ZMP
si:dkey-85g17.2
Ensembl ID:
ZFIN ID:
Description:
cell division cycle and apoptosis regulator protein 1 [Source:RefSeq peptide;Acc:NP_001139071]
Human Orthologue:
CCAR1
Human Description:
cell division cycle and apoptosis regulator 1 [Source:HGNC Symbol;Acc:24236]
Mouse Orthologue:
Ccar1
Mouse Description:
cell division cycle and apoptosis regulator 1 Gene [Source:MGI Symbol;Acc:MGI:1914750]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22266 | Nonsense | Available for shipment | Available now |
sa22267 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22266
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109579 | Nonsense | 850 | 1194 | 17 | 24 |
ENSDART00000111129 | Nonsense | 894 | 1238 | 18 | 25 |
ENSDART00000133057 | Nonsense | 850 | 1194 | 18 | 25 |
ENSDART00000138172 | None | None | 282 | None | 7 |
The following transcripts of ENSDARG00000074759 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 18467305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18287340 |
GRCz11 | 13 | 18418332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTCCAACCAAGGATGAGAAGAAGGACAAAAAAGAGAGAGCTAAAAAA[G/T]AGGCCGAAAGAAGGGATATAAAGAAAGAAAGAGATGAAGACAATGGAGAG
Long Flanking Sequence:
GTTGTCTTTCCTTGTCTATGGCTAGGCAGAACCTCGGTTTTTAGCACTACAAAGTTTTGAATGTGGTAATCATGGAACATTTTCTTGCACATGACCACACAGAACAAACTTGTTGGCATCCAAAGACTTGTAGGCTTTTAACTTCTCTTGAAAAATCACTTGAAGTTTCAATGAGGTAGTTTTATGTTTCTTATCCAATATCCATTGGGAGGGTGCTAGCGCAAATGGACCTGTCAGACGAACGCGGCTCACTTTAACGTTAATTTTGCTTATCTGTGCTTTACTTCACTGTGCTTATCACTGGGTGAGAAAACAATTGTTAATATCTGGCCGCGACGAGGCATAAACAGCACTGGTCATTTGTTCTGTTTCAGGTGTCATTGTTTGCTGAATTGTTCAACGAAATGCTTCAACGAGACTTCGGCTACAGGATTTACAAAGCTCTCGCTTCTCTTCCAACCAAGGATGAGAAGAAGGACAAAAAAGAGAGAGCTAAAAAA[G/T]AGGCCGAAAGAAGGGATATAAAGAAAGAAAGAGATGAAGACAATGGAGAGCCGGTCGCAAAGAGAATAAGAGAGGAAGATGACAAGAGGAAGGTGAGGACGTACTTCAGTGTGAATTGGATCTTTAGGTGTTATCTTAAATGAATGTAAAAGTAAGCCACTCAATTTGTGTTTCCGGGATAAAGGATGAGGAAAAGGAGAGAGGAATAAAGAGAGAAGAATCCAAAGATGACGACGATAATGAAGATGGAAGCAGCAACAACAATGCAGATGAATACGATCCTTTGGAGGCAGAAGATGCAGACGATTATGATGACGATGGTAGGGCTGTTGAAATAATATAGCTGAATTCAAAGAAAAGTTTTGATTAGGGATAAATGTGTTTTATTTTATATTACATTTAAATATTTAAACAAATAATTTTTGTTTAAATTAGGTTTTATGAGAAGTACGTTATCTATAAATAAGGCATTATTCTTTGATAATATTTCTATATGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22267
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109579 | Nonsense | 1020 | 1194 | 21 | 24 |
ENSDART00000111129 | Nonsense | 1064 | 1238 | 22 | 25 |
ENSDART00000133057 | Nonsense | 1020 | 1194 | 22 | 25 |
ENSDART00000138172 | None | None | 282 | None | 7 |
The following transcripts of ENSDARG00000074759 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 18476756)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 18296791 |
GRCz11 | 13 | 18427783 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGTGAAGAAGTTGTTAAACAAACCTTTGGTTAAAGAGTCGTGCCATTA[T/A]CGAAAGCTGACGGACAGGCCTAAAGATGAGCCTTGCCCCGCACTGATCTC
Long Flanking Sequence:
CTGTATTATTATTATTACCATTTCAAACTAATATTCATGTAATAATAATGCTTAAAATAACTTTCATATTTTGTAAAAAAAAAAAAAATAATAATAATATATATATATATATATATATATATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATGTATGTATGTATATGTATGTATCATTTATGTATCAAAGTAATTGATTAAAAGGAAAAGATGTTTGTTGCATCATGCCTGATCACAATATAATGTGTTACTAGTAATTTTCTAATTGAACGCAATGTAGCATATTTATTAAAAGACTGTTTTTTTTCTATCTTTTCAGGTGAAGAAGTTGTTAAACAAACCTTTGGTTAAAGAGTCGTGCCATTA[T/A]CGAAAGCTGACGGACAGGCCTAAAGATGAGCCTTGCCCCGCACTGATCTCTGAGGCTCACATAGACAACCTTTTAGGTGTGCAAAGAGGAGGATGACTGAAACTGAGAAGCTCATTTGTAACAATAGAGCACATATCAATGACAAACTCTCTGTGCCCACAGGTAACCAGATTTTACTGACCAGCCAGAAGATCAAGCGAGAGCCAGATGAGAGCGGTGAGTCAGGGAGTCTAATCGTCTACAAGGGAGCTCTGGTGGATGTGGGAAGTATGATGCAGAAGCTGGAGAAGAGCGAGAAAACACGAGAGGACATTGAGCAAAAGCTCATGCAGCAAGATGTTAAAATGGGTAACACTTTTTTTATTACATTCAAATGACTGTCATGAGCAGTTTGATTTGTGGTCAGTGAACCTTAGTGACCCATTATGTTTATTTTTTTGATGGGATAATAATAGTTGCTCCTTTTTAGATCCAGGTTGTAGCACATTTTGTCTTCACAA
Associated Phenotype:
Not determined