ZMP
atad5a
Ensembl ID:
ZFIN ID:
Description:
Si:ch211-11k18.10 protein [Source:UniProtKB/TrEMBL;Acc:A9JSS3]
Human Orthologue:
ATAD5
Human Description:
ATPase family, AAA domain containing 5 [Source:HGNC Symbol;Acc:25752]
Mouse Orthologue:
Atad5
Mouse Description:
ATPase family, AAA domain containing 5 Gene [Source:MGI Symbol;Acc:MGI:2442925]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20016 | Essential Splice Site | Available for shipment | Available now |
sa15159 | Nonsense | Available for shipment | Available now |
sa14858 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20016
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103733 | Essential Splice Site | 17 | 1778 | None | 23 |
ENSDART00000103734 | Essential Splice Site | None | 766 | None | 9 |
ENSDART00000103737 | Essential Splice Site | 17 | 1778 | None | 22 |
The following transcripts of ENSDARG00000070568 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 26790151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 26114085 |
GRCz11 | 3 | 26244956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGGGGTTGTTGCATTGCCAGCTGTCATGGAGGATTTCGAGGGTCAGG[T/G]ATGTGTCTTATTAATAATGTGTAACTGTTAATCTGTTATGGCTGTGTTTT
Long Flanking Sequence:
AAAGTAATTTTCCACGCGGAGCGGGTTTGTGGGTTGGTTCTTACAACGCGTTATGCTTGTTTTCGCCGGGAAGTATATCGTTGTTTGGTAAATGTGTCGATAGATAGGCTTTGTGTTTACTCGGAGTCGTTGCTGGATTCATATTTATGCACTCTTCACTGTAATTCATGGATTATGTATCAGCAGATCCCCGAGGGAAATAAAACAACAGGTGAGTGTCTGCAATTTAAATACATTTCTTCAAACACACTTTGACTAACTTACACTTTTACCAGCGTTATGCTAACATATTAAGCAACATTCACCCAAACTGTTACAGTAGCTGTTTATGAATTATAACATTTATAATAACATTTTAAATCTTTCATGACACTTTTGTTTGGCGTGCTCGCGTTTAACCTCTTTTAAAATCCTTCTTAAATGCAGATCTTTAGTTTTAGGGTGAAAGATGGCTGGGGTTGTTGCATTGCCAGCTGTCATGGAGGATTTCGAGGGTCAGG[T/G]ATGTGTCTTATTAATAATGTGTAACTGTTAATCTGTTATGGCTGTGTTTTAGTTATATAATCAGAAAAGTGTAATATTTATATTAAATTAAAATTGTTGCTTTTCCAGCCGTGCAAAAAAATGAGAAAGGATGGCGATGCACCATCTGTCAGAACTATCACTAACTACTTTGCACCCAAGATAGTGGAGAAACCGTTCTCACCGCCTCGATCCAACAACATCATGGACTTCTTCAAGAAGACCTCGCCTGCACCAGAAATAAAAAACTGCTCTCTGAAAGCTAAAGAAAACTCGCCGCATTCTTCAGAGCAAGTAAGTCAAGAAGTCTCAGGGAAACCTGTTCGAGGACGAGGGCAGAAGCGCACCAGGAAGACTAAAGACAAGAAGAAATCTAAAGAGGAGGATGCACAGGTGGTCACAGATGATGTTGTGCTTATTGAGAGTCCCGGTGATTCAAAGGAAAGTGAAACTGCTGGACTTCCAGATAGAACTTGTCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15159
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 |
---|---|---|---|---|---|
ENSDART00000103733 | Nonsense | 1605 | 1778 | 21 | 23 |
ENSDART00000103734 | Nonsense | 593 | 766 | 7 | 9 |
ENSDART00000103737 | Nonsense | 1605 | 1778 | 20 | 22 |
The following transcripts of ENSDARG00000070568 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 26772269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 26131967 |
GRCz11 | 3 | 26262838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTKGACTCCTCACTASACTATCAAGCCTCGCAGTCRGARGGGTTTTGC[C/T]GACCCCAGGATTCTGGCTGGACYRGTGCAGAGATCAAGAGCGGGATGACT
Long Flanking Sequence:
GAGGAGTGAATCTTCTCCATTCGAATATGGAGAGTCTGCTTCCACTGCCAACTCGTCTTTTACCCCAGTCCACATTTAAACCACAAGCAGCACCAGCTCCACAGTCCCAGCCTGAGCAACTACCTCAAACTGTGAGATTAGAAAGTTTGGACGAGCCCTCTGATGACGGCAGTCCTCTCAAAGTGTCCGCGAGAATGAAGGGGCGTAAGAAGATGAGCATTAACCACAAAGATGTTTTCCAGTCTGATTCAGAGTCTGAGGAAGACTTCCTCCCACTGCCAAAAAACAGCAGAGATCCTGCTCAAAGCACTAATGTAGAAACAGCCGACGTGCCTGAAGCTGCCCCCAAAAAATCAAGGTGTATTGTGTTAACTGAAGCCGAAAAGAAGAAGAGCAAGCCAGTGATGCAGTGCTTGAGTGGTTTGGCAGAGTTTTTAGACCACATGTCCTTCCTTGACTCCTCACTACACTATCAAGCCTCGCAGTCAGAGGGGTTTTGC[C/T]GACCCCAGGATTCTGGCTGGACCAGTGCAGAGATCAAGAGCGGGATGACTGATGATATTCGGTTAGAGTCTGTCAAGCAGGCCAATAGTGTTAGTGTTGAAGAAGTGCATGCTGTTTTGGAGCATTTGAGTTTTAAGAAGTGCAAGGCTGTAGTGTCTGATGCCTGGGACAGAGTGCAGCAGCTGGAGGCCGAGATCAGAGGAAAAGCTGAGGAGGAGCTCACACTCTCCGTGGCTCCACACAGACAGAGCTTCAGCCTCACACAGACTACACCTTGTGAACCAAGGTAGGAATGAGATTTTTTTTTTTGGGTTAATTTCATTTATATATATCTTTTCATCATGGAAAAAATAATGGATTAGCAAAGCAGTGTTCCTCGGAATGAATGAGTTACCCGTTATATGTTGCCCACCCGTTATATGTTGCACAACTAGTGGCTGATTTAGTTAGGATTATTAGGCTATATCATTGAAGAAATAATTTCATATTGAAGCAACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14858
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 |
---|---|---|---|---|---|
ENSDART00000103733 | Nonsense | 1687 | 1778 | 21 | 23 |
ENSDART00000103734 | Nonsense | 675 | 766 | 7 | 9 |
ENSDART00000103737 | Nonsense | 1687 | 1778 | 20 | 22 |
The following transcripts of ENSDARG00000070568 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 26772023)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 26132213 |
GRCz11 | 3 | 26263084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGAGGARAAGCTGAGGAGGAGCTCACACTCTCYGTGGCTCCACACAGA[C/T]AGAGCTTCAGCCTCACACAGACTACACCTTGTGAACCAAGGTAGGAATGA
Long Flanking Sequence:
ATTCAGAGTCTGAGGAAGACTTCCTCCCACTGCCAAAAAACAGCAGAGATCCTGCTCAAAGCACTAATGTAGAAACAGCCGACGTGCCTGAAGCTGCCCCCAAAAAATCAAGGTGTATTGTGTTAACTGAAGCCGAAAAGAAGAAGAGCAAGCCAGTGATGCAGTGCTTGAGTGGTTTGGCAGAGTTTTTAGACCACATGTCCTTCCTTGACTCCTCACTACACTATCAAGCCTCGCAGTCAGAGGGGTTTTGCCGACCCCAGGATTCTGGCTGGACCAGTGCAGAGATCAAGAGCGGGATGACTGATGATATTCGGTTAGAGTCTGTCAAGCAGGCCAATAGTGTTAGTGTTGAAGAAGTGCATGCTGTTTTGGAGCATTTGAGTTTTAAGAAGTGCAAGGCTGTAGTGTCTGATGCCTGGGACAGAGTGCAGCAGCTGGAGGCCGAGATCAGAGGAAAAGCTGAGGAGGAGCTCACACTCTCCGTGGCTCCACACAGA[C/T]AGAGCTTCAGCCTCACACAGACTACACCTTGTGAACCAAGGTAGGAATGAGATTTTTTTTTTTGGGTTAATTTCATTTATATATATCTTTTCATCATGGAAAAAATAATGGATTAGCAAAGCAGTGTTCCTCGGAATGAATGAGTTACCCGTTATATGTTGCCCACCCGTTATATGTTGCACAACTAGTGGCTGATTTAGTTAGGATTATTAGGCTATATCATTGAAGAAATAATTTCATATTGAAGCAACTAAAAAAGTCTGTAAACTCTCAAAAAGAGACAAGCAAGAAAAATTTCTTGAAAAATAGGCAATTGTTTCGGTTACCTTGACCATTGTCAATGCCAAGATATCCATGTTAGGACAGGAAGCCATCTTAACTGAAAAAAAATCTGCGCACACTCAAAAATCAGAAAGACACAAGCGAGATGAAGTGACAAGCAATTGTACACACCTATTGGATTGTTTTTAAGGAGCGCTGAGTCTTAAGTTGCCTTTATC
Associated Phenotype:
Not determined