DCDC1 (doublecortin domain containing 1) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: DCDC1 (doublecortin domain containing 1) Homo sapiens
Analyze
Symbol: DCDC1
Name: doublecortin domain containing 1
RGD ID: 1351849
HGNC Page HGNC:20625
Description: Enables microtubule binding activity. Involved in regulation of mitotic cytokinesis. Located in Flemming body and mitotic spindle.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: DCDC5; DKFZp779D068; doublecortin domain containing 5; doublecortin domain-containing protein 1; doublecortin domain-containing protein 5; FLJ44078; FLJ46154; KIAA1493; MGC190499; MGC190811
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381130,863,603 - 31,369,739 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1130,830,369 - 31,369,810 (-)EnsemblGRCh38hg38GRCh38
GRCh371130,885,150 - 31,391,286 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361131,240,747 - 31,347,897 (-)NCBINCBI36Build 36hg18NCBI36
Build 341131,240,747 - 31,347,897NCBI
Celera1131,431,602 - 31,538,744 (-)NCBICelera
Cytogenetic Map11p14.1-p13NCBI
HuRef1130,977,492 - 31,085,706 (-)NCBIHuRef
CHM1_11131,283,686 - 31,390,898 (-)NCBICHM1_1
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
cytoplasm  (IEA)
cytoskeleton  (IEA)
Flemming body  (IDA,IEA)
microtubule  (IEA)
midbody  (IBA,IDA,IEA)
mitotic spindle  (IDA)
spindle  (IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10819331   PMID:11181995   PMID:12477932   PMID:12820024   PMID:14702039   PMID:16344560   PMID:16554811   PMID:16869982   PMID:19801982   PMID:20236041   PMID:20379614   PMID:20700443  
PMID:21321669   PMID:21873635   PMID:22159412   PMID:22504420   PMID:22797727   PMID:26460568   PMID:30021884   PMID:31753913   PMID:33961781   PMID:37827155  


Genomics

Comparative Map Data
DCDC1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381130,863,603 - 31,369,739 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1130,830,369 - 31,369,810 (-)EnsemblGRCh38hg38GRCh38
GRCh371130,885,150 - 31,391,286 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361131,240,747 - 31,347,897 (-)NCBINCBI36Build 36hg18NCBI36
Build 341131,240,747 - 31,347,897NCBI
Celera1131,431,602 - 31,538,744 (-)NCBICelera
Cytogenetic Map11p14.1-p13NCBI
HuRef1130,977,492 - 31,085,706 (-)NCBIHuRef
CHM1_11131,283,686 - 31,390,898 (-)NCBICHM1_1
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBIT2T-CHM13v2.0
Gm9342
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm392105,833,679 - 106,236,532 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl2105,868,563 - 106,234,411 (+)EnsemblGRCm39 Ensembl
GRCm382106,080,864 - 106,409,743 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl2106,003,336 - 106,406,151 (+)EnsemblGRCm38mm10GRCm38
MGSCv372106,065,822 - 106,241,378 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv362106,184,519 - 106,206,972 (+)NCBIMGSCv36mm8
Celera2107,444,081 - 107,617,831 (+)NCBICelera
Cytogenetic Map2E3NCBI
cM Map255.49NCBI
Dcdc1-ps1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr83112,940,793 - 113,351,417 (+)NCBIGRCr8
mRatBN7.2392,486,054 - 92,896,696 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl392,718,047 - 92,896,542 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.0397,207,500 - 97,435,067 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl397,256,881 - 97,433,651 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.03103,873,584 - 104,052,850 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4391,716,409 - 91,896,083 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera391,766,794 - 91,943,987 (+)NCBICelera
Cytogenetic Map3q33NCBI
DCDC1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2933,082,524 - 33,580,111 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11133,087,008 - 33,584,582 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01130,837,264 - 31,333,462 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11130,726,365 - 31,223,089 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1130,755,366 - 31,181,807 (-)Ensemblpanpan1.1panPan2
DCDC1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11836,024,054 - 36,484,119 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1836,024,107 - 36,480,774 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1835,672,839 - 36,155,172 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01836,667,003 - 37,146,388 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1836,667,620 - 37,126,604 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11836,240,867 - 36,723,748 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01835,822,607 - 36,306,181 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01836,457,705 - 36,940,478 (+)NCBIUU_Cfam_GSD_1.0
Dcdc1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494733,215,775 - 33,703,190 (+)NCBIHiC_Itri_2
SpeTri2.0NW_0049365336,559,484 - 6,827,979 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LOC100517025
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl229,365,195 - 29,792,979 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1229,365,181 - 29,796,389 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2231,872,562 - 32,293,072 (+)NCBISscrofa10.2Sscrofa10.2susScr3
DCDC1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1133,812,925 - 34,311,269 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666038130,980,259 - 131,486,665 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in DCDC1
86 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11p14.3-12(chr11:22550115-38199159)x1 copy number loss See cases [RCV000052648] Chr11:22550115..38199159 [GRCh38]
Chr11:22571661..38220709 [GRCh37]
Chr11:22528237..38177285 [NCBI36]
Chr11:11p14.3-12
pathogenic
GRCh38/hg38 11p13(chr11:31096480-31726083)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052649]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052649]|See cases [RCV000052649] Chr11:31096480..31726083 [GRCh38]
Chr11:31118027..31747631 [GRCh37]
Chr11:31074603..31704207 [NCBI36]
Chr11:11p13
pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13
pathogenic
NM_181807.3(DCDC1):c.437T>C (p.Val146Ala) single nucleotide variant Malignant melanoma [RCV000062194] Chr11:31306386 [GRCh38]
Chr11:31327933 [GRCh37]
Chr11:31284509 [NCBI36]
Chr11:11p13
not provided
GRCh38/hg38 11p14.2-13(chr11:26368962-35252976)x1 copy number loss See cases [RCV000135295] Chr11:26368962..35252976 [GRCh38]
Chr11:26390509..35274523 [GRCh37]
Chr11:26347085..35231099 [NCBI36]
Chr11:11p14.2-13
pathogenic
GRCh38/hg38 11p13(chr11:31299323-31790071)x1 copy number loss See cases [RCV000135618] Chr11:31299323..31790071 [GRCh38]
Chr11:31320870..31811619 [GRCh37]
Chr11:31277446..31768195 [NCBI36]
Chr11:11p13
pathogenic
GRCh38/hg38 11p13(chr11:31299323-31726083)x1 copy number loss See cases [RCV000136946] Chr11:31299323..31726083 [GRCh38]
Chr11:31320870..31747631 [GRCh37]
Chr11:31277446..31704207 [NCBI36]
Chr11:11p13
uncertain significance
GRCh38/hg38 11p13(chr11:31070635-31535274)x1 copy number loss See cases [RCV000137512] Chr11:31070635..31535274 [GRCh38]
Chr11:31092182..31556821 [GRCh37]
Chr11:31048758..31513397 [NCBI36]
Chr11:11p13
uncertain significance
GRCh38/hg38 11p13(chr11:31189295-31701133)x1 copy number loss See cases [RCV000139992] Chr11:31189295..31701133 [GRCh38]
Chr11:31210842..31722681 [GRCh37]
Chr11:31167418..31679257 [NCBI36]
Chr11:11p13
pathogenic
GRCh38/hg38 11p15.1-13(chr11:20079474-34463996)x1 copy number loss See cases [RCV000142499] Chr11:20079474..34463996 [GRCh38]
Chr11:20101020..34485543 [GRCh37]
Chr11:20057596..34442119 [NCBI36]
Chr11:11p15.1-13
pathogenic
NC_000011.10:g.31130456_31671718del deletion Congenital aniridia [RCV000257311] Chr11:31130456..31671718 [GRCh38]
Chr11:31152003..31693266 [GRCh37]
Chr11:31108579..31649842 [NCBI36]
Chr11:11p13
pathogenic
NC_000011.10:g.30896521_31676711del deletion Congenital aniridia [RCV000257640] Chr11:30896521..31676711 [GRCh38]
Chr11:30918066..31698257 [GRCh37]
Chr11:30874642..31654833 [NCBI36]
Chr11:11p14.1-13
pathogenic
NC_000011.8:g.31199000_31914000del715001 deletion Congenital aniridia [RCV000257713] Chr11:31242424..31957424 [GRCh37]
Chr11:31199000..31914000 [NCBI36]
Chr11:11p13
pathogenic
NC_000011.10:g.30988877_31725876del deletion Congenital aniridia [RCV000256800] Chr11:30988877..31725876 [GRCh38]
Chr11:31010424..31747424 [GRCh37]
Chr11:30967000..31704000 [NCBI36]
Chr11:11p14.1-13
pathogenic
NC_000011.10:g.31256273_31773692del deletion Congenital aniridia [RCV000257783] Chr11:31256273..31773692 [GRCh38]
Chr11:31277819..31795239 [GRCh37]
Chr11:31234395..31751815 [NCBI36]
Chr11:11p13
pathogenic
NC_000011.8:g.31199000_31849000del650001 deletion Congenital aniridia [RCV000257160] Chr11:31242424..31892424 [GRCh37]
Chr11:31199000..31849000 [NCBI36]
Chr11:11p13
pathogenic
GRCh37/hg19 11p13(chr11:31312348-31454239)x1 copy number loss See cases [RCV000240129] Chr11:31312348..31454239 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p13(chr11:31312348-31345582)x1 copy number loss See cases [RCV000239817] Chr11:31312348..31345582 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p13(chr11:31284306-32458309)x1 copy number loss See cases [RCV000240076] Chr11:31284306..32458309 [GRCh37]
Chr11:11p13
pathogenic
GRCh37/hg19 11p14.1-12(chr11:30615127-40606139)x1 copy number loss See cases [RCV000240268] Chr11:30615127..40606139 [GRCh37]
Chr11:11p14.1-12
pathogenic
GRCh37/hg19 11p13(chr11:31311902-31349768)x1 copy number loss See cases [RCV000240582] Chr11:31311902..31349768 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p13(chr11:31210842-35436121)x1 copy number loss See cases [RCV000446864] Chr11:31210842..35436121 [GRCh37]
Chr11:11p13
pathogenic
GRCh37/hg19 11p13(chr11:31292909-31357084)x1 copy number loss See cases [RCV000446137] Chr11:31292909..31357084 [GRCh37]
Chr11:11p13
likely benign
GRCh37/hg19 11p15.1-13(chr11:18536224-31923308)x1 copy number loss Aniridia 1 [RCV000420782] Chr11:18536224..31923308 [GRCh37]
Chr11:11p15.1-13
pathogenic
GRCh37/hg19 11p13(chr11:31186493-31698208)x1 copy number loss Aniridia 1 [RCV000445122] Chr11:31186493..31698208 [GRCh37]
Chr11:11p13
pathogenic
GRCh37/hg19 11p15.1-13(chr11:21586131-33168232)x1 copy number loss Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome [RCV000435400] Chr11:21586131..33168232 [GRCh37]
Chr11:11p15.1-13
pathogenic
GRCh37/hg19 11p14.1-11.2(chr11:29238811-45494063)x1 copy number loss See cases [RCV000445800] Chr11:29238811..45494063 [GRCh37]
Chr11:11p14.1-11.2
pathogenic
GRCh37/hg19 11p13(chr11:31147306-31714853)x1 copy number loss Aniridia 1 [RCV000426648] Chr11:31147306..31714853 [GRCh37]
Chr11:11p13
pathogenic
GRCh37/hg19 11p14.1-13(chr11:29750813-32752091)x1 copy number loss 11p partial monosomy syndrome [RCV000433834] Chr11:29750813..32752091 [GRCh37]
Chr11:11p14.1-13
pathogenic
GRCh37/hg19 11p13(chr11:31083877-31704548)x1 copy number loss Aniridia 1 [RCV000427112] Chr11:31083877..31704548 [GRCh37]
Chr11:11p13
pathogenic
GRCh37/hg19 11p14.1-13(chr11:27895487-34494489)x1 copy number loss See cases [RCV000448524] Chr11:27895487..34494489 [GRCh37]
Chr11:11p14.1-13
pathogenic
GRCh37/hg19 11p13(chr11:31210842-31312348)x1 copy number loss See cases [RCV000448413] Chr11:31210842..31312348 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p14.2-11.12(chr11:26574629-50508019)x3 copy number gain See cases [RCV000448603] Chr11:26574629..50508019 [GRCh37]
Chr11:11p14.2-11.12
pathogenic
GRCh37/hg19 11p14.3-13(chr11:25771208-35614978)x1 copy number loss See cases [RCV000512014] Chr11:25771208..35614978 [GRCh37]
Chr11:11p14.3-13
pathogenic
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12
pathogenic
GRCh37/hg19 11p14.1-12(chr11:27588560-41770792)x1 copy number loss See cases [RCV000511434] Chr11:27588560..41770792 [GRCh37]
Chr11:11p14.1-12
pathogenic|uncertain significance
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
NM_001387274.1(DCDC1):c.182A>G (p.Gln61Arg) single nucleotide variant not specified [RCV004293691] Chr11:31307891 [GRCh38]
Chr11:31329438 [GRCh37]
Chr11:11p13
uncertain significance
GRCh38/hg38 11p14.3-13(chr11:24595399-31096539)x3 copy number gain See cases [RCV000134877] Chr11:24595399..31096539 [GRCh38]
Chr11:24616945..31118086 [GRCh37]
Chr11:24573521..31074662 [NCBI36]
Chr11:11p14.3-13
pathogenic
GRCh38/hg38 11p14.1-13(chr11:30446855-31031357)x3 copy number gain See cases [RCV000137846] Chr11:30446855..31031357 [GRCh38]
Chr11:30468402..31052904 [GRCh37]
Chr11:30424978..31009480 [NCBI36]
Chr11:11p14.1-13
uncertain significance
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13
pathogenic
Single allele deletion not provided [RCV000677913] Chr11:31290802..31432693 [GRCh38]
Chr11:31312348..31454239 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p13(chr11:31325456-31501794)x1 copy number loss not provided [RCV000683312] Chr11:31325456..31501794 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p13(chr11:31351185-31573646)x3 copy number gain not provided [RCV000683318] Chr11:31351185..31573646 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p14.1-13(chr11:29883001-33865721)x1 copy number loss not provided [RCV000683364] Chr11:29883001..33865721 [GRCh37]
Chr11:11p14.1-13
pathogenic
NC_000011.9:g.(?_31284590)_(32456911_?)del deletion Aniridia 1 [RCV000708019]|Drash syndrome [RCV001386651] Chr11:31284590..32456911 [GRCh37]
Chr11:11p13
pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p14.3-12(chr11:24469451-37524085)x1 copy number loss not provided [RCV000737457] Chr11:24469451..37524085 [GRCh37]
Chr11:11p14.3-12
pathogenic
GRCh37/hg19 11p14.3-13(chr11:25196998-34196484)x1 copy number loss not provided [RCV000737466] Chr11:25196998..34196484 [GRCh37]
Chr11:11p14.3-13
pathogenic
GRCh37/hg19 11p13(chr11:31390733-31414949)x1 copy number loss not provided [RCV000737473] Chr11:31390733..31414949 [GRCh37]
Chr11:11p13
benign
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25
pathogenic
GRCh37/hg19 11p14.2-13(chr11:27154853-33302474)x1 copy number loss not provided [RCV000749997] Chr11:27154853..33302474 [GRCh37]
Chr11:11p14.2-13
pathogenic
GRCh37/hg19 11p13(chr11:31385819-31397428)x0 copy number loss not provided [RCV000750003] Chr11:31385819..31397428 [GRCh37]
Chr11:11p13
benign
GRCh37/hg19 11p13(chr11:31389267-31397428)x0 copy number loss not provided [RCV000750004] Chr11:31389267..31397428 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.4481A>G (p.Lys1494Arg) single nucleotide variant DCDC5-related condition [RCV004758745]|not provided [RCV000891777] Chr11:30903511 [GRCh38]
Chr11:30925058 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.5101T>C (p.Ser1701Pro) single nucleotide variant DCDC5-related condition [RCV004758744]|not provided [RCV000891776] Chr11:30881290 [GRCh38]
Chr11:30902837 [GRCh37]
Chr11:11p14.1
benign
GRCh37/hg19 11p13(chr11:31326349-31415981)x3 copy number gain not provided [RCV000849970] Chr11:31326349..31415981 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p15.3-13(chr11:11053978-34732891)x3 copy number gain not provided [RCV001006387] Chr11:11053978..34732891 [GRCh37]
Chr11:11p15.3-13
pathogenic
NC_000011.9:g.(?_31284590)_(31832374_?)del deletion Aniridia 1 [RCV000801986] Chr11:31284590..31832374 [GRCh37]
Chr11:11p13
pathogenic
NM_001387274.1(DCDC1):c.4291G>A (p.Ala1431Thr) single nucleotide variant DCDC5-related condition [RCV004758746]|not provided [RCV000891778] Chr11:30904978 [GRCh38]
Chr11:30926525 [GRCh37]
Chr11:11p14.1
benign
GRCh37/hg19 11p14.3-13(chr11:22079154-35597645)x1 copy number loss not provided [RCV000849589] Chr11:22079154..35597645 [GRCh37]
Chr11:11p14.3-13
pathogenic
NM_001387274.1(DCDC1):c.4701G>C (p.Trp1567Cys) single nucleotide variant DCDC5-related condition [RCV004758748]|not provided [RCV000895310] Chr11:30899605 [GRCh38]
Chr11:30921152 [GRCh37]
Chr11:11p14.1
benign
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13
pathogenic
NM_001387274.1(DCDC1):c.247G>A (p.Val83Met) single nucleotide variant DCDC1-related disorder [RCV003973025]|Head and neck cancer [RCV001004028]|not provided [RCV002068801] Chr11:31307826 [GRCh38]
