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UGID:717231     UniGene Hs.502072     Homo sapiens (human)   USH1C
Usher syndrome 1C (autosomal recessive, severe) (USH1C)

Human protein-coding gene USH1C. Represented by 126 ESTs from 69 cDNA libraries. EST representation biased toward adult. Corresponds to 2 reference sequences (different isoforms). [UniGene 717231 - Hs.502072]

Tissues and development stages from this gene's sequences survey gene expression. Links to other NCBI expression resources.
Restricted Expression: adult [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: intestine; brain; kidney; cervix; pancreas; uncharacterized tissue; mixed; uterus; connective tissue; ascites; muscle; lung; stomach; testis; bladder; blood; eye; liver
Genomic location specified by transcript mapping, radiation hybrid mapping, genetic mapping or cytogenetic mapping.
Chromosome: 11
Map position: 11p14.3
Sequences representing this gene; mRNAs, ESTs, and gene predictions supported by transcribed sequences.

mRNA sequences (11)

AF039699.1 Homo sapiens antigen NY-CO-37 (NY-CO-38) mRNA, complete cds PA
AF039700.1 Homo sapiens antigen NY-CO-38 (NY-CO-38) mRNA, complete cds PA
AB006955.1 Homo sapiens mRNA for AIE-75, complete cds PA
AB018687.1 Homo sapiens mRNA for autoimmune enteropathy-related antigen AIE-75, complete cds P
BX641129.1 Homo sapiens mRNA; cDNA DKFZp686A09227 (from clone DKFZp686A09227) A
NM_005709.3 Homo sapiens Usher syndrome 1C (autosomal recessive, severe) (USH1C), transcript variant 1, mRNA PA
NM_153676.3 Homo sapiens Usher syndrome 1C (autosomal recessive, severe) (USH1C), transcript variant b3, mRNA PA
AK225614.1 Homo sapiens mRNA for harmonin isoform a variant, clone: REC01285 PA
BC016057.1 Homo sapiens Usher syndrome 1C (autosomal recessive, severe), mRNA (cDNA clone MGC:23100 IMAGE:4867369), complete cds PA
AK290788.1 Homo sapiens cDNA FLJ77086 complete cds, highly similar to Homo sapiens Usher syndrome 1C (autosomal recessive, severe) (USH1C), transcript variant 1, mRNA P
AK300936.1 Homo sapiens cDNA FLJ51329 complete cds, highly similar to Harmonin P

EST sequences (10 of 126) [Show all sequences]

BX099952.1 Clone IMAGp998N215291_;_IMAGE:2143700 pancreas A
AI269960.1 Clone IMAGE:1869333 kidney 3' read P
AI270726.1 Clone IMAGE:1962829 intestine 3' read A
AI272081.1 Clone IMAGE:1865611 kidney 3' read A
AI453367.1 Clone IMAGE:2143700 pancreas 3' read A
AI628985.1 Clone IMAGE:2285282 kidney 3' read
AI629007.1 Clone IMAGE:2285306 kidney 3' read
AI738958.1 Clone IMAGE:2390044 intestine 3' read A
AI738967.1 Clone IMAGE:2390043 intestine 3' read A
AI739238.1 Clone IMAGE:2390268 intestine 3' read A

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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