[Wormbase] The icl-1 gene encodes, through alternative splicing, two alternative forms (ICL-1A, or 'IClnN1', and ICL-1B, or 'IClnN2'), with distinct electrophysiological properties, of an anion channel homolog.
Wormbase predicts 2 models, but Caenorhabditis elegans cDNA sequences in GenBank, dbEST, Trace and SRA, filtered against clone rearrangements, coaligned on the genome and clustered in a minimal non-redundant way by the manually supervised AceView program, support at least 3 spliced variants
AceView synopsis, each blue text links to tables and details
According to AceView, this gene is expressed at very high level
, 7.3 times the average gene in this release, at all stages of development [Kohara cDNAs]. The expression profile for the gene, derived from the proportion of animals at each stage in each Kohara library is: embryos 19%, L1 or L2 larvae 36%, L3 to adult (including dauer) 45%. See the in situ hybridization pattern in Kohara NextDB
. The sequence
of this gene is defined by 6 cDNA clones
and 90 elements defined by RNA-seq, some from embryo (seen once), l1 (once), l2 (once), mixed (once).
Alternative mRNA variants and regulation:
The gene contains 7 distinct gt-ag introns
. Transcription produces 3 alternatively spliced mRNAs
. Variant a is transpliced to SL1, SL2, SL3, SL4, SL5, SL7, SL8, b to SL7, SL2. There are 4 validated alternative polyadenylation sites
(see the diagram
). The mRNAs appear to differ by presence or absence of a cassette exon
, overlapping exons with different boundaries.
There are 5 articles
specifically referring to this gene in PubMed. In addition we point below
to 2 abstracts. This essential gene is associated to a phenotype
(Embryonic Lethal, SLow growth). Functionally, the gene has been proposed to participate in processes
(chloride transport, regulation of cell volume). Proteins are expected to localize
in cytoplasm. These proteins appear to interact
with other proteins (SNR-1, SNR-3, SNR-6, SNR-7).
Protein coding potential:
The 3 spliced mRNAs putatively encode good proteins
, altogether 3 different isoforms (2 complete, 1 partial
), some containing Nucleotide-sensitive chloride conductance regulator domain
[Pfam], a second peroximal domain, a vacuolar domain, a coiled coil stretch [Psort2]
Please quote: AceView: a comprehensive cDNA-supported gene and transcripts annotation, Genome Biology 2006, 7(Suppl 1):S12
Map on chromosome IV, links to other databases and other names
This essential gene icl-1 maps on chomosome IV at position +4.63 (interpolated). In AceView, it covers 1.12 kb
, from 9095633 to 9094515 (WS190), on the reverse strand.
Links to: WormBase
The gene is also known in Wormgenes/AceView by its positional name 4J860, in Wormbase by its cosmid.number name C01F6.8, in NextDB, the Nematode expression pattern database, as CEYK6358.
Closest AceView homologs in other species
The closest human gene
, according to BlastP, is the AceView gene CLNS1A
The closest mouse gene
, according to BlastP, is the AceView gene Clns1a
The closest A.thaliana gene
, according to BlastP, is the AceView gene AT5G62290
Alternative mRNAs are shown aligned from 5' to 3' on a virtual genome where introns have been shrunk to a minimal length. Exon size is proportional to length, intron height reflects the number of cDNAs supporting each intron, the small numbers show the support of the introns in deep sequencing (with details in mouse-over) . Introns of the same color are identical, of different colors are different. 'Good proteins' are pink, partial or not-good proteins are yellow, uORFs are green. 5' cap or3' poly A flags show completeness of the transcript.
Mouse over the ending of each transcript gives tissues from which the supporting cDNAs were extracted. Details on tissue of origin for each intron and exon is available from the intron and exons table
Click on any transcript to open the specific mRNA page, to see the exact cDNA clone support and eventual SNPs and to get details on tissues, sequences, mRNA and protein annotations. Proteins supported by a single continuous cDNA sequence lead to underlining the name/ending of the variant. Names not underlined result from cDNA concatenation in the coding region and should be experimentally checked.
are depicted by broken lines; the height of the top of each intron reflects the relative number of clones supporting this intron. ]^[ A pink broken line
denotes an intron with standard boundaries (gt-ag or gc-ag) that is exactly supported (i.e. a cDNA sequence exactly matches the genome over 16 bp, 8 on both sides of the intron). ] ^ ] A blue broken line
denotes non-standard introns, exactly supported, but with non-standard at-ac or any other boundaries. ]-[ Pink
and ] - ] blue
straight lines represent 'fuzzy' introns of the standard and non-standard types respectively, those introns do not follow the 16 bp rule. Black straight lines ]-[denote gaps in the alignments.
Wide filled pink areas represent putative protein coding regions, narrow empty pink boxes represent the 5'UTR (on the left) and 3' UTR (on the right). Flags identify validated endings: cap site on the 5' side, polyadenylation site on the 3' side. Filled flags correspond to frequent events while empty flags have lesser supporting cDNAs (yet all are validated); at the 3' side, black flags are associated to the main AATAAA signal, blue flags
to any single letter variant of the main . More explanations are given in the gene help file