ZMP

Ensembl ID:

ZFIN ID:

Description:

neurotrimin isoform 1 [Source:RefSeq peptide;Acc:NP_001003852]

Human Orthologues:

IGLON5, LSAMP, NEGR1, NTM, OPCML

Human Descriptions:

IgLON family member 5 [Source:HGNC Symbol;Acc:34550]
limbic system-associated membrane protein [Source:HGNC Symbol;Acc:6705]
neuronal growth regulator 1 [Source:HGNC Symbol;Acc:17302]
neurotrimin [Source:HGNC Symbol;Acc:17941]
opioid binding protein/cell adhesion molecule-like [Source:HGNC Symbol;Acc:8143]

Mouse Orthologues:

Iglon5, Lsamp, Negr1, Ntm, Opcml

Mouse Descriptions:

IgLON family member 5 Gene [Source:MGI Symbol;Acc:MGI:2686277]
limbic system-associated membrane protein Gene [Source:MGI Symbol;Acc:MGI:1261760]
neuronal growth regulator 1 Gene [Source:MGI Symbol;Acc:MGI:2444846]
neurotrimin Gene [Source:MGI Symbol;Acc:MGI:2446259]
opioid binding protein/cell adhesion molecule-like Gene [Source:MGI Symbol;Acc:MGI:97397]

Allele Name:

sa27629

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000011317	Nonsense	67	305	3	7
ENSDART00000064097	Nonsense	50	358	2	9
ENSDART00000099964	Nonsense	67	317	3	8
ENSDART00000113912	Nonsense	31	301	2	7

The following transcripts of ENSDARG00000018065 do not overlap with this mutation:

• ENSDART00000136398

Genomic Location (Zv9):

Chromosome 10 (position 31510285)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	30611634
GRCz11	10	30497974

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

Flanking Sequence:

Long Flanking Sequence:

Associated Phenotype: