CDK13 (cyclin dependent kinase 13) - Rat Genome Database

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Gene: CDK13 (cyclin dependent kinase 13) Homo sapiens
Analyze
Symbol: CDK13
Name: cyclin dependent kinase 13
RGD ID: 1322573
HGNC Page HGNC
Description: Enables RNA polymerase II CTD heptapeptide repeat kinase activity and cyclin binding activity. Involved in hemopoiesis and phosphorylation of RNA polymerase II C-terminal domain. Located in Golgi apparatus; cytosol; and nuclear speck. Part of cyclin K-CDK13 complex. Implicated in congenital heart defects, dysmorphic facial features, and intellectual developmental disorder.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CDC2-related protein kinase 5; CDC2L; CDC2L5; cell division cycle 2-like protein kinase 5; cell division protein kinase 13; CHDFIDD; CHED; cholinesterase-related cell division controller; cyclin-dependent kinase 13; FLJ35215; hCDK13; KIAA1791
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 Ensembl739,950,121 - 40,099,580 (+)EnsemblGRCh38hg38GRCh38
GRCh38739,949,664 - 40,099,580 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37739,989,855 - 40,139,179 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36739,956,484 - 40,101,679 (+)NCBINCBI36hg18NCBI36
Build 34739,763,348 - 39,908,385NCBI
Celera739,978,186 - 40,124,932 (+)NCBI
Cytogenetic Map7p14.1NCBI
HuRef739,873,916 - 40,020,642 (+)NCBIHuRef
CHM1_1739,992,473 - 40,139,235 (+)NCBICHM1_1
CRA_TCAGchr7v2740,028,472 - 40,175,171 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

References

Additional References at PubMed
PMID:1731328   PMID:8125298   PMID:8889548   PMID:9847074   PMID:11162436   PMID:11347906   PMID:12477932   PMID:12853948   PMID:14702039   PMID:14968112   PMID:15144186   PMID:15231748  
PMID:15302935   PMID:15635413   PMID:16721827   PMID:16730941   PMID:16964243   PMID:17081983   PMID:17620599   PMID:18480452   PMID:19884882   PMID:20811636   PMID:20952539   PMID:21873635  
PMID:22012619   PMID:22547058   PMID:22664934   PMID:22681889   PMID:22912832   PMID:22939629   PMID:22990118   PMID:23602568   PMID:24457600   PMID:25216700   PMID:25561469   PMID:25852190  
PMID:25921289   PMID:26167880   PMID:26186194   PMID:26344197   PMID:26496610   PMID:26748711   PMID:26886422   PMID:26949251   PMID:27479907   PMID:27634302   PMID:28065597   PMID:28514442  
PMID:28515276   PMID:28611215   PMID:28807008   PMID:28986522   PMID:29021403   PMID:29117863   PMID:29121065   PMID:29222009   PMID:29393965   PMID:29507755   PMID:29509190   PMID:29845934  
PMID:29996118   PMID:30021884   PMID:30209976   PMID:30319007   PMID:30404004   PMID:30702837   PMID:30804502   PMID:30890647   PMID:31297882   PMID:31527615   PMID:32296183   PMID:32416067  
PMID:32694731   PMID:32877691   PMID:34079125  


Genomics

Comparative Map Data
CDK13
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl739,950,121 - 40,099,580 (+)EnsemblGRCh38hg38GRCh38
GRCh38739,949,664 - 40,099,580 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37739,989,855 - 40,139,179 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36739,956,484 - 40,101,679 (+)NCBINCBI36hg18NCBI36
Build 34739,763,348 - 39,908,385NCBI
Celera739,978,186 - 40,124,932 (+)NCBI
Cytogenetic Map7p14.1NCBI
HuRef739,873,916 - 40,020,642 (+)NCBIHuRef
CHM1_1739,992,473 - 40,139,235 (+)NCBICHM1_1
CRA_TCAGchr7v2740,028,472 - 40,175,171 (+)NCBI
Cdk13
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391317,885,309 - 17,979,960 (-)NCBIGRCm39mm39
GRCm39 Ensembl1317,884,900 - 17,979,682 (-)Ensembl
GRCm381317,711,676 - 17,805,212 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1317,710,315 - 17,805,097 (-)EnsemblGRCm38mm10GRCm38
MGSCv371317,807,796 - 17,896,931 (-)NCBIGRCm37mm9NCBIm37
MGSCv361317,500,876 - 17,590,239 (-)NCBImm8
Celera1318,019,147 - 18,109,011 (-)NCBICelera
Cytogenetic Map13A2NCBI
Cdk13
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21747,251,145 - 47,344,675 (+)NCBImRatBN7.2
Rnor_6.0 Ensembl1749,833,400 - 49,921,550 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01749,833,194 - 49,922,932 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01747,889,843 - 47,979,627 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41755,146,130 - 55,235,545 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11755,071,862 - 55,237,672 (+)NCBI
Celera1743,336,076 - 43,426,801 (+)NCBICelera
Cytogenetic Map17q11NCBI
Cdk13
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_0049554603,590,854 - 3,701,148 (-)NCBIChiLan1.0ChiLan1.0
CDK13
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1744,177,940 - 44,324,319 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl744,177,204 - 44,324,683 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0744,138,345 - 44,285,606 (-)NCBIMhudiblu_PPA_v0panPan3
CDK13
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1189,801,350 - 9,920,401 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl189,803,535 - 9,920,281 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha189,647,410 - 9,768,703 (-)NCBI
ROS_Cfam_1.0189,847,718 - 9,969,056 (-)NCBI
UMICH_Zoey_3.1189,825,425 - 9,946,650 (-)NCBI
UNSW_CanFamBas_1.0189,795,209 - 9,922,569 (-)NCBI
UU_Cfam_GSD_1.0189,909,730 - 10,031,244 (-)NCBI
Cdk13
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440511896,084,330 - 96,178,160 (+)NCBI
SpeTri2.0NW_00493647815,296,055 - 15,387,749 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CDK13
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1854,308,144 - 54,429,939 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11854,310,311 - 54,430,060 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21859,602,083 - 59,696,059 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CDK13
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12118,551,273 - 18,688,889 (-)NCBI
ChlSab1.1 Ensembl2118,553,446 - 18,688,525 (-)Ensembl
Vero_WHO_p1.0NW_0236660623,715,053 - 3,852,971 (+)NCBI
