ZMP
CDH16
Ensembl ID:
Description:
cadherin 16, KSP-cadherin [Source:HGNC Symbol;Acc:1755]
Human Orthologue:
CDH16
Human Description:
cadherin 16, KSP-cadherin [Source:HGNC Symbol;Acc:1755]
Mouse Orthologue:
Cdh16
Mouse Description:
cadherin 16 Gene [Source:MGI Symbol;Acc:MGI:106671]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7280 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30891 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34157 | Essential Splice Site | Available for shipment | Available now |
sa21051 | Nonsense | Available for shipment | Available now |
sa34156 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21050 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7280
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109534 | Essential Splice Site | 91 | 831 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 45940813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 44613641 |
GRCz11 | 7 | 44952866 |
KASP Assay ID:
554-4669.1 (used for ordering genotyping assays)
KASP Sequence:
AAATTGAGCAGAMGAATGTACATWTTCCCAGAGCTATTTGTCTTTATTTC[A/T]AGCTACNNNNNNNNNNNNNNNTGTCACATGKGTCCCTGACTCTCAGTTSA
Long Flanking Sequence:
CAGATCTCCCTCTGACCTATTCTGATCTGACTGTAAATGGTGATGATGAAGGGATTTTTGGTGTGGAGTCAGGTTTTCTGTATGCCCTTAAACCTCTGGACCGAGAAAAACAGCCATCTTACTCCTTACAGGTAAGAATCCTAAAGAGATGTCTGTCTGTCTGTCTGTCTATCTGTTCAAAATAAAACCAGCATCCACTTCAATTATTTTATTCAGTTACATTGCTGTTAACAGATGTGTTATGATGAAAATAGGAATTAGTTTTGCTTTTTAATATACTACTAATCTGTCTTCAAACTTTGAAATAAGAATATTGTAATTTAGGCCATTTATTTGCTGAAAGTGACAATAGGTCAACTTACATTTATCATTAGAATGTTTATATAGTGTTTTACAAAATTTTATATTTACATATTTATTTTTGTCGAGCTATTATTGATTTAGACAAATAAATTGAGCAGACGAATGTACATATTCCCAGAGCTATTTGTCTTTATTTC[A/T]AGCTACATTCAAAACACTGACTGTCACATGGGTCCCTGACTCTCAGTTGAAATAAAACCTACGTCATTGATTTGCTAGATTTTCAAAATGCAAAAAAAAAAAAACACATCCGGAGGTAGTCCAAAAATAACAAACGCTGACAGAAATTGCAGGCCAATGAAACGTGAACCCAAAAGGGTTTGAGCTCTAATAAGACATGCTGCTTGAGTGCTTTGACCTGAGTGCTTTTTTTCCAGGTGTCCTTCACAAAGTCCATGCACACTCAGAGCTTCACCGTAGAGGTGTGCGTCATCGATAAGAACGACAACGTACCGGTGTTCCTGGAAGAGAGCATGAGAGGCAGCGTGCAGCTGGGTCTTCTCAAAGGTGGGTGTGTGGAGCTCAGCGGGCTCTGACTGACAACTCTTTCTGCTGGATGACTTCTGCTTACACTAATTGCAACACTTGACTTTTTCTTATTTTTCAGCCATGACATGCCATGCTAAATGAGATGCTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30891
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109534 | Essential Splice Site | 109 | 831 | 7 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 45940535)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 44613363 |
GRCz11 | 7 | 44952588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTCCAGGTGTCCTTCACAAAGTCCATGCACACTCAGAGCTTCACCGT[A/T]GAGGTGTGCGTCATCGATAAGAACGACAACGTACCGGTGTTCCTGGAAGA
Long Flanking Sequence:
CTACTAATCTGTCTTCAAACTTTGAAATAAGAATATTGTAATTTAGGCCATTTATTTGCTGAAAGTGACAATAGGTCAACTTACATTTATCATTAGAATGTTTATATAGTGTTTTACAAAATTTTATATTTACATATTTATTTTTGTCGAGCTATTATTGATTTAGACAAATAAATTGAGCAGACGAATGTACATATTCCCAGAGCTATTTGTCTTTATTTCAAGCTACATTCAAAACACTGACTGTCACATGGGTCCCTGACTCTCAGTTGAAATAAAACCTACGTCATTGATTTGCTAGATTTTCAAAATGCAAAAAAAAAAAAACACATCCGGAGGTAGTCCAAAAATAACAAACGCTGACAGAAATTGCAGGCCAATGAAACGTGAACCCAAAAGGGTTTGAGCTCTAATAAGACATGCTGCTTGAGTGCTTTGACCTGAGTGCTTTTTTTCCAGGTGTCCTTCACAAAGTCCATGCACACTCAGAGCTTCACCGT[A/T]GAGGTGTGCGTCATCGATAAGAACGACAACGTACCGGTGTTCCTGGAAGAGAGCATGAGAGGCAGCGTGCAGCTGGGTCTTCTCAAAGGTGGGTGTGTGGAGCTCAGCGGGCTCTGACTGACAACTCTTTCTGCTGGATGACTTCTGCTTACACTAATTGCAACACTTGACTTTTTCTTATTTTTCAGCCATGACATGCCATGCTAAATGAGATGCTAATTTGTTAGTCTGAATGTCAAACATTTTCCACACTATACCATGAATTGGAGTAGCGTAATAGCACACAGTAGTTGTAACTGAGTGCTGTATATATTTATCTATAAATGAGCAATATCACACGAGCAGCAGTGTGATATGGCTGTATAACAGCACTGGTGGGATGCGTGTGTTGGTGCGAGGCCGCAGGCTGAGTGCCTTAGTGTCCCACCAGTGATGATATACAGCCATATCACACTTCTCTGAGTGAAGTATTGTGTTTATAAAATAGTTTGACAACATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34157
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109534 | Essential Splice Site | 191 | 831 | 8 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 45934874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 44607702 |
GRCz11 | 7 | 44946927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTCTCAATCGACTCCATCACTGGAGAAGTGTCCCTCACAGAAGATGG[T/C]AATACTTGTCTCTGACTAACATGATGATTAATGAATAGTCTGACTCATAT
Long Flanking Sequence:
CACAGTAAATAGAAGATGACATTTCTCTGTTTCATTTTTTTATTTATTTATTTACTTTCAAACATTTGAATTGTAAGTGGTATTTGCTTTTAAATGTTGCTTTGTGACCAATTCTGTTTGCTTCCTGTTTCCTTTCACACTGTCTGTATTAATAAAATGCACAGAATTATATTTCTTAGAAAGAGCTATTTCTGAAATTCAGTTGTGTTAATATGCAAATAAACACCATTTGCTCATCAGTCTAAATGTGTCAATCCAGTCTCTTCATATAGATTGTAATAAAAAAATAAATAAAAATAAAAATCTGCTGTCTGTCTGTGTGTTTGTGTCATTTTCACAGGTATCCCGTTCATGCAGGTGGAAGCGCTGGACCGAGACGACCGAAACACTGCCCACGCAGACCTGCGCTTTAGTCTTCTGGACCAGATACCGCGCATCCCTGCCAGCCACATGTTCTCAATCGACTCCATCACTGGAGAAGTGTCCCTCACAGAAGATGG[T/C]AATACTTGTCTCTGACTAACATGATGATTAATGAATAGTCTGACTCATATATTCGGTAAAGAAGAATTAATAATGTATTAGATCAGTTAGTGCCTCCATGTCATTGCGTTGACTAATCAGACCTTGAAAATATGGAATACTTAATCTGTTATGTGAGTATTGGGTTACATTTTAATTTGGGCACCAATCAACAGTATTAGAAAAATGTTATGAAAAAGGAGAGTTCCAGTCCTTGATTCTGATTGGCTGAGCCAAATGGGATGCTGTTGTTAAGTACTCTACAAGCATATGCCTTTGACTGTTGCATGGCAACCATTCCACTATTGAAAAAATGCACAAAAGCATGCACATAACTTTAAATGACTGCTCAGCCAAACAGCAAAAATTGCAAAATCATATATTCAAAAAGGCAGCAATACCAAAGCTCCAAAAATAGCAATTTATTGAATTAAAAAATTAATTTGTATTTGAAATATGACATGCCTTCTAACAATTCCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21051
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109534 | Nonsense | 234 | 831 | 9 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 45929626)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 44602454 |
GRCz11 | 7 | 44941679 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTTCTTCTCCACTGGAACTGTGCTGGTGGAAGTGACTGGGAATGCAT[G/A]GGCCTCTCCAGACCCTGTGAGGCTGCAGGAGAATCTGCCTGGACCATATC
Long Flanking Sequence:
ATTTTTTCTCTGAAAGCATTTTAAAGTTTCCTTGGCTGTGTTTTGGATCATTGTCTTGCTGTCTTGTCTCACCCTGGTTTCATCTTCATCATAATGTAGGCTGCTGAAAAACTACTGAGAGATTTCAGCTGCTGTCGGGCTTTCATTACCTTTTTACACCTCCCTTTCTTTGTGTTTTCAATACTTTTTCTCTGCATCATTTCATTTCATTACACATAACTTATTTCTTTGATTGTTACTAACATCTGGTGAAAATTTCAAGTCAACGACACCTTTAGGAATGTGTGTTCAAAGAAAAAAGGTGGCTTGTTCAATACATATTTTCCCCGCTGTAAGCATAGATACCTTTGTAAACGTATCCATCTGTGCAGGTGCTTCAACATTGGATCCAGAGATGTGTGGCCGCTACAAGCTCTCTGTAATGGTGCAGGACATGGCAGGCAAGGCCAATGCTTTCTTCTCCACTGGAACTGTGCTGGTGGAAGTGACTGGGAATGCAT[G/A]GGCCTCTCCAGACCCTGTGAGGCTGCAGGAGAATCTGCCTGGACCATATCCCATCCCAATCTCACAGGTATGATGAAAAGAGCACTGGCGGCATGACACAGATGGGCATAGGTGAGTATGTTTCATATTGCGTGCATCCTCTTCAAAGGCGAGTGTGGCAACATCCCATAATTGCACAAGGCTTTCATCATCACATGACCTCTTGTTAGATGTTCAGATTTTGTGATATTATTCATGACTCACTGCCATCTTAGCAAAAATTCCCATATTTGAAACACCTAATATTGTGATGGTAAATATGCTATATATCATACTGCATAATATATTTATAAGAATATGTACGGTTTATATTAGGACTACCGAATGCTAAGGAACATTCTGTTGTTCTCAGTTATCTTCAGTGAAACTCATAGCTATAGTATTTCCATTAGCTGACCATTTTTGTTGTTTAGTGAAATGCCCTGTCAATCATCTTCTCACGTCCTCCACATGTATATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34156
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109534 | Nonsense | 669 | 831 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 45858321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 44531149 |
GRCz11 | 7 | 44870374 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACACATTCTGGATGTGAATGACAACAGCCCGGTTCTGGTGGGCGATTA[T/A]TCCTGGAAGTACCTGTGCACACCTCGCTGGGAGGATCAGGCTCTGGTTCT
Long Flanking Sequence:
TGTGATAATGAATGGATTATCATGCACCCACAGTTAAAGTTAGGCCTATAATCTGTTCAAAGAATGGTTAAAGCAAAAGCGGGAACTACTGCTGCTTATAAAAAGACATTTTTAGTTACATGCCTAATGTTTCAGGTTTTTTTATATAAAACTATGTAGCAAAATAAAAGAACAATAGAAGGCAAAATAAATGTTTTGCTAATAAATACAGCTTTAAAATAAGCATTTTCTCTAGACAACCAGTTTGGGCCTTTAAAAAAATATTCTGAGAAAAAGGTGGGCCTTGAAGTGAAAAAGGTTGAGAACCCCTGCCATAGTGGACCACAAGTAAATTCATGGAACAAGTGTTGCATGGACACCTTAAGATAGTCTCACCACAAATGATTGATATTTCTTCATCTACTGTCTCCTCTAGGTAACTCCTCTCTGTCCGCCTCCACACTGGTGACTGTACACATTCTGGATGTGAATGACAACAGCCCGGTTCTGGTGGGCGATTA[T/A]TCCTGGAAGTACCTGTGCACACCTCGCTGGGAGGATCAGGCTCTGGTTCTGGCCTCTCGGGACAGTGATGGCCCTCAGCATGGAGGAAGGCTCAACTTCTCCCTCCGCAGTGATGCCACTGTCCGCCGCACCTGGAAACTCACCCCCATCAATGGTTCGTGTATCCTACTCTTCCACCTGTTGAGCAATAGCTGTGTTGAGTAAGAAGGGACAAACTCACCAAGAACTACATGACCCATCTTTTAAAAACCTAGTCTGTCAGTCATTTTAAAAAGCACACGCTTCTCCAGTGTATAATTCCTGTAATGTTCCCAAACCTTCAATAATCACAATAGCGCTGACACCAGTTGTGCTGACCTCCGCTAGCAATGACGTCAATGTGGATAAAATTAGAGATCTGAAAACAGAAAAAAGTGCTGTTCGGTAGATGTAGCGTCCAGGCAGTCAAACTGAAACGTCATCTGAATTGGGTGTAATGCTTACAACCCGCTGAATCACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21050
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109534 | Essential Splice Site | 720 | 831 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 45858166)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 44530994 |
GRCz11 | 7 | 44870219 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCAGTGATGCCACTGTCCGCCGCACCTGGAAACTCACCCCCATCAATG[G/T]TTCGTGTATCCTACTCTTCCACCTGTTGAGCAATAGCTGTGTTGAGTAAG
Long Flanking Sequence:
GTAGCAAAATAAAAGAACAATAGAAGGCAAAATAAATGTTTTGCTAATAAATACAGCTTTAAAATAAGCATTTTCTCTAGACAACCAGTTTGGGCCTTTAAAAAAATATTCTGAGAAAAAGGTGGGCCTTGAAGTGAAAAAGGTTGAGAACCCCTGCCATAGTGGACCACAAGTAAATTCATGGAACAAGTGTTGCATGGACACCTTAAGATAGTCTCACCACAAATGATTGATATTTCTTCATCTACTGTCTCCTCTAGGTAACTCCTCTCTGTCCGCCTCCACACTGGTGACTGTACACATTCTGGATGTGAATGACAACAGCCCGGTTCTGGTGGGCGATTATTCCTGGAAGTACCTGTGCACACCTCGCTGGGAGGATCAGGCTCTGGTTCTGGCCTCTCGGGACAGTGATGGCCCTCAGCATGGAGGAAGGCTCAACTTCTCCCTCCGCAGTGATGCCACTGTCCGCCGCACCTGGAAACTCACCCCCATCAATG[G/T]TTCGTGTATCCTACTCTTCCACCTGTTGAGCAATAGCTGTGTTGAGTAAGAAGGGACAAACTCACCAAGAACTACATGACCCATCTTTTAAAAACCTAGTCTGTCAGTCATTTTAAAAAGCACACGCTTCTCCAGTGTATAATTCCTGTAATGTTCCCAAACCTTCAATAATCACAATAGCGCTGACACCAGTTGTGCTGACCTCCGCTAGCAATGACGTCAATGTGGATAAAATTAGAGATCTGAAAACAGAAAAAAGTGCTGTTCGGTAGATGTAGCGTCCAGGCAGTCAAACTGAAACGTCATCTGAATTGGGTGTAATGCTTACAACCCGCTGAATCACACACACACACGGCGCAGAGTGTACTGACAAAGAAGGAAATTGCCCTCCATGTCTAGTGTCTTCAGATGAATCTGTCTTGGACGTAATAAGCGTAATGGCTCTCGTCCTGATAGCTTTAGGCATCATTAATGTGCCAAGCTGATGCCGGTGAGCAGGT
Associated Phenotype:
Not determined