ZMP
znf516
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 516 [Source:RefSeq peptide;Acc:NP_001153141]
Human Orthologue:
ZNF516
Human Description:
zinc finger protein 516 [Source:HGNC Symbol;Acc:28990]
Mouse Orthologue:
Zfp516
Mouse Description:
zinc finger protein 516 Gene [Source:MGI Symbol;Acc:MGI:2443957]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43267 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12406 | Essential Splice Site | Available for shipment | Available now |
sa45669 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15699 | Nonsense | Available for shipment | Available now |
sa39243 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43267
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 |
---|---|---|---|---|---|
ENSDART00000076716 | Nonsense | 426 | 1045 | 1 | 10 |
ENSDART00000104279 | Nonsense | 428 | 1084 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 22197609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 22130989 |
GRCz11 | 19 | 21715312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAGGGCTGGGAAGAAAGGTTAGCTGATGCGGATGTAGCATACGACAGG[G/T]AAAAAGGCGAGTATGTCTTACTCAGACAGGACAAGCGGAAGAAATCACTT
Long Flanking Sequence:
TCTGTGGACGTCGTTTTCGTGAGCCCTGGTTCCTACGTAGTCACATGAAGACCCACAACACCAAGGTAAAACCAAGGAGTAACTCTTACCTTCCGGCCACTGTCAACGAGGTGGCGCAGGACGAGTCCAACTTGGTGAATGAAGTGTGTCTGTATGAACTCTGTGCCAAGTGTGGTAACTTCTTCCATGACCGCAAAAGCTTGCAATTGCATGAGCAGGTTCACAAAAATATTGAGCAGCCTCTTAAAAACAAAAACTGCAATGAAAACAACTTTCCATCTGTCACCAAGACAAGCTTCCTGCAATGCCTAAACTTGAAACCTGCAGGAAATATTGAGAACCCTAGTGAGGGAACCATAGGGAAAAGAATCCCAGAGCTTGATCCTGTAAGCAGCTACCAAGCTTGGCAACTGGCAACAAGAGGCAAATTGGTGGAGGTAACAGAGAGAAGCCAGGGCTGGGAAGAAAGGTTAGCTGATGCGGATGTAGCATACGACAGG[G/T]AAAAAGGCGAGTATGTCTTACTCAGACAGGACAAGCGGAAGAAATCACTTGATTCCACTGTGAGTATCCCAACCAAGAAACGGAGAGGGGCTGTTACCCAAGGCTGCACTCCAGATCAGCACAGCAATGGAGAAAAGAACAGCCATGTTTCAACAGGTGAGCGAAGCCCTGAAAATCTGAGTGACTCTGAGTATCGCCCTACTTCTCGCCCTAGCCGTAAAAATTCCCAGAAAACTTCAGAGTGCTTGGAGTGTGGAAAGGGCTTCCGCACACAGCAACAGATGGTGATCCACATGCTCATCAGACATGGTGGCTTGGGTGAAACCATTGGTGGAAATGGACTGTTCCGCAAAACAACGTCTAGCCCATCTAAAACAGGGGAATCTGCAGGACACTTCAGGGATCAAAGACGGGCTGGGTTCTTGGGGGACACAGGTAAGGGAATCCCTTCTTGTTTTTACAAATATAGAAAACTCAAAGATTGAGTAATCTTACACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12406
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076716 | Essential Splice Site | 456 | 1045 | None | 10 |
ENSDART00000104279 | None | 479 | 1084 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 22197454)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 22130834 |
GRCz11 | 19 | 21715157 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCACTCCAGATCAGCACAGCAATGGAGAAAAGAACAGCCATGTTTCAAC[A/T]GGTGAGCGAAGCCCTGAAAATCTGAGTGACTCTGAGTATCGCCCTACTTC
Long Flanking Sequence:
GAACTCTGTGCCAAGTGTGGTAACTTCTTCCATGACCGCAAAAGCTTGCAATTGCATGAGCAGGTTCACAAAAATATTGAGCAGCCTCTTAAAAACAAAAACTGCAATGAAAACAACTTTCCATCTGTCACCAAGACAAGCTTCCTGCAATGCCTAAACTTGAAACCTGCAGGAAATATTGAGAACCCTAGTGAGGGAACCATAGGGAAAAGAATCCCAGAGCTTGATCCTGTAAGCAGCTACCAAGCTTGGCAACTGGCAACAAGAGGCAAATTGGTGGAGGTAACAGAGAGAAGCCAGGGCTGGGAAGAAAGGTTAGCTGATGCGGATGTAGCATACGACAGGGAAAAAGGCGAGTATGTCTTACTCAGACAGGACAAGCGGAAGAAATCACTTGATTCCACTGTGAGTATCCCAACCAAGAAACGGAGAGGGGCTGTTACCCAAGGCTGCACTCCAGATCAGCACAGCAATGGAGAAAAGAACAGCCATGTTTCAAC[A/T]GGTGAGCGAAGCCCTGAAAATCTGAGTGACTCTGAGTATCGCCCTACTTCTCGCCCTAGCCGTAAAAATTCCCAGAAAACTTCAGAGTGCTTGGAGTGTGGAAAGGGCTTCCGCACACAGCAACAGATGGTGATCCACATGCTCATCAGACATGGTGGCTTGGGTGAAACCATTGGTGGAAATGGACTGTTCCGCAAAACAACGTCTAGCCCATCTAAAACAGGGGAATCTGCAGGACACTTCAGGGATCAAAGACGGGCTGGGTTCTTGGGGGACACAGGTAAGGGAATCCCTTCTTGTTTTTACAAATATAGAAAACTCAAAGATTGAGTAATCTTACACAAATTTGACAAAAACTTCAAGTGAAACTTGTTTGCATATCATAAACTATCATTAAGCTTTCAACAAACACTTTGAGCAGGCAGTATCATTAATGAAATGCTGTGTGGATGCTCAAAATCTGAAAGGGGTTTTATTGTTACATTGGGCAGATGTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45669
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076716 | Essential Splice Site | 682 | 1045 | 7 | 10 |
ENSDART00000104279 | None | 662 | 1084 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 22194386)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 22127766 |
GRCz11 | 19 | 21712089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCACCTCAACTCACCTGGAGAGGGCAGCACTGAGTGACGCCGCTTTAAA[G/A]ACAGAGGAAGAAAAGAGCAAGGGTTTGGAGGAAAGCAGCTCCACAGATAA
Long Flanking Sequence:
TTGTTGAATAAAAATTTGTTAATATGTTTCTCTATTTAAGATCTAAAAACGAAATTAGAAAGTTTTACTGAAATACAGCTACAGTACATGGGTATGTGGTGCCATCTTGTGGTGAAACTCTGGAATTGTTTTGAATGTCAATGCTCACTGTTATTAAAATTAGCTCATTTTAATACATTCAGAGATAATTCACTACTGTTCTGTGTTTTTTTTGTGTGTGTTTTTATGACAGATAAAAAGCCATACACCTGTGAGCACTGTGACTTTTGCACCTCGGAGCCCTCAGCCATCGCTGCCCATATCCAAACGCATCAATCGGCGGTCAGGGACTGGGGCCAGAGGAGTGATGCCTTAACCAGCTCACTCAGCCAAAGCCAAACTCACCAAACCAATCACACAGGCTTCCCAAGGCTGAGAAATGCTCTTCTCCAACAGCCCTACTGGCCCTACACCACCTCAACTCACCTGGAGAGGGCAGCACTGAGTGACGCCGCTTTAAA[G/A]ACAGAGGAAGAAAAGAGCAAGGGTTTGGAGGAAAGCAGCTCCACAGATAAAGCGGAGTCTAATCTGCTTAATCTCTCAGTGGACGTGGATAACAAAAAAGAAGTTTCGTCCATTCTTTTGAACAATTTGGTTAGACACCAGTGCCCTTATTGCTCCTATGCAACACACTACCCAGAAGTTCTCTGGATCCACCAACGAATCGCACACAAAATTGACAGCACTACGTTGGTGCCGAAGTGGGCCCCAAAAAATGGCCTTAAGGGGCCCAAAACGCTTCTTGATTTCAAGAGACGCACCGGGCCACCTCCATTTCTGGAGGGTAAGGACTGCCCGTCTCTGCCTCAGATGAGAAGTTACAGAACCAGTCCACCTGATTGCAGCCCTGGAGGGACGAAGAAATCAAAACCTCTGACAAGTACTGTAGAGTCCAGCTCTTCGCAAAACAAGAGCTGGCACACAGCCACAGCGCCAGGGGCATCATCGCACTCGTCCAAACACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15699
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000076716 | Nonsense | 848 | 1045 | 7 | 10 |
ENSDART00000104279 | Nonsense | 829 | 1084 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 22193887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 22127267 |
GRCz11 | 19 | 21711590 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGCACACAGCCRCAGCGCCAGGGGCAKCATCGCACTCGTCCAAACAC[A/T]AAACCAGCAAGTCCAGGACAGATGAGTTGGCAGGYAGTAAACAYAAAACA
Long Flanking Sequence:
AGACAGAGGAAGAAAAGAGCAAGGGTTTGGAGGAAAGCAGCTCCACAGATAAAGCGGAGTCTAATCTGCTTAATCTCTCAGTGGACGTGGATAACAAAAAAGAAGTTTCGTCCATTCTTTTGAACAATTTGGTTAGACACCAGTGCCCTTATTGCTCCTATGCAACACACTACCCAGAAGTTCTCTGGATCCACCAACGAATCGCACACAAAATTGACAGCACTACGTTGGTGCCGAAGTGGGCCCCAAAAAATGGCCTTAAGGGGCCCAAAACGCTTCTTGATTTCAAGAGACGCACCGGGCCACCTCCATTTCTGGAGGGTAAGGACTGCCCGTCTCTGCCTCAGATGAGAAGTTACAGAACCAGTCCACCTGATTGCAGCCCTGGAGGGACGAAGAAATCAAAACCTCTGACAAGTACTGTAGAGTCCAGCTCTTCGCAAAACAAGAGCTGGCACACAGCCACAGCGCCAGGGGCATCATCGCACTCGTCCAAACAC[A/T]AAACCAGCAAGTCCAGGACAGATGAGTTGGCAGGCAGTAAACACAAAACAGACATCCATCAAAACAACTCCTCACGGCCCATGGCAAGTCCACAGAAGACTGGAAACCCAAAGACAGGTAGCCGAGTGGTGGAGAGTAGTTTGCTACCTCAAGAGGGACTTCATTTTATGCTCTCTAGCAAACACAACCTCTCGGATCAGAGGAGCTCCAAAGCTCACGCTCCTCAGACCCCCAGTAAGTCTGATTCTCAAGCTCAGGATACACCGTCTGTGGCTGGGTACGACCCCTGGAACAGACTGGGCCTGAGTGGCCCGTCACCTCACTCTCAGTCCAAGAGACAGTCAACAGCCGATGGTGCAGAAGGTGTGACGGACATCCTGAGTTTTTTAAAGAACTGTAACCCTCACGATCTTGCTGCCCTCTACCACCACTGGGGCTACAGTAGTGCCATGACAGAGCAAGCAGGTAAAATATTTCAGTATTATATAATGCTGTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39243
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 |
---|---|---|---|---|---|
ENSDART00000076716 | Nonsense | 933 | 1045 | 7 | 10 |
ENSDART00000104279 | Nonsense | 914 | 1084 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 22193632)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 22127012 |
GRCz11 | 19 | 21711335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCAAAGCTCACGCTCCTCAGACCCCCAGTAAGTCTGATTCTCAAGCT[C/T]AGGATACACCGTCTGTGGCTGGGTACGACCCCTGGAACAGACTGGGCCTG
Long Flanking Sequence:
GCCTTAAGGGGCCCAAAACGCTTCTTGATTTCAAGAGACGCACCGGGCCACCTCCATTTCTGGAGGGTAAGGACTGCCCGTCTCTGCCTCAGATGAGAAGTTACAGAACCAGTCCACCTGATTGCAGCCCTGGAGGGACGAAGAAATCAAAACCTCTGACAAGTACTGTAGAGTCCAGCTCTTCGCAAAACAAGAGCTGGCACACAGCCACAGCGCCAGGGGCATCATCGCACTCGTCCAAACACAAAACCAGCAAGTCCAGGACAGATGAGTTGGCAGGCAGTAAACACAAAACAGACATCCATCAAAACAACTCCTCACGGCCCATGGCAAGTCCACAGAAGACTGGAAACCCAAAGACAGGTAGCCGAGTGGTGGAGAGTAGTTTGCTACCTCAAGAGGGACTTCATTTTATGCTCTCTAGCAAACACAACCTCTCGGATCAGAGGAGCTCCAAAGCTCACGCTCCTCAGACCCCCAGTAAGTCTGATTCTCAAGCT[C/T]AGGATACACCGTCTGTGGCTGGGTACGACCCCTGGAACAGACTGGGCCTGAGTGGCCCGTCACCTCACTCTCAGTCCAAGAGACAGTCAACAGCCGATGGTGCAGAAGGTGTGACGGACATCCTGAGTTTTTTAAAGAACTGTAACCCTCACGATCTTGCTGCCCTCTACCACCACTGGGGCTACAGTAGTGCCATGACAGAGCAAGCAGGTAAAATATTTCAGTATTATATAATGCTGTTTTTTTTTTTAATCCAGTAAGCTTTTATTTTACAATGAATAATATACATTTTATAGTCTAATGAAATGACACATCAACCTAATATTGGCCCTGTTTATACCTTTTATTTATTGTTTACCTTGTATTATTTCTTGTGTGCTGTTGGGGATGTTTTCGTCCACTCTGGGGTGATTTTTAGTCTTAATTTGGTCACAACTTTTTTCGGATTAGCAAATGGAATGATTTTAGTTTTTTATTTGGAAACATTTTTTAGGAAAATG
Associated Phenotype:
Not determined