ZMP

celsr2l

Ensembl ID:

ENSDARG00000019726

ZFIN ID:

ZDB-GENE-050208-404

Description:

cadherin EGF LAG seven-pass G-type receptor 2 [Source:RefSeq peptide;Acc:NP_001074046]

Human Orthologues:

CELSR1, CELSR2, CELSR3

Human Descriptions:

cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac
cadherin, EGF LAG seven-pass G-type receptor 2 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac
cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac

Mouse Orthologues:

Celsr1, Celsr2, Celsr3

Mouse Descriptions:

cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo
cadherin, EGF LAG seven-pass G-type receptor 2 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo
cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa24043	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa24043

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

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082453	Nonsense	166	1478	4	29
ENSDART00000136491	Nonsense	167	1272	4	25

Genomic Location (Zv9):

Chromosome 22 (position 416671)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	403779
GRCz11	22	441502

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCGGCTGCATGAAGGACCTGCGCATTGACGAGCGGCACGTCGACATGGCC[G/T]GATTCATCGCTAATAACGGAACGCTACCCGGTGAGCTGTCGCTTGCAATG

Long Flanking Sequence:

ATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTATCTGTCTGTCCGTCCATCCATCTCTCTCTCTCTCTTCATCAGCCGGTGCTGAACCGCGCAGGTCTTCCTCAGGGGCCGTCGGATCAGAAGGTTGTCGTGGTAACGGTTGACGACTGTGACTCGTCAGTCGCTCTGCGCTTTGGCCATGTGGTGGGAAACTACTCCTGCTCCGCCCAGGGCAGCCAATCAGGATCCAAGAAGTAAGAGCGTTGGCAAGACGTCATCGGCGAACGTTCACCATACGAAACCCTTATATGGTCGTGTTTCCGTGCAGGTCTCTGGATCTGACGGGTCCTCTGCTGCTCGGAGGCGTCCCCAAACTGCCTGAGGAATTCCCCGTGCAGAACCGGCAGTTCATCGGCTGCATGAAGGACCTGCGCATTGACGAGCGGCACGTCGACATGGCC[G/T]GATTCATCGCTAATAACGGAACGCTACCCGGTGAGCTGTCGCTTGCAATGTTTTTAGTATTTTTAATTATTTAGTGAAGTGTCTTGAAATGTGTGTATGTTATTGGATGATTGACGTATTCTCAACTGAAACATGAAGAGAGGGTGGGGCATAGCATAGCTCCTCCCCTTTTTAAAAAAAATCAGCCAATAGTGTTTAGTTTTATCACAGCTCTGCCAGTGAGAGTGGTTGAGCTCAAGCGCATCACATCTAAAGGGCAGGGCGTGTCAGACACCAGAGAGCATTTGATTGGTCAGAAGATTGGATGAGAATCTGAAGTATGAGGAGATGACAAAAAACAGTGACGCATTTAGTTGGAAGTGACGAACTGCAAACTTTAGATGTTTATATCAGGTTTAGTTCTACTACATGTGGATTTTGTCAGTTTCGTCAGACTGACTTAAAATATTAAGTTATTATGGTGGCTTGAGAAAGTCAACATACTGTTATACTACATTAAC

Associated Phenotype:

Not determined