ZMP
zgc:73290
Ensembl ID:
ZFIN ID:
Description:
enhanced at puberty protein 1 [Source:RefSeq peptide;Acc:NP_997852]
Human Orthologue:
C14orf4
Human Description:
chromosome 14 open reading frame 4 [Source:HGNC Symbol;Acc:14282]
Mouse Orthologue:
6430527G18Rik
Mouse Description:
RIKEN cDNA 6430527G18 gene Gene [Source:MGI Symbol;Acc:MGI:2442463]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42878 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28815 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42878
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 |
---|---|---|---|---|---|
ENSDART00000015418 | Nonsense | 108 | 661 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 11192974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 11175496 |
GRCz11 | 17 | 11329562 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACCATGTGGACGGCTCGTCTAAATCGCAACAGCAGCAGCAGCAGCAA[C/T]AACAACAGTCCGGCTTGGACCGATACGCGCTCGCCACCGAAAGATCACGC
Long Flanking Sequence:
GGAGTGGTTAGCGCATGCGCACTCGCATGGCAACAAGTGGCTTGTCATTTGTAACAGAAAAAGGAACTGCGGAACGTGGTGCTGACGTCACCGGCCCAGCCAGGTGGCATTCCGAGCAGCAGAAGAGGCGCATTCGCCTCCTAGTAACCGTATAACGGGTCCGAGAGGAGCAGCTCAACATGTCTTCGGCGCAGGTCTCCTCGTCGAGGAGACAGTCGTGTTATCTGTGCGACCTGCCGCGCATGCCGTGGGCGATGATTTGGGATTTTACGGAGCCCGTGTGCAGGGGTTGCGTGAATTACGAGGGCGCGGATCGGATCGAGTTTGTTATCGAGACCGCGCGCCATCTCAAGCGGGCTCATGGCTTCCAGGAGGGGAGATCCCCGGGTCCAGCGCCGCCGCCTGCGGTCAAAGCACAAGCGGTCATGTCATCCAAGGAGTCTGTGCAGATGAACCATGTGGACGGCTCGTCTAAATCGCAACAGCAGCAGCAGCAGCAA[C/T]AACAACAGTCCGGCTTGGACCGATACGCGCTCGCCACCGAAAGATCACGCTTTGATTATTCCAGCATCGGCGCGCACAGGCTTCCGAACGGGCTCGGTGGACCGAACGGCTTCCCCAAATCAGACGACGGACCCCCCGAGCTTAACCGACAGAGCCCGAACTCGCGTCGCAATCACGGGCTGGTGGCGGTGTCGGGGCAGATGAGCGTGCCGCCGAACCTCCTCCCGCAGACGCTCCTGAACGGCCCACCGTCGTCGGCGAGTATAGCGCAGCACAGCCTTTCCGGACGAGCCCCTCCAGCCCCGGCCAGCATCGGACCCGCGCTCGCGCTCTCTGAACAAGGTAAACGACCCGGCTCGGTGTCCAGCACGGACCAAGAGAGAGATCTGAAAGAGAAACAGCGTAACGCTGAAGCTTTGACTGAACTCGGTGAAAGTTTGAGGAACAGGTCAGAGGAATGGACGAATAAACCCAAAATAGTGAGAGACACACTGATCACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28815
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 |
---|---|---|---|---|---|
ENSDART00000015418 | Nonsense | 110 | 661 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 11192968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 11175490 |
GRCz11 | 17 | 11329556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGGACGGCTCGTCTAAATCGCAACAGCAGCAGCAGCAGCAACAACAA[C/T]AGTCCGGCTTGGACCGATACGCGCTCGCCACCGAAAGATCACGCTTTGAT
Long Flanking Sequence:
GTTAGCGCATGCGCACTCGCATGGCAACAAGTGGCTTGTCATTTGTAACAGAAAAAGGAACTGCGGAACGTGGTGCTGACGTCACCGGCCCAGCCAGGTGGCATTCCGAGCAGCAGAAGAGGCGCATTCGCCTCCTAGTAACCGTATAACGGGTCCGAGAGGAGCAGCTCAACATGTCTTCGGCGCAGGTCTCCTCGTCGAGGAGACAGTCGTGTTATCTGTGCGACCTGCCGCGCATGCCGTGGGCGATGATTTGGGATTTTACGGAGCCCGTGTGCAGGGGTTGCGTGAATTACGAGGGCGCGGATCGGATCGAGTTTGTTATCGAGACCGCGCGCCATCTCAAGCGGGCTCATGGCTTCCAGGAGGGGAGATCCCCGGGTCCAGCGCCGCCGCCTGCGGTCAAAGCACAAGCGGTCATGTCATCCAAGGAGTCTGTGCAGATGAACCATGTGGACGGCTCGTCTAAATCGCAACAGCAGCAGCAGCAGCAACAACAA[C/T]AGTCCGGCTTGGACCGATACGCGCTCGCCACCGAAAGATCACGCTTTGATTATTCCAGCATCGGCGCGCACAGGCTTCCGAACGGGCTCGGTGGACCGAACGGCTTCCCCAAATCAGACGACGGACCCCCCGAGCTTAACCGACAGAGCCCGAACTCGCGTCGCAATCACGGGCTGGTGGCGGTGTCGGGGCAGATGAGCGTGCCGCCGAACCTCCTCCCGCAGACGCTCCTGAACGGCCCACCGTCGTCGGCGAGTATAGCGCAGCACAGCCTTTCCGGACGAGCCCCTCCAGCCCCGGCCAGCATCGGACCCGCGCTCGCGCTCTCTGAACAAGGTAAACGACCCGGCTCGGTGTCCAGCACGGACCAAGAGAGAGATCTGAAAGAGAAACAGCGTAACGCTGAAGCTTTGACTGAACTCGGTGAAAGTTTGAGGAACAGGTCAGAGGAATGGACGAATAAACCCAAAATAGTGAGAGACACACTGATCACGCTTTCT
Associated Phenotype:
Not determined