Busch Lab

ZMP

celsr1a

Ensembl ID:
ENSDARG00000069185
ZFIN ID:
ZDB-GENE-030616-78
Description:
SI:bZ6L08.1 (Novel protein similar to human cadherin, EGF LAG seven-pass G-type receptor (CELSR)) [S
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 8 alleles of this gene:

Allele Name Consequence Status Availability
sa18077 Nonsense Available for shipment Available now
sa33484 Nonsense Available for shipment Available now
sa31402 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa18077
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000187 None None 1767 None 34
ENSDART00000043737 None None 1224 None 26
ENSDART00000123617 Nonsense 284 1664 6 35
Genomic Location (Zv9):
Chromosome 4 (position 27543073)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 28243350
GRCz11 4 28232638
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCATGAGRAACCTGACAATTGACAGTAAATCARTTGACATGGCCAGTTA[C/A]ATTGCCAACAAWGGCACTACCGAAGGTTAGCCACAAATCATTACATTGCT
Long Flanking Sequence:
AAACTGTGTACCTGTTTATAATTTATTTGTACTGCAAAAACTTTAAGAAATTACCTGTTTTATTATATAATATATCAATAAATCACCCAATGAGGTAAACAAAATAATCATATGTCAAAAGAAAAAACAATTATAATTTTGCTTACCCAATTGGTTGATTATTTTGTTTGTTTTAAGGAAAAACTCTCCTAATTGTGGCATATTATTTTTTTAAGACAAGACAATATTTTTGCTTGTCTAAAAACACTTCTTGATTTAAGAACTTGTAGAAATTGGGACTACAAAAAAGACAAAAAGTAAGAAAAGCTTTTTTTTTTTGCAGTGTACTATGGTGGATATTTAAGTGTTTCATCTCTCTTCAGGTCTTTGGATCTCACTGGACCACTTTTACTTGGCGGTGTTCCAAATCTTCCGGAGGATTTCCCCATACGGAACCGGGACTTCGTGGGTTGCATGAGGAACCTGACAATTGACAGTAAATCAGTTGACATGGCCAGTTA[C/A]ATTGCCAACAATGGCACTACCGAAGGTTAGCCACAAATCATTACATTGCTTGCTGATCAACTTTCGAATAGTTGTAATTCCTTAACTCTTGTATTCTGATTTTGAGGCTTTGGCCACAGCTTTCACAGTGTTTCAGCAAATAGACTAATTGTTTATGACACAGATTTTGTGAAAATGCTTTGGAATTTTTAAAAACTCAACAATACACTCAGGGTAAATTGTATTCTAGTGGTTGTTTTTGCTCTTTTTACTTTCATTATAATGACTTTTTTTTTCAAAGCAGTGACACTATATAGTCGTGCATTCTTGATTGTTGGTGGTTTGGAGGTACACTTTATCATTTTACTGTTGATCAGCAGTTACAGTGCTAAATAAAGCGTATTTTCTGGGTTTTATAAGCATTATAGTGTGAGTGTAAGAGAGTGTAAGAGTGCACACCTACCTTGAAATGTTTGAGAAAATCAAAAATAAGCAACTCTTAGAACATGGTAAACATAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33484
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000187 Nonsense 750 1767 14 34
ENSDART00000043737 Nonsense 320 1224 7 26
ENSDART00000123617 Nonsense 655 1664 14 35
Genomic Location (Zv9):
Chromosome 4 (position 27527707)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 28227984
GRCz11 4 28217272
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATCAGCCAAAAGACAGTGACACCTGTTTCCCCTGTGACTGCTTTCATT[T/A]GGGCGCCAACTCGCGAACATGTGACCCAGAGACGGGACAGTGCCCTTGCA
Long Flanking Sequence:
