ZMP
ENSDARG00000091395
Ensembl ID:
Human Orthologues:
CDH10, CDH6, CDH9
Human Descriptions:
cadherin 10, type 2 (T2-cadherin) [Source:HGNC Symbol;Acc:1749]
cadherin 6, type 2, K-cadherin (fetal kidney) [Source:HGNC Symbol;Acc:1765]
cadherin 9, type 2 (T1-cadherin) [Source:HGNC Symbol;Acc:1768]
cadherin 6, type 2, K-cadherin (fetal kidney) [Source:HGNC Symbol;Acc:1765]
cadherin 9, type 2 (T1-cadherin) [Source:HGNC Symbol;Acc:1768]
Mouse Orthologues:
Cdh10, Cdh6, Cdh9
Mouse Descriptions:
cadherin 10 Gene [Source:MGI Symbol;Acc:MGI:107436]
cadherin 6 Gene [Source:MGI Symbol;Acc:MGI:107435]
cadherin 9 Gene [Source:MGI Symbol;Acc:MGI:107433]
cadherin 6 Gene [Source:MGI Symbol;Acc:MGI:107435]
cadherin 9 Gene [Source:MGI Symbol;Acc:MGI:107433]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14525 | Nonsense | Available for shipment | Available now |
sa14677 | Essential Splice Site | Available for shipment | Available now |
sa22164 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14525
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 |
---|---|---|---|---|---|
ENSDART00000128298 | Nonsense | 47 | 776 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 41246364)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 39511264 |
GRCz11 | 12 | 39685765 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCGGATCGGGATGGACGGACTCTACACCGCACTAAACGAGGATGGATGT[G/A]GAATAGTTTCTTTCTCTTAGAGGAATGGACAGGAACTGGAAAGCAGTATG
Long Flanking Sequence:
ATGGTCAACCTTGTGAGGTTCGTCAATTAGAGACCACCAAGTGACTGCTGGGTGCTAAAAAACACTTAATCTTTGTGTAATCAATCTATACTAACGATTAAGTTTCTAGTTAGCCGACACGATTTTTAGTCAGCTAACATAAATTTAAGAGCAGGTAATTTAGCTAGGTTGCTGCATTGGAATGGTCTCTTAAAGATCTTTTTTTTTCCATCTGTCACAGGCCTCAAGAAGACAGAATTGAGGAGAATTAAGGATAAGATGCCCCATTTCGTCAGCCCTGCCATTCAGCAGTATCTTCGACGCAGAGCTCTGTTTCTTAATTGATTTCTTATCAAGGACTCTCCAGGAGTGATCGGATACAATGATAATCAATCAACTTACTTTCCTCCTGTTGTTCTGCTTGCTGGGCTGGAGCAGCGCAATGATCCGGCCGGTGCCTGGAATTAGCACGTCGGATCGGGATGGACGGACTCTACACCGCACTAAACGAGGATGGATGT[G/A]GAATAGTTTCTTTCTCTTAGAGGAATGGACAGGAACTGGAAAGCAGTATGTCGGAAAGGTATGGGCTGTCACTCTTTAAAACTTTTTTTTTCTTTGCTTTTTTAAACATTAACCGTGTAGATCTGGGTGTCCACATAATTTTGTACAAAGTGAATCTAGTGATCTTTACTCAGTGGATATACCATGGCATGACTATGAACAAAGATCCAAGATTATAATACAATGATGTTCTTTCAGTAACCTCAATGTTACAACAAACTGATACAAGACTATAGTAGTTCTACTGCATATGAGTAAACTAACATGAGTATGATTGTATATAGTGTCCCACCAGTGACAACACACAGCCATATTCCACTGCTTTGAGTTCAATGACATAATCGTGTGTATAGAAAAGAAAATCAAACACGAGAGTCTAAAAACCCTTTGGTATGAGGAACTACTTTCTTCCGCCATTCATTCACATCTGCAGCTGATGTCAGAACAGCAGAAACCATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14677
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128298 | Essential Splice Site | 67 | 776 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 41284762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 39592373 |
