ZMP
zgc:66441
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 710 [Source:RefSeq peptide;Acc:NP_956086]
Human Orthologue:
ZNF710
Human Description:
zinc finger protein 710 [Source:HGNC Symbol;Acc:25352]
Mouse Orthologue:
Zfp710
Mouse Description:
zinc finger protein 710 Gene [Source:MGI Symbol;Acc:MGI:1921747]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43117 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43118 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43119 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16083 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43117
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015712 | Nonsense | 259 | 700 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 25875304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26104987 |
GRCz11 | 18 | 26089507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTGAAAACCACAGACGAGGATGTGAACCCAGCTATAAGGCGGTACTA[T/G]GAATCCAGCATGACAGCATATGAAGCTGCTGAGATTGGTCTGCCGGGAGA
Long Flanking Sequence:
CCTCATGGGGAGAACCGGAAACCTGAAGGGGTCTATGGGGAAGAGCGCAGACGACCGGGTCCCCGAGGGAGGACCAAGAGGCCCTTGACTGAAGGAGAACCAGAGGAGTCTTCAGAGAGGTCTCTGGAGGCACAGAGTCACGTGAAAGGGGAGAGGCCTGACTTCTCTATCCCCTGTTATCTCTCAAATCCCCAGCAAACTGACAACGAGCCAGAAGTGTTGGATCTTGCACCTCAGAGACAGCCAAAGAAAGAAGAGCAGTGCAACAAAGGGTACCCTGAACCCTCAAGAGAGCCATGCAGCCAACAGGTTGACTCTGACACTAAAGTATCTCAAACCCATCAAATTCAAGTGGGGCATGGAAAGGTGCTGGTGGAATCATCTGAGGAACTGCGGGGAAAAGAGGAGGAACGAGAAGAAGAGGATGAGGAAGTGGAGGAGAGAGCACTGAACCTGAAAACCACAGACGAGGATGTGAACCCAGCTATAAGGCGGTACTA[T/G]GAATCCAGCATGACAGCATATGAAGCTGCTGAGATTGGTCTGCCGGGAGATTATGAAGAGGGTGGCCAGCCCATGGTTTGGGCTGAGAGTGAAAACTCCCTCGGTAGACGGATGCAGATCGACCGGCTAGATATCAACGTGCAAATTGACGAATCGTACTGTGTGGATGTGGGTGAAGGTTTGAAGAGATGGAAGTGTCGCATGTGTGAGAAGTCCTACACTTCAAAGTACAACTTGGTTACGCACATTCTAGGTCACAATGGCATTAAACCACATGAGTGTATGCACTGTGGGAAACTCTTCAAGCAGCCCAGCCACCTTCAGACACATTTGCTTACTCACCAGGGCACACGGCCACACAAGTGCACTGTCTGCAAGAAGGCCTTTACCCAGACTAGTCACCTTAAACGCCATATGTTGCAGCATAGCGACATCAAGCCTTACAGTTGCCGTTTCTGTGGCCGAGGCTTTGCCTATCCTAGTGAGCTGCGCACCCACGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43118
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 |
---|---|---|---|---|---|
ENSDART00000015712 | Nonsense | 277 | 700 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 25875358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26105041 |
GRCz11 | 18 | 26089561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAGCATGACAGCATATGAAGCTGCTGAGATTGGTCTGCCGGGAGATTA[T/A]GAAGAGGGTGGCCAGCCCATGGTTTGGGCTGAGAGTGAAAACTCCCTCGG
Long Flanking Sequence:
CCGGGTCCCCGAGGGAGGACCAAGAGGCCCTTGACTGAAGGAGAACCAGAGGAGTCTTCAGAGAGGTCTCTGGAGGCACAGAGTCACGTGAAAGGGGAGAGGCCTGACTTCTCTATCCCCTGTTATCTCTCAAATCCCCAGCAAACTGACAACGAGCCAGAAGTGTTGGATCTTGCACCTCAGAGACAGCCAAAGAAAGAAGAGCAGTGCAACAAAGGGTACCCTGAACCCTCAAGAGAGCCATGCAGCCAACAGGTTGACTCTGACACTAAAGTATCTCAAACCCATCAAATTCAAGTGGGGCATGGAAAGGTGCTGGTGGAATCATCTGAGGAACTGCGGGGAAAAGAGGAGGAACGAGAAGAAGAGGATGAGGAAGTGGAGGAGAGAGCACTGAACCTGAAAACCACAGACGAGGATGTGAACCCAGCTATAAGGCGGTACTATGAATCCAGCATGACAGCATATGAAGCTGCTGAGATTGGTCTGCCGGGAGATTA[T/A]GAAGAGGGTGGCCAGCCCATGGTTTGGGCTGAGAGTGAAAACTCCCTCGGTAGACGGATGCAGATCGACCGGCTAGATATCAACGTGCAAATTGACGAATCGTACTGTGTGGATGTGGGTGAAGGTTTGAAGAGATGGAAGTGTCGCATGTGTGAGAAGTCCTACACTTCAAAGTACAACTTGGTTACGCACATTCTAGGTCACAATGGCATTAAACCACATGAGTGTATGCACTGTGGGAAACTCTTCAAGCAGCCCAGCCACCTTCAGACACATTTGCTTACTCACCAGGGCACACGGCCACACAAGTGCACTGTCTGCAAGAAGGCCTTTACCCAGACTAGTCACCTTAAACGCCATATGTTGCAGCATAGCGACATCAAGCCTTACAGTTGCCGTTTCTGTGGCCGAGGCTTTGCCTATCCTAGTGAGCTGCGCACCCACGAAACCAAGCACGAGAGTGGACACTGTCATGTCTGCACACAGTGTGGAATGGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43119
