ZMP
ankrd28
Ensembl ID:
ZFIN ID:
Human Orthologue:
ANKRD28
Human Description:
ankyrin repeat domain 28 [Source:HGNC Symbol;Acc:29024]
Mouse Orthologues:
Ankrd28, E230028L10Rik
Mouse Descriptions:
RIKEN cDNA E230028L10 gene Gene [Source:MGI Symbol;Acc:MGI:2685285]
ankyrin repeat domain 28 Gene [Source:MGI Symbol;Acc:MGI:2145661]
ankyrin repeat domain 28 Gene [Source:MGI Symbol;Acc:MGI:2145661]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42703 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9605 | Essential Splice Site | Available for shipment | Available now |
sa1392 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa42703
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027020 | Essential Splice Site | 302 | 1054 | 7 | 27 |
ENSDART00000146436 | Essential Splice Site | 302 | 1052 | 8 | 28 |
Genomic Location (Zv9):
Chromosome 16 (position 22214368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 20320811 |
GRCz11 | 16 | 20126630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTGCCTTGAGCTGCTTGTGGGCAATGGTGCAGATGTCAATATCAAGG[T/C]AAGGTGGCACATGCAGATCTGAATTGACATTTATACTTAACTTGTTTTAG
Long Flanking Sequence:
AAACTCACAATGTGCTTTGCTTTCACTCACACATTTGCGTACTGAGGGCGATTTAGCCAGAATAGCTTTCAGATGGCACCATGCTAACCTTTTCATCCAGAGCACCACTTTAGAAGGAACCTTTTGGGCATTTAAATAAACATGCATTTTGTGTTTGGTCAATACATATTCATGGTTATATAAGCTCTTTTTCAGTTGTATTAAATGTAGATCTCTAATTAAACCATTCTGCAAGCAAATGTGAATGTTTTATAGTTAAACATTTGAACTGTGCACGTGCTTTCAGATGAATGAGCCAAACGCGTATGGAAACACACCGCTGCACGTGGCTTGCTACAATGGTCAGGATGTGGTGGTGAACGAGTTGATCGAGTGTGGCGCCAATGTGAACCAGGTTAATGAGAAGGGCTTCGCACCCCTGCACTTCACCGCCGCCTCACGACATGGAGCACTTTGCCTTGAGCTGCTTGTGGGCAATGGTGCAGATGTCAATATCAAGG[T/C]AAGGTGGCACATGCAGATCTGAATTGACATTTATACTTAACTTGTTTTAGGTTAACTATGCCTTTAAGATGACATGACGCCGAAGCCATTAAATACTACATCCGACTAAATCAATATGCAGTATCGTTTTTGTAAAAAGACAAGATTAAAATGTAGTTAAAATAGAAAAATAGAATCCCAAATCCAACTGAAAATAACAAGCATTCATGTTTTTTGTCCTGACTTTGATTTTTAGTGTCTAATAAATAGGGTTGGATACCGAAACCTACCTTTGAAACCAGTATGCACCTGACCGAATTAGCATATGAATTTCGGTGCCTAATTCCGGTGCCACTGGCATTTTAGAATTTGCAAGTCAGAGGCTGTCCGCAGCGCCCAGCCACGACTCATGACTGTTTAGTTTTCTGTCGCGCCAAAGACCACCATCTGAATAGTTTCATTTTAAATATTATGCAAATGTGCGCGTCTGATGTGTGATACTATCAACTGTCATGTGCGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9605
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027020 | Essential Splice Site | 523 | 1054 | 14 | 27 |
ENSDART00000146436 | Essential Splice Site | 523 | 1052 | 15 | 28 |
Genomic Location (Zv9):
Chromosome 16 (position 22222779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 20329222 |
GRCz11 | 16 | 20135041 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCAGTGCATTACGCCTCTGCSTATGGACACCGTCTGTGTCTGGARYTG[G/A]TAAGTTACTGGTRAACTTAAAACCACAYAATTCGGTAATTCACATAATTT
