ZMP
atad5b
Ensembl ID:
ZFIN ID:
Description:
ATPase family, AAA domain containing 5b [Source:RefSeq peptide;Acc:NP_001076298]
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 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17344 | Nonsense | Available for shipment | Available now |
| sa40667 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1125 | Nonsense | F2 line generated | Not yet available |
| sa15284 | Nonsense | Available for shipment | Available now |
| sa16554 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17344
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:
Founder:
SL4_09_F2
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015996 | Nonsense | 160 | 1060 | 1 | 14 |
| ENSDART00000135710 | Nonsense | 163 | 1060 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 6 (position 19365000)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 22074071 |
| GRCz11 | 6 | 18545392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCATTGATCATTTTGGATCTAATAAAGAGGGGTTGACCAGATTTTTA[C/T]AAACAGAGATAGATGATGGGGACCACTTGATAGATCAGCMAAAAATGAAC
Long Flanking Sequence:
AGTTTAAAATATTTATGGCAACAATGGATTCGTCGCTCTTTCCTCTGGCTGTTGTAAAAATAATGAACTCTTCCGGAAGTGTCTGCAACAGAAGGAATTTTCATGCTGGAGTCCTACAATCAGAAGGCAACCCCCAAACCCAAATGCACCCGAAACGTAACAGACTGAAACTAGCAAAAACGTACAGAACATCGGATAATATTGTCGGGAACAATCCCAGCCATGTAACTGGGAGCTACGAATCGACTACCTTTTGTAAAGGAACATTTTTTACAGATGCTGTAAGAACTACTGACGATAAAGACAACTTGACTCAGAAAGAACACTTTTCTCAAAGAGTGCAAAACAGCAATAAGGTGACATCAAAGAGGACGAGTAATAATATGAGCGTGCAGCTCGTCTGCACTCCTGCAAAGAGAGAGCATGCCTCTAGTGACAGTAGTTTAAAGCCAGCCATTGATCATTTTGGATCTAATAAAGAGGGGTTGACCAGATTTTTA[C/T]AAACAGAGATAGATGATGGGGACCACTTGATAGATCAGCCAAAAATGAACATTGGCCAAATCCAAGAGACCTCAAAACATGATCCTATCCAAAACTTGAGGTCCTCAAACAACAGCACGTCTTCATGTAGAGAACCACCCAACGTCAGAACCGTCAAAGAAATGGTGGGTTAGCTTAAAGATGTCACACTGGTGTAACAATATAATTTTCTCACAGTATTGTGCATCAACTCTTTATTTTTGGAATATCTTCTAAAAGTGTTTTATTTTACATGGCTGTTTTATTGTCCAACACGTTACATTACAACTTAAATTTGCATGTTAAAATAATGTAGTTAATAATTTTATTATGTAATCATATATTTTTACATTTTAATACCCTCTACTGTGTAAAAGATGCTAAGAATTTATTCTGACAGCATTACCTATTTCAACACAACAGATTGGTTGGTCTTCAAGTCAAAAAGATCAGGTTTCACTCTTGTAGGATTTAAATTGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40667
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
Founder:
SL7_02_F7
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015996 | Nonsense | 179 | 1060 | 1 | 14 |
| ENSDART00000135710 | Nonsense | 182 | 1060 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 6 (position 19364943)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 22074128 |
| GRCz11 | 6 | 18545449 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATAGATGATGGGGACCACTTGATAGATCAGCCAAAAATGAACATTGGC[C/T]AAATCCAAGAGACCTCAAAACATGATCCTATCCAAAACTTGAGGTCCTCA
Long Flanking Sequence:
AAATAATGAACTCTTCCGGAAGTGTCTGCAACAGAAGGAATTTTCATGCTGGAGTCCTACAATCAGAAGGCAACCCCCAAACCCAAATGCACCCGAAACGTAACAGACTGAAACTAGCAAAAACGTACAGAACATCGGATAATATTGTCGGGAACAATCCCAGCCATGTAACTGGGAGCTACGAATCGACTACCTTTTGTAAAGGAACATTTTTTACAGATGCTGTAAGAACTACTGACGATAAAGACAACTTGACTCAGAAAGAACACTTTTCTCAAAGAGTGCAAAACAGCAATAAGGTGACATCAAAGAGGACGAGTAATAATATGAGCGTGCAGCTCGTCTGCACTCCTGCAAAGAGAGAGCATGCCTCTAGTGACAGTAGTTTAAAGCCAGCCATTGATCATTTTGGATCTAATAAAGAGGGGTTGACCAGATTTTTACAAACAGAGATAGATGATGGGGACCACTTGATAGATCAGCCAAAAATGAACATTGGC[C/T]AAATCCAAGAGACCTCAAAACATGATCCTATCCAAAACTTGAGGTCCTCAAACAACAGCACGTCTTCATGTAGAGAACCACCCAACGTCAGAACCGTCAAAGAAATGGTGGGTTAGCTTAAAGATGTCACACTGGTGTAACAATATAATTTTCTCACAGTATTGTGCATCAACTCTTTATTTTTGGAATATCTTCTAAAAGTGTTTTATTTTACATGGCTGTTTTATTGTCCAACACGTTACATTACAACTTAAATTTGCATGTTAAAATAATGTAGTTAATAATTTTATTATGTAATCATATATTTTTACATTTTAATACCCTCTACTGTGTAAAAGATGCTAAGAATTTATTCTGACAGCATTACCTATTTCAACACAACAGATTGGTTGGTCTTCAAGTCAAAAAGATCAGGTTTCACTCTTGTAGGATTTAAATTGAACTATTAATTTATTGTTCTTTGTACAGTGCTGTTTTTTTATTGTTGTTTTTTGGCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1125
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
Founder:
mrf138
KASP Assay Location:
Project 554.15, Plate 22, Well A05
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015996 | Nonsense | 240 | 1060 | 2 | 14 |
| ENSDART00000135710 | Nonsense | 243 | 1060 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 6 (position 19364369)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 22074702 |
| GRCz11 | 6 | 18546023 |
KASP Assay ID:
554-1036.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGTGAAAATAGCTGTGAGTTGCTGAAAGACATTCAAAAACTCAATTTG[C/T]AGTTTCCTGTCCAAAGGTTTTTCACCCTTCTTCTGAAGAAGGGAACTTCA
Long Flanking Sequence:
AGAACCACCCAACGTCAGAACCGTCAAAGAAATGGTGGGTTAGCTTAAAGATGTCACACTGGTGTAACAATATAATTTTCTCACAGTATTGTGCATCAACTCTTTATTTTTGGAATATCTTCTAAAAGTGTTTTATTTTACATGGCTGTTTTATTGTCCAACACGTTACATTACAACTTAAATTTGCATGTTAAAATAATGTAGTTAATAATTTTATTATGTAATCATATATTTTTACATTTTAATACCCTCTACTGTGTAAAAGATGCTAAGAATTTATTCTGACAGCATTACCTATTTCAACACAACAGATTGGTTGGTCTTCAAGTCAAAAAGATCAGGTTTCACTCTTGTAGGATTTAAATTGAACTATTAATTTATTGTTCTTTGTACAGTGCTGTTTTTTTATTGTTGTTTTTTGGCAGAGGTTGAGCTGGAGAAAGGAAATTCCCAGTGAAAATAGCTGTGAGTTGCTGAAAGACATTCAAAAACTCAATTTG[C/T]AGTTTCCTGTCCAAAGGTTTTTCACCCTTCTTCTGAAGAAGGGAACTTCATCTATGGAGGAGAGCTCTGCTTTAGGTAGGCAATTATATTTGCAAATGAATATAAATGGTTGTTTTTTGTTTAAAATAATGATCATCAGGACAAACAGTCTTACGCAACTCCTTGCTGAAATCTGCCTTTATTTTTTTAGAAGCAGAAATGTCTGAAAATTACAAGCATCATTCAGATTATTGTGTTCAGAGGAAGAGAAAGCTGGAGCTGGAGGATCAGTACAGGACATACAAACGTTACAGAATGAACAAAGGAATTAGATTTGCCATTAAGGATTTTGAGCTATTTTCTGATGTTTTGGTCAACCCTCATTCAAAGTACACAAACCGACTGAGTCGAACAAAGTGCAGACAGCAACAAACTACATTCTGTGCTATAGTCACTGAACCAGTACAAAATGACTCTGTTTATCAGAACCAAAGGCTAAGAGTGGATGATGTTCTTTGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15284
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:
Founder:
SL4_07_F10
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015996 | Nonsense | 328 | 1060 | 3 | 14 |
| ENSDART00000135710 | Nonsense | 331 | 1060 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 6 (position 19363990)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 22075081 |
