Busch Lab

ZMP

cdon

Ensembl ID:
ENSDARG00000061328
ZFIN ID:
ZDB-GENE-021115-4
Description:
cell adhesion molecule-related/down-regulated by oncogenes [Source:RefSeq peptide;Acc:NP_001075097]
Human Orthologue:
CDON
Human Description:
Cdon homolog (mouse) [Source:HGNC Symbol;Acc:17104]
Mouse Orthologue:
Cdon
Mouse Description:
cell adhesion molecule-related/down-regulated by oncogenes Gene [Source:MGI Symbol;Acc:MGI:1926387]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa10351 Essential Splice Site Available for shipment Available now
sa36720 Nonsense Mutation detected in F1 DNA Not yet available
sa36719 Nonsense Mutation detected in F1 DNA Not yet available
sa23371 Nonsense Available for shipment Available now
sa43164 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10351
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087339 Essential Splice Site 24 1125 2 19
ENSDART00000110633 Essential Splice Site 24 348 2 8

The following transcripts of ENSDARG00000061328 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 42505980)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44111352
GRCz11 18 44104806
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTCMGCTGTGCTTTGTGTGTGCCATACTCTGCTCCTCAACTGCCCAA[G/A]TGAGTATCACAMTCAAAAAAAGTYATTGCAATTGAAACACTTACTAAGAA
Long Flanking Sequence:
TCGCTTGACGCAGAAGTATAAACCAGGTATACGTGTCTCCTGGTTCTGCTGTACTTTAGTGTTGGTGAAAGACTGTCCAGCACATGCAGTGAATTGTGCACAGTTGTCTGCTTTTCAAGTAGTTGGAGCATTTTAAATACTCGCCCTTGCCTCATTCGAATAGTCTACCGTGACAGCGCATATAAGATAAATGACGTAGTACGTAATAATCGGTAATGATCTAATAATGAACCAATAACGAATTGTCCACTTCTGCATTGTGGTACATCGAAGAAACAATTGATTTTGACACCCCTACAAAATATCAATATTGTATCGCCCATGAGCATTTTTTAATGAATGTGTTTGACTATGTTTCAGGTGTGGAGTTTATGTGGAGGGGGTGTGTGTGAGGCCCCAGGTTAGTGCACAGACGTGAAACAGCGTCATGGAGGACGGTGGCCTGAGATTATTGTCCGCTGTGCTTTGTGTGTGCCATACTCTGCTCCTCAACTGCCCAA[G/A]TGAGTATCACACTCAAAAAAAGTCATTGCAATTGAAACACTTACTAAGAAGCAGCATTCAGCCATCAAAGTTATTCTTCCTAGCAGGCTGAAGAATGTAGATGAAATGTTTTTAATTTACTTCATTTTATTTTTCAGCTGTTCTTTCTTTCTCTTTCCGTGCGGAGCCTCTCTCAGCGATTCTGAAGCAAGGTTCTTCAGTCCACCTACATTGCACAACACATCCAGCCACTGCCAGAATCAGCTGGCTGTTTCAAGGGCAACCACTAGATCCCAGTCACCATTCTGGAGTGGAACTAAGTCAAGACTCCCTCTCACTGTCAAACCTCCAACCGGCTCTCACAGGCTCCTACCAGTGCTCGGCTCGCTCTGAGACAGGCTCCATCATCAGCAGGCATGCACGAGTTACCATTGCAGGTAAGCACATCTGATCACATGTATATTGTGCCAACAAGTACACTTTGAACTGTAAGATCAATTCTACAAACAACAATGCACTTC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa1179
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087339 Essential Splice Site 214 1125 5 19
ENSDART00000110633 Essential Splice Site 214 348 5 8
ENSDART00000087339 Essential Splice Site 214 1125 5 19
ENSDART00000110633 Essential Splice Site 214 348 5 8

The following transcripts of ENSDARG00000061328 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 42503001)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44108373
GRCz11 18 44101827
KASP Assay ID:
554-1089.1 (used for ordering genotyping assays)
KASP Sequence:
AACTCGAGAGACTCGMGTAGAGGCTCATGGCACTAAACTCTTAGTCAAAG[G/A]TTGGTTGAACAAACTGACTTGTCTTTCTCTAAGTTTCAATTAAGTATATT
Long Flanking Sequence:
TACAATCCAAATCAATACTGCATTTTCAGTGATTTGTTTACATCATAGATTGACTAAAACTTTAGTCTGCCTATTTCTGTTTTGCTATGAAGTGATTGATCACTCTTTGATTTATTCCTTTAGATATTGAGGAGTTTGCGGAAACCCATCGGAGGTCATTTACTGTAAATAAGGGCGACACTGCTGTTATTGAATGTCCACTTCCGCGCAGCAATCCACCTGCTCTTCCACGCTTCCGGATACGGGGGAAATGGCTGGAACAGTCTACAGGTAGATCAGATGATCTGCAATGCCAAACCCTCCAGAAATGCATGAAGATACATTTGAACGCTTTGTCTCTTTTGTATTTCTTTCAGACGAGTATTTAATACTGCCCTCCGGGAACCTTCAGATTGTGTCTGTGTCTTCAGAACATCAGGGAATGTATAAATGTGGAGCTTATAATCCTTTAACTCGAGAGACTCGCGTAGAGGCTCATGGCACTAAACTCTTAGTCAAAG[G/A]TTGGTTGAACAAACTGACTTGTCTTTCTCTAAGTTTCAATTAAGTATATTCTATTATTTCTTTGGTATGCTAGATTTTCTGTGTACTGTAAATATAAATTGTACTGTTATAAACTATAATAAAGCCATTGCTTCATTTCTTTGACGTAGATTCAGAAAGCTCTTCACCTGTAAGGATTGTCTATCCCATCACACCTCGCAGTCTTACTGTGGACCAGTCTGGATCTCTAACCCTTGAGTGTGTTGTATCAGGAAGTCTTTCTTCAAAGGTCAAATGGATGAAAAATGGGGCAGAGCTATCACTGAGCTCCAAAAGGATGTTATCGCATAGCAACCTGGTGTTGAATGACATTCAGCCGGGTGATGGAGGACATTATAGCTGCTCTGTTCCTACTGACCGTGGAGCTGTGGTCAGTGTCAACTACACTGTGAATGTGCTTGGTGAGGAGTTAATATTTATACCTTCACTTTGGTAATTTTAGCAATGTTTAGGGCAGTTTG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5642
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087339 Essential Splice Site 214 1125 5 19
ENSDART00000110633 Essential Splice Site 214 348 5 8
ENSDART00000087339 Essential Splice Site 214 1125 5 19
ENSDART00000110633 Essential Splice Site 214 348 5 8

The following transcripts of ENSDARG00000061328 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 42503001)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44108373
GRCz11 18 44101827
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCGAGAGACTCGMGTAGAGGCTCATGGCACTAAACTCTTAGTCAAAG[G/A]TTGGTTGAACAAACTGACTTGTCTTTCTCTAAGTTTCAATTAAGTATATT
Long Flanking Sequence:
TACAATCCAAATCAATACTGCATTTTCAGTGATTTGTTTACATCATAGATTGACTAAAACTTTAGTCTGCCTATTTCTGTTTTGCTATGAAGTGATTGATCACTCTTTGATTTATTCCTTTAGATATTGAGGAGTTTGCGGAAACCCATCGGAGGTCATTTACTGTAAATAAGGGCGACACTGCTGTTATTGAATGTCCACTTCCGCGCAGCAATCCACCTGCTCTTCCACGCTTCCGGATACGGGGGAAATGGCTGGAACAGTCTACAGGTAGATCAGATGATCTGCAATGCCAAACCCTCCAGAAATGCATGAAGATACATTTGAACGCTTTGTCTCTTTTGTATTTCTTTCAGACGAGTATTTAATACTGCCCTCCGGGAACCTTCAGATTGTGTCTGTGTCTTCAGAACATCAGGGAATGTATAAATGTGGAGCTTATAATCCTTTAACTCGAGAGACTCGCGTAGAGGCTCATGGCACTAAACTCTTAGTCAAAG[G/A]TTGGTTGAACAAACTGACTTGTCTTTCTCTAAGTTTCAATTAAGTATATTCTATTATTTCTTTGGTATGCTAGATTTTCTGTGTACTGTAAATATAAATTGTACTGTTATAAACTATAATAAAGCCATTGCTTCATTTCTTTGACGTAGATTCAGAAAGCTCTTCACCTGTAAGGATTGTCTATCCCATCACACCTCGCAGTCTTACTGTGGACCAGTCTGGATCTCTAACCCTTGAGTGTGTTGTATCAGGAAGTCTTTCTTCAAAGGTCAAATGGATGAAAAATGGGGCAGAGCTATCACTGAGCTCCAAAAGGATGTTATCGCATAGCAACCTGGTGTTGAATGACATTCAGCCGGGTGATGGAGGACATTATAGCTGCTCTGTTCCTACTGACCGTGGAGCTGTGGTCAGTGTCAACTACACTGTGAATGTGCTTGGTGAGGAGTTAATATTTATACCTTCACTTTGGTAATTTTAGCAATGTTTAGGGCAGTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36720
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087339 Nonsense 354 1125 7 19
ENSDART00000110633 None None 348 None 8

The following transcripts of ENSDARG00000061328 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 42502106)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44107478
GRCz11 18 44100932
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGGCAATCCAACCCCCAACATCACATGGCTCCTTAACGCTGCCCCTT[T/A]ATCTTCTTCACCCCGCCTCAAAATCTCTGGCACCTCCCTTCTCATCTCTT
Long Flanking Sequence:
GACCGTGGAGCTGTGGTCAGTGTCAACTACACTGTGAATGTGCTTGGTGAGGAGTTAATATTTATACCTTCACTTTGGTAATTTTAGCAATGTTTAGGGCAGTTTGATGCTAGGAGATCAGGGTTTTCTCAGGTTTCTTAAAGGTGTAGTAGGTGATCTGCCTAAATGCTAACTGGCTATTGTAATATGTTCAAAACACGATAAATAAGTAGACTGAACAAACAGCAGTTTGAGTGTACTTTCCAACCAACAATCAACTAAATGATCAGATGCTAAAAATATTAATTAGCCATGAACAACAGTTCACTTAAAAATTTGAAGTAGTTGCATCATTATGGTGTAAAATAACTCTAGCATGCTTCTCTACTTTACAGCACATGTATCCATCCTGCGAGGTTTGTCAGATCAGGCTGCAGTTGCTGGATCCTCTGTGAGATTTACCTGTGCTGCCAGTGGCAATCCAACCCCCAACATCACATGGCTCCTTAACGCTGCCCCTT[T/A]ATCTTCTTCACCCCGCCTCAAAATCTCTGGCACCTCCCTTCTCATCTCTTCAACAACGCTTCAAGATCAGGGAATCTACCAGTGCATGTTTGATAATGGCATTAGCTCTGCACAATCCACAGGAAGACTCAGTATCCAATCAGGTAAGATACCTAAAACACTCATGTACAGTATATGTGTATGAACTTCACAGGGGGCTTCAGTCACTAGATCTTGAATCGGGTCCTTCACCTAATTAAAGTTTAAAGGGCCATGAAACCCCCTCTTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTCTGTTTAGGGGGGAGTGTCGGAGGAACTAAAGTGGGAGAGTGTGGGAGTGTCTATTTGGGCACGCGCGAGTTTCAGTCAAAATACTCACACACAGGAGTGATGGTGTTTAACCTACATGGACATCTGTAGTCGAATTATTTGCCAAATTATTAAATGGTGGACTTTAACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36719
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087339 Nonsense 392 1125 7 19
ENSDART00000110633 None None 348 None 8