Cdk13
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474021,100,780 - 21,202,147 (-)NCBI

Position Markers
GDB:1318631  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,132,969 - 40,133,125UniSTSGRCh37
Build 36740,099,494 - 40,099,650RGDNCBI36
Celera740,121,168 - 40,121,324RGD
Cytogenetic Map7p13UniSTS
HuRef740,016,878 - 40,017,034UniSTS
CRA_TCAGchr7v2740,171,407 - 40,171,563UniSTS
RH93376  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,136,118 - 40,136,261UniSTSGRCh37
Build 36740,102,643 - 40,102,786RGDNCBI36
Celera740,124,317 - 40,124,460RGD
Cytogenetic Map7p13UniSTS
HuRef740,020,027 - 40,020,170UniSTS
CRA_TCAGchr7v2740,174,556 - 40,174,699UniSTS
GeneMap99-GB4 RH Map7186.1UniSTS
RH93929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,136,489 - 40,136,663UniSTSGRCh37
Build 36740,103,014 - 40,103,188RGDNCBI36
Celera740,124,688 - 40,124,862RGD
Cytogenetic Map7p13UniSTS
HuRef740,020,398 - 40,020,572UniSTS
CRA_TCAGchr7v2740,174,927 - 40,175,101UniSTS
GeneMap99-GB4 RH Map7183.82UniSTS
RH120012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,092,489 - 40,092,782UniSTSGRCh37
Build 36740,059,014 - 40,059,307RGDNCBI36
Celera740,080,697 - 40,080,990RGD
Cytogenetic Map7p13UniSTS
HuRef739,976,646 - 39,976,939UniSTS
CRA_TCAGchr7v2740,130,937 - 40,131,230UniSTS
TNG Radiation Hybrid Map719620.0UniSTS
RH119268  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,017,113 - 40,017,453UniSTSGRCh37
Build 36739,983,638 - 39,983,978RGDNCBI36
Celera740,005,341 - 40,005,681RGD
Cytogenetic Map7p13UniSTS
HuRef739,901,205 - 39,901,545UniSTS
CRA_TCAGchr7v2740,055,624 - 40,055,964UniSTS
TNG Radiation Hybrid Map719579.0UniSTS
D7S3089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,017,077 - 40,017,496UniSTSGRCh37
Build 36739,983,602 - 39,984,021RGDNCBI36
Celera740,005,305 - 40,005,724RGD
Cytogenetic Map7p13UniSTS
HuRef739,901,169 - 39,901,588UniSTS
CRA_TCAGchr7v2740,055,588 - 40,056,007UniSTS
RH139622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,134,693 - 40,134,889UniSTSGRCh37
Build 36740,101,218 - 40,101,414RGDNCBI36
Celera740,122,891 - 40,123,087RGD
HuRef740,018,601 - 40,018,797UniSTS
CRA_TCAGchr7v2740,173,130 - 40,173,326UniSTS
HSC209_(7Gr397mb)  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,042,705 - 40,042,849UniSTSGRCh37
Build 36740,009,230 - 40,009,374RGDNCBI36
Celera740,030,927 - 40,031,071RGD
Cytogenetic Map7p13UniSTS
HuRef739,926,791 - 39,926,935UniSTS
CRA_TCAGchr7v2740,081,199 - 40,081,343UniSTS
GDB:1318476  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,083,244 - 40,083,380UniSTSGRCh37
Build 36740,049,769 - 40,049,905RGDNCBI36
Celera740,071,452 - 40,071,588RGD
Cytogenetic Map7p13UniSTS
HuRef739,967,398 - 39,967,534UniSTS
CRA_TCAGchr7v2740,121,692 - 40,121,828UniSTS
RH45694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,134,440 - 40,134,580UniSTSGRCh37
Build 36740,100,965 - 40,101,105RGDNCBI36
Celera740,122,638 - 40,122,778RGD
Cytogenetic Map7p13UniSTS
HuRef740,018,348 - 40,018,488UniSTS
CRA_TCAGchr7v2740,172,877 - 40,173,017UniSTS
GeneMap99-GB4 RH Map7186.0UniSTS
NCBI RH Map7626.9UniSTS
RH66471  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,104,988 - 40,105,185UniSTSGRCh37
Build 36740,071,513 - 40,071,710RGDNCBI36
Celera740,093,192 - 40,093,389RGD
Cytogenetic Map7p13UniSTS
HuRef739,988,912 - 39,989,109UniSTS
CRA_TCAGchr7v2740,143,431 - 40,143,628UniSTS
GeneMap99-GB4 RH Map7183.32UniSTS
NCBI RH Map7623.0UniSTS
RH47846  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,133,270 - 40,133,389UniSTSGRCh37
Build 36740,099,795 - 40,099,914RGDNCBI36
Celera740,121,469 - 40,121,588RGD
Cytogenetic Map7p13UniSTS
HuRef740,017,179 - 40,017,298UniSTS
CRA_TCAGchr7v2740,171,708 - 40,171,827UniSTS
GeneMap99-GB4 RH Map7183.51UniSTS
G16022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37739,990,921 - 39,991,106UniSTSGRCh37
Build 36739,957,446 - 39,957,631RGDNCBI36
Celera739,979,148 - 39,979,333RGD
Cytogenetic Map7p13UniSTS
HuRef739,874,878 - 39,875,063UniSTS
CRA_TCAGchr7v2740,029,431 - 40,029,616UniSTS
RH36512  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,051,170 - 40,051,362UniSTSGRCh37
Build 36740,017,695 - 40,017,887RGDNCBI36
Celera740,039,388 - 40,039,580RGD
Cytogenetic Map7p13UniSTS
HuRef739,935,314 - 39,935,506UniSTS
CRA_TCAGchr7v2740,089,660 - 40,089,852UniSTS
GeneMap99-GB4 RH Map7183.32UniSTS
NCBI RH Map7623.0UniSTS
CDC2L5_3913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,134,428 - 40,135,285UniSTSGRCh37
Build 36740,100,953 - 40,101,810RGDNCBI36
Celera740,122,626 - 40,123,484RGD
HuRef740,018,336 - 40,019,194UniSTS
CRA_TCAGchr7v2740,172,865 - 40,173,723UniSTS
CDC2L5  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37740,027,411 - 40,027,578UniSTSGRCh37
Celera740,015,638 - 40,015,805UniSTS
HuRef739,911,502 - 39,911,669UniSTS
CRA_TCAGchr7v2740,065,922 - 40,066,089UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR133Bhsa-miR-133bMirtarbaseexternal_infoLuciferase reporter assayFunctional MTI23451058

Predicted Target Of
Summary Value
Count of predictions:1873
Count of miRNA genes:894
Interacting mature miRNAs:1065
Transcripts:ENST00000181839, ENST00000340829, ENST00000465643, ENST00000478563, ENST00000484589
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


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 2233 1482 1374 317 1143 167 3722 1146 1969 269 1420 1578 164 1150 2169 4
Low 206 1503 352 307 802 298 634 1051 1765 150 40 35 11 1 54 619 2 2
Below cutoff 6 6

