CWC25 (CWC25 spliceosome associated protein homolog) - Rat Genome Database

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Gene: CWC25 (CWC25 spliceosome associated protein homolog) Homo sapiens
Analyze
Symbol: CWC25
Name: CWC25 spliceosome associated protein homolog
RGD ID: 1603211
HGNC Page HGNC:25989
Description: Involved in mRNA splicing, via spliceosome. Located in nuclear speck. Part of U2-type catalytic step 1 spliceosome.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: CCDC49; coiled-coil domain containing 49; coiled-coil domain-containing protein 49; CWC25 spliceosome-associated protein homolog; DKFZp779M0968; FLJ20291; pre-mRNA-splicing factor CWC25 homolog; spliceosome-associated protein homolog CWC25
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
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
GRCh381738,800,441 - 38,825,321 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1738,800,441 - 38,825,355 (-)EnsemblGRCh38hg38GRCh38
GRCh371736,956,694 - 36,981,574 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361734,210,972 - 34,235,115 (-)NCBINCBI36Build 36hg18NCBI36
Celera1733,618,412 - 33,642,555 (-)NCBICelera
Cytogenetic Map17q12NCBI
HuRef1732,752,758 - 32,776,922 (-)NCBIHuRef
CHM1_11737,191,993 - 37,216,912 (-)NCBICHM1_1
T2T-CHM13v2.01739,663,526 - 39,688,404 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8125298   PMID:12477932   PMID:16189514   PMID:19941820   PMID:20195357   PMID:21145461   PMID:21873635   PMID:21988832   PMID:24981860   PMID:26496610   PMID:27173435   PMID:29301961  
PMID:29395067   PMID:30021884   PMID:31586073   PMID:31980649   PMID:32296183   PMID:32994395   PMID:33536335   PMID:33961781   PMID:34079125   PMID:34672954   PMID:34732716   PMID:35013218  
PMID:35337019   PMID:35384245   PMID:35944360   PMID:36244648   PMID:36373674   PMID:38113892  


Genomics

Comparative Map Data
CWC25
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381738,800,441 - 38,825,321 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1738,800,441 - 38,825,355 (-)EnsemblGRCh38hg38GRCh38
GRCh371736,956,694 - 36,981,574 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361734,210,972 - 34,235,115 (-)NCBINCBI36Build 36hg18NCBI36
Celera1733,618,412 - 33,642,555 (-)NCBICelera
Cytogenetic Map17q12NCBI
HuRef1732,752,758 - 32,776,922 (-)NCBIHuRef
CHM1_11737,191,993 - 37,216,912 (-)NCBICHM1_1
T2T-CHM13v2.01739,663,526 - 39,688,404 (-)NCBIT2T-CHM13v2.0
Cwc25
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391197,636,296 - 97,657,439 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1197,636,307 - 97,657,382 (-)EnsemblGRCm39 Ensembl
GRCm381197,745,470 - 97,766,613 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1197,745,481 - 97,766,556 (-)EnsemblGRCm38mm10GRCm38
MGSCv371197,606,784 - 97,627,927 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361197,561,705 - 97,582,646 (-)NCBIMGSCv36mm8
Celera11107,395,235 - 107,416,163 (-)NCBICelera
Cytogenetic Map11DNCBI
cM Map1161.09NCBI
Cwc25
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81083,232,052 - 83,256,722 (-)NCBIGRCr8
mRatBN7.21082,735,698 - 82,760,373 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1082,736,995 - 82,760,354 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1087,683,936 - 87,708,652 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01087,182,022 - 87,206,740 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01082,574,601 - 82,599,319 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01085,684,898 - 85,709,568 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1085,684,898 - 85,709,568 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01085,475,897 - 85,499,557 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41086,491,167 - 86,515,834 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11086,507,374 - 86,537,704 (-)NCBI
Celera1081,491,290 - 81,515,794 (-)NCBICelera
Cytogenetic Map10q31NCBI
Cwc25
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545113,868,845 - 13,884,267 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495545113,867,570 - 13,884,433 (-)NCBIChiLan1.0ChiLan1.0
CWC25
