Imported Disease Annotations - MGITerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | infertility | | ISS | Cdc23 (Mus musculus) | 13592920 | | MouseDO | | |
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Imported Disease Annotations - MGITerm | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | infertility | | ISS | Cdc23 (Mus musculus) | 13592920 | | MouseDO | | |
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# | Reference Title | Reference Citation |
1. | GOAs Human GO annotations | GOA_HUMAN data from the GO Consortium |
2. | KEGG Annotation Import Pipeline | Pipeline to import KEGG annotations from KEGG into RGD |
3. | Data Import for Chemical-Gene Interactions | RGD automated import pipeline for gene-chemical interactions |
PMID:8125298 | PMID:9469815 | PMID:9790767 | PMID:10318877 | PMID:10500174 | PMID:10548110 | PMID:10793135 | PMID:10922056 | PMID:11076961 | PMID:11256614 | PMID:11285280 | PMID:11340163 |
PMID:11535616 | PMID:11742988 | PMID:12070128 | PMID:12188893 | PMID:12477932 | PMID:12629511 | PMID:12956947 | PMID:14593737 | PMID:14657031 | PMID:15029244 | PMID:15302935 | PMID:15345747 |
PMID:15489334 | PMID:15678131 | PMID:16189514 | PMID:16364912 | PMID:16565220 | PMID:16648845 | PMID:16921029 | PMID:16964243 | PMID:17081983 | PMID:17609108 | PMID:17942546 | PMID:18162579 |
PMID:18485873 | PMID:18997788 | PMID:19322201 | PMID:19531213 | PMID:20360068 | PMID:20467437 | PMID:20686030 | PMID:21043528 | PMID:21336306 | PMID:21516116 | PMID:21549307 | PMID:21873635 |
PMID:21926987 | PMID:21990323 | PMID:22014574 | PMID:22193957 | PMID:22280307 | PMID:22658674 | PMID:22792066 | PMID:22939629 | PMID:22990118 | PMID:23007861 | PMID:23022380 | PMID:23078409 |
PMID:23160376 | PMID:23443559 | PMID:23455924 | PMID:23508102 | PMID:23667531 | PMID:23708001 | PMID:23979597 | PMID:24163370 | PMID:24464857 | PMID:24711643 | PMID:24722188 | PMID:25043029 |
PMID:25064703 | PMID:25306918 | PMID:25306923 | PMID:25416956 | PMID:25458010 | PMID:25490258 | PMID:25544563 | PMID:25859049 | PMID:25910212 | PMID:26083744 | PMID:26186194 | PMID:26299517 |
PMID:26344197 | PMID:26496610 | PMID:26673895 | PMID:26811472 | PMID:26871637 | PMID:26949251 | PMID:27030811 | PMID:27107014 | PMID:27114510 | PMID:27120157 | PMID:27173435 | PMID:27229929 |
PMID:27248496 | PMID:28404789 | PMID:28514442 | PMID:28700943 | PMID:28786561 | PMID:28813667 | PMID:28883622 | PMID:29183995 | PMID:29229926 | PMID:29509190 | PMID:29549242 | PMID:29568061 |
PMID:29863498 | PMID:29955894 | PMID:30033366 | PMID:30553447 | PMID:30585266 | PMID:30737378 | PMID:30804502 | PMID:30945288 | PMID:31024071 | PMID:31073040 | PMID:31091453 | PMID:31420536 |
PMID:31586073 | PMID:31753913 | PMID:32076268 | PMID:32129710 | PMID:32152539 | PMID:32296183 | PMID:32416067 | PMID:32707033 | PMID:32814053 | PMID:32877691 | PMID:32934012 | PMID:32989298 |
PMID:33187986 | PMID:33306668 | PMID:33705438 | PMID:33729478 | PMID:33853758 | PMID:33961781 | PMID:34011540 | PMID:34079125 | PMID:34244565 | PMID:34373451 | PMID:34595750 | PMID:34709266 |
PMID:34831298 | PMID:35271311 | PMID:35509820 | PMID:35831314 | PMID:35952650 | PMID:36215168 | PMID:36736316 | PMID:37768355 | PMID:37827155 | PMID:38280479 |
CDC23 (Homo sapiens - human) |
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Cdc23 (Mus musculus - house mouse) |
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Cdc23 (Rattus norvegicus - Norway rat) |
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Cdc23 (Chinchilla lanigera - long-tailed chinchilla) |
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CDC23 (Pan paniscus - bonobo/pygmy chimpanzee) |
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CDC23 (Canis lupus familiaris - dog) |
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Cdc23 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
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CDC23 (Sus scrofa - pig) |
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CDC23 (Chlorocebus sabaeus - green monkey) |
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Cdc23 (Heterocephalus glaber - naked mole-rat) |
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Variants in CDC23
10 total Variants |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 | copy number gain | See cases [RCV000051193] | Chr5:130860928..155321811 [GRCh38] Chr5:130196621..154701371 [GRCh37] Chr5:130224520..154681564 [NCBI36] Chr5:5q23.3-33.2 |
pathogenic |
GRCh38/hg38 5q31.1-31.2(chr5:133401565-138437038)x1 | copy number loss | See cases [RCV000052114] | Chr5:133401565..138437038 [GRCh38] Chr5:132737257..137772727 [GRCh37] Chr5:132765156..137800626 [NCBI36] Chr5:5q31.1-31.2 |
pathogenic |
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 | copy number loss | See cases [RCV000053524] | Chr5:106619588..156124387 [GRCh38] Chr5:105955289..155551397 [GRCh37] Chr5:105983188..155483975 [NCBI36] Chr5:5q21.3-33.2 |
pathogenic |
GRCh38/hg38 5q31.1-31.3(chr5:135297294-140106003)x3 | copy number gain | See cases [RCV000133750] | Chr5:135297294..140106003 [GRCh38] Chr5:134632984..139485588 [GRCh37] Chr5:134660883..139465772 [NCBI36] Chr5:5q31.1-31.3 |
pathogenic |
GRCh38/hg38 5q31.2-31.3(chr5:137836682-140696361)x3 | copy number gain | See cases [RCV000134725] | Chr5:137836682..140696361 [GRCh38] Chr5:137172371..140075946 [GRCh37] Chr5:137200270..140056130 [NCBI36] Chr5:5q31.2-31.3 |
pathogenic |
GRCh38/hg38 5q31.2(chr5:138179894-139039890)x3 | copy number gain | See cases [RCV000135679] | Chr5:138179894..139039890 [GRCh38] Chr5:137515583..138375579 [GRCh37] Chr5:137543482..138403478 [NCBI36] Chr5:5q31.2 |
uncertain significance |
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 | copy number gain | See cases [RCV000138808] | Chr5:129847794..153353546 [GRCh38] Chr5:129183487..152733106 [GRCh37] Chr5:129211386..152713299 [NCBI36] Chr5:5q23.3-33.2 |
pathogenic |
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 | copy number gain | not provided [RCV000487658] | Chr5:94844077..178830410 [GRCh37] Chr5:5q15-35.3 |
likely benign |
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 | copy number gain | See cases [RCV000449349] | Chr5:130125085..157574910 [GRCh37] Chr5:5q23.3-33.3 |
pathogenic |
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) | copy number gain | See cases [RCV000510723] | Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 | copy number gain | See cases [RCV000448245] | Chr5:106716357..180687338 [GRCh37] Chr5:5q21.3-35.3 |
pathogenic |
NC_000005.9:g.(?_86400000)_(154000000_?)del | deletion | Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] | Chr5:86400000..154000000 [GRCh37] Chr5:5q14.3-33.2 |
pathogenic |
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 | copy number loss | See cases [RCV000511978] | Chr5:17628741..176575720 [GRCh37] Chr5:5p15.1-q35.2 |
pathogenic |
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 | copy number gain | See cases [RCV000512039] | Chr5:113577..180719789 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
NM_004661.4(CDC23):c.1690A>G (p.Thr564Ala) | single nucleotide variant | Inborn genetic diseases [RCV003280347] | Chr5:138189082 [GRCh38] Chr5:137524771 [GRCh37] Chr5:5q31.2 |
uncertain significance |
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 | copy number gain | not provided [RCV000744323] | Chr5:25328..180693344 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 | copy number gain | not provided [RCV000744317] | Chr5:13648..180905029 [GRCh37] Chr5:5p15.33-q35.3 |