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015712 | Nonsense | 495 | 700 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 25876010)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26105693 |
GRCz11 | 18 | 26090213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGAACCATCTGATGAAGCACCAGAATGTGCGGCCCTATGTCTGCTCA[G/T]AGTGCGGCATGGAGTTTGTGCAGATCCACCACCTGAAGCAGCACATGCTT
Long Flanking Sequence:
GTGAGAAGTCCTACACTTCAAAGTACAACTTGGTTACGCACATTCTAGGTCACAATGGCATTAAACCACATGAGTGTATGCACTGTGGGAAACTCTTCAAGCAGCCCAGCCACCTTCAGACACATTTGCTTACTCACCAGGGCACACGGCCACACAAGTGCACTGTCTGCAAGAAGGCCTTTACCCAGACTAGTCACCTTAAACGCCATATGTTGCAGCATAGCGACATCAAGCCTTACAGTTGCCGTTTCTGTGGCCGAGGCTTTGCCTATCCTAGTGAGCTGCGCACCCACGAAACCAAGCACGAGAGTGGACACTGTCATGTCTGCACACAGTGTGGAATGGAGTTCCCCACACATGCTCACCTCAAGCGCCACCAGGTCAGCCACCAGGGCCCAACAACCTTTCAGTGCACTGAATGTCATAAGTCCTTTGCCTACCGTAGCCAGCTTCAGAACCATCTGATGAAGCACCAGAATGTGCGGCCCTATGTCTGCTCA[G/T]AGTGCGGCATGGAGTTTGTGCAGATCCACCACCTGAAGCAGCACATGCTTACACACAAGGTACTGACACAGCAGGCCCCCGAACACAAGGTACTTGAACCTCATTATTAGTTTATTTTGTAATCTTCCCCCCAACCATCCTATTAGAAATTACTCCCCAAAGACTTTCAGATCCAGAACCCACCTACATTGTCAACTGCTACATATTTTCATAAAACCATAGGTTAATGTGTCTTCTTCAGTTGTGTCTCTGGTATTGCCAAAGCAAGTTTCAGTGTAAATAGAGGCATTTCTGTCAGTCCCTTCTAGCCATCAGCCCACTTCCGACCCTGTCATTTACTCGTTCTGTTTCTCTGTCTCTTGCACTAGTATGGAGCTGTTTTGTGTGTGCTTTGTGCAGTGAAGTGCGTCTCTCAAGCTGATACTTCCTTCTTTCATTTTTCTCTCTCCTTGAGTATGATTCATCTTATCATGACTGCGGTGTCAGTAAACAGAATGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16083
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 |
---|---|---|---|---|---|
ENSDART00000015712 | Nonsense | 508 | 700 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 25876049)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 26105732 |
GRCz11 | 18 | 26090252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTCTGCTCAGAGTGCGGCATGGAGTTTGTGCAGATCCACCACCTGAAG[C/T]AGCACATGCTTACACACAAGGTACTGACACAGCAGGCCCCCGAACACAAG
Long Flanking Sequence:
ACATTCTAGGTCACAATGGCATTAAACCACATGAGTGTATGCACTGTGGGAAACTCTTCAAGCAGCCCAGCCACCTTCAGACACATTTGCTTACTCACCAGGGCACACGGCCACACAAGTGCACTGTCTGCAAGAAGGCCTTTACCCAGACTAGTCACCTTAAACGCCATATGTTGCAGCATAGCGACATCAAGCCTTACAGTTGCCGTTTCTGTGGCCGAGGCTTTGCCTATCCTAGTGAGCTGCGCACCCACGAAACCAAGCACGAGAGTGGACACTGTCATGTCTGCACACAGTGTGGAATGGAGTTCCCCACACATGCTCACCTCAAGCGCCACCAGGTCAGCCACCAGGGCCCAACAACCTTTCAGTGCACTGAATGTCATAAGTCCTTTGCCTACCGTAGCCAGCTTCAGAACCATCTGATGAAGCACCAGAATGTGCGGCCCTATGTCTGCTCAGAGTGCGGCATGGAGTTTGTGCAGATCCACCACCTGAAG[C/T]AGCACATGCTTACACACAAGGTACTGACACAGCAGGCCCCCGAACACAAGGTACTTGAACCTCATTATTAGTTTATTTTGTAATCTTCCCCCCAACCATCCTATTAGAAATTACTCCCCAAAGACTTTCAGATCCAGAACCCACCTACATTGTCAACTGCTACATATTTTCATAAAACCATAGGTTAATGTGTCTTCTTCAGTTGTGTCTCTGGTATTGCCAAAGCAAGTTTCAGTGTAAATAGAGGCATTTCTGTCAGTCCCTTCTAGCCATCAGCCCACTTCCGACCCTGTCATTTACTCGTTCTGTTTCTCTGTCTCTTGCACTAGTATGGAGCTGTTTTGTGTGTGCTTTGTGCAGTGAAGTGCGTCTCTCAAGCTGATACTTCCTTCTTTCATTTTTCTCTCTCCTTGAGTATGATTCATCTTATCATGACTGCGGTGTCAGTAAACAGAATGTGCCACAGGTCAACAGGGTTATAAACAAAAACACTCAGCAGT
Associated Phenotype:
Not determined