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21926,122,697 - 26,147,986 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11728,006,272 - 28,031,553 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01718,446,107 - 18,471,059 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11718,719,907 - 18,745,213 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1718,719,907 - 18,745,213 (+)Ensemblpanpan1.1panPan2
CWC25
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1923,426,005 - 23,443,512 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl923,426,038 - 23,443,040 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha922,897,724 - 22,915,507 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0924,221,176 - 24,238,855 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl924,221,297 - 24,239,757 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1922,993,244 - 23,010,863 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0923,254,139 - 23,271,927 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0923,380,031 - 23,397,696 (+)NCBIUU_Cfam_GSD_1.0
Cwc25
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560222,848,443 - 22,871,673 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493649014,202,679 - 14,226,704 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493649014,201,851 - 14,226,724 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CWC25
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1223,298,065 - 23,316,238 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11223,298,050 - 23,315,445 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
CWC25
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11667,357,118 - 67,389,809 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1667,357,125 - 67,391,550 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366607738,358,971 - 38,387,272 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Cwc25
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247953,890,848 - 3,905,960 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247953,891,607 - 3,907,160 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CWC25
26 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2		 pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3		 pathogenic
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
NM_017748.5(CWC25):c.707G>A (p.Arg236His) single nucleotide variant not specified [RCV004333733] Chr17:38806960 [GRCh38]
Chr17:36963213 [GRCh37]
Chr17:17q12		 likely benign
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q12(chr17:36972794-38033708)x4 copy number gain not provided [RCV000683933] Chr17:36972794..38033708 [GRCh37]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17p11.2-q21.2(chr17:21690653-38772647)x3 copy number gain not provided [RCV000846852] Chr17:21690653..38772647 [GRCh37]
Chr17:17p11.2-q21.2		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17q12(chr17:36906480-36996181)x3 copy number gain not provided [RCV000739507] Chr17:36906480..36996181 [GRCh37]
Chr17:17q12		 benign
NM_017748.5(CWC25):c.1166G>C (p.Arg389Pro) single nucleotide variant not specified [RCV004309840] Chr17:38802204 [GRCh38]
Chr17:36958457 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.248G>A (p.Arg83His) single nucleotide variant not specified [RCV004286543] Chr17:38815041 [GRCh38]
Chr17:36971294 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.401T>C (p.Ile134Thr) single nucleotide variant not specified [RCV004305566] Chr17:38814888 [GRCh38]
Chr17:36971141 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.1002A>G (p.Arg334=) single nucleotide variant not specified [RCV004317893] Chr17:38802861 [GRCh38]
Chr17:36959114 [GRCh37]
Chr17:17q12		 likely benign
GRCh37/hg19 17q12(chr17:36710984-37295662)x3 copy number gain not provided [RCV001006899] Chr17:36710984..37295662 [GRCh37]
Chr17:17q12		 uncertain significance
NC_000017.10:g.(?_36891476)_(37009963_?)dup duplication not provided [RCV003109613] Chr17:36891476..37009963 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.187G>A (p.Val63Ile) single nucleotide variant not specified [RCV004245702] Chr17:38820905 [GRCh38]
Chr17:36977158 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.404G>A (p.Arg135Gln) single nucleotide variant not specified [RCV004149229] Chr17:38814885 [GRCh38]
