ZMP
si:dkey-73n10.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A3KQ83]
Human Orthologue:
C15orf39
Human Description:
chromosome 15 open reading frame 39 [Source:HGNC Symbol;Acc:24497]
Mouse Orthologue:
1700017B05Rik
Mouse Description:
RIKEN cDNA 1700017B05 gene Gene [Source:MGI Symbol;Acc:MGI:1921461]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23281 | Nonsense | Available for shipment | Available now |
sa9924 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23281
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 |
---|---|---|---|---|---|
ENSDART00000100458 | Nonsense | 314 | 986 | 2 | 4 |
ENSDART00000139015 | None | None | 160 | None | 2 |
ENSDART00000141378 | Nonsense | 88 | 760 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 18719784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18950007 |
GRCz11 | 18 | 18939073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCGTGCCCCAGTTCCTCCACAGATGTACAAGGGATATCCACATGCTTA[T/A]GACCCAAGGACATTGGCACACCCTGAAGTTTCTTCAAAAGTGTATCAGGG
Long Flanking Sequence:
CCAAGACAGCACAGTCCAAGGGCAGCAAGAGTTGTCTCGCCAGTGGCAATTCCTAATGGTCATATTAGAGGCTCTGATGCAGAGAGATGTGTTGGATTGGCTATTCCAAAACCAGTATACAGTCATAGCCCTTGCTGTACTGAGCGTGGCTGTACTGCCGGGCACAACTATGGCATGGAACATGGCCCGCATAGGATGTCCCCTCACATATATGATGAGGATTGGGCTGCTCATTATAGCCGCCTGGCTTATCTGCATAAAAAAGGCCAGGAAGCACTGGCACAACAGAGGGGTTTGCAGTTGGAGCATGGTGTGGAGGGTATAAAGGATGGAAAGACCGGGGGCTACAATACTGGATCGAATGGGCCAAGGAGGCCACTTCCTGTAATGGAACCAAGCTATACTTATAATGCTCCGCATCCATTTATTAGTGCCACACCAGAGTATTGCCATCGTGCCCCAGTTCCTCCACAGATGTACAAGGGATATCCACATGCTTA[T/A]GACCCAAGGACATTGGCACACCCTGAAGTTTCTTCAAAAGTGTATCAGGGTCGTTCCCCCATATCCAAATACACACCAGTGCCTCCATGTCCCAATATCTATTATCCTCAGAGTCACCCTGAGACTTACAGAACCAATTCCAGTGCTCTTACAAATGAGCATGGTCAGCGCCACCACATGGGTCAGTTTCATTCGCCTAGAACAGACTTGATATCACCACCCTGCTCTGCTGTGCCCACTCACCATCCACTGATCTCAAAATATTCTTCTTATCATCCATATGGGGTCCATTTAACTACTAACCAAGCACCCACCAATGAACAGACACATCCACCTTTTCCAGTGGATCAGTCAGAACGGCCACTTGATTTCTCGACACGAAGGGTCCAGACACCAGACTCTCCTCGAGAGCTTTGTAAAACATATGGAACTTCTGGGGCTTTCCATCCTACTCTATCCCACAACAGATGTCTCAGTAATACCCCTACCACTGAACACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9924
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100458 | Nonsense | 956 | 986 | 2 | 4 |
ENSDART00000139015 | Nonsense | 113 | 160 | 1 | 2 |
ENSDART00000141378 | Nonsense | 730 | 760 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 18 (position 18717858)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 18948081 |
GRCz11 | 18 | 18937147 |
KASP Assay ID:
2261-2073.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTCAAAACTCCGGAGACTTCTGTCCCTTAAACACCTGCCTGACATATA[C/A]CCTGATGTCCTCAACCTCCTCTACTATGCCAATGTCTGCAAGTTCCTCGG
Long Flanking Sequence:
ACTAGCAGCAAGCATGCCCGTTATCAGTTTATGGAGCTTCACCAGTCCCTCTGTAGACTTTTACACTGCAATGTTACTCAAACCCCATGTCAGGTGCTCAGGGACTGGTTATGCAAACTGGACGTATGTGAGTCAGGCAAAGCTCAGAAAGTTTCTTGCCTCTTGGGGTCAAAAATGAGGGAAGTGTGGCTTAAAGGGGATGAGATGGAGGTGGCTCTTCAAAGGGTGGTCCGCCAGCTTCAAATGTACATTGACATCAGTGAATGCCCCTTTCCTCATGTCATGAGGGCTGGTGCTGTGTTCGTTCCCATGTTGGTGGTCAAAGAGGTGCTGTTTCCTCAGGTTCAAGGCACATATATAGACCAGGTTCTTCAGGAGCATCGGGTGGAGCTCCGGCCCACCACGCTCTCAGAGGAAAGGCAACTCACTCAACTCCACAGAAAGGCTTTCTCTTCAAAACTCCGGAGACTTCTGTCCCTTAAACACCTGCCTGACATATA[C/A]CCTGATGTCCTCAACCTCCTCTACTATGCCAATGTCTGCAAGTTCCTCGGTGAGTGCTAAATGCTTGATCATTGTTAATTGCATAAGAACTCCTGGTTGTTTAGTGTTGCAGTAGGTGAATTTTGCATTTGTGAGCTGGGCTCAGATTACAGGAGTTTCTAACCAATTCATCCCACATGTGAGTAGGAATTTAACAGATTGTCTTCCCTCAAATCTCTAAGATGCACATGACAATCTAAAAATTGTGATGCATCAAACTTTACAAGAAACTATTAAGTTTATCATGGCAGAGTAGACGTGACAATATTCAATTAATCAATATATCATGAAAATGAACATGCTCTATATTGATATCATAGGCACTTTAGAATACATTGAGTTATTTATTTTTACATCATTATTTATTTATTTATTTATTTTATTTTAGGAAATGAATGTTGTATTTGCAGTGGTGTTATAACAGCCCCAAATGCTTGGAGACTTAATTGTTTAGCTTAATA
Associated Phenotype:
Not determined