Long Flanking Sequence:
ATTCATTTGAGAAGTGTGAGTGTTCTAAATCTGGCTCAGGCACGGTGCAGTTAGCCGGCCCTGCCCTGGCTGGAAGAGTTGTACCAGAAAGCTGTTCACTTGGGCTGTGGCGCGGTACAATTTTAGTGTAATTGCAAATCGCCCCTGAGCCTGAAACTGATCACGAAATGTAACTTTTAAGGGACTGTTTCCTATGGATTGATTAATCATTACAAGCGTGCTTCGGCACGGTTCAAAAGCAACTGTACATAGTGTGAGTATACCCTTAAAAACCAAGCCCAAAATCCATTCAAGAGAACATAATGAGTCTCTCATTTTGAAAATCTCAGATTTAATTTCACAGACATGTCTTTCTAGTAGTTACCAGTCTTTCTCTTTCCCTAACTAGGTGCCTGGAATATTTGCTGAGGAATGATGCTAACCCAGGGATCCGAGACAATCAGGGCTACAATGCAGTGCATTACGCCTCTGCGTATGGACACCGTCTGTGTCTGGAGTTG[G/A]TAAGTTACTGGTGAACTTAAAACCACATAATTCGGTAATTCACATAATTTGTAAATATTTTCAGCTGATTGTTTCTTTTCTCTTCATTAGATTGCGAGTGAAACTCCGTTAGATGTGGTAAGAACTGTAATGCTTAACATAAAACTTCCTGATATATCATGGCCTTTAAGATGTTTAAGTTCTTCATTTAGGCCACAGGAGTCAAAGCCAATTTCTGGAGGGCCGCAACCCTGCACAGTTTAGTTCTAACCCTGCTTCAACACACTTACCTGTAAGTTTCAAACAAGCCTGAAGGACTCAATTAGTTTGATCAAGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGAGCTGCGGCCCTCCAGGAACTGGCTTTGACACCTGTGATTTTAGGGGGACCAAAAGAAGTTAAGCACTTTGTAAGGCAAGCAGCTGTGCGATATTATCCCTTTATCGCATATAATCACACTGGTGTGATCAGACAAGCGTGTGTATGATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1392
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027020 | Essential Splice Site | 875 | 1054 | 23 | 27 |
ENSDART00000146436 | Essential Splice Site | 873 | 1052 | 24 | 28 |
Genomic Location (Zv9):
Chromosome 16 (position 22236242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 20342685 |
GRCz11 | 16 | 20148504 |
KASP Assay ID:
554-1304.1 (used for ordering genotyping assays)
KASP Sequence:
AAAACCCCGCTCATGATGGCCGCTGAGAACGGCCAGACTAATGCAGTTGG[T/C]AGGAGTTTGACACTGGATGCCTYAAATGTTTCTGGTTAACTGGGTGTGTG
Long Flanking Sequence:
AGCCACCTTTTGTTTTGCAATAAATACCTGCACATTTTGCATACAGCTATTTTTGTTTGCATGATACTTTAAAATTGTGCTCCTTACAAATTCATTAAAATTTTACAAATATTTAAATTCTAGATTTACAGACATTATTTTTGACATTATTTAAAATGTGTGACTAAGAAAAAGCTATTCACTTTTTTTGGTGAGGCAAGTAAACATTTTTGAAAAAGCAAGTAAAAATCTGAACCACTGGCCCAATCAAATCCATAGTGTTGAATCCTGCATAGGTTAACGAATAAATATCATATTAAATAACATTCAGTGGGACTGAGGTCTATACTGTAACTGTTTTCTGTCTGCAACAGGACTCCTCTTCACGCTGCTGCATTCACCGATCATGTGGAGTGCCTGCAGCTCCTGCTGGGCCACAATGCACAGGTGAACTGTGTGGATGCTGGAGGAAAAACCCCGCTCATGATGGCCGCTGAGAACGGCCAGACTAATGCAGTTGG[T/C]AGGAGTTTGACACTGGATGCCTCAAATGTTTCTGGTTAACTGGGTGTGTGTTTGGGTTTGATGTGTCACGATGTCTGTTTGTTTGGCAGAGGTGTTGGTGAGCAGTGCTAAAGCAGATCTCACGCTACAGGACGCCAACAAAAACACTGCTCTCCATCTGGCCTGCAGTAAGGTAACAAACACTCTGCTCTCTTGTGTCTTAATTCCTCGAATGAAACCATGGGGCAAGATGGGAAATGACATTTTGTGTAGATTTAGCATGTTTAAATTAGCACTGGGTGGTATGATGGTATATATCATTGCTGCAGAATGAAATTTGTATCTTAAAAGATTTTATTTTATTCCATGTGTACTGTGAATGTAAATAAGTGCATGTAGCCAACTCGCAATATGCATGAGGTCAAGAAAAAAGACACTACTTGGGCTCTATGTTAATGATCTAGGTGCAAAGTCTGAAGCGCATGGCACAAAGCATTAAGGGCATATCCGAATCCATTTAA
Associated Phenotype:
Not determined