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_052965 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003718 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_031267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011515597 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012750 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017012751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB058694 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC006023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC072061 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ297709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ297710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK025500 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092534 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK130653 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK223053 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY679523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC080601 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BF707421 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM699295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM727913 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BU686489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647326 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH236951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471073 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR748837 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M80629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000181839   ⟹   ENSP00000181839
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,950,256 - 40,099,580 (+)Ensembl
RefSeq Acc Id: ENST00000340829   ⟹   ENSP00000340557
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,950,121 - 40,095,555 (+)Ensembl
RefSeq Acc Id: ENST00000465643
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl740,092,247 - 40,095,532 (+)Ensembl
RefSeq Acc Id: ENST00000478563
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl740,059,215 - 40,093,168 (+)Ensembl
RefSeq Acc Id: ENST00000484589   ⟹   ENSP00000494206
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,987,836 - 40,073,143 (+)Ensembl
RefSeq Acc Id: ENST00000611390   ⟹   ENSP00000484610
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,951,713 - 40,093,023 (+)Ensembl
RefSeq Acc Id: ENST00000613626   ⟹   ENSP00000480835
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,950,360 - 40,069,346 (+)Ensembl
RefSeq Acc Id: ENST00000642213
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,998,837 - 40,002,249 (+)Ensembl
RefSeq Acc Id: ENST00000642592   ⟹   ENSP00000494207
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl740,045,930 - 40,067,973 (+)Ensembl
RefSeq Acc Id: ENST00000642626   ⟹   ENSP00000493853
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,987,599 - 39,997,983 (+)Ensembl
RefSeq Acc Id: ENST00000642660
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,987,599 - 39,999,386 (+)Ensembl
RefSeq Acc Id: ENST00000643859   ⟹   ENSP00000496440
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,951,751 - 40,095,520 (+)Ensembl
RefSeq Acc Id: ENST00000643868   ⟹   ENSP00000495083
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,951,018 - 39,952,918 (+)Ensembl
RefSeq Acc Id: ENST00000643915   ⟹   ENSP00000496187
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,988,074 - 40,095,508 (+)Ensembl
RefSeq Acc Id: ENST00000644221
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl740,060,820 - 40,095,546 (+)Ensembl
RefSeq Acc Id: ENST00000644561
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl740,062,511 - 40,095,482 (+)Ensembl
RefSeq Acc Id: ENST00000645470   ⟹   ENSP00000495036
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,999,389 - 40,066,882 (+)Ensembl
RefSeq Acc Id: ENST00000645826
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl740,078,414 - 40,095,462 (+)Ensembl
RefSeq Acc Id: ENST00000646039   ⟹   ENSP00000494168
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,951,302 - 40,095,519 (+)Ensembl
RefSeq Acc Id: ENST00000646437   ⟹   ENSP00000496618
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,987,769 - 39,999,456 (+)Ensembl
RefSeq Acc Id: ENST00000647453
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,998,250 - 40,049,206 (+)Ensembl
RefSeq Acc Id: ENST00000647518
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl739,984,105 - 40,002,031 (+)Ensembl
RefSeq Acc Id: NM_003718   ⟹   NP_003709
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,950,256 - 40,099,580 (+)NCBI
GRCh37739,989,959 - 40,136,733 (+)RGD
Build 36739,956,484 - 40,101,679 (+)NCBI Archive
Celera739,978,186 - 40,124,932 (+)RGD
HuRef739,873,916 - 40,020,642 (+)RGD
CHM1_1739,992,473 - 40,139,235 (+)NCBI
CRA_TCAGchr7v2740,028,472 - 40,175,171 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: NM_031267   ⟹   NP_112557
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,950,360 - 40,097,134 (+)NCBI
GRCh37739,989,959 - 40,136,733 (+)RGD
Build 36739,956,484 - 40,101,679 (+)NCBI Archive
Celera739,978,186 - 40,124,932 (+)RGD
HuRef739,873,916 - 40,020,642 (+)RGD
CHM1_1739,992,473 - 40,139,235 (+)NCBI
CRA_TCAGchr7v2740,028,472 - 40,175,171 (+)ENTREZGENE
Sequence:
RefSeq Acc Id: XM_011515597   ⟹   XP_011513899
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,949,664 - 40,054,623 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017012750   ⟹   XP_016868239
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,949,664 - 40,097,134 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017012751   ⟹   XP_016868240
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,949,664 - 40,095,532 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_003709   ⟸   NM_003718
- Peptide Label: isoform 1
- UniProtKB: Q14004 (UniProtKB/Swiss-Prot),   A0A024RA85 (UniProtKB/TrEMBL),   Q9BVE2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_112557   ⟸   NM_031267
- Peptide Label: isoform 2
- UniProtKB: Q14004 (UniProtKB/Swiss-Prot),   A0A024RA66 (UniProtKB/TrEMBL),   Q9BVE2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011513899   ⟸   XM_011515597
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_016868239   ⟸   XM_017012750
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_016868240   ⟸   XM_017012751
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000484610   ⟸   ENST00000611390
RefSeq Acc Id: ENSP00000480835   ⟸   ENST00000613626
RefSeq Acc Id: ENSP00000181839   ⟸   ENST00000181839
RefSeq Acc Id: ENSP00000494206   ⟸   ENST00000484589
RefSeq Acc Id: ENSP00000493853   ⟸   ENST00000642626
RefSeq Acc Id: ENSP00000494207   ⟸   ENST00000642592
RefSeq Acc Id: ENSP00000496187   ⟸   ENST00000643915
RefSeq Acc Id: ENSP00000495083   ⟸   ENST00000643868
RefSeq Acc Id: ENSP00000496440   ⟸   ENST00000643859
RefSeq Acc Id: ENSP00000340557   ⟸   ENST00000340829
RefSeq Acc Id: ENSP00000495036   ⟸   ENST00000645470
RefSeq Acc Id: ENSP00000494168   ⟸   ENST00000646039
RefSeq Acc Id: ENSP00000496618   ⟸   ENST00000646437
Protein Domains
Protein kinase

Promoters
RGD ID:7210423
Promoter ID:EPDNEW_H10958
Type:initiation region
Name:CDK13_4
Description:cyclin dependent kinase 13
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10959  EPDNEW_H10962  EPDNEW_H10960  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,949,652 - 39,949,712EPDNEW
RGD ID:7210425
Promoter ID:EPDNEW_H10959
Type:initiation region
Name:CDK13_2
Description:cyclin dependent kinase 13
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10958  EPDNEW_H10962  EPDNEW_H10960  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,949,795 - 39,949,855EPDNEW
RGD ID:7210437
Promoter ID:EPDNEW_H10960
Type:initiation region
Name:CDK13_1
Description:cyclin dependent kinase 13
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10958  EPDNEW_H10959  EPDNEW_H10962  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,950,080 - 39,950,140EPDNEW
RGD ID:6805399
Promoter ID:HG_KWN:57122
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:ENST00000310016,   ENST00000326351,   NM_031267,   OTTHUMT00000250726
Position:
Human AssemblyChrPosition (strand)Source
Build 36739,955,446 - 39,957,967 (+)MPROMDB
RGD ID:7210431
Promoter ID:EPDNEW_H10962
Type:initiation region
Name:CDK13_3
Description:cyclin dependent kinase 13
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10958  EPDNEW_H10959  EPDNEW_H10960  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38739,987,882 - 39,987,942EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
CDK13, VAL874LEU variation Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000578219] Chr7:7p14.1 pathogenic
GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3 copy number gain See cases [RCV000051159] Chr7:54185..41875885 [GRCh38]
Chr7:54185..41915483 [GRCh37]
Chr7:149268..41882008 [NCBI36]
Chr7:7p22.3-14.1
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 7p14.1-12.3(chr7:39814159-45749735)x1 copy number loss See cases [RCV000053132] Chr7:39814159..45749735 [GRCh38]
Chr7:39853758..45789334 [GRCh37]
Chr7:39820283..45755859 [NCBI36]
Chr7:7p14.1-12.3
pathogenic
GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3 copy number gain See cases [RCV000053532] Chr7:33328312..62377476 [GRCh38]
Chr7:33367924..61831899 [GRCh37]
Chr7:33334449..61469334 [NCBI36]
Chr7:7p14.3-q11.21
pathogenic
NM_003718.4(CDK13):c.1625C>T (p.Pro542Leu) single nucleotide variant Malignant melanoma [RCV000061643] Chr7:39988012 [GRCh38]
Chr7:40027611 [GRCh37]
Chr7:39994136 [NCBI36]
Chr7:7p14.1
not provided
NM_003718.4(CDK13):c.3236-888A>T single nucleotide variant Lung cancer [RCV000106038] Chr7:40091897 [GRCh38]
Chr7:40131496 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.2440del (p.His813_Ile814insTer) deletion not provided [RCV001291589] Chr7:40045922 [GRCh38]
Chr7:40085521 [GRCh37]
Chr7:7p14.1
likely 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 7p14.1-12.1(chr7:40020598-50543500)x1 copy number loss See cases [RCV000136904] Chr7:40020598..50543500 [GRCh38]
Chr7:40060197..50611198 [GRCh37]
Chr7:40026722..50578692 [NCBI36]
Chr7:7p14.1-12.1
pathogenic
GRCh38/hg38 7p14.1(chr7:39670747-40871336)x3 copy number gain See cases [RCV000137688] Chr7:39670747..40871336 [GRCh38]
Chr7:39710346..40910935 [GRCh37]
Chr7:39676871..40877460 [NCBI36]
Chr7:7p14.1
uncertain significance
GRCh38/hg38 7p14.1-12.3(chr7:37303478-48660738)x1 copy number loss See cases [RCV000137139] Chr7:37303478..48660738 [GRCh38]
Chr7:37343082..48700334 [GRCh37]
Chr7:37309607..48670880 [NCBI36]
Chr7:7p14.1-12.3
pathogenic
GRCh38/hg38 7p14.1-13(chr7:39063400-45363096)x1 copy number loss See cases [RCV000137305] Chr7:39063400..45363096 [GRCh38]
Chr7:39103000..45402695 [GRCh37]
Chr7:39069525..45369220 [NCBI36]
Chr7:7p14.1-13
pathogenic
GRCh38/hg38 7p14.2-14.1(chr7:35460776-42013800)x1 copy number loss See cases [RCV000138190] Chr7:35460776..42013800 [GRCh38]
Chr7:35500386..42053399 [GRCh37]
Chr7:35466911..42019924 [NCBI36]
Chr7:7p14.2-14.1
pathogenic
GRCh38/hg38 7p14.3-14.1(chr7:32678391-41044983)x1 copy number loss See cases [RCV000140283] Chr7:32678391..41044983 [GRCh38]
Chr7:32718003..41084581 [GRCh37]
Chr7:32684528..41051106 [NCBI36]
Chr7:7p14.3-14.1
pathogenic
GRCh38/hg38 7p14.1(chr7:39251052-40641073)x1 copy number loss See cases [RCV000140653] Chr7:39251052..40641073 [GRCh38]
Chr7:39290651..40680672 [GRCh37]
Chr7:39257176..40647197 [NCBI36]
Chr7:7p14.1
uncertain significance
GRCh38/hg38 7p14.1(chr7:39968852-40055511)x3 copy number gain See cases [RCV000140736] Chr7:39968852..40055511 [GRCh38]
Chr7:40008451..40095110 [GRCh37]
Chr7:39974976..40061635 [NCBI36]
Chr7:7p14.1
likely benign
GRCh38/hg38 7p14.1-13(chr7:38177999-45304100)x1 copy number loss See cases [RCV000142297] Chr7:38177999..45304100 [GRCh38]
Chr7:38217601..45343699 [GRCh37]
Chr7:38184126..45310224 [NCBI36]
Chr7:7p14.1-13
pathogenic
NM_003718.5(CDK13):c.4097G>A (p.Arg1366His) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000656730] Chr7:40094538 [GRCh38]
Chr7:40134137 [GRCh37]
Chr7:7p14.1
uncertain significance
CDK13, ASN842ASP variation Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000578215] Chr7:7p14.1 pathogenic
