ZMP
celsr3
Ensembl ID:
ZFIN ID:
Description:
Cadherin, EGF LAG seven-pass G-type receptor 3 [Source:UniProtKB/TrEMBL;Acc:A9C3S7]
Human Orthologue:
CELSR3
Human Description:
cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac
Mouse Orthologue:
Celsr3
Mouse Description:
cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34415 | Nonsense | Available for shipment | Available now |
sa11108 | Essential Splice Site | Available for shipment | Available now |
sa10576 | Essential Splice Site | Available for shipment | Available now |
sa21306 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34415
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 |
---|---|---|---|---|---|
ENSDART00000078334 | Nonsense | 127 | 2916 | 1 | 40 |
ENSDART00000131888 | None | None | 441 | None | 4 |
ENSDART00000137391 | None | None | 407 | None | 9 |
ENSDART00000145095 | Nonsense | 157 | 2065 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 26978629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26106547 |
GRCz11 | 8 | 26125686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGACCGAAATGATCACTCACCTGTGTTTGAGCAAACAGAGTATCGT[G/T]AGACCATTCGGGAGAATGTAGAAGAGGGATATCCGATACTACAGCTGCGA
Long Flanking Sequence:
AAAGCGAAGTTGGGGTGGGTAATCAGTACAGCGAAAAACAAAAATATAAAGATAGTGATGAAGTGCTCAGGGAAGAGGGACAGGAATACAGTGAAGAGCAGACAGGTATCCCTTCTGCCGGGCGCTCCCGTAGAGCTGCTAATCGACAACCCCAATTCCCCCAGTATAACTACCAGGTTCAGGTTGCTGAGAACCAGCCTCCTGGTACCTCAGTTATAGCTATGACAGCTGAGGACCATGATGCTGGTGAGGCAGGCAGACTCAGTTACAGCATGGCCCCTTTAATGAACAGCAGGTCCATGGATTATTTTCAAATCGACCCAATTACTGGCCTTCTCACCACCACACACATTCTGGATCGTGAACACATGGACCTGCACTACTTTAGAGTTACTGCCGCAGACCACGGCTCTCCACATCTTTCAGGGACGACTATGGTGACCATCACTGTGGCTGACCGAAATGATCACTCACCTGTGTTTGAGCAAACAGAGTATCGT[G/T]AGACCATTCGGGAGAATGTAGAAGAGGGATATCCGATACTACAGCTGCGAGCAACAGATCTTGACTCAACAGCAAATGCCAACATACGCTACAGATTCGTCGGAGAAAGTGCAGCTGTCGCACGCTCTGCTTTTGAAATTGATCCACGGTCAGGCTTGATCACAACACGAGGTATTGTTGATAGAGAAACAAACGAGCGCTATACATTGTTGGTGGAAGCCAGCGACCAGGGGAGAGAGCCAGGGCCACGGTCGGCTACTGTTAGCGTCCATATCACTGTGCTGGATGAGAATGACAACGTTCCACAGTTCAGTCAAAAACGATATGTAGTAGCAGTTCGAGAAGATGTCCGACCACATTCCGAAATACTTAGAATCAGCGCTACGGACCAGGATAAAGATGGCAATGCTGCTGTGCACTACAACATAATCAGTGGGAACAGCCGTGGACAGTTTGCGATTGACAGTGTTACTGGAGAAATCCAGGTGGTTGCGCCGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11108
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078334 | Essential Splice Site | 1695 | 2916 | 14 | 40 |
ENSDART00000131888 | None | None | 441 | None | 4 |
ENSDART00000137391 | None | None | 407 | None | 9 |
ENSDART00000145095 | Essential Splice Site | 1725 | 2065 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 27032694)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26160612 |
GRCz11 | 8 | 26179751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAWCTGTGACTGTGAGGATAGTCAYTATGGACAATAYTGCCAACACAGG[T/C]ACACATTCACAAACACTGCATGCGTTCACACTATTACGCCCCAAGTCTNN
Long Flanking Sequence:
GGTTCACAAAACGGTTCACGCTGAAACGTGTTGCTCAAACTGTTGAGCTTGAATGGATGTGATCAGTCATAAAGTTGTGCAGTGAGCTGTTTTATGCAGTTTACTTTCAATGGATGATTGTTTTGAAGCTCTGAATGTACATGTTTTCATTATATGACGCAAATAAACAGTAAATAACGCTGTGCAGCTAGTCTGCAGCAAAATGGACGGTATGAATTTTGTGTTCTACTCAACACAACCCATAATACAGCACAGCCTTGATCTCTGAGTATAGCACACTTCACCTTTAAGTGATAATGTTTGTTTTTTTTATAATTCGAGGTTTGTGTTGTAACAGTTCTCTATTTTTCTATTTAGGATTCTATGGTAAAAGCTGTATGGATGCTTGTCAACTGAACCCATGTGAGAATCAAGCAAAGTGCCACAGGAAGCCCAGCTCCTCTCACGGATACATCTGTGACTGTGAGGATAGTCACTATGGACAATATTGCCAACACAGG[T/C]ACACATTCACAAACACTGCATGCGTTCACACTATTACGCCCCAAGTCTAGGGGACAAAAAATGACCTAAAGGGAATATTAAATATTTGGGTTGCGGTGGTGGATTTCCTAAAAAGATCCCCTTCGATTAACAACTAAACACAGACACTCAAAATTAAATGGATTTATTGTACTGTAGGTAGAAAAATATTAAGGAGCAACTCTTCAGGGTGACCACTGGCCAAAATAAGAAACAAAATAATATTTAAGCAAAATAAACTAAATTACCTATAAATCTTTAAAAAAAAAATACAGGAGCGTACATCACTCCCTAAACATAACCATATTAATCAAAATAAATAGGCAGGCCACCCCTACCACTACAAAGTTTTGGGTCATCAGTCGAAGGCGCAAAATCCACAAGCTCTTTCCCAGACCACTGGACACTGCCATTGCAAGGTACATACAAATAAAGAGTTCAGACACACACACACACACACACGCACACACACACACACACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10576
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078334 | Essential Splice Site | 2045 | 2916 | 21 | 40 |
ENSDART00000131888 | None | None | 441 | None | 4 |
ENSDART00000137391 | None | None | 407 | None | 9 |
ENSDART00000145095 | None | None | 2065 | None | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 27043509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26171427 |
GRCz11 | 8 | 26190566 |
KASP Assay ID:
2260-0666.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCATGTTGTGCTGCCCCCTGCTGCACTAGTGCCACAACGCAATGTCTG[T/A]AAGTCACACAYKCACAAGTTATTAAAGTWCTYCAACAAAGCATAGTAACA
Long Flanking Sequence:
TTCTATTAAGTATTTAATAAATAATGAAGTCATAAAATCACAATACAGTATAATTCAACACAATCCCAATCGCAACACTTATAATAAATCTGGGCCTTTGTTATGCTACACCTGGCAACATATTTAAAGCATTAGTTTTTTTTCAAAGTATAAACTCTGGAGGAAAGCAAGTCTTAGTGAGCTCATGGTTATAAAAATTAAATATTAAAAATATTCAGTCAGGTCCAGTGTGAGAAAGATGAGAAAGATCAATGTGAGACCAATACCTGCAATGCATCAGCAGAAAAACTGCAGCACTACAGAGACACCATCTATTAAAGAAATGCCTGTGTTTGTTTGTTTGTTACAGTCATGACTCTGGATCGTGTTGACAACCACACACACGTGCGGCGCCGCTTTCCACGGTATCACAGTCCTCTGTTCAGGGGTCAAGCGCTCTGGGATGCTCACACTCATGTTGTGCTGCCCCCTGCTGCACTAGTGCCACAACGCAATGTCTG[T/A]AAGTCACACACGCACAAGTTATTAAAGTTCTCCAACAAAGCATAGTAACACTTTCTATGAAGCCTGTATATATAATTCTTAGTAAAATATTATATTGCATGCATAGTCTCTTATAAACAACATTACAATATCGTCTTATAACCACATCATGCTATTTTACGACTGCTTAAAATAACAATGACCTTTGTAATTTTACTTAAAGCAGACAGTACACTTATAAATTATGCATAACACTTTACAACGGAAAGCATATGCTAATTATTATCCATGACTTTTGCATAAAACCCCTAATTTGCTGCTTGTTTATGGTTAATGTAGTTGTTAAGTTAAGCTAAGATATGGTAAAGGATTAGGGGATGTAGAAAATGGTCAAGTAAAATAATTACTAATAAACAGACAATATGCAAGCTAATATGCATATATCTAAAGTTAGAATTGGCTCCCATACTGAAGTGTTATTATTATATGAGAGATTTTTTGTTTCGTTTTGTCACTTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21306
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078334 | Nonsense | 2828 | 2916 | 40 | 40 |
ENSDART00000131888 | Nonsense | 322 | 441 | 4 | 4 |
ENSDART00000137391 | None | None | 407 | None | 9 |
ENSDART00000145095 | None | None | 2065 | None | 21 |
Genomic Location (Zv9):
Chromosome 8 (position 27063620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26191538 |
GRCz11 | 8 | 26210677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGATGAGCAGTCGGTCCCGCGAGCAGCTGGAGTCTAATGGTGGAGCA[C/T]AGCCCTGCAGAGAGTGGCTGAGGACCCTGCCGCCCCGCCAGCTCTCACAC
Long Flanking Sequence:
TGAAGAATCGTCTGGGCTGTCCTCCAGCTCTGCAGGGTCTGTCTGCTGTGGGTCGTGCTCCCAGCGAGATGTCCTGGTATAGGACCTCCACACTGGGCCACCGAGGCGTTCCAGCCGCCTCCTACGGTCGCATGTACTCTGGCACTGGCTCACTGTCCCAACCCGCTTCACGATACTCGTCCCGTGAACACCTGGATTCATTAGCAAGACGACAGCGGTCTAGAGACAACCTGGACCTGCTACCCCGACGGCGCGAGCTCGGTGCAGAACACCTGGGTGGGTCCAGAGAGAGGCTGGGTCCTGTTCACAGCATCCACGCATCCAGAGAAGACCTGGTGGGCAGGGGAGGTTTAGCAGGGTTAATGGGGGCCGAGGGGTCATTAAGCGGTTCCAGAACGCAGCTTAACACCCTAACAAGGCAGCAGGCCTCTCGGGAGCACCTTGGAGGGGCTCTGATGAGCAGTCGGTCCCGCGAGCAGCTGGAGTCTAATGGTGGAGCA[C/T]AGCCCTGCAGAGAGTGGCTGAGGACCCTGCCGCCCCGCCAGCTCTCACACCCTGACCCACACCCGCCCTCCTCACCCCCTCCACCAATCACAGAGGAGCCCCACGAATCCCTGCCCTCTCGCCGTGGACGCCTAGACTCTGCGCCCCCGTGTAGGTACCCGTCATCATCTGCGGCTGCACCCGGAGCCCCGTCCAGTCGACCGCCCTCTAGTGAACACCTGGATATCCTGTCGTCCATACTCGCCTCCTTCAGCTCCTCTGTGTTAACCCCGCCCCCTAACCCCGCTGGCCCCTCCCCTTCCCCACCTCCTCCTCTCTCTGCAACCTCTCAGAGCGTCTCCGAAGTGTCACCTGACTCTGAGTAAGTCCTGCCCCTTTTGTGTCACTGAGTGTCCACTTCCTTGTTGATTGACGGTCATCTTTGTGTGCTCATCAAAGATGATTGATTCTGTAGTTCTGCAATTGTATGTCGTAGATTAGAATTTAATGAGTTTTTCATA
Associated Phenotype:
Not determined