Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79883
Gene name Gene Name - the full gene name approved by the HGNC.
Podocan like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PODNL1
Synonyms (NCBI Gene) Gene synonyms aliases
SLRR5B
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029802 hsa-miR-26b-5p Microarray 19088304
MIRT1246393 hsa-miR-1254 CLIP-seq
MIRT1246394 hsa-miR-129-5p CLIP-seq
MIRT1246395 hsa-miR-1307 CLIP-seq
MIRT1246396 hsa-miR-3116 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005615 Component Extracellular space IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
621043 26275 ENSG00000132000
Protein
UniProt ID Q6PEZ8
Protein name Podocan-like protein 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 74 136 Leucine rich repeat Repeat
PF13855 LRR_8 216 278 Leucine rich repeat Repeat
PF13855 LRR_8 358 420 Leucine rich repeat Repeat
PF13855 LRR_8 429 483 Leucine rich repeat Repeat
Sequence
MAESGLAMWPSLLLLLLLPGPPPVAGLEDAAFPHLGESLQPLPRACPLRCSCPRVDTVDC
DGLDLRVFPDNITRAAQHLSLQNNQLQELPYNELSRLSGLRTLNLHNNLISSEGLPDEAF
ESLTQLQHLCVAHNKL
SVAPQFLPRSLRVADLAANQVMEIFPLTFGEKPALRSVYLHNNQ
LSNAGLPPDAFRGSEAIATLSLSNNQLSYLPPSLPPSLERLHLQNNLISKVPRGALSRQT
QLRELYLQHNQLTDSGLDATTFSKLHSLEYLDLSHNQL
TTVPAGLPRTLAILHLGRNRIR
QVEAARLHGARGLRYLLLQHNQLGSSGLPAGALRPLRGLHTLHLYGNGLDRVPPALPRRL
RALVLPHNHVAALGARDLVATPGLTELNLAYNRLASARVHHRAFRRLRALRSLDLAGNQL

TRLPMGLPTGLRTLQLQRNQLRMLEPEPLAGLDQLRELSLAHNRLRVGDIGPGTWHELQA
LQV
RHRLVSHTVPRAPPSPCLPCHVPNILVSW
Sequence length 512
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Retinal dystrophy Retinal Dystrophies rs267606794, rs200691042, rs397704718, rs202193201, rs794728002, rs121965036, rs121965057, rs121918129, rs137853190, rs386834252, rs121918165, rs137853113, rs137853114, rs121918328, rs587777803
View all (2328 more)
28041643
Associations from Text Mining
Disease Name Relationship Type References
Glioma Associate 34830454
Neoplasms Stimulate 37284741