DDX24 (DEAD-box helicase 24) - Rat Genome Database

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Gene: DDX24 (DEAD-box helicase 24) Homo sapiens
Analyze
Symbol: DDX24
Name: DEAD-box helicase 24
RGD ID: 1353174
HGNC Page HGNC:13266
Description: Enables RNA binding activity. Located in nucleolus.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: ATP-dependent RNA helicase DDX24; DEAD (Asp-Glu-Ala-Asp) box helicase 24; DEAD (Asp-Glu-Ala-Asp) box polypeptide 24; DEAD box protein 24; DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 24; S. cerevisiae CHL1-like helicase
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: LOC644303  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381494,048,287 - 94,081,202 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1494,048,287 - 94,081,202 (-)EnsemblGRCh38hg38GRCh38
GRCh371494,514,633 - 94,547,548 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361493,587,021 - 93,617,311 (-)NCBINCBI36Build 36hg18NCBI36
Build 341493,587,021 - 93,617,311NCBI
Celera1474,571,013 - 74,601,331 (-)NCBICelera
Cytogenetic Map14q32.12NCBI
HuRef1474,697,258 - 74,727,325 (-)NCBIHuRef
CHM1_11494,455,281 - 94,485,555 (-)NCBICHM1_1
T2T-CHM13v2.01488,275,602 - 88,308,519 (-)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
membrane  (HDA)
nucleolus  (IBA,IDA)

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. DExD/H-box RNA helicases in ribosome biogenesis. Martin R, etal., RNA Biol. 2013 Jan;10(1):4-18. doi: 10.4161/rna.21879. Epub 2012 Aug 24.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10936056   PMID:11076863   PMID:11230166   PMID:11256614   PMID:12477932   PMID:14702039   PMID:15014966   PMID:15302935   PMID:15489334   PMID:15489336   PMID:15561718   PMID:15635413  
PMID:16051665   PMID:16169070   PMID:16226712   PMID:16381901   PMID:16964243   PMID:17081983   PMID:17353931   PMID:18029348   PMID:18289627   PMID:18954305   PMID:19454010   PMID:19615732  
PMID:19946888   PMID:20237496   PMID:21044950   PMID:21145461   PMID:21150319   PMID:21654808   PMID:21873635   PMID:21988832   PMID:22113938   PMID:22174317   PMID:22586326   PMID:22658674  
PMID:22681889   PMID:22751105   PMID:22939629   PMID:22990118   PMID:23443559   PMID:24163370   PMID:24457600   PMID:24623722   PMID:24980433   PMID:24981860   PMID:25609649   PMID:25665578  
PMID:25693804   PMID:25867071   PMID:25921289   PMID:26186194   PMID:26209609   PMID:26344197   PMID:26496610   PMID:26499835   PMID:26638075   PMID:26678539   PMID:26687479   PMID:26949251  
PMID:27173435   PMID:27248496   PMID:27684187   PMID:27926873   PMID:28302793   PMID:28380382   PMID:28514442   PMID:28515276   PMID:28695742   PMID:28977666   PMID:29117863   PMID:29229926  
PMID:29298432   PMID:29346117   PMID:29395067   PMID:29467282   PMID:29490077   PMID:29507755   PMID:29509190   PMID:29568061   PMID:29802200   PMID:29955894   PMID:30063812   PMID:30209976  
PMID:30367141   PMID:30404004   PMID:30415952   PMID:30462309   PMID:30463901   PMID:30745168   PMID:30804394   PMID:30804502   PMID:30833792   PMID:30940648   PMID:30948266   PMID:31091453  
PMID:31586073   PMID:31665637   PMID:31685992   PMID:31753913   PMID:31822558   PMID:31980649   PMID:32460013   PMID:32538781   PMID:32572027   PMID:32687490   PMID:32707033   PMID:32744500  
PMID:32807901   PMID:32877691   PMID:33106477   PMID:33301849   PMID:33306668   PMID:33462405   PMID:33567341   PMID:33729478   PMID:33754909   PMID:33957083   PMID:33961781   PMID:34079125  
PMID:34373451   PMID:34591612   PMID:34718347   PMID:35013218   PMID:35140242   PMID:35241646   PMID:35271311   PMID:35384245   PMID:35439318   PMID:35509820   PMID:35563538   PMID:35654790  
PMID:35763670   PMID:35819319   PMID:35831314   PMID:35850772   PMID:35864588   PMID:35906200   PMID:35944360   PMID:36089195   PMID:36114006   PMID:36215168   PMID:36232890   PMID:36243803  
PMID:36298642   PMID:36373674   PMID:36424410   PMID:36526897   PMID:36774506   PMID:36779763   PMID:36912080   PMID:37536630   PMID:37689310   PMID:37705750   PMID:37827155   PMID:38043669  
