ZMP
si:dkey-71b5.10
Ensembl ID:
ZFIN ID:
Human Orthologue:
ZNF687
Human Description:
zinc finger protein 687 [Source:HGNC Symbol;Acc:29277]
Mouse Orthologue:
Zfp687
Mouse Description:
zinc finger protein 687 Gene [Source:MGI Symbol;Acc:MGI:1925516]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36109 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7422 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36109
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112368 | Nonsense | 175 | 1246 | 1 | 10 |
| ENSDART00000135689 | None | None | 630 | None | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 24112197)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22117047 |
| GRCz11 | 16 | 21921299 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACATAATGACGCTTTTACTAATCACCCTGCCAGCACTTTTCAGTCTT[T/A]ACCTCTGAGTGATCACCCCAGCGTATCTTCACGTTTAATTAGTCCAAACT
Long Flanking Sequence:
TTTCGATGATCTGCTTGCAGCATTTGATATTCCAGACATTGATGCCAAAGAAGCAATTCAGTCTGACACTCATGGCAATCATAATGAACACAGTAGTGTAGTTGAAAAGGAGAGAAGTGGAAGTCCTTCCCTAAGACCTTCAGGAAGTCCTGATCCTCCTCACAATGACCCTTCCGTGGTCAGCGTGATTGTAAAAAACAGTGTACATTCAGATGACAAAGCCGAAGGGAATGAAACTGGGGAGTTTTCTAGTGCAGATGAATCACAAAAGTCTCCCCAGAAAGGTCCCAGTAAAGATAGCTCAGTGCCTACGGATCAATTTATCTATAATGGACTCAAAAGCGTCTCAGGTGGGTCTACAGAATCCTCTCCATCACTAGATCTAGCACCGGGGCAGCCTAATGGCCCCCTTTGGGCTCTTTCTGCTTCTAAAGCTACTGGTGATGATGACAAACATAATGACGCTTTTACTAATCACCCTGCCAGCACTTTTCAGTCTT[T/A]ACCTCTGAGTGATCACCCCAGCGTATCTTCACGTTTAATTAGTCCAAACTTTTCTTCCAAAGTTGATTCTGAGGAAGCACAAGCAATAAATGGCACTTTAAGAGCAGGAGTTCGTCGGCACCTGTCTGAAGATGAAGAATCTGAACCAGACCTGGGCAGTCCTGCTCTTGTCATACAAGAGAGCCCCAATTCCCAGCTGTGCCCTGCTCCCAAGGTCCCACGCATGCAGCGGTCCCCTTCAAGTGTGTTTCAACCGCTTTCTCCCTCATCACCTTCCTTACCTGTGAGTAACACCCAAATGGAGGAACCCTCTGTCCAGCATCCAAAACTACACAGCAGCACCAACCCAACATCTCTGACCTCCACAAATAATCTACCAGTTGAAGAAAAAGATCTGGAGCATATAATTGAGGAGAGAGATTCTCCTGAGAGCCCTGAGCCAGAAATCTCTCAATCTCGTACATCTCTTCCCTCAAATTCACAAGGAGCCATTGAGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7422
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 > T
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112368 | Missense | 730 | 1246 | 4 | 10 |
| ENSDART00000135689 | Missense | 216 | 630 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 24119417)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 22124070 |
| GRCz11 | 16 | 21928322 |
KASP Assay ID:
554-4233.1 (used for ordering genotyping assays)
KASP Sequence:
GATTTTCCAAATGTNNNNNNNNNNTTTTTTTCTGTAGTGCTGTCTGCAGT[G/T]TTCTCCACCAATGCCACTCTGGAACTCGTGCTGTGCTGCAGCTCACCGTC
Long Flanking Sequence:
AATTTTCACAGTATGTTTGAATATTTTTTTCTTCTAGAGAAAGTCTTATTTGTTTTATTTCAGCTAGAATAAAAGCAGTTTTTAATTAAAAAAACATTTTAAGATCAATATTATTAGCCCCCTTTAGCAATAAATAATATTTGATTGTCTACAGAAGAGACCAGTGTTCTACAATAATTTACCTAATTACCCTAACTTGTACAATTAACCAAGTTGAGCCTTTAAATTGCACTTTACTAGTATCTTAAAAACATCTGGTAAAATATTATTTACTGTCTTCATGGCAAATATAAAATAAATCAGATATTAGTAATGAGTTATTAAAACTATTATGTTTAGAAATCTGCTGAAAAAAAAATAATTCAGTCAAAAAGAAATTGGGGGGAAAATATACGGGGGGTGGGTTTAATAAGGAGGGCTAATAATTATGACTTCAATTGAATATATATTGATTTTCCAAATGTGTTGTTGTTGTTTTTTTCTGTAGTGCTGTCTGCAGT[G/T]TTCTCCACCAATGCCACTCTGGAACTCGTGCTGTGCTGCAGCTCACCGTCGGATGCACCAGCAGCTCCCTCCTCTCGTGTGCCCTGAATGTGGACTCATCTGTCAGACTCATGAGCTCAACACTCACCTCAAACAAACCTGCCTGCACTACTCACGCCGCCTTGGATACAAGTATGCGCTCAATCATGCTCACAATACTGCCAAAACCCTCAGTTTCAGCTGTGGTTTTTGGTAAAAGTGCAATCTCCTCTGTTCTTTGCAGATGTGCCTGTTGTCATTTGGTGTTTGGAGGAGTGAATAGTCAGAATGCGGTAAAGACGCACATGCAGACGGCTCACTGTGAGATCTTTCATAAATGTCCCTCCTGCCCAATGGCTTTCAAATCTTCTTCTGGTGCTGAAAGCCACTGCGCATCCCAGCATCCTGAGCTGTCTGAAACTGCGAGACAGTCCAAGTAAGTGCAAGAATATTATAATAGTGATTAAATAAGTGTAAAATAA
Associated Phenotype:
Not determined