ZMP
ankrd33ba
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q7T168]
Human Orthologue:
ANKRD33B
Human Description:
ankyrin repeat domain 33B [Source:HGNC Symbol;Acc:35240]
Mouse Orthologue:
Ankrd33b
Mouse Description:
ankyrin repeat domain 33B Gene [Source:MGI Symbol;Acc:MGI:1917904]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30096 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44136 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30096
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 |
|---|---|---|---|---|---|
| ENSDART00000081220 | Nonsense | 402 | 510 | 4 | 4 |
| ENSDART00000132390 | Nonsense | 262 | 370 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 24 (position 22666959)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 21913837 |
| GRCz11 | 24 | 22059011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTTTTCAGAACTCCCGCGTCCTGCTGGTGCCCAAACCGAAAGATCGG[C/T]GAGCGAGTTTACAGCCTAATGCTCAAGCAGAGGATTCATCCACACTGACC
Long Flanking Sequence:
AAGCAAGGGACAACGGGCGGAAGTTCACAGCTCGAGAGTGGGCCATCTTCACCAGCCGACACGAGACCGTCTTAACCATTATGCGGCTCATGCATCAGCCATGTGCAGATCAGTTCTGTGACAGCTATCGACCCGAATGGCCCCTTCTACCCGCACTGGTGGCCAAAGCACAGGCTCCCAAAGGCTGCATCCAAAAAATCTCAGAGACACTACGCGACTTCTTTGACATCAGCAACGTCACGGAGGCTTCAGAGGACGGTGTTCTCGATCACATGGTACGCATGACCACAGCGCTAGGCAGTCCATTCATTGCGACGTCATGTCGAACGGTGTGTCCTGGCAGCCCACCATGTGTGGGCAAACGTCGTTATGCTGTTCAGGAGATATTAAAAAAGCGACGCATTGAGCAGCTTAAAATACTCGGACCTGAACGCATCGAGAACTATAAACGTCTTTTTCAGAACTCCCGCGTCCTGCTGGTGCCCAAACCGAAAGATCGG[C/T]GAGCGAGTTTACAGCCTAATGCTCAAGCAGAGGATTCATCCACACTGACCATCCGCAGGACCAGTCTACTGCCATTACACCTGCTGAGGAGGAGCAGCGTCAGACCAGGTCTGGTGGTGCCCAAAGTGAGGATCACCAAGGCTCCGACTCCAACCTATGTGCCGGAGAGAGTGCGGCGGAAAAGCAGCTGTGTAGAAGAACAGTTCCTTCAGATCCCCAAGTGGAGATACAAAGAACTGAAAGAAGAGCGAAAGAAAGCAGAAGAGGCGGAAAGGAAAAGACTGGAGGCCATAACGAAAAGACAGCTCACCACTGGCAAGAGGAAATAAGTGTTTGCAAATATACTACTCACCATTTGATACTTGAAATGCTTATGTTAGATTGCGATTTATTTTTATTACCTATTTATTATATTTTTGATAGTTAAAGGCTTCTAAGCTCCTTTTTAAAATGGGGTTAATTGAATGGTTTAAAGGGAGCTGCTCTTTTAAGGGCCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44136
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 |
|---|---|---|---|---|---|
| ENSDART00000081220 | Nonsense | 414 | 510 | 4 | 4 |
| ENSDART00000132390 | Nonsense | 274 | 370 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 24 (position 22666996)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 21913874 |
| GRCz11 | 24 | 22059048 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGAAAGATCGGCGAGCGAGTTTACAGCCTAATGCTCAAGCAGAGGATT[C/A]ATCCACACTGACCATCCGCAGGACCAGTCTACTGCCATTACACCTGCTGA
Long Flanking Sequence:
GTGGGCCATCTTCACCAGCCGACACGAGACCGTCTTAACCATTATGCGGCTCATGCATCAGCCATGTGCAGATCAGTTCTGTGACAGCTATCGACCCGAATGGCCCCTTCTACCCGCACTGGTGGCCAAAGCACAGGCTCCCAAAGGCTGCATCCAAAAAATCTCAGAGACACTACGCGACTTCTTTGACATCAGCAACGTCACGGAGGCTTCAGAGGACGGTGTTCTCGATCACATGGTACGCATGACCACAGCGCTAGGCAGTCCATTCATTGCGACGTCATGTCGAACGGTGTGTCCTGGCAGCCCACCATGTGTGGGCAAACGTCGTTATGCTGTTCAGGAGATATTAAAAAAGCGACGCATTGAGCAGCTTAAAATACTCGGACCTGAACGCATCGAGAACTATAAACGTCTTTTTCAGAACTCCCGCGTCCTGCTGGTGCCCAAACCGAAAGATCGGCGAGCGAGTTTACAGCCTAATGCTCAAGCAGAGGATT[C/A]ATCCACACTGACCATCCGCAGGACCAGTCTACTGCCATTACACCTGCTGAGGAGGAGCAGCGTCAGACCAGGTCTGGTGGTGCCCAAAGTGAGGATCACCAAGGCTCCGACTCCAACCTATGTGCCGGAGAGAGTGCGGCGGAAAAGCAGCTGTGTAGAAGAACAGTTCCTTCAGATCCCCAAGTGGAGATACAAAGAACTGAAAGAAGAGCGAAAGAAAGCAGAAGAGGCGGAAAGGAAAAGACTGGAGGCCATAACGAAAAGACAGCTCACCACTGGCAAGAGGAAATAAGTGTTTGCAAATATACTACTCACCATTTGATACTTGAAATGCTTATGTTAGATTGCGATTTATTTTTATTACCTATTTATTATATTTTTGATAGTTAAAGGCTTCTAAGCTCCTTTTTAAAATGGGGTTAATTGAATGGTTTAAAGGGAGCTGCTCTTTTAAGGGCCCTGACACACCAGAAAACTAGCGACGTCACTTGTTTTCAGTT
Associated Phenotype:
Not determined