GRCz11 | 12 | 39724163 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTAATTCKGGAACTGTTAATTCCAGCAAAACTCTCTTTGCTCTTTTTAA[A/G]GCTTCACTCAGACATGGACACGGAAGATGGAAATGTGAAGTACGTCCTCA
Long Flanking Sequence:
AACCGAAGGGGAACCCATTATAAATATGCTGTCATGTAAATGTTTACATCCAGGTGCATGTTCTGCTCTGAAGGAGCATTTGCCGTAATTGTGACTACAGTGTGAAGGTAAAGGAGTCAATTCACAAGTTTTCTGAGATATCTGCCATATGTCGTTAACCACGGCAAACACAGAGCTTTTTGAAATTCTGAAATTATTACTGACACTGCTGTGAAATTTCCAAAGAAAGAAAATTAAACCAAGTGGAGCCTTTGAGCAAATTCACATTCATATTCACATATTCATGACTCATTTAAAAAACATTGCTCAAGAAACTTGGGCCAGAAAGGGCTTAAACTGTGTTTAGCAAATGGTTTAATTTCTGTTTCCCTTTGCACAAGGTTTAGGAACATTTTTCCCTGACAGACTAAGCATATTTGCGCACAATTTGCCAGTCGCGCTAGGAAAACACTTAATTCGGGAACTGTTAATTCCAGCAAAACTCTCTTTGCTCTTTTTAA[A/G]GCTTCACTCAGACATGGACACGGAAGATGGAAATGTGAAGTACGTCCTCACCGGAGAAGGAGCTGGAACTGTTTTCGAGATTGATGAGAACTCAGGCGATATTCATGCCACCAGGAGGCTTGACAGGGAAGAGAAAGCGTCGTACACTCTGAGCGCTAAAGCCGTCAACAAAACCTCTGGACAGGATCTGGAGAGGGCCTCCGAATTCATCATCAAAATCCATGACATCAATGACAACGAGCCAAAGTTCGCCAAGGACACCTACGTGGCCAGCGTATCTGAGATGTCCAATGTTGGTGAGTTCAACATGTTCCTGTCAGATTCACAAAGATGAAAGGCTCAGTTCACCCAAAAATGAAAACTCGGTCAACATTCGATTTACTTCTACCAGAGTTATTTGAGTTGCTTTATTCTGTTGAATGTTGAAATGTGATAACAATTGACTCTAGAAGTGAATAGCTACCGGCTTCCAACATTCTTCAAAATATGTTTTGTTTTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22164
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 |
---|---|---|---|---|---|
ENSDART00000128298 | Nonsense | 624 | 776 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 41344636)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGCCTCTGTCTCCATAGTGATTGTGGTATTGTTTGCGGCCCTGCGG[C/T]GACAAAAGAAAAAGGAGCCCCTGATCATCTCAAAAGAAGACGTTCGCGAC
Long Flanking Sequence:
GTTTTTCATATTTGACCCAATATTGAGTAACAAAATCCAGCATTTTTAGAGGATAAAAATGTACACTACATAATTTTTTTGCAATAAATATATTTATTTAAATGTAATAAATACATGTATTAATATGGAATAATAAATATAATGAATGTCTAAATCAAAAAAATAAATAAAAATACATAGACAAATGTGACTTTTTTGTTACAAGCTAGAAAAAGAATTGGTAAAGTATAATGTACAAAAAAAATGTATGGATTGTCAAGTTCAAATGTATATGAAATGGAAATGATAAATTGTTAATAAAAATAGCATGTTCACACACATTATCCAGCAAAACCTGCCGAAAGCAGTGCCTCAGTACAGTGTCAGGTGTCTCTGTCACACTCAGCATGCATGACTATCACACAGCTTTGTTCGGCTTGATTTGCACAGTGCTGATGATATCATTTTGTTCATCTGCCTCTGTCTCCATAGTGATTGTGGTATTGTTTGCGGCCCTGCGG[C/T]GACAAAAGAAAAAGGAGCCCCTGATCATCTCAAAAGAAGACGTTCGCGACAACGTGGTGTCCTACAACGATGAGGGCGGCGGAGAGGAGGACACACAGGCCTTCGACATCGGAACTCTGCGCAACCCCGAAGTCATTGACACCAACAAACTCCGACGGGACATCATGCCCGAAATGCTGTTCCCTTACCGCCGCACATCTCCCCTAAAAGACAACACGGATGTCAGAGACTTCATCAACGGACGGCTGCAAGAAAACGACTTGGACCCAACAGCACCTCCTTATGACTCCTTGGCTACGTACGCCTACGAAGGCAACGGATCCTTGGCGGAGTCGCTCAGCTCTCTCGAATCCGCCGCCACCGAAGGCGACCAAGAGTTCGATTATTTGAGTCACTGGGGTCCACAGTTCAAAAAACTGGCGGATATGTATATAGGGCAGGAATCCCAGAGAGAGACTTAAAGCGGATATGCAACACAGCACACTTAAATATATCTCAGA
Associated Phenotype:
Not determined