PMID:38113892  


Genomics

Comparative Map Data
DDX24
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381494,048,287 - 94,081,202 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1494,048,287 - 94,081,202 (-)EnsemblGRCh38hg38GRCh38
GRCh371494,514,633 - 94,547,548 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361493,587,021 - 93,617,311 (-)NCBINCBI36Build 36hg18NCBI36
Build 341493,587,021 - 93,617,311NCBI
Celera1474,571,013 - 74,601,331 (-)NCBICelera
Cytogenetic Map14q32.12NCBI
HuRef1474,697,258 - 74,727,325 (-)NCBIHuRef
CHM1_11494,455,281 - 94,485,555 (-)NCBICHM1_1
T2T-CHM13v2.01488,275,602 - 88,308,519 (-)NCBIT2T-CHM13v2.0
Ddx24
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3912103,374,235 - 103,392,106 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl12103,374,241 - 103,392,089 (-)EnsemblGRCm39 Ensembl
GRCm3812103,407,976 - 103,425,847 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl12103,407,982 - 103,425,830 (-)EnsemblGRCm38mm10GRCm38
MGSCv3712104,646,186 - 104,664,077 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3612103,809,033 - 103,826,830 (-)NCBIMGSCv36mm8
Celera12104,624,733 - 104,642,624 (-)NCBICelera
Cytogenetic Map12ENCBI
cM Map1252.92NCBI
Ddx24
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr86128,329,554 - 128,346,818 (-)NCBIGRCr8
mRatBN7.26122,564,767 - 122,582,032 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl6122,564,767 - 122,581,927 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx6122,705,614 - 122,722,897 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.06123,000,876 - 123,018,159 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.06122,335,418 - 122,352,763 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.06127,302,201 - 127,319,382 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl6127,302,201 - 127,319,362 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl6128,996,616 - 129,001,614 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.06136,522,732 - 136,539,906 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.46127,699,436 - 127,716,597 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.16127,703,182 - 127,720,344 (-)NCBI
Celera6120,045,460 - 120,062,621 (-)NCBICelera
Cytogenetic Map6q32NCBI
Ddx24
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543816,100,594 - 16,114,657 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543816,100,345 - 16,116,377 (-)NCBIChiLan1.0ChiLan1.0
DDX24
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21595,208,308 - 95,241,312 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11494,424,813 - 94,457,787 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01474,683,068 - 74,713,394 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11494,016,438 - 94,046,635 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1494,016,438 - 94,046,635 (-)Ensemblpanpan1.1panPan2
DDX24
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1863,115,740 - 63,136,402 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl863,115,746 - 63,165,905 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha862,692,199 - 62,712,845 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0863,386,682 - 63,407,257 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl863,386,683 - 63,406,313 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1863,064,220 - 63,084,820 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0863,115,645 - 63,136,269 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0863,445,847 - 63,466,503 (-)NCBIUU_Cfam_GSD_1.0
Ddx24
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440864011,534,965 - 11,553,604 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049367331,913,437 - 1,932,869 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049367331,913,439 - 1,932,027 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
DDX24
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl7115,328,121 - 115,352,929 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.17115,328,122 - 115,347,355 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.27122,186,509 - 122,207,174 (-)NCBISscrofa10.2Sscrofa10.2susScr3
DDX24
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12471,808,721 - 71,838,268 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2471,808,995 - 71,838,262 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366605359,048,089 - 59,078,195 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ddx24
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473410,405,656 - 10,422,101 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in DDX24
47 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 14q32.11-32.13(chr14:90255156-95274696)x1 copy number loss See cases [RCV000051551] Chr14:90255156..95274696 [GRCh38]
Chr14:90721500..95741033 [GRCh37]
Chr14:89791253..94810786 [NCBI36]
Chr14:14q32.11-32.13
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 14q31.3-32.33(chr14:86094030-106832642)x3 copy number gain See cases [RCV000052295] Chr14:86094030..106832642 [GRCh38]
Chr14:86560374..107240869 [GRCh37]
Chr14:85630127..106311914 [NCBI36]
Chr14:14q31.3-32.33
pathogenic
GRCh38/hg38 14q31.2-32.33(chr14:83912345-106855405)x3 copy number gain See cases [RCV000052294] Chr14:83912345..106855405 [GRCh38]
Chr14:84378689..107263620 [GRCh37]
Chr14:83448442..106334665 [NCBI36]
Chr14:14q31.2-32.33
pathogenic
GRCh38/hg38 14q32.12-32.33(chr14:91455861-106832642)x3 copy number gain See cases [RCV000052296] Chr14:91455861..106832642 [GRCh38]
Chr14:91922205..107240869 [GRCh37]
Chr14:90991958..106311914 [NCBI36]
Chr14:14q32.12-32.33
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 14q32.12-32.33(chr14:92540983-104863658)x3 copy number gain See cases [RCV000135896] Chr14:92540983..104863658 [GRCh38]
Chr14:93007328..105329995 [GRCh37]
Chr14:92077081..104401040 [NCBI36]
Chr14:14q32.12-32.33
pathogenic
GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3 copy number gain See cases [RCV000138230] Chr14:77222795..106879298 [GRCh38]
Chr14:77689138..107287505 [GRCh37]
Chr14:76758891..106358550 [NCBI36]
Chr14:14q24.3-32.33
pathogenic
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
NM_020414.4(DDX24):c.1035C>G (p.Ile345Met) single nucleotide variant Inborn genetic diseases [RCV003266970] Chr14:94062305 [GRCh38]
Chr14:94528651 [GRCh37]
Chr14:14q32.12
uncertain significance
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 14q32.12-32.13(chr14:93498930-96059698)x3 copy number gain See cases [RCV000511246] Chr14:93498930..96059698 [GRCh37]
Chr14:14q32.12-32.13
uncertain significance
NM_020414.4(DDX24):c.110A>G (p.Asn37Ser) single nucleotide variant Inborn genetic diseases [RCV003271935] Chr14:94079633 [GRCh38]
Chr14:94545979 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.386G>A (p.Gly129Glu) single nucleotide variant Inborn genetic diseases [RCV003242109] Chr14:94079357 [GRCh38]
Chr14:94545703 [GRCh37]
Chr14:14q32.12
uncertain significance
GRCh37/hg19 14q31.3-32.13(chr14:88401076-94725706)x1 copy number loss not provided [RCV003312295] Chr14:88401076..94725706 [GRCh37]
Chr14:14q31.3-32.13
pathogenic
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 14q31.2-32.2(chr14:84783137-96908198)x1 copy number loss not provided [RCV000683625] Chr14:84783137..96908198 [GRCh37]
Chr14:14q31.2-32.2
pathogenic
GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3 copy number gain not provided [RCV000848687] Chr14:91969028..107285437 [GRCh37]
Chr14:14q32.12-32.33
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 14q11.1-32.33(chr14:19000422-107289053)x3 copy number gain not provided [RCV000738412] Chr14:19000422..107289053 [GRCh37]
Chr14:14q11.1-32.33
pathogenic
NM_020414.4(DDX24):c.125G>C (p.Gly42Ala) single nucleotide variant Inborn genetic diseases [RCV003273122] Chr14:94079618 [GRCh38]
Chr14:94545964 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1667A>G (p.Asn556Ser) single nucleotide variant Inborn genetic diseases [RCV003242108] Chr14:94060344 [GRCh38]
Chr14:94526690 [GRCh37]
Chr14:14q32.12
uncertain significance
GRCh37/hg19 14q31.2-32.2(chr14:84783523-96907490)x1 copy number loss Deletion syndrome [RCV001004048] Chr14:84783523..96907490 [GRCh37]
Chr14:14q31.2-32.2
pathogenic
NC_000014.8:g.(?_93687728)_(95560403_?)del deletion DICER1-related tumor predisposition [RCV002044285] Chr14:93687728..95560403 [GRCh37]
Chr14:14q32.12-32.13
likely pathogenic
GRCh37/hg19 14q32.12-32.13(chr14:94442454-95185710) copy number gain not specified [RCV002052454] Chr14:94442454..95185710 [GRCh37]
Chr14:14q32.12-32.13
uncertain significance
GRCh37/hg19 14q32.12-32.13(chr14:94400492-96192218) copy number gain not specified [RCV002052453] Chr14:94400492..96192218 [GRCh37]
Chr14:14q32.12-32.13
uncertain significance
GRCh37/hg19 14q31.3-32.13(chr14:88345625-94773741) copy number loss not specified [RCV002053117] Chr14:88345625..94773741 [GRCh37]
Chr14:14q31.3-32.13
pathogenic
NC_000014.8:g.(?_90429459)_(97347545_?)dup duplication not provided [RCV003109490] Chr14:90429459..97347545 [GRCh37]
Chr14:14q32.11-32.2
uncertain significance
NC_000014.8:g.(?_90429459)_(94856914_?)dup duplication Achondrogenesis, type IA [RCV003113413] Chr14:90429459..94856914 [GRCh37]
Chr14:14q32.11-32.13
uncertain significance
NM_020414.4(DDX24):c.809C>T (p.Thr270Ile) single nucleotide variant Inborn genetic diseases [RCV003276427] Chr14:94062531 [GRCh38]
Chr14:94528877 [GRCh37]
Chr14:14q32.12
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
NM_020414.4(DDX24):c.227G>T (p.Arg76Ile) single nucleotide variant Inborn genetic diseases [RCV003295566] Chr14:94079516 [GRCh38]
Chr14:94545862 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.665C>T (p.Thr222Ile) single nucleotide variant Inborn genetic diseases [RCV003261532] Chr14:94079078 [GRCh38]
Chr14:94545424 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.751A>G (p.Met251Val) single nucleotide variant Inborn genetic diseases [RCV003012988] Chr14:94062589 [GRCh38]
Chr14:94528935 [GRCh37]
Chr14:14q32.12
likely benign
GRCh37/hg19 14q31.1-32.2(chr14:81593708-97059276)x3 copy number gain not provided [RCV002472541] Chr14:81593708..97059276 [GRCh37]
Chr14:14q31.1-32.2
likely pathogenic
GRCh37/hg19 14q31.2-32.33(chr14:84537502-107285437)x3 copy number gain not provided [RCV002472581] Chr14:84537502..107285437 [GRCh37]
Chr14:14q31.2-32.33
pathogenic
NM_020414.4(DDX24):c.1103A>C (p.Asn368Thr) single nucleotide variant Inborn genetic diseases [RCV002751923] Chr14:94062237 [GRCh38]
Chr14:94528583 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.347A>G (p.Lys116Arg) single nucleotide variant Inborn genetic diseases [RCV002997396] Chr14:94079396 [GRCh38]
Chr14:94545742 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.2494T>C (p.Cys832Arg) single nucleotide variant Inborn genetic diseases [RCV002732684] Chr14:94051277 [GRCh38]
Chr14:94517623 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.275C>G (p.Ser92Cys) single nucleotide variant Inborn genetic diseases [RCV002784128] Chr14:94079468 [GRCh38]
Chr14:94545814 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.845G>C (p.Gly282Ala) single nucleotide variant Inborn genetic diseases [RCV002844376] Chr14:94062495 [GRCh38]
Chr14:94528841 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1058A>G (p.Gln353Arg) single nucleotide variant Inborn genetic diseases [RCV002978450] Chr14:94062282 [GRCh38]
Chr14:94528628 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1538T>A (p.Val513Glu) single nucleotide variant Inborn genetic diseases [RCV002757250] Chr14:94060473 [GRCh38]
Chr14:94526819 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1472T>C (p.Met491Thr) single nucleotide variant Inborn genetic diseases [RCV002977904] Chr14:94060539 [GRCh38]
Chr14:94526885 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1132G>A (p.Ala378Thr) single nucleotide variant Inborn genetic diseases [RCV002951062] Chr14:94062208 [GRCh38]
Chr14:94528554 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1387C>T (p.Arg463Trp) single nucleotide variant Inborn genetic diseases [RCV002692593] Chr14:94060923 [GRCh38]
