ZMP
dok7
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens DOK7, docking protein 7 (DOK7) [Source:UniProtKB/TrEMBL;Acc:B7ZDE
Human Orthologue:
DOK7
Human Description:
docking protein 7 [Source:HGNC Symbol;Acc:26594]
Mouse Orthologue:
Dok7
Mouse Description:
docking protein 7 Gene [Source:MGI Symbol;Acc:MGI:3584043]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45078 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45077 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45078
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084665 | Nonsense | 19 | 663 | 2 | 11 |
ENSDART00000135369 | Nonsense | 19 | 394 | 2 | 7 |
ENSDART00000137166 | None | None | 95 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 41572857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 40489098 |
GRCz11 | 1 | 41191885 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCCATGTTCGAACTCTGCCTTTGTTTTGTTTCCTTACGTTAACAGTG[G/A]AAAAACAGATGGGTGATTCTTCGGAAACCTTCGCCGGTAGCAGGTAAATC
Long Flanking Sequence:
ATATTTTTTTCTCTGTACATTTTTGTGATGTACCATCCCCTCAAACCAGATCTGACTGTCTGAGACTTGCCAGAATGGCCAGGTCATGTGTTGTAAATTAATTAGGAGCATATAACTTGTCACCTTGAATGGACAACTGTAAAAACCGTTCTGGTGTGTGTTCAGAGAGGGTGGCCCTGTGCATGTGTGAGTATTGTGGGGGAGAGAGAGTTTGCGTGTGTGTTACAGCAGAGCAGACAGTGAATTCTGGAGGTTATTTTGAAAGTGACCCCCTCACTCACTCACTGCCGCGGACCGCACACAGCTGTCGGGAAACATGACACAAGATGACGGATACGGTTGTCGTAGAGGGACAAGTCAAACTCCGAGAAGGCAAAAAGGTGGTTAAAAGCAACGCAAACTACTTTTACTGCATCATTCATTGCTGTGCCAAAAGTTAAGTGGTTATTTGTTTCCATGTTCGAACTCTGCCTTTGTTTTGTTTCCTTACGTTAACAGTG[G/A]AAAAACAGATGGGTGATTCTTCGGAAACCTTCGCCGGTAGCAGGTAAATCCTATAAATTCTGCTTGGGAAAAGTTTCTACGCTGTTCTTTTAAGTGTTGGGGTGAATAAAGTGTTTCAAAATAGCCGTTTTGTTTGATAAACGTACTTACCATGTTTGAAGTCCTGTCATGTAGCGCTGTCACGTTTTTTTTACCTCATGATGGCATGTAGGATATTGGCATGTTCGTTATGTGGAATATTGGAATGACACAGTTAATACACGTGTCAAGATGTCGCAATTCACTTGGACTCGAGCTGTTTTAGCACCAGAATTGAAATGTAGCTAAGTTTTAAATGTTAAGTGTTAAAGAAAATGAAGCTAGTTGTCTTTAGCTAGTTGTTACATGAGCTGTATATGATTTTTTTTTGTCTTGGTCTGAAACTACAATATAAGAATGCTTAAATCTAGAAAGCTTTTTTTTTTTTGGGTTCTGTCCCACAAACTAAACTTAAACAAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45077
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084665 | Nonsense | 527 | 663 | 7 | 11 |
ENSDART00000135369 | None | None | 394 | None | 7 |
ENSDART00000137166 | None | None | 95 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 41536675)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 40452916 |
GRCz11 | 1 | 41155703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCCACCACAACACGCTTACAACCCATCATCTGTCCTGACTGTGGCGGA[C/T]GAAAGGTCATTTCAAAATTGTTTTTATGTTGATTTATCGATATATTTATT
Long Flanking Sequence:
GACGGCAGAGCTCCACAGACAGCGGCATCGCCACCGGAAGCCACTCCTCATATTCGGGAAGCTTCTCCTCTTACACTGGGAGCATGGATATTGGCCATGGAGAGACTGACGAGTTTGGATCCTTAATAAGCCTTCCTCAAAACCCCAATTCAGTCTCTATTATAAACACTCCAGTAAGGACAGTTCCCCAGATTCCTGAGGACAACCCATGTGTGTGTTCTCTCCGAGAGGCTGATCAAACACAGGCCAACGTATACACAAGTTCACCTCTGCAGCATTACGATGTCCCTCGCAGGTTCCTACAACACAATCAGGAGCAGTGTTCCACTGGTGTGGTTCAGGACAGAGGGTCTGAATGTGGAGCGGAGAGTGTCCCTGCTGACAACGTCATAAGACAGACTGTCCTGAGGAGATTGAACTCTTGTGGAGTAGACGCAGTGCCACCTGAAGGTCCCACCACAACACGCTTACAACCCATCATCTGTCCTGACTGTGGCGGA[C/T]GAAAGGTCATTTCAAAATTGTTTTTATGTTGATTTATCGATATATTTATTTTTAGGGATGCACCAAAATAAAAATAAAAAATAGGCAGAAACCAGAAATTCTGAATGAACTTGAGCGAAAACTGAAACCAATATGCCTTGTAATCATTAATTAATTTTCTTTTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGTGGAATAAACCGCCAACTTATCCAGCACCGCGGATGCCCTTCCAGCTACAACCCATCTCTGGGAAATATCCACACACACTCATCCACGACGGACAATTTAGCCTACCTAATTCACCTGTACCATGTCTTTGGACTGTGGGGGAAAACCGGAGCACCCAGAGGAAACCCACGCGAATGCAGGGAGAACATGCAAACTCCACAGAGAAACGCTAACTGACCCAGCCGAGGCTCGAACCATCGACCCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCTCTGCGTCGCCCCT
Associated Phenotype:
Not determined