Chr11:31329373 [GRCh37]
Chr11:11p13
benign|uncertain significance
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3
pathogenic
NC_000011.9:g.(?_31284590)_(31824402_?)del deletion Aniridia 1 [RCV001385451] Chr11:31284590..31824402 [GRCh37]
Chr11:11p13
pathogenic
NM_001387274.1(DCDC1):c.600G>A (p.Glu200=) single nucleotide variant not provided [RCV001710343] Chr11:31305769 [GRCh38]
Chr11:31327316 [GRCh37]
Chr11:11p13
benign
NC_000011.9:g.(?_31284610)_(31828475_?)del deletion Aniridia 1 [RCV001959123] Chr11:31284610..31828475 [GRCh37]
Chr11:11p13
pathogenic
NM_001387274.1(DCDC1):c.474G>T (p.Arg158=) single nucleotide variant not provided [RCV001918549] Chr11:31306349 [GRCh38]
Chr11:31327896 [GRCh37]
Chr11:11p13
likely benign|uncertain significance
NM_001387274.1(DCDC1):c.591+13C>T single nucleotide variant not provided [RCV002096023] Chr11:31306219 [GRCh38]
Chr11:31327766 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.672C>G (p.Leu224=) single nucleotide variant not provided [RCV002179252] Chr11:31305697 [GRCh38]
Chr11:31327244 [GRCh37]
Chr11:11p13
benign
NC_000011.9:g.(?_30253450)_(32460464_?)del deletion not provided [RCV003113910] Chr11:30253450..32460464 [GRCh37]
Chr11:11p14.1-13
uncertain significance
NC_000011.9:g.(?_31284610)_(31671789_?)del deletion not provided [RCV003119949] Chr11:31284610..31671789 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p14.1-13(chr11:27547893-31656604)x1 copy number loss not provided [RCV002265529] Chr11:27547893..31656604 [GRCh37]
Chr11:11p14.1-13
not provided
GRCh37/hg19 11p13-12(chr11:31372721-38259316)x1 copy number loss not provided [RCV002472502] Chr11:31372721..38259316 [GRCh37]
Chr11:11p13-12
pathogenic
NM_001387274.1(DCDC1):c.205A>G (p.Thr69Ala) single nucleotide variant not specified [RCV004194944] Chr11:31307868 [GRCh38]
Chr11:31329415 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.592-18C>T single nucleotide variant not provided [RCV002685961] Chr11:31305795 [GRCh38]
Chr11:31327342 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.880T>C (p.Ser294Pro) single nucleotide variant not specified [RCV004137127] Chr11:31290727 [GRCh38]
Chr11:31312274 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.717G>A (p.Thr239=) single nucleotide variant not provided [RCV002907912] Chr11:31305652 [GRCh38]
Chr11:31327199 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.745A>C (p.Lys249Gln) single nucleotide variant not specified [RCV004107556] Chr11:31305624 [GRCh38]
Chr11:31327171 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.815A>T (p.Asp272Val) single nucleotide variant not specified [RCV004094656] Chr11:31290792 [GRCh38]
Chr11:31312339 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.534T>G (p.Ala178=) single nucleotide variant DCDC1-related disorder [RCV003963327]|not provided [RCV002695034] Chr11:31306289 [GRCh38]
Chr11:31327836 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.1001C>A (p.Pro334Gln) single nucleotide variant not specified [RCV004086229] Chr11:31265560 [GRCh38]
Chr11:31287107 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.949A>G (p.Thr317Ala) single nucleotide variant not provided [RCV003992736]|not specified [RCV004218119] Chr11:31290658 [GRCh38]
Chr11:31312205 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.262G>A (p.Val88Ile) single nucleotide variant not provided [RCV002705453] Chr11:31307811 [GRCh38]
Chr11:31329358 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.1030A>G (p.Arg344Gly) single nucleotide variant not specified [RCV004232641] Chr11:31265531 [GRCh38]
Chr11:31287078 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.716C>T (p.Thr239Met) single nucleotide variant not provided [RCV002890583]|not specified [RCV004065978] Chr11:31305653 [GRCh38]
Chr11:31327200 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.754+9G>T single nucleotide variant DCDC1-related disorder [RCV003961155]|not provided [RCV002900056] Chr11:31305606 [GRCh38]
Chr11:31327153 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.20A>G (p.Glu7Gly) single nucleotide variant DCDC1-related disorder [RCV003936299]|not provided [RCV002722021] Chr11:31328261 [GRCh38]
Chr11:31349808 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.961-9C>T single nucleotide variant not provided [RCV002587853] Chr11:31265609 [GRCh38]
Chr11:31287156 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.851T>C (p.Ile284Thr) single nucleotide variant not specified [RCV004271977] Chr11:31290756 [GRCh38]
Chr11:31312303 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.811A>G (p.Thr271Ala) single nucleotide variant not specified [RCV004261177] Chr11:31290796 [GRCh38]
Chr11:31312343 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p13(chr11:31260027-31639671)x1 copy number loss not provided [RCV003334142] Chr11:31260027..31639671 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.4687G>A (p.Glu1563Lys) single nucleotide variant DCDC5-related condition [RCV004731531]|not provided [RCV003394795] Chr11:30899619 [GRCh38]
Chr11:30921166 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.648C>G (p.Phe216Leu) single nucleotide variant not specified [RCV004359192] Chr11:31305721 [GRCh38]
Chr11:31327268 [GRCh37]
Chr11:11p13
uncertain significance
GRCh37/hg19 11p13(chr11:31296614-31466509)x1 copy number loss not provided [RCV003483119] Chr11:31296614..31466509 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.4090A>G (p.Ile1364Val) single nucleotide variant not provided [RCV003390031] Chr11:30906554 [GRCh38]
Chr11:30928101 [GRCh37]
Chr11:11p14.1
likely benign
NM_001387274.1(DCDC1):c.476A>G (p.Asn159Ser) single nucleotide variant not provided [RCV003561915] Chr11:31306347 [GRCh38]
Chr11:31327894 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.1054+2435A>G single nucleotide variant not provided [RCV003863968] Chr11:31263072 [GRCh38]
Chr11:31284619 [GRCh37]
Chr11:11p13
benign
GRCh37/hg19 11p13(chr11:31158395-31677662)x1 copy number loss not specified [RCV003986954] Chr11:31158395..31677662 [GRCh37]
Chr11:11p13
pathogenic
NM_001387274.1(DCDC1):c.1668del (p.Phe556fs) deletion DCDC1-related disorder [RCV003941387] Chr11:31106880 [GRCh38]
Chr11:31128427 [GRCh37]
Chr11:11p13
benign
GRCh37/hg19 11p13(chr11:31001762-31555701)x1 copy number loss not specified [RCV003986933] Chr11:31001762..31555701 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.960+13T>C single nucleotide variant not provided [RCV003565794] Chr11:31290634 [GRCh38]
Chr11:31312181 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.3989G>A (p.Arg1330Lys) single nucleotide variant not specified [RCV004373238] Chr11:30906655 [GRCh38]
Chr11:30928202 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.2946T>A (p.Asn982Lys) single nucleotide variant not specified [RCV004373245] Chr11:30925360 [GRCh38]
Chr11:30946907 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.2933G>A (p.Arg978Gln) single nucleotide variant not specified [RCV004373244] Chr11:30925373 [GRCh38]
Chr11:30946920 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.1015T>A (p.Tyr339Asn) single nucleotide variant not specified [RCV004373236] Chr11:31265546 [GRCh38]
Chr11:31287093 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.4379C>T (p.Thr1460Ile) single nucleotide variant not specified [RCV004373240] Chr11:30903613 [GRCh38]
Chr11:30925160 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.562G>T (p.Ala188Ser) single nucleotide variant not specified [RCV004373247] Chr11:31306261 [GRCh38]
Chr11:31327808 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.827G>A (p.Arg276Gln) single nucleotide variant not specified [RCV004373249] Chr11:31290780 [GRCh38]
Chr11:31312327 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.4115C>T (p.Ser1372Leu) single nucleotide variant not specified [RCV004373239] Chr11:30905154 [GRCh38]
Chr11:30926701 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.4822C>A (p.Gln1608Lys) single nucleotide variant not provided [RCV003993063] Chr11:30894328 [GRCh38]
