ZMP
si:ch211-245h14.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human zinc finger protein 512 (ZNF512) [Source:UniProtKB/TrEMBL;Acc:Q5RHA4]
Human Orthologue:
ZNF512
Human Description:
zinc finger protein 512 [Source:HGNC Symbol;Acc:29380]
Mouse Orthologue:
Zfp512
Mouse Description:
zinc finger protein 512 Gene [Source:MGI Symbol;Acc:MGI:1917345]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5956 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25143 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3063 | Nonsense | F2 line generated | Not yet available |
sa13791 | Nonsense | Available for shipment | Available now |
sa39297 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5956
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 |
---|---|---|---|---|---|
ENSDART00000061413 | Nonsense | 129 | 374 | 5 | 11 |
ENSDART00000147787 | Nonsense | 116 | 418 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 38556768)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38629180 |
GRCz11 | 20 | 38532059 |
KASP Assay ID:
554-3648.1 (used for ordering genotyping assays)
KASP Sequence:
AATGGTTTGTTCTAGGGCTGCACTGGAAGTTTCACTAGTATAATGGGTTA[T/A]GTATACMATATGAAGAAATGTGGCAAAGAGTCGTCCGAGCTGGAGAAACT
Long Flanking Sequence:
TTAAAAATCAAGACATAATTATATTTTATTTTGTTAAAATAAGCATAATCTAGAGGCCTTTGCCTTTCATATAAGCCACTTCTGATACCAAATGATCAACTAGACCTCAAGTTATTATTAGTGGGTCCTAAGACTTGGATAGGCGACAAGACTTTTGTCAGGTAGTGTATATTAACATAAAATATAATACTTTTTAGTAATAAACAAGAAAATTTAAATAAGGTATGCCACTATTTCACATGTAAGATATTTTTATTAAAGCTAAATTGTTTACAACATTGTTAAGAAATGCTGAAATCAGTTACAGTTTAAAATATATTAAAAAGAAACTATTTGAAATTGGTAATTTAAATAGTTTAATCAATAAATTAGTTTAAATAGTCCTTTAAATCAAATTTTTGTACTGACCACATGGAACTATGCATGTTTTTATGCATGTTACCTCAAAGGAATGGTTTGTTCTAGGGCTGCACTGGAAGTTTCACTAGTATAATGGGTTA[T/A]GTATACCATATGAAGAAATGTGGCAAAGAGTCGTCCGAGCTGGAGAAACTTTTATTGAATTGTAAACACTGTGGAAAAGCATATCGTTCCAGAGCGGGCCTGGAGTATCATCTCAAAAATGAACACAGTCCAGTGAGTCCTAATAGCTTTATTCAGTTCTCCTGTATCTCATATTCTTTCACATTCTGTTTTCCACAAATAAATTCTCATGTTTACCTGCTGTTGCAGGTAGCTGAGGAAAGTGAGGAGGTAAAACCCCAGAAAGAGCCGGTGCCAGAACGGACACAGAGCGGACGGGCCAAACGTTTGTCGGCGCAGGTCGCCGGGTTTTACCTGAGAGAAATCGCCAGCGAGGAGCTGCTAAAGGAATGGCCCAAAAGAAAAGTCCAACGAGACCTGGTGCCAGATGACAGGAAGGTGCTGCAAAATATACACATCTGACTGTGGCAATAAATGTTGCTTTTGCAGGGCTGTGAAGATGTCAAAACCTGTGTGAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25143
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 |
---|---|---|---|---|---|
ENSDART00000061413 | Nonsense | 157 | 374 | 5 | 11 |
ENSDART00000147787 | Nonsense | 144 | 418 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 38556852)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38629264 |
GRCz11 | 20 | 38532143 |
KASP Assay ID:
554-7705.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGAGCTGGAGAAACTTTTATTGAATTGTAAACACTGTGGAAAAGCATA[T/A]CGTTCCAGAGCGGGCCTGGAGTATCATCTCAAAAATGAACACAGTCCAGT
Long Flanking Sequence:
