [RCV000240532] Chr7:73591993..75914797 [GRCh37]
Chr7:7q11.23
likely pathogenic
GRCh37/hg19 7q11.23(chr7:75058408-77082896)x1 copy number loss See cases [RCV000449141] Chr7:75058408..77082896 [GRCh37]
Chr7:7q11.23
pathogenic
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) copy number gain See cases [RCV000510686] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:75155154-75729363)x1 copy number loss See cases [RCV000511396] Chr7:75155154..75729363 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 copy number gain See cases [RCV000511549] Chr7:43361..159119707 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:72456604-76007380)x1 copy number loss See cases [RCV000510782] Chr7:72456604..76007380 [GRCh37]
Chr7:7q11.23
pathogenic
Single allele deletion not provided [RCV000677988] Chr7:73591993..93683437 [GRCh37]
Chr7:7q11.23-21.3
uncertain significance
GRCh37/hg19 7q11.23(chr7:75384846-76279036)x3 copy number gain not provided [RCV000682872] Chr7:75384846..76279036 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.23(chr7:75085013-75995207)x3 copy number gain not provided [RCV000682874] Chr7:75085013..75995207 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.23(chr7:75082354-76007380)x1 copy number loss not provided [RCV000682875] Chr7:75082354..76007380 [GRCh37]
Chr7:7q11.23
likely pathogenic
NC_000007.13:g.(20954043_21001537)_(114528369_114556605)inv inversion Speech-language disorder 1 [RCV000234948] Chr7:21001537..114528369 [GRCh37]
Chr7:7p15.3-q31.1
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 copy number gain not provided [RCV000746280] Chr7:44935..159126310 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 copy number gain not provided [RCV000746278] Chr7:10704..159122532 [GRCh37]
Chr7:7p22.3-q36.3
pathogenic
GRCh37/hg19 7q11.23(chr7:75155747-75445377)x3 copy number gain not provided [RCV000746815] Chr7:75155747..75445377 [GRCh37]
Chr7:7q11.23
benign
GRCh37/hg19 7q11.23(chr7:72744494-76038818) copy number loss Williams syndrome [RCV000767638] Chr7:72744494..76038818 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:75076890-76007283)x3 copy number gain not provided [RCV000849303] Chr7:75076890..76007283 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.23(chr7:75233243-76007283)x3 copy number gain not provided [RCV000849638] Chr7:75233243..76007283 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.23(chr7:75091878-76117614)x1 copy number loss not provided [RCV000848509] Chr7:75091878..76117614 [GRCh37]
Chr7:7q11.23
uncertain significance
GRCh37/hg19 7q11.23(chr7:72621722-76007380)x1 copy number loss not provided [RCV001005967] Chr7:72621722..76007380 [GRCh37]
Chr7:7q11.23
pathogenic
GRCh37/hg19 7q11.23(chr7:72403117-76709600)x1 copy number loss not provided [RCV001258798] Chr7:72403117..76709600 [GRCh37]
Chr7:7q11.23
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:10623 AgrOrtholog
COSMIC CCL24 COSMIC
Ensembl Genes ENSG00000106178 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000222902 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000400533 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000222902 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000416943 ENTREZGENE, UniProtKB/Swiss-Prot
GTEx ENSG00000106178 GTEx
HGNC ID HGNC:10623 ENTREZGENE
Human Proteome Map CCL24 Human Proteome Map
InterPro Chemokine_b/g/d UniProtKB/Swiss-Prot
  Chemokine_IL8-like_dom UniProtKB/Swiss-Prot
  Interleukin_8-like_sf UniProtKB/Swiss-Prot
KEGG Report hsa:6369 UniProtKB/Swiss-Prot
NCBI Gene 6369 ENTREZGENE
OMIM 602495 OMIM
PANTHER PTHR12015 UniProtKB/Swiss-Prot
Pfam IL8 UniProtKB/Swiss-Prot
PharmGKB PA35555 PharmGKB
SMART SCY UniProtKB/Swiss-Prot
Superfamily-SCOP SSF54117 UniProtKB/Swiss-Prot
UniProt CCL24_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary B2R5K2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-07 CCL24  C-C motif chemokine ligand 24    chemokine (C-C motif) ligand 24  Symbol and/or name change 5135510 APPROVED
2011-08-16 CCL24  chemokine (C-C motif) ligand 24  CCL24  chemokine (C-C motif) ligand 24  Symbol and/or name change 5135510 APPROVED