ZMP
zgc:172142
Ensembl ID:
ZFIN ID:
Description:
ankyrin repeat and SAM domain-containing protein 3 [Source:RefSeq peptide;Acc:NP_001108037]
Human Orthologue:
ANKS3
Human Description:
ankyrin repeat and sterile alpha motif domain containing 3 [Source:HGNC Symbol;Acc:29422]
Mouse Orthologue:
Anks3
Mouse Description:
ankyrin repeat and sterile alpha motif domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1919865]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24546 | Nonsense | Available for shipment | Available now |
sa3261 | Nonsense | Available for shipment | Available now |
sa37949 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37948 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24546
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078828 | Nonsense | 201 | 622 | 5 | 14 |
ENSDART00000131342 | Nonsense | 201 | 622 | 6 | 16 |
Genomic Location (Zv9):
Chromosome 24 (position 39177515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37786604 |
GRCz11 | 24 | 37674501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCAGTCATTTTGATTGTGTGTATGATTCAGGGCGCGCGAACAAAGGAC[C/T]GAAACATGAAGGGAGAAACGGCGAGAGCTCTGGCTATGATGTACGGACAC
Long Flanking Sequence:
ATTATGGTTTTCTTTGGCTAACCGCTTGTTAAGTGTGACGTCACGCGAAGCGGCTTCCGGGTCCAATAGCTCTATCAAACTGTATGGAGAGACTCGAGAAATGATAATAATAAACATTTACAAAGCGATGTAACACTTTCGAAAATCACGATCGCAATATATATGTCCATGCCTAATATCCGATGGCCAGAAAGTCATTATTTTTTTATAAATTGTAAAAATTTTGGTATTTGTGATGCAGCAAGCCCAGAGATTGTTGTGTACACTATGATTTTATATAAAATTAACTTTAATGTGTGATAGGAATAAAAAGTGATCATAAACAAATATTTTCTTAACTCAAATGAGTCGCAGCTTGGACGCGGAAACAGTATTACATACGTCACCAACACGTCACCACTTAACAAGCGGAAAGTAACGCTGATCAGGGAATAGTCAGGTGAACAGTATTATCAGTCATTTTGATTGTGTGTATGATTCAGGGCGCGCGAACAAAGGAC[C/T]GAAACATGAAGGGAGAAACGGCGAGAGCTCTGGCTATGATGTACGGACACATCAAAATCGCCAGCCTCATCGACATGCACGTCATAAGAGCCAAATCATGTCAGTCGCTGCACACTTTAGTGTTTGTCGTTTTCCCCTTTTAGTCCTGCCTGCAGAGAATAACTCAAGCTGATGTCTGTGTGTAGCTATGTATGAGGAGCTGAGCTCGTCTGAAGAAGAAAACCCAAGTCCTAGAGTCCGTTCAGCTCACAGCAGAACCAGAGGACCCAGCATTCACGATGGCCCACAGGCTATCGCACGATTCAGAGTCGGATCCAAACACGGTAAATACTGGAGCAAACAAGGTCAATTTTATAAATGCATTAGATTGGTTTATGCTAATTCGATGTTTTACATAATCTCAACTGAAACATGAAGACAAGGTGGGGCATATTATAGCCCCTCCCCTTTTTTAAATCAGCCAATAGGGTTTGTTTTAATCACAACTCCTCCAGAGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3261
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078828 | Nonsense | 272 | 622 | 6 | 14 |
ENSDART00000131342 | Nonsense | 272 | 622 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 24 (position 39177216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37786305 |
GRCz11 | 24 | 37674202 |
KASP Assay ID:
554-2871.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGCAGAACCAGAGGACCCAGCATTCACGATGGCCCACAGGCTATCGCA[C/T]GATTCAGAGTCGGATCCAAACACGGTAAATACTGGAGCAAACAAGGTCAA
Long Flanking Sequence:
ATAGGAATAAAAAGTGATCATAAACAAATATTTTCTTAACTCAAATGAGTCGCAGCTTGGACGCGGAAACAGTATTACATACGTCACCAACACGTCACCACTTAACAAGCGGAAAGTAACGCTGATCAGGGAATAGTCAGGTGAACAGTATTATCAGTCATTTTGATTGTGTGTATGATTCAGGGCGCGCGAACAAAGGACCGAAACATGAAGGGAGAAACGGCGAGAGCTCTGGCTATGATGTACGGACACATCAAAATCGCCAGCCTCATCGACATGCACGTCATAAGAGCCAAATCATGTCAGTCGCTGCACACTTTAGTGTTTGTCGTTTTCCCCTTTTAGTCCTGCCTGCAGAGAATAACTCAAGCTGATGTCTGTGTGTAGCTATGTATGAGGAGCTGAGCTCGTCTGAAGAAGAAAACCCAAGTCCTAGAGTCCGTTCAGCTCACAGCAGAACCAGAGGACCCAGCATTCACGATGGCCCACAGGCTATCGCA[C/T]GATTCAGAGTCGGATCCAAACACGGTAAATACTGGAGCAAACAAGGTCAATTTTATAAATGCATTAGATTGGTTTATGCTAATTCGATGTTTTACATAATCTCAACTGAAACATGAAGACAAGGTGGGGCATATTATAGCCCCTCCCCTTTTTTAAATCAGCCAATAGGGTTTGTTTTAATCACAACTCCTCCAGAGACAGTACTTGAGCTCAAGCGCATCAAATAATAAGCAAATGAGAAGTGTCTTGAAAGGGGGCGGGGCATGTCAGATACTAAAAAGCATTTGATTGGTCAGAAGATTCGATGAGAAAGTATGAGGTGATGCCAGAAAAAAACATTAAGGCGGAAGTGAAACTGCAAGCTTTGGATGTTTATATCAGGTTTATATCTGGTCACTGTTTTGAAGCATGCTAGCTTATAGATATACTTAAAGCTAACATACTGATGCTAACATCTAATTTCACTGGAACTTTAATTGCAGAAGTTCCTGCAGCTCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37949
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 |
---|---|---|---|---|---|
ENSDART00000078828 | Nonsense | 561 | 622 | 12 | 14 |
ENSDART00000131342 | Nonsense | 561 | 622 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 24 (position 39168641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37777730 |
GRCz11 | 24 | 37665627 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGCAGACGCTGAACGCAAAACTACACACTCTACAGAACACGCACACA[C/T]AACTCAAACAGATCACACAGGATGACGGTCGATCTGTGGGAAAAGGTGTG
Long Flanking Sequence:
CAGTTTGAGTGACCAATCAAATGCTCTCTAGTATCCGACATGCCCCTCCCACTTCAAGACGTTTTTCATTTTCTGCACTTGAACTCAATCATTCTCACTGGCAGAGCGCTGATCAAACAAAACACTATTGGATTTTTTAATGGGGTGGAGCTACACTAAATCCTGCCCTCTTTTTTGTGTTTCGGTTGAGATTACGCCAAAGATCGAATAACAATGCCTATATTTCAAAGCGCTTCACAGGAGCTTAACATTTTAATTTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCCAGCGTTGCGTGGAGGTGGAGTCTTTTCAGGGTCAAGTGACCCAGGAGAAAGAGCTGCGTGCTGTGATGGAGGGATGCCTGATGGAGGAGAAGATGGCATGGAAAAGGGTTCAGGCAGAACTGAAGGAAAACGCTAAACGCATGCAGACGCTGAACGCAAAACTACACACTCTACAGAACACGCACACA[C/T]AACTCAAACAGATCACACAGGATGACGGTCGATCTGTGGGAAAAGGTGTGCAGAACCTAACAAAATTTACATTTAGTATCTAATGCAAAAAAAAATCTGAAATTCCTACAACCTCTCAGAATAATCCAACAACAGCCTAGCAACCATTCAGGACACCCTAACAACCATCCACCAACCTCTCAAAACTGACTTTTTTCATAATTAGGATTTATTTTACAATTACCTTAGAGTTTTGAATCCGTTCAGCCGATCTCTGGGTCTTGCGGAGCACTTTCAGCTTAGCTTAGCTTAGCATACATCATTGAATCGGATTAGACCAGTAGCATCCCATTAAGCGTAATGATCAAGGAGCTTTGCTGCTGTACCATGGCTGAAACAGGCACAATGATATCACACAGCCCATGAAAATAGTCCACAGCTAGGTAACAGCACTAATGCAATTGCACCTGCTGCAACCAGGGTACGGCAGCAATGTTGCTTGATTATTACGCCAGAATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37948
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 |
---|---|---|---|---|---|
ENSDART00000078828 | Essential Splice Site | 576 | 622 | 12 | 14 |
ENSDART00000131342 | Essential Splice Site | 576 | 622 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 24 (position 39168594)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37777683 |
GRCz11 | 24 | 37665580 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACAACTCAAACAGATCACACAGGATGACGGTCGATCTGTGGGAAAAGG[T/C]GTGCAGAACCTAACAAAATTTACATTTAGTATCTAATGCAAAAAAAAATC
Long Flanking Sequence:
CCCACTTCAAGACGTTTTTCATTTTCTGCACTTGAACTCAATCATTCTCACTGGCAGAGCGCTGATCAAACAAAACACTATTGGATTTTTTAATGGGGTGGAGCTACACTAAATCCTGCCCTCTTTTTTGTGTTTCGGTTGAGATTACGCCAAAGATCGAATAACAATGCCTATATTTCAAAGCGCTTCACAGGAGCTTAACATTTTAATTTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCCAGCGTTGCGTGGAGGTGGAGTCTTTTCAGGGTCAAGTGACCCAGGAGAAAGAGCTGCGTGCTGTGATGGAGGGATGCCTGATGGAGGAGAAGATGGCATGGAAAAGGGTTCAGGCAGAACTGAAGGAAAACGCTAAACGCATGCAGACGCTGAACGCAAAACTACACACTCTACAGAACACGCACACACAACTCAAACAGATCACACAGGATGACGGTCGATCTGTGGGAAAAGG[T/C]GTGCAGAACCTAACAAAATTTACATTTAGTATCTAATGCAAAAAAAAATCTGAAATTCCTACAACCTCTCAGAATAATCCAACAACAGCCTAGCAACCATTCAGGACACCCTAACAACCATCCACCAACCTCTCAAAACTGACTTTTTTCATAATTAGGATTTATTTTACAATTACCTTAGAGTTTTGAATCCGTTCAGCCGATCTCTGGGTCTTGCGGAGCACTTTCAGCTTAGCTTAGCTTAGCATACATCATTGAATCGGATTAGACCAGTAGCATCCCATTAAGCGTAATGATCAAGGAGCTTTGCTGCTGTACCATGGCTGAAACAGGCACAATGATATCACACAGCCCATGAAAATAGTCCACAGCTAGGTAACAGCACTAATGCAATTGCACCTGCTGCAACCAGGGTACGGCAGCAATGTTGCTTGATTATTACGCCAGAATGAGAGTCTAGTTCCAAAAAATATCAGCTAGAAAATTATTTTTCTTAGATT
Associated Phenotype:
Not determined