Chr11:30915875 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.3410A>G (p.Glu1137Gly) single nucleotide variant not specified [RCV004373248] Chr11:30916912 [GRCh38]
Chr11:30938459 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.285A>T (p.Gln95His) single nucleotide variant not specified [RCV004373246] Chr11:31307788 [GRCh38]
Chr11:31329335 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.4736C>T (p.Thr1579Ile) single nucleotide variant not specified [RCV004373242] Chr11:30899570 [GRCh38]
Chr11:30921117 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.4447G>A (p.Glu1483Lys) single nucleotide variant not specified [RCV004373241] Chr11:30903545 [GRCh38]
Chr11:30925092 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.2797T>C (p.Tyr933His) single nucleotide variant not specified [RCV004373237] Chr11:30931871 [GRCh38]
Chr11:30953418 [GRCh37]
Chr11:11p14.1
uncertain significance
NM_001387274.1(DCDC1):c.844C>T (p.Leu282Phe) single nucleotide variant not specified [RCV004373250] Chr11:31290763 [GRCh38]
Chr11:31312310 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.1616A>G (p.Gln539Arg) single nucleotide variant DCDC1-related disorder [RCV003968910] Chr11:31106932 [GRCh38]
Chr11:31128479 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.961-10dup duplication DCDC1-related disorder [RCV003924186] Chr11:31265609..31265610 [GRCh38]
Chr11:31287156..31287157 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.2052A>G (p.Ala684=) single nucleotide variant DCDC1-related disorder [RCV003961654] Chr11:31094116 [GRCh38]
Chr11:31115663 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.164+3A>G single nucleotide variant DCDC1-related disorder [RCV003944704] Chr11:31328114 [GRCh38]
Chr11:31349661 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.2308C>G (p.Gln770Glu) single nucleotide variant DCDC1-related disorder [RCV003957179] Chr11:31065144 [GRCh38]
Chr11:31086691 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.1657A>G (p.Met553Val) single nucleotide variant DCDC1-related disorder [RCV003916909] Chr11:31106891 [GRCh38]
Chr11:31128438 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.2492C>A (p.Thr831Asn) single nucleotide variant DCDC1-related disorder [RCV003917023] Chr11:31064568 [GRCh38]
Chr11:31086115 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.1955A>G (p.Asp652Gly) single nucleotide variant DCDC1-related disorder [RCV003937189] Chr11:31102205 [GRCh38]
Chr11:31123752 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.1457C>T (p.Thr486Met) single nucleotide variant DCDC1-related disorder [RCV003937232] Chr11:31127497 [GRCh38]
Chr11:31149044 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.616C>T (p.Leu206=) single nucleotide variant DCDC1-related disorder [RCV003927019] Chr11:31305753 [GRCh38]
Chr11:31327300 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.2193T>C (p.Ala731=) single nucleotide variant DCDC1-related disorder [RCV003932057] Chr11:31091437 [GRCh38]
Chr11:31112984 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.1983+10T>C single nucleotide variant DCDC1-related disorder [RCV003932154] Chr11:31102167 [GRCh38]
Chr11:31123714 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.2653A>G (p.Asn885Asp) single nucleotide variant DCDC1-related disorder [RCV003926764] Chr11:30952507 [GRCh38]
Chr11:30974054 [GRCh37]
Chr11:11p14.1
likely benign
NM_001387274.1(DCDC1):c.2254T>G (p.Ser752Ala) single nucleotide variant DCDC1-related disorder [RCV003933854] Chr11:31077909 [GRCh38]
Chr11:31099456 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.2592G>T (p.Arg864Ser) single nucleotide variant DCDC1-related disorder [RCV003977269] Chr11:30952568 [GRCh38]
Chr11:30974115 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.3178C>T (p.Leu1060Phe) single nucleotide variant DCDC1-related disorder [RCV003929704] Chr11:30920891 [GRCh38]
Chr11:30942438 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.3718G>A (p.Glu1240Lys) single nucleotide variant DCDC5-related condition [RCV004759039] Chr11:30911356 [GRCh38]
Chr11:30932903 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.2716-10C>A single nucleotide variant DCDC5-related condition [RCV004759100] Chr11:30931962 [GRCh38]
Chr11:30953509 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.1421A>G (p.Tyr474Cys) single nucleotide variant DCDC1-related disorder [RCV003957078] Chr11:31127533 [GRCh38]
Chr11:31149080 [GRCh37]
Chr11:11p13
likely benign
NM_001387274.1(DCDC1):c.2887C>T (p.Arg963Trp) single nucleotide variant not specified [RCV004373243] Chr11:30931781 [GRCh38]
Chr11:30953328 [GRCh37]
Chr11:11p14.1
likely benign
NM_001387274.1(DCDC1):c.2298+8C>T single nucleotide variant DCDC1-related disorder [RCV003917356] Chr11:31077857 [GRCh38]
Chr11:31099404 [GRCh37]
Chr11:11p13
benign
NM_001387274.1(DCDC1):c.533C>T (p.Ala178Val) single nucleotide variant not specified [RCV004611380] Chr11:31306290 [GRCh38]
Chr11:31327837 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.826C>T (p.Arg276Trp) single nucleotide variant not specified [RCV004611379] Chr11:31290781 [GRCh38]
Chr11:31312328 [GRCh37]
Chr11:11p13
uncertain significance
NC_000011.9:g.(?_31349644)_(31832375_?)del deletion not provided [RCV004580379] Chr11:31349644..31832375 [GRCh37]
Chr11:11p13
uncertain significance
NC_000011.9:g.(?_31305244)_(31349768_?)del deletion not provided [RCV004580380] Chr11:31305244..31349768 [GRCh37]
Chr11:11p13
uncertain significance
NM_001387274.1(DCDC1):c.5097C>A (p.Cys1699Ter) single nucleotide variant Susceptibility to severe COVID-19 [RCV004598584] Chr11:30881294 [GRCh38]
Chr11:30902841 [GRCh37]
Chr11:11p14.1
likely pathogenic
NM_001387274.1(DCDC1):c.2867G>T (p.Gly956Val) single nucleotide variant DCDC5-related condition [RCV004759077] Chr11:30931801 [GRCh38]
Chr11:30953348 [GRCh37]
Chr11:11p14.1
likely benign
NM_001387274.1(DCDC1):c.2894C>T (p.Thr965Met) single nucleotide variant DCDC5-related condition [RCV004759221] Chr11:30931774 [GRCh38]
Chr11:30953321 [GRCh37]
Chr11:11p14.1
likely benign
NM_001387274.1(DCDC1):c.3036C>T (p.Asp1012=) single nucleotide variant DCDC5-related condition [RCV004759206] Chr11:30922600 [GRCh38]
Chr11:30944147 [GRCh37]
Chr11:11p14.1
likely benign
NM_001387274.1(DCDC1):c.3037C>T (p.Leu1013=) single nucleotide variant DCDC5-related condition [RCV004759085] Chr11:30922599 [GRCh38]
Chr11:30944146 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.5234-7_5234-6del deletion DCDC5-related condition [RCV004730684] Chr11:30878717..30878718 [GRCh38]
Chr11:30900264..30900265 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.4710G>A (p.Lys1570=) single nucleotide variant DCDC5-related condition [RCV004759097] Chr11:30899596 [GRCh38]
Chr11:30921143 [GRCh37]
Chr11:11p14.1
benign
NM_001387274.1(DCDC1):c.5233+7A>G single nucleotide variant DCDC5-related condition [RCV004759264] Chr11:30881151 [GRCh38]
Chr11:30902698 [GRCh37]
Chr11:11p14.1
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:18
Count of miRNA genes:6
Interacting mature miRNAs:6
Transcripts:ENST00000303697, ENST00000339794, ENST00000342355, ENST00000429306, ENST00000444572, ENST00000534021, ENST00000534722
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407312711GWAS961687_Hblood phosphate measurement QTL GWAS961687 (human)4e-09blood phosphate amount (VT:0001565)blood phosphate level (CMO:0000504)113092421030924211Human
1576345LVC1_HLeft ventricular contractility QTL 1 (human)3.93Left ventricular contractility11797076733970767Human
407369542GWAS1018518_Hmajor depressive disorder QTL GWAS1018518 (human)3e-10major depressive disorder113130275131302752Human
407392591GWAS1041567_Hthalamus volume QTL GWAS1041567 (human)7e-17thalamus volumeboth kidneys wet weight to body weight ratio (CMO:0000340)113120998731209988Human
407289167GWAS938143_Hcystatin C measurement QTL GWAS938143 (human)4e-11cystatin C measurementblood cystatin C level (CMO:0002777)113092421030924211Human
407010632GWAS659608_Hhemoglobin measurement QTL GWAS659608 (human)7e-20hemoglobin measurementhemoglobin measurement (CMO:0000508)113088189530881896Human