The following transcripts of ENSDARG00000061328 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 42501993)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44107365
GRCz11 18 44100819
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGATCAGGGAATCTACCAGTGCATGTTTGATAATGGCATTAGCTCTGCA[C/T]AATCCACAGGAAGACTCAGTATCCAATCAGGTAAGATACCTAAAACACTC
Long Flanking Sequence:
GAGATCAGGGTTTTCTCAGGTTTCTTAAAGGTGTAGTAGGTGATCTGCCTAAATGCTAACTGGCTATTGTAATATGTTCAAAACACGATAAATAAGTAGACTGAACAAACAGCAGTTTGAGTGTACTTTCCAACCAACAATCAACTAAATGATCAGATGCTAAAAATATTAATTAGCCATGAACAACAGTTCACTTAAAAATTTGAAGTAGTTGCATCATTATGGTGTAAAATAACTCTAGCATGCTTCTCTACTTTACAGCACATGTATCCATCCTGCGAGGTTTGTCAGATCAGGCTGCAGTTGCTGGATCCTCTGTGAGATTTACCTGTGCTGCCAGTGGCAATCCAACCCCCAACATCACATGGCTCCTTAACGCTGCCCCTTTATCTTCTTCACCCCGCCTCAAAATCTCTGGCACCTCCCTTCTCATCTCTTCAACAACGCTTCAAGATCAGGGAATCTACCAGTGCATGTTTGATAATGGCATTAGCTCTGCA[C/T]AATCCACAGGAAGACTCAGTATCCAATCAGGTAAGATACCTAAAACACTCATGTACAGTATATGTGTATGAACTTCACAGGGGGCTTCAGTCACTAGATCTTGAATCGGGTCCTTCACCTAATTAAAGTTTAAAGGGCCATGAAACCCCCTCTTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTCTGTTTAGGGGGGAGTGTCGGAGGAACTAAAGTGGGAGAGTGTGGGAGTGTCTATTTGGGCACGCGCGAGTTTCAGTCAAAATACTCACACACAGGAGTGATGGTGTTTAACCTACATGGACATCTGTAGTCGAATTATTTGCCAAATTATTAAATGGTGGACTTTAACTGCAGTTTGGCTCTTTCATTCAGGGAATTCATTCATGCCCCTCGCGACAAACGAGATATTTGATTCGAGGATCTGCTCTAAGTGTGTATTTTTCATGCAATGTTTGATACCGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23371
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087339 Nonsense 634 1125 11 19
ENSDART00000110633 None None 348 None 8

