ZMP
pknox1.1
Ensembl ID:
ZFIN ID:
Description:
pbx/knotted 1 homeobox 1.1 [Source:RefSeq peptide;Acc:NP_571966]
Human Orthologue:
PKNOX1
Human Description:
PBX/knotted 1 homeobox 1 [Source:HGNC Symbol;Acc:9022]
Mouse Orthologue:
Pknox1
Mouse Description:
Pbx/knotted 1 homeobox Gene [Source:MGI Symbol;Acc:MGI:1201409]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25422 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25422
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053210 | Missense | 369 | 433 | 10 | 11 |
ENSDART00000111771 | Nonsense | 369 | 377 | 11 | 12 |
The following transcripts of ENSDARG00000078080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 20584076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 19737953 |
GRCz11 | 9 | 19548822 |
KASP Assay ID:
554-7590.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTCCGACTCCATCGCCTCAACAGGAAGCCAGCAGCAGCTCACAATGC[C/T]AGACGGTACAATTTAAGTTCTTCTAACTTGACCCATGACCCAGTTGTCTT
Long Flanking Sequence:
CGCGTGGGTTTTCCCCGGGTTCTCCGGTTTCCTCCCACCATCCAAAGACATTCAACATACATAACAATCAAGCTTGTCTAATTCCTTACGTTCCCTTAGCTACAGCAGCAGGGGAGTTCTGAGATCCACCGAGCTCGGGCTCCCTTCTTGCTCTGCCAACGGGAGGAAGCCCCGGGCTCGAGGAGCCCTTGAGCTCGGGGCTCTCTCCCGGGACAGCATGCCAAATAAGCTTTGTAAATCATCAGCTAAGTGTGAACTCTTGAAACAGGAAATTTTATATTTATTTCTTGATAACCTGGTATGCAGTATACAAGTTACATATTGCCTGCATTTTGCCTACAGGTTTATTAATGCTCGAAGACGAATACTGCAGCCAATGCTGGATGCCAACTCAACAGAGGCATCTAAAAGCAAGAAAAAGGTGGCTCAGAGTCGCCCGCTGCACCGCTTCTGGTCCGACTCCATCGCCTCAACAGGAAGCCAGCAGCAGCTCACAATGC[C/T]AGACGGTACAATTTAAGTTCTTCTAACTTGACCCATGACCCAGTTGTCTTGGTTTGGTTTTACAGGGTTTGCCCTTGCGTGATTGTGTGCAGGGAGTTTGGTTACTGTGGGAATGAATGTTGACGGCTTCCAGGCGCTTTCTTCAGATGGAGCCACTCTCGCCATGCAGCAGGTCTTGATGGGAAATCACAGCGAGGATGAGACTGATGAAAGCGGCAATGAAGACGACACAGATATGTCAACCGCCAACATGCCCGGTCTGGGTTTAGACGTCAGCGACTAAGACGCATGGATTGCAGGTCACACACTGCATGCTTACATTTACATTGGAAAACTTGCAGATGATGCTTGTTGCAAGAGATCCGCTCCCTATGTAGATTTTCAGCAAAGCTGATACTTGTGCACTACAAAAAGAATTAAGTACTGTATGTTGACCTTTATGTTACACAAAACACAAGTGAACAGTTTACAGAGAGCACAACGTTACTGAAAGCAGCAAA
Associated Phenotype:
Not determined