ZMP
si:ch211-221b16.9
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate kelch repeat and BTB (POZ) domain [Source:UniProtKB/TrEMBL;Acc:A
Human Orthologues:
KBTBD6, KBTBD7
Human Descriptions:
kelch repeat and BTB (POZ) domain containing 6 [Source:HGNC Symbol;Acc:25340]
kelch repeat and BTB (POZ) domain containing 7 [Source:HGNC Symbol;Acc:25266]
kelch repeat and BTB (POZ) domain containing 7 [Source:HGNC Symbol;Acc:25266]
Mouse Orthologues:
Gm5465, Kbtbd7
Mouse Descriptions:
kelch repeat and BTB (POZ) domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2685141]
predicted gene 5465 Gene [Source:MGI Symbol;Acc:MGI:3643058]
predicted gene 5465 Gene [Source:MGI Symbol;Acc:MGI:3643058]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34600 | Nonsense | Available for shipment | Available now |
sa15388 | Nonsense | Available for shipment | Available now |
sa21458 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34600
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 |
---|---|---|---|---|---|
ENSDART00000112884 | Nonsense | 51 | 617 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 9 (position 17940384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 17416454 |
GRCz11 | 9 | 17424166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAGTGGACGTGACCATAGAAGTGGAGCCTGACACCGAAACAGCAGAG[C/T]GAAGTGTTTCCTCTGGTGCTGGAAAAGTGTTTCAGTGTAGCAGGAATATA
Long Flanking Sequence:
GCCGCGGCCGATGTGACCAATCAGCGCCCTATGTTGCAGCTCAGGGGTAGCAAGTTTGAGTGAGACGTACAACGTCGATGTCTCAAGATCAAAAGCCGAACGATATGAAATTAAACGGGACTGACATCGCCAGTGTATGTAGTTTGCCCCGATTAGTAAAGTCGAAAATGACTGCGTTTCATTCATAAAACATGCGCGGGCTTTCATGCAACACAGACGCAGCACCAGCAGATCGCATCTTGTTGTTTTCATGACGTTTTAAATCATCACAGCGGCAAAGCCGATGGAGATTTGATGTCACCTTCGTCAACGGGATTTAGTTGCGTTTGGACGGAGAAAGCAAGCTCGACATGGCTTCAGTGAACAGCTTCGGTGGTCCGGAGGAACTTGAGGACACGAATCACGCTCTAAGTTTGATGAAAGAGATGAAATTATTCTACGACTCGCAGCTGTTAGTGGACGTGACCATAGAAGTGGAGCCTGACACCGAAACAGCAGAG[C/T]GAAGTGTTTCCTCTGGTGCTGGAAAAGTGTTTCAGTGTAGCAGGAATATACTGGCAGCAGCGAGCCCTTATTTTAAGAGCATGTTTACAGGAGGACTGTACGAGAGCACGCAGAGAAAGGTCACCATTCACGACGTGGACGCCGATTCGATGGCGGTCATAATTGATTACTGCTACACTGGCAAAGTGACAATCACTGAAAGCAACGTGCAGAGGCTTTATGCAGCTGCAAACATGCTGCAGCTGGAGTACATCCGGCAAGCCTGTGCTAACTTCATGACAAGAAGGCTGGACCTTTCTAACTGTGCAGGGATTTTGAAGTTTGCGGACACCTTTGACAATCTGGAGTTGAAGAGAGAAGCTCAGGCATTCATCGCAAAGAACTTTGTCCAGCTTGGTGCCAGCGTGAAAGAGCTTTGTGAGCTGGACCAGAGGCAGATTAAAGAGATCCTCATGCTGGATTCTTTGGATGTTGACTGTGAGCGTAAAGTGTGCTCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15388
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112884 | Nonsense | 74 | 617 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 9 (position 17940455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 17416525 |
GRCz11 | 9 | 17424237 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAAAGTGTTYCAGTGTAGCAGGAATATACTGGCAGCRGCGAGCCCTTA[T/G]TTTAAGAGCATGTTTACAGGAGGACTGTACGAGAGCACGCAGAGAAAGGT
Long Flanking Sequence:
ACGTCGATGTCTCAAGATCAAAAGCCGAACGATATGAAATTAAACGGGACTGACATCGCCAGTGTATGTAGTTTGCCCCGATTAGTAAAGTCGAAAATGACTGCGTTTCATTCATAAAACATGCGCGGGCTTTCATGCAACACAGACGCAGCACCAGCAGATCGCATCTTGTTGTTTTCATGACGTTTTAAATCATCACAGCGGCAAAGCCGATGGAGATTTGATGTCACCTTCGTCAACGGGATTTAGTTGCGTTTGGACGGAGAAAGCAAGCTCGACATGGCTTCAGTGAACAGCTTCGGTGGTCCGGAGGAACTTGAGGACACGAATCACGCTCTAAGTTTGATGAAAGAGATGAAATTATTCTACGACTCGCAGCTGTTAGTGGACGTGACCATAGAAGTGGAGCCTGACACCGAAACAGCAGAGCGAAGTGTTTCCTCTGGTGCTGGAAAAGTGTTTCAGTGTAGCAGGAATATACTGGCAGCAGCGAGCCCTTA[T/G]TTTAAGAGCATGTTTACAGGAGGACTGTACGAGAGCACGCAGAGAAAGGTCACCATTCACGACGTGGACGCCGATTCGATGGCGGTCATAATTGATTACTGCTACACTGGCAAAGTGACAATCACTGAAAGCAACGTGCAGAGGCTTTATGCAGCTGCAAACATGCTGCAGCTGGAGTACATCCGGCAAGCCTGTGCTAACTTCATGACAAGAAGGCTGGACCTTTCTAACTGTGCAGGGATTTTGAAGTTTGCGGACACCTTTGACAATCTGGAGTTGAAGAGAGAAGCTCAGGCATTCATCGCAAAGAACTTTGTCCAGCTTGGTGCCAGCGTGAAAGAGCTTTGTGAGCTGGACCAGAGGCAGATTAAAGAGATCCTCATGCTGGATTCTTTGGATGTTGACTGTGAGCGTAAAGTGTGCTCATTCGCAGTACAGTGGATTGAAAGTAATTTACATGAAAATTCAGAAGATGCGCTGCAGGTCCTTAAATGTGTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21458
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 |
---|---|---|---|---|---|
ENSDART00000112884 | Nonsense | 455 | 617 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 9 (position 17941598)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 17417668 |
GRCz11 | 9 | 17425380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTTAATGAACGCCTTTATGTGGTAAACAAGAGGAGGATGCTGTGCTA[C/A]GAGCCAAAGAAAAACCACTGGCTCCAGCGGGCCTCTCTGAAGCGCAGTAA
Long Flanking Sequence:
AAACAAAGAATCGGCAAGAGTGCAAAAGAAATGGTGCTATTCCTCGGACGGCCAAATCAACCCATCATGTGCTATGACCCCTATGTGGAGGACATCTATTCCATGGCATCCCCGGTCATTAACCTCACCAGTCAGAACTTCAAACGTTCCCCTATGGAGACCTTTTTGGTCTGCACCACACCAGAAAACAATCTGTATCTCGCCTCACAGCTGTCCAAGCACTTTTGGGTCTACAATCCCTTGTTGGATTGTTGGCAGGAGCTTGCAGAAAGACTTCTTGGAAGAATGCAGTCTTACATCGGCTACCTCAATGGACACCTGTATATTTTGGGTGGCAGAGATCCAGTATCGGATGCCAGGCTTAAGGAAGTAGAATGCTACAGCATTCAAAGGAATCAGTGGGTTTTTGTGGCCCCTTTGCCTCATTCTTTGGGAAAGATGCAGGTTGTGACAGTTAATGAACGCCTTTATGTGGTAAACAAGAGGAGGATGCTGTGCTA[C/A]GAGCCAAAGAAAAACCACTGGCTCCAGCGGGCCTCTCTGAAGCGCAGTAAACTCCACAATGCCTGTGTCTTCCAAGAGCAGATTATCTGTTTGTGCGATATTCCTGTCGTCAAAGCATATAACCCAGTTCGTGGAGAATGGAGGCGGATCGGAGACATTCCTATTGACAGCTGTGCTCTCAACTATCAAGTTGTGCAACACAGCAGCAAACTGCTGCTTTTAACTATAGCAGTTGTTCATCACAACAAAAACAGGCTTGTTATACATGAATATGATCCCACTCGCGACTCATGGAAAAATGTTTCCACCCTCTTAGGATCTTTCTTCGGATCCATAAGTCTCTCCACCCGGTTGTATACTGCATGTTTGGGGTCTGGTCGGAAATTTGTTTTGGAGGAGGATGACGACAGCGGCTCCAGCGCTGACTGGGACTTTGATGGACTGACTGACGCAGACTCGGACTCCGGCAGCTCAAGCTCTTTTTCGGATGAGAACTGGTA
Associated Phenotype:
Not determined