CCDC28A (coiled-coil domain containing 28A) - Rat Genome Database

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Gene: CCDC28A (coiled-coil domain containing 28A) Homo sapiens
Analyze
Symbol: CCDC28A
Name: coiled-coil domain containing 28A
RGD ID: 1351078
HGNC Page HGNC:21098
Description: This gene encodes a coiled-coil domain containing protein. Although the specific function of this gene has not yet been determined, this gene is a known translocation partner of nucleoporin 98 in acute leukemias. The resulting fusion gene produces a nucleoporin 98-coiled-coil domain-containing protein 28A chimeric protein which may be involved in promoting myeloproliferative neoplasms. [provided by RefSeq, Jan 2017]
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: C6orf80; CCRL1AP; chemokine C-C motif receptor-like 1 adjacent; coiled-coil domain-containing protein 28A; DKFZp586D0623; MGC131913
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
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
GRCh386138,773,769 - 138,793,319 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6138,773,769 - 138,793,319 (+)EnsemblGRCh38hg38GRCh38
GRCh376139,094,906 - 139,114,456 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 366139,136,350 - 139,156,149 (+)NCBINCBI36Build 36hg18NCBI36
Build 346139,136,349 - 139,156,147NCBI
Celera6139,834,761 - 139,854,557 (+)NCBICelera
Cytogenetic Map6q24.1NCBI
HuRef6136,656,063 - 136,675,758 (+)NCBIHuRef
CHM1_16139,357,677 - 139,377,457 (+)NCBICHM1_1
T2T-CHM13v2.06139,962,307 - 139,981,863 (+)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

Molecular Function

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
Additional References at PubMed
PMID:12477932   PMID:14574404   PMID:15489334   PMID:16028218   PMID:19322201   PMID:22058212   PMID:23602568   PMID:25416956   PMID:26673895   PMID:27432908   PMID:31515488   PMID:31871319  
PMID:32296183   PMID:33060197   PMID:33961781   PMID:35944360   PMID:36724073  