Chr17:36971138 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.991G>A (p.Gly331Arg) single nucleotide variant not specified [RCV004211559] Chr17:38806307 [GRCh38]
Chr17:36962560 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.371C>G (p.Ala124Gly) single nucleotide variant not specified [RCV004242125] Chr17:38814918 [GRCh38]
Chr17:36971171 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.1028G>A (p.Arg343Gln) single nucleotide variant not specified [RCV004238808] Chr17:38802835 [GRCh38]
Chr17:36959088 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.452G>A (p.Arg151Gln) single nucleotide variant not specified [RCV004093329] Chr17:38812841 [GRCh38]
Chr17:36969094 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.899A>C (p.Lys300Thr) single nucleotide variant not specified [RCV004116904] Chr17:38806768 [GRCh38]
Chr17:36963021 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.800C>T (p.Pro267Leu) single nucleotide variant not specified [RCV004238175] Chr17:38806867 [GRCh38]
Chr17:36963120 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.1115G>A (p.Arg372Gln) single nucleotide variant not specified [RCV004101328] Chr17:38802748 [GRCh38]
Chr17:36959001 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.682G>A (p.Gly228Ser) single nucleotide variant not specified [RCV004169335] Chr17:38809710 [GRCh38]
Chr17:36965963 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.374A>G (p.Asn125Ser) single nucleotide variant not specified [RCV004072998] Chr17:38814915 [GRCh38]
Chr17:36971168 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.1099G>T (p.Ala367Ser) single nucleotide variant not specified [RCV004175505] Chr17:38802764 [GRCh38]
Chr17:36959017 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.403C>T (p.Arg135Trp) single nucleotide variant not specified [RCV004220587] Chr17:38814886 [GRCh38]
Chr17:36971139 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.733A>G (p.Thr245Ala) single nucleotide variant not specified [RCV004096667] Chr17:38806934 [GRCh38]
Chr17:36963187 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.503A>T (p.Gln168Leu) single nucleotide variant not specified [RCV004257765] Chr17:38810591 [GRCh38]
Chr17:36966844 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.1033C>T (p.Arg345Trp) single nucleotide variant not specified [RCV004249520] Chr17:38802830 [GRCh38]
Chr17:36959083 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.603C>G (p.Ser201Arg) single nucleotide variant not specified [RCV004353631] Chr17:38810491 [GRCh38]
Chr17:36966744 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.143G>A (p.Arg48Lys) single nucleotide variant not specified [RCV004357093] Chr17:38820949 [GRCh38]
Chr17:36977202 [GRCh37]
Chr17:17q12		 uncertain significance
GRCh37/hg19 17q12(chr17:36836115-37099066)x3 copy number gain not provided [RCV003485156] Chr17:36836115..37099066 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.997A>T (p.Thr333Ser) single nucleotide variant not specified [RCV004367499] Chr17:38806301 [GRCh38]
Chr17:36962554 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.221A>T (p.Tyr74Phe) single nucleotide variant not specified [RCV004367495] Chr17:38815068 [GRCh38]
Chr17:36971321 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.604G>A (p.Glu202Lys) single nucleotide variant not specified [RCV004367497] Chr17:38810490 [GRCh38]
Chr17:36966743 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.383T>C (p.Leu128Pro) single nucleotide variant not specified [RCV004367496] Chr17:38814906 [GRCh38]
Chr17:36971159 [GRCh37]
Chr17:17q12		 uncertain significance
NM_017748.5(CWC25):c.691G>T (p.Val231Phe) single nucleotide variant not specified [RCV004367498] Chr17:38806976 [GRCh38]
Chr17:36963229 [GRCh37]
Chr17:17q12		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2926
Count of miRNA genes:867
Interacting mature miRNAs:1038
Transcripts:ENST00000225428, ENST00000536127, ENST00000578906, ENST00000581092, ENST00000582713, ENST00000583435, ENST00000584007, ENST00000585298
Prediction methods:Miranda, Pita, 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.

