ZMP
celsr2l
Ensembl ID:
ZFIN ID:
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
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
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 are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24043 | Nonsense | Available for shipment | Available now |
| sa43735 | Nonsense | Mutation detected in F1 DNA | Not yet available |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Mutation Details
Allele Name:
sa43735
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082453 | Nonsense | 365 | 1478 | 8 | 29 |
| ENSDART00000136491 | None | None | 1272 | None | 25 |
Genomic Location (Zv9):
Chromosome 22 (position 421462)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 408570 |
| GRCz11 | 22 | 446293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCGTCGGTGGCATCTCGGACGGCAGGAATCGTGTGATTGGTGGATTC[A/T]GAGGATGCATTCAGGTCATTATTACACACACACACACACACACACAGCGT
Long Flanking Sequence:
TCGTGTTGATGATGTCACAGTGAGTGATGGCCAATGGCATCACGTCTCTCTTGAACTCAAAGGCCCGACGACAGGTGGCGTCACGGCAACACTGAGCCTTGACTACGGTCTCTACACGGTCAGTCCAACTGCAGACAATGATGGAGCACACACACTAATGTCAGTGACATGACGCCTGTGTGTGTGGGGGTGTGTGTGTGTGTATATGTGTGTGTGTTCGTGTGTTTGTACGTACATGTGTGTTTATGTATGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCGTGTGTGTTTGTACGGACATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTACGTACATGTGTTTATGTATGTGTGTGTGTGTGTGTGTGCAGTCCTCTATGGATCTGGACTCGAAGCTGAAGGGTGTAAGGCTGAAGACTCTGAGCGTCGGTGGCATCTCGGACGGCAGGAATCGTGTGATTGGTGGATTC[A/T]GAGGATGCATTCAGGTCATTATTACACACACACACACACACACACAGCGTTTTCAGCAGTACGTACATTCCTTTAATAATATTACGTCGCATATTGAACATTGTTTGTCTGTTCTCATAGTTTTTACATGTCTCATAGTTTTTCATATTAAATAAGCTGGAATTTAAATCACCTGCATTGTCAACAACATCTCTTCTCTGATTGGTGTTTAATGACATGAGGGCGGAGTCTCTTATGGGATCCACCAATAGCAAAACCACAACTATCCAATTTAATCCACAGAGGCAAAATCAAGCCCCGCCCACATTTATTCTTCACTCATAAGCAGAGGTGCAGCACAATAGAGTTTCGCTTTCGCTTTCTCAGGGTTTGCGTATTGGCGGCGACTCCTCGACTCCTGCATTTCCCAGCATGCCCCAGGCGCGTGTGCTGAACGTGGAGTCGGGCTGCAGTCTGCCGAACACCTGCGGATCGAACCCGTGTCCGGCTCACAGCGACTG
Associated Phenotype:
Not determined