pathogenic |
Single allele | deletion | Neurodevelopmental disorder [RCV000787436] | Chr5:14685137..149511942 [GRCh37] Chr5:5p15.2-q32 |
uncertain significance |
NM_004661.4(CDC23):c.1286+10G>A | single nucleotide variant | not provided [RCV000949502] | Chr5:138192259 [GRCh38] Chr5:137527948 [GRCh37] Chr5:5q31.2 |
benign |
NM_004661.4(CDC23):c.1623T>C (p.Asp541=) | single nucleotide variant | not provided [RCV000964935] | Chr5:138189633 [GRCh38] Chr5:137525322 [GRCh37] Chr5:5q31.2 |
benign |
NC_000005.9:g.(?_136633338)_(140998481_?)dup | duplication | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] | Chr5:136633338..140998481 [GRCh37] Chr5:5q31.2-31.3 |
uncertain significance |
GRCh37/hg19 5q31.2(chr5:136409875-137739167) | copy number loss | Microcephaly [RCV001352638] | Chr5:136409875..137739167 [GRCh37] Chr5:5q31.2 |
pathogenic |
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) | copy number gain | not specified [RCV002053526] | Chr5:130125085..157574910 [GRCh37] Chr5:5q23.3-33.3 |
pathogenic |
GRCh37/hg19 5q31.1-31.2(chr5:132031902-137623639) | copy number loss | not specified [RCV002053530] | Chr5:132031902..137623639 [GRCh37] Chr5:5q31.1-31.2 |
pathogenic |
NC_000005.9:g.(?_136957787)_(140078137_?)dup | duplication | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV003116437] | Chr5:136957787..140078137 [GRCh37] Chr5:5q31.2-31.3 |
uncertain significance |
NC_000005.9:g.(?_136957787)_(138861289_?)del | deletion | STING-associated vasculopathy with onset in infancy [RCV003113978] | Chr5:136957787..138861289 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_004661.4(CDC23):c.21G>T (p.Met7Ile) | single nucleotide variant | Inborn genetic diseases [RCV002823161] | Chr5:138213292 [GRCh38] Chr5:137548981 [GRCh37] Chr5:5q31.2 |
likely benign |
NM_004661.4(CDC23):c.1595G>T (p.Cys532Phe) | single nucleotide variant | Inborn genetic diseases [RCV002793219] | Chr5:138189661 [GRCh38] Chr5:137525350 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_004661.4(CDC23):c.286G>A (p.Val96Ile) | single nucleotide variant | Inborn genetic diseases [RCV002936796] | Chr5:138206633 [GRCh38] Chr5:137542322 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_004661.4(CDC23):c.1742A>G (p.Asn581Ser) | single nucleotide variant | Inborn genetic diseases [RCV002674146] | Chr5:138189030 [GRCh38] Chr5:137524719 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_004661.4(CDC23):c.343T>A (p.Tyr115Asn) | single nucleotide variant | Inborn genetic diseases [RCV003256492] | Chr5:138206576 [GRCh38] Chr5:137542265 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_004661.4(CDC23):c.322G>A (p.Gly108Ser) | single nucleotide variant | Inborn genetic diseases [RCV003214874] | Chr5:138206597 [GRCh38] Chr5:137542286 [GRCh37] Chr5:5q31.2 |
uncertain significance |
NM_004661.4(CDC23):c.1270C>T (p.Arg424Trp) | single nucleotide variant | Inborn genetic diseases [RCV003195012] | Chr5:138192285 [GRCh38] Chr5:137527974 [GRCh37] Chr5:5q31.2 |
uncertain significance |
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. |
RH48651 |
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WI-14323 |
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RH91186 |
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D5S1673E |
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RH48461 |
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RH44568 |
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alimentary part of gastrointestinal system | circulatory system | endocrine system | exocrine system | hemolymphoid system | hepatobiliary system | integumental system | musculoskeletal system | nervous system | renal system | reproductive system | respiratory system | sensory system | visual system | adipose tissue | appendage | entire extraembryonic component | pharyngeal arch | |
High | ||||||||||||||||||
Medium | 2082 | 1387 | 1345 | 318 | 1152 | 186 | 3547 | 937 | 1974 | 336 | 1422 | 1540 | 149 | 1 | 1069 | 2005 | 6 | |
Low | 357 | 1591 | 381 | 306 | 787 | 279 | 810 | 1259 | 1760 | 83 | 38 | 73 | 26 | 135 | 783 | 2 | ||
Below cutoff | 13 | 12 | 1 |
RefSeq Transcripts | NM_004661 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
GenBank Nucleotide | AB011472 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC106752 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AF053977 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AF191341 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK223250 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK291610 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK304635 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AY603103 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC005258 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC010944 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC017713 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BT009810 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471062 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CP068273 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | ENST00000394884 ⟹ ENSP00000378348 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000394886 ⟹ ENSP00000378350 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000464806 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000471692 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000475021 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000482948 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000483961 ⟹ ENSP00000422505 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000505120 ⟹ ENSP00000423704 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | ENST00000511383 ⟹ ENSP00000422902 | ||||||||
Type: | CODING | ||||||||
Position: |
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RefSeq Acc Id: | NM_004661 ⟹ NP_004652 | ||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||
Position: |
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Sequence: |
Protein RefSeqs | NP_004652 | (Get FASTA) | NCBI Sequence Viewer |
GenBank Protein | AAC70920 | (Get FASTA) | NCBI Sequence Viewer |
AAF05755 | (Get FASTA) | NCBI Sequence Viewer | |
AAH05258 | (Get FASTA) | NCBI Sequence Viewer | |
AAH10944 | (Get FASTA) | NCBI Sequence Viewer | |
AAH17713 | (Get FASTA) | NCBI Sequence Viewer | |
AAP88812 | (Get FASTA) | NCBI Sequence Viewer | |
AAS99353 | (Get FASTA) | NCBI Sequence Viewer | |
BAA75628 | (Get FASTA) | NCBI Sequence Viewer | |
BAD96970 | (Get FASTA) | NCBI Sequence Viewer | |
BAF84299 | (Get FASTA) | NCBI Sequence Viewer | |
BAG65414 | (Get FASTA) | NCBI Sequence Viewer | |
EAW62154 | (Get FASTA) | NCBI Sequence Viewer | |
EAW62155 | (Get FASTA) | NCBI Sequence Viewer | |
EAW62156 | (Get FASTA) | NCBI Sequence Viewer | |
Ensembl Protein | ENSP00000378348.3 | ||
ENSP00000378350 | |||
ENSP00000378350.2 | |||
ENSP00000422505.1 | |||
ENSP00000422902.1 | |||
ENSP00000423704.1 | |||
GenBank Protein | Q9UJX2 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_004652 ⟸ NM_004661 |
- UniProtKB: | Q53FN2 (UniProtKB/Swiss-Prot), O75433 (UniProtKB/Swiss-Prot), D3DQB7 (UniProtKB/Swiss-Prot), B7WP05 (UniProtKB/Swiss-Prot), B4E3A2 (UniProtKB/Swiss-Prot), A8K6E5 (UniProtKB/Swiss-Prot), Q9BS73 (UniProtKB/Swiss-Prot), Q9UJX2 (UniProtKB/Swiss-Prot) |
- Sequence: |
RefSeq Acc Id: | ENSP00000423704 ⟸ ENST00000505120 |
RefSeq Acc Id: | ENSP00000422505 ⟸ ENST00000483961 |
RefSeq Acc Id: | ENSP00000422902 ⟸ ENST00000511383 |
RefSeq Acc Id: | ENSP00000378350 ⟸ ENST00000394886 |
RefSeq Acc Id: | ENSP00000378348 ⟸ ENST00000394884 |
Name | Modeler | Protein Id | AA Range | Protein Structure |
AF-Q9UJX2-F1-model_v2 | AlphaFold | Q9UJX2 | 1-597 | view protein structure |
RGD ID: | 6802947 | ||||||||
Promoter ID: | HG_KWN:51199 | ||||||||
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: | ENST00000394884, NM_004661, OTTHUMT00000314050, OTTHUMT00000314051 | ||||||||
Position: |
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RGD ID: | 6852356 | ||||||||
Promoter ID: | EP73985 | ||||||||
Type: | multiple initiation site | ||||||||
Name: | HS_CDC23 | ||||||||
Description: | CDC23 (cell division cycle 23, yeast, homolog). | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Experiment Methods: | Mammalian gene collection (MGC) full-length cDNA cloning | ||||||||
Position: |
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RGD ID: | 6870696 | ||||||||
Promoter ID: | EPDNEW_H8513 | ||||||||
Type: | initiation region | ||||||||
Name: | CDC23_1 | ||||||||
Description: | cell division cycle 23 | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
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Database | Acc Id | Source(s) |
AGR Gene | HGNC:1724 | AgrOrtholog |
COSMIC | CDC23 | COSMIC |
Ensembl Genes | ENSG00000094880 | Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
Ensembl Transcript | ENST00000394884.7 | UniProtKB/Swiss-Prot |
ENST00000394886 | ENTREZGENE | |
ENST00000394886.7 | UniProtKB/Swiss-Prot | |
ENST00000483961.6 | UniProtKB/TrEMBL | |
ENST00000505120.1 | UniProtKB/TrEMBL | |
ENST00000511383.5 | UniProtKB/TrEMBL | |
Gene3D-CATH | 1.25.40.10 | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL |
GTEx | ENSG00000094880 | GTEx |
HGNC ID | HGNC:1724 | ENTREZGENE |
Human Proteome Map | CDC23 | Human Proteome Map |
InterPro | APC8 | UniProtKB/Swiss-Prot |
TPR-like_helical_dom_sf | UniProtKB/Swiss-Prot, UniProtKB/TrEMBL | |
TPR_repeat | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:8697 | UniProtKB/Swiss-Prot |
NCBI Gene | 8697 | ENTREZGENE |
OMIM | 603462 | OMIM |
PANTHER | CELL DIVISION CYCLE 16,23,27 | UniProtKB/Swiss-Prot |
CELL DIVISION CYCLE PROTEIN 23 HOMOLOG | UniProtKB/Swiss-Prot | |
Pfam | ANAPC8 | UniProtKB/Swiss-Prot |
TPR_11 | UniProtKB/Swiss-Prot | |
TPR_8 | UniProtKB/Swiss-Prot | |
PharmGKB | PA26258 | PharmGKB |
PROSITE | TPR | UniProtKB/Swiss-Prot |
TPR_REGION | UniProtKB/Swiss-Prot | |
SMART | TPR | UniProtKB/Swiss-Prot |
Superfamily-SCOP | SSF48452 | UniProtKB/Swiss-Prot |
UniProt | A8K6E5 | ENTREZGENE |
B4E3A2 | ENTREZGENE | |
B7WP05 | ENTREZGENE | |
CDC23_HUMAN | UniProtKB/Swiss-Prot | |
D3DQB7 | ENTREZGENE | |
D6RBY8_HUMAN | UniProtKB/TrEMBL | |
D6RCF8_HUMAN | UniProtKB/TrEMBL | |
H0Y936_HUMAN | UniProtKB/TrEMBL | |
O75433 | ENTREZGENE | |
Q53FN2 | ENTREZGENE | |
Q9BS73 | ENTREZGENE | |
Q9UJX2 | ENTREZGENE | |
UniProt Secondary | A8K6E5 | UniProtKB/Swiss-Prot |
B4E3A2 | UniProtKB/Swiss-Prot | |
B7WP05 | UniProtKB/Swiss-Prot | |
D3DQB7 | UniProtKB/Swiss-Prot | |
O75433 | UniProtKB/Swiss-Prot | |
Q53FN2 | UniProtKB/Swiss-Prot | |
Q9BS73 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2013-01-22 | CDC23 | cell division cycle 23 | cell division cycle 23 homolog (S. cerevisiae) | Symbol and/or name change | 5135510 | APPROVED | |
2011-08-17 | CDC23 | cell division cycle 23 homolog (S. cerevisiae) | CDC23 | cell division cycle 23 homolog (S. cerevisiae) | Symbol and/or name change | 5135510 | APPROVED |