ZMP
znf503
Ensembl ID:
ZFIN ID:
Description:
Zinc finger protein 503 [Source:UniProtKB/Swiss-Prot;Acc:Q6UFS5]
Human Orthologue:
ZNF503
Human Description:
zinc finger protein 503 [Source:HGNC Symbol;Acc:23589]
Mouse Orthologue:
Zfp503
Mouse Description:
zinc finger protein 503 Gene [Source:MGI Symbol;Acc:MGI:1353644]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11014 | Nonsense | Available for shipment | Available now |
sa19057 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12639 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11014
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 |
---|---|---|---|---|---|
ENSDART00000008906 | Nonsense | 325 | 563 | 2 | 2 |
ENSDART00000008906 | Nonsense | 325 | 563 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 17519047)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 17339082 |
GRCz11 | 13 | 17470074 |
KASP Assay ID:
2260-6225.1 (used for ordering genotyping assays)
KASP Sequence:
CCGGCTATCCCCAACACTTCTTGCCCCACGGTGGAAGCCTGGTYAACGCA[C/T]AGCTCGCCAGCTCACTGGGCTGCAGTAAAGCWGGCTCRAGCCCTCTAGCC
Long Flanking Sequence:
CTTCTGGGGTGTCGAGCGGAGAGAAGTCTGGTTTCCGTGTGCCTAGCGCCACCTGCCAGCCGTTCACTCCCAGGACTGGCAGCCCGAATTCCAGCACTTCTGCTTCCCCGATGCCGTCAGATGGCAAAGGAGAGAGAGATGAAAAGAAAGATTCTGATTGTAATAAAAACTGCTCCTCAGACGGATCTGCACCGACCAGTGTCAGCCACAGCAGGATAAGCGTGAGCTGTGCGGGAATTAACGTGGAGGTCAACCAGCACCAGGAGACCACCTCAGGATCCAAAGCATCGGCGACGTCGGACTCGGTGTCGTGTGTCACCTCTTCTTCCTCGGCCTCCGTCCTGGGGTCAGGACTTGTAGCTCCCGTTTCTCCATACAAACCTGGCCAGACTGTTTTTCCCCTACCCCCGGCAGGCATGACGTACCCTGGAAGTTTAGCAGGGGCCTACGCCGGCTATCCCCAACACTTCTTGCCCCACGGTGGAAGCCTGGTCAACGCA[C/T]AGCTCGCCAGCTCACTGGGCTGCAGTAAAGCTGGCTCAAGCCCTCTAGCCGGGGCATCTCCCCCGTCCATAATGTCTGCTAGCCTTTGTAGAGACCCTTACTGCTTGAGTTACCACTGTGCCAGCCACTTAGCGGGCGCAGCCGGAGCTTCCTGCACACACGACTCGGCGGCTGCGGCGGCCGCGTCCGCTTTGAAGTCCGGATATCCACTCATGTACCCGACACACCCTTTGCACGGGGTTCACTCCTCGCCGCCATCTTTTGGTGGACACCCTTTGTATCCCTATGGTTTCATGCTGCCCAACGACCCTCTTCCGCATGTGTGTAACTGGGTGTCAGCTAATGGACCTTGTGATAAGCGTTTCTCGTCCTCCGAAGAACTTCTTAACCACCTGCGGACGCACACCGCGTTCACCGGGACTGAAAAGTTGATATCGGGTTATCCCAGTTCATCATCGTTAGCTAGTGCTGCAGCCGCAGCTATGGCGTGCCATATGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19057
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 |
---|---|---|---|---|---|
ENSDART00000008906 | Nonsense | 325 | 563 | 2 | 2 |
ENSDART00000008906 | Nonsense | 325 | 563 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 17519047)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 17339082 |
GRCz11 | 13 | 17470074 |
KASP Assay ID:
2260-6225.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGCTATCCCCAACACTTCTTGCCCCACGGTGGAAGCCTGGTCAACGCA[C/T]AGCTCGCCAGCTCACTGGGCTGCAGTAAAGCTGGCTCAAGCCCTCTAGCC
Long Flanking Sequence:
CTTCTGGGGTGTCGAGCGGAGAGAAGTCTGGTTTCCGTGTGCCTAGCGCCACCTGCCAGCCGTTCACTCCCAGGACTGGCAGCCCGAATTCCAGCACTTCTGCTTCCCCGATGCCGTCAGATGGCAAAGGAGAGAGAGATGAAAAGAAAGATTCTGATTGTAATAAAAACTGCTCCTCAGACGGATCTGCACCGACCAGTGTCAGCCACAGCAGGATAAGCGTGAGCTGTGCGGGAATTAACGTGGAGGTCAACCAGCACCAGGAGACCACCTCAGGATCCAAAGCATCGGCGACGTCGGACTCGGTGTCGTGTGTCACCTCTTCTTCCTCGGCCTCCGTCCTGGGGTCAGGACTTGTAGCTCCCGTTTCTCCATACAAACCTGGCCAGACTGTTTTTCCCCTACCCCCGGCAGGCATGACGTACCCTGGAAGTTTAGCAGGGGCCTACGCCGGCTATCCCCAACACTTCTTGCCCCACGGTGGAAGCCTGGTCAACGCA[C/T]AGCTCGCCAGCTCACTGGGCTGCAGTAAAGCTGGCTCAAGCCCTCTAGCCGGGGCATCTCCCCCGTCCATAATGTCTGCTAGCCTTTGTAGAGACCCTTACTGCTTGAGTTACCACTGTGCCAGCCACTTAGCGGGCGCAGCCGGAGCTTCCTGCACACACGACTCGGCGGCTGCGGCGGCCGCGTCCGCTTTGAAGTCCGGATATCCACTCATGTACCCGACACACCCTTTGCACGGGGTTCACTCCTCGCCGCCATCTTTTGGTGGACACCCTTTGTATCCCTATGGTTTCATGCTGCCCAACGACCCTCTTCCGCATGTGTGTAACTGGGTGTCAGCTAATGGACCTTGTGATAAGCGTTTCTCGTCCTCCGAAGAACTTCTTAACCACCTGCGGACGCACACCGCGTTCACCGGGACTGAAAAGTTGATATCGGGTTATCCCAGTTCATCATCGTTAGCTAGTGCTGCAGCCGCAGCTATGGCGTGCCATATGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12639
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008906 | Nonsense | 513 | 563 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 13 (position 17519612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 17339647 |
GRCz11 | 13 | 17470639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCCCTGGGAGCCCCGGGACACTGGCACTCAGGAGCCCGCATCATGCGT[T/A]AGGACTAAGCAGCCGCTATCACCCGTATTCAAAGAGCCCGTTGCCTACTC
Long Flanking Sequence:
GTCCATAATGTCTGCTAGCCTTTGTAGAGACCCTTACTGCTTGAGTTACCACTGTGCCAGCCACTTAGCGGGCGCAGCCGGAGCTTCCTGCACACACGACTCGGCGGCTGCGGCGGCCGCGTCCGCTTTGAAGTCCGGATATCCACTCATGTACCCGACACACCCTTTGCACGGGGTTCACTCCTCGCCGCCATCTTTTGGTGGACACCCTTTGTATCCCTATGGTTTCATGCTGCCCAACGACCCTCTTCCGCATGTGTGTAACTGGGTGTCAGCTAATGGACCTTGTGATAAGCGTTTCTCGTCCTCCGAAGAACTTCTTAACCACCTGCGGACGCACACCGCGTTCACCGGGACTGAAAAGTTGATATCGGGTTATCCCAGTTCATCATCGTTAGCTAGTGCTGCAGCCGCAGCTATGGCGTGCCATATGCACATGCCGCCCTCAGGAGCCCCTGGGAGCCCCGGGACACTGGCACTCAGGAGCCCGCATCATGCGT[T/A]AGGACTAAGCAGCCGCTATCACCCGTATTCAAAGAGCCCGTTGCCTACTCCCGGCGCGCCGGTTCCAGTACCTGCCGCCACCGGCCCTTATTACTCTCCCTATGCACTGTATGGTCAAAGACTCACCACAGCATCAGCGCTTGGATACCAGTGAAAAACCAACAGACTTTGTTCAAATTTATAGATTATAAAGATTGAAATATAAAGACTTTTATATCATCGCGCCACTGAAGGACTGGATCCGTGGACTCACTGTATTTATTTATGTCAGCTTAAAGCGGACGATAATACAAATGAAAATATTTGAGCAACTCAAAAGTGCATTACATTTGAACTGAACTCTGTAGATAAAGTGAAACACATGTTAGAGTACTAATAAAATAGGGGTCTTCAGTTGGATGTTGATTTGGAATTGCTATGATTGTATTGTTCGTTATTATTTAATGTCTCATTGAAAAAAGATGATAATTTACATGCATGTTTGTTTCTTAAATCCCAAA
Associated Phenotype:
Not determined