NM_003718.5(CDK13):c.2525A>G (p.Asn842Ser) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000417211]|Global developmental delay [RCV001526523]|Inborn genetic diseases [RCV000622786]|Marfanoid habitus and intellectual disability [RCV000850464]|not provided [RCV000498452] Chr7:40046007 [GRCh38]
Chr7:40085606 [GRCh37]
Chr7:7p14.1
pathogenic|likely pathogenic
NM_003718.5(CDK13):c.2524A>G (p.Asn842Asp) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000625958]|not provided [RCV001383184] Chr7:40046006 [GRCh38]
Chr7:40085605 [GRCh37]
Chr7:7p14.1
pathogenic|likely pathogenic
NM_003718.5(CDK13):c.2141G>A (p.Gly714Asp) single nucleotide variant Global developmental delay [RCV001255404]|not provided [RCV000522705] Chr7:39999459 [GRCh38]
Chr7:40039058 [GRCh37]
Chr7:7p14.1
pathogenic
NM_003718.5(CDK13):c.484dup (p.Ala162fs) duplication Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000786912]|not provided [RCV000598864] Chr7:39951117..39951118 [GRCh38]
Chr7:39990716..39990717 [GRCh37]
Chr7:7p14.1
pathogenic|uncertain significance
NM_003718.5(CDK13):c.1152del (p.Ser385fs) deletion not provided [RCV000599056] Chr7:39951793 [GRCh38]
Chr7:39991392 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.2626A>G (p.Thr876Ala) single nucleotide variant not provided [RCV000521638] Chr7:40062851 [GRCh38]
Chr7:40102450 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.2866dup (p.Tyr956fs) duplication not provided [RCV000599271] Chr7:40078089..40078090 [GRCh38]
Chr7:40117688..40117689 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.2912C>T (p.Ala971Val) single nucleotide variant not specified [RCV000414433] Chr7:40078734 [GRCh38]
Chr7:40118333 [GRCh37]
Chr7:7p14.1
uncertain significance
TMEM106B-BRAF fusion deletion Pleomorphic xanthoastrocytoma [RCV000454357] Chr7:12258147..140494267 [GRCh37]
Chr7:7p21.3-q34
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 7p14.3-13(chr7:32911003-44576005)x1 copy number loss See cases [RCV000446955] Chr7:32911003..44576005 [GRCh37]
Chr7:7p14.3-13
pathogenic
GRCh37/hg19 7p14.1(chr7:40095110-40256612)x1 copy number loss See cases [RCV000447190] Chr7:40095110..40256612 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2140G>C (p.Gly714Arg) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000417209] Chr7:39999458 [GRCh38]
Chr7:40039057 [GRCh37]
Chr7:7p14.1
pathogenic
NM_003718.5(CDK13):c.2149G>A (p.Gly717Arg) single nucleotide variant Autism spectrum disorder [RCV001527382]|Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000417213]|Inborn genetic diseases [RCV000622659]|not provided [RCV000489190] Chr7:39999467 [GRCh38]
Chr7:40039066 [GRCh37]
Chr7:7p14.1
pathogenic
NM_003718.5(CDK13):c.2252G>A (p.Arg751Gln) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000417212] Chr7:40001930 [GRCh38]
Chr7:40041529 [GRCh37]
Chr7:7p14.1
pathogenic
GRCh37/hg19 7p21.3-12.1(chr7:11048840-52863626)x3 copy number gain See cases [RCV000512091] Chr7:11048840..52863626 [GRCh37]
Chr7:7p21.3-12.1
pathogenic
NM_003718.5(CDK13):c.2200A>G (p.Lys734Glu) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001200020]|not provided [RCV000482250] Chr7:40001878 [GRCh38]
Chr7:40041477 [GRCh37]
Chr7:7p14.1
pathogenic|likely pathogenic
NM_003718.5(CDK13):c.2209C>T (p.Arg737Cys) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001174959]|not provided [RCV000478032] Chr7:40001887 [GRCh38]
Chr7:40041486 [GRCh37]
Chr7:7p14.1
pathogenic
GRCh37/hg19 7p14.1(chr7:38619347-40542932)x1 copy number loss See cases [RCV000512076] Chr7:38619347..40542932 [GRCh37]
Chr7:7p14.1
likely 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 7p14.1(chr7:38619347-40542932)x1 copy number loss not provided [RCV000509377] Chr7:38619347..40542932 [GRCh37]
Chr7:7p14.1
not provided
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
NM_003718.5(CDK13):c.2995C>T (p.Arg999Ter) single nucleotide variant not provided [RCV000578663] Chr7:40078817 [GRCh38]
Chr7:40118416 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.1066C>G (p.Pro356Ala) single nucleotide variant not provided [RCV000514635] Chr7:39951707 [GRCh38]
Chr7:39991306 [GRCh37]
Chr7:7p14.1
benign|likely benign
NM_003718.5(CDK13):c.181del (p.Leu61fs) deletion Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000791281]|Inborn genetic diseases [RCV000623626] Chr7:39950821 [GRCh38]
Chr7:39990420 [GRCh37]
Chr7:7p14.1
likely pathogenic|uncertain significance
NM_003718.5(CDK13):c.2716G>A (p.Glu906Lys) single nucleotide variant Inborn genetic diseases [RCV000623723] Chr7:40063036 [GRCh38]
Chr7:40102635 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.478G>C (p.Gly160Arg) single nucleotide variant Inborn genetic diseases [RCV000623922] Chr7:39951119 [GRCh38]
Chr7:39990718 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.425dup (p.Leu143fs) duplication not provided [RCV000627452] Chr7:39951062..39951063 [GRCh38]
Chr7:39990661..39990662 [GRCh37]
Chr7:7p14.1
uncertain significance
GRCh37/hg19 7p14.1(chr7:40043298-40324829)x1 copy number loss not provided [RCV000682815] Chr7:40043298..40324829 [GRCh37]
Chr7:7p14.1
uncertain significance
GRCh37/hg19 7p14.3-13(chr7:30463886-43470805)x3 copy number gain not provided [RCV000682909] Chr7:30463886..43470805 [GRCh37]
Chr7:7p14.3-13
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 7p14.1(chr7:37213108-40255122)x3 copy number gain not provided [RCV000746632] Chr7:37213108..40255122 [GRCh37]
Chr7:7p14.1
pathogenic
NC_000007.13:g.39999692_40144263dup duplication Primary amenorrhea [RCV000754437] Chr7:39960093..40104664 [GRCh38]
Chr7:39999692..40144263 [GRCh37]
Chr7:7p14.1
likely benign
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
NM_003718.5(CDK13):c.3168C>A (p.Thr1056=) single nucleotide variant not provided [RCV000940484] Chr7:40088264 [GRCh38]
Chr7:40127863 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.2442A>T (p.Ile814=) single nucleotide variant not provided [RCV000940630] Chr7:40045924 [GRCh38]
Chr7:40085523 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.498G>A (p.Thr166=) single nucleotide variant not provided [RCV000936290] Chr7:39951139 [GRCh38]
Chr7:39990738 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.3645A>G (p.Ser1215=) single nucleotide variant not provided [RCV000938812] Chr7:40093194 [GRCh38]
Chr7:40132793 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.3073C>T (p.Arg1025Ter) single nucleotide variant not provided [RCV000760635] Chr7:40088169 [GRCh38]
Chr7:40127768 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.3955G>A (p.Gly1319Ser) single nucleotide variant not provided [RCV000905520] Chr7:40094396 [GRCh38]
Chr7:40133995 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.115C>T (p.Leu39=) single nucleotide variant not provided [RCV000899138] Chr7:39950756 [GRCh38]
Chr7:39990355 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.240C>T (p.Cys80=) single nucleotide variant not provided [RCV000903123] Chr7:39950881 [GRCh38]
Chr7:39990480 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.792A>G (p.Thr264=) single nucleotide variant not provided [RCV000902469] Chr7:39951433 [GRCh38]
Chr7:39991032 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2715C>T (p.Gly905=) single nucleotide variant not provided [RCV000885255] Chr7:40063035 [GRCh38]
Chr7:40102634 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.993C>A (p.Ala331=) single nucleotide variant not provided [RCV000928118] Chr7:39951634 [GRCh38]
Chr7:39991233 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.4266C>T (p.Asp1422=) single nucleotide variant not provided [RCV000905168] Chr7:40094707 [GRCh38]
Chr7:40134306 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.3483T>A (p.Pro1161=) single nucleotide variant not provided [RCV000921610] Chr7:40093032 [GRCh38]
Chr7:40132631 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.652C>A (p.Arg218=) single nucleotide variant not provided [RCV000923398] Chr7:39951293 [GRCh38]
Chr7:39990892 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1459G>T (p.Ala487Ser) single nucleotide variant not provided [RCV000880263] Chr7:39987846 [GRCh38]
Chr7:40027445 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1824A>C (p.Pro608=) single nucleotide variant not provided [RCV000976145] Chr7:39988211 [GRCh38]
Chr7:40027810 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2124C>T (p.Ile708=) single nucleotide variant not provided [RCV000879972] Chr7:39999442 [GRCh38]
Chr7:40039041 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.1959T>G (p.Pro653=) single nucleotide variant not provided [RCV000924494] Chr7:39997581 [GRCh38]
Chr7:40037180 [GRCh37]
Chr7:7p14.1
likely benign
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
NM_003718.5(CDK13):c.3182G>A (p.Gly1061Asp) single nucleotide variant not provided [RCV001043630] Chr7:40088278 [GRCh38]
Chr7:40127877 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.462G>A (p.Glu154=) single nucleotide variant not provided [RCV000929239] Chr7:39951103 [GRCh38]
Chr7:39990702 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1128C>T (p.Tyr376=) single nucleotide variant not provided [RCV000929370] Chr7:39951769 [GRCh38]
Chr7:39991368 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.3508G>A (p.Val1170Met) single nucleotide variant not provided [RCV000952536] Chr7:40093057 [GRCh38]
Chr7:40132656 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.2246C>A (p.Ala749Glu) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000767530] Chr7:40001924 [GRCh38]
Chr7:40041523 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.552C>T (p.Ser184=) single nucleotide variant not provided [RCV000982222] Chr7:39951193 [GRCh38]
Chr7:39990792 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1242G>A (p.Pro414=) single nucleotide variant not provided [RCV000914596] Chr7:39987629 [GRCh38]
Chr7:40027228 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1401C>T (p.Ala467=) single nucleotide variant not provided [RCV000899038] Chr7:39987788 [GRCh38]
Chr7:40027387 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1413G>A (p.Ala471=) single nucleotide variant not provided [RCV000903286] Chr7:39987800 [GRCh38]
Chr7:40027399 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1207C>T (p.Leu403Phe) single nucleotide variant not provided [RCV000894171] Chr7:39951848 [GRCh38]
Chr7:39991447 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.486C>T (p.Ala162=) single nucleotide variant not provided [RCV000922359] Chr7:39951127 [GRCh38]
Chr7:39990726 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2027G>A (p.Ser676Asn) single nucleotide variant not provided [RCV000938982] Chr7:39997649 [GRCh38]
Chr7:40037248 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.1833T>G (p.Pro611=) single nucleotide variant not provided [RCV000909845] Chr7:39988220 [GRCh38]
Chr7:40027819 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.2985C>T (p.Cys995=) single nucleotide variant not provided [RCV000973398] Chr7:40078807 [GRCh38]
Chr7:40118406 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.813C>G (p.Arg271=) single nucleotide variant not provided [RCV000938135] Chr7:39951454 [GRCh38]
Chr7:39991053 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.3030-9T>C single nucleotide variant not provided [RCV000937863] Chr7:40088117 [GRCh38]
Chr7:40127716 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1989G>A (p.Lys663=) single nucleotide variant not provided [RCV000915592] Chr7:39997611 [GRCh38]
Chr7:40037210 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.4050T>A (p.Val1350=) single nucleotide variant not provided [RCV000914102] Chr7:40094491 [GRCh38]
Chr7:40134090 [GRCh37]
Chr7:7p14.1
benign
GRCh37/hg19 7p14.1(chr7:40081970-40611718)x1 copy number loss not provided [RCV000846641] Chr7:40081970..40611718 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.2570G>A (p.Gly857Glu) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000850539] Chr7:40047847 [GRCh38]
Chr7:40087446 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.2201A>G (p.Lys734Arg) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001200021] Chr7:40001879 [GRCh38]
Chr7:40041478 [GRCh37]
Chr7:7p14.1
pathogenic
NM_003718.5(CDK13):c.509C>T (p.Ala170Val) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001198674] Chr7:39951150 [GRCh38]
Chr7:39990749 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.1149C>T (p.Ser383=) single nucleotide variant not provided [RCV000911017] Chr7:39951790 [GRCh38]
Chr7:39991389 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.3888C>T (p.Ala1296=) single nucleotide variant not provided [RCV000907801] Chr7:40094329 [GRCh38]
Chr7:40133928 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1671C>T (p.Ala557=) single nucleotide variant not provided [RCV000881254] Chr7:39988058 [GRCh38]
Chr7:40027657 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.1878A>G (p.Arg626=) single nucleotide variant not provided [RCV000936687] Chr7:39997500 [GRCh38]
Chr7:40037099 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2897+9G>T single nucleotide variant not provided [RCV000888246] Chr7:40078130 [GRCh38]
Chr7:40117729 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.441G>A (p.Glu147=) single nucleotide variant not provided [RCV000908048] Chr7:39951082 [GRCh38]
Chr7:39990681 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1870A>G (p.Ser624Gly) single nucleotide variant not provided [RCV000958979] Chr7:39988257 [GRCh38]
Chr7:40027856 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.1260A>G (p.Ser420=) single nucleotide variant not provided [RCV000950412] Chr7:39987647 [GRCh38]
Chr7:40027246 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.642C>T (p.Arg214=) single nucleotide variant not provided [RCV000953251] Chr7:39951283 [GRCh38]
Chr7:39990882 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.3271G>A (p.Glu1091Lys) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001336069]|not provided [RCV000880412] Chr7:40092820 [GRCh38]
Chr7:40132419 [GRCh37]
Chr7:7p14.1
likely benign|uncertain significance
NM_003718.5(CDK13):c.2180C>T (p.Thr727Ile) single nucleotide variant not provided [RCV000971141] Chr7:39999498 [GRCh38]
Chr7:40039097 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2511T>G (p.Asp837Glu) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001249357] Chr7:40045993 [GRCh38]
Chr7:40085592 [GRCh37]
Chr7:7p14.1
not provided
NM_003718.5(CDK13):c.3185T>C (p.Val1062Ala) single nucleotide variant not provided [RCV000890055] Chr7:40088281 [GRCh38]
Chr7:40127880 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1479T>C (p.Ser493=) single nucleotide variant not provided [RCV000934678] Chr7:39987866 [GRCh38]
Chr7:40027465 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.3401G>T (p.Gly1134Val) single nucleotide variant not provided [RCV000891425] Chr7:40092950 [GRCh38]
Chr7:40132549 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.858C>T (p.Ser286=) single nucleotide variant not provided [RCV000911157] Chr7:39951499 [GRCh38]
Chr7:39991098 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.806del (p.Ser269fs) deletion Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV000984968] Chr7:39951447 [GRCh38]
Chr7:39991046 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.2421T>A (p.Val807=) single nucleotide variant not provided [RCV000911480] Chr7:40045903 [GRCh38]
Chr7:40085502 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.3184G>A (p.Val1062Met) single nucleotide variant not provided [RCV000912556] Chr7:40088280 [GRCh38]
Chr7:40127879 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1928G>A (p.Arg643Gln) single nucleotide variant not provided [RCV000998789] Chr7:39997550 [GRCh38]
Chr7:40037149 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.891C>T (p.Pro297=) single nucleotide variant not provided [RCV000911479] Chr7:39951532 [GRCh38]
Chr7:39991131 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.2009C>G (p.Thr670Arg) single nucleotide variant not provided [RCV000889754] Chr7:39997631 [GRCh38]
Chr7:40037230 [GRCh37]
Chr7:7p14.1
benign
NM_003718.5(CDK13):c.2194G>A (p.Ala732Thr) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001027706] Chr7:40001872 [GRCh38]
Chr7:40041471 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.2210G>A (p.Arg737His) single nucleotide variant not provided [RCV001092566] Chr7:40001888 [GRCh38]
Chr7:40041487 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.2898-1G>A single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001200022] Chr7:40078719 [GRCh38]
Chr7:40118318 [GRCh37]
Chr7:7p14.1
pathogenic
NM_003718.5(CDK13):c.2638C>T (p.Arg880Cys) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001254124] Chr7:40062863 [GRCh38]
Chr7:40102462 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.1654T>G (p.Leu552Val) single nucleotide variant Intellectual disability [RCV001252191] Chr7:39988041 [GRCh38]
Chr7:40027640 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1462A>G (p.Lys488Glu) single nucleotide variant Intellectual disability [RCV001252190] Chr7:39987849 [GRCh38]
Chr7:40027448 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.1219G>A (p.Gly407Arg) single nucleotide variant Intellectual disability [RCV001252189] Chr7:39987606 [GRCh38]
Chr7:40027205 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.3094G>A (p.Gly1032Ser) single nucleotide variant Intellectual disability [RCV001252192]|not provided [RCV001463224] Chr7:40088190 [GRCh38]
Chr7:40127789 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2140G>T (p.Gly714Cys) single nucleotide variant Global developmental delay [RCV001255381] Chr7:39999458 [GRCh38]
Chr7:40039057 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.1012C>T (p.Arg338Cys) single nucleotide variant Inborn genetic diseases [RCV001267562] Chr7:39951653 [GRCh38]
