ZMP
NP_571161.1
Ensembl ID:
Description:
cadherin 4, retinal isoform 1 [Source:RefSeq peptide;Acc:NP_571161]
Human Orthologue:
CDH4
Human Description:
cadherin 4, type 1, R-cadherin (retinal) [Source:HGNC Symbol;Acc:1763]
Mouse Orthologue:
Cdh4
Mouse Description:
cadherin 4 Gene [Source:MGI Symbol;Acc:MGI:99218]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17776 | Nonsense | Available for shipment | Available now |
| sa6204 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17776
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097934 | Nonsense | 55 | 864 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 21011680)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 20534938 |
| GRCz11 | 11 | 20636250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGAACCCATCCAGTTCATGGTGACAGCCAGAGACAGAGCAGGAGAGTA[T/G]ATCTGGGAGACCACTGTTAAACTGGCCCTCGCCGGACACCCACTTTCACC
Long Flanking Sequence:
TCCAGTACATTACTTATAGTATTGGATTTAGTCCATGATTTATTAGATATATAATTCATTTTATTTAGTTATTGGTCTGTGTGACTCTGAATGAAGAATCAATAATATGCTGCTCGCTTTAACTGTAATAACTACAGTTTGTTCTATTTATTTTGTATCGTATATAGTCTTGATGTTTTATTTAATAAGCCGGGGAAATAGACCTTGACAAATGTATGAATAAGAGCATGAAAGATCATATTAAACCAATTTTAAAGTCTGTCAGCAATAATACTTTCATTGTTATTTTGTTTTTCTCACACTTTATGCTTCTCTTTCTTTTATTTTTTCCCTGCAGTGAAGTTTGAAACCTGTCACCGAATAGAGGAGCTTTCTTTTGAGAGCAGTGACCCAAAGTTCAGCGTTCGGCCTGATGGCTCTCTTTACGCAGAGCAAGATGTGACGAATCTAACAGAACCCATCCAGTTCATGGTGACAGCCAGAGACAGAGCAGGAGAGTA[T/G]ATCTGGGAGACCACTGTTAAACTGGCCCTCGCCGGACACCCACTTTCACCTCCTTTTAACCAGGCAAGAACCTTTTTTTGTCATTTATGTCAAGTATTATTTTTGACTATTGTTTTCTGCACTCACTCACTAGTAGCTAAATCATGTAATATACTTTAAAGTACTTTAGTTCTTCTAATTAGATTATATCACATTTTAAAAATGCTTGTACTCGGATAACATGCACTTTTTAGGAAGTACACGATTCATACACTGGCAGCATATTATTATTAATTTATTAATCCCCCTAATTACTTTTTCCCTCTTATTTATTTATTTATTTATTTATTTGTTTATTATTTAAAAAATGCTCGTTTCAATGTAACCTAAGTAAATTTGCAATGCTTCTGAAATTCTGAAATCTCTGTCAATTTTATCATGTGAGATAATTTCAGGCTTGACTGTATGTATGTATGTATGTATGTGTGTGTGTGTGTGTATGTATGTATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6204
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097934 | Nonsense | 141 | 864 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 11 (position 21076064)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 20599322 |
| GRCz11 | 11 | 20700634 |
KASP Assay ID:
554-4689.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTTGATTATCTATAAAACTGCTGTCATTGTGCTGTTTTATTGCAGATT[C/T]GATCGGACCAGGACAAAAAGATTGAGATCCGGTACAGTATAACAGGAGCT
Long Flanking Sequence:
TTCATTTCTAAAATGGAGACTAAGTCGAAGGAAATGAACGATATGAACGATATGGTTAGTTTTGACCATATTTGGAAGGGTCATGAATATTAATGTGCTCTACTCTGTTGCTCAAGCAGCACGTCAGTGCCTTGTGGCTAATAAAACTCTGTCTAAGGCATGCATTTTAGTGATTATGGATCGCCACAGTTGGTGTTTCCTATTTTTTAACCAGGATTTTACACTCACAGAAATTACATAAAAATGAGGAAACTATTTAGTATCAGGCTCATGTCATTCCCATGTTCTGAATCTTTATTTTTAAGCAGATTTTTTTTTTCTTTTTTTTTTTTTAGCAGAATTTCATGCTTCTTTGTTGTCCACAATGTTGGTCCTGAAATCAAAACCTGGTTAGAATATCTTCCCCATGTGAGCACTAAATTGACAGGTTAAACGTAGCAACGCATTTTGTGTTTGATTATCTATAAAACTGCTGTCATTGTGCTGTTTTATTGCAGATT[C/T]GATCGGACCAGGACAAAAAGATTGAGATCCGGTACAGTATAACAGGAGCTGGAGCAGATCAGCCTCCCAATGACGTCTTTAATATTGATCCTGTGACAGGGAAAATGTCTGTCACAAAACCTTTGGACAGAGAAGATAGAGCTTCTTACCATGTAAGTGCTTCTCTTTCTTCGACTCAAGATCATTTTTCCCCCTGTTCAGATCCTATTTAAAGTTGAACTGGCCTCAAACCAATTTAAGAAACATGCTCTAGTTTGCAAGAGTTGATGGCCTTTTGCCAGTTGGAATAAATCTAAAACTTTAATATATGCAGTGATCCCAAAAGATATGTGGACACTTAAGGCACTTTTTTAAGTGCATTCATAATTTTGAATTATACAACCAAATAGCAGTATCAAGGCAGAATAATGACAGAAAACATTGTGCAAACAGTGCAAATTATTACCCATGTGAACTGTATGCTCAATATCTGATTATAAATCTAAACGAAAGCCCCCCAA
Associated Phenotype:
Not determined