The following transcripts of ENSDARG00000061328 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 42481879)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44087251
GRCz11 18 44080705
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCCAATGGTGGCTCTCCCATCACTGCATTTCGCGTGGAGTACAGAAAA[C/T]AGGGGCGTAATGGAGACTGGATCATTGCAGCTGATAACATCTCACCGCTT
Long Flanking Sequence:
GCATATACACATATACAGACATGATACAATTTATACACTGAGTTACTGGAGGTTAATGAAGACCTCATTTGTGCATGTGTATTAAGTGTATCATGTCTTTAAATGTATCAGGAATGTATCAGGTGTGTATATGTAAAGAATGTATCAGGTGTGTATATGCATGGCTGTCTTCATCAACCTCCAGTAGCTCAGTGGTAATGTCACTCACTTCTCAATCCAGAGACCTGGGTTCTATCCCAGACACATAAATACAGTAATTCAATATAATTCTTTAGTTCCTGGTCCAACTATAGATGTGCACGTTGCGATAATGATGCTGAAACAATATGTTGTTTTTATTTTTTTCCTAATTTCTTATTGGTTGGATTCATTCTCTAGTTCCTGAGGCTCCAGACCGCCCCACAATCTCAATGGCGACAGAAAGTTCTGTTTACGTCACATGGATACCTCGGGCCAATGGTGGCTCTCCCATCACTGCATTTCGCGTGGAGTACAGAAAA[C/T]AGGGGCGTAATGGAGACTGGATCATTGCAGCTGATAACATCTCACCGCTTAAACTGTCAGTGGAAGTGCGCAACCTTGAGCCAGGTGAGGTTACTGCAGTATGTTTTAAAATTTTTATAGAAAAACTTGAGGAACTTTGAGCTGCATGATTTAAAGCAGGGATCTCAAACTCGCGGCCCGCAGGCCATTTGCGGCCCTCAGTGCAATATTTTGTGGCCCGCGCCGACCACTGTACACTGACAGAATCTGACAGCGCTCTCTCTCCCCGCTCCGCTGATTCTATCCGTACACAGCGGTCACTGGCATTCCCCGCCCGCCGTGTAAACAAAGGGGCGGGGATGCCGGTGACGTCACCACGCACCCCGCCCCTTTGTTAGACGCTGTGACGGGCGGGAAGTGTTAGGAGGGAACTCACGCCGGCCAGAACCAAGGTAAGCTGTTCCTGCCCCTGCCTGCCACTTAGCTACCTATCTGCAGCCTGCATCTTATATATATTATAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43164
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087339 Essential Splice Site 798 1125 14 19
ENSDART00000110633 None None 348 None 8

The following transcripts of ENSDARG00000061328 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 42472513)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 44077885
GRCz11 18 44071339
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGGCGGCGAGAGCGAATACAGTAACGTCATGATCTGCGAGACCAAAG[G/A]TGAGAGTCTGAAGTACCGTCACAGGAATGCTATACTTAACATGCAGACAG
Long Flanking Sequence:
GGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTCTGCCTGTATGTTTGTGTATATGTGAATATGTGTGTGTCTGTATGTATATGTGTGTTTAAATAGGTGTGTATGTGTGTAAATAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTCTGCCTGTATGTTTGTGTATATGTGAATATGTGTGTGTCTGTATGTATATGTGTGTTTAAATAGGTGTGTATGTGTGTAAATGATAGAGAAAACGGAGACAAAGCAAATGAATTGTGGTTAGGATTTATCAACACATGCTTTGAAAGAAGAAGTCCATGTCCTTCAGTACAGCCGCTCTCATTGCATCCTGTCACTTCCTCCCCTCAGGCTTCAAATTCTGGCACATGATTGGTGAACTCCAACCCGAGACATCTTATGACATCAAGATGCAGTGCTATAATGACGGCGGCGAGAGCGAATACAGTAACGTCATGATCTGCGAGACCAAAG[G/A]TGAGAGTCTGAAGTACCGTCACAGGAATGCTATACTTAACATGCAGACAGGAACCCATAAAGCCCCGGTGCTAATGACAGAGGGAAGCGAGCAATGGTTTTATTATCGGGTAGACAAAGAGAGACATTGTGCTGCGTCTCCTTGACATCATTCACTGATAACTGGCCTTAATGCAACACTGTTGAAATCCAAGCAGAGTGTCATTCACAGCCAGAGCAAATAAAAACATCGGACTTGCTGCTACAACAGACTTTAAGACTGACAACAGATGCATTGTTGTATGCTAGCACTTGTTAGGGTTCTGGATTATTGCTAATACTTGGGGATAGACATTTCAACAAATCCATGATCCTAAGAATTAAAGCATTAGTATTAAACGCTGCATAATTAATCCTGTTTAATTAGTTCTACAGTGCATCAAATCAAGCACTTTATAAGCAACAGATCTTTAAAGGTGCTATATGTACGTGTTGACTCTTCTAAAGCATGAAAATACCATA
Associated Phenotype:
Not determined