GAATGAGATTAAAGTTTTTCGATTGTCCAACAGGCTGCAGAAGATGTTCTCAACCTTACACCACATTCTGTCTTTATATTACGCACTTAGCCATAAAGTGCTCTGCGTTGTGAGACAAAGGGGGAAAAAAAAAACTCTCAAAAAAAACTCTTTTTGGGACAACTTGAATGTTCTATGTGCCTTCCACATGAATTTGTAAAAATGCTTTCTTACAAAAGTCAACTTAAATGATTTGTGTTGGCACAACATGAAGGTATTATGTGGAACACTTGCTACTTCTAAAAAAAAAGCAAAAGAAAAAAAAAACAATTTTTTTTTCATTTACATAAACGAAAGTGTCAGAGGTAAACGTGTAAATGTAAATGTGGTTGACTCAACATGAAGTCAAATTTATTTTGAACTTTAGAGATTGTTACATTACTACAGTGTTTCTTTCACACAGGACAACTACTATCAGCCAAAAGACAGTGACACCTGTTTCCCCTGTGACTGCTTTCATT[T/A]GGGCGCCAACTCGCGAACATGTGACCCAGAGACGGGACAGTGCCCTTGCAAGGCGGGTGTGATTGGGCGACAGTGCAACCGCTGTGACAACCCTTTCTCTGAAGTGACTAGCACCGGCTGTGAGGGTATGTACCAATTTTTGTTCATTCAAGTATCTTTTTGCAGAAATTATATATATAAAGTACCAACATAATGTTTTCTGTGTTGTTACCTACTAGTTGGATATGAGGGCTGTCCAAAAGCCTTTGATTCTGGAATCTGGTGGCCCAGGACTAATTTTGGTTTCCCTGTGGCAATGAATTGCCCCAAGGGATCTATTGGTGAGTGAAACAGGCCTTTTTATCTTCACAAAATTATTGTATTTAAGCTAAAGAACAAAAATGACAGACACATTTGAGGTTTAATCAATAACTTTTTGTATTTTATTTTAGGCTTCAACTTTTTATATGTTATGTGGTGCATCAATTATTTTATTTCAACCATTATGCTATTATTCGGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31402
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000187 Essential Splice Site 989 1767 18 34
ENSDART00000043737 Essential Splice Site 559 1224 11 26
ENSDART00000123617 Essential Splice Site 894 1664 18 35
Genomic Location (Zv9):
Chromosome 4 (position 27523854)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 28224131
GRCz11 4 28213419
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGGAAGACTTACCTGAAACCCTTCATCATCGTAACAGAGAATATGGG[T/A]GAGCATTGCTAAAAGTATCTTGCGTAGAACTTAAATGTAGTTTTAAGCAT
Long Flanking Sequence:
TTTAGGGGGATTTTTCTGTTGGTCTTTGCTGGGCTTGAAAAAAAAGTCTTTAGCAGCCCAAAATTGCATGCTTTTAGTGGTTTAGCAGATTAGTGTAAATAACACAGTGTATAGTGACTACTGTCATGAGAACGAAAACGCCCACGTTTAAAGCGCATCTGGCAACATGAACATGCTTATCATGATACATGGTTTTAGGATAAGGATGCGTTTTAGGGCCGCATTCATTATGTCTAGCCTTGGAACAGATTCAGACTTCTAATGGCTCTCAAATGTCCAGAATTTGACCCTGAAATATGTTTCTGAATGCTGTAGAACCTAGTGAAGGCTGGCAGCGCAATCCTGGATGCCAGTAATAAAGAGCACTGGGATCAGATACAGAGAACAGAAGGGGGCACGGCAAATCTGCTCAAACACTTTGAGGAATATGCCAACACTCTGGCTCAGAACATGAGGAAGACTTACCTGAAACCCTTCATCATCGTAACAGAGAATATGGG[T/A]GAGCATTGCTAAAAGTATCTTGCGTAGAACTTAAATGTAGTTTTAAGCATGGTTTTGAAAACTGGACAGTTCTTTATTAACCTTTTTTTATGACAGTTTTTGCAGTGGATTACTTGGTCACTTATCCAGATGCAACAAAAGTACCCAATTTCCAAACTACTGACCAGGAGTGTCCCAAAGACCTCAAGTCTTCTGTACTTTTCCCAGAATTCAGCTTCAAATCATCAGAGCATAAAGGTAAAACTTACAATATGGCAACAAAAAGACATTGAATTTGGAATTTCTGTAATAAATATCTTCTAAATTGGACATGACAATATAAAATTAATGAGAATAAATATTATATTTCAATACATTTGTGTTCACTCTCGTATATACTTAATCACTAAAAAAAACTTGAGTTTTCCCACAAAAACTTTGTTTCCTAGAAATGTAGCATTTATTGTAAATATCATTAAACAAAATCTCTTATTATATTAAAAAGGTCTTAAAATGGCGAG
Associated Phenotype:
Not determined