| GRCz11 | 6 | 18546402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAGCTATTTTCTGATGTTTTGGTCAACCCTCATTCAAAGTACACAAAC[C/T]GACTGAGTCGAACAAAGTGCAGACAGCAAYAAACTACATTCTGTGYTATA
Long Flanking Sequence:
ATTGTTCTTTGTACAGTGCTGTTTTTTTATTGTTGTTTTTTGGCAGAGGTTGAGCTGGAGAAAGGAAATTCCCAGTGAAAATAGCTGTGAGTTGCTGAAAGACATTCAAAAACTCAATTTGCAGTTTCCTGTCCAAAGGTTTTTCACCCTTCTTCTGAAGAAGGGAACTTCATCTATGGAGGAGAGCTCTGCTTTAGGTAGGCAATTATATTTGCAAATGAATATAAATGGTTGTTTTTTGTTTAAAATAATGATCATCAGGACAAACAGTCTTACGCAACTCCTTGCTGAAATCTGCCTTTATTTTTTTAGAAGCAGAAATGTCTGAAAATTACAAGCATCATTCAGATTATTGTGTTCAGAGGAAGAGAAAGCTGGAGCTGGAGGATCAGTACAGGACATACAAACGTTACAGAATGAACAAAGGAATTAGATTTGCCATTAAGGATTTTGAGCTATTTTCTGATGTTTTGGTCAACCCTCATTCAAAGTACACAAAC[C/T]GACTGAGTCGAACAAAGTGCAGACAGCAACAAACTACATTCTGTGCTATAGTCACTGAACCAGTACAAAATGACTCTGTTTATCAGAACCAAAGGCTAAGAGTGGATGATGTTCTTTGGACAGATAAATATCAACCTCAGCAGTCAAGTGAAGTCATTGGAAACTCTGCATCTGTACGGCAATTGCACAGGTAAAAATGAATCACTGTAATATTACAGCCTATAGTAACATGGAATGTTAACCAAAAAAAATAAGTTTAATTTAATCATTCTTTTTCATACAACACACAAACATGTATCCACAATTTGCATAATGTTGGGTTTAATTAGTTACAAAAGAACATAGTTACTGTAATTAAACTACTTTTCATTTTTAGATGAATTTAACGGTCCAATTTAAATAAATTCAGAGAAGCAGGGTAATTGTAAATGTACTAATTAAACAATTTAGCTAAAAAATAAATACATAACTTTTAAATATTAAAAATATTAGATTTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16554
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:
Founder:
SL4_08_H9
KASP Assay Location:
Unknown
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000015996 | Nonsense | 338 | 1060 | 3 | 14 |
| ENSDART00000135710 | Nonsense | 341 | 1060 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 6 (position 19363960)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 22075111 |
| GRCz11 | 6 | 18546432 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCATTCAAAGTACACAAACYGACTGAGTCGAACAAAGTGCAGACAGCAA[C/T]AAACTACATTCTGTGYTATAGTCACTGAACCAGTACAAAATGACTCTGTT
Long Flanking Sequence:
TGTTGTTTTTTGGCAGAGGTTGAGCTGGAGAAAGGAAATTCCCAGTGAAAATAGCTGTGAGTTGCTGAAAGACATTCAAAAACTCAATTTGCAGTTTCCTGTCCAAAGGTTTTTCACCCTTCTTCTGAAGAAGGGAACTTCATCTATGGAGGAGAGCTCTGCTTTAGGTAGGCAATTATATTTGCAAATGAATATAAATGGTTGTTTTTTGTTTAAAATAATGATCATCAGGACAAACAGTCTTACGCAACTCCTTGCTGAAATCTGCCTTTATTTTTTTAGAAGCAGAAATGTCTGAAAATTACAAGCATCATTCAGATTATTGTGTTCAGAGGAAGAGAAAGCTGGAGCTGGAGGATCAGTACAGGACATACAAACGTTACAGAATGAACAAAGGAATTAGATTTGCCATTAAGGATTTTGAGCTATTTTCTGATGTTTTGGTCAACCCTCATTCAAAGTACACAAACCGACTGAGTCGAACAAAGTGCAGACAGCAA[C/T]AAACTACATTCTGTGCTATAGTCACTGAACCAGTACAAAATGACTCTGTTTATCAGAACCAAAGGCTAAGAGTGGATGATGTTCTTTGGACAGATAAATATCAACCTCAGCAGTCAAGTGAAGTCATTGGAAACTCTGCATCTGTACGGCAATTGCACAGGTAAAAATGAATCACTGTAATATTACAGCCTATAGTAACATGGAATGTTAACCAAAAAAAATAAGTTTAATTTAATCATTCTTTTTCATACAACACACAAACATGTATCCACAATTTGCATAATGTTGGGTTTAATTAGTTACAAAAGAACATAGTTACTGTAATTAAACTACTTTTCATTTTTAGATGAATTTAACGGTCCAATTTAAATAAATTCAGAGAAGCAGGGTAATTGTAAATGTACTAATTAAACAATTTAGCTAAAAAATAAATACATAACTTTTAAATATTAAAAATATTAGATTTTGCTAAATGGATTTGCTAAATTTATTTACATAGC
Associated Phenotype:
Not determined