ZMP
zgc:158327
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100009645 [Source:RefSeq peptide;Acc:NP_001076483]
Human Orthologue:
C14orf49
Human Description:
chromosome 14 open reading frame 49 [Source:HGNC Symbol;Acc:19861]
Mouse Orthologue:
4831426I19Rik
Mouse Description:
RIKEN cDNA 4831426I19 gene Gene [Source:MGI Symbol;Acc:MGI:2442408]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10496 | Nonsense | Available for shipment | Available now |
| sa44870 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa13773 | Essential Splice Site | Available for shipment | Available now |
| sa17025 | Essential Splice Site | Available for shipment | Available now |
| sa6466 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10496
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 |
|---|---|---|---|---|---|
| ENSDART00000033706 | Nonsense | 94 | 1038 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 15752354)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15903182 |
| GRCz11 | 17 | 15911115 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATTAAAGAATCAGACTCATTSCAAACTCAAAGATYTGAAGGCKTTTTA[T/A]GATGACACGTTAACTTACATCATTCACTGTCACAGGTACAGACTGAGSAT
Long Flanking Sequence:
CACTTGTGGCTAATAGAGAAAGTAAAGTAAAGCAAATGTTAGCGGGAAACAGAAGTTTTTAAAATTTCATTAGTGATTGGTACTGAACTCAATACTTTTAACAACCCTGCTGTTAGTAAAGCTTTACTGTAAAGAGTTACTCAAAAGGCCTGTAAATAGTCACAGAATCTTTAATATGGAAGGCTAGATTAAATGTTCAAAATGGTCAGGTTAAAAATAAATTAGACTTTTTAAAGGTTTAAAACGCTTTTCTAAGCATCTGTTGCTTTGATGAACAACCACTGCCAATACAACAATATCAATATTTTTACATACTTTCTTATATATTGAATTATTGAATATCGACATATGTCTGCCTTTTAGAAAATCCACAGCTTGGAGCCTGACGGCCAAGTGAAGATGGACCGAGTGCTTGTTGCTTCTGAAGCACTTCTTCGGAATGGAGATGAAGAATTAAAGAATCAGACTCATTGCAAACTCAAAGATTTGAAGGCTTTTTA[T/A]GATGACACGTTAACTTACATCATTCACTGTCACAGGTACAGACTGAGGATAGTGAGGATAATGACACAAAGATATTTATCGTCAACGTAATGTCTAAGGGAAACCATTGTTTTATTTTCTCAGTTTATTAGTGTGATCTCTTTCATGCTCTCTGACAGTCGTATCGAGTGGGTTTGGCTGCACTGGAGTGAGTACTTAAAGGCTCATGAGGAGTTTGGCCTGTGGCTGGAGAAGATGCACCGCTCTCTGGAGCCTTTGCTGGAGATGCAGCTGGGTCTGCAAGAGAAGCTGTGGCAGGTGGATCATCTGCGGGTTCTCCACAGCGACATCCAGGGCCAGGCCCAGTTTCTGGAGAGGCTCCTGGATGAGGCCGCAGCTCTGTTCAACCGTACAGGAGACCCAAGTGTGGATGAGCAGACTCAGCAGGGTCTTCAAGAGGCCTACAACCACATTCGAGACCGAGCACAGGTAAACCTGCCTCTCTTTAAACCAACTAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44870
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033706 | Essential Splice Site | 106 | 1038 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 15752512)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15903340 |
| GRCz11 | 17 | 15911273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTATTTTCTCAGTTTATTAGTGTGATCTCTTTCATGCTCTCTGACA[G/T]TCGTATCGAGTGGGTTTGGCTGCACTGGAGTGAGTACTTAAAGGCTCATG
Long Flanking Sequence:
GTCACAGAATCTTTAATATGGAAGGCTAGATTAAATGTTCAAAATGGTCAGGTTAAAAATAAATTAGACTTTTTAAAGGTTTAAAACGCTTTTCTAAGCATCTGTTGCTTTGATGAACAACCACTGCCAATACAACAATATCAATATTTTTACATACTTTCTTATATATTGAATTATTGAATATCGACATATGTCTGCCTTTTAGAAAATCCACAGCTTGGAGCCTGACGGCCAAGTGAAGATGGACCGAGTGCTTGTTGCTTCTGAAGCACTTCTTCGGAATGGAGATGAAGAATTAAAGAATCAGACTCATTGCAAACTCAAAGATTTGAAGGCTTTTTATGATGACACGTTAACTTACATCATTCACTGTCACAGGTACAGACTGAGGATAGTGAGGATAATGACACAAAGATATTTATCGTCAACGTAATGTCTAAGGGAAACCATTGTTTTATTTTCTCAGTTTATTAGTGTGATCTCTTTCATGCTCTCTGACA[G/T]TCGTATCGAGTGGGTTTGGCTGCACTGGAGTGAGTACTTAAAGGCTCATGAGGAGTTTGGCCTGTGGCTGGAGAAGATGCACCGCTCTCTGGAGCCTTTGCTGGAGATGCAGCTGGGTCTGCAAGAGAAGCTGTGGCAGGTGGATCATCTGCGGGTTCTCCACAGCGACATCCAGGGCCAGGCCCAGTTTCTGGAGAGGCTCCTGGATGAGGCCGCAGCTCTGTTCAACCGTACAGGAGACCCAAGTGTGGATGAGCAGACTCAGCAGGGTCTTCAAGAGGCCTACAACCACATTCGAGACCGAGCACAGGTAAACCTGCCTCTCTTTAAACCAACTAAAGTCAAAGATTTTACGGTGGAACTTCATTTGGTTGCATGTTATTTTACAGTATGAGTGCTTTATGTGTTCTTCCAGTGTATTTACCTAAGCAAGTATTAGGTTACAGTATATAAGGTAACTACAAGGTCTGCATTGAGCTAATAAAAGTATCTTCTCTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13773
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033706 | Essential Splice Site | 541 | 1038 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 15772824)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15923652 |
| GRCz11 | 17 | 15931585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAGAGTTACTCCACAGCCAGCTCCAGCAGCGCAAGAACCGCCTGCAGG[T/C]ACACCAACAGCCTCCGCTCGCAATCTGACCGTAAATGCCTGCGATACAGT
Long Flanking Sequence:
TGGCTTCCAGTGAATCGCTCTTATATCAGGCTTTTGTTGCGCCGTCATGCAGAGATCTGAACTGTACTAAAGATCAGCTTTTTAACTCTTGACTGTTGTTTGATGTTCTAACATTCTGTATTTTTGACATTTGATTTCCACTTTGTTTCTTAGAAAATAAAGGTTACGGATCCTGTTTATTTTGTGGATGTGATTATATTGTGTTTTAAGCATTTGTAGCGCTTCATCTCGACGGTTTAATTCTGTGTTAGTGCTTTGTTGGCTTTGAAGTGATCGTGTGTGCTCCTTCTTCTGTTTTGTTTTTGTTCTTTTGTAGAAGTTGCTTAAAAACAGCGTGCAGCTCCAGGAGCGCTTGAGTTTGCTCCAGGTGAAGAGTGATCTGCTCAGCGCAGTTTTTGGCCAGGAGAAAGCTGAAGATCTGTTGGGGGAGCTCAGCGGGGATATGAGGAAGAGAGAGTTACTCCACAGCCAGCTCCAGCAGCGCAAGAACCGCCTGCAGG[T/C]ACACCAACAGCCTCCGCTCGCAATCTGACCGTAAATGCCTGCGATACAGTAACAGACTTTACACCTGCTGTTAGACATGCAGCATGTAGAGTCTTGCATAGTCGTGCATAACAAAAAAAAAATTATCATTTTGATCAGAGCTTGTCTTGTCCAGCTGGAAAAAAAGAGAAGTGTGGAGATGGTTAAGATGTGTGGCTAATAAAATCAACATAGTCTGTAATTGATAGCCCTTTTTTTTTTTTTTTTTTTTGTTGTTATTTTGTGTTATTTTGTTTTATTCTATTTAAATTTATTTTGTTTTGTTTTATTTTGTTCTATTTAGTTTTATTTTGTTTTGTTTATTTTATTTTGTTTTCTTTTATTCTGTTTTGTTTTATTTTTATAAGAACAATTGTTATTTTATTTTATTCTATTTCGTTTTATTTTTAGTTTTATTTTATTCTATTCTATTTTGTTTTATTTTATTTTTATTTTATTTTTGTTTTTTTTTGTTTTTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17025
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:
G > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000033706 | Essential Splice Site | 746 | 1038 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 15782323)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15933151 |
| GRCz11 | 17 | 15941084 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCGAGAGTCCTGGATGTCCCTCCAMACGCTCAGTCTCAATCTGTACAG[G/C]TTAGGAGATGAAGTRATTTCTTTTAYAGAGGTTGTTGTTGSGATTCAGTG
Long Flanking Sequence:
AAAACTTGACAAACATATTTAATTATTAATTTTAAACAGTGTCAACAGCAGATATCATCTAAAAAAGTTTTTAAAAATTTTTAATTACTGTTACAAGTAAAAATAAATGTTAATTGTTAATGTATACTTTTTGTCCTAAATCATTTTATTAATTTTTTTTTCACTATTTTATTAAGAGATAAATAAAGTTTATACTGAGGGCTTTAAAAAAAAAAGAAGAAAAAAGTATGCCATATTTTTTGTCATGTCACATAATCAAAGGAATGCTTGCCTGTGCATTGCATTATTTGAGATTCTGCCTTGCATATAACTGTGTTTGTCCTCTAGAGGGCGCTAGGAGAGTTTCCAGAGAAGGAACTTCAGCTTCATCAGACAGAGGCTCAGGGTCATACTGTGCTGGCCAAAACCTCGGAAGAAGGCAAAGTGCACATTCTGCAAGACCTCAAACGTCTCCGAGAGTCCTGGATGTCCCTCCACACGCTCAGTCTCAATCTGTACAG[G/C]TTAGGAGATGAAGTAATTTCTTTTACAGAGGTTGTTGTTGGGATTCAGTGGAGATAAACTGTGACTCAAGTGTAATTAAGATATACATTTACCAAACCCGTTGAACAAATCTCGTTCCAAGAGACATATTTCACATTGAGTTTAGATTGATTGCTCTGTAAATCATTGCTGTGTTTACAAGGATTTTTTTAAGCTGTGTCAAACATGTTTAAGCTGTGACTTTCTAAAAAAAAGTAAAATAAAAATCCATTGTAAAAACCAAGCAGTTTTTTGTTGGTCATCTAAACATGGACATCTTGGTTAAAACAAGGGCTGTCAGTGAAATCTTATAGATGTCCAATTATAGTCAATAAATAGACTAGTCATCAAATAGACAGATCAGATGAACTTCACAATTGTAGTCATTCTGTTATTTCTGTTTGATGACTAAACAGACTAAAAAGATTAGACATCTATTACAAACACACAAAAAAAGTGCTTGCTGGGAAGTGAACAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6466
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 |
|---|---|---|---|---|---|
| ENSDART00000033706 | Essential Splice Site | 971 | 1038 | 15 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 15787075)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15937903 |
| GRCz11 | 17 | 15945836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGATCCCTGAGCGCTAAAGAACTGAGGATAAGACAGAATACACTCAAG[G/A]TTGGTGGTGTTTGTTACAWTTTTTTTTWTTTTTTGCTTTCTTTTTTWTCT
Long Flanking Sequence:
TGTACCAAATTGTGATTTTAATTTAATGGTAAATAAATAGGAAAAAAACGAATCATTTTAAATTTGTAAATTTGACAAATTTTAAATTTGTAAATATGTACGAATCATTTTAAATTAAAATTTGGATTTGTACTGTAATTTACTACTAAGAGAAAAACTTTTAAGGTCATTTCAGACCAAATACATAAAAAAAGAAGTGAAAATTCATCAAAAGACTTGGAAAAACATCAAAATAATTTTTTTAGCTAGATCACCCAGCCCTGAAGCCACTATTAAGCGAGCGATACCTTAGCTGCAATCATAATCGGACAGAGGGATGTTTCTTTTCATTCCTCCCGCAGACGGGTTCTCAGGGGCCCCGACGTCCTGCTGATACGGAGGCCCAGAGGAGCCAGTTTGAAGCGTGGCTTCACAAGCAAAACGACAAACTCACAGGAATTTTGAGCAACCAAAGATCCCTGAGCGCTAAAGAACTGAGGATAAGACAGAATACACTCAAG[G/A]TTGGTGGTGTTTGTTACATTTTTTTTTATTTTTTGCTTTCTTTTTTATCTGTTTTTGATTAAAGTTTCATGTCGAGTCCAAAATATCAAAAAGTGTTAGCGTAGAAAACAATCTTTGATAGCTTTGATATCTTATTCAACAAAGCGCAGTGTGATGTTTTACTTTGGTCACACTCAGAACATGCTGGATCATTTTTCAGTATATGAAGACGCATGTCTGTGTGAATCTGGTGTGTAGAGTGCCATACGTACCTTTACATCAGTGCAGTTGCTGATCTGTGAAGCTCTTTTGAAGGCCGGGCTCAGGTTTTTTACCTCAGGCTTTGAGAAATTCAAGCTTTACAACTACCTAGAATCTGTCACATCTGATGATAGCTGAGCTGACAGACTCGGCGTCATGCTGTTTTTTTGTTCAGTCACAGCTTCACAGCTCAGATTTGAGAAAGCTTTTAAACGGCGGTTCATATGCGGTCTTCCTGTTGAATATGCCATGCAGATAGA
Associated Phenotype:
Not determined