ZMP
zgc:162148
Ensembl ID:
ZFIN ID:
Description:
Calcium uptake protein 1, mitochondrial [Source:UniProtKB/Swiss-Prot;Acc:A4IG32]
Human Orthologue:
CBARA1
Human Description:
calcium binding atopy-related autoantigen 1 [Source:HGNC Symbol;Acc:1530]
Mouse Orthologue:
Cbara1
Mouse Description:
calcium binding atopy-related autoantigen 1 Gene [Source:MGI Symbol;Acc:MGI:2384909]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42129 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa31903 | Nonsense | Available for shipment | Available now |
| sa42130 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42129
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092521 | Essential Splice Site | None | 488 | None | 12 |
| ENSDART00000124667 | None | None | 489 | None | 12 |
| ENSDART00000132301 | Essential Splice Site | None | 489 | None | 13 |
| ENSDART00000145940 | None | None | 202 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 4548787)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 4743565 |
| GRCz11 | 13 | 4872151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACATCTTTCCTGCAGGACTTTATCTGACGTTGCCTTAAGTGTCTGAG[T/A]AAGTGTATAATACCCGCTCGCTTTAACACCAAGGGGCTAAGTTAGACTAG
Long Flanking Sequence:
TATAATGAGGGATGTTGTTATGTAGAACAAAATCATACTTCATAACCATTGTTAACCATTTGCAGCGTTTTAAAGGATGACAACCCTAATTAAGTAATTTTTGTCGTGTGTGAAAATGTAACGCCATGTCAACAAGCCTCTTCTAAAAGAACAAAACAGGTTTTTAACGTCCTCACCTATCAAACTGAGTGTTTAGAAATACACCATTTTGTTGTTTGTCAACCGCCAATATATTGAAGAAGAAGAAGAAGAAGAAGAAGAAGAACGGAGTGTTTACAAACTGATGGAAGATCCCACAGACTGAGCAGATAAGGGGAGGCGGAGGCTTGACGTTTGCTGTGGGTGTGTTTGTGTGTGTTCGGCCTCCGTAGACGCGGAACTTCAGCGCAGAAAGTCAACGCGACTAACGTTAAAGCAGAATCGTAGGGGGAATCTGCAGTTCTTACAGAAAAAACATCTTTCCTGCAGGACTTTATCTGACGTTGCCTTAAGTGTCTGAG[T/A]AAGTGTATAATACCCGCTCGCTTTAACACCAAGGGGCTAAGTTAGACTAGCCAAATCTAGTGTGATTTCAGATAGGAGAGTTTTCCCTGTAACGTTACGTGACTGGTCGTATCTTCATGGCATGCTTAAGCTGAAAGGTCTAGAATGACAAATCCCCATGTTGCTAGACGTCTTATAATAGTATATTTAATGTTTCTCAGTAAAGGAAGCAGTTAAATATGTAATCGCTGTGTAGCTCATGCTAATGCTCCAGCTGCACATCGCCTCAGATCATCATAATAACAACTTCAGCTCAATATTAAAGCTGATGTAACGTTAGTGTCCATGTTGAAAAGAGACATAGAAAAACACAGTTTATGTTATAATTGTGAGGCAGTGACATCGTTATTTGACTGTTTTTGTTTTTAAACATTGACAAGTGTTTATAAAATATCGTGTTGACATTGTTGGTATTAATGTATATGTCATATCTCGCGATACATACCATGTTTTTTGGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31903
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092521 | Nonsense | 153 | 488 | 4 | 12 |
| ENSDART00000124667 | Nonsense | 153 | 489 | 3 | 12 |
| ENSDART00000132301 | Nonsense | 153 | 489 | 4 | 13 |
| ENSDART00000145940 | Nonsense | 48 | 202 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 4576265)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 4771043 |
| GRCz11 | 13 | 4899629 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTTTGCCACCCTGAAGATCATCAATGAACACGGAGACGCAGAAGTGTA[C/A]ATGACACCGCAGGACTTTGTGCGCTCCATCACACCAAACGAGAAACAGCC