ATACCAAATGATCAACTAGACCTCAAGTTATTATTAGTGGGTCCTAAGACTTGGATAGGCGACAAGACTTTTGTCAGGTAGTGTATATTAACATAAAATATAATACTTTTTAGTAATAAACAAGAAAATTTAAATAAGGTATGCCACTATTTCACATGTAAGATATTTTTATTAAAGCTAAATTGTTTACAACATTGTTAAGAAATGCTGAAATCAGTTACAGTTTAAAATATATTAAAAAGAAACTATTTGAAATTGGTAATTTAAATAGTTTAATCAATAAATTAGTTTAAATAGTCCTTTAAATCAAATTTTTGTACTGACCACATGGAACTATGCATGTTTTTATGCATGTTACCTCAAAGGAATGGTTTGTTCTAGGGCTGCACTGGAAGTTTCACTAGTATAATGGGTTATGTATACCATATGAAGAAATGTGGCAAAGAGTCGTCCGAGCTGGAGAAACTTTTATTGAATTGTAAACACTGTGGAAAAGCATA[T/A]CGTTCCAGAGCGGGCCTGGAGTATCATCTCAAAAATGAACACAGTCCAGTGAGTCCTAATAGCTTTATTCAGTTCTCCTGTATCTCATATTCTTTCACATTCTGTTTTCCACAAATAAATTCTCATGTTTACCTGCTGTTGCAGGTAGCTGAGGAAAGTGAGGAGGTAAAACCCCAGAAAGAGCCGGTGCCAGAACGGACACAGAGCGGACGGGCCAAACGTTTGTCGGCGCAGGTCGCCGGGTTTTACCTGAGAGAAATCGCCAGCGAGGAGCTGCTAAAGGAATGGCCCAAAAGAAAAGTCCAACGAGACCTGGTGCCAGATGACAGGAAGGTGCTGCAAAATATACACATCTGACTGTGGCAATAAATGTTGCTTTTGCAGGGCTGTGAAGATGTCAAAACCTGTGTGAAGCTAGTTTTGGTTACGCTGCATGCATCATTCCTTCCATCATTCATTCATTTTCTTTTCGGCTTAGTTCCTTTATTAATCAGGGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3063
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000061413 | Nonsense | 227 | 374 | 6 | 11 |
ENSDART00000147787 | Nonsense | 214 | 418 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 38557156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38629568 |
GRCz11 | 20 | 38532447 |
KASP Assay ID:
554-2774.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAAATCGCCAGCGAGGAGCTGCTAAAGGAATGGCCCAAAAGAAAAGTC[C/T]AACGAGACCTGGTGCCAGATGACAGGAAGGTGCTGCAAAATATACACATC
Long Flanking Sequence:
AATCAAATTTTTGTACTGACCACATGGAACTATGCATGTTTTTATGCATGTTACCTCAAAGGAATGGTTTGTTCTAGGGCTGCACTGGAAGTTTCACTAGTATAATGGGTTATGTATACCATATGAAGAAATGTGGCAAAGAGTCGTCCGAGCTGGAGAAACTTTTATTGAATTGTAAACACTGTGGAAAAGCATATCGTTCCAGAGCGGGCCTGGAGTATCATCTCAAAAATGAACACAGTCCAGTGAGTCCTAATAGCTTTATTCAGTTCTCCTGTATCTCATATTCTTTCACATTCTGTTTTCCACAAATAAATTCTCATGTTTACCTGCTGTTGCAGGTAGCTGAGGAAAGTGAGGAGGTAAAACCCCAGAAAGAGCCGGTGCCAGAACGGACACAGAGCGGACGGGCCAAACGTTTGTCGGCGCAGGTCGCCGGGTTTTACCTGAGAGAAATCGCCAGCGAGGAGCTGCTAAAGGAATGGCCCAAAAGAAAAGTC[C/T]AACGAGACCTGGTGCCAGATGACAGGAAGGTGCTGCAAAATATACACATCTGACTGTGGCAATAAATGTTGCTTTTGCAGGGCTGTGAAGATGTCAAAACCTGTGTGAAGCTAGTTTTGGTTACGCTGCATGCATCATTCCTTCCATCATTCATTCATTTTCTTTTCGGCTTAGTTCCTTTATTAATCAGGGGTTATCGCAATGGAATGAACTGCCAACTCATGCAACATATGTTTTACACAGCAGATGCCCTTTCAGCTGCAACCCATCACTGGGAAACATCAATAAACTCTTGCATTCACACAAATGCACTACAGACAATTTAGCTTCTTCAATTCACCTATAGCACATGCCTTTGGACTGTGGGGGGAAACCGGAGCACCCGGAGAAAAAAAACCCACGCAAACACGGGTAGAACATACCTGTACCTGCACTGTGGAAGCAGTCTACAGTCATTCCTGTGTCAAAAAAAAAAAGAAGCCACAGAAGTTAGAGGACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13791
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 |
---|---|---|---|---|---|
ENSDART00000061413 | Nonsense | 228 | 374 | 6 | 11 |
ENSDART00000147787 | Nonsense | 215 | 418 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 38557159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38629571 |
