ZMP
cdh2
Ensembl ID:
ZFIN ID:
Description:
Cadherin-2 [Source:UniProtKB/Swiss-Prot;Acc:Q90275]
Human Orthologue:
CDH2
Human Description:
cadherin 2, type 1, N-cadherin (neuronal) [Source:HGNC Symbol;Acc:1759]
Mouse Orthologue:
Cdh2
Mouse Description:
cadherin 2 Gene [Source:MGI Symbol;Acc:MGI:88355]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa206 | Nonsense | F2 line generated | Not yet available |
sa16882 | Essential Splice Site | Available for shipment | Available now |
sa15918 | Nonsense | Available for shipment | Available now |
sa32283 | Nonsense | Available for shipment | Available now |
sa11989 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa206
Status:
F2 line generated
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024627 | Nonsense | 28 | 893 | 2 | 16 |
The following transcripts of ENSDARG00000018693 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 17789419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 17843919 |
GRCz11 | 20 | 17743502 |
KASP Assay ID:
554-0152.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTGTGTTTTTGGCAGGTGGCGGTCCAGGGCACAGGGGCGATGCCATGT[C/T]AGCCTGGTTTCACCGAGAACGAGTACAACGTCATGACAGCCGACGTCATC
Long Flanking Sequence:
CCTGACCTCATCAGTCTAATTACACCCACCTCAAAATAACAGATGCCCCAGTGCCGGAGGGGGGAGGGGGGCAAACCCTCACCATCCTTGAAGGAAGAATAATTCAAAGCCAAGCCAGCAAATCGTCATGCAATGAACCTTATTTAATTTCGCCGATCTGCTGCAAATTAGCGAGTAATCGTTGAAAAATACAATAGCATAGCTAATTCAAAGAGTTCATTTCGAGCGTGATCAATGGACTTGGCGGCTCTGGAAAGGCTCATCACGGTGCTTTTCTTGAGCGGAGTTCTGCCTCATTTCCTCTGTTTATGGTGAAAGAGCGTGATCGTTATGTCCATCGATTCCTCTTGGGATTCGGGATATTTGGCTCTCGCTGTGGTGTAGGTTGGCCCGCGCTGAGGGGCGATGTGTATTAATCACCATTAATCGGGGGATTAATTTGTCTGGTGCTTTTGTGTTTTTGGCAGGTGGCGGTCCAGGGCACAGGGGCGATGCCATGT[C/T]AGCCTGGTTTCACCGAGAACGAGTACAACGTCATGACAGCCGACGTCATCACCGAGGGACAAGTTCTGCTCAAAGGTAAACAAAGACGTTTTCTTTACATGCATACTTAGAATAAACGGACCAATCCAAGCGGTGAGGCAGAGCGCTCCCTTACCAGGCTTGGGTTTCCAGTGTGAAGAGAAAAAGAGTTGGGGGAAGGGTGGGCTTTATGCTTGTATGTGAAAGAACGAGAGGGGGAGGAGGGTTAAGTGTTAGGGTTGCTTTAGTAGGGGGTGTTTATAGAGGGTGATATGTGTGCGAGAGAAAGAAAGGAGCAGGAGGAGGAGAACAGCTCTGTGTTTTGGTGGAATGTGTTTTGAAGCTTCACAGTGTGAAGTATCTGGGTGCTTGAATCACCCTCCCCCACTGTGGATGAATCCCTGTTGTGATCGATAGCATTGATTAGACCAGCCCATATCCATACAATTAGTCGATGGCACACATCCCAGTCAGCCATCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16882
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024627 | Essential Splice Site | 52 | 893 | 2 | 16 |
The following transcripts of ENSDARG00000018693 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 17789495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 17843995 |
GRCz11 | 20 | 17743578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACGTCATGACAGCCGAMGTCATCACCGAGGGACAAGTTCTGCTCAAAG[G/A]TAAACAAAGACGTTTTCTTTACATGCATACTTAGAATAAACGGACCAATC
Long Flanking Sequence:
CCTCACCATCCTTGAAGGAAGAATAATTCAAAGCCAAGCCAGCAAATCGTCATGCAATGAACCTTATTTAATTTCGCCGATCTGCTGCAAATTAGCGAGTAATCGTTGAAAAATACAATAGCATAGCTAATTCAAAGAGTTCATTTCGAGCGTGATCAATGGACTTGGCGGCTCTGGAAAGGCTCATCACGGTGCTTTTCTTGAGCGGAGTTCTGCCTCATTTCCTCTGTTTATGGTGAAAGAGCGTGATCGTTATGTCCATCGATTCCTCTTGGGATTCGGGATATTTGGCTCTCGCTGTGGTGTAGGTTGGCCCGCGCTGAGGGGCGATGTGTATTAATCACCATTAATCGGGGGATTAATTTGTCTGGTGCTTTTGTGTTTTTGGCAGGTGGCGGTCCAGGGCACAGGGGCGATGCCATGTCAGCCTGGTTTCACCGAGAACGAGTACAACGTCATGACAGCCGACGTCATCACCGAGGGACAAGTTCTGCTCAAAG[G/A]TAAACAAAGACGTTTTCTTTACATGCATACTTAGAATAAACGGACCAATCCAAGCGGTGAGGCAGAGCGCTCCCTTACCAGGCTTGGGTTTCCAGTGTGAAGAGAAAAAGAGTTGGGGGAAGGGTGGGCTTTATGCTTGTATGTGAAAGAACGAGAGGGGGAGGAGGGTTAAGTGTTAGGGTTGCTTTAGTAGGGGGTGTTTATAGAGGGTGATATGTGTGCGAGAGAAAGAAAGGAGCAGGAGGAGGAGAACAGCTCTGTGTTTTGGTGGAATGTGTTTTGAAGCTTCACAGTGTGAAGTATCTGGGTGCTTGAATCACCCTCCCCCACTGTGGATGAATCCCTGTTGTGATCGATAGCATTGATTAGACCAGCCCATATCCATACAATTAGTCGATGGCACACATCCCAGTCAGCCATCTCAATACGCTCAGTCAATCCGGCAGGGGCCACATTTGTGCTGCGGTTGTAAACTTGGGAGGCCTTATAACATCCCAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15918
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 |
---|---|---|---|---|---|
ENSDART00000024627 | Nonsense | 517 | 893 | 10 | 16 |
The following transcripts of ENSDARG00000018693 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 17848927)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 17903427 |
GRCz11 | 20 | 17803010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCRATGCTAACGACTTTYACAGCTCATGATCCAGACAGATATATGCAG[C/T]AGACTATTAGGTATTAAAGMAMACACATCTRCATATATACAYATGGTTTC
Long Flanking Sequence:
CCATAGACATGGGTTCAAATGCAGAGCAAAAGACGGTCTCCATGGAAACAGCTTCCACCTGCTGTTCAGCCGAGTTAATGGTTTATATGTCTCTTAATTGAGAATGAGTTATTCATTAATTATTATTCAAACATTTCTCTCCTGTGTATTTAATTGCAACACAATTCATTTATTGTATCGTTTCGATTCTTTCCCCTAACAGATTGTGAAGCGGAGTTAACTTGATTGTGTGTCTGCTTGTGTGTTCTTGTGTACAGCCAGTTGATTTCGAGATGAATCGATCATTCATGCTGACTGTTGTCGCTGACAATGAAGTGCCACTAGCGAGTGGAATCCATCGCACACGCCAGTCTACAGCCACCGTATCCATCCGCGTCATCGATGTGAACGAAAGCCCCAACTTTGACCCCAACCCCAAACAGATCAAACTGGAGGAGGGTCTTCCGCAGTGGTCAATGCTAACGACTTTCACAGCTCATGATCCAGACAGATATATGCAG[C/T]AGACTATTAGGTATTAAAGAAAACACATCTGCATATATACATATGGTTTCTAGCAATGGAAAGCATTTTTGGAAGTGTAATGCATTTTTATAAACTATTTACAGTTTACAAAAATAAAACTAATATGAAATAGTGTTGTCAGGCGATCAAATTATTTTAAAGGTTTTATTTAACAAAGGATTTCCTGTTATAATTATAGACAGATTATTATTGATAAAGTGCATTTTTATAGCACTTAATAATGTTTTTTTTTTTTATTTGTTTGCACCTTTATATTTATATAATATATGTTAAATATAAATGTTAAATGTAAATTCTTAACGCACTGTTCGTTTCATTTTGACAAATATTCTATACAGTCTAAACACAACAGAAGTAGTAGACTAATTTAAAAATTGGCTACTCCACATATAACCATTGTGAAAATGTAAACGAAATGAAAACGTTAACCACATCTTCTTGTGTGTTTGTGTTTTAAAGTTACTCTAAATTATACGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32283
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 |
---|---|---|---|---|---|
ENSDART00000024627 | Nonsense | 558 | 893 | 11 | 16 |
The following transcripts of ENSDARG00000018693 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 17849522)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 17904022 |
GRCz11 | 20 | 17803605 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATTGCTGTTTTGGATCGAGAATCTCCTTACGTGAAAAATAACCTTTA[C/A]AACGCCACATTCATGGCTTCAGACAATGGTAAGAGCAATGTTGTGTGTGT
Long Flanking Sequence:
CTATTTACAGTTTACAAAAATAAAACTAATATGAAATAGTGTTGTCAGGCGATCAAATTATTTTAAAGGTTTTATTTAACAAAGGATTTCCTGTTATAATTATAGACAGATTATTATTGATAAAGTGCATTTTTATAGCACTTAATAATGTTTTTTTTTTTTATTTGTTTGCACCTTTATATTTATATAATATATGTTAAATATAAATGTTAAATGTAAATTCTTAACGCACTGTTCGTTTCATTTTGACAAATATTCTATACAGTCTAAACACAACAGAAGTAGTAGACTAATTTAAAAATTGGCTACTCCACATATAACCATTGTGAAAATGTAAACGAAATGAAAACGTTAACCACATCTTCTTGTGTGTTTGTGTTTTAAAGTTACTCTAAATTATACGACCCCGCCAACTGGTTGGAGATCGACCCAAACAACGGACGAATTTCCACCATTGCTGTTTTGGATCGAGAATCTCCTTACGTGAAAAATAACCTTTA[C/A]AACGCCACATTCATGGCTTCAGACAATGGTAAGAGCAATGTTGTGTGTGTCTGTGTGTGTGTGTGTGTGTATGCATAAGCAGTTAAGATTGAGTGATTGAGTGATTCCATTGATTTTAGCTCTAGGGTGGAACTGCAACCGAACAGACTCAGAAATATACCCATGCCCACACATCCATGCTTAATGATCACACCAATGACAAATGCAAACTCATTCCCAACGTCTGCGTGTTCACTTTCCCTGGGTGGCTCTTTGAAGCAGCTCTTCTTTCTAACACACACATATGCACATACACTACCCGCTGTGTGAAAGAGTCTACAGAAGTCTGCTAGGCCGCTATTCTGCTGCCGTGTTTAACATTCTTGCTGCATCAGAGCTGTGAAACAACCCCCCTCTCTCACACACACACACACACACGCTGTAAATTTGAAAGCTTGTCTCCAGAAACACTCACAAAGCAGTTGTGCCGTTTTCGTATACGGTATTCCAGCACAAAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11989
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 |
---|---|---|---|---|---|
ENSDART00000024627 | Essential Splice Site | 568 | 893 | 11 | 16 |
The following transcripts of ENSDARG00000018693 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 17849552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 17904052 |
GRCz11 | 20 | 17803635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACGTGAAAAATAACCTTTACAACGCCAYATTCATGGCTTCAGACAATGG[T/A]AAGAGCAATGTTGTGTGTGTCNNNNTGTGTGTGTGTGTGTATGCATAAGC
Long Flanking Sequence:
ATGAAATAGTGTTGTCAGGCGATCAAATTATTTTAAAGGTTTTATTTAACAAAGGATTTCCTGTTATAATTATAGACAGATTATTATTGATAAAGTGCATTTTTATAGCACTTAATAATGTTTTTTTTTTTTATTTGTTTGCACCTTTATATTTATATAATATATGTTAAATATAAATGTTAAATGTAAATTCTTAACGCACTGTTCGTTTCATTTTGACAAATATTCTATACAGTCTAAACACAACAGAAGTAGTAGACTAATTTAAAAATTGGCTACTCCACATATAACCATTGTGAAAATGTAAACGAAATGAAAACGTTAACCACATCTTCTTGTGTGTTTGTGTTTTAAAGTTACTCTAAATTATACGACCCCGCCAACTGGTTGGAGATCGACCCAAACAACGGACGAATTTCCACCATTGCTGTTTTGGATCGAGAATCTCCTTACGTGAAAAATAACCTTTACAACGCCACATTCATGGCTTCAGACAATGG[T/A]AAGAGCAATGTTGTGTGTGTCTGTGTGTGTGTGTGTGTGTATGCATAAGCAGTTAAGATTGAGTGATTGAGTGATTCCATTGATTTTAGCTCTAGGGTGGAACTGCAACCGAACAGACTCAGAAATATACCCATGCCCACACATCCATGCTTAATGATCACACCAATGACAAATGCAAACTCATTCCCAACGTCTGCGTGTTCACTTTCCCTGGGTGGCTCTTTGAAGCAGCTCTTCTTTCTAACACACACATATGCACATACACTACCCGCTGTGTGAAAGAGTCTACAGAAGTCTGCTAGGCCGCTATTCTGCTGCCGTGTTTAACATTCTTGCTGCATCAGAGCTGTGAAACAACCCCCCTCTCTCACACACACACACACACACGCTGTAAATTTGAAAGCTTGTCTCCAGAAACACTCACAAAGCAGTTGTGCCGTTTTCGTATACGGTATTCCAGCACAAAACCCACCTGTAATCCAGTTTCAGCACACACTAAA
Associated Phenotype:
Not determined