ZMP
cecr1a
Ensembl ID:
ZFIN ID:
Description:
Adenosine deaminase CECR1-A [Source:UniProtKB/Swiss-Prot;Acc:P58781]
Human Orthologue:
CECR1
Human Description:
cat eye syndrome chromosome region, candidate 1 [Source:HGNC Symbol;Acc:1839]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38038 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44262 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38038
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073416 | Essential Splice Site | 474 | 503 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 17056941)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 16603485 |
| GRCz11 | 25 | 16699885 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGCTTTAATTTAGGCACATTGAAAGAGCTAGCTTTAAACTCCCTCAG[G/A]TAGGAAATGACCACAATTTAAACAAAAAAGAGACTGTATATGCAAGCTTG
Long Flanking Sequence:
CTTCTTGCTGTGAGGCTAACCACCGTGTCACCCTGCAAATTTATAACACAAAATTATTAGCCCTTCTCTGAAATTTAAATACTTTTTCAAATATTTCATAAGTGATGTTTAACACAGCAAGGAAAGATTGCGCGATTCGATATAATATTGTTTATTAGCACTACTTTAGCTAAAAACTAACATTGAATTGAACTATACTAAATCATATTTCATTTTCGTTTATAAGAAATAAAACATAATGTATTCAATACAATATTAAATAGCATTTTACCTGAAAATTGTTTTCTTCTCTTTCAGGTGTTGAAGCTGGTCTCAGACCTGCGGGATCATCCGGCTGCAGTGCTGATGGCTGAAGGTCATCCTCTGGTGATCAGCTCTGATGATCCTGCTGTTTTTGGAGCCACGGCTCTTTCACACGATTTTTATGAAGCTTTTATGGGTTTTGGAGGAATGAGCTTTAATTTAGGCACATTGAAAGAGCTAGCTTTAAACTCCCTCAG[G/A]TAGGAAATGACCACAATTTAAACAAAAAAGAGACTGTATATGCAAGCTTGTACATTTAGGTGTCCTCAATATTTAATGTGTGCTCTGGTTCTTCATTTATAGGTACAGCACATTGCCAAGTCAAAGAAAGGAGGAAGCTATCGACGCTCTGCTAGTAAAATGGGACAAGTTTGTTTGGGAAAGTTTACTTTGACAGGACGTTACCACATCAGGACGTTTTTAATTAGGAGGCCATTGTTTACAAGACATCTACGTCATTTGTTTGTCGTATTGGTGATACTGAGGTGCGAAAACGCCAATTTATGCTGAGAGAAACAGAATGTAATGCCTTGAACTGATCTGTGCTGCCATCTTGTGGAGAATCTGAAGCAGTGCTTTTGTGAATATTAATCGTGGTTTCAGATTTATATAAATGTAAAGTCACACAATCTGAACGGGGTTAACTACTTAACTACTCAGGATGCGTGATAAACCTTGTCTTGTTGTAAGTGTGCATTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44262
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000073416 | Nonsense | 500 | 503 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 25 (position 17057120)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 16603664 |
| GRCz11 | 25 | 16700064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGAAGCTATCGACGCTCTGCTAGTAAAATGGGACAAGTTTGTTTGG[G/T]AAAGTTTACTTTGACAGGACGTTACCACATCAGGACGTTTTTAATTAGGA
Long Flanking Sequence:
ACATTGAATTGAACTATACTAAATCATATTTCATTTTCGTTTATAAGAAATAAAACATAATGTATTCAATACAATATTAAATAGCATTTTACCTGAAAATTGTTTTCTTCTCTTTCAGGTGTTGAAGCTGGTCTCAGACCTGCGGGATCATCCGGCTGCAGTGCTGATGGCTGAAGGTCATCCTCTGGTGATCAGCTCTGATGATCCTGCTGTTTTTGGAGCCACGGCTCTTTCACACGATTTTTATGAAGCTTTTATGGGTTTTGGAGGAATGAGCTTTAATTTAGGCACATTGAAAGAGCTAGCTTTAAACTCCCTCAGGTAGGAAATGACCACAATTTAAACAAAAAAGAGACTGTATATGCAAGCTTGTACATTTAGGTGTCCTCAATATTTAATGTGTGCTCTGGTTCTTCATTTATAGGTACAGCACATTGCCAAGTCAAAGAAAGGAGGAAGCTATCGACGCTCTGCTAGTAAAATGGGACAAGTTTGTTTGG[G/T]AAAGTTTACTTTGACAGGACGTTACCACATCAGGACGTTTTTAATTAGGAGGCCATTGTTTACAAGACATCTACGTCATTTGTTTGTCGTATTGGTGATACTGAGGTGCGAAAACGCCAATTTATGCTGAGAGAAACAGAATGTAATGCCTTGAACTGATCTGTGCTGCCATCTTGTGGAGAATCTGAAGCAGTGCTTTTGTGAATATTAATCGTGGTTTCAGATTTATATAAATGTAAAGTCACACAATCTGAACGGGGTTAACTACTTAACTACTCAGGATGCGTGATAAACCTTGTCTTGTTGTAAGTGTGCATTAAAGGGAATGTTCACGCAACAATGGTAAATTCAGTCATCAACTTGCTTGAGTTTCTTCCGTTGAACACAAAGAAGTTTTTAGGCATTCTGCAAAGTACCATTTTTGTTTTCAACAGAAGAAAGGAACTCCTGAAGGTCTGTAACTATTTAAAGAGGAAATAGTGAGTATTTTTGGTGTGAAC
Associated Phenotype:
Not determined