ZMP
ankk1
Ensembl ID:
ZFIN ID:
Description:
ankyrin repeat and kinase domain containing 1 [Source:RefSeq peptide;Acc:NP_001124137]
Human Orthologue:
ANKK1
Human Description:
ankyrin repeat and kinase domain containing 1 [Source:HGNC Symbol;Acc:21027]
Mouse Orthologue:
Ankk1
Mouse Description:
ankyrin repeat and kinase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:3045301]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8927 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5880 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22635 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8927
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079504 | Nonsense | 24 | 733 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 20975760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 22078386 |
GRCz11 | 15 | 22014118 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTGAAGGACTCTTTTAAAGATGGCAGCCTGGAGGGGTTTAGTTATTTT[A/T]AAAAAGATGAGTTTGAAAGTGACTGGGAGAAACTGGTTGAGCGCAAGTTT
Long Flanking Sequence:
TAATAATTACAACGTGCTGAAAATGTGGCAAGCACTTTTTAAATGTGTTGAGCAGTAAGCTGTTATAGAACCTAATTAATATGTAGCATCAAAATATATTTAGCTTAATTACGCTAAATAAAATGAAACTGCTTCCCTAACCCCAAACATGCACACATGCCATACTGTATGAGGAAATCTGTACTGTTATATAAATACATGAAGCAGGTATAACCGGTTATCAGTTGCCCCACACAGATCTGTCAACCTCACCTGTGCGACTGATTCAAAACTGGCTTTGTTACATTTCTGTTCACATAATCAGTGCTTTGACTCCTCCTAGAGCCTTTGGAAGTTTCCTTGACCTGCTTTTTGTTTGCCAAGAAGAAATGTCGAAGGGCTGAAGAGAGAGCTACTGGCAGAGTCTTCATTTCCTGAGACGGGAAAACAACATGACAGACGCAAACTCCGATGTGAAGGACTCTTTTAAAGATGGCAGCCTGGAGGGGTTTAGTTATTTT[A/T]AAAAAGATGAGTTTGAAAGTGACTGGGAGAAACTGGTTGAGCGCAAGTTTGGTCGGGTCTATAAGGTGAAGCTTAAAGTCTTGCGTGAAACATGTGCTCTGAAGACCACAACCAATGACTACAGGTACTGATACATATGAGAGATCATATAATGGTAAAAGTAGTTGTAAGTCGTTGTTATAGTTTAACAGTTATAATATTACCACTTTTGCTTTTAAGTAAAACAATAACTTGTGTTGTCCTTGTAAATATGTTTTCAAAATTTCAAATGAGAAAATGATCAGTTAATTCCACTAAATCACAACCGGTTAATATAAATGAATGATTTCAGATTTTGTATGCTGGAAAATAATTATTATATTGAATTATTATTATCTGTATATTATGTATCTTTTATATGTTTATTTTATTTGCATTATGATTTTTATTTTTGCATTATTAGTTATTATATACTTTATGGCCCAACAGGAACATAATGGAGATTTCCAAAATTGGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5880
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079504 | Essential Splice Site | 308 | 733 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 20984976)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 22087602 |
GRCz11 | 15 | 22023334 |
KASP Assay ID:
554-3893.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTAAAATCCATGACAATAAAATGAATTCAATTGTGCTTTCCCTCCATT[A/C]GCCCAAGAAAACGGCTGACTCCTCAGGCAAGTATTTTTCAATGCATTCAA
Long Flanking Sequence:
TCAGTTATTAGAAATGAGTTATTAAAACTATTACGATTAGAAATGTGTTTAAAAAATCTCTTCTTTAAACAGAAACTGAGAAAAAAAAACAGGGGGGCTAATAATTCTGACTTTAACTGTATCTCCCCTCTCTCTCTTTCAAAAACTCCTATTCTAGCACTAAATTCTCTGAGTACAAACAAGTTACTTTGTATAATTAGCACTTCTTGTACGTATTGCGTAAAGAAATGTATATTGTTATGTTTTCACTTTAATTACTGCAGTTGTGAAATCTTAACAGATCTAGAAGAGCCTGACTCTGTTTCAAGCCTATAAATGTTAAACAAACTTAAGTTGGCTCCAGTGTTGTGAACTTTTCAAAAAGTCTGAGATGTACAATGGGTGTTACTATGCAAATAAATAAATTACTGTGACTGCTATATTGACCAACACAACATTCAGACTAACACATTTTAAAATCCATGACAATAAAATGAATTCAATTGTGCTTTCCCTCCATT[A/C]GCCCAAGAAAACGGCTGACTCCTCAGGCAAGTATTTTTCAATGCATTCAATCTTTTGTGCTGTCTCTCTGAACAATCCTTCCACATTTTACTGTATATATATAACAGTCCTCTAACCCATTTCCCCTATGCACTATAGATGATTCAAGCATTCAGTCTCTGCTTGTAAGAAAAGACTTTAATAGTTTCAAGAAAGTTGTACGAAAAGAGCATGTGTCAATGCTCTTTCAAGACAACAACTCTCTCCTTCATCACGCCGTGGCAGGCGGGGACAGAGAAAGTGTGCAGATGGTCCTGAATCTGGGAGCCTCGGTGAATTGCCAGAGTGTAAAAGGCTACACTCCTCTCATCGTCGCAGTTCTGCACAAGTTTTATGAGATCTGCAGCTTGCTGACAGACTGTGGGGCTGACGTCAACCTCAGCGATGGCGACCAGTGGACCGCGCTACATTTTGCCGTACAGGCTGGCGACGACCGAGCCACTCGATTTTTGCTAGACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22635
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 |
---|---|---|---|---|---|
ENSDART00000079504 | Nonsense | 605 | 733 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 15 (position 20985982)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 22088608 |
GRCz11 | 15 | 22024340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGAAAGGCCATCCGGAGATTATCCTCACCTTGGAGGAACACCAAGGCT[C/A]AGTCAACATTCAAGGGAAAAACGGCTGGACGCCTTTGCATCTTGCCTGTC
Long Flanking Sequence:
GAGAGCTGATGCCAAGGAAAAGGATGGATGGACGCCTTTGCATCTAGCAGCTCAAAATGGGCACGAGAACATTGTGAGAATCTTACTCCGCCGTCTTGACAGCGTGGATGTGCAGGAGCACCAATCATGCCGTACAGCGCTTCATGTAGCTTCTATTTATGGCCACATAAACATCGTCAAGCTCTTGCTCAATAAAGGAGCTGACATCGACAAACAGGATAACAACCAATCCACTGCCCTACACCTGGCGGCAGAGGAGGGGCACTTCAGGGTGGTCCGTTTACTGGTTAATAGTGGAGCTGATGTGAATAAAGTTGATGAGCAAAGCTACAGCTCTCTTCATTTTGCAGCTCTGAACGGTTATACAGGTATCTGTAGACTCCTCTTAAGTAAAGGAATCGACCCCAACAGCAGAACTAATAAGAACTGGACCGCCATGCACCTGGCAGCCCTGAAAGGCCATCCGGAGATTATCCTCACCTTGGAGGAACACCAAGGCT[C/A]AGTCAACATTCAAGGGAAAAACGGCTGGACGCCTTTGCATCTTGCCTGTCATCATGGACAAGAGGAGGTGGTGACTGGGCTGCTGACAGCAGGTGCTGATCCAAACTTGGCTGAGGATAACGGCTGGACTCCCCTCCATTTAGCCTGTAATAGCAGCAGCTTCCCTAGCGTGCTGCAGTTGATATCCCATAAAGCTAATGTGAATGCTCAGAATAACAGCCAGTCAACACCCTTGCATTTAGCCGCCCAGCTCAGCAACATCCCCATCATCAAAGCCCTTCTGATGAATAATGCACAGCGGGAGATGCAGGACTCCAAAGGATGTACCGCCTTAACCTTGGCTCAACAGTGCAACAATTCAGAAGCCGTGGAGCTCCTGGACAGCTAGTGCTTGGGTTGAGAGCGAGCCATGTTCGGTGACAGATAACTCGGCCATTAGAGGGAGTACAACATTGATTTCTCCCATCGATTTCCTTCCTCCTGCAAAGCCTGCTCTTATA
Associated Phenotype:
Not determined