ZMP
si:dkeyp-27c8.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
CDH24
Human Description:
cadherin 24, type 2 [Source:HGNC Symbol;Acc:14265]
Mouse Orthologue:
Cdh24
Mouse Description:
cadherin-like 24 Gene [Source:MGI Symbol;Acc:MGI:1928330]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24402 | Nonsense | Available for shipment | Available now |
sa37780 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24403 | Nonsense | Available for shipment | Available now |
sa13405 | Nonsense | Available for shipment | Available now |
sa5983 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37781 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24402
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114959 | Nonsense | 885 | 1870 | 2 | 13 |
ENSDART00000141958 | Nonsense | 88 | 643 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 40929811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 40762665 |
GRCz11 | 23 | 40655569 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCGTGCAGGACATCAACGATAATCCACCGCTGTTCCAGAGCGGCCCCTA[C/A]AGCGCCACCGTACCCGAGATGGCCAACATTGGTATTACAAGTCTCTTTTA
Long Flanking Sequence:
TTTACTGAGAGATTAAAACTCAAGAGTTTTCGGTTTCAGAATAGCTGATCTGAGTTTGGTCAATCAACTTTGAGTAGATCAACTGTTTTTTGCTAGATTCTATTCAATTATAATCCATTTTGTTCTGTTCATGAATAGTTTCCACATCATTTTTTTTTCTCTCGACAGGGTTTTACAGAAAGAGAATCTATTAATTGCTTTAACATACTTGCTGTCTTTCTTTTCCCATTCCTCCAGCTTCATTCCAGTGTGGACAAGGGCGATGGCCGGACCAAATATATTTTAAAGGGCGAAGGGGCTGGATCTGTGTTCGTCATCGACAGCCGTACTGGGAACATCCACGTCACCAAACCCTTAGACCGAGAGGAGAAGGACCAATATCGCCTTATCGCCACTGCAACAGACCGGCAGACGGGTCGAGCCCTGGAGCCCTCGTCCCAGTTCATCATCCGCGTGCAGGACATCAACGATAATCCACCGCTGTTCCAGAGCGGCCCCTA[C/A]AGCGCCACCGTACCCGAGATGGCCAACATTGGTATTACAAGTCTCTTTTACATGCAAGATTGAAATAGATGTCCTTAGATGTAAGCAAAATAATCTTGTTTTTGCTCTGAAATAAGATTATTTTGCTTGTTTTAGGGAAAAACTCACTTTATTTTGACTTATTAATTCTGAAAACAAAACAATAGTTTTAACTTAAATAGAAAATGTTTTTTGATTTCTGAATTTTGGACTAAAAACTCTAAATAAGAAAAGCATTTTGTAAACAGTGTTAATCAGCAATTCCACTTTTAAAGTAAAGTGTGACCAACATTTTTAATGGCAAATGTTTTGGAATTTATAGTGGCGTTTCCATCCAGCATTCTTTGATGCAAAACCCCTACATGTGCAAAATTTAAACAGTGCATAAAACAGAGAATAAAAATCAGCCAATATTTTGTGTTAGTTAAACTTTATATTGGCTATCTTGCTATTTAAGAAACATGACACAAACTGTAAATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37780
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114959 | Essential Splice Site | 1183 | 1870 | 7 | 13 |
ENSDART00000141958 | Essential Splice Site | 386 | 643 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 40981629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 40814483 |
GRCz11 | 23 | 40707387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGAGAGCAGGAGCAATGGCACAACATTACTGTCATCGCCACACAGAGAG[G/A]TACCAGAGCTCCTCGCCTCCGCTCTTAAAGGGACACGCCGTCAATTCTGC
Long Flanking Sequence:
CTCAGTCTACATAAACAAAAGCACCTACATTTAAATTATTATTATTGTTTTGCATGACAGTAATGAGAATTATAGTATATTTTTTATTATCATTTCAATTCTGCTGTAAAATCTCACTAGAATTTGTTCTCGACATGTTTTAATAAGCTTTTCCTCACACTGCTCATGCAGTTTTTCATTATCAGTGTAAAAAAAACACTCATATTGCATCACGTTTCAGTCTGCAACAGGAAATCCGTGAGCTGTTTTCACTTCAAGCCGGTCGGTTTCGCTTGCTTAACTGCGTTATTGATGCACCGGCTTCTCTTTATATCTTGTAATCTGTCTGCCCTCCTCCTTTTATTCCTGTCCATTTCTTCTCAGGTACTCGATTGATCCCGAGTCGGACCCCGAGGCTCTGTTCCGCATCGCCTCTGACAATGGCCTCATCACCACGGCCATGGAATTGGATCGAGAGCAGGAGCAATGGCACAACATTACTGTCATCGCCACACAGAGAG[G/A]TACCAGAGCTCCTCGCCTCCGCTCTTAAAGGGACACGCCGTCAATTCTGCGCGCCTGACAATCTCACACAGGTCGCAGCGTGAAATCGGCCCACAGGAAAGCTATTACTGCTGCAGAGGCTCATCCGCAAACAGAGAAAAAGATAATCAAATGACAACTCAGATTGCTTTTAAAGTCCCCGTGAAATCAGAATTGAAGTTTTATAGGTGCTCATTTCACTATGTAAGCCTTAAAAGGGTTAGTTCACTCAAAAATAAGAATTTATACTTTTTTACTCACCGTCAAGGCGTCTTATTGTAGGTGTATATTACTGTCAACTTGAAGCCAAATCCAGTTGAAGTTAATTTTGAGTTATTTTAAGTGATCTTGGGTTTTTCCAGCTGATGGATGAATGGATGCAGCAGATGGATGGATGGATGGATACAGCAGATAAATGGAGGGATATAGCTTATATATAGCTAATACACACCTGATCAAACTAATTGAGTCCTTCAGGCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24403
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 |
---|---|---|---|---|---|
ENSDART00000114959 | Nonsense | 1384 | 1870 | 11 | 13 |
ENSDART00000141958 | Nonsense | 587 | 643 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 41005844)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 40838698 |
GRCz11 | 23 | 40731602 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTTTTATCTGATAGTGGTGACGGCTCTCTCGCTATCATTGCGAAAG[C/T]AAAAACGGGACACTCAGTCTCCTGTGGAAGATGATGAGATCCGGGAGAAC
Long Flanking Sequence:
GCTCAAACATAAAAAATGTTGAAATACGTGAAGCGCTATGAATACTTTCCGCATGCACTGTGACTCAGTTTTTCGACCACACTTTGTTATCATTGCTCATTTATTCGTGCTGGAATTTTATTTATATTTATTTGCAGGAAATTAGAACTGAATTTAGAATTAGTTTTGAAACAAATCTTTGCGTTAACAAATGAAATTAAACATGTAGGCTAATGGATGTATTCAGTGGAGATCGGACAACACCGTTTCCCTATCCTTGAAAGTAAAGGAGTAAAGAGTAAAAATTAGTAAAAAGAAAGTAAAGAGGCCGAATGGAGGAGGCTCGTTCTTTATCTTCATGCTGCAAATGCTCTGTTTAACTGTCTTCTCGCTAGTGAAGCTTTCAGTTTTTCCACTTTTCCTATTGGCCGTGGGAGATGAGACTCTGATTGGTTTAATGTTATGTTTTATTCTTCTTTTATCTGATAGTGGTGACGGCTCTCTCGCTATCATTGCGAAAG[C/T]AAAAACGGGACACTCAGTCTCCTGTGGAAGATGATGAGATCCGGGAGAACATCATCACGTATGACGATGAGGGAGGAGGAGAGGCGGATACAGCCGCTTTCGACATTGCCGCGCTAAAGAGCGCCCCGCAGAGCATGAGGAGGGTACAGCGCCTACAAAACACCAACAACATGTGAGTCAACCCTATTTATATATTTAACAGTCTTTTGGGAGGCACGGTGGCTCAGTGTTTAGCACTGTCGCCACACAGCATGAAGGTCACTGGTTTGAGTCTAGGCTGAGCAAGTTCGCATTTCTGTGTGGAGTTTGCATGTTATCCCTGTGTTGGCGTGGGTTTCCTCTGGGTGATCCGGTTACCCCCACAGACCAAACACATGTGCTGTAGGTGAATTGAATAAATTAAATGGGCCATAGTGAATGTGTGTGTATGAATAAGAGTGTGTATTGGTGTTCCTCAGTGTTGAATTGCGGCTCGAAGACCATTCTCTGTATAAAACGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13405
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 |
---|---|---|---|---|---|
ENSDART00000114959 | Nonsense | 1604 | 1870 | 13 | 13 |
ENSDART00000141958 | None | None | 643 | None | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 41015857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 40848711 |
GRCz11 | 23 | 40741615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCATCGGCGGGCCACAAACTAGAGTCGTCCCCTCACGGTTTAAATACA[C/T]GAGCCTCCATTTCCACCATCACCACAGACGACTCAACTCCTGTATCAGCA
Long Flanking Sequence:
AATGCAGAGAACAGACTTGTGTTCTTGTAAAGAGCGGTCTTGCCAGGTCAGCTCGGAAGAGCAAACTCAGGAGACCACGAGAACACATCACTTCCTGATGGTCACATGACCTTCATGCATTTTTAAGAGAAAATTTAAACATTACAGCATTCATACAATTTTTTTTCTCTCTTTTCTATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTCAGTTGAGATTACTTCAAACATTTAATAAAACATGTACATTTCATAGCACTTCACAGACCTTTAATGCTATAAATATGTGGTTTTAGCAGATTTAATTATTCAGTTTTCCTTCCCTCACCAAAACCTGTCTTTTTCTCTCTCAGTCTGTTCATTCAGATCAAGTTCTGTTCGTGAAGGGCTCCAGTCAGAGCGGCTCCTGTTCAGAGGCTTCCAGCTCATCGGCGGGCCACAAACTAGAGTCGTCCCCTCACGGTTTAAATACA[C/T]GAGCCTCCATTTCCACCATCACCACAGACGACTCAACTCCTGTATCAGCAGTGGACAAGAATGGAGATATTACGCTCATCAGCACCAGCCAGAGCTCAACCAGCCTCAGCACCACAGATATACCATTCAGAACGATGGAGGGAACGCTACTGAGAAATGGTAGAGGAATAGCTTTAAACACAACCACTCTTCTTTATCCAGAAGCTGCCGCTGCCACTGCTGCTGCTGGGCTTATGGGATTATATGGAGTAAGTGGGCGGAACTATGTGCCACAGTTAGTGATGCCCCTCCCAGGTGGGGCGGGGCTTTATGAAAGTAGATGGGGCTTAGGGAATGGGAAAGTTGGACAAGCGAGCTCAGATAAAGCATCCGCCGATTCGTTGACAAATCGAATGGGCGATTTCCTGCAACACCGTCTGGCGATGGTGACCTTTGACCCCATGCAGCCGCCGTATGACTCGCTGCAGACGTACGGATTGGAGGGTGGCGGCTCACAGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5983
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114959 | Nonsense | 1662 | 1870 | 13 | 13 |
ENSDART00000141958 | None | None | 643 | None | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 41016032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 40848886 |
GRCz11 | 23 | 40741790 |
KASP Assay ID:
554-3840.1 (used for ordering genotyping assays)
KASP Sequence:
ATTCAGAACGATGGAGGGAACGCTAYTGAGAAATGGTAGAGGAATAGCTT[T/G]AAACACAACCACTCTTCTTTATCCAGAAGCTGCCGCTGCCACTGCTGCTG
Long Flanking Sequence:
CTATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTCAGTTGAGATTACTTCAAACATTTAATAAAACATGTACATTTCATAGCACTTCACAGACCTTTAATGCTATAAATATGTGGTTTTAGCAGATTTAATTATTCAGTTTTCCTTCCCTCACCAAAACCTGTCTTTTTCTCTCTCAGTCTGTTCATTCAGATCAAGTTCTGTTCGTGAAGGGCTCCAGTCAGAGCGGCTCCTGTTCAGAGGCTTCCAGCTCATCGGCGGGCCACAAACTAGAGTCGTCCCCTCACGGTTTAAATACACGAGCCTCCATTTCCACCATCACCACAGACGACTCAACTCCTGTATCAGCAGTGGACAAGAATGGAGATATTACGCTCATCAGCACCAGCCAGAGCTCAACCAGCCTCAGCACCACAGATATACCATTCAGAACGATGGAGGGAACGCTACTGAGAAATGGTAGAGGAATAGCTT[T/G]AAACACAACCACTCTTCTTTATCCAGAAGCTGCCGCTGCCACTGCTGCTGCTGGGCTTATGGGATTATATGGAGTAAGTGGGCGGAACTATGTGCCACAGTTAGTGATGCCCCTCCCAGGTGGGGCGGGGCTTTATGAAAGTAGATGGGGCTTAGGGAATGGGAAAGTTGGACAAGCGAGCTCAGATAAAGCATCCGCCGATTCGTTGACAAATCGAATGGGCGATTTCCTGCAACACCGTCTGGCGATGGTGACCTTTGACCCCATGCAGCCGCCGTATGACTCGCTGCAGACGTACGGATTGGAGGGTGGCGGCTCACAGGCCACGTCTCTCAGCTCGCTGGAAAGCGAGGCAGAAAAAGACACGCAGGGCCAGAAACACAGTTTTGAGGAATGGGGACCCAAGTTTGACAGGTTGCTTGATATTTTTAGGGAACGAGCGACGGAAAAGGAGGATAATGCAAAGCATGAGGGCGAACGTTTGAAGGGAGAGGAAACGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37781
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114959 | Nonsense | 1755 | 1870 | 13 | 13 |
ENSDART00000141958 | None | None | 643 | None | 10 |
Genomic Location (Zv9):
Chromosome 23 (position 41016312)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 40849166 |
GRCz11 | 23 | 40742070 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAACACCGTCTGGCGATGGTGACCTTTGACCCCATGCAGCCGCCGTA[T/A]GACTCGCTGCAGACGTACGGATTGGAGGGTGGCGGCTCACAGGCCACGTC
Long Flanking Sequence:
TCGGCGGGCCACAAACTAGAGTCGTCCCCTCACGGTTTAAATACACGAGCCTCCATTTCCACCATCACCACAGACGACTCAACTCCTGTATCAGCAGTGGACAAGAATGGAGATATTACGCTCATCAGCACCAGCCAGAGCTCAACCAGCCTCAGCACCACAGATATACCATTCAGAACGATGGAGGGAACGCTACTGAGAAATGGTAGAGGAATAGCTTTAAACACAACCACTCTTCTTTATCCAGAAGCTGCCGCTGCCACTGCTGCTGCTGGGCTTATGGGATTATATGGAGTAAGTGGGCGGAACTATGTGCCACAGTTAGTGATGCCCCTCCCAGGTGGGGCGGGGCTTTATGAAAGTAGATGGGGCTTAGGGAATGGGAAAGTTGGACAAGCGAGCTCAGATAAAGCATCCGCCGATTCGTTGACAAATCGAATGGGCGATTTCCTGCAACACCGTCTGGCGATGGTGACCTTTGACCCCATGCAGCCGCCGTA[T/A]GACTCGCTGCAGACGTACGGATTGGAGGGTGGCGGCTCACAGGCCACGTCTCTCAGCTCGCTGGAAAGCGAGGCAGAAAAAGACACGCAGGGCCAGAAACACAGTTTTGAGGAATGGGGACCCAAGTTTGACAGGTTGCTTGATATTTTTAGGGAACGAGCGACGGAAAAGGAGGATAATGCAAAGCATGAGGGCGAACGTTTGAAGGGAGAGGAAACGAACAAGACAGAGGATGAAAGTGAGACAGAAGTGCGAAATGAGATTACAATTGAATCGAAGGAGACACGTCAGGCTGAGGAGGAAAGCACGGAAGACACGGAGCAAACGCAAAACGGAAAGAGACACTAGAGAGGGAATGGGAGGATGTGATGTCACATCTTAAACGTTCTAAAGCAATAAGTGCTGAAGGGAGAAAATGAGCACAATCTGGACAAAAGAGAATTTTATATGGACCTGCCAAAAACCCAGTATGTCATTGTTGTAGAGGAGCTGAAGGTCTT
Associated Phenotype:
Not determined