ZMP
zgc:175171
Ensembl ID:
ZFIN IDs:
Description:
Zgc:175171 protein [Source:UniProtKB/TrEMBL;Acc:A9JRY5]
Human Orthologue:
ZNF740
Human Description:
zinc finger protein 740 [Source:HGNC Symbol;Acc:27465]
Mouse Orthologue:
Zfp740
Mouse Description:
zinc finger protein 740 Gene [Source:MGI Symbol;Acc:MGI:1915994]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41756 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11563 | Essential Splice Site | Available for shipment | Available now |
sa18580 | Essential Splice Site | Available for shipment | Available now |
sa27709 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41756
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 |
---|---|---|---|---|---|
ENSDART00000104570 | None | None | 273 | None | 11 |
ENSDART00000109026 | Nonsense | 203 | 268 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 2255229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2253639 |
GRCz11 | 11 | 2277061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATAAATCTTAAGTATATTCTGCTCTGGTCATTCAGGGGTGAAGCCGTA[T/A]GCTTGCTCCATGTGTGACAGGCGTTTTTTCCAACGTTACCACCTCCAGAG
Long Flanking Sequence:
AACCTGATGTGGAATATATAATTAAACAAAGTCATCAATAGATTGTTTTGGTGCACAAAAGTGTTCTTGAAGCTTCATATGAACCTCTGAAGTTACATAGATTGTTTTGACAATATCTTGGTTTCTTTTCTGGACTTTGAGTGTCTCTTGTTGCCTATGGAGGATGAGGGAGCTCTCTGATTTCATTTGAAATGTCTTGAGGAGATTGGAACTAAATAAGCGTAATTAATACCAAAATTGTAATTTTGGGTGCACTCTAACTAAGAATGAGCATTAATATAATGGGTTTGCATTATTAGCAGGAAGATTGTAAGCTGGCACCACATTAAGCTGCGCATTCATCTTTTTGTGCTTTTTATGTGCTTGCAAGCATCTTTTGCTCTCTGTTCTTGTGACGCATGCAGTTTCAGCAACATTCAGCCTTTATGTTGACGTAAATGTGTTGCATATATATAAATCTTAAGTATATTCTGCTCTGGTCATTCAGGGGTGAAGCCGTA[T/A]GCTTGCTCCATGTGTGACAGGCGTTTTTTCCAACGTTACCACCTCCAGAGACACAGCCTCACTCATACGGGTACGAGCCGTCTCTTTTTACTCTTTGTATTCACCTGACTACACCAATGCACAGCTTGGCACTGTTGCCATCTTATTTGTGTTTGTCAGTATTCTCAGACAAGCCTTTGGGCCTGTTGCCTTTGCAATGAAGACAGTTGTATTTTTTTGGACTCGGTACTCAGTATTTCTAAAAAGTTTTCATAGCCAAAATTTTCATAGCCAAAATGCATATATGATTTTATTAATCAAGTTCTGGCTTCAACAAACTCGAGTTTGGTAATAGTTACAGACCATGCATTGGGGTGTTGGACATACTGAAATCCAAACTTAACACTACGATGCTCTGTGTTTAGGGGTGAAGCCGTATGCTTGTTCCATATGCGACATGAGGTTTTTTCAGCGTTACCATCTGCAGAGACACAGCCTCACCCACACGGGTATGAGATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11563
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104570 | None | None | 273 | None | 11 |
ENSDART00000109026 | Essential Splice Site | 255 | 268 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 2254564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2252974 |
GRCz11 | 11 | 2276396 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCATTGTCCTCAATTTAATTGCTCCCTTAAATTATTACTTTGTTTATTT[A/C]GAGATWAAGCCATTTGCTTGCACAATATGCCACWTTGACTNTTTTCCCCCC
Long Flanking Sequence:
TCAGACAAGCCTTTGGGCCTGTTGCCTTTGCAATGAAGACAGTTGTATTTTTTTGGACTCGGTACTCAGTATTTCTAAAAAGTTTTCATAGCCAAAATTTTCATAGCCAAAATGCATATATGATTTTATTAATCAAGTTCTGGCTTCAACAAACTCGAGTTTGGTAATAGTTACAGACCATGCATTGGGGTGTTGGACATACTGAAATCCAAACTTAACACTACGATGCTCTGTGTTTAGGGGTGAAGCCGTATGCTTGTTCCATATGCGACATGAGGTTTTTTCAGCGTTACCATCTGCAGAGACACAGCCTCACCCACACGGGTATGAGATGAGGGATCAATGCACTTTAAACATGTATTAAACACTTTAGTTCTCAGCCTTCACTGCAGGCACAGTCTTCATGGTTCTCCATGGCCATTTTGGCTATTTAATGCCATGGATTAAACATTCATTGTCCTCAATTTAATTGCTCCCTTAAATTATTACTTTGTTTATTT[A/C]GAGATTAAGCCATTTGCTTGCACAATATGCCACATTGACTTTTTCCCCCCATCCGCCCCATCATTTCATAATTTCCCCAAATTCTGGCCCATTCTCAGGGAACTATGCTATATTTTCAACAAAGCATTCATTACTTTTTTTCTAATTGAATCCTTTTTTTGCATTGAGAGACCATTTTGGGGTGCAGATCTCCACAGTGTTCATGTTAGTGGTCAGCCAGTGTATTTTCCTCATGCCTGACCCACATGGGTTGTCAGCGTCAATGCTTCCTATTCACTTTGAATGGGTGACTTTGATCATTGTCAAGCTGAATTGTGGATCCGTCGGTGCCGCGTCAGTGGCGTTGCTCACTGCAGAAGTTGGGAATTTTAAAACTTTTCAAGTGCCATGCATCAGCCAATCAGATTGCTTAATGCAAATATAGTTTAAAAGTGGTAAACAGGATGAATTTAAAATGGGAGAAAACTATTATTGCGGTGGGCAATCACCCTGTCCTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18580