Chr7:39991252 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.1497C>A (p.Asn499Lys) single nucleotide variant Seizures [RCV001256046] Chr7:39987884 [GRCh38]
Chr7:40027483 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.1526C>G (p.Thr509Arg) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001332313] Chr7:39987913 [GRCh38]
Chr7:40027512 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.1187del (p.Arg396fs) deletion not provided [RCV001268314] Chr7:39951828 [GRCh38]
Chr7:39991427 [GRCh37]
Chr7:7p14.1
pathogenic
NM_003718.5(CDK13):c.4403A>G (p.Glu1468Gly) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329118] Chr7:40094844 [GRCh38]
Chr7:40134443 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.3190C>T (p.Pro1064Ser) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329115] Chr7:40088286 [GRCh38]
Chr7:40127885 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.2251C>T (p.Arg751Ter) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329114] Chr7:40001929 [GRCh38]
Chr7:40041528 [GRCh37]
Chr7:7p14.1
likely pathogenic
NM_003718.5(CDK13):c.521C>G (p.Thr174Arg) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329119] Chr7:39951162 [GRCh38]
Chr7:39990761 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.796A>G (p.Ser266Gly) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001336070] Chr7:39951437 [GRCh38]
Chr7:39991036 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.875C>T (p.Ala292Val) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329120] Chr7:39951516 [GRCh38]
Chr7:39991115 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.1583G>C (p.Ser528Thr) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329113] Chr7:39987970 [GRCh38]
Chr7:40027569 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.748AGC[6] (p.Ser254dup) microsatellite not provided [RCV001358406] Chr7:39951386..39951387 [GRCh38]
Chr7:39990985..39990986 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.3481C>G (p.Pro1161Ala) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329116] Chr7:40093030 [GRCh38]
Chr7:40132629 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.4081C>G (p.Pro1361Ala) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001329117] Chr7:40094522 [GRCh38]
Chr7:40134121 [GRCh37]
Chr7:7p14.1
uncertain significance
NM_003718.5(CDK13):c.1499C>T (p.Thr500Met) single nucleotide variant not provided [RCV001467690] Chr7:39987886 [GRCh38]
Chr7:40027485 [GRCh37]
Chr7:7p14.1
likely benign
NM_003718.5(CDK13):c.2510A>G (p.Asp837Gly) single nucleotide variant Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder [RCV001420349] Chr7:40045992 [GRCh38]
Chr7:40085591 [GRCh37]
Chr7:7p14.1
likely pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1733 AgrOrtholog
COSMIC CDK13 COSMIC
Ensembl Genes ENSG00000065883 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000181839 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000340557 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000480835 UniProtKB/TrEMBL
  ENSP00000484610 UniProtKB/TrEMBL
  ENSP00000493853 UniProtKB/TrEMBL
  ENSP00000494168 UniProtKB/TrEMBL
  ENSP00000494206 UniProtKB/TrEMBL
  ENSP00000494207 UniProtKB/TrEMBL
  ENSP00000495036 UniProtKB/TrEMBL
  ENSP00000495083 UniProtKB/TrEMBL
  ENSP00000496187 UniProtKB/TrEMBL
  ENSP00000496440 UniProtKB/TrEMBL
  ENSP00000496618 UniProtKB/TrEMBL
Ensembl Transcript ENST00000181839 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000340829 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000484589 UniProtKB/TrEMBL
  ENST00000611390 UniProtKB/TrEMBL
  ENST00000613626 UniProtKB/TrEMBL
  ENST00000642592 UniProtKB/TrEMBL
  ENST00000642626 UniProtKB/TrEMBL
  ENST00000643859 UniProtKB/TrEMBL
  ENST00000643868 UniProtKB/TrEMBL
  ENST00000643915 UniProtKB/TrEMBL
  ENST00000645470 UniProtKB/TrEMBL
  ENST00000646039 UniProtKB/TrEMBL
  ENST00000646437 UniProtKB/TrEMBL
GTEx ENSG00000065883 GTEx
HGNC ID HGNC:1733 ENTREZGENE
Human Proteome Map CDK13 Human Proteome Map
InterPro Kinase-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_kinase_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protein_kinase_ATP_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ser/Thr_kinase_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:8621 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8621 ENTREZGENE
OMIM 603309 OMIM
  617360 OMIM
Pfam Pkinase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA26264 PharmGKB
PROSITE PROTEIN_KINASE_ATP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_DOM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEIN_KINASE_ST UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART S_TKc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF56112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024RA66 ENTREZGENE, UniProtKB/TrEMBL
  A0A024RA85 ENTREZGENE, UniProtKB/TrEMBL
  A0A087X209_HUMAN UniProtKB/TrEMBL
  A0A2R8Y4Z0_HUMAN UniProtKB/TrEMBL
  A0A2R8Y644_HUMAN UniProtKB/TrEMBL
  A0A2R8Y7W5_HUMAN UniProtKB/TrEMBL
  A0A2R8Y7Y0_HUMAN UniProtKB/TrEMBL
  A0A2R8YCQ1_HUMAN UniProtKB/TrEMBL
  A0A2R8YD28_HUMAN UniProtKB/TrEMBL
  A0A2R8YEB7_HUMAN UniProtKB/TrEMBL
  A0A2R8YF61_HUMAN UniProtKB/TrEMBL
  A0A2R8YFE7_HUMAN UniProtKB/TrEMBL
  CDK13_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q9BVE2 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary Q53G78 UniProtKB/Swiss-Prot
  Q6DKQ9 UniProtKB/Swiss-Prot
  Q75MH4 UniProtKB/Swiss-Prot
  Q75MH5 UniProtKB/Swiss-Prot
  Q96JN4 UniProtKB/Swiss-Prot
  Q9H4A0 UniProtKB/Swiss-Prot
  Q9H4A1 UniProtKB/Swiss-Prot
  Q9UDR4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-06-21 CDK13  cyclin dependent kinase 13  CDK13  cyclin-dependent kinase 13  Symbol and/or name change 5135510 APPROVED
2011-07-27 CDK13  cyclin-dependent kinase 13  CDC2L5  cell division cycle 2-like 5 (cholinesterase-related cell division controller)  Symbol and/or name change 5135510 APPROVED