ZMP
zgc:100980
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC437012 [Source:RefSeq peptide;Acc:NP_001002739]
Human Orthologue:
C17orf28
Human Description:
chromosome 17 open reading frame 28 [Source:HGNC Symbol;Acc:15736]
Mouse Orthologue:
C630004H02Rik
Mouse Description:
RIKEN cDNA C630004H02 gene Gene [Source:MGI Symbol;Acc:MGI:2445087]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35375 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa24922 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35375
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027032 | Essential Splice Site | 624 | 803 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 12 (position 47635708)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 46264947 |
| GRCz11 | 12 | 46565939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACCAGCTCAAACAGGCACTCTGAACGCAAGCTTGAAGGACATACCAC[G/A]TATGTGAATCACAGCTTCTGTATGTTAATAAGTATAAATTACAACAGGGT
Long Flanking Sequence:
TTTACTAGATATTTTTCAAGATTTTAGTATTCAGCTTTTAAAGGCTTCACTAGGTTAATTAGGGTAAAGTTAGGGTAATTAGGCAAGTTATTGTATAACAGTGGTTTGTTCTGGAGACGATCCAAAACTAACATTGCTTAAGGGGGCTAATAATATTGACCTTAAAATAGGTATAATAAAATTATAGGCGAATAATTGACTTCAGCTGTATGAGTTATTAATAAGTCTGAAAATAAGTGCTTGTACGTGTCTGTAAATATCAGGTAACTCTAACCTGGTGTACGGCATCATCCGCAAGCGCAGCCTCTTCCACCAGCTGGCTAACTTACCCACAGACATCACCCTCATCCAGAAAGCTCTGCAGAGGAAAAAGAGCAGGAGCAACAGCATCCATAATGCAGTTTTCATGGAGATCAGCAACCCTTACAGCAGCGAGGGTCTGAGTAAAACCACACCAGCTCAAACAGGCACTCTGAACGCAAGCTTGAAGGACATACCAC[G/A]TATGTGAATCACAGCTTCTGTATGTTAATAAGTATAAATTACAACAGGGTTGCCAGGTCCAATAAAAGTTTTCACCCCATTGACAACTTAAAAGTGTGCAAAACAAGTTAACAGTAGCCTGATTTTGTTTGTTTGTTTGTTTGGTTGGTTGGTTGGTTTTTGCTTTGACAAATAATGTATTTCAACCATGTTAACAAACTAATATAGTTTGTATTAATCAAACCAAAGTGTTGCCAAATGTTTCACTTCACTAATTTCACTTTTTGTTTTGATTTGTTCTGTTTTTGTTCTGTTTTTAAATGATAATGATTTATTTTAAAGATATTATAAGTGACTTATTTTTCAAAAGGTTTCACAGGAATGCATTTTTGAAGATATTGCATTAAAAACATGTATTTATTTATTTTTTTTAAATGCACATCAAAAATATATACTCAGTTGAGACAGAAAAGACATGCATGCATGCACACAAACACCATTCATTCATTTATTCATAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24922
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000027032 | Essential Splice Site | 783 | 803 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 12 (position 47649407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 46278647 |
| GRCz11 | 12 | 46579639 |
KASP Assay ID:
554-7482.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTACATGTTAAAATGTGGTATAACATGATGTGTTTGTTGTTGTTTTA[G/A]TAATGTGGATCCTCCTGTTTGGTACGACACTGATGTCAAGCTGTTTGAGA
Long Flanking Sequence:
GCACAAATGATCAAATTCTTAAAGTTATACACAAGCAGGACCTTCACATTAATCTAAAAGTTTGGAAATTGAACACAAATAGACAGTTTTAAGGGTCTTTTTATTAGTAATATGTTCAATAGTAAAGAAGTATTTTTTTTCAATTGCTTAAACACAAGAAAGCGGAGTTTCTATTGGAAAATTTACACTTATGAATATGAAAAATATCAACTAAATAATCAAATACATTAGCCTTCCTGTAATTTGTTTTCTTTCAAATATTTCCAAAGTTATATTTAACAGAGCAAGGAATTTTTTTTACAGTATTTCCTAAAATGTTTGTTCTTTTTTTTCCTCTGTGGACCCGTTCAGTGAAGTGTATTAAGTGTACATTACATCATCACACCCAAAAGCATGAGTGCAAAAAGCAGCACAACTTACCTTTTATATATTCAGCTCTATTTTTGAATGCATGTACATGTTAAAATGTGGTATAACATGATGTGTTTGTTGTTGTTTTA[G/A]TAATGTGGATCCTCCTGTTTGGTACGACACTGATGTCAAGCTGTTTGAGATCCAGAGAGTTTAATGACAGAAGAAACTCTGCACAGCCTTTTCTTTACCGCTGAACACATTGTGGATGATGAATGAGCTCTGCATTTGTTCTCCAAAATCGAGTTCAATGAAGTCTAAGATGTCCTCTTATTTTTTTTCTTTGTTTCTGGTGTATATATTGGCACTGTTGTTTCTGAAACATGCTGTTTTATTTTCCACTGAGTCAAACCGTGAGAAAGACACGCACTTGATTTCATGAGCAATGGGTTGTCTTTCTTTTTGTGTGTCTGTCTGTATCTGTGCGTGTTATTTTTACTGTAATACTCTTCTGCAGGTGGAGGACTGAGAGTGACTTCTGCATAAATGAAGCACAAAAAATGTGCAAAAGCTGCAAACTTAAATGCTGCATGTACAGAAATACTATAAAAATATTCATAAATGCGGTTTTGTTTACTTTATTTGCAAATGCA
Associated Phenotype:
Not determined