Busch Lab

ZMP

si:dkey-30k22.7

Ensembl ID:
ENSDARG00000037286
ZFIN ID:
ZDB-GENE-090313-302
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 are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa19502 Nonsense Available for shipment Available now
sa19501 Nonsense Available for shipment Available now
sa39615 Nonsense Mutation detected in F1 DNA Not yet available
sa9493 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa19502
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032841 None None 1091 None 11
ENSDART00000125204 Nonsense 94 107 2 2
ENSDART00000126068 None None 189 None 2
ENSDART00000126076 None None 644 None 2
ENSDART00000135763 Nonsense 716 1204 4 6
Genomic Location (Zv9):
Chromosome 1 (position 24488808)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 24940579
GRCz11 1 25631408
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCGGTCTACCTGAGCTCTTCTCTAATGCAGCTGCGCAGTAGCAGTGTG[A/T]AGCTGTCTGTTTCTGCTCGAGATGGAGGAGGCATGTCTGCTGCTTATCCT
Long Flanking Sequence:
AGCCGAGGCTCGAAACAGCAACGTTCTTGCTGTGAGGCGATTGTGCTATCCACTGTGCCAGTGCGTCGCCACACATTATTATTAAAGAACGTAATGCTGTTGTGATTTAGATATCTAAATCAAATTTGTATAAGTCATAATATACTTAAAAATAAACCCAAAGGCATTGTGTGGACATCTCCGTTCCTAAAGTGCTTTCCAATTTTAGTATTAGATTTGAGTGTTGTCCAACTGTTGTAGCCACTACTCAACTTTTGACTATGTTTTGATTGTTATACTTCAGCAGAAAGTTGATGCCTAATCAAATTTAAAAATAACATACCACCTACACGTCACCAATCCTATTCCTAAAGACCTTCCTCCAGATTTCTGTACTTATCAATTGCTGCTTCAGGTCCAAATAGATCACCTATAGGCAAGATGTTAATGTTGGTTTTGTGTGTTCGGCAGGTTCGGTCTACCTGAGCTCTTCTCTAATGCAGCTGCGCAGTAGCAGTGTG[A/T]AGCTGTCTGTTTCTGCTCGAGATGGAGGAGGCATGTCTGCTGCTTATCCTGCTAACATCACTGTGAACATCTTGCAGAGCGACCAGCCTCCTGCCCTCTTCCAGAAAGCTCAATACACCTTCTCCATCTCTGAGGACGCACCAGTGGGCTCTTCTGTGGGTTTGGTTCAGGCCATTACCCCTGCCAGTGAGTTATTTTGTGGGGAATATTGTGACACATTCACTGTAAACCCTAATAAGTAAGAATTCATGTCTCTGTTTAAAACCATCGGGTAAGCTGGTTTAAAACCCCTATGTAACCACTTTCCTCAAATGATCTGAGGAAAGTGATGACCTCATTTGGTTTGAGTAATGGGAAATTGACAACTCAATTAATTGAGTTGACCAAATATGGTTTCTTCATTGAATTAGCTTAAATGTTCAATTAAAGATAACTTAAATGTTTAAGTATAGATAACTTAAAATGGCTAATAGACTAAACTTCCAAATTTTTCGTCGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19501
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032841 Nonsense 362 1091 5 11
ENSDART00000125204 None None 107 None 2
ENSDART00000126068 None None 189 None 2
ENSDART00000126076 None None 644 None 2
ENSDART00000135763 None None 1204 None 6
Genomic Location (Zv9):
Chromosome 1 (position 24477397)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 24929168
GRCz11 1 25619997
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAGTTTGCAGTTTGGCATTAAAAGTTCTAGTGGCGAGCTTTATGTGGCA[C/T]AACATCTGGACTACGAAGTCACTCAGCGTTACTTCCTGGTTGTACGTGCA
Long Flanking Sequence:
GAAGGTCCGTTTGTTGAATTAAGGTTTCATTGCATCTACATACCAACTAATTCACATTAGATTATAAGTAGACTGTTAGGTTAGGGTTAGGGTTAGGGTTAGTGTAAGTTGACATGTACTTGCAAAGTTCCTTATAGTCAGTTAAATGTCTGTTAAAAGAGCAGTTTCAACAGATATCAGGCAGACAGTGAACTAATACTTAAATGGACCATCAAAATAAAGTGTTACTGAATGTCTTGTCTCTAGTGTTTAAAAAATTATAACAAATTTTGTTTTAAAATTTTGTTTTCTTCCAGGTTTATGTCTTGGATCAACAAAAAGAGAATTTCCAGAGCAGCTTTCAGCACTTTACTGTTCTAGAAGATGTGGGACTGGGAACTATCATTGGGTCTCTCGGTGTTTCAAATGCACCAGATACAGAACTACGATATTCCATTGTTGAGGGTAATGGTAGTTTGCAGTTTGGCATTAAAAGTTCTAGTGGCGAGCTTTATGTGGCA[C/T]AACATCTGGACTACGAAGTCACTCAGCGTTACTTCCTGGTTGTACGTGCAGAAGCCTTTCCCACTTTTAATGTCACTGTATTTGCTGCAGTCAGCATTCTCGATGTCAATGACCACAACCCCTGGTTCCCTAGCAATGGCAACATTGTGATATTTGGTGTTCATGAGGATGTTTCCAATGGAACAGTGGTATATGTGTTTAATGCACGAGATGGTGATGGAAGTCTACACTACAGTGAGCTTTATTATTCTTTGACTTTCGACCCCAGCCCTGCCATTGAGGGGCTGCCTTTACACATTGACCCTCACACTGGAGTTGTGACAACAAACGGACAACTGGACCGTGAACGAACTGAGAACATTATATTTAGAGTGACAGCCAGCGATAGCTTGAAAGAGCCCAATGAAAGGAAAAATGCATCAATCATAGCTCAAATGATTGTGCTGGATATCAATGACAACAGTCCTACATTTGTCTCCATGGATATAGCATGTGTCCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39615
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032841 Nonsense 403 1091 5 11
ENSDART00000125204 None None 107 None 2
ENSDART00000126068 None None 189 None 2
ENSDART00000126076 None None 644 None 2
ENSDART00000135763 None None 1204 None 6
Genomic Location (Zv9):
Chromosome 1 (position 24477273)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 24929044
GRCz11 1 25619873
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGTATTTGCTGCAGTCAGCATTCTCGATGTCAATGACCACAACCCCT[G/A]GTTCCCTAGCAATGGCAACATTGTGATATTTGGTGTTCATGAGGATGTTT
Long Flanking Sequence:
AAGTTCCTTATAGTCAGTTAAATGTCTGTTAAAAGAGCAGTTTCAACAGATATCAGGCAGACAGTGAACTAATACTTAAATGGACCATCAAAATAAAGTGTTACTGAATGTCTTGTCTCTAGTGTTTAAAAAATTATAACAAATTTTGTTTTAAAATTTTGTTTTCTTCCAGGTTTATGTCTTGGATCAACAAAAAGAGAATTTCCAGAGCAGCTTTCAGCACTTTACTGTTCTAGAAGATGTGGGACTGGGAACTATCATTGGGTCTCTCGGTGTTTCAAATGCACCAGATACAGAACTACGATATTCCATTGTTGAGGGTAATGGTAGTTTGCAGTTTGGCATTAAAAGTTCTAGTGGCGAGCTTTATGTGGCACAACATCTGGACTACGAAGTCACTCAGCGTTACTTCCTGGTTGTACGTGCAGAAGCCTTTCCCACTTTTAATGTCACTGTATTTGCTGCAGTCAGCATTCTCGATGTCAATGACCACAACCCCT[G/A]GTTCCCTAGCAATGGCAACATTGTGATATTTGGTGTTCATGAGGATGTTTCCAATGGAACAGTGGTATATGTGTTTAATGCACGAGATGGTGATGGAAGTCTACACTACAGTGAGCTTTATTATTCTTTGACTTTCGACCCCAGCCCTGCCATTGAGGGGCTGCCTTTACACATTGACCCTCACACTGGAGTTGTGACAACAAACGGACAACTGGACCGTGAACGAACTGAGAACATTATATTTAGAGTGACAGCCAGCGATAGCTTGAAAGAGCCCAATGAAAGGAAAAATGCATCAATCATAGCTCAAATGATTGTGCTGGATATCAATGACAACAGTCCTACATTTGTCTCCATGGATATAGCATGTGTCCCAGAGGACACAGAAGTTGGACTTTTGGTTCATCATGTGATGGCCAAAGATAAAGATGAAGGAAGAAACGGGCATGTCACTTACAGTGTGTCTTCAGGGAACGAGAAGAGCTACTTTCACATGGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9493
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000032841 Nonsense 444 1091 5 11
ENSDART00000125204 None None 107 None 2
ENSDART00000126068 None None 189 None 2
ENSDART00000126076 None None 644 None 2
ENSDART00000135763 None None 1204 None 6
Genomic Location (Zv9):
Chromosome 1 (position 24477149)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 24928920
GRCz11 1 25619749
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTAATGCACGAGATGGTGATGGAAGTCTACACTACAGTGAGCTTTATTA[T/G]TCTTTGACTTWCGACCCCAGCCCTGCCATTGAGGGGCTGCCTTTACACAT
Long Flanking Sequence:
TTTAAAAAATTATAACAAATTTTGTTTTAAAATTTTGTTTTCTTCCAGGTTTATGTCTTGGATCAACAAAAAGAGAATTTCCAGAGCAGCTTTCAGCACTTTACTGTTCTAGAAGATGTGGGACTGGGAACTATCATTGGGTCTCTCGGTGTTTCAAATGCACCAGATACAGAACTACGATATTCCATTGTTGAGGGTAATGGTAGTTTGCAGTTTGGCATTAAAAGTTCTAGTGGCGAGCTTTATGTGGCACAACATCTGGACTACGAAGTCACTCAGCGTTACTTCCTGGTTGTACGTGCAGAAGCCTTTCCCACTTTTAATGTCACTGTATTTGCTGCAGTCAGCATTCTCGATGTCAATGACCACAACCCCTGGTTCCCTAGCAATGGCAACATTGTGATATTTGGTGTTCATGAGGATGTTTCCAATGGAACAGTGGTATATGTGTTTAATGCACGAGATGGTGATGGAAGTCTACACTACAGTGAGCTTTATTA[T/G]TCTTTGACTTTCGACCCCAGCCCTGCCATTGAGGGGCTGCCTTTACACATTGACCCTCACACTGGAGTTGTGACAACAAACGGACAACTGGACCGTGAACGAACTGAGAACATTATATTTAGAGTGACAGCCAGCGATAGCTTGAAAGAGCCCAATGAAAGGAAAAATGCATCAATCATAGCTCAAATGATTGTGCTGGATATCAATGACAACAGTCCTACATTTGTCTCCATGGATATAGCATGTGTCCCAGAGGACACAGAAGTTGGACTTTTGGTTCATCATGTGATGGCCAAAGATAAAGATGAAGGAAGAAACGGGCATGTCACTTACAGTGTGTCTTCAGGGAACGAGAAGAGCTACTTTCACATGGAAAGCACAGGTATTGTGGTTTTAGGGATGTAGATGAATGTTGTGATAAGGAAAAAAAAGTCTAGGTTATATAGTTCATCCTAAAAAAAAACAATGCTGTTTTCATTTTCATATCTTCACATAATTCC
Associated Phenotype:
Not determined