Gene: KAL1 ENSG00000011201

Description

Kallmann syndrome 1 sequence [Source:HGNC Symbol;Acc:6211]

Gene Synonyms

ADMLX, HH1, HHA, KAL, KALIG-1, KALIG1, KMS, WFDC19

Location

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants) and is associated with 2 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000262648.3	KAL1-001	6314	680aa	ENSP00000262648.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS14130	P23352	NM_000216.2	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000481896.1	KAL1-003	797	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-
ENST00000488294.1	KAL1-002	704	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

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