Genomics

Comparative Map Data
CCDC28A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386138,773,769 - 138,793,319 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6138,773,769 - 138,793,319 (+)EnsemblGRCh38hg38GRCh38
GRCh376139,094,906 - 139,114,456 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 366139,136,350 - 139,156,149 (+)NCBINCBI36Build 36hg18NCBI36
Build 346139,136,349 - 139,156,147NCBI
Celera6139,834,761 - 139,854,557 (+)NCBICelera
Cytogenetic Map6q24.1NCBI
HuRef6136,656,063 - 136,675,758 (+)NCBIHuRef
CHM1_16139,357,677 - 139,377,457 (+)NCBICHM1_1
T2T-CHM13v2.06139,962,307 - 139,981,863 (+)NCBIT2T-CHM13v2.0
Ccdc28a
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391018,089,424 - 18,110,940 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1018,089,424 - 18,110,746 (-)EnsemblGRCm39 Ensembl
GRCm381018,213,676 - 18,235,805 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1018,213,676 - 18,234,998 (-)EnsemblGRCm38mm10GRCm38
MGSCv371017,933,491 - 17,954,787 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361017,906,343 - 17,924,394 (-)NCBIMGSCv36mm8
MGSCv361018,092,971 - 18,111,028 (-)NCBIMGSCv36mm8
Celera1018,112,973 - 18,144,756 (-)NCBICelera
Cytogenetic Map10A3NCBI
cM Map107.53NCBI
Ccdc28a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8114,677,451 - 14,692,729 (-)NCBIGRCr8
mRatBN7.2112,857,668 - 12,872,944 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl112,857,666 - 12,873,003 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx112,629,455 - 12,644,028 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0118,631,379 - 18,645,952 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0112,837,959 - 12,852,996 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0113,384,153 - 13,395,643 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl113,384,156 - 13,395,370 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0115,072,108 - 15,083,495 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4113,269,164 - 13,284,200 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1113,269,225 - 13,284,298 (-)NCBI
Celera111,314,407 - 11,329,332 (-)NCBICelera
Cytogenetic Map1p12NCBI
Ccdc28a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543620,846,227 - 20,873,552 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543620,849,493 - 20,875,284 (-)NCBIChiLan1.0ChiLan1.0
CCDC28A
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25158,740,208 - 158,759,522 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16156,637,791 - 156,657,108 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v06136,533,841 - 136,553,303 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16140,619,716 - 140,638,830 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl6140,619,716 - 140,638,830 (+)Ensemblpanpan1.1panPan2
CCDC28A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1131,044,102 - 31,058,173 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl131,044,126 - 31,057,800 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha131,920,945 - 31,935,141 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0131,207,239 - 31,221,442 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl131,207,395 - 31,221,439 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1131,084,696 - 31,098,895 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0130,966,784 - 30,981,007 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0131,276,492 - 31,290,694 (+)NCBIUU_Cfam_GSD_1.0
CCDC28A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl125,647,000 - 25,663,273 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1125,646,997 - 25,663,277 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2128,782,282 - 28,798,563 (-)NCBISscrofa10.2Sscrofa10.2susScr3
CCDC28A
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11334,596,584 - 34,615,633 (-)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_0236660406,769,559 - 6,788,468 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Ccdc28a
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462475315,157,391 - 15,185,029 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462475315,157,509 - 15,185,253 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CCDC28A
7 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_015439.3(CCDC28A):c.11G>A (p.Arg4Gln) single nucleotide variant Inborn genetic diseases [RCV003357447] Chr6:138776131 [GRCh38]
Chr6:139097268 [GRCh37]
Chr6:6q24.1
uncertain significance
GRCh38/hg38 6q23.3-25.3(chr6:135358150-155455117)x3 copy number gain See cases [RCV000136826] Chr6:135358150..155455117 [GRCh38]
Chr6:135679288..155776251 [GRCh37]
Chr6:135720981..155817943 [NCBI36]
Chr6:6q23.3-25.3
pathogenic
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 copy number gain See cases [RCV000139729] Chr6:74382807..142040500 [GRCh38]
Chr6:75092523..142361637 [GRCh37]
Chr6:75149243..142403330 [NCBI36]
Chr6:6q13-24.1
pathogenic
GRCh38/hg38 6q23.2-27(chr6:133537271-165875545)x3 copy number gain See cases [RCV000143444] Chr6:133537271..165875545 [GRCh38]
Chr6:133858409..166289033 [GRCh37]
Chr6:133900102..166209023 [NCBI36]
Chr6:6q23.2-27
pathogenic
GRCh37/hg19 6q23.3-24.3(chr6:135239633-146997510) copy number loss not provided [RCV000767713] Chr6:135239633..146997510 [GRCh37]
Chr6:6q23.3-24.3
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6q23.2-24.2(chr6:133077239-143761582)x1 copy number loss See cases [RCV000510451] Chr6:133077239..143761582 [GRCh37]
Chr6:6q23.2-24.2
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6q24.1(chr6:139102366-139328765)x3 copy number gain not provided [RCV000746058] Chr6:139102366..139328765 [GRCh37]
Chr6:6q24.1
benign
GRCh37/hg19 6q23.2-24.1(chr6:133817341-140038401)x1 copy number loss not provided [RCV001005848] Chr6:133817341..140038401 [GRCh37]
Chr6:6q23.2-24.1
pathogenic
NM_015439.3(CCDC28A):c.-155G>A single nucleotide variant Inborn genetic diseases [RCV003289968] Chr6:138773790 [GRCh38]
Chr6:139094927 [GRCh37]
Chr6:6q24.1
uncertain significance
GRCh37/hg19 6q23.3-24.1(chr6:135936688-140660269)x1 copy number loss not provided [RCV001249247] Chr6:135936688..140660269 [GRCh37]
Chr6:6q23.3-24.1
not provided
GRCh37/hg19 6q23.2-24.1(chr6:133810210-140046615)x1 copy number loss not provided [RCV001537931] Chr6:133810210..140046615 [GRCh37]
Chr6:6q23.2-24.1
pathogenic
GRCh37/hg19 6q24.1(chr6:139093282-140660265) copy number gain not specified [RCV002053629] Chr6:139093282..140660265 [GRCh37]
Chr6:6q24.1
uncertain significance
Single allele deletion Autoinflammatory syndrome, familial, Behcet-like [RCV002247731] Chr6:134838331..142160056 [GRCh38]
Chr6:6q23.3-24.1
pathogenic
NM_015439.3(CCDC28A):c.29G>A (p.Ser10Asn) single nucleotide variant Inborn genetic diseases [RCV003280873] Chr6:138776149 [GRCh38]
Chr6:139097286 [GRCh37]
Chr6:6q24.1
uncertain significance
GRCh37/hg19 6q24.1(chr6:139063032-139273184)x3 copy number gain not provided [RCV002474990] Chr6:139063032..139273184 [GRCh37]
Chr6:6q24.1
uncertain significance
NM_015439.3(CCDC28A):c.61G>A (p.Val21Ile) single nucleotide variant Myoepithelial tumor [RCV002463908] Chr6:138776181 [GRCh38]
Chr6:139097318 [GRCh37]
Chr6:6q24.1
uncertain significance
NM_015439.3(CCDC28A):c.-62C>G single nucleotide variant Inborn genetic diseases [RCV002969047] Chr6:138773883 [GRCh38]
Chr6:139095020 [GRCh37]
Chr6:6q24.1
uncertain significance
NM_015439.3(CCDC28A):c.-129G>A single nucleotide variant Inborn genetic diseases [RCV002762226] Chr6:138773816 [GRCh38]
Chr6:139094953 [GRCh37]
Chr6:6q24.1
uncertain significance
NM_015439.3(CCDC28A):c.475G>T (p.Asp159Tyr) single nucleotide variant Inborn genetic diseases [RCV002813723] Chr6:138785379 [GRCh38]
Chr6:139106516 [GRCh37]
Chr6:6q24.1
uncertain significance
NM_015439.3(CCDC28A):c.529G>C (p.Asp177His) single nucleotide variant Inborn genetic diseases [RCV003379252] Chr6:138792777 [GRCh38]
Chr6:139113914 [GRCh37]
Chr6:6q24.1
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:206
Count of miRNA genes:188
Interacting mature miRNAs:196
Transcripts:ENST00000332797
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.

Markers in Region
RH46863  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376139,114,224 - 139,114,381UniSTSGRCh37
Build 366139,155,917 - 139,156,074RGDNCBI36
Celera6139,854,325 - 139,854,482RGD
Cytogenetic Map6q23.1-q24.1UniSTS
HuRef6136,675,526 - 136,675,683UniSTS
GeneMap99-GB4 RH Map6555.33UniSTS
NCBI RH Map61561.4UniSTS
SHGC-31193  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376139,114,295 - 139,114,395UniSTSGRCh37
Build 366139,155,988 - 139,156,088RGDNCBI36
Celera6139,854,396 - 139,854,496RGD
Cytogenetic Map6q23.1-q24.1UniSTS
HuRef6136,675,597 - 136,675,697UniSTS
Stanford-G3 RH Map65791.0UniSTS
GeneMap99-GB4 RH Map6554.94UniSTS
Whitehead-RH Map6777.8UniSTS
NCBI RH Map61561.4UniSTS
GeneMap99-G3 RH Map66094.0UniSTS
STS-N33316  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376139,114,186 - 139,114,370UniSTSGRCh37
Build 366139,155,879 - 139,156,063RGDNCBI36
Celera6139,854,287 - 139,854,471RGD
Cytogenetic Map6q23.1-q24.1UniSTS
HuRef6136,675,488 - 136,675,672UniSTS
GeneMap99-GB4 RH Map6552.47UniSTS
NCBI RH Map61561.4UniSTS


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 2423 2547 1713 614 1925 456 3916 1499 3571 410 1439 1600 170 1171 2367 4
Low 9 437 10 8 23 8 439 694 137 8 9 8 33 421
Below cutoff

Sequence


RefSeq Acc Id: ENST00000332797   ⟹   ENSP00000332716
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6138,773,520 - 138,793,319 (+)Ensembl
RefSeq Acc Id: ENST00000611852   ⟹   ENSP00000479060
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6138,773,509 - 138,793,317 (+)Ensembl
RefSeq Acc Id: ENST00000617445   ⟹   ENSP00000482946
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6138,773,769 - 138,793,319 (+)Ensembl
RefSeq Acc Id: NM_001379071   ⟹   NP_001366000
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386138,773,769 - 138,783,155 (+)NCBI
T2T-CHM13v2.06139,962,307 - 139,971,693 (+)NCBI
Sequence:
RefSeq Acc Id: NM_015439   ⟹   NP_056254
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386138,773,769 - 138,793,319 (+)NCBI
GRCh376139,094,657 - 139,114,456 (+)RGD
Build 366139,136,350 - 139,156,149 (+)NCBI Archive
Celera6139,834,761 - 139,854,557 (+)RGD
HuRef6136,656,063 - 136,675,758 (+)ENTREZGENE
CHM1_16139,357,677 - 139,377,457 (+)NCBI
T2T-CHM13v2.06139,962,307 - 139,981,863 (+)NCBI
Sequence:
RefSeq Acc Id: NP_056254   ⟸   NM_015439
- Peptide Label: isoform 1
- UniProtKB: B4DUJ5 (UniProtKB/TrEMBL),   Q7Z6N9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001366000   ⟸   NM_001379071
- Peptide Label: isoform 2
RefSeq Acc Id: ENSP00000332716   ⟸   ENST00000332797
RefSeq Acc Id: ENSP00000479060   ⟸   ENST00000611852
RefSeq Acc Id: ENSP00000482946   ⟸   ENST00000617445

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8IWP9-F1-model_v2 AlphaFold Q8IWP9 1-274 view protein structure

Promoters
RGD ID:7209267
Promoter ID:EPDNEW_H10379
Type:initiation region
Name:CCDC28A_1
Description:coiled-coil domain containing 28A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386138,773,769 - 138,773,829EPDNEW
RGD ID:6803875
Promoter ID:HG_KWN:55194
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:ENST00000026464,   NM_015439
Position:
Human AssemblyChrPosition (strand)Source
Build 366139,135,996 - 139,136,687 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:21098 AgrOrtholog
COSMIC CCDC28A COSMIC
Ensembl Genes ENSG00000024862 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
Ensembl Transcript ENST00000617445 ENTREZGENE
  ENST00000617445.5 UniProtKB/TrEMBL
GTEx ENSG00000024862 GTEx
HGNC ID HGNC:21098 ENTREZGENE
Human Proteome Map CCDC28A Human Proteome Map
InterPro CCDC28 UniProtKB/TrEMBL, UniProtKB/Swiss-Prot
NCBI Gene 25901 ENTREZGENE
OMIM 615353 OMIM
PANTHER COILED-COIL DOMAIN-CONTAINING PROTEIN 28A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR13400 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam DUF4061 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134939277 PharmGKB
UniProt B4DUJ5 ENTREZGENE, UniProtKB/TrEMBL
  CC28A_HUMAN UniProtKB/Swiss-Prot
  Q7Z6N9 ENTREZGENE, UniProtKB/TrEMBL
  Q8IWP9 ENTREZGENE
  R9RSM4_HUMAN UniProtKB/TrEMBL
  R9RUD5_HUMAN UniProtKB/TrEMBL
  R9RUZ6_HUMAN UniProtKB/TrEMBL
UniProt Secondary E1P591 UniProtKB/Swiss-Prot
  Q32NC7 UniProtKB/Swiss-Prot
  Q66K67 UniProtKB/Swiss-Prot
  Q96E23 UniProtKB/Swiss-Prot
  Q9Y430 UniProtKB/Swiss-Prot