ZMP
si:ch211-216l23.1
Ensembl ID:
ZFIN ID:
Description:
Zinc finger protein 423 [Source:UniProtKB/Swiss-Prot;Acc:A1L1R6]
Human Orthologue:
ZNF423
Human Description:
zinc finger protein 423 [Source:HGNC Symbol;Acc:16762]
Mouse Orthologue:
Zfp423
Mouse Description:
zinc finger protein 423 Gene [Source:MGI Symbol;Acc:MGI:1891217]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7445 | Missense | Mutation detected in F1 DNA | Not yet available |
sa6510 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7445
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083296 | Missense | 28 | 1365 | 2 | 8 |
ENSDART00000128003 | Missense | 28 | 1365 | 2 | 8 |
ENSDART00000146133 | Missense | 28 | 1275 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 17487120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17838886 |
GRCz11 | 18 | 17827952 |
KASP Assay ID:
554-4082.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCGGTAGCGGTGGAAGAGGCCGARTCTACAGAGTGCGCCAGTGGTTGG[G/A]ACTCTTCTGTTCAGACAGGTATGATTTCGCTAGCGTGGCGTCCTGCACGA
Long Flanking Sequence:
TGTTTCCATTTCTAGACTGTGTGCCAAAGTGCTTCCAGGCTATGGGGAGTTTTGTAGAGACCGGTAGTATGTGTGTATGTGTGTGTGTTAATGGTGGTGAGGCTATGGGGGGTGGTCCAGATTCTTATTGTGTCCTGAACACTGCTGCTTCCTGTTTGTGTGCCAGTGGGGCTTCCTTCCTTGACTATGCCCAGGAAAACCTTCATCACACATTCCTCCTCTCATCTCACTGCCTCCCGTTACCTGTTTTTGCACCTCCAAAATTAGCACACAGGCAAACAAAGAGCACATACACACAATAAAGTCCTTTGATGTGCATCCAACTTTCAGATTGAGCGCATCACAGACTCATGATGGAACGTGGATTATGTGGCGCACTTCTGAGAAGAATGCCGTAAATGTTGTGTGTGGTTTGGCTACGCAAGCGCTCTAATACGCTCTCTCTCTCTTTTTCGGTAGCGGTGGAAGAGGCCGAATCTACAGAGTGCGCCAGTGGTTGG[G/A]ACTCTTCTGTTCAGACAGGTATGATTTCGCTAGCGTGGCGTCCTGCACGATACATCCAACCCCCTGCTCCTTCAGGGACGACCCGCTGCATCACAATCTCTAATATCAATTCCACATGGCCTGCAGCCCTGCACACAGAGGGAGGGAGGGAGGAAGGGAGGGAAGGAGGGAGAGTTTTTCATAAGGCACTAGAGGATGGCGTCCAGGTGCATGCCGGACTGGAAGCTTAGCGGCGCTTCCTGTCTGAACGTACAGGCACATTGCCGCACTCAGAATGTAATATCGCACAACTTGACAAGTTTGATTACACCTCCCCTCTGGAGAGGAACATTTCTGTCCTGCAAAATTCAAGCGGGCTGATTTAGACTGTGCATCTCTCTGACTATTACATTTTTCAACGGTTACCTCAGAAGACCTTTTTCAAATAAGCACACGTATTTAGATATATTTGGATTGGAGAATGAAAACTTTAAAGGATGCATTGGTTGACAAAGTTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6510
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 |
---|---|---|---|---|---|
ENSDART00000083296 | Nonsense | 1177 | 1365 | 4 | 8 |
ENSDART00000128003 | Nonsense | 1177 | 1365 | 4 | 8 |
ENSDART00000146133 | Nonsense | 1177 | 1275 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 17543413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17895179 |
GRCz11 | 18 | 17884245 |
KASP Assay ID:
554-4945.1 (used for ordering genotyping assays)
KASP Sequence:
AGATAGATGTCAAYGGCCTGCCTTATGGTCTTTGTGCTGGCTGCATGAGT[C/T]GAGGGACAAACGGCCAGTCCCCAACAGTTGTTGTCACCCCACARGAGGCT
Long Flanking Sequence:
TTTCTGAGAATGGCTTGAGGGAACATGCCCAGACGCATCGTGGCCCAGCAAAGCACTACATGTGTCCCATCTGTGGCGAACGCTTTCCTTCACTTCTTACTCTCACTGAGCACAAGGTCACCCACAGCAAGAGCTTGGACACAGGCACCTGCCGTATCTGCAAGATGCCCCTGCAGAGCGAGGAAGAGTTTATTGAGCACTGCCAGATGCACCCTGACCTGAGGAACTCTCTCACAGGCTTCCGCTGTGTTGTTTGCATGCAAACTGTCACCTCAACGCTCGAATTGAAGATACATGGAACCTTTCACATGCAGAAGCTCTCATCCTCTGGGGGTAGTGGTGGAGGTGGAGGATCAGCCTCATCATCTCCAAACGGCCAGCTGCAGGCCCACAAACTCTATAAATGTGCCCTTTGTCTCAAAGACTTCAAGAACAAGCAAGAGCTGGTCAAGATAGATGTCAATGGCCTGCCTTATGGTCTTTGTGCTGGCTGCATGAGT[C/T]GAGGGACAAACGGCCAGTCCCCAACAGTTGTTGTCACCCCACAAGAGGCTGGGGATAAGGGAACCACTGGACTGCGCTGCTCAGAGTGTGCTGTTAAATTTGAGACCCTGGAAGACCTGGAAAGTCACATTCAGGTGGACCATACCGAGATGAGCCCTGAGACCAGTGGAGCTAAAAAAGTTACAGACGCTTCTCCTGTTCCAAAGGTAAGTGTCAAGACCTCACTCTTATAAGCTAATATACTTTACATTTAAACTTAATCTCAATTACATGTTGGTTTTCTCCTGAAAGGAAAGTTAAATGTATGTGATAGTTCAATATAAAACCAGAAGATCAAAGATTACTCAGCCATTGTCAACAAGCACAGGGCCTTTTGACAGAAATGTTCTTTTATAAAATGATTTGTATTCACTTCGGGTATTTTGGGGGTCATTTGAGGTTTTCCTCTAGTGCTCAAATTTGTGTTCTTTCTCTACCTTTTCTTTTTTGTGTGCGTCTCT
Associated Phenotype:
Not determined