Long Flanking Sequence:
CGTAATATGCCTAGAACAGTAGCAAAGCTCCTTTATTATTACGCCAGAATGAAAGTATAGTTCCTATCCACATCAGCTTAGAAGCAAATAGCAACTTTTTCAGTCAGTAATTTCAGAAGAGTAATTTTTTAAATAGGAAAACTATCAAATCTTTTTCTTTTGTGTGTGTTTTTTAGTGAGATGCTAATGGTCTAATCCGATTCAATGATTTATGCTAAGCTAAGCTAAAAGTGCTCCTGCTAACTAAATGGGTTCAAAAATGGTAAAGCCAAAGAGTTGAACTCTAGGAGACTTGTAAAATTAGACTATTTCCAAAAAAAGTGGGGTGTTCCTTCTACATCTACTCTTCTTCTGTTCTGGTAAATGTGCTTAATATGATTATATGTGTTACAGGTGATGGAGTATGAGAACAGGATCAGAGCTTACTCTACCCCTGACAAGATATTTCGTTACTTTGCCACCCTGAAGATCATCAATGAACACGGAGACGCAGAAGTGTA[C/A]ATGACACCGCAGGACTTTGTGCGCTCCATCACACCAAACGAGAAACAGCCAGAGAGTGAGTCTCAGTCCTTTTCCTCTTCAGGGTTTCAGAAAGTTGATCTTTGTATGTACTTCATAGCCTAAAAGAGTGGTCCTTAACCTTTTTATCACCAAAGAGACTGAGCAACGCTTGAAAATTTTATTACGGCCCTGTGGGGTGTGGTTCAAAATAGATTGCTAGACGGCCATCAATGTTTTCTCAGAGGAGGTCAAGCTGACAAAGCATTGAGCCGAGGTCATTTTCTCAAAATAAAAGATCGTTCAGACACAGATAATAAATAAAATGTAAATAATTAATTATTTCTTTTGCAACCCGCTACCAATTAATCCACCGACCGGTACTGGTCTAAGGCCTTGGGGGTTGGGGACCACTAGCCTAAAACACATGATACAGGACCATTCACTTGGCATGGCCATATTTCATATGTCAGCATCTGTAATGGTCAAATGAGAGGGGCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42130
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092521 | Essential Splice Site | 322 | 488 | 8 | 12 |
| ENSDART00000124667 | Essential Splice Site | 323 | 489 | 8 | 12 |
| ENSDART00000132301 | Essential Splice Site | 323 | 489 | 9 | 13 |
| ENSDART00000145940 | None | None | 202 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 4628469)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 4823247 |
| GRCz11 | 13 | 4951833 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCTGGAGTTCCAGAGGAAATTACAGCATGATGTGCTTAAACTGGAGG[T/A]AAGGCGTATACGTCGAGGAAGATGGAGAAATGTAGACTTTTTATATGAGG
Long Flanking Sequence:
GTGTTTCGTGACCCTTTAAGTTTTATTGTCCAGCCCCTGTATATGTGAAGTTACAAATCACTGAGTTATATACATATAGTTCACCGTACTAGTACCGGGTTGGTCACTTAAATCCCCTTCCTTCCCCATTCTGATGCTCAGTTTGAACTGCAACAGATCGTCTTGACCATGTCTACATGCCTAAATGCATTGAGTTGCTGCCCTGTGATTGGCTGATTAAAAATTCCGTTAACGAGCAGTTGGACAGGTGTACCTAATAAGTGTAATAATAAATAAGTGTATGTTGTTTTTTTTCCAGGTTCAGAGTATCATTCGCTCTCAGACCAGTATGGGGATGAGACACCGAGATCGCTCCACTACAGGAAACACTCTGAAAACCGGCGGCTGCAGCTCAGCTCTCACCACCTACTTTTTTGGGGCTGATCTGAAGGGCAAACTCACTATAAGCAGCTTCCTGGAGTTCCAGAGGAAATTACAGCATGATGTGCTTAAACTGGAGG[T/A]AAGGCGTATACGTCGAGGAAGATGGAGAAATGTAGACTTTTTATATGAGGGATGACAGAAAAAAATGAATCGAGGTTGAAAGTTGTCTGCCAAAGTCTCCGCTGGAATCTTAACCTCATGCATAATTTAAAGCTGCAGATTCATTCAGCACAGAATATTGTGTGCTGTCCTGGAAGTAAGAAGGCGTTAATCAGGATTTGGGGTGGTGGGATGGAGAAAAAAAAGAAAAGAAGGAGAACTGTTCAGTAGGTACTTATAAGTAGTGATAAAAAGTGTCAGTTCCTCCTTTTGCTTGTTGCAAAAATAAACTGTAGAAAGAGTAATGTTTCCAATTTGTTAATTTTGAGTAAATATTGTGGGGGGAAAACTTTTGCTGATATGTTTTCTGAGAGTGATGAATAACTGTTCAAATCCTCATTGATTTATCCAACTTATTTAAATTGCACACATTTTTTGGAGTCCATCTCCTATAGCGAAACCTCACATTCAGTATTGTTAAA
Associated Phenotype:
Not determined