Markers in Region
RH76647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371736,957,780 - 36,958,011UniSTSGRCh37
Build 361734,211,306 - 34,211,537RGDNCBI36
Celera1733,618,746 - 33,618,977RGD
Cytogenetic Map17q12UniSTS
HuRef1732,753,851 - 32,754,082UniSTS
RH94016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371736,957,472 - 36,957,627UniSTSGRCh37
Build 361734,210,998 - 34,211,153RGDNCBI36
Celera1733,618,438 - 33,618,593RGD
Cytogenetic Map17q12UniSTS
HuRef1732,753,543 - 32,753,698UniSTS
GeneMap99-GB4 RH Map17305.08UniSTS
RH45659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371736,956,822 - 36,956,971UniSTSGRCh37
Build 361734,210,348 - 34,210,497RGDNCBI36
Celera1733,617,787 - 33,617,936RGD
Cytogenetic Map17q12UniSTS
HuRef1732,752,893 - 32,753,042UniSTS
GeneMap99-GB4 RH Map17306.73UniSTS
D8S2278  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map3p25.3-p24.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map10q11UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map12q21.31UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic MapXp22.1UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map10q22UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map6p21.33UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map4q34.1UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map6q25UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map6p22UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map8q24UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic MapYp11.3UniSTS
Cytogenetic Map2p23.1UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map12p12.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map15q22.1UniSTS
Cytogenetic Map1p34-p33UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map3q25.31UniSTS
Cytogenetic Map14q22UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map12p13.3UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map3q26.32UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map13q11UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map14q12-q13UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map17q11.2-q12UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map4q31UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map15q15-q21.1UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map4q22.1-q23UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map17q22-q23.2UniSTS
Cytogenetic Map3q21UniSTS
Cytogenetic Map18q22.3UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic MapXq26.1UniSTS
Cytogenetic Map4q21.21UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic MapXq22.3UniSTS
Cytogenetic Map3q13.13UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map10p11.23UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map13q33.1UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map1q31-q41UniSTS
Cytogenetic Map2p16.1UniSTS
Cytogenetic Map14q23UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map11q12.2UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map9p21UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map3p12.1UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map17q24.1UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic Map12q14.3-q15UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map12q15UniSTS
Cytogenetic Map3q28UniSTS
Cytogenetic Map6p25.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic Map11q24UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map19q13.13UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map2p25.1-p24.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map16p12.3UniSTS
Cytogenetic Map2p25.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map21q21.1UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map12q23.1UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map17q24UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map7q31.3UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1p13-p12UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map10q21.1UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map14q31UniSTS


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 adipose tissue appendage entire extraembryonic component
High
Medium 2317 2017 1400 354 1563 198 3975 1431 1755 153 1259 1462 169 1204 2447 3
Low 34 967 84 79 212 77 343 762 1909 29 1 1 2 341 1
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_017748 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_073428 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_001752548 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007065311 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007065312 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008484847 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008484848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008485633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC006449 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK000298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK302983 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK316077 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW612704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC003085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471152 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068261 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CR749362 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY021361 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000611845
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1738,806,503 - 38,809,808 (-)Ensembl
RefSeq Acc Id: ENST00000614790   ⟹   ENSP00000478070
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1738,800,441 - 38,825,321 (-)Ensembl
RefSeq Acc Id: ENST00000618122   ⟹   ENSP00000478244
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1738,802,815 - 38,815,735 (-)Ensembl
RefSeq Acc Id: ENST00000619299   ⟹   ENSP00000482247
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1738,801,725 - 38,825,315 (-)Ensembl
RefSeq Acc Id: ENST00000619462   ⟹   ENSP00000479527
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1738,802,840 - 38,810,595 (-)Ensembl
RefSeq Acc Id: ENST00000619818
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1738,806,800 - 38,825,355 (-)Ensembl
RefSeq Acc Id: ENST00000622665   ⟹   ENSP00000481539
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1738,810,354 - 38,825,306 (-)Ensembl
RefSeq Acc Id: NM_017748   ⟹   NP_060218
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381738,800,441 - 38,825,321 (-)NCBI
GRCh371736,956,687 - 36,981,603 (-)NCBI
Build 361734,210,972 - 34,235,115 (-)NCBI Archive
Celera1733,618,412 - 33,642,555 (-)RGD
HuRef1732,752,758 - 32,776,922 (-)NCBI
CHM1_11737,191,993 - 37,216,912 (-)NCBI
T2T-CHM13v2.01739,663,526 - 39,688,404 (-)NCBI
Sequence:
RefSeq Acc Id: NR_073428
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381738,800,441 - 38,825,321 (-)NCBI
HuRef1732,752,758 - 32,776,922 (-)NCBI
CHM1_11737,191,993 - 37,216,912 (-)NCBI
T2T-CHM13v2.01739,663,526 - 39,688,404 (-)NCBI
Sequence:
RefSeq Acc Id: XR_007065311
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381738,806,939 - 38,825,321 (-)NCBI
RefSeq Acc Id: XR_007065312
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381738,806,939 - 38,825,321 (-)NCBI
RefSeq Acc Id: XR_008484847
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01739,670,023 - 39,688,404 (-)NCBI
RefSeq Acc Id: XR_008484848
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01739,670,023 - 39,688,404 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_060218   ⟸   NM_017748
- UniProtKB: A0JLM3 (UniProtKB/Swiss-Prot),   Q68DK5 (UniProtKB/Swiss-Prot),   Q9NXE8 (UniProtKB/Swiss-Prot),   B4DJK2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000481539   ⟸   ENST00000622665
RefSeq Acc Id: ENSP00000478070   ⟸   ENST00000614790
RefSeq Acc Id: ENSP00000478244   ⟸   ENST00000618122
RefSeq Acc Id: ENSP00000479527   ⟸   ENST00000619462
RefSeq Acc Id: ENSP00000482247   ⟸   ENST00000619299
Protein Domains
CBF1-interacting co-repressor CIR N-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9NXE8-F1-model_v2 AlphaFold Q9NXE8 1-425 view protein structure

Promoters
RGD ID:6793900
Promoter ID:HG_KWN:25960
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:NM_017748
Position:
Human AssemblyChrPosition (strand)Source
Build 361734,234,976 - 34,235,476 (-)MPROMDB
RGD ID:7234797
Promoter ID:EPDNEW_H23144
Type:initiation region
Name:CWC25_1
Description:CWC25 spliceosome associated protein homolog
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23145  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381738,825,321 - 38,825,381EPDNEW
RGD ID:7234799
Promoter ID:EPDNEW_H23145
Type:multiple initiation site
Name:CWC25_2
Description:CWC25 spliceosome associated protein homolog
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H23144  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381738,825,514 - 38,825,574EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:25989 AgrOrtholog
COSMIC CWC25 COSMIC
Ensembl Genes ENSG00000273559 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000276761 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000614790 ENTREZGENE
  ENST00000614790.5 UniProtKB/Swiss-Prot
  ENST00000614868.2 UniProtKB/Swiss-Prot
  ENST00000619299.4 UniProtKB/TrEMBL
  ENST00000619462.4 UniProtKB/TrEMBL
  ENST00000622665.1 UniProtKB/TrEMBL
  ENST00000631731.1 UniProtKB/TrEMBL
  ENST00000632717.1 UniProtKB/TrEMBL
  ENST00000633854.1 UniProtKB/TrEMBL
GTEx ENSG00000273559 GTEx
  ENSG00000276761 GTEx
HGNC ID HGNC:25989 ENTREZGENE
Human Proteome Map CWC25 Human Proteome Map
InterPro CIR_N_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CWC25 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:54883 UniProtKB/Swiss-Prot
NCBI Gene 54883 ENTREZGENE
PANTHER CELL CYCLE CONTROL PROTEIN CWF25 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PRE-MRNA-SPLICING FACTOR CWC25 HOMOLOG UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Cir_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CWC25 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA165431769 PharmGKB
SMART Cir_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WVL7_HUMAN UniProtKB/TrEMBL
  A0A087WY60_HUMAN UniProtKB/TrEMBL
  A0JLM3 ENTREZGENE
  B4DJK2 ENTREZGENE, UniProtKB/TrEMBL
  CWC25_HUMAN UniProtKB/Swiss-Prot
  Q68DK5 ENTREZGENE
  Q9NXE8 ENTREZGENE
UniProt Secondary A0JLM3 UniProtKB/Swiss-Prot
  Q68DK5 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-07-05 CWC25  CWC25 spliceosome associated protein homolog    CWC25 spliceosome-associated protein homolog  Symbol and/or name change 5135510 APPROVED
2015-07-07 CWC25  CWC25 spliceosome-associated protein homolog    CWC25 spliceosome-associated protein homolog (S. cerevisiae)  Symbol and/or name change 5135510 APPROVED
2011-07-27 CWC25  CWC25 spliceosome-associated protein homolog (S. cerevisiae)  CCDC49  coiled-coil domain containing 49  Symbol and/or name change 5135510 APPROVED