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104570 | Essential Splice Site | 227 | 273 | 8 | 11 |
ENSDART00000109026 | None | None | 268 | None | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 2241629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2240039 |
GRCz11 | 11 | 2263461 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WGGTTTTTCCAACGTTACCACTTGGAAAGACACAGCCTCACTCACACTGG[T/C]ATGTGTCCTTTCACTGCACTCTGATTCTTGGATTGGGGCTGGAGTTTRTA
Long Flanking Sequence:
CAAAGCTGCTTGATGTGTAACTACTAGTGAACTTGGGTTTTAATAATCAATTATTAAAATGAATCTATATTAAACCAGGAGTATCAAATTAAGCTATGCACATGCAGTGGTTAAAATGACACACATGACAACACATGCGTACCAAGCCAAAAGACCCATGCCGAATAAGTGTACCATTACACCCCTACTAAACTAAAGAAAACATTTGCTTTAACCCTAAAAAACGAAAAAATATCATATCAGTATTCATATTTTAAACCGCTCTCACAATATTTGCTTTTGTAATACGGCAAGTGTAAACCATAATGAGTAAAAAATGCAGAATTGAATATACTTATTGTTAAAGCATTTAAAAAATGTTTGCTGCTTTGGATGTTTTGCAAAGACATTCACTAAAAATTGACTCTACATTTAGGGGTGAAGCCGTATGCTTGTTCCATGTGCGACATGAGGTTTTTCCAACGTTACCACTTGGAAAGACACAGCCTCACTCACACTGG[T/C]ATGTGTCCTTTCACTGCACTCTGATTCTTGGATTGGGGCTGGAGTTTGTATATATTTTGTGGATCGGAAACAAACACAATGATGTAGCTTTTTAACAACTATTTTTTGCATTAGTTATTTCCCTTTTGTTTGATAACATCAAGTTTTGCATTATCTAGGTCTCATTTCTCTGTGGAGGTGTTTGATTTCTGTGCATATTGCATTTGTTTGCTGTCATTTATGTGTTGCATACTGATATAGCAGTGTCTTTTTAAGCATTTATACTTTAAAGTAAGTACGCACAACCTCAGTCTCAAACCAGGTTAGCTGAAACCAAAACCTCAGTGTGCCATTTTAAAGCCCATTCACACCAAGGATGATAGCTGTAATGATAAAGATGTAGTGGAGAGTTTACACCAGTGGTTCACAACCTTTTTCCTGCAAACTCCTATTTCAACATTCAGTTTTCCTAATGACCCCTTTCAAAAAAAAAGATGAAGATTTAAAGGGCCATGACACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27709
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 |
---|---|---|---|---|---|
ENSDART00000104570 | Nonsense | 266 | 273 | 9 | 11 |
ENSDART00000109026 | None | None | 268 | None | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 2236284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 2234694 |
GRCz11 | 11 | 2258116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGCGCGTTCACAGCGGAGAAAAGCCTTACCAGTGTGAGCGCTGCCAA[C/T]AGGTGAGAGCATGCTGGGTTTTCAGGATTATTAGGCTTTTTTCCACACAA
Long Flanking Sequence:
TATCTATTATGGTAATATCACAGAGAGGAATAATATCATTTGAATTAATTCTGAACGTTTAGCTAATCAGAATTAATCCTGCTTTAACGAGCTTAAGTGTTAAAGGGACAGAAGGCAGAACTACTGAACGTTATATTGCATTGATGTGGATGTTAATATACAGTAGTTATTCTTACAGTTTTCATTCTTGGTGAGAACAGGTCTTCACTAATAAGCAGTTTTTCACTCGAATTTGAATATACTCTACAAACTCGAGTTTGTATGAAGTCATACTTATTGCTAAGCTTGAATATACTCTGTATTTAAGGTTTTTATTGTGTGTTGTGGCATGCTGTGGGACTGACGGTGTACTTTGCTTTAATAACCAGTGTGTTCCTCTGACAGGAGAGAAGCCGTTTGCGTGTGACATGTGTGACATGCGCTTCATTCAGAGGTATCATCTGGAGCGACACAAGCGCGTTCACAGCGGAGAAAAGCCTTACCAGTGTGAGCGCTGCCAA[C/T]AGGTGAGAGCATGCTGGGTTTTCAGGATTATTAGGCTTTTTTCCACACAAACATGAAAAAAATCTCCAGACTGATATTTTTCTGATCTCATAACTCTGTGGTTGGTAGTTTTGGCAAATATATACAGATGTTTCAATATAATGTGAACAGACTTTCTCTGTGCATTTGATTCGAGTTTTTAACTGCAGATGTCTCCTCTCTAATGATGGAGTTGCTCAGTGTCAGGTGACTGAAACCGAAACTTTCTGAAAACTCCAGTCATGGTAAAGGTTTTCTGAAACTTCGGTTGCAGTGTGATCGTGTGTCCACTTTTTACTTCTTTCTGATTGGCCAACGTGGCTGGGTTCACACCAATCATGGAAGACGCAATTTCAGAAAACTTTCGCACACTTTGTCATTTTCACCGCAGGATAGTAATCTACCTTTGATCTCACGTTTGCATTGACTTGTAGGCAATTTACTTGCGCAAATGCTACGCCGTTTGGTATGAACTCAGCACA
Associated Phenotype:
Not determined