> Polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1 (PKHD1L1)
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UGID:157513     UniGene Hs.170128     Homo sapiens (human)   PKHD1L1
Polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1 (PKHD1L1)

Human protein-coding gene PKHD1L1. Represented by 39 ESTs from 20 cDNA libraries. EST representation biased toward uterine tumor; fetus. Corresponds to reference sequence NM_177531.4. [UniGene 157513 - Hs.170128]

SELECTED PROTEIN SIMILARITIES
Comparison of cluster transcripts with RefSeq proteins. The alignments can suggest function of the cluster.
Best Hits and Hits from model organismsSpeciesId(%)Len(aa)
NP_803875.2 PKHD1L1 gene product H. sapiens 100.0 4242
NP_619615.2 fibrocystin-L precursor M. musculus 82.9 4246
NP_001073509.2 polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1 precursor D. rerio 55.0 4169
Other hits (2 of 23) [Show all]SpeciesId(%)Len(aa)
XP_520034.4 PREDICTED: fibrocystin-L P. troglodytes 98.9 4250
XP_003903125.1 PREDICTED: fibrocystin-L-like, partial P. anubis 96.8 3411

GENE EXPRESSION
Tissues and development stages from this gene's sequences survey gene expression. Links to other NCBI expression resources.
Restricted Expression: uterine tumor [show more like this]
fetus [show more like this]
EST Profile: Approximate expression patterns inferred from EST sources.
[Show more entries with profiles like this]
GEO Profiles: Experimental gene expression data (Gene Expression Omnibus).
cDNA Sources: uterus; mixed; pancreas; muscle; brain; uncharacterized tissue; adrenal gland; trachea; testis; connective tissue; lymph node; liver; larynx; adipose tissue
MAPPING POSITION
Genomic location specified by transcript mapping, radiation hybrid mapping, genetic mapping or cytogenetic mapping.
Chromosome: 8
Map position: 8q23
SEQUENCES
Sequences representing this gene; mRNAs, ESTs, and gene predictions supported by transcribed sequences.

mRNA sequences (5)

AY219181.1 Homo sapiens fibrocystin L mRNA, complete cds P
NM_177531.4 Homo sapiens polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1 (PKHD1L1), mRNA P
AL133640.1 Homo sapiens mRNA; cDNA DKFZp586C1021 (from clone DKFZp586C1021) PA
AK131338.1 Homo sapiens cDNA FLJ16352 fis, clone TESTI4000155 P
BC093096.1 Homo sapiens polycystic kidney and hepatic disease 1 (autosomal recessive)-like 1, mRNA (cDNA clone IMAGE:30330124), partial cds PA

EST sequences (10 of 39) [Show all sequences]

BX094313.1 Clone IMAGp998A18363_;_IMAGE:191897 mixed
BX103043.1 Clone IMAGp998K122037_;_IMAGE:824579 lymph node PA
BX116053.1 Clone IMAGp998F16525_;_IMAGE:243855 mixed P
AI240377.1 Clone IMAGE:1856262 mixed 3' read
AI564413.1 Clone IMAGE:2214598 uterus 3' read P
AI565137.1 Clone IMAGE:2212808 uterus 3' read A
AI571042.1 Clone IMAGE:2180156 uterus 3' read
AI682988.1 Clone IMAGE:2262900 uterus 3' read
AI860430.1 Clone IMAGE:2424827 uterus 3' read
AI889793.1 Clone IMAGE:2440616 uterus 3' read P


Key to Symbols

P Has similarity to known Proteins (after translation)
A Contains a poly-Adenylation signal
S Sequence is a Suboptimal member of this cluster
M Clone is putatively CDS-complete by MGC criteria

 
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