ZMP

zgc:85942

Ensembl ID:

ENSDARG00000062262

ZFIN ID:

ZDB-GENE-040426-2364

Description:

hypothetical protein LOC405866 [Source:RefSeq peptide;Acc:NP_998095]

Human Orthologue:

EDNRA

Human Description:

endothelin receptor type A [Source:HGNC Symbol;Acc:3179]

Mouse Orthologue:

Ednra

Mouse Description:

endothelin receptor type A Gene [Source:MGI Symbol;Acc:MGI:105923]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44063	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa16023	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa44063

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089837	Essential Splice Site	208	328	None	6
ENSDART00000089841	Essential Splice Site	278	363	None	8
ENSDART00000111996	Essential Splice Site	278	363	None	8

Genomic Location (Zv9):

Chromosome 23 (position 46049720)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	45964546
GRCz11	23	45699741

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATGTGTGTGTTTTTTATATAAATGTGTGTGTGTGTGTGTGTGTGTGTGT[A/G]GAGGCGGGAGGTGGCCAAAGCCGTGTTCTCTCTGGTGCTGATCTTCGCTC

Long Flanking Sequence:

TGTTTATATACGTGTGTTTGTGTTTCAATACATATATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATGCAGGTGTCTGTATGTGTCGGCATTTAAATACGTGTGTGTCTGTCTGTCTATAAATGTGTGTGTGCGTCTGTTTATATACGTCTGTATCTGTATATATAGACGCATGTGTGTGTGTTCGCGCACGTCTGTTTATACATGTTTGTGTCTGATTATATAGATGTGTGTGTGTGTGTGTGTGTTTATACTGTATACATTTGTGTGTGTCTGTTTACATAAGTGTGTGTCTTTGTTCATATAGACAAGTGTGTCTCTGTCTATTTAATACACACGTGTATGTGTCAGTTAGTTGGTTTATATATATATTAGGGGTGTGTGTGTCATTTAAATACATATATGCATGTGTCCATTTATGTAAATGTGTGTGTTTTTTATATAAATGTGTGTGTGTGTGTGTGTGTGTGTGT[A/G]GAGGCGGGAGGTGGCCAAAGCCGTGTTCTCTCTGGTGCTGATCTTCGCTCTCTGCTGGTTTCCTCTTCATCTGAGTCGAATCCTGAAGAAGATGGTGTACTTCCAGAACGATGTTGGCCGCTGCGACCTGCTCAAGTAAACACACACACACACACACACACACATACTCTATACACATTCACACACATGCATAAACACACACATACTGTACACAAAGACATACTATATACAGTACACACAAACACACACTTACACAATATACCTGTACACACACACACATACTCTACATACACACAGACTGTATAACATTTACACATCCATATGCACACACAAAAAGCATATTGTATATACACACACACATGCATAAATACACACAATGTTCAAACACACTACAGTATATGCACACATACTGTACACACACACACACACACACACACATACTATACACACATATTGTACACACACATGGACTGTATACATATGCACACACATACACACAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16023

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089837	Essential Splice Site	289	328	None	6
ENSDART00000089841	Essential Splice Site	311	363	None	8
ENSDART00000111996	Essential Splice Site	311	363	None	8

Genomic Location (Zv9):

Chromosome 23 (position 46054903)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	45959363
GRCz11	23	45694558

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTGTGTGTGTGTGTGTGTGNNTCATCTCATGTGTGTGTGGTCTCTCCTC[A/T]GTCGTGTCTGTGCTGCTGGTGTTACTCAGACRGGTCTCTGATGGGCAGYG

Long Flanking Sequence:

TGTATGTGTGTTTGACTATATATTTATGTGTGTGCGTGTGTATGTGTGTGTGTTAAGTTAATTTACGTTAAACACTCAAATGTGTATGTGTGTTTGACTATATATTTATGTGTGTGCGTGTGTATGTGTGTGTGTGTGTTAAGTTAATTTACGTTAAACACTCAAATGTGTATGTGTGTTTGACTATATATTTATGTGTGTGTGTGTGTATGTGTGTGTGTGTGTTAAGTTAATTTACGTTAAACACTCAAATTTGTATGTGTGTTTGACTATATATTTATGTGTGTGCGTGTGTATGTGTGTGTGTGTTAAGTTAATTTACATTAAACACTCAAATGTGTATGTGTGTTTGACTATATATTTATGTGTGTGTGTGAATGTGTGTGTGTTAATTTAATTTACGTTAAACACTCAAATGTGTATGTGTGTTTGACTATATATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTCATCTCATGTGTGTGTGGTCTCTCCTC[A/T]GTCGTGTCTGTGCTGCTGGTGTTACTCAGACGGGTCTCTGATGGGCAGCGGCGCTCCACTCAACGCCACCAGCCTACAATACAAGAGTCCAGAACACAACCAGCGCAAGGACAGCTACAACTGACACACACACACACACACACTCACACACCTGACATGCAACTGACACACACACACACACACAACCAGCGACAAAGACAGCTACACATGACATACACACAGCGCATAGGCAGCTACAACTGACACACACACACACACCATACTGCACAATGACAGCTACAACTGACACACACATTCACATGTATATAACATATAACACACACACACCTGTATAATACACACTTTTCTTCTCGTTTTCACAGCATGTTGTCTTCTGTCCATATATATGTATATACCCTGCTGCGTCCTCTTTAAAGATGCTGTAATAGTGAGTGTTTGTTATAAATGTGCCGTCTTCAGAACTCAATGAATCAAATGTATTAAAGATTATTTACAAACAG

Associated Phenotype:

Not determined