Chr14:94527269 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1222G>A (p.Asp408Asn) single nucleotide variant Inborn genetic diseases [RCV003004063] Chr14:94062118 [GRCh38]
Chr14:94528464 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.524A>G (p.Lys175Arg) single nucleotide variant Inborn genetic diseases [RCV002702171] Chr14:94079219 [GRCh38]
Chr14:94545565 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1253C>T (p.Thr418Ile) single nucleotide variant Inborn genetic diseases [RCV002916595] Chr14:94061057 [GRCh38]
Chr14:94527403 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1340G>A (p.Arg447Gln) single nucleotide variant Inborn genetic diseases [RCV002699833] Chr14:94060970 [GRCh38]
Chr14:94527316 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.665C>G (p.Thr222Ser) single nucleotide variant Inborn genetic diseases [RCV002802525] Chr14:94079078 [GRCh38]
Chr14:94545424 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.941C>T (p.Ala314Val) single nucleotide variant Inborn genetic diseases [RCV002709722] Chr14:94062399 [GRCh38]
Chr14:94528745 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1003G>A (p.Asp335Asn) single nucleotide variant Inborn genetic diseases [RCV002989482] Chr14:94062337 [GRCh38]
Chr14:94528683 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1765C>T (p.Arg589Cys) single nucleotide variant Inborn genetic diseases [RCV002935911] Chr14:94060246 [GRCh38]
Chr14:94526592 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.2198G>A (p.Arg733Gln) single nucleotide variant Inborn genetic diseases [RCV002747118] Chr14:94053108 [GRCh38]
Chr14:94519454 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1033A>G (p.Ile345Val) single nucleotide variant Inborn genetic diseases [RCV003202692] Chr14:94062307 [GRCh38]
Chr14:94528653 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.682C>G (p.Arg228Gly) single nucleotide variant Inborn genetic diseases [RCV003202978] Chr14:94079061 [GRCh38]
Chr14:94545407 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.995T>G (p.Phe332Cys) single nucleotide variant Inborn genetic diseases [RCV003194888] Chr14:94062345 [GRCh38]
Chr14:94528691 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1111C>A (p.Gln371Lys) single nucleotide variant Inborn genetic diseases [RCV003201001] Chr14:94062229 [GRCh38]
Chr14:94528575 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1309C>T (p.Arg437Cys) single nucleotide variant Inborn genetic diseases [RCV003188955] Chr14:94061001 [GRCh38]
Chr14:94527347 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1547C>T (p.Ala516Val) single nucleotide variant Inborn genetic diseases [RCV003199757] Chr14:94060464 [GRCh38]
Chr14:94526810 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.2504A>G (p.Lys835Arg) single nucleotide variant Inborn genetic diseases [RCV003175362] Chr14:94051267 [GRCh38]
Chr14:94517613 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.2405C>T (p.Thr802Met) single nucleotide variant Inborn genetic diseases [RCV003213410] Chr14:94051366 [GRCh38]
Chr14:94517712 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1453C>T (p.Leu485Phe) single nucleotide variant Inborn genetic diseases [RCV003192536] Chr14:94060558 [GRCh38]
Chr14:94526904 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.1147T>C (p.Tyr383His) single nucleotide variant Inborn genetic diseases [RCV003175869] Chr14:94062193 [GRCh38]
Chr14:94528539 [GRCh37]
Chr14:14q32.12
likely benign
NM_020414.4(DDX24):c.2021G>A (p.Arg674Gln) single nucleotide variant Inborn genetic diseases [RCV003206251] Chr14:94055153 [GRCh38]
Chr14:94521499 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.394A>G (p.Met132Val) single nucleotide variant Inborn genetic diseases [RCV003262514] Chr14:94079349 [GRCh38]
Chr14:94545695 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.2068C>T (p.Leu690Phe) single nucleotide variant Inborn genetic diseases [RCV003308473] Chr14:94055106 [GRCh38]
Chr14:94521452 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.438C>A (p.Asn146Lys) single nucleotide variant Inborn genetic diseases [RCV003338355] Chr14:94079305 [GRCh38]
Chr14:94545651 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.962C>G (p.Thr321Ser) single nucleotide variant Inborn genetic diseases [RCV003370691] Chr14:94062378 [GRCh38]
Chr14:94528724 [GRCh37]
Chr14:14q32.12
uncertain significance
NM_020414.4(DDX24):c.2479G>A (p.Glu827Lys) single nucleotide variant Inborn genetic diseases [RCV003378027] Chr14:94051292 [GRCh38]
Chr14:94517638 [GRCh37]
Chr14:14q32.12
uncertain significance
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 14q31.3-32.33(chr14:88580184-107285437)x3 copy number gain not provided [RCV003485051] Chr14:88580184..107285437 [GRCh37]
Chr14:14q31.3-32.33
pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1303
Count of miRNA genes:429
Interacting mature miRNAs:479
Transcripts:ENST00000330836, ENST00000544005, ENST00000553400, ENST00000553451, ENST00000555054, ENST00000555324, ENST00000555762, ENST00000556635
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
SGC34995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,522,806 - 94,522,905UniSTSGRCh37
Build 361493,592,559 - 93,592,658RGDNCBI36
Celera1474,576,556 - 74,576,655RGD
Cytogenetic Map14q32UniSTS
HuRef1474,702,672 - 74,702,771UniSTS
GeneMap99-GB4 RH Map14248.9UniSTS
Whitehead-RH Map14323.1UniSTS
NCBI RH Map14978.5UniSTS
D14S638E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,527,361 - 94,528,526UniSTSGRCh37
Build 361493,597,114 - 93,598,279RGDNCBI36
Celera1474,581,111 - 74,582,276RGD
Cytogenetic Map14q32UniSTS
HuRef1474,707,225 - 74,708,390UniSTS
D14S652E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,545,452 - 94,545,575UniSTSGRCh37
Build 361493,615,205 - 93,615,328RGDNCBI36
Celera1474,599,225 - 74,599,348RGD
Cytogenetic Map14q32UniSTS
HuRef1474,725,219 - 74,725,342UniSTS
D14S708E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,526,555 - 94,526,661UniSTSGRCh37
Build 361493,596,308 - 93,596,414RGDNCBI36
Celera1474,580,305 - 74,580,411RGD
Cytogenetic Map14q32UniSTS
HuRef1474,706,419 - 74,706,525UniSTS
D14S798  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,522,366 - 94,522,466UniSTSGRCh37
Build 361493,592,119 - 93,592,219RGDNCBI36
Celera1474,576,116 - 74,576,216RGD
Cytogenetic Map14q32UniSTS
HuRef1474,702,232 - 74,702,332UniSTS
D14S832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,517,289 - 94,517,491UniSTSGRCh37
Build 361493,587,042 - 93,587,244RGDNCBI36
Celera1474,571,034 - 74,571,236RGD
Cytogenetic Map14q32UniSTS
HuRef1474,697,279 - 74,697,481UniSTS
GeneMap99-GB4 RH Map14248.7UniSTS
Whitehead-RH Map14323.0UniSTS
Whitehead-YAC Contig Map14 UniSTS
D14S667E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,517,379 - 94,517,478UniSTSGRCh37
Build 361493,587,132 - 93,587,231RGDNCBI36
Celera1474,571,124 - 74,571,223RGD
Cytogenetic Map14q32UniSTS
HuRef1474,697,369 - 74,697,468UniSTS
GeneMap99-GB4 RH Map14249.02UniSTS
NCBI RH Map14985.2UniSTS
RH1626  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,517,374 - 94,517,533UniSTSGRCh37
Build 361493,587,127 - 93,587,286RGDNCBI36
Celera1474,571,119 - 74,571,278RGD
Cytogenetic Map14q32UniSTS
HuRef1474,697,364 - 74,697,523UniSTS
GeneMap99-GB4 RH Map14249.02UniSTS
NCBI RH Map14987.5UniSTS
A002F39  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,517,421 - 94,517,556UniSTSGRCh37
Build 361493,587,174 - 93,587,309RGDNCBI36
Celera1474,571,166 - 74,571,306RGD
Cytogenetic Map14q32UniSTS
HuRef1474,697,411 - 74,697,551UniSTS
GeneMap99-GB4 RH Map14246.79UniSTS
Whitehead-RH Map14323.5UniSTS
RH46093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,522,449 - 94,522,582UniSTSGRCh37
Build 361493,592,202 - 93,592,335RGDNCBI36
Celera1474,576,199 - 74,576,332RGD
Cytogenetic Map14q32UniSTS
HuRef1474,702,315 - 74,702,448UniSTS
GeneMap99-GB4 RH Map14248.7UniSTS
D14S900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371494,517,315 - 94,517,397UniSTSGRCh37
Build 361493,587,068 - 93,587,150RGDNCBI36
Celera1474,571,060 - 74,571,142RGD
Cytogenetic Map14q32UniSTS
HuRef1474,697,305 - 74,697,387UniSTS
GeneMap99-GB4 RH Map14249.7UniSTS


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 2438 2771 1681 579 1793 420 4357 2133 3684 416 1460 1613 175 1 1204 2788 6 2
Low 1 220 45 45 158 45 64 50 3
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_020414 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF134475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF145022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF161446 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF214731 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK025162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294613 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK297232 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304504 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL079302 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL136886 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000778 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009406 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC096826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000330836   ⟹   ENSP00000328690
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,050,938 - 94,081,183 (-)Ensembl
RefSeq Acc Id: ENST00000544005   ⟹   ENSP00000440623
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,050,923 - 94,081,202 (-)Ensembl
RefSeq Acc Id: ENST00000553400
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,050,922 - 94,051,824 (-)Ensembl
RefSeq Acc Id: ENST00000553451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,050,922 - 94,056,163 (-)Ensembl
RefSeq Acc Id: ENST00000555054   ⟹   ENSP00000452145
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,050,965 - 94,081,202 (-)Ensembl
RefSeq Acc Id: ENST00000555324
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,078,966 - 94,081,146 (-)Ensembl
RefSeq Acc Id: ENST00000555762
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,050,920 - 94,081,198 (-)Ensembl
RefSeq Acc Id: ENST00000556635
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,051,188 - 94,053,378 (-)Ensembl
RefSeq Acc Id: ENST00000621632   ⟹   ENSP00000481495
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,048,287 - 94,081,202 (-)Ensembl
RefSeq Acc Id: ENST00000622786   ⟹   ENSP00000481317
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,050,953 - 94,062,253 (-)Ensembl
RefSeq Acc Id: ENST00000640432   ⟹   ENSP00000492621
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1494,051,020 - 94,081,212 (-)Ensembl
RefSeq Acc Id: NM_020414   ⟹   NP_065147
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381494,048,287 - 94,081,202 (-)NCBI
GRCh371494,517,268 - 94,547,558 (-)RGD
Build 361493,587,021 - 93,617,311 (-)NCBI Archive
Celera1474,571,013 - 74,601,331 (-)RGD
HuRef1474,697,258 - 74,727,325 (-)ENTREZGENE
CHM1_11494,455,281 - 94,485,555 (-)NCBI
T2T-CHM13v2.01488,275,602 - 88,308,519 (-)NCBI
Sequence:
RefSeq Acc Id: NP_065147   ⟸   NM_020414
- UniProtKB: E7EMJ4 (UniProtKB/Swiss-Prot),   Q4V9L5 (UniProtKB/Swiss-Prot),   Q9GZR7 (UniProtKB/Swiss-Prot),   G3V529 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000452145   ⟸   ENST00000555054
RefSeq Acc Id: ENSP00000328690   ⟸   ENST00000330836
RefSeq Acc Id: ENSP00000481495   ⟸   ENST00000621632
RefSeq Acc Id: ENSP00000440623   ⟸   ENST00000544005
RefSeq Acc Id: ENSP00000481317   ⟸   ENST00000622786
RefSeq Acc Id: ENSP00000492621   ⟸   ENST00000640432
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9GZR7-F1-model_v2 AlphaFold Q9GZR7 1-859 view protein structure

Promoters
RGD ID:6791643
Promoter ID:HG_KWN:20070
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:ENST00000298901,   NM_020414,   NM_145249
Position:
Human AssemblyChrPosition (strand)Source
Build 361493,616,246 - 93,617,357 (+)MPROMDB
RGD ID:6852118
Promoter ID:EP73865
Type:initiation region
Name:HS_DDX24
Description:DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 24.
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 361493,617,301 - 93,617,361EPD
RGD ID:7228487
Promoter ID:EPDNEW_H19989
Type:initiation region
Name:DDX24_1
Description:DEAD-box helicase 24
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381494,081,202 - 94,081,262EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:13266 AgrOrtholog
COSMIC DDX24 COSMIC
Ensembl Genes ENSG00000089737 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000273761 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000544005.5 UniProtKB/TrEMBL
  ENST00000555054.1 UniProtKB/TrEMBL
  ENST00000613280.4 UniProtKB/Swiss-Prot
  ENST00000614817.3 UniProtKB/TrEMBL
  ENST00000618456.2 UniProtKB/Swiss-Prot
  ENST00000619833.4 UniProtKB/TrEMBL
  ENST00000621632 ENTREZGENE
  ENST00000621632.5 UniProtKB/Swiss-Prot
  ENST00000626330.2 UniProtKB/TrEMBL
  ENST00000639269.1 UniProtKB/TrEMBL
Gene3D-CATH 3.40.50.300 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000089737 GTEx
  ENSG00000273761 GTEx
HGNC ID HGNC:13266 ENTREZGENE
Human Proteome Map DDX24 Human Proteome Map
InterPro DEAD/DEAH_box_helicase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Helicase_ATP-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Helicase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  P-loop_NTPase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RNA-helicase_DEAD-box_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RNA_helicase_DEAD_Q_motif UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:57062 UniProtKB/Swiss-Prot
NCBI Gene 57062 ENTREZGENE
OMIM 606181 OMIM
PANTHER ATP-DEPENDENT RNA HELICASE DDX24 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RNA HELICASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DEAD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Helicase_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27211 PharmGKB
PROSITE DEAD_ATP_HELICASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HELICASE_ATP_BIND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HELICASE_CTER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Q_MOTIF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DEXDc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HELICc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF52540 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WXU8_HUMAN UniProtKB/TrEMBL
  A0A1W2PRR2_HUMAN UniProtKB/TrEMBL
  DDX24_HUMAN UniProtKB/Swiss-Prot
  E7EMJ4 ENTREZGENE
  F5GYL3_HUMAN UniProtKB/TrEMBL
  G3V529 ENTREZGENE, UniProtKB/TrEMBL
  Q4V9L5 ENTREZGENE
  Q9GZR7 ENTREZGENE
UniProt Secondary E7EMJ4 UniProtKB/Swiss-Prot
  Q4V9L5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-12 DDX24  DEAD-box helicase 24  DDX24  DEAD (Asp-Glu-Ala-Asp) box helicase 24  Symbol and/or name change 5135510 APPROVED
2013-07-23 DDX24  DEAD (Asp-Glu-Ala-Asp) box helicase 24  DDX24  DEAD (Asp-Glu-Ala-Asp) box polypeptide 24  Symbol and/or name change 5135510 APPROVED