Imported Annotations - OMIM | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bardet-Biedl syndrome 19 | IAGP | 7240710 | OMIM |



![]() |
Create Name: | |
Description: |
![]() |
Save what matters to you |
{{ loginError }} |
Sign in with your RGD account |
Create New Account | Recover Password |
Analyze GeneStrainQTL List |
![]() Gene Annotator (Functional Annotation) unavailable |
![]() Gene Annotator (Annotation Distribution) unavailable |
![]() Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable |
Gene Annotator (Functional Annotation) |
Gene Annotator (Annotation Distribution) |
Variant Visualizer (Genomic Variants) |
![]() InterViewer (Protein-Protein Interactions) unavailable |
![]() Gviewer (Genome Viewer) unavailable |
![]() Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable |
InterViewer (Protein-Protein Interactions) |
GViewer (Genome Viewer) |
Variant Visualizer (Damaging Variants) |
![]() Gene Annotator (Annotation Comparison) unavailable |
![]() OLGA (Gene List Generator) unavailable |
![]() |
Gene Annotator (Annotation Comparison) |
OLGA (Gene List Generator) |
Excel (Download) |
![]() MOET (Multi-Ontology Enrichement) unavailable |
![]() GOLF (Gene-Ortholog Location Finder) unavailable |
|
MOET (Multi-Ontology Enrichement) |
GOLF (Gene-Ortholog Location Finder) |
Imported Annotations - OMIM | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bardet-Biedl syndrome 19 | IAGP | 7240710 | OMIM |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1. | GOA_HUMAN data from the GO Consortium |
2. | OMIM Disease Annotation Pipeline |
3. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
4. | RGD automated import pipeline for gene-chemical interactions |
5. | RGD automated import pipeline for human HPO-to-gene-to-disease annotations |
PubMed | 8889548 10591208 12477932 12529303 14702039 15461802 15489334 16189514 16751776 17276912 20301537 21873635 22022256 22939629 24488770 25416956 25443296 26389662 26638075 27173435 27432908 28514442 29229926 29704304 |
IFT27 (Homo sapiens - human) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ift27 (Mus musculus - house mouse) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ift27 (Rattus norvegicus - Norway rat) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ift27 (Chinchilla lanigera - long-tailed chinchilla) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IFT27 (Pan paniscus - bonobo/pygmy chimpanzee) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IFT27 (Canis lupus familiaris - dog) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ift27 (Ictidomys tridecemlineatus - thirteen-lined ground squirrel) |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
IFT27 (Sus scrofa - pig) |
|
RH45587 |
|
||||||||||||||||||||||||||||||||||||||||
WI-15209 |
|
||||||||||||||||||||||||||||||||||||||||
STS-T69764 |
|
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. |
RefSeq Transcripts | NG_034205 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
NM_001177701 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_001363003 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NM_006860 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
NR_033531 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
XM_017028540 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
GenBank Nucleotide | AA809074 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AB209424 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AI215119 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK090708 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK307105 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AK307382 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AL022729 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
AW236857 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC000566 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BM711121 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BT006815 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BX537634 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH471095 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CR456558 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DB457924 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
DB502180 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KF457438 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
Z80897 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_001177701 ⟹ NP_001171172 | |||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | |||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||
Position: |
|
|||||||||||||||||||||||||||||
Sequence: |
GAGGAGGAGGCGGGGCAGGTGGGCTATGGTTGCTTGGAGAGTGCATCCGGCCCGGTACTTGTGAhide sequence |
RefSeq Acc Id: | NM_001363003 ⟹ NP_001349932 | |||||||||
RefSeq Status: | REVIEWED | |||||||||
Type: | CODING | |||||||||
Position: |
|
RefSeq Acc Id: | NM_006860 ⟹ NP_006851 | ||||||||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | ||||||||||||||||||||||||||||||||||
Type: | CODING | ||||||||||||||||||||||||||||||||||
Position: |
|
||||||||||||||||||||||||||||||||||
Sequence: |
GAGGAGGAGGCGGGGCAGGTGGGCTATGGTTGCTTGGAGAGTGCATCCGGCCCGGTACTTGTGAhide sequence |
RefSeq Acc Id: | NR_033531 | |||||||||||||||||||||||||||||
RefSeq Status: | REVIEWED | |||||||||||||||||||||||||||||
Type: | NON-CODING | |||||||||||||||||||||||||||||
Position: |
|
|||||||||||||||||||||||||||||
Sequence: |
GAGGAGGAGGCGGGGCAGGTGGGCTATGGTTGCTTGGAGAGTGCATCCGGCCCGGTACTTGTGAhide sequence |
RefSeq Acc Id: | XM_017028540 ⟹ XP_016884029 | |||||||||
RefSeq Status: | ||||||||||
Type: | CODING | |||||||||
Position: |
|
|||||||||
Sequence: |
TGTACTTCAGCCTGCGTGACAGAGACTCCATCTCAAAACAAGAAAAGTGTCAGAAGTGGTCCCThide sequence |
Protein RefSeqs | NP_001171172 | (Get FASTA) | NCBI Sequence Viewer |
NP_001349932 | (Get FASTA) | NCBI Sequence Viewer | |
NP_006851 | (Get FASTA) | NCBI Sequence Viewer | |
XP_016884029 | (Get FASTA) | NCBI Sequence Viewer | |
GenBank Protein | AAH00566 | (Get FASTA) | NCBI Sequence Viewer |
AAP35461 | (Get FASTA) | NCBI Sequence Viewer | |
BAD92661 | (Get FASTA) | NCBI Sequence Viewer | |
CAA18787 | (Get FASTA) | NCBI Sequence Viewer | |
CAG30444 | (Get FASTA) | NCBI Sequence Viewer | |
EAW60114 | (Get FASTA) | NCBI Sequence Viewer | |
EAW60115 | (Get FASTA) | NCBI Sequence Viewer | |
EAW60116 | (Get FASTA) | NCBI Sequence Viewer | |
EAW60117 | (Get FASTA) | NCBI Sequence Viewer | |
Q9BW83 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_006851 ⟸ NM_006860 |
- Peptide Label: | isoform 2 |
- UniProtKB: | Q9BW83 (UniProtKB/Swiss-Prot) |
- Sequence: |
MVKLAAKCILADPAVGKTALAQIFRSDGAHFQKSYTLTTGMDLVVKTVPVPDTGDSVELFIFDShide sequence |
RefSeq Acc Id: | NP_001171172 ⟸ NM_001177701 |
- Peptide Label: | isoform 1 |
- UniProtKB: | Q9BW83 (UniProtKB/Swiss-Prot) |
- Sequence: |
MVKLAAKCILAGDPAVGKTALAQIFRSDGAHFQKSYTLTTGMDLVVKTVPVPDTGDSVELFIFDhide sequence |
RefSeq Acc Id: | XP_016884029 ⟸ XM_017028540 |
- Peptide Label: | isoform X2 |
- Sequence: |
MDLVVKTVPVPDTGDSVELFIFDSAGKELFSEMLDKLWESPNVLCLVYDVTNEESFNNCSKWLEhide sequence |
RefSeq Acc Id: | NP_001349932 ⟸ NM_001363003 |
- Peptide Label: | isoform 1 |
RGD ID: | 6800277 | |||||||||
Promoter ID: | HG_KWN:42623 | |||||||||
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: | ENST00000216198, NM_001177701, OTTHUMT00000318834, OTTHUMT00000318835, OTTHUMT00000318837, OTTHUMT00000318838, OTTHUMT00000318840, OTTHUMT00000318844, UC010GWY.1 | |||||||||
Position: |
|
RGD ID: | 13603908 | |||||||||
Promoter ID: | EPDNEW_H28138 | |||||||||
Type: | initiation region | |||||||||
Name: | IFT27_1 | |||||||||
Description: | intraflagellar transport 27 | |||||||||
SO ACC ID: | SO:0000170 | |||||||||
Source: | EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | |||||||||
Experiment Methods: | Single-end sequencing. | |||||||||
Position: |
|
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 22q12.3-13.1(chr22:35333993-38900177)x1 | copy number loss | Polydactyly [RCV000051364]|See cases [RCV000051364] | Chr22:35333993..38900177 [GRCh38] Chr22:35729986..39296182 [GRCh37] Chr22:34059986..37626128 [NCBI36] Chr22:22q12.3-13.1 |
pathogenic |
GRCh38/hg38 22q12.3-13.1(chr22:36552376-37669915)x1 | copy number loss | Cleft palate, isolated [RCV000051365]|See cases [RCV000051365] | Chr22:36552376..37669915 [GRCh38] Chr22:36948423..38065922 [GRCh37] Chr22:35278369..36395868 [NCBI36] Chr22:22q12.3-13.1 |
pathogenic |
GRCh38/hg38 22q12.3-13.1(chr22:36068124-38002382)x3 | copy number gain | Hearing impairment [RCV000051683]|See cases [RCV000051683] | Chr22:36068124..38002382 [GRCh38] Chr22:36464172..38398389 [GRCh37] Chr22:34794118..36728335 [NCBI36] Chr22:22q12.3-13.1 |
pathogenic |
GRCh38/hg38 22q12.3-13.33(chr22:33768441-50739977)x3 | copy number gain | Failure to thrive [RCV000051682]|See cases [RCV000051682] | Chr22:33768441..50739977 [GRCh38] Chr22:34164428..51178405 [GRCh37] Chr22:32494428..49525271 [NCBI36] Chr22:22q12.3-13.33 |
pathogenic |
NM_001177701.2(IFT27):c.174+73C>T | single nucleotide variant | Malignant melanoma [RCV000072956] | Chr22:36767233 [GRCh38] Chr22:37163277 [GRCh37] Chr22:35493223 [NCBI36] Chr22:22q12.3 |
not provided |
GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3 | copy number gain | See cases [RCV000133646] | Chr22:16916608..50739836 [GRCh38] Chr22:17397498..51178264 [GRCh37] Chr22:15777498..49525130 [NCBI36] Chr22:22q11.1-13.33 |
pathogenic |
NM_001177701.3(IFT27):c.299G>A (p.Cys100Tyr) | single nucleotide variant | BARDET-BIEDL SYNDROME 19 [RCV000128641]|Bardet-Biedl syndrome 19 [RCV000128641] | Chr22:36763972 [GRCh38] Chr22:37160016 [GRCh37] Chr22:22q12.3 |
pathogenic |
GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3 | copy number gain | See cases [RCV000134730] | Chr22:16916743..50739785 [GRCh38] Chr22:17397633..51178213 [GRCh37] Chr22:15777633..49525079 [NCBI36] Chr22:22q11.1-13.33 |
pathogenic |
GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3 | copy number gain | See cases [RCV000137926] | Chr22:20907226..37187347 [GRCh38] Chr22:21261514..37583387 [GRCh37] Chr22:19591514..35913333 [NCBI36] Chr22:22q11.21-12.3 |
pathogenic |
GRCh37/hg19 22q12.3-13.1(chr22:37090025-39601950)x3 | copy number gain | See cases [RCV000446037] | Chr22:37090025..39601950 [GRCh37] Chr22:22q12.3-13.1 |
uncertain significance |
GRCh37/hg19 22q12.3-13.1(chr22:35680095-38098981)x1 | copy number loss | See cases [RCV000207444] | Chr22:35680095..38098981 [GRCh37] Chr22:22q12.3-13.1 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3 | copy number gain | See cases [RCV000240091] | Chr22:16054691..51237518 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q12.3-13.33(chr22:35728929-51220961)x3 | copy number gain | See cases [RCV000240469] | Chr22:35728929..51220961 [GRCh37] Chr22:22q12.3-13.33 |
pathogenic |
NM_001177701.3(IFT27):c.234+1G>A | single nucleotide variant | not provided [RCV000722443] | Chr22:36766137 [GRCh38] Chr22:37162181 [GRCh37] Chr22:22q12.3 |
uncertain significance |
NM_001177701.3(IFT27):c.121G>A (p.Gly41Arg) | single nucleotide variant | not provided [RCV000722460] | Chr22:36767359 [GRCh38] Chr22:37163403 [GRCh37] Chr22:22q12.3 |
uncertain significance |
NM_001177701.3(IFT27):c.107A>G (p.Tyr36Cys) | single nucleotide variant | Bardet-Biedl syndrome [RCV000757976] | Chr22:36767790 [GRCh38] Chr22:37163834 [GRCh37] Chr22:22q12.3 |
pathogenic |
NM_001177701.3(IFT27):c.352+1G>T | single nucleotide variant | Bardet-Biedl syndrome [RCV000757977] | Chr22:36763918 [GRCh38] Chr22:37159962 [GRCh37] Chr22:22q12.3 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3 | copy number gain | See cases [RCV000446956] | Chr22:16054691..51220902 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
NM_001177701.3(IFT27):c.415C>T (p.Arg139Trp) | single nucleotide variant | not provided [RCV000443592] | Chr22:36762951 [GRCh38] Chr22:37158995 [GRCh37] Chr22:22q12.3 |
benign |
GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3 | copy number gain | See cases [RCV000448847] | Chr22:16054691..51237463 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q12.3-13.1(chr22:36877226-38548989)x1 | copy number loss | See cases [RCV000512008] | Chr22:36877226..38548989 [GRCh37] Chr22:22q12.3-13.1 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838) | copy number gain | See cases [RCV000510873] | Chr22:16888900..51197838 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3 | copy number gain | See cases [RCV000512333] | Chr22:16888900..51197838 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q12.3-13.1(chr22:35674826-39466442)x3 | copy number gain | See cases [RCV000512385] | Chr22:35674826..39466442 [GRCh37] Chr22:22q12.3-13.1 |
likely pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16054667-51243435)x3 | copy number gain | not provided [RCV000741689] | Chr22:16054667..51243435 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51195728)x3 | copy number gain | not provided [RCV000741691] | Chr22:16114244..51195728 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16114244-51211392)x3 | copy number gain | not provided [RCV000741692] | Chr22:16114244..51211392 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3 | copy number gain | not provided [RCV000846344] | Chr22:16888899..51197838 [GRCh37] Chr22:22q11.1-13.33 |
pathogenic |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:18626 | AgrOrtholog |
COSMIC | IFT27 | COSMIC |
Ensembl Genes | ENSG00000100360 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSP00000343593 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSP00000390016 | UniProtKB/TrEMBL | |
ENSP00000392016 | UniProtKB/TrEMBL | |
ENSP00000393541 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENSP00000399606 | UniProtKB/TrEMBL | |
ENSP00000404556 | UniProtKB/TrEMBL | |
Ensembl Transcript | ENST00000340630 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENST00000415653 | UniProtKB/TrEMBL | |
ENST00000417951 | UniProtKB/TrEMBL | |
ENST00000430701 | UniProtKB/TrEMBL | |
ENST00000433985 | ENTREZGENE, UniProtKB/Swiss-Prot | |
ENST00000440696 | UniProtKB/TrEMBL | |
ENST00000476548 | ENTREZGENE | |
GTEx | ENSG00000100360 | GTEx |
HGNC ID | HGNC:18626 | ENTREZGENE |
Human Proteome Map | IFT27 | Human Proteome Map |
InterPro | P-loop_NTPase | UniProtKB/Swiss-Prot |
RabL4_euk | UniProtKB/Swiss-Prot | |
Small_GTP-bd_dom | UniProtKB/Swiss-Prot | |
Small_GTPase | UniProtKB/Swiss-Prot | |
Small_GTPase_Ras-type | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:11020 | UniProtKB/Swiss-Prot |
NCBI Gene | 11020 | ENTREZGENE |
OMIM | 615870 | OMIM |
615996 | OMIM | |
PANTHER | PTHR24070 | UniProtKB/Swiss-Prot |
Pfam | Ras | UniProtKB/Swiss-Prot |
PharmGKB | PA38609 | PharmGKB |
PROSITE | RAB | UniProtKB/Swiss-Prot |
Superfamily-SCOP | SSF52540 | UniProtKB/Swiss-Prot |
TIGRFAMs | small_GTP | UniProtKB/Swiss-Prot |
UniGene | Hs.415172 | ENTREZGENE |
UniProt | B1AH56_HUMAN | UniProtKB/TrEMBL |
B1AH58_HUMAN | UniProtKB/TrEMBL | |
F5GZ09_HUMAN | UniProtKB/TrEMBL | |
H0Y6C7_HUMAN | UniProtKB/TrEMBL | |
IFT27_HUMAN | UniProtKB/Swiss-Prot, ENTREZGENE | |
UniProt Secondary | F6SIY6 | UniProtKB/TrEMBL |
F6X9B7 | UniProtKB/TrEMBL | |
O60897 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2014-07-08 | IFT27 | intraflagellar transport 27 | intraflagellar transport 27 homolog (Chlamydomonas) | Symbol and/or name change | 5135510 | APPROVED | |
2011-07-27 | IFT27 | intraflagellar transport 27 homolog (Chlamydomonas) | RABL4 | RAB, member of RAS oncogene family-like 4 | Symbol and/or name change | 5135510 | APPROVED |
![]() |
More on IFT27 | |
![]() |
Alliance Gene |
![]() |
NCBI Gene |
![]() |
Ensembl Gene |
![]() |
JBrowse: hg19 hg38 |
![]() |
HGNC Report |
![]() |
NCBI Genome Data Viewer |
CRRD Object Information | |
CRRD ID: | 1318628 |
Created: | 2005-01-12 |
Species: | Homo sapiens |
Last Modified: | 2019-11-26 |
Status: | ACTIVE |
![]() |
![]() |
![]() |
![]() |
RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.