ZMP
cldnd
Ensembl ID:
ZFIN ID:
Description:
Claudin-like protein ZF-A89 [Source:UniProtKB/Swiss-Prot;Acc:Q9YH91]
Human Orthologue:
CLDN4
Human Description:
claudin 4 [Source:HGNC Symbol;Acc:2046]
Mouse Orthologue:
Cldn4
Mouse Description:
claudin 4 Gene [Source:MGI Symbol;Acc:MGI:1313314]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa3121 | Nonsense | F2 line generated | Not yet available |
| sa37321 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa3121
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000021620 | Nonsense | 64 | 208 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 21 (position 25157703)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 25741040 |
| GRCz11 | 21 | 25777645 |
KASP Assay ID:
554-2953.1 (used for ordering genotyping assays)
KASP Sequence:
GAAGGCCTCTGGATGAACTGTGTGCAGCAAAGCACAGGTCAGATGCAGTG[C/A]AAGGTTTATGACTCCATGCTGGCTCTACCTCAAGACCTCCAGGCCGCCCG
Long Flanking Sequence:
GCCTTTAAAGCTAATTATCTGCACCCCATTCACTACCTACTAAACACCTTTTTATACTTATTATTTTATTATATTTGTTAAACAAATCTTTCATCTTTATTGACTGTAAAAAAGTCTTCAGTTGCAATACCGAGCTAGTTAGTATTCGGAAGAGCTTGTACGTGAAATCAATTAGGCAACGAGCGCGTGAACCACCACCAGCTGCATCCAATCCCATTAATTAAAACCCAACCTCCAAAGGCCACTATAAATAATCGTGCCGTCTACTCGAAAGATAGAGTCGGGTTCTTTACACTATCAAAATCTACAATGGCATCTGTTGGGCTTCAGCTTCTGGCCACTGTCCTGGCGATCATCGGCTGGTTGGGTGAAATCGTCATTTGCGCGCTGCCCATGTGGAAGGTGACGGCTTTCATTGGCAACAACATCGTGACCGCGCAGATTTTCTGGGAAGGCCTCTGGATGAACTGTGTGCAGCAAAGCACAGGTCAGATGCAGTG[C/A]AAGGTTTATGACTCCATGCTGGCTCTACCTCAAGACCTCCAGGCCGCCCGAGCTCTCGTGGTCATCTCCATAATCGTCACTTTCATGGGCGTTTTCCTGACCATCGCTGGAGGAAAGTGCACCAACTGCATTGAGGACCAGGACGCGAAGGCTAAAGTCGTGGTCGCCGCTGGAGTGTTCTTCCTGGTTGGTGGAATTCTTTGTTTGATCCCGGTGTGCTGGTCCGCGAACTCCGTCATCAAGGATTTCTACAACCCCACCCTGTCCGATGCTCAGAAACGGGAGCTGGGAGCGTCACTCTTCATCGGCTGGTGCGCGTCCGGTCTGCTGCTGCTCGGCGGAGCACTGCTCTGCTGCCAGTGCCCGAAGAACGAGGGTCGCGCTTATTCTGTTAAGTACTCTGCTCCCAGGTCTGCTCCAGGAGCTTATGTGTGACGCACCGACTTTCTGGACTAGTGTTATCGTCTCCTGTTTGTGTAGGAAGAGATTTTTATGTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37321
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000021620 | Nonsense | 104 | 208 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 21 (position 25157823)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 25741160 |
| GRCz11 | 21 | 25777765 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATCGTCACTTTCATGGGCGTTTTCCTGACCATCGCTGGAGGAAAGTG[C/A]ACCAACTGCATTGAGGACCAGGACGCGAAGGCTAAAGTCGTGGTCGCCGC
Long Flanking Sequence:
GTTGCAATACCGAGCTAGTTAGTATTCGGAAGAGCTTGTACGTGAAATCAATTAGGCAACGAGCGCGTGAACCACCACCAGCTGCATCCAATCCCATTAATTAAAACCCAACCTCCAAAGGCCACTATAAATAATCGTGCCGTCTACTCGAAAGATAGAGTCGGGTTCTTTACACTATCAAAATCTACAATGGCATCTGTTGGGCTTCAGCTTCTGGCCACTGTCCTGGCGATCATCGGCTGGTTGGGTGAAATCGTCATTTGCGCGCTGCCCATGTGGAAGGTGACGGCTTTCATTGGCAACAACATCGTGACCGCGCAGATTTTCTGGGAAGGCCTCTGGATGAACTGTGTGCAGCAAAGCACAGGTCAGATGCAGTGCAAGGTTTATGACTCCATGCTGGCTCTACCTCAAGACCTCCAGGCCGCCCGAGCTCTCGTGGTCATCTCCATAATCGTCACTTTCATGGGCGTTTTCCTGACCATCGCTGGAGGAAAGTG[C/A]ACCAACTGCATTGAGGACCAGGACGCGAAGGCTAAAGTCGTGGTCGCCGCTGGAGTGTTCTTCCTGGTTGGTGGAATTCTTTGTTTGATCCCGGTGTGCTGGTCCGCGAACTCCGTCATCAAGGATTTCTACAACCCCACCCTGTCCGATGCTCAGAAACGGGAGCTGGGAGCGTCACTCTTCATCGGCTGGTGCGCGTCCGGTCTGCTGCTGCTCGGCGGAGCACTGCTCTGCTGCCAGTGCCCGAAGAACGAGGGTCGCGCTTATTCTGTTAAGTACTCTGCTCCCAGGTCTGCTCCAGGAGCTTATGTGTGACGCACCGACTTTCTGGACTAGTGTTATCGTCTCCTGTTTGTGTAGGAAGAGATTTTTATGTTTTACTTTCTGGTCTTGCATGACCGTTTTTAATTTAATAAACGTCTTAATGATTTTTATATATTTGTCTCTTGGGATTTATTTTAAGTGAAGTTGCTCCGTTTCCAAAAGTCAGAACAGGCTTA
Associated Phenotype:
Not determined