ZMP
zgc:152778
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC553349 [Source:RefSeq peptide;Acc:NP_001071004]
Human Orthologue:
ZNF185
Human Description:
zinc finger protein 185 (LIM domain) [Source:HGNC Symbol;Acc:12976]
Mouse Orthologue:
Zfp185
Mouse Description:
zinc finger protein 185 Gene [Source:MGI Symbol;Acc:MGI:108095]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30980 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42375 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30980
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106564 | Essential Splice Site | 76 | 1091 | 3 | 24 |
ENSDART00000126693 | Essential Splice Site | 76 | 609 | 4 | 13 |
ENSDART00000131084 | Essential Splice Site | 76 | 616 | 3 | 13 |
ENSDART00000143388 | Essential Splice Site | 76 | 1086 | 4 | 21 |
ENSDART00000106564 | Essential Splice Site | 76 | 1091 | 3 | 24 |
ENSDART00000126693 | Essential Splice Site | 76 | 609 | 4 | 13 |
ENSDART00000131084 | Essential Splice Site | 76 | 616 | 3 | 13 |
ENSDART00000143388 | Essential Splice Site | 76 | 1086 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 14 (position 18539712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14334165 |
GRCz11 | 14 | 14639728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCATCACCCACGACCAAATCGCCTCAGCCCAAAACTGACACAGAGAA[G/T]TATGATCTATACCCCTGTACAACATCCATATTTGTATTTATTCAATGAGC
Long Flanking Sequence:
CAGCATCAAATCCTGTCATGCAGCATGTCACACATTGCTTAACACACTCACTAACATTCATTTGTACCTTTTCGTTTGAACATTTAGAGTAGTCATCCTGACACTGAATGAATTAAAATAATAGTCTTGTGCTATTAAAAGATGTCTTTATGCATTGATAAACTGCTTTGTTTGCAGAGGGAGACAGACAGTCGGTTTTCCAAACCACTAAAGTCCGCACTGCTCTGAAAGGAGATGGCAGCTGGATACAGAGACAAGAGCCAGAAAATACTGACGTGGAGAAACCATGGTGAGGAGTTGCTGTACTATTTACAAGGACATTAATTAATCTATGTAATCAAATGGGAAAACATGGTAACGCCTTACCAATATTTGTAACGTTTTCTTCTTTGTAGGCTTGCTGAGGTGCGAGCAAACCGCTCTAGTAGTGTTTTCGAAGAAACAAGTCCTGTTTCATCACCCACGACCAAATCGCCTCAGCCCAAAACTGACACAGAGAA[G/T]TATGATCTATACCCCTGTACAACATCCATATTTGTATTTATTCAATGAGCAGGTCAGAGCTACAAATGTTTAAATGAGAAAGTGTAGTCTTCTTTGGGGTTTATTTAAGGTGTTTATGCTGGCACAGCAATGTTATCAGTTTATAGTTACAGAAGAATGGAATAAGAGAAAAAAAAGCTGCACGACTTGTCTTTTGGGATGTTGTCTGTGGAGTTGAGCTGCCAGTCGAACACTACACCCAAATTTTTGATAGATCTGGATGTGTTAACTAAATGTTTGTGTGCTCTGAACTTCATCAGAAGATGATAAGCTTTGACTCCACTAGGTTTTTAACTGAGATGACCACCAGAAAAATCAAGGGGCTCTTTTTTGACAATCCATGCGCAAAGTGAAAAGCGCAGGGCGCAAACGCATTCAGGGCGTGTCAGAATCCACTTTTGCTAATATAAGGACGGAAAAATCCGCTTTGCGCCGTGGCGCATGGTCTAAAAGTGTTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42375
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106564 | Essential Splice Site | 76 | 1091 | 3 | 24 |
ENSDART00000126693 | Essential Splice Site | 76 | 609 | 4 | 13 |
ENSDART00000131084 | Essential Splice Site | 76 | 616 | 3 | 13 |
ENSDART00000143388 | Essential Splice Site | 76 | 1086 | 4 | 21 |
ENSDART00000106564 | Essential Splice Site | 76 | 1091 | 3 | 24 |
ENSDART00000126693 | Essential Splice Site | 76 | 609 | 4 | 13 |
ENSDART00000131084 | Essential Splice Site | 76 | 616 | 3 | 13 |
