ZMP
znf536
Ensembl ID:
ZFIN ID:
Description:
Novel zinc finger protein [Source:UniProtKB/TrEMBL;Acc:Q1LYK4]
Human Orthologue:
ZNF536
Human Description:
zinc finger protein 536 [Source:HGNC Symbol;Acc:29025]
Mouse Orthologue:
Zfp536
Mouse Description:
zinc finger protein 536 Gene [Source:MGI Symbol;Acc:MGI:1926102]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34159 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34160 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa18888 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34159
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034068 | None | 191 | 1389 | 1 | 4 |
| ENSDART00000126085 | Essential Splice Site | 90 | 610 | None | 3 |
Genomic Location (Zv9):
Chromosome 7 (position 47982563)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 46100674 |
| GRCz11 | 7 | 46373040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGGTAATCTGAAAATCCACCTCCGCACCCATAAGCTGGGAAATCTTGG[T/A]AAGGGCCGTGGTCGTGTACGTGAGGAAAATAGGCTTCTTCATGAACTTGA
Long Flanking Sequence:
GTACTTAACGGCCGCTATCCAATCAGTCAGAAACTGCATCAGCTGACTGCTCAGCTGGGTCATGCCTTTCCTGAACTACAGAGTCGCCAGCAGATCCCAGAGGAAAAGGCAGCAACCCCACTGGATGAGAAAACCCATGCTGCCTTAGCTAGTCAGCCAATCAGCAGCCAGATGGCCTTACTGGCCAACCAGCTCAATCGTGACATGGATGTGGGCGCCTTGAGTGGTCTCAATGGCCGTGTTGATTTGCAACAATTTCTCAATGGACAGAATTTAGGAATCATGTCTCAGATGAATGATATTGAAGATGATGCACGCAAGAACCGCAAATATCCCTGTCCTCTTTGTGGCAAGCGATTCCGCTTCAACAGCATTCTGTCACTTCATATGCGTACACACACTGGAGAGAAGCCTTTCAAATGTCCATATTGTGACCACCGAGCTGCTCAGAAGGGTAATCTGAAAATCCACCTCCGCACCCATAAGCTGGGAAATCTTGG[T/A]AAGGGCCGTGGTCGTGTACGTGAGGAAAATAGGCTTCTTCATGAACTTGAAGAGAGAGCCATTCTACGTGATAAGCAAATGAGGAACAGCTTGCTGCAGCCACCTCAACCTCTTCCACCCCACTTGGGTATCCAGACTCATAGCCAACAACAGCCTGGCTCTGCCTGTGGCCTGCTCACTCCAACCAGTATTGGTAACTCACCTGAGGGACTGACCCAGCCGTCTGCCTCACCTAAGCCTGCTTCTAACAACCTACAAGATGAGCAAGCCCTCAATCCAGCCCAAGGATACCGGTGCACTTTTTGCAAGGGTAAATTTAAGAAGCGCGAGGAGCTAGACCGCCACATTCGCATTCTCCACAAACCCTACAAATGTACCCTGTGTGAATTTGCTGCTTCACAGGAGGAGGACCTGATCAGCCATGTGGAGAAAACACATATCACCGCTGAATCAGCCCAGGGACAGGGCACAGGAGCTGGCAATGGAGAGAAACCCAGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34160
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000034068 | Nonsense | 293 | 1389 | 1 | 4 |
| ENSDART00000126085 | Nonsense | 152 | 610 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 7 (position 47982869)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 46100980 |
| GRCz11 | 7 | 46373346 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGATGAGCAAGCCCTCAATCCAGCCCAAGGATACCGGTGCACTTTTTG[C/A]AAGGGTAAATTTAAGAAGCGCGAGGAGCTAGACCGCCACATTCGCATTCT
Long Flanking Sequence:
GATGATGCACGCAAGAACCGCAAATATCCCTGTCCTCTTTGTGGCAAGCGATTCCGCTTCAACAGCATTCTGTCACTTCATATGCGTACACACACTGGAGAGAAGCCTTTCAAATGTCCATATTGTGACCACCGAGCTGCTCAGAAGGGTAATCTGAAAATCCACCTCCGCACCCATAAGCTGGGAAATCTTGGTAAGGGCCGTGGTCGTGTACGTGAGGAAAATAGGCTTCTTCATGAACTTGAAGAGAGAGCCATTCTACGTGATAAGCAAATGAGGAACAGCTTGCTGCAGCCACCTCAACCTCTTCCACCCCACTTGGGTATCCAGACTCATAGCCAACAACAGCCTGGCTCTGCCTGTGGCCTGCTCACTCCAACCAGTATTGGTAACTCACCTGAGGGACTGACCCAGCCGTCTGCCTCACCTAAGCCTGCTTCTAACAACCTACAAGATGAGCAAGCCCTCAATCCAGCCCAAGGATACCGGTGCACTTTTTG[C/A]AAGGGTAAATTTAAGAAGCGCGAGGAGCTAGACCGCCACATTCGCATTCTCCACAAACCCTACAAATGTACCCTGTGTGAATTTGCTGCTTCACAGGAGGAGGACCTGATCAGCCATGTGGAGAAAACACATATCACCGCTGAATCAGCCCAGGGACAGGGCACAGGAGCTGGCAATGGAGAGAAACCCAGCAATGAATTCCGCTGTGAGGTTTGTGGCCAGGTTTTTAGTCAAGCTTGGTTTCTGAAAGGCCACATGCGGAAACACAAGGACTCCTTTGAACATTGCTGCCAGATCTGTGGACGTCGTTTCAAGGAGCCCTGGTTCCTGAAGAATCACATGAAGGTGCATCTCAACAAGCTGGCCATCAAGAGCAAGCCTCCTGTTGGTGGAGGAGCTGATGATGAAGGACACGCCGTGAACAGCATGAGCAGCCTTGCTCAAGAAGCTCATGCAAACCTGTATTCACGTTATATTTCTTGTTTGCAAAGTGGTTTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18888
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 |
|---|---|---|---|---|---|
| ENSDART00000034068 | Nonsense | 543 | 1389 | 1 | 4 |
| ENSDART00000126085 | Nonsense | 402 | 610 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 7 (position 47983619)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 46101730 |
| GRCz11 | 7 | 46374096 |
KASP Assay ID:
554-6151.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTTGCAAGCTGCAGCTAAGGTAGCAGAAATGGACCCCCTAAACAGTTA[T/A]CAAGCCTGGCAAATCATGGCACGTGGAATGGCAATGGAGCGCTCCTTCAT
Long Flanking Sequence:
GGCCACATGCGGAAACACAAGGACTCCTTTGAACATTGCTGCCAGATCTGTGGACGTCGTTTCAAGGAGCCCTGGTTCCTGAAGAATCACATGAAGGTGCATCTCAACAAGCTGGCCATCAAGAGCAAGCCTCCTGTTGGTGGAGGAGCTGATGATGAAGGACACGCCGTGAACAGCATGAGCAGCCTTGCTCAAGAAGCTCATGCAAACCTGTATTCACGTTATATTTCTTGTTTGCAAAGTGGTTTCCTCACACCCGACAAACAAGGCCTGGCTGAACAGCAGCACCAGATGCTGGCCAAAGCCGGTATTGCTATGAAGGAGAAGGAGATGCTTGGAAAGCTCCTAAGTCCAATGGCCAGCATGGGCCATGGCTTAGGGGAAAATGAAAAGCGATCACTTTTAGGTTGCCTGAACCTAGTGCCCCCTCTGAAGTCTAGCTGTATGGAGCGCTTGCAAGCTGCAGCTAAGGTAGCAGAAATGGACCCCCTAAACAGTTA[T/A]CAAGCCTGGCAAATCATGGCACGTGGAATGGCAATGGAGCGCTCCTTCATGCCAAAAGAGCAGCACCATGGTGTGCATGGACAAGAAGATGAACTTGCCAATGCAGCTGGGATTGTTCCCTTTGGTAAAGACAAGCCTGACCACCCAACCTTAGGCTCTAATGATGGTTCCAAGCTGAAGCAACATCCTGATGTGCTTCATGGAGTGAAGACAAGTGGAGGCATGATGCCCTTGAAAGATGAAGGTTTAACCTTTGATAGTCACCGTGAGTTCTTGCCTCACCATGGTGGTCTAGGCCTGGGCCAAGGGCTTGAGTACAGCCTAGCCAGCCTAAAGGAGAAAGCAACTGAGTGTCCTGACTGTGGCAGAGTCTTCAGAACCTACCATCAAATGGTGGTCCACTCTCGAGTGCACAACAAGGATCGCCGAACCCTAGAAGACAGCTCCCAGCACATTCTAGATGAACGGCGTGGCTCAGCTAGCGACCCTGAATCTCAGTC
Associated Phenotype:
Not determined