GRCz11 | 20 | 38532450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATCGCCAGCGAGGAGCTGCTAAAGGAATGGCCCAAAAGAAAAGTCYAA[C/T]GAGACCTGGTGCCAGATGACAGGAAGGTGCTGCAAAATATACACATCTGA
Long Flanking Sequence:
CAAATTTTTGTACTGACCACATGGAACTATGCATGTTTTTATGCATGTTACCTCAAAGGAATGGTTTGTTCTAGGGCTGCACTGGAAGTTTCACTAGTATAATGGGTTATGTATACCATATGAAGAAATGTGGCAAAGAGTCGTCCGAGCTGGAGAAACTTTTATTGAATTGTAAACACTGTGGAAAAGCATATCGTTCCAGAGCGGGCCTGGAGTATCATCTCAAAAATGAACACAGTCCAGTGAGTCCTAATAGCTTTATTCAGTTCTCCTGTATCTCATATTCTTTCACATTCTGTTTTCCACAAATAAATTCTCATGTTTACCTGCTGTTGCAGGTAGCTGAGGAAAGTGAGGAGGTAAAACCCCAGAAAGAGCCGGTGCCAGAACGGACACAGAGCGGACGGGCCAAACGTTTGTCGGCGCAGGTCGCCGGGTTTTACCTGAGAGAAATCGCCAGCGAGGAGCTGCTAAAGGAATGGCCCAAAAGAAAAGTCCAA[C/T]GAGACCTGGTGCCAGATGACAGGAAGGTGCTGCAAAATATACACATCTGACTGTGGCAATAAATGTTGCTTTTGCAGGGCTGTGAAGATGTCAAAACCTGTGTGAAGCTAGTTTTGGTTACGCTGCATGCATCATTCCTTCCATCATTCATTCATTTTCTTTTCGGCTTAGTTCCTTTATTAATCAGGGGTTATCGCAATGGAATGAACTGCCAACTCATGCAACATATGTTTTACACAGCAGATGCCCTTTCAGCTGCAACCCATCACTGGGAAACATCAATAAACTCTTGCATTCACACAAATGCACTACAGACAATTTAGCTTCTTCAATTCACCTATAGCACATGCCTTTGGACTGTGGGGGGAAACCGGAGCACCCGGAGAAAAAAAACCCACGCAAACACGGGTAGAACATACCTGTACCTGCACTGTGGAAGCAGTCTACAGTCATTCCTGTGTCAAAAAAAAAAAGAAGCCACAGAAGTTAGAGGACTTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39297
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 |
---|---|---|---|---|---|
ENSDART00000061413 | None | None | 374 | None | 11 |
ENSDART00000147787 | Nonsense | 387 | 418 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 38563001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38635413 |
GRCz11 | 20 | 38538292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACAGCGACTCAAGAACTGAAAATGAAGAGGAAAGAGAGACGAAACCAA[C/T]AGAAACGGAAAGCAAGCGGACAGGAGAAAGACTGCTATGAATTCAGTGGC
Long Flanking Sequence:
GATATTTATATATAATTTGTATCATATTATATATAATATCTAAATACAAATAAACATTTTCCTAAATCTACATGCGTGTATATAAAGTGTTTATATATATTTTACACACTTAAATTATGTCAAAACAAACTTTTATTTATTTTATTTCGATGTGATTATGTTAATTATGTTATATCTATTTTTTATTTTAAAAAATGTATTAATACCTAATTTTATGCTCATTTGTATAATCAGAATGTACATTTTCTAATGATTTCCATGATTATTTTACACAGGACTGGTTTGTTGTTCGGTCCAAGTCTAAGAGCTTAAAGTTTGAAAAACTGGACAAGACTCAAGCAAAGGAAGATTCAGACCTTCCCTCGCCGGACTCAGAAACTCTCAGTTTCCCCCAGGGCTCCAGCAGCACTTGGCAGGACAGACAGACGTCAGCGGTGCCCATCTCAAGTGGCACAGCGACTCAAGAACTGAAAATGAAGAGGAAAGAGAGACGAAACCAA[C/T]AGAAACGGAAAGCAAGCGGACAGGAGAAAGACTGCTATGAATTCAGTGGCAATGAGAGTCAGAGCAGCAGCGGCAGCAGCAGCTCCAGCTCCAGCAGTGAGTCTGAACCCGAGACCCACAAACAGGATGAATGGACCCTCAGCAGACCCCTCTCCAGCCAGAGACCCGAAAGTGACCCGTAAAACATTCCTGTTCCGTCATATGTGGAGTTCTCCAAAGATTAAAGAGGTACATTACTGTTCAGAAGTTTTGAGTAAAAGGGATAGTTAACCCAAAAATTAAAATTTACTCAGTATTTACTCACCCTCAAGTGCTTCCCTACAACCATTGACTTCAATAGTAAGAAAAACAATACTATGGAAGTCAATGGTCACAGTTTTCAGCATTTTTCTAAATATCTGCTTTTGTAAGAATCTCATAAAGGTTAATTAATGATGACAGGATTTTCATTTTTGTGTGAACCATCCCTTTAAGAGAAAAAAGACGTCTCTTTTGCTCAC
Associated Phenotype:
Not determined