ZMP
zgc:101121
Ensembl ID:
ZFIN ID:
Description:
AN1-type zinc finger protein 6 [Source:RefSeq peptide;Acc:NP_991323]
Human Orthologues:
ZFAND5, ZFAND6
Human Descriptions:
zinc finger, AN1-type domain 5 [Source:HGNC Symbol;Acc:13008]
zinc finger, AN1-type domain 6 [Source:HGNC Symbol;Acc:30164]
zinc finger, AN1-type domain 6 [Source:HGNC Symbol;Acc:30164]
Mouse Orthologues:
Zfand5, Zfand6
Mouse Descriptions:
zinc finger, AN1-type domain 5 Gene [Source:MGI Symbol;Acc:MGI:1278334]
zinc finger, AN1-type domain 6 Gene [Source:MGI Symbol;Acc:MGI:1929510]
zinc finger, AN1-type domain 6 Gene [Source:MGI Symbol;Acc:MGI:1929510]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa26892 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14322 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26892
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062263 | Essential Splice Site | None | 232 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 11466185)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 10320191 |
| GRCz11 | 7 | 10562298 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTATTAACCCCATTTGAAATCGATATATCCATCTTCGGGAGTCAGGAG[G/A]TGAGTTTATAACGTTTGCCGCCGCCGCCGCTATGAACTGAGTCAGTGAAA
Long Flanking Sequence:
TCATATGCACATATATTTTACATCTAAATATAAATAAAAATTTTATCAAATATATGCATGCCTGTGTGTATTTAAATACAGTAAGCCAATGCAAATATACAAAGTAAATATAAATAGATAAATATAAATATACAAAGTGCACACATTTAAATTGTCAAAATAATCTTTTATTTTAATAAACAGCCCAGCACTAAAAATTAAAACATCTTTTGAGTTCACGTTAAAACGTCAACATAGGATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAACGTCAACATAGGAAAACTTTAAAGTCCCTTCCTCGTGACGTCACCGGGTAGGTTAAAGTGGGGGCTGGAGTGTCAAAACTAACAAACAGGCAGTTTTCTCGGTGGGGGAAGGGACGCTGGTCAACGTCGAAAACACTTAGCAAACACTTTAATAGTGCTGGACTACAAAAGCAAACTCTATTAACCCCATTTGAAATCGATATATCCATCTTCGGGAGTCAGGAG[G/A]TGAGTTTATAACGTTTGCCGCCGCCGCCGCTATGAACTGAGTCAGTGAAACAGCTGCGGCGTTTTGAGACCTGTTAGCTAATTTGACAAGAGCTAACGTTAAACCTGCTGTTGTAAACTGTACTTAATAATTATGAATTCATTTGGTAAATATCATCCATTAGCGTTAACAACGTACCGTGTAGCTTTGTAACTAGCAAGCTAATAGCAAAGTTATCAAAAGGAAACATTAGTGGATTTGAAACTCGTACGCCGTCAGTTTGCTTAAATGTATCAATCCGCATAGGATTGTAAGGTATGTTCAAAAACAGCCGAGGAACTATACATGCCAGCTGTTTAACTTCTGATGATGTCTTTAGGGAAGCATATGTGATTAACTTCTGATATATGATGAATCTGCTTCTAATAATCCTCAAAGTTGTACGTTACACGCCATTGATCAAGGCTTTGGTGATTACTTCGTCTTACAATTTAAGTCCTTTTTTAAATAAAGAAAATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14322
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 |
|---|---|---|---|---|---|
| ENSDART00000062263 | Nonsense | 67 | 232 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 11453153)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 10333223 |
| GRCz11 | 7 | 10575330 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCCAGCTTAAGCAGTAAAGGAGAATCTCTGACTGTACAATCGAYGTCA[C/T]AGCATGAACAAAACAGGTACAACGTCTTCCTCTTTAATACCCACCCCTAC
Long Flanking Sequence:
CTCATTTATGCTTGCTTGTTTACAGTTGGTTACTAGGTTACCAATACTACATTCAGCCTCTCTAAAACTTGATAGAAATGCACATGATTCACATTTGGGATTTTTTTTTTTCCTTTCCTTTCTACAATGTTATGTTGCATGATAGATTGGAAACCCTCACCCGGCTAGTGACTCATGTGCTTGGTTCCTTTATTTTGTTATGTTGTGCCACGTTGCACTGCCTACAATGAAATATAATTATTCGAAACCCAGCTTATCCACATCAAAGTGTTTTTGCTGAGCTGTAATTTCATTATCTACAGCGTTTATTCCAAAATGGGCCACCGTTGGAAACATCTCCTAAAACAAACCATCACTTCTCTTATACTGTTATCAGGATCTTAAGAATAAGGAGAACTTAAAATGGGTGTTGACATTTTGGGTTTCCTGCTTTCTCATTGCTTACAGTGTCTTCCAGCTTAAGCAGTAAAGGAGAATCTCTGACTGTACAATCGACGTCA[C/T]AGCATGAACAAAACAGGTACAACGTCTTCCTCTTTAATACCCACCCCTACATCATTTCTCATAACGGTTGCATAAGCCATTTCAATTGATGAGATGTGGTTTATTTGTGCAACTTCAATAGTGCATGACAACTTGTTTTCTTTGTTATGACACCTTCTGTGTGACACAAACCTGTTTTGGGAATTGGTAGGTATATTGTAGAAATACAACAGATTCTGCTGTAGCATTTATATAATCATATATTTAAATGGTAATCAGTGTACATTTGGTAGAGTTTTTAATTCGTCTCAAACAAAAAAATGAGAAAAAATGAGTTTTTACACGAAAATGTGATTGTAAATGGCCTTAAAGGCACAATATTGCCACTAGAGGGCGTGTGTTCACAACAAAGAAAGCCACATTTTGATGACTGAGTGACCAAGTGTGGAATCATGGGAGTTGTGCCAATCATTACATCCTTCGGCAGTGGTCCCCAACCCCTGGGGATCAATTGGTACTGG
Associated Phenotype:
Not determined