407020498GWAS669474_Hbone density QTL GWAS669474 (human)2e-09bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)113118922431189225Human
407285334GWAS934310_Hcreatinine measurement QTL GWAS934310 (human)2e-11creatinine measurementblood creatinine measurement (CMO:0000767)113126373731263738Human
407166293GWAS815269_Hunipolar depression QTL GWAS815269 (human)4e-10unipolar depression113095407930954080Human
406974290GWAS623266_Hseasonal gut microbiome measurement QTL GWAS623266 (human)0.000002seasonal gut microbiome measurement113087127730871278Human
406954457GWAS603433_Hhematocrit QTL GWAS603433 (human)2e-11hematocrithematocrit (CMO:0000037)113088189530881896Human
407244638GWAS893614_Haortic measurement QTL GWAS893614 (human)1e-08aortic measurementaorta measurement (CMO:0001474)113092361730923618Human
407087450GWAS736426_Hbone density QTL GWAS736426 (human)2e-08bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)113088944430889445Human
407288794GWAS937770_Hcreatinine measurement QTL GWAS937770 (human)1e-10creatinine measurementblood creatinine measurement (CMO:0000767)113092421030924211Human
407364315GWAS1013291_Hsystolic blood pressure QTL GWAS1013291 (human)0.0000007systolic blood pressuresystolic blood pressure (CMO:0000004)113109026331090264Human
407090527GWAS739503_Hosteoarthritis, knee QTL GWAS739503 (human)5e-08osteoarthritis, knee113118888631188887Human
407291738GWAS940714_Hglomerular filtration rate QTL GWAS940714 (human)4e-11glomerular filtration rateglomerular filtration rate (CMO:0000490)113126373731263738Human
407216601GWAS865577_Hunipolar depression QTL GWAS865577 (human)0.000009unipolar depression113135208231352083Human
407416168GWAS1065144_Hdiastolic blood pressure QTL GWAS1065144 (human)7e-10diastolic blood pressurediastolic blood pressure (CMO:0000005)113109026331090264Human
407346021GWAS994997_Hcortical thickness QTL GWAS994997 (human)7e-09cortical thickness113116855231168553Human
407326191GWAS975167_Htestosterone measurement QTL GWAS975167 (human)4e-08testosterone measurementserum testosterone level (CMO:0000568)113097636030976361Human
407315822GWAS964798_Hglomerular filtration rate QTL GWAS964798 (human)3e-10glomerular filtration rateglomerular filtration rate (CMO:0000490)113092421030924211Human
407141102GWAS790078_Heducational attainment QTL GWAS790078 (human)2e-10educational attainment113124604931246050Human
406982632GWAS631608_Hwhite matter microstructure measurement QTL GWAS631608 (human)5e-08white matter microstructure measurement113125041931250420Human
406967146GWAS616122_Hhemoglobin measurement QTL GWAS616122 (human)2e-10hemoglobin measurementhemoglobin measurement (CMO:0000508)113088189530881896Human
407318507GWAS967483_Hcystatin C measurement QTL GWAS967483 (human)6e-10cystatin C measurementblood cystatin C level (CMO:0002777)113098754130987542Human
407100270GWAS749246_Herythrocyte count QTL GWAS749246 (human)5e-15erythrocyte countred blood cell count (CMO:0000025)113110660531106606Human
406919406GWAS568382_Hcup-to-disc ratio measurement QTL GWAS568382 (human)3e-08cup-to-disc ratio measurement113091314430913145Human
406924657GWAS573633_Hdiastolic blood pressure, systolic blood pressure QTL GWAS573633 (human)1e-08diastolic blood pressure, systolic blood pressuresystolic blood pressure (CMO:0000004)113094552430945525Human
406943487GWAS592463_Hhemoglobin measurement QTL GWAS592463 (human)2e-08hemoglobin measurementhemoglobin measurement (CMO:0000508)113118922431189225Human
406924672GWAS573648_Hvisual cortical surface area measurement QTL GWAS573648 (human)2e-08visual cortical surface area measurement113098890830988909Human
407294979GWAS943955_Hdiastolic blood pressure QTL GWAS943955 (human)3e-11diastolic blood pressurediastolic blood pressure (CMO:0000005)113109026331090264Human
406913803GWAS562779_Hbreast density QTL GWAS562779 (human)0.000004breast density113090963830909639Human
407022472GWAS671448_Hcigarettes per day measurement QTL GWAS671448 (human)2e-14cigarettes per day measurement113121231031212311Human
407022473GWAS671449_Hcigarettes per day measurement QTL GWAS671449 (human)6e-16cigarettes per day measurement113132793631327937Human
407044622GWAS693598_Hbone density QTL GWAS693598 (human)2e-11bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)113093012730930128Human
407063181GWAS712157_Hheel bone mineral density QTL GWAS712157 (human)1e-11heel bone mineral densitybone mineral density (CMO:0001226)113094141730941418Human
406904080GWAS553056_Hunipolar depression QTL GWAS553056 (human)5e-10unipolar depression113087127730871278Human
406933905GWAS582881_Hoptic disc size measurement QTL GWAS582881 (human)4e-15optic disc size measurement113126373731263738Human
1559104SCL15_HSerum cholesterol level QTL 15 (human)2.60.06Lipid levelhyperlipidemia susceptibility111589236841892368Human
406900889GWAS549865_Hneuroimaging measurement QTL GWAS549865 (human)7e-13neuroimaging measurement113102239231022393Human
406997912GWAS646888_Hbiological sex QTL GWAS646888 (human)5e-12biological sex113108517831085179Human
407234086GWAS883062_Hbone density QTL GWAS883062 (human)4e-16bone mineral mass (VT:0005007)bone mineral density (CMO:0001226)113097622130976222Human
407294382GWAS943358_Hcigarettes per day measurement QTL GWAS943358 (human)3e-08cigarettes per day measurement113131387731313878Human
407241135GWAS890111_Hbrain measurement QTL GWAS890111 (human)4e-10brain measurementbrain measurement (CMO:0000911)113129433931294340Human
406928808GWAS577784_Hcigarettes per day measurement QTL GWAS577784 (human)1e-13cigarettes per day measurement113131387731313878Human
407201327GWAS850303_Hattention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement QTL GWAS850303 (human)6e-09attention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement113106296731062968Human
407288236GWAS937212_Hcystatin C measurement QTL GWAS937212 (human)3e-12cystatin C measurementblood cystatin C level (CMO:0002777)113126373731263738Human
407080239GWAS729215_Hsodium measurement QTL GWAS729215 (human)3e-12sodium measurementblood sodium level (CMO:0000499)113128988231289883Human
407361450GWAS1010426_Hinsomnia QTL GWAS1010426 (human)2e-09insomnia113111695231116953Human
407361449GWAS1010425_Hinsomnia QTL GWAS1010425 (human)1e-08insomnia113097922730979228Human
406983085GWAS632061_Hunipolar depression QTL GWAS632061 (human)4e-15unipolar depression113087127730871278Human
406943408GWAS592384_Hhemoglobin measurement QTL GWAS592384 (human)6e-11hemoglobin measurementhemoglobin measurement (CMO:0000508)113088134630881347Human
406983984GWAS632960_Hbrain measurement, neuroimaging measurement QTL GWAS632960 (human)2e-09brain measurement, neuroimaging measurementbrain measurement (CMO:0000911)113106884331068844Human
406919348GWAS568324_Hdiastolic blood pressure, systolic blood pressure QTL GWAS568324 (human)1e-08diastolic blood pressure, systolic blood pressuresystolic blood pressure (CMO:0000004)113089694030896941Human
406923319GWAS572295_Hsmoking initiation QTL GWAS572295 (human)1e-14smoking initiation113104656331046564Human
407047487GWAS696463_Hplasma betaine measurement QTL GWAS696463 (human)0.000008plasma betaine measurement113102713631027137Human

Markers in Region
D11S914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371131,363,290 - 31,363,565UniSTSGRCh37
GRCh371131,363,289 - 31,363,550UniSTSGRCh37
Build 361131,319,865 - 31,320,126RGDNCBI36
Celera1131,510,720 - 31,510,983RGD
Celera1131,510,721 - 31,510,998UniSTS
Cytogenetic Map11p13UniSTS
HuRef1131,056,624 - 31,056,887UniSTS
HuRef1131,056,625 - 31,056,902UniSTS
Marshfield Genetic Map1137.62RGD
Genethon Genetic Map1142.0UniSTS
TNG Radiation Hybrid Map1114844.0UniSTS
deCODE Assembly Map1147.08UniSTS
Stanford-G3 RH Map111450.0UniSTS
GeneMap99-GB4 RH Map11120.2UniSTS
Whitehead-RH Map11109.5UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map11184.2UniSTS
GeneMap99-G3 RH Map111450.0UniSTS
D11S2001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371131,362,903 - 31,363,043UniSTSGRCh37
Build 361131,319,479 - 31,319,619RGDNCBI36
