CWF19L2 (CWF19 like cell cycle control factor 2) - Rat Genome Database

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Gene: CWF19L2 (CWF19 like cell cycle control factor 2) Homo sapiens
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Symbol: CWF19L2
Name: CWF19 like cell cycle control factor 2
RGD ID: 1320784
HGNC Page HGNC:26508
Description: Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be part of post-mRNA release spliceosomal complex.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: CWF19 like 2, cell cycle control; CWF19 like 2, cell cycle control (S. pombe); CWF19-like 2, cell cycle control (S. pombe); CWF19-like protein 2; FLJ32343
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
GRCh3811107,326,360 - 107,457,825 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11107,326,360 - 107,457,825 (-)EnsemblGRCh38hg38GRCh38
GRCh3711107,197,086 - 107,328,551 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3611106,702,293 - 106,830,406 (-)NCBINCBI36Build 36hg18NCBI36
Build 3411106,702,292 - 106,830,406NCBI
Celera11104,362,890 - 104,483,437 (-)NCBICelera
Cytogenetic Map11q22.3NCBI
HuRef11103,133,370 - 103,254,160 (-)NCBIHuRef
CHM1_111107,080,175 - 107,211,650 (-)NCBICHM1_1
T2T-CHM13v2.011107,333,512 - 107,464,989 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
3. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
Additional References at PubMed
PMID:14702039   PMID:16344560   PMID:18398821   PMID:20379614   PMID:20677014   PMID:21832049   PMID:21873635   PMID:24623722   PMID:25184681   PMID:25416956   PMID:25921289   PMID:26186194  
PMID:26496610   PMID:27433848   PMID:28514442   PMID:28700943   PMID:29395067   PMID:29773831   PMID:30196744   PMID:31586073   PMID:32296183   PMID:32433965   PMID:32814053   PMID:33961781  
PMID:34079125   PMID:34349018   PMID:34795231   PMID:35271311   PMID:35439318   PMID:35944360   PMID:36273042   PMID:36373674   PMID:37071664   PMID:37689310   PMID:38113892   PMID:38334954  
PMID:38580884   PMID:38697112  


Genomics

Comparative Map Data
CWF19L2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811107,326,360 - 107,457,825 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl11107,326,360 - 107,457,825 (-)EnsemblGRCh38hg38GRCh38
GRCh3711107,197,086 - 107,328,551 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3611106,702,293 - 106,830,406 (-)NCBINCBI36Build 36hg18NCBI36
Build 3411106,702,292 - 106,830,406NCBI
Celera11104,362,890 - 104,483,437 (-)NCBICelera
Cytogenetic Map11q22.3NCBI
HuRef11103,133,370 - 103,254,160 (-)NCBIHuRef
CHM1_111107,080,175 - 107,211,650 (-)NCBICHM1_1
T2T-CHM13v2.011107,333,512 - 107,464,989 (-)NCBIT2T-CHM13v2.0
Cwf19l2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm3993,403,592 - 3,479,236 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl93,403,592 - 3,479,236 (+)EnsemblGRCm39 Ensembl
GRCm3893,403,592 - 3,479,236 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl93,403,592 - 3,479,236 (+)EnsemblGRCm38mm10GRCm38
MGSCv3793,404,085 - 3,479,236 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv3693,404,085 - 3,479,236 (+)NCBIMGSCv36mm8
Celera3119,215,796 - 119,285,730 (-)NCBICelera
Cytogenetic Map9A1NCBI
cM Map92.06NCBI
Cwf19l2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr866,036,158 - 6,102,686 (-)NCBIGRCr8
mRatBN7.26290,148 - 356,636 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl6281,685 - 356,604 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx6506,515 - 572,953 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.06815,805 - 882,242 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.06340,227 - 406,631 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0618,970,616 - 19,037,176 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl618,970,564 - 19,055,924 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0628,868,716 - 28,935,276 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47418,368 - 485,802 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.17418,367 - 482,123 (+)NCBI
Celera6115,555 - 181,554 (-)NCBICelera
Cytogenetic Map6q11NCBI
Cwf19l2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554129,766,910 - 9,861,027 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554129,758,751 - 9,861,019 (-)NCBIChiLan1.0ChiLan1.0
CWF19L2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v29108,025,853 - 108,203,804 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan111109,157,101 - 109,297,820 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v011102,219,339 - 102,345,865 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.111105,702,934 - 105,828,168 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl11105,702,934 - 105,828,149 (-)Ensemblpanpan1.1panPan2
CWF19L2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1524,936,700 - 25,080,927 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl524,833,373 - 25,080,451 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha524,852,125 - 25,005,758 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0524,963,467 - 25,107,620 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl524,963,519 - 25,107,618 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1525,015,519 - 25,159,677 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0524,902,624 - 25,047,003 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0524,964,115 - 25,111,783 (+)NCBIUU_Cfam_GSD_1.0
Cwf19l2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494790,229,976 - 90,343,408 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049365511,193,109 - 1,306,533 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CWF19L2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl935,967,204 - 36,059,749 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1935,967,198 - 36,059,780 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2940,006,188 - 40,106,971 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CWF19L2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1198,749,892 - 98,885,698 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl198,766,109 - 98,885,671 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604327,061,434 - 27,186,945 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Cwf19l2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247842,113,153 - 2,253,466 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CWF19L2
64 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3 copy number gain See cases [RCV000053638] Chr11:100348599..135040246 [GRCh38]
Chr11:100219331..134910140 [GRCh37]
Chr11:99724541..134415350 [NCBI36]
Chr11:11q22.1-25		 pathogenic
NM_152434.2(CWF19L2):c.1434-600A>C single nucleotide variant Lung cancer [RCV000109577] Chr11:107418887 [GRCh38]
Chr11:107289613 [GRCh37]
Chr11:11q22.3		 uncertain significance
GRCh38/hg38 11q14.3-22.3(chr11:91086659-109595582)x1 copy number loss See cases [RCV000138038] Chr11:91086659..109595582 [GRCh38]
Chr11:90819827..109466308 [GRCh37]
Chr11:90459475..108971518 [NCBI36]
Chr11:11q14.3-22.3		 pathogenic
GRCh37/hg19 11q22.3(chr11:106959465-107537265)x1 copy number loss See cases [RCV000239992] Chr11:106959465..107537265 [GRCh37]
Chr11:11q22.3		 uncertain significance
GRCh37/hg19 11q14.2-22.3(chr11:88152458-109414650)x1 copy number loss See cases [RCV000510457] Chr11:88152458..109414650 [GRCh37]
Chr11:11q14.2-22.3		 pathogenic
GRCh37/hg19 11q22.3(chr11:106767102-107561488)x3 copy number gain See cases [RCV000511621] Chr11:106767102..107561488 [GRCh37]
Chr11:11q22.3		 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
GRCh37/hg19 11q22.3(chr11:107072930-107283027)x1 copy number loss See cases [RCV000511100] Chr11:107072930..107283027 [GRCh37]
Chr11:11q22.3		 uncertain significance
GRCh37/hg19 11q22.2-22.3(chr11:102578709-107230611)x1 copy number loss not provided [RCV000683366] Chr11:102578709..107230611 [GRCh37]
Chr11:11q22.2-22.3		 likely pathogenic
GRCh37/hg19 11q13.4-23.3(chr11:71588805-116680918)x3 copy number gain not provided [RCV000683374] Chr11:71588805..116680918 [GRCh37]
Chr11:11q13.4-23.3		 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 11q14.1-23.2(chr11:80053454-113316236)x1 copy number loss not provided [RCV000737595] Chr11:80053454..113316236 [GRCh37]
Chr11:11q14.1-23.2		 pathogenic
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 11q22.3-23.3(chr11:104101411-116680918)x1 copy number loss not provided [RCV000848741] Chr11:104101411..116680918 [GRCh37]
Chr11:11q22.3-23.3		 pathogenic
NM_152434.3(CWF19L2):c.2498A>G (p.His833Arg) single nucleotide variant not specified [RCV004302175] Chr11:107329961 [GRCh38]
Chr11:107200687 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1037C>T (p.Thr346Met) single nucleotide variant not specified [RCV004309461] Chr11:107429195 [GRCh38]
Chr11:107299921 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.421T>G (p.Ser141Ala) single nucleotide variant not specified [RCV004286209] Chr11:107442968 [GRCh38]
Chr11:107313694 [GRCh37]
Chr11:11q22.3		 uncertain significance
GRCh37/hg19 11q22.3-23.3(chr11:105699599-114524876)x1 copy number loss not provided [RCV001006445] Chr11:105699599..114524876 [GRCh37]
Chr11:11q22.3-23.3		 pathogenic
GRCh37/hg19 11q22.3-23.2(chr11:103320065-114349787)x1 copy number loss not provided [RCV001006439] Chr11:103320065..114349787 [GRCh37]
Chr11:11q22.3-23.2		 pathogenic
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
NC_000011.9:g.(?_94153285)_(111965700_?)del deletion Ataxia-telangiectasia syndrome [RCV001389105] Chr11:94153285..111965700 [GRCh37]
Chr11:11q21-23.1		 pathogenic
NC_000011.9:g.104288964_134937416dup duplication Distal trisomy 11q [RCV001250234] Chr11:104288964..134937416 [GRCh37]
Chr11:11q22.3-25		 pathogenic
GRCh37/hg19 11q14.1-23.3(chr11:85422071-118022671)x1 copy number loss not provided [RCV001832892] Chr11:85422071..118022671 [GRCh37]
Chr11:11q14.1-23.3		 uncertain significance
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
GRCh37/hg19 11q22.1-22.3(chr11:101371503-109306519)x1 copy number loss not provided [RCV002472494] Chr11:101371503..109306519 [GRCh37]
Chr11:11q22.1-22.3		 pathogenic
NM_152434.3(CWF19L2):c.1709A>C (p.Gln570Pro) single nucleotide variant not specified [RCV004202518] Chr11:107392804 [GRCh38]
Chr11:107263530 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1690G>A (p.Gly564Arg) single nucleotide variant not specified [RCV004092521] Chr11:107392823 [GRCh38]
Chr11:107263549 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1276G>C (p.Gly426Arg) single nucleotide variant not specified [RCV004094655] Chr11:107428956 [GRCh38]
Chr11:107299682 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1928A>G (p.Lys643Arg) single nucleotide variant not specified [RCV004118012] Chr11:107353681 [GRCh38]
Chr11:107224407 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1082T>C (p.Phe361Ser) single nucleotide variant not specified [RCV004166879] Chr11:107429150 [GRCh38]
Chr11:107299876 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2367A>G (p.Ile789Met) single nucleotide variant not specified [RCV004217202] Chr11:107334953 [GRCh38]
Chr11:107205679 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1084G>C (p.Gly362Arg) single nucleotide variant not specified [RCV004166529] Chr11:107429148 [GRCh38]
Chr11:107299874 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.661A>G (p.Lys221Glu) single nucleotide variant not specified [RCV004076242] Chr11:107439093 [GRCh38]
Chr11:107309819 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2555G>C (p.Gly852Ala) single nucleotide variant not specified [RCV004100235] Chr11:107327040 [GRCh38]
Chr11:107197766 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1913A>G (p.Asp638Gly) single nucleotide variant not specified [RCV004150573] Chr11:107353696 [GRCh38]
Chr11:107224422 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.276A>T (p.Glu92Asp) single nucleotide variant not specified [RCV004224562] Chr11:107454513 [GRCh38]
Chr11:107325239 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.70C>A (p.Gln24Lys) single nucleotide variant not specified [RCV004122330] Chr11:107457747 [GRCh38]
Chr11:107328473 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1984A>G (p.Ile662Val) single nucleotide variant not specified [RCV004081998] Chr11:107353625 [GRCh38]
Chr11:107224351 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1261C>T (p.Arg421Cys) single nucleotide variant not specified [RCV004135456] Chr11:107428971 [GRCh38]
Chr11:107299697 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.599C>T (p.Pro200Leu) single nucleotide variant not specified [RCV004145609] Chr11:107439155 [GRCh38]
Chr11:107309881 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2252G>A (p.Cys751Tyr) single nucleotide variant not specified [RCV004106415] Chr11:107336664 [GRCh38]
Chr11:107207390 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1634A>G (p.Glu545Gly) single nucleotide variant not specified [RCV004159429] Chr11:107392879 [GRCh38]
Chr11:107263605 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1469T>C (p.Val490Ala) single nucleotide variant not specified [RCV004175662] Chr11:107418252 [GRCh38]
Chr11:107288978 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2203A>G (p.Met735Val) single nucleotide variant not specified [RCV004107044] Chr11:107336713 [GRCh38]
Chr11:107207439 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.52A>G (p.Ile18Val) single nucleotide variant not specified [RCV004114097] Chr11:107457765 [GRCh38]
Chr11:107328491 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.44C>T (p.Ala15Val) single nucleotide variant not specified [RCV004225930] Chr11:107457773 [GRCh38]
Chr11:107328499 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2456C>T (p.Pro819Leu) single nucleotide variant not specified [RCV004124298] Chr11:107330003 [GRCh38]
Chr11:107200729 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.157C>T (p.Arg53Trp) single nucleotide variant not specified [RCV004137039] Chr11:107455725 [GRCh38]
Chr11:107326451 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.489A>T (p.Lys163Asn) single nucleotide variant not specified [RCV004222016] Chr11:107441584 [GRCh38]
Chr11:107312310 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2503A>G (p.Ile835Val) single nucleotide variant not specified [RCV004147266] Chr11:107329956 [GRCh38]
Chr11:107200682 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2288A>G (p.Gln763Arg) single nucleotide variant not specified [RCV004075356] Chr11:107336628 [GRCh38]
Chr11:107207354 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.947A>T (p.Asp316Val) single nucleotide variant not specified [RCV004279548] Chr11:107429285 [GRCh38]
Chr11:107300011 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2564A>C (p.Asp855Ala) single nucleotide variant not specified [RCV004278927] Chr11:107327031 [GRCh38]
Chr11:107197757 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.658A>G (p.Thr220Ala) single nucleotide variant not specified [RCV004270209] Chr11:107439096 [GRCh38]
Chr11:107309822 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1115C>T (p.Ser372Phe) single nucleotide variant not specified [RCV004248739] Chr11:107429117 [GRCh38]
Chr11:107299843 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2621A>G (p.Lys874Arg) single nucleotide variant not specified [RCV004253683] Chr11:107326974 [GRCh38]
Chr11:107197700 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1721G>T (p.Arg574Ile) single nucleotide variant not specified [RCV004251975] Chr11:107392792 [GRCh38]
Chr11:107263518 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.83C>T (p.Ala28Val) single nucleotide variant not specified [RCV004345229] Chr11:107457734 [GRCh38]
Chr11:107328460 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.136C>T (p.Arg46Cys) single nucleotide variant not specified [RCV004340742] Chr11:107455746 [GRCh38]
Chr11:107326472 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1518G>A (p.Met506Ile) single nucleotide variant not specified [RCV004341873] Chr11:107418203 [GRCh38]
Chr11:107288929 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1607C>T (p.Ser536Phe) single nucleotide variant not specified [RCV004339471] Chr11:107416219 [GRCh38]
Chr11:107286945 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2303A>G (p.Tyr768Cys) single nucleotide variant not specified [RCV004361219] Chr11:107336613 [GRCh38]
Chr11:107207339 [GRCh37]
Chr11:11q22.3		 uncertain significance
Single allele duplication not provided [RCV003448710] Chr11:102134973..134945611 [GRCh37]
Chr11:11q22.2-25		 pathogenic
NM_152434.3(CWF19L2):c.429A>G (p.Lys143=) single nucleotide variant not provided [RCV003396059] Chr11:107442960 [GRCh38]
Chr11:107313686 [GRCh37]
Chr11:11q22.3		 likely benign
NM_152434.3(CWF19L2):c.201T>C (p.Ile67=) single nucleotide variant not provided [RCV003396060] Chr11:107455681 [GRCh38]
Chr11:107326407 [GRCh37]
Chr11:11q22.3		 likely benign
NM_152434.3(CWF19L2):c.1439C>T (p.Pro480Leu) single nucleotide variant not specified [RCV004367510] Chr11:107418282 [GRCh38]
Chr11:107289008 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1975A>G (p.Lys659Glu) single nucleotide variant not specified [RCV004367512] Chr11:107353634 [GRCh38]
Chr11:107224360 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2279T>G (p.Met760Arg) single nucleotide variant not specified [RCV004367517] Chr11:107336637 [GRCh38]
Chr11:107207363 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.950G>T (p.Arg317Ile) single nucleotide variant not specified [RCV004367523] Chr11:107429282 [GRCh38]
Chr11:107300008 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2110C>T (p.Arg704Trp) single nucleotide variant not specified [RCV004367514] Chr11:107349029 [GRCh38]
Chr11:107219755 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2153A>G (p.His718Arg) single nucleotide variant not specified [RCV004367515] Chr11:107348986 [GRCh38]
Chr11:107219712 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2289G>C (p.Gln763His) single nucleotide variant not specified [RCV004367518] Chr11:107336627 [GRCh38]
Chr11:107207353 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2623A>G (p.Lys875Glu) single nucleotide variant not specified [RCV004367519] Chr11:107326972 [GRCh38]
Chr11:107197698 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.611A>G (p.Asp204Gly) single nucleotide variant not specified [RCV004367520] Chr11:107439143 [GRCh38]
Chr11:107309869 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1461C>G (p.Ile487Met) single nucleotide variant not specified [RCV004367511] Chr11:107418260 [GRCh38]
Chr11:107288986 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1232A>G (p.Asn411Ser) single nucleotide variant not specified [RCV004367509] Chr11:107429000 [GRCh38]
Chr11:107299726 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1999A>T (p.Ser667Cys) single nucleotide variant not specified [RCV004367513] Chr11:107353610 [GRCh38]
Chr11:107224336 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2221G>T (p.Val741Leu) single nucleotide variant not specified [RCV004367516] Chr11:107336695 [GRCh38]
Chr11:107207421 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.673G>A (p.Val225Ile) single nucleotide variant not specified [RCV004367521] Chr11:107433741 [GRCh38]
Chr11:107304467 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.710A>T (p.Tyr237Phe) single nucleotide variant not specified [RCV004367522] Chr11:107433704 [GRCh38]
Chr11:107304430 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1694A>C (p.Lys565Thr) single nucleotide variant not specified [RCV004616168] Chr11:107392819 [GRCh38]
Chr11:107263545 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1819A>G (p.Lys607Glu) single nucleotide variant not specified [RCV004616166] Chr11:107390127 [GRCh38]
Chr11:107260853 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2465C>T (p.Ser822Phe) single nucleotide variant not specified [RCV004616167] Chr11:107329994 [GRCh38]
Chr11:107200720 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2341G>A (p.Ala781Thr) single nucleotide variant not specified [RCV004616170] Chr11:107336575 [GRCh38]
Chr11:107207301 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.1411G>T (p.Asp471Tyr) single nucleotide variant not specified [RCV004616172] Chr11:107428821 [GRCh38]
Chr11:107299547 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2517C>G (p.His839Gln) single nucleotide variant not specified [RCV004616165] Chr11:107329942 [GRCh38]
Chr11:107200668 [GRCh37]
Chr11:11q22.3		 uncertain significance
NM_152434.3(CWF19L2):c.2078G>T (p.Gly693Val) single nucleotide variant not specified [RCV004616169] Chr11:107353531 [GRCh38]
Chr11:107224257 [GRCh37]
Chr11:11q22.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:932
Count of miRNA genes:413
Interacting mature miRNAs:439
Transcripts:ENST00000282251, ENST00000431778, ENST00000433523, ENST00000462890, ENST00000532251
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
406978994GWAS627970_Hpars opercularis volume measurement QTL GWAS627970 (human)0.0000008frontal lobe morphology trait (VT:0000798)11107391784107391785Human
407285255GWAS934231_Hphysical activity measurement QTL GWAS934231 (human)9e-10physical activity measurementvoluntary body movement measurement (CMO:0000954)11107450430107450431Human
407359734GWAS1008710_Hpulse pressure measurement QTL GWAS1008710 (human)4e-14pulse pressure measurementpulse pressure (CMO:0000292)11107370011107370012Human
406904322GWAS553298_Hsmoking initiation QTL GWAS553298 (human)6e-10smoking initiation11107434056107434057Human
407087702GWAS736678_Hcoronary artery disease QTL GWAS736678 (human)9e-08coronary artery disease11107326914107326915Human
407115937GWAS764913_Hcognitive decline measurement QTL GWAS764913 (human)0.000008cognitive behavior trait (VT:0010450)11107326880107326881Human
406979736GWAS628712_Hfourth ventricle volume measurement QTL GWAS628712 (human)0.000009fourth ventricle size trait (VT:0000829)11107449918107449919Human
407267885GWAS916861_HC-reactive protein measurement QTL GWAS916861 (human)1e-08C-reactive protein measurementblood C-reactive protein level (CMO:0003160)11107373196107373197Human
1559115SCL20_HSerum cholesterol level QTL 20 (human)3.220.001213Lipid levelLDL cholesterol11100442501126442501Human
406904319GWAS553295_Hsmoking initiation QTL GWAS553295 (human)2e-11smoking initiation11107430784107430785Human
406980109GWAS629085_Hbrain cortex volume measurement QTL GWAS629085 (human)0.000004brain cortex volume measurement11107391784107391785Human

Markers in Region
RH92467  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711107,197,116 - 107,197,285UniSTSGRCh37
Build 3611106,702,326 - 106,702,495RGDNCBI36
Celera11104,362,935 - 104,363,104RGD
Cytogenetic Map11q22.3UniSTS
HuRef11103,133,415 - 103,133,584UniSTS
GeneMap99-GB4 RH Map11362.08UniSTS
D11S2228E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711107,198,621 - 107,198,734UniSTSGRCh37
Build 3611106,703,831 - 106,703,944RGDNCBI36
Celera11104,364,440 - 104,364,553RGD
Cytogenetic Map11q22.3UniSTS
HuRef11103,134,920 - 103,135,033UniSTS
GeneMap99-GB4 RH Map11361.98UniSTS
NCBI RH Map11934.8UniSTS
SHGC-145207  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711107,202,834 - 107,203,167UniSTSGRCh37
Build 3611106,708,044 - 106,708,377RGDNCBI36
Celera11104,368,640 - 104,368,973RGD
Cytogenetic Map11q22.3UniSTS
HuRef11103,139,124 - 103,139,457UniSTS
TNG Radiation Hybrid Map1149016.0UniSTS
RH36538  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711107,197,117 - 107,197,255UniSTSGRCh37
Build 3611106,702,327 - 106,702,465RGDNCBI36
Celera11104,362,936 - 104,363,074RGD
Cytogenetic Map11q22.3UniSTS
HuRef11103,133,416 - 103,133,554UniSTS
GeneMap99-GB4 RH Map11362.08UniSTS
D11S4021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh3711107,299,030 - 107,299,256UniSTSGRCh37
Build 3611106,804,240 - 106,804,466RGDNCBI36
Celera11104,453,902 - 104,454,128RGD
Cytogenetic Map11q22.3UniSTS
HuRef11103,224,320 - 103,224,546UniSTS
Whitehead-RH Map11486.4UniSTS
Whitehead-YAC Contig Map11 UniSTS


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
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2438 2788 2253 4974 1726 2351 6 624 1951 465 2270 7305 6472 53 3734 1 852 1744 1617 175 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_152434 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011542620 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017017239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047426419 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367763 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054367764 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_007062452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008488344 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_947795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AI148333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK056905 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK126881 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK293001 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP000766 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AP001823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016611 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC028043 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC056241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC070142 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC107418 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC110439 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC110440 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC110441 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC110442 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC118669 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX647832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648704 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX649022 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471065 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA291472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000282251   ⟹   ENSP00000282251
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11107,326,360 - 107,457,825 (-)Ensembl
Ensembl Acc Id: ENST00000431778   ⟹   ENSP00000411736
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11107,326,360 - 107,443,031 (-)Ensembl
Ensembl Acc Id: ENST00000462890
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11107,348,711 - 107,353,730 (-)Ensembl
Ensembl Acc Id: ENST00000532251   ⟹   ENSP00000434704
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl11107,326,797 - 107,443,031 (-)Ensembl
RefSeq Acc Id: NM_152434   ⟹   NP_689647
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811107,326,360 - 107,457,825 (-)NCBI
GRCh3711107,197,071 - 107,328,572 (-)RGD
Build 3611106,702,293 - 106,830,406 (-)NCBI Archive
Celera11104,362,890 - 104,483,437 (-)RGD
HuRef11103,133,370 - 103,254,160 (-)ENTREZGENE
CHM1_111107,080,175 - 107,211,650 (-)NCBI
T2T-CHM13v2.011107,333,512 - 107,464,989 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011542620   ⟹   XP_011540922
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811107,424,773 - 107,457,825 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047426419   ⟹   XP_047282375
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811107,326,360 - 107,433,741 (-)NCBI
RefSeq Acc Id: XM_054367763   ⟹   XP_054223738
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011107,431,867 - 107,464,989 (-)NCBI
RefSeq Acc Id: XM_054367764   ⟹   XP_054223739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011107,333,512 - 107,440,900 (-)NCBI
RefSeq Acc Id: XR_007062452
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811107,336,627 - 107,457,825 (-)NCBI
RefSeq Acc Id: XR_008488344
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.011107,343,780 - 107,464,989 (-)NCBI
RefSeq Acc Id: NP_689647   ⟸   NM_152434
- UniProtKB: Q6PHW1 (UniProtKB/Swiss-Prot),   A8KAD6 (UniProtKB/Swiss-Prot),   A4FU68 (UniProtKB/Swiss-Prot),   A4FU67 (UniProtKB/Swiss-Prot),   A4FU66 (UniProtKB/Swiss-Prot),   Q96MI1 (UniProtKB/Swiss-Prot),   Q2TBE0 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011540922   ⟸   XM_011542620
- Peptide Label: isoform X1
- Sequence:
Ensembl Acc Id: ENSP00000282251   ⟸   ENST00000282251
Ensembl Acc Id: ENSP00000434704   ⟸   ENST00000532251
Ensembl Acc Id: ENSP00000411736   ⟸   ENST00000431778
RefSeq Acc Id: XP_047282375   ⟸   XM_047426419
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054223739   ⟸   XM_054367764
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054223738   ⟸   XM_054367763
- Peptide Label: isoform X1
Protein Domains
Cwf19-like C-terminal   Cwf19-like protein C-terminal

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q2TBE0-F1-model_v2 AlphaFold Q2TBE0 1-894 view protein structure

Promoters
RGD ID:6788665
Promoter ID:HG_KWN:14097
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_152434
Position:
Human AssemblyChrPosition (strand)Source
Build 3611106,833,466 - 106,833,966 (-)MPROMDB
RGD ID:7221987
Promoter ID:EPDNEW_H16739
Type:initiation region
Name:CWF19L2_2
Description:CWF19 like 2, cell cycle control
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H16740  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811107,443,030 - 107,443,090EPDNEW
RGD ID:7221989
Promoter ID:EPDNEW_H16740
Type:initiation region
Name:CWF19L2_1
Description:CWF19 like 2, cell cycle control
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H16739  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh3811107,457,825 - 107,457,885EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26508 AgrOrtholog
COSMIC CWF19L2 COSMIC
Ensembl Genes ENSG00000152404 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000282251 ENTREZGENE
  ENST00000282251.10 UniProtKB/Swiss-Prot
  ENST00000431778.5 UniProtKB/TrEMBL
  ENST00000532251.1 UniProtKB/TrEMBL
Gene3D-CATH 3.30.428.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000152404 GTEx
HGNC ID HGNC:26508 ENTREZGENE
Human Proteome Map CWF19L2 Human Proteome Map
InterPro Cwf19-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cwf19-like_C_dom-1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cwf19-like_C_dom-2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HIT-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:143884 UniProtKB/Swiss-Prot
NCBI Gene 143884 ENTREZGENE
PANTHER CWF19-LIKE PROTEIN 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR12072 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam CwfJ_C_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CwfJ_C_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134914164 PharmGKB
Superfamily-SCOP SSF54197 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A4FU66 ENTREZGENE
  A4FU67 ENTREZGENE
  A4FU68 ENTREZGENE
  A8KAD6 ENTREZGENE
  C19L2_HUMAN UniProtKB/Swiss-Prot
  H0YE03_HUMAN UniProtKB/TrEMBL
  H7C3G7_HUMAN UniProtKB/TrEMBL
  Q2TBE0 ENTREZGENE
  Q6PHW1 ENTREZGENE
  Q6PIV4_HUMAN UniProtKB/TrEMBL
  Q96MI1 ENTREZGENE
UniProt Secondary A4FU66 UniProtKB/Swiss-Prot
  A4FU67 UniProtKB/Swiss-Prot
  A4FU68 UniProtKB/Swiss-Prot
  A8KAD6 UniProtKB/Swiss-Prot
  Q6PHW1 UniProtKB/Swiss-Prot
  Q96MI1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2018-07-10 CWF19L2  CWF19 like cell cycle control factor 2    CWF19 like 2, cell cycle control (S. pombe)  Symbol and/or name change 5135510 APPROVED
2017-02-28 CWF19L2  CWF19 like 2, cell cycle control (S. pombe)    CWF19-like 2, cell cycle control (S. pombe)  Symbol and/or name change 5135510 APPROVED