Transcript: ENST00000485305.1 NHS-002

Description

Nance-Horan syndrome (congenital cataracts and dental anomalies) [Source:HGNC Symbol;Acc:7820]

Gene Synonyms

CTRCT40, CXN, SCML1

Location

About this transcript

This transcript has 3 exons, is associated with 1600 variant alleles and maps to 76 oligo probes.

Gene

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000380060.3	NHS-001	8761	1630aa	ENSP00000369400.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14181	Q6T4R5	NM_198270.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000398097.3	NHS-003	8213	1474aa	ENSP00000381170.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS48087	Q6T4R5	NM_001136024.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000485305.1	NHS-002	409	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

Summary

Statistics

Exons: 3, Coding exons: 0, Transcript length: 409 bps,

Version

ENST00000485305.1

Type

Processed transcript

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:	OTTHUMT00000055933 (version 1)