Celera1131,510,334 - 31,510,474RGD
Cytogenetic Map11p13UniSTS
HuRef1131,056,242 - 31,056,378UniSTS
Marshfield Genetic Map1137.62UniSTS
Marshfield Genetic Map1137.62RGD
TNG Radiation Hybrid Map1114815.0UniSTS
deCODE Assembly Map1147.08UniSTS
Stanford-G3 RH Map111460.0UniSTS
Whitehead-RH Map11106.9UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map11184.2UniSTS
STS-AA017167  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371131,303,085 - 31,303,354UniSTSGRCh37
Build 361131,259,661 - 31,259,930RGDNCBI36
Celera1131,450,514 - 31,450,783RGD
Cytogenetic Map11p13UniSTS
HuRef1130,996,422 - 30,996,691UniSTS
GeneMap99-GB4 RH Map11120.2UniSTS
SHGC-32530  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371131,303,027 - 31,303,132UniSTSGRCh37
Build 361131,259,603 - 31,259,708RGDNCBI36
Celera1131,450,456 - 31,450,561RGD
Cytogenetic Map11p13UniSTS
HuRef1130,996,364 - 30,996,469UniSTS
Stanford-G3 RH Map111470.0UniSTS
Whitehead-RH Map11109.4UniSTS
NCBI RH Map11184.2UniSTS
GeneMap99-G3 RH Map111470.0UniSTS
D11S2369  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371131,362,814 - 31,363,043UniSTSGRCh37
Build 361131,319,390 - 31,319,619RGDNCBI36
Celera1131,510,245 - 31,510,474RGD
Cytogenetic Map11p13UniSTS
HuRef1131,056,153 - 31,056,378UniSTS
AU046597  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X137,595,264 - 137,596,506UniSTSGRCh37
GRCh371131,306,651 - 31,307,230UniSTSGRCh37
CeleraX137,961,245 - 137,962,487UniSTS
Celera1131,454,079 - 31,454,658UniSTS
HuRef1130,999,989 - 31,000,568UniSTS
HuRefX126,862,225 - 126,863,467UniSTS
D11S914  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map11p13UniSTS
Marshfield Genetic Map1137.62UniSTS
Genethon Genetic Map1142.0UniSTS
deCODE Assembly Map1147.08UniSTS
GeneMap99-GB4 RH Map11120.2UniSTS
Whitehead-RH Map11109.5UniSTS
Whitehead-YAC Contig Map11 UniSTS
NCBI RH Map11213.4UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
1137 2106 2355 1992 4845 1671 2205 1 570 774 418 2154 5278 4952 43 3682 789 1667 1527 164

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001367979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_020869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_181807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448476 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448477 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448478 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448479 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448481 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448482 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448483 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448485 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448488 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024448489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426876 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368639 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368641 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368642 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368645 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368647 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368649 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368651 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054368653 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002957144 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_002957145 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA846321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AA954541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB040926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126066 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK128035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL133349 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL133376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL135932 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL137160 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL137804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW340116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY247970 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX097338 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX116244 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX117620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647348 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CV569749 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CV574283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB090201 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB528022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF455358 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000303697   ⟹   ENSP00000306898
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,863,603 - 30,906,705 (-)Ensembl
Ensembl Acc Id: ENST00000342355   ⟹   ENSP00000343496
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,943,202 - 31,369,810 (-)Ensembl
Ensembl Acc Id: ENST00000406071   ⟹   ENSP00000385936
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,863,604 - 30,992,686 (-)Ensembl
Ensembl Acc Id: ENST00000429306
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,906,315 - 30,909,104 (-)Ensembl
Ensembl Acc Id: ENST00000437348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,931,771 - 31,127,665 (-)Ensembl
Ensembl Acc Id: ENST00000444572   ⟹   ENSP00000404672
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,830,369 - 30,925,408 (-)Ensembl
Ensembl Acc Id: ENST00000452803   ⟹   ENSP00000389792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1131,262,624 - 31,369,774 (-)Ensembl
Ensembl Acc Id: ENST00000483396
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,864,942 - 30,992,684 (-)Ensembl
Ensembl Acc Id: ENST00000534021
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1131,155,903 - 31,241,616 (-)Ensembl
Ensembl Acc Id: ENST00000534722
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1131,106,894 - 31,241,758 (-)Ensembl
Ensembl Acc Id: ENST00000597505   ⟹   ENSP00000472625
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,878,584 - 31,328,280 (-)Ensembl
Ensembl Acc Id: ENST00000684477   ⟹   ENSP00000507427
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1130,863,603 - 31,369,739 (-)Ensembl
RefSeq Acc Id: NM_001367979   ⟹   NP_001354908
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,369,739 (-)NCBI
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001387274   ⟹   NP_001374203
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,369,739 (-)NCBI
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001387275   ⟹   NP_001374204
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 30,992,525 (-)NCBI
T2T-CHM13v2.01130,997,893 - 31,128,615 (-)NCBI
Sequence:
RefSeq Acc Id: NM_020869   ⟹   NP_065920
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 30,992,525 (-)NCBI
CHM1_11130,884,126 - 31,013,345 (-)NCBI
T2T-CHM13v2.01130,997,893 - 31,128,615 (-)NCBI
Sequence:
RefSeq Acc Id: NM_181807   ⟹   NP_861523
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,262,626 - 31,369,739 (-)NCBI
GRCh371131,284,171 - 31,391,357 (-)ENTREZGENE
Build 361131,240,747 - 31,347,897 (-)NCBI Archive
Celera1131,431,602 - 31,538,744 (-)RGD
HuRef1130,977,492 - 31,085,706 (-)ENTREZGENE
CHM1_11131,283,686 - 31,390,898 (-)NCBI
T2T-CHM13v2.01131,398,475 - 31,505,576 (-)NCBI
Sequence:
RefSeq Acc Id: NR_170625
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,942,208 - 31,369,739 (-)NCBI
T2T-CHM13v2.01131,078,295 - 31,505,576 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448471   ⟹   XP_024304239
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,343,052 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448472   ⟹   XP_024304240
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,865,348 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448473   ⟹   XP_024304241
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448475   ⟹   XP_024304243
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448476   ⟹   XP_024304244
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448477   ⟹   XP_024304245
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448478   ⟹   XP_024304246
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448480   ⟹   XP_024304248
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,305,699 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448481   ⟹   XP_024304249
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,863,603 - 31,305,697 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448482   ⟹   XP_024304250
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,912,732 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448483   ⟹   XP_024304251
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,942,208 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448484   ⟹   XP_024304252
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,931,809 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448485   ⟹   XP_024304253
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,041,787 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448486   ⟹   XP_024304254
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,102,200 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448487   ⟹   XP_024304255
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,103,650 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448488   ⟹   XP_024304256
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,118,491 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024448489   ⟹   XP_024304257
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,135,289 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047426876   ⟹   XP_047282832
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381130,878,543 - 31,369,739 (-)NCBI
RefSeq Acc Id: XM_054368632   ⟹   XP_054224607
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368633   ⟹   XP_054224608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,012,832 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368634   ⟹   XP_054224609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,999,639 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368635   ⟹   XP_054224610
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,478,888 (-)NCBI
RefSeq Acc Id: XM_054368636   ⟹   XP_054224611
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368637   ⟹   XP_054224612
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368638   ⟹   XP_054224613
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368639   ⟹   XP_054224614
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368640   ⟹   XP_054224615
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368641   ⟹   XP_054224616
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368642   ⟹   XP_054224617
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368643   ⟹   XP_054224618
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,441,529 (-)NCBI
RefSeq Acc Id: XM_054368644   ⟹   XP_054224619
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,441,529 (-)NCBI
RefSeq Acc Id: XM_054368645   ⟹   XP_054224620
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01130,997,893 - 31,441,527 (-)NCBI
RefSeq Acc Id: XM_054368646   ⟹   XP_054224621
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,047,025 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368647   ⟹   XP_054224622
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,074,289 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368648   ⟹   XP_054224623
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,067,904 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368649   ⟹   XP_054224624
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,177,879 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368650   ⟹   XP_054224625
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,238,292 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368651   ⟹   XP_054224626
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,239,742 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368652   ⟹   XP_054224627
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,254,586 - 31,505,576 (-)NCBI
RefSeq Acc Id: XM_054368653   ⟹   XP_054224628
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,271,070 - 31,505,576 (-)NCBI
RefSeq Acc Id: XR_002957144
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,041,783 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XR_002957145
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381131,110,280 - 31,369,739 (-)NCBI
Sequence:
RefSeq Acc Id: XR_008488391
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,177,875 - 31,505,576 (-)NCBI
RefSeq Acc Id: XR_008488392
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01131,246,370 - 31,505,576 (-)NCBI
Protein Sequences
Protein RefSeqs NP_001354908 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374203 (Get FASTA)   NCBI Sequence Viewer  
  NP_001374204 (Get FASTA)   NCBI Sequence Viewer  
  NP_065920 (Get FASTA)   NCBI Sequence Viewer  
  NP_861523 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304239 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304240 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304241 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304243 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304244 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304245 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304246 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304248 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304249 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304250 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304251 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304252 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304253 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304254 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304255 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304256 (Get FASTA)   NCBI Sequence Viewer  
  XP_024304257 (Get FASTA)   NCBI Sequence Viewer  
  XP_047282832 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224607 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224608 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224609 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224610 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224611 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224612 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224613 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224614 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224615 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224616 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224617 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224618 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224619 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224620 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224621 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224622 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224623 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224624 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224625 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224626 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224627 (Get FASTA)   NCBI Sequence Viewer  
  XP_054224628 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAP75563 (Get FASTA)   NCBI Sequence Viewer  
  BAA96017 (Get FASTA)   NCBI Sequence Viewer  
  BAC86423 (Get FASTA)   NCBI Sequence Viewer  
  BAC87240 (Get FASTA)   NCBI Sequence Viewer  
  EAW68248 (Get FASTA)   NCBI Sequence Viewer  
  EAW68252 (Get FASTA)   NCBI Sequence Viewer  
  EAW68253 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000306898.4
  ENSP00000343496.4
  ENSP00000385936
  ENSP00000385936.3
  ENSP00000389792
  ENSP00000389792.1
  ENSP00000404672.2
  ENSP00000472625
  ENSP00000472625.1
  ENSP00000507427
  ENSP00000507427.1
GenBank Protein M0R2J8 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_861523   ⟸   NM_181807
- Peptide Label: isoform 2
- UniProtKB: P59894 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_065920   ⟸   NM_020869
- Peptide Label: isoform 3
- UniProtKB: B6ZDN3 (UniProtKB/TrEMBL),   H7C298 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304246   ⟸   XM_024448478
- Peptide Label: isoform X12
- Sequence:
RefSeq Acc Id: XP_024304244   ⟸   XM_024448476
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: XP_024304243   ⟸   XM_024448475
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_024304245   ⟸   XM_024448477
- Peptide Label: isoform X11
- Sequence:
RefSeq Acc Id: XP_024304241   ⟸   XM_024448473
- Peptide Label: isoform X8
- UniProtKB: A0A804HJA9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304239   ⟸   XM_024448471
- Peptide Label: isoform X8
- UniProtKB: A0A804HJA9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304248   ⟸   XM_024448480
- Peptide Label: isoform X13
- Sequence:
RefSeq Acc Id: XP_024304249   ⟸   XM_024448481
- Peptide Label: isoform X14
- Sequence:
RefSeq Acc Id: XP_024304240   ⟸   XM_024448472
- Peptide Label: isoform X8
- UniProtKB: A0A804HJA9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_024304250   ⟸   XM_024448482
- Peptide Label: isoform X15
- Sequence:
RefSeq Acc Id: XP_024304252   ⟸   XM_024448484
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_024304251   ⟸   XM_024448483
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024304253   ⟸   XM_024448485
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_024304254   ⟸   XM_024448486
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_024304255   ⟸   XM_024448487
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_024304256   ⟸   XM_024448488
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_024304257   ⟸   XM_024448489
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: NP_001354908   ⟸   NM_001367979
- Peptide Label: isoform 4
- UniProtKB: Q6ZU04 (UniProtKB/Swiss-Prot),   Q6ZRR9 (UniProtKB/Swiss-Prot),   P59894 (UniProtKB/Swiss-Prot),   M0R2J8 (UniProtKB/Swiss-Prot),   B7WNX6 (UniProtKB/Swiss-Prot),   B1AL47 (UniProtKB/Swiss-Prot),   A6PVL6 (UniProtKB/Swiss-Prot)
Ensembl Acc Id: ENSP00000472625   ⟸   ENST00000597505
Ensembl Acc Id: ENSP00000389792   ⟸   ENST00000452803
Ensembl Acc Id: ENSP00000404672   ⟸   ENST00000444572
Ensembl Acc Id: ENSP00000385936   ⟸   ENST00000406071
Ensembl Acc Id: ENSP00000343496   ⟸   ENST00000342355
Ensembl Acc Id: ENSP00000306898   ⟸   ENST00000303697
RefSeq Acc Id: NP_001374203   ⟸   NM_001387274
- Peptide Label: isoform 6
- UniProtKB: A0A804HJA9 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374204   ⟸   NM_001387275
- Peptide Label: isoform 7
- UniProtKB: H7C298 (UniProtKB/TrEMBL)
Ensembl Acc Id: ENSP00000507427   ⟸   ENST00000684477
RefSeq Acc Id: XP_047282832   ⟸   XM_047426876
- Peptide Label: isoform X8
- UniProtKB: A0A804HJA9 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054224617   ⟸   XM_054368642
- Peptide Label: isoform X22
RefSeq Acc Id: XP_054224615   ⟸   XM_054368640
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054224612   ⟸   XM_054368637
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054224614   ⟸   XM_054368639
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054224616   ⟸   XM_054368641
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054224613   ⟸   XM_054368638
- Peptide Label: isoform X18
RefSeq Acc Id: XP_054224607   ⟸   XM_054368632
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054224611   ⟸   XM_054368636
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054224610   ⟸   XM_054368635
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054224619   ⟸   XM_054368644
- Peptide Label: isoform X24
RefSeq Acc Id: XP_054224618   ⟸   XM_054368643
- Peptide Label: isoform X23
RefSeq Acc Id: XP_054224620   ⟸   XM_054368645
- Peptide Label: isoform X25
RefSeq Acc Id: XP_054224609   ⟸   XM_054368634
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054224608   ⟸   XM_054368633
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054224621   ⟸   XM_054368646
- Peptide Label: isoform X26
RefSeq Acc Id: XP_054224623   ⟸   XM_054368648
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054224622   ⟸   XM_054368647
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054224624   ⟸   XM_054368649
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054224625   ⟸   XM_054368650
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054224626   ⟸   XM_054368651
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054224627   ⟸   XM_054368652
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054224628   ⟸   XM_054368653
- Peptide Label: isoform X7
Protein Domains
Doublecortin   Ricin B-type lectin

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-M0R2J8-F1-model_v2 AlphaFold M0R2J8 1-1783 view protein structure

Promoters
RGD ID:6788730
Promoter ID:HG_KWN:12556
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:ENST00000342355,   ENST00000354034,   ENST00000399333,   NM_181706,   UC001MSW.1,   UC009YJM.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361131,347,796 - 31,348,296 (+)MPROMDB
RGD ID:7219923
Promoter ID:EPDNEW_H15707
Type:initiation region
Name:DCDC1_1
Description:doublecortin domain containing 1
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
GRCh381131,369,739 - 31,369,799EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20625 AgrOrtholog
COSMIC DCDC1 COSMIC
Ensembl Genes ENSG00000170959 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000303697.8 UniProtKB/TrEMBL
  ENST00000342355.8 UniProtKB/Swiss-Prot
  ENST00000406071 ENTREZGENE
  ENST00000406071.6 UniProtKB/TrEMBL
  ENST00000444572.6 UniProtKB/TrEMBL
  ENST00000452803 ENTREZGENE
  ENST00000452803.1 UniProtKB/Swiss-Prot
  ENST00000597505 ENTREZGENE
  ENST00000597505.5 UniProtKB/Swiss-Prot
  ENST00000684477 ENTREZGENE
  ENST00000684477.1 UniProtKB/TrEMBL
Gene3D-CATH 2.80.10.50 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  3.10.20.230 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000170959 GTEx
HGNC ID HGNC:20625 ENTREZGENE
Human Proteome Map DCDC1 Human Proteome Map
InterPro DCDC1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Doublecortin_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Doublecortin_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ricin_B-like_lectins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ricin_B_lectin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:341019 UniProtKB/Swiss-Prot
NCBI Gene DCDC1 ENTREZGENE
OMIM 608062 OMIM
PANTHER DOUBLECORTIN DOMAIN-CONTAINING PROTEIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  DOUBLECORTIN DOMAIN-CONTAINING PROTEIN 1 UniProtKB/TrEMBL
  PTHR46302 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134970075 PharmGKB
PROSITE PS50309 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RICIN_B_LECTIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART DCX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50370 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF89837 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A804HJA9 ENTREZGENE, UniProtKB/TrEMBL
  A6PVL6 ENTREZGENE
  B1AL47 ENTREZGENE
  B6ZDN3 ENTREZGENE, UniProtKB/TrEMBL
  B7WNX6 ENTREZGENE
  DCDC1_HUMAN UniProtKB/Swiss-Prot
  H0Y2Q8_HUMAN UniProtKB/TrEMBL
  H7C298 ENTREZGENE, UniProtKB/TrEMBL
  M0R2J8 ENTREZGENE
  P59894 ENTREZGENE
  Q6ZRR9 ENTREZGENE
  Q6ZU04 ENTREZGENE
UniProt Secondary A6PVL6 UniProtKB/Swiss-Prot
  B1AL47 UniProtKB/Swiss-Prot
  B7WNX6 UniProtKB/Swiss-Prot
  P59894 UniProtKB/Swiss-Prot
  Q6ZRR9 UniProtKB/Swiss-Prot
  Q6ZU04 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-11-21 DCDC1  doublecortin domain containing 1  DCDC5  doublecortin domain containing 5  Data merged from RGD:1603545 737654 PROVISIONAL
2011-07-27 DCDC5  doublecortin domain containing 5  DCDC5  doublecortin domain containing 5  Symbol and/or name change 5135510 APPROVED