ENSDART00000143388 | Essential Splice Site | 76 | 1086 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 14 (position 18539712)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14334165 |
GRCz11 | 14 | 14639728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCATCACCCACGACCAAATCGCCTCAGCCCAAAACTGACACAGAGAA[G/T]TATGATCTATACCCCTGTACAACATCCATATTTGTATTTATTCAATGAGC
Long Flanking Sequence:
CAGCATCAAATCCTGTCATGCAGCATGTCACACATTGCTTAACACACTCACTAACATTCATTTGTACCTTTTCGTTTGAACATTTAGAGTAGTCATCCTGACACTGAATGAATTAAAATAATAGTCTTGTGCTATTAAAAGATGTCTTTATGCATTGATAAACTGCTTTGTTTGCAGAGGGAGACAGACAGTCGGTTTTCCAAACCACTAAAGTCCGCACTGCTCTGAAAGGAGATGGCAGCTGGATACAGAGACAAGAGCCAGAAAATACTGACGTGGAGAAACCATGGTGAGGAGTTGCTGTACTATTTACAAGGACATTAATTAATCTATGTAATCAAATGGGAAAACATGGTAACGCCTTACCAATATTTGTAACGTTTTCTTCTTTGTAGGCTTGCTGAGGTGCGAGCAAACCGCTCTAGTAGTGTTTTCGAAGAAACAAGTCCTGTTTCATCACCCACGACCAAATCGCCTCAGCCCAAAACTGACACAGAGAA[G/T]TATGATCTATACCCCTGTACAACATCCATATTTGTATTTATTCAATGAGCAGGTCAGAGCTACAAATGTTTAAATGAGAAAGTGTAGTCTTCTTTGGGGTTTATTTAAGGTGTTTATGCTGGCACAGCAATGTTATCAGTTTATAGTTACAGAAGAATGGAATAAGAGAAAAAAAAGCTGCACGACTTGTCTTTTGGGATGTTGTCTGTGGAGTTGAGCTGCCAGTCGAACACTACACCCAAATTTTTGATAGATCTGGATGTGTTAACTAAATGTTTGTGTGCTCTGAACTTCATCAGAAGATGATAAGCTTTGACTCCACTAGGTTTTTAACTGAGATGACCACCAGAAAAATCAAGGGGCTCTTTTTTGACAATCCATGCGCAAAGTGAAAAGCGCAGGGCGCAAACGCATTCAGGGCGTGTCAGAATCCACTTTTGCTAATATAAGGACGGAAAAATCCGCTTTGCGCCGTGGCGCATGGTCTAAAAGTGTTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7232
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000106564 | Nonsense | 616 | 1091 | 12 | 24 |
ENSDART00000126693 | None | None | 609 | None | 13 |
ENSDART00000131084 | None | None | 616 | None | 13 |
ENSDART00000143388 | Nonsense | 652 | 1086 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 14 (position 18535168)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 14329621 |
GRCz11 | 14 | 14635184 |
KASP Assay ID:
554-4715.1 (used for ordering genotyping assays)
KASP Sequence:
CTACGGCACAAGCTAAAACAGCAGCAGAGTCTAAACTAATGGAAGAAATT[A/T]AAGCTTCAATAAAAACAACAWCAGCAAGTGATGCTAAATCCACATCAGAA
Long Flanking Sequence:
CGGTAACTGAAACTAAATCCACATCTCAGCCTAAACCACTTGCTGAAACTAAACCTACTATACAGATTACAGCAGCATCAGAACCTAAATCAGCAACTGAAACCAAACCTACAACACAAACTACAACAGCAACTGAACCTAAACTTACATCAGAAACTAAGACAGTTGTTGAAACTAAACCCACCACACAAGTAACAAAAACAACTGAAATTAAACCTATAATGAAAACTCGAGAAGCAAGTGATTCCAAACCAACACTGATACCTACAGTGGTTGTAACAAAGCCTACAGAGACAACTGAAGTTAAACCTACAACACAAACTAAAACAGCAACTGACTCCAAACTTGTGGAGGAAACTAAAACTACAATAGTTACAGCAAGTGACCCTAAACCAACATCAGAACCTAAAGCAGTTGAAACCAAACCTGCAACAACAGCTGAACCTAAACCTACGGCACAAGCTAAAACAGCAGCAGAGTCTAAACTAATGGAAGAAATT[A/T]AAGCTTCAATAAAAACAACAACAGCAAGTGATGCTAAATCCACATCAGAACCTAAACCAGTTGAAATCAAACCAACAACAACAGCTGACCCTAAATCCTCCACTGAAACTAAACCTACGGCACAAACTAAAACAGCAACTGAGTCTAAACTACTTGAAGAAATTAAAACTACAATAAAATTGAGCACAGAAAGTGATTCGAAACCCACATCAGAACCTAAGCCAGTTGAAACCAAGCCTTCAACAACAACTGAATCAAAATCCACAACTGAACCTAAACCTACAGCACAAGCTAAAACCGCAACTGAGTCTAAACTATTGGAAGAAATTAAAACTACGATAAAAATGAGCACAGAAAGTGATCCTAAACCCACACCAGAGCCTAAAACAGTTGAAACTAAGCCTACAACAACAGCTGAACCTAAATCTGCAACTGAAACTAAGCCTACAACACAAACTAAAACAGCAACTGACTCTAAATTAGTGGAAGAAATTAAAACT
Associated Phenotype:
Not determined