ZMP
si:ch211-204d2.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A9C3U2]
Human Orthologue:
C10orf18
Human Description:
chromosome 10 open reading frame 18 [Source:HGNC Symbol;Acc:23484]
Mouse Orthologue:
BC016423
Mouse Description:
cDNA sequence BC016423 Gene [Source:MGI Symbol;Acc:MGI:2145274]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21207 | Nonsense | Available for shipment | Available now |
sa16911 | Nonsense | Available for shipment | Available now |
sa9993 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21207
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111957 | Nonsense | 1512 | 2967 | 17 | 24 |
ENSDART00000137039 | None | None | 175 | None | 6 |
ENSDART00000141560 | None | None | 104 | None | 2 |
ENSDART00000147817 | None | None | 1186 | None | 6 |
The following transcripts of ENSDARG00000074168 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 11520423)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11148701 |
GRCz11 | 8 | 11186406 |
KASP Assay ID:
2260-0197.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCAACAAAGCATTCATCTGCTGGGACAAGTGGCTCCCCAAGTCAAGTT[G/T]AAGCCTTGATGGTAACTGTATTGTACAATTTTTGTTACACTGTTCACAAT
Long Flanking Sequence:
TGGTAACCATTCCAGTCATCATAATCAATAATTACACATTCAGCATTTGAATTTCCAAATTTCTTTTTCTTAATGTTTACAGGAAATGGAACTTCAATATTGAAGACACCTTTGAGGATGTTCATCTCATTTTTCACATGTGGATTGGTCTTTTCTATAGTAAATCCACTTCCAGATTATTTCACCTTGAAAATAGTACTATACTTCCAAAGGGGAAGGATATAGAAAAGGTCCATCTGGATAAAAATGCCATTCAGAGTGCGGTGTCATTGCTCAATGTTGAGTTAAACACGAAAGAAGGCTCGCCCAAGCCTGCACATCTGTCATCAGGGGTTTTAGATCTATCTGTGAAAAATGGTGAGCCCGTGACTCCCTGTTCAATCTCAGATCAAAGCAGAACAAAGGACACCGCATCAGAGCCTGTGGGAATATCATCTAAAAAACATGAAACGCCAACAAAGCATTCATCTGCTGGGACAAGTGGCTCCCCAAGTCAAGTT[G/T]AAGCCTTGATGGTAACTGTATTGTACAATTTTTGTTACACTGTTCACAATATATAAACTGTTCTGTGCTATTCTCAGTTATTTTTTTCAGCATGACTGTGCAATTTGATGTTGATTTTGATTTATTATGTTACAGAATTACAGATCGGCTGTTGACACGCCACAGGAAAAGTCAGTGCCTGACAGTGACACGGACACTGATGAAGAAAATGATATCGCCACTGACCACTCCTATTCTCAGATTATGGAAGGAAACAGTGCGTACACCCAGTTGTGTGATCAAGCATCAAATATGAGAATAGGTGTCCGGATACATCTGCCAAAGATCAGAAGCGTTTCAAATAACAAAGCATCCACTTCGGATCCTAAAAAAATCTGTGTGTTCCATCAAGTACTTAAACCGGCAGAATTCTCAAGTCCAAGTCGGCTGATTTTGGGACAGAAACATTTTGATTTAAGTTTAAATAACAAAACTGACCATGCAACACAGCAAAAGAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16911
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111957 | Nonsense | 1548 | 2967 | 18 | 24 |
ENSDART00000137039 | None | None | 175 | None | 6 |
ENSDART00000141560 | None | None | 104 | None | 2 |
ENSDART00000147817 | None | None | 1186 | None | 6 |
The following transcripts of ENSDARG00000074168 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 11520657)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11148467 |
GRCz11 | 8 | 11186172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGACACGGACACTGATGAAGAAAATGATATCGCCACTGACCACTCCTA[T/G]TCTCAGATTATGGAAGGAAACAGTGCGTACACCCAGTTGTGTGATCAAGC
Long Flanking Sequence:
ATCTGGATAAAAATGCCATTCAGAGTGCGGTGTCATTGCTCAATGTTGAGTTAAACACGAAAGAAGGCTCGCCCAAGCCTGCACATCTGTCATCAGGGGTTTTAGATCTATCTGTGAAAAATGGTGAGCCCGTGACTCCCTGTTCAATCTCAGATCAAAGCAGAACAAAGGACACCGCATCAGAGCCTGTGGGAATATCATCTAAAAAACATGAAACGCCAACAAAGCATTCATCTGCTGGGACAAGTGGCTCCCCAAGTCAAGTTGAAGCCTTGATGGTAACTGTATTGTACAATTTTTGTTACACTGTTCACAATATATAAACTGTTCTGTGCTATTCTCAGTTATTTTTTTCAGCATGACTGTGCAATTTGATGTTGATTTTGATTTATTATGTTACAGAATTACAGATCGGCTGTTGACACGCCACAGGAAAAGTCAGTGCCTGACAGTGACACGGACACTGATGAAGAAAATGATATCGCCACTGACCACTCCTA[T/G]TCTCAGATTATGGAAGGAAACAGTGCGTACACCCAGTTGTGTGATCAAGCATCAAATATGAGAATAGGTGTCCGGATACATCTGCCAAAGATCAGAAGCGTTTCAAATAACAAAGCATCCACTTCGGATCCTAAAAAAATCTGTGTGTTCCATCAAGTACTTAAACCGGCAGAATTCTCAAGTCCAAGTCGGCTGATTTTGGGACAGAAACATTTTGATTTAAGTTTAAATAACAAAACTGACCATGCAACACAGCAAAAGAAAGATGTGTCTGACAGTTCAGACAGTAAAGGGATTTTTAGATCACATGGAATGAAAGAAGGTTGCCCAAAAAATATGGCTGACGGAAATCTTGACAAGACTTCAGAATTTAAAACTGGAGACACAGCCTCTGTTTCTTTACAAAAACAGAGTCCATCTGCAACTGCAGAGATTGAAAAGGTCTCTGATGAAGATATCCTGAATGAACCTCTGACGATTGTGGAAAACATGACTTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9993
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 |
---|---|---|---|---|---|
ENSDART00000111957 | Nonsense | 2188 | 2967 | 19 | 24 |
ENSDART00000137039 | None | None | 175 | None | 6 |
ENSDART00000141560 | None | None | 104 | None | 2 |
ENSDART00000147817 | Nonsense | 407 | 1186 | 1 | 6 |
The following transcripts of ENSDARG00000074168 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 11522751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 11146373 |
GRCz11 | 8 | 11184078 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACAGCATGTGCTCTACTCCTACTCAAGATGAAATTCCTGAAATATGTTA[T/A]CCAGAAGTAAACAAAGAGTTGAGGGTAGAAGATCTGGACAGAAAACTKTG
Long Flanking Sequence:
TATAATATCCTTCAAGAATTTGCTAATGATTCATGCTCAGATGAGGATCAACCCATGCCTGