Gene Symbol | Lhfpl5 |
Entrez Gene ID | 294303 |
Full Name | LHFPL tetraspan subfamily member 5 |
Synonyms | Tmhs |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
ORF » Species Summary » Rattus norvegicus » Lhfpl5 cDNA ORF clone
Gene Symbol | Lhfpl5 |
Entrez Gene ID | 294303 |
Full Name | LHFPL tetraspan subfamily member 5 |
Synonyms | Tmhs |
General protein information |
|
Gene Type | protein-coding |
Organism | Rattus norvegicus(Norway rat) |
Genome |
mRNA | Protein | Name |
---|---|---|
NM_001013906.1 | NP_001013928.1 | LHFPL tetraspan subfamily member 5 protein |
LOC718952 | XP_001112357.2 | |
Canis lupus familiaris (dog) | LHFPL5 | XP_005627321.1 |
Rattus norvegicus (Norway rat) | Lhfpl5 | NP_001013928.1 |
Gallus gallus (chicken) | LHFPL5 | NP_989729.1 |
Danio rerio (zebrafish) | lhfpl5a | XP_686620.5 |
Homo sapiens (human) | LHFPL5 | NP_872354.1 |
Caenorhabditis elegans (roundworm) | F26D10.11 | NP_503066.1 |
Bos taurus (cattle) | LHFPL5 | NP_001192875.1 |
Mus musculus (house mouse) | Lhfpl5 | NP_080847.2 |
Xenopus tropicalis (tropical clawed frog) | lhfpl5 | NP_001017269.1 |
TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells.
Xiong W, Grillet N, Elledge HM, Wagner TF, Zhao B, Johnson KR, Kazmierczak P, M?ller U
Cell151(6)1283-95(2012 Dec)
Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation.
Longo-Guess CM, Gagnon LH, Fritzsch B, Johnson KR
Mammalian genome : official journal of the International Mammalian Genome Society18(9)646-56(2007 Sep)
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.
Kalay E, Li Y, Uzumcu A, Uyguner O, Collin RW, Caylan R, Ulubil-Emiroglu M, Kersten FF, Hafiz G, van Wijk E, Kayserili H, Rohmann E, Wagenstaller J, Hoefsloot LH, Strom TM, N?rnberg G, Baserer N, den Hollander AI, Cremers FP, Cremers CW, Becker C, Brunner HG, N?rnberg P, Karaguzel A, Basaran S, Kubisch C, Kremer H, Wollnik B
Human mutation27(7)633-9(2006 Jul)
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
Longo-Guess CM, Gagnon LH, Cook SA, Wu J, Zheng QY, Johnson KR
Proceedings of the National Academy of Sciences of the United States of America102(22)7894-9(2005 May)
GeneRIFs: Gene References Into Functions What's a GeneRIF?
LHFPL5 is essential for normal function of the human cochlea.
Title: Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.
The following Lhfpl5 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the Lhfpl5 cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.
CloneID | ORa04198 | |
Clone ID Related Accession (Same CDS sequence) | NM_001013906.1 | |
Accession Version | NM_001013906.1 Latest version! | Documents for ORF clone product in default vector |
Sequence Information | ORF Nucleotide Sequence (Length: 660bp) Protein sequence SNP |
|
Vector | pcDNA3.1-C-(k)DYK or customized vector | User Manual |
Clone information | Clone Map | MSDS |
Tag on pcDNA3.1+/C-(K)DYK | C terminal DYKDDDDK tags | |
ORF Insert Method | CloneEZ™ Seamless cloning technology | |
Insert Structure | linear | |
Update Date | 2018-09-15 | |
Organism | Rattus norvegicus(Norway rat) | |
Product | LHFPL tetraspan subfamily member 5 protein | |
Comment | Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from BC087673.1. On Apr 20, 2005 this sequence version replaced XM_228037.3. ##Evidence-Data-START## Transcript exon combination :: BC087673.1, BP483179.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMD00052296, SAMD00052297 [ECO:0000348] ##Evidence-Data-END## |
1 | ATGGTGAAGT TGCTGCCAGC CCAGGAGGCC GCCAAGATCT ACCACACCAA CTATGTGCGA |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq | NP_001013928.1 |
CDS | 247..906 |
Translation |
Target ORF information:
Target ORF information:
|
NM_001013906.1 |
1 | ATGGTGAAGT TGCTGCCAGC CCAGGAGGCC GCCAAGATCT ACCACACCAA CTATGTGCGA |
The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells. |
Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation. |
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss. |
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice. |