WDR97 (WD repeat domain 97) - Rat Genome Database

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Gene: WDR97 (WD repeat domain 97) Homo sapiens
Analyze
Symbol: WDR97
Name: WD repeat domain 97
RGD ID: 1601920
HGNC Page HGNC
Description: The function and protein-coding potential of this gene is unknown. The exon combination is based on AB058778.1 for which two possible open reading frames can be predicted (with start codons at nucleotide 26 or 2614). The position of the first ORF stop codon is consistent with a prediction of nonsense-mediated decay. Given the observation of the first ORF and its length, a predicted translation of the second ORF is inconsistent with the translation leaky scanning theory. Therefore, this gene is represented as a non-protein-coding transcript. [provided by RefSeq, Oct 2008]
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: KIAA1875; WD repeat-containing protein 97; WD repeat-containing protein KIAA1875
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8144,107,726 - 144,118,328 (+)EnsemblGRCh38hg38GRCh38
GRCh388144,107,739 - 144,118,328 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh378145,162,642 - 145,173,231 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 368145,234,623 - 145,245,206 (+)NCBINCBI36hg18NCBI36
Celera8141,500,152 - 141,510,742 (+)NCBI
Cytogenetic Map8q24.3NCBI
HuRef8140,438,512 - 140,449,102 (+)NCBIHuRef
CHM1_18145,203,012 - 145,213,602 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

References - curated
1. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:11347906   PMID:14702039   PMID:16169070   PMID:28675297  


Genomics

Comparative Map Data
WDR97
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl8144,107,726 - 144,118,328 (+)EnsemblGRCh38hg38GRCh38
GRCh388144,107,739 - 144,118,328 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh378145,162,642 - 145,173,231 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 368145,234,623 - 145,245,206 (+)NCBINCBI36hg18NCBI36
Celera8141,500,152 - 141,510,742 (+)NCBI
Cytogenetic Map8q24.3NCBI
HuRef8140,438,512 - 140,449,102 (+)NCBIHuRef
CHM1_18145,203,012 - 145,213,602 (+)NCBICHM1_1
Gm35339
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391576,238,649 - 76,249,141 (+)NCBIGRCm39mm39
GRCm39 Ensembl1576,238,632 - 76,249,401 (+)Ensembl
GRCm381576,354,449 - 76,364,941 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1576,354,432 - 76,365,201 (+)EnsemblGRCm38mm10GRCm38
MGSCv371576,184,974 - 76,192,269 (+)MERGEGRCm37mm9NCBIm37
Celera1577,854,510 - 77,863,925 (+)NCBICelera
Cytogenetic Map15D3NCBI
Wdr97
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.27108,078,280 - 108,087,028 (+)NCBI
Rnor_6.0 Ensembl7117,420,788 - 117,429,504 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.07117,420,779 - 117,429,497 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.07117,408,407 - 117,417,227 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47114,405,497 - 114,414,108 (+)NCBIRGSC3.4rn4RGSC3.4
Celera7104,430,636 - 104,439,354 (+)NCBICelera
Cytogenetic Map7q34NCBI
Wdr97
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554542,769,387 - 2,777,921 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554542,769,356 - 2,778,024 (+)NCBIChiLan1.0ChiLan1.0
WDR97
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.18143,865,981 - 143,874,738 (+)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v08140,874,055 - 140,882,725 (+)NCBIMhudiblu_PPA_v0panPan3
WDR97
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11337,601,804 - 37,612,044 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1337,565,502 - 37,577,451 (+)NCBI
ROS_Cfam_1.01338,078,032 - 38,090,010 (+)NCBI
UMICH_Zoey_3.11337,750,090 - 37,760,466 (+)NCBI
UNSW_CanFamBas_1.01337,878,770 - 37,889,123 (+)NCBI
UU_Cfam_GSD_1.01338,354,949 - 38,366,912 (+)NCBI
Wdr97
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303638,033 - 647,015 (-)NCBI
SpeTri2.0NW_0049364708,064,132 - 8,073,157 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
WDR97
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.14588,629 - 597,333 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24741,756 - 750,444 (-)NCBISscrofa10.2Sscrofa10.2susScr3
WDR97
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.18138,322,976 - 138,327,761 (+)NCBI
Wdr97
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462473512,706,710 - 12,715,795 (-)NCBI

Position Markers
RH79825  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378145,162,267 - 145,162,498UniSTSGRCh37
Build 368145,234,255 - 145,234,486RGDNCBI36
Celera8141,499,790 - 141,500,021RGD
Cytogenetic Map8q24.3UniSTS
HuRef8140,438,150 - 140,438,381UniSTS
RH65611  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh378145,160,874 - 145,161,088UniSTSGRCh37
Build 368145,232,862 - 145,233,076RGDNCBI36
Celera8141,498,397 - 141,498,611RGD
Cytogenetic Map8q24.3UniSTS
HuRef8140,436,757 - 140,436,971UniSTS
GeneMap99-GB4 RH Map8563.39UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4651
Count of miRNA genes:1111
Interacting mature miRNAs:1384
Transcripts:ENST00000323662, ENST00000525150, ENST00000528691, ENST00000529209, ENST00000533108, ENST00000534167
Prediction methods:Microtar, 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.


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 46 3 1 238 363 17
Low 1895 1779 1540 544 1183 394 3182 1055 3145 225 985 1457 158 913 2039 1
Below cutoff 536 1204 133 72 741 64 1170 1136 348 185 100 128 13 291 749 3

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000323662   ⟹   ENSP00000320648
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,107,739 - 144,118,328 (+)Ensembl
RefSeq Acc Id: ENST00000525150
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,109,699 - 144,116,390 (+)Ensembl
RefSeq Acc Id: ENST00000528691
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,109,727 - 144,116,382 (+)Ensembl
RefSeq Acc Id: ENST00000529209
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,112,469 - 144,116,383 (+)Ensembl
RefSeq Acc Id: ENST00000533108
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,109,727 - 144,111,205 (+)Ensembl
RefSeq Acc Id: ENST00000534167   ⟹   ENSP00000435391
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl8144,107,726 - 144,118,315 (+)Ensembl
RefSeq Acc Id: NM_001316309   ⟹   NP_001303238
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,107,739 - 144,118,328 (+)NCBI
Sequence:
RefSeq Acc Id: XM_024447145   ⟹   XP_024302913
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh388144,108,871 - 144,116,392 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001303238   ⟸   NM_001316309
- UniProtKB: A6NE52 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_024302913   ⟸   XM_024447145
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000435391   ⟸   ENST00000534167
RefSeq Acc Id: ENSP00000320648   ⟸   ENST00000323662
Protein Domains
WD_REPEATS_REGION

Promoters
RGD ID:6806825
Promoter ID:HG_KWN:62315
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:NR_024207
Position:
Human AssemblyChrPosition (strand)Source
Build 368145,234,261 - 145,234,942 (+)MPROMDB
RGD ID:6806826
Promoter ID:HG_KWN:62316
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:UC010MFQ.1,   UC010MFR.1
Position:
Human AssemblyChrPosition (strand)Source
Build 368145,235,461 - 145,236,647 (+)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 8q22.1-24.3(chr8:94682154-145068656)x3 copy number gain See cases [RCV000134353] Chr8:94682154..145068656 [GRCh38]
Chr8:95694382..146294042 [GRCh37]
Chr8:95763558..146264846 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.22-24.3(chr8:130639182-145068712)x3 copy number gain See cases [RCV000137644] Chr8:130639182..145068712 [GRCh38]
Chr8:131651428..146294098 [GRCh37]
Chr8:131720610..146264902 [NCBI36]
Chr8:8q24.22-24.3
pathogenic|conflicting data from submitters
GRCh38/hg38 8q24.3(chr8:139236824-145068712)x3 copy number gain See cases [RCV000137466] Chr8:139236824..145068712 [GRCh38]
Chr8:140249067..146294098 [GRCh37]
Chr8:140318249..146264902 [NCBI36]
Chr8:8q24.3
likely pathogenic
GRCh38/hg38 8q24.3(chr8:139004218-145049449)x3 copy number gain See cases [RCV000137340] Chr8:139004218..145049449 [GRCh38]
Chr8:140016461..146274835 [GRCh37]
Chr8:140085643..146245639 [NCBI36]
Chr8:8q24.3
likely pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124498498-145068712)x3 copy number gain See cases [RCV000137346] Chr8:124498498..145068712 [GRCh38]
Chr8:125510739..146294098 [GRCh37]
Chr8:125579920..146264902 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3 copy number gain See cases [RCV000138643] Chr8:241605..145054781 [GRCh38]
Chr8:191605..146280167 [GRCh37]
Chr8:181605..146250971 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.3-24.3(chr8:87931152-145068712)x3 copy number gain See cases [RCV000138551] Chr8:87931152..145068712 [GRCh38]
Chr8:88943380..146294098 [GRCh37]
Chr8:89012496..146264902 [NCBI36]
Chr8:8q21.3-24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:77480050-145068712)x3 copy number gain See cases [RCV000139036] Chr8:77480050..145068712 [GRCh38]
Chr8:78392286..146294098 [GRCh37]
Chr8:78554841..146264902 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:97382873-145070385)x3 copy number gain See cases [RCV000140447] Chr8:97382873..145070385 [GRCh38]
Chr8:98395101..146295771 [GRCh37]
Chr8:98464277..146266575 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:141738068-144140607)x1 copy number loss See cases [RCV000140913] Chr8:141738068..144140607 [GRCh38]
Chr8:142764538..145195510 [GRCh37]
Chr8:142823655..145267498 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3 copy number gain See cases [RCV000141808] Chr8:208048..145070385 [GRCh38]
Chr8:158048..146295771 [GRCh37]
Chr8:148048..146266575 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:100867343-145070385)x3 copy number gain See cases [RCV000141694] Chr8:100867343..145070385 [GRCh38]
Chr8:101879571..146295771 [GRCh37]
Chr8:101948747..146266575 [NCBI36]
Chr8:8q22.3-24.3
pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3 copy number gain See cases [RCV000142021] Chr8:21291522..145070385 [GRCh38]
Chr8:21149033..146295771 [GRCh37]
Chr8:21193313..146266575 [NCBI36]
Chr8:8p21.3-q24.3
pathogenic
GRCh38/hg38 8q22.3-24.3(chr8:103306336-145068712)x3 copy number gain See cases [RCV000142810] Chr8:103306336..145068712 [GRCh38]
Chr8:104318564..146294098 [GRCh37]
Chr8:104387740..146264902 [NCBI36]
Chr8:8q22.3-24.3
pathogenic|likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3 copy number gain See cases [RCV000142858] Chr8:226452..145068712 [GRCh38]
Chr8:176452..146294098 [GRCh37]
Chr8:166452..146264902 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.13-24.3(chr8:78614077-145054634)x3 copy number gain See cases [RCV000142597] Chr8:78614077..145054634 [GRCh38]
Chr8:79526312..146280020 [GRCh37]
Chr8:79688867..146250824 [NCBI36]
Chr8:8q21.13-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000148092] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q21.2-24.3(chr8:85765999-145070385)x3 copy number gain See cases [RCV000143659] Chr8:85765999..145070385 [GRCh38]
Chr8:86778228..146295771 [GRCh37]
Chr8:86863079..146266575 [NCBI36]
Chr8:8q21.2-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000148117] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8q24.21-24.3(chr8:128220912-145049449)x3 copy number gain See cases [RCV000050830] Chr8:128220912..145049449 [GRCh38]
Chr8:129233158..146274835 [GRCh37]
Chr8:129302340..146245639 [NCBI36]
Chr8:8q24.21-24.3
pathogenic
GRCh38/hg38 8q23.3-24.3(chr8:113580402-145054634)x3 copy number gain See cases [RCV000050638] Chr8:113580402..145054634 [GRCh38]
Chr8:114592631..146280020 [GRCh37]
Chr8:114661807..146250824 [NCBI36]
Chr8:8q23.3-24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3 copy number gain See cases [RCV000051206] Chr8:241530..145049449 [GRCh38]
Chr8:191530..146274835 [GRCh37]
Chr8:181530..146245639 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:144002671-144796947)x3 copy number gain See cases [RCV000050640] Chr8:144002671..144796947 [GRCh38]
Chr8:145076839..146022332 [GRCh37]
Chr8:145148827..145993136 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8q22.1-24.3(chr8:95606052-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053677]|See cases [RCV000053677] Chr8:95606052..145054775 [GRCh38]
Chr8:96618280..146280161 [GRCh37]
Chr8:96687456..146250965 [NCBI36]
Chr8:8q22.1-24.3
pathogenic
GRCh38/hg38 8q24.13-24.3(chr8:124514090-145054634)x3 copy number gain See cases [RCV000053678] Chr8:124514090..145054634 [GRCh38]
Chr8:125526331..146280020 [GRCh37]
Chr8:125595512..146250824 [NCBI36]
Chr8:8q24.13-24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:139447227-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053701]|See cases [RCV000053701] Chr8:139447227..145054775 [GRCh38]
Chr8:140459470..146280161 [GRCh37]
Chr8:140528652..146250965 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:144002671-145054634)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053702]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053702]|See cases [RCV000053702] Chr8:144002671..145054634 [GRCh38]
Chr8:145076839..146280020 [GRCh37]
Chr8:145148827..146250824 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3 copy number gain See cases [RCV000053602] Chr8:241530..145054634 [GRCh38]
Chr8:191530..146280020 [GRCh37]
Chr8:181530..146250824 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]|See cases [RCV000053604] Chr8:244417..145054775 [GRCh38]
Chr8:194417..146280161 [GRCh37]
Chr8:184417..146250965 [NCBI36]
Chr8:8p23.3-q24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:143684819-144287978)x1 copy number loss See cases [RCV000054310] Chr8:143684819..144287978 [GRCh38]
Chr8:144940777..145511679 [GRCh37]
Chr8:144838977..145482487 [NCBI36]
Chr8:8q24.3
pathogenic
GRCh38/hg38 8q24.3(chr8:144002471-145054775)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054311]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054311]|See cases [RCV000054311] Chr8:144002471..145054775 [GRCh38]
Chr8:145076639..146280161 [GRCh37]
Chr8:145148627..146250965 [NCBI36]
Chr8:8q24.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26959 AgrOrtholog
COSMIC WDR97 COSMIC
Ensembl Genes ENSG00000179698 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000320648 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000435391 UniProtKB/TrEMBL
Ensembl Transcript ENST00000323662 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000534167 UniProtKB/TrEMBL
Gene3D-CATH 2.130.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000179698 GTEx
HGNC ID HGNC:26959 ENTREZGENE
Human Proteome Map WDR97 Human Proteome Map
InterPro G-protein_beta_WD-40_rep UniProtKB/TrEMBL
  WD40/YVTN_repeat-like_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD40_repeat_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:340390 UniProtKB/Swiss-Prot
NCBI Gene 340390 ENTREZGENE
Pfam WD40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA142671601 PharmGKB
PRINTS GPROTEINBRPT UniProtKB/TrEMBL
PROSITE WD_REPEATS_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD_REPEATS_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WD_REPEATS_REGION UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART WD40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF50978 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6NE52 ENTREZGENE
  E9PKB8_HUMAN UniProtKB/TrEMBL
  WDR97_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary Q96JF2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-10-20 WDR97  WD repeat domain 97  KIAA1875  KIAA1875  Symbol and/or name change 5135510 APPROVED
2011-09-01 KIAA1875  KIAA1875  KIAA1875  KIAA1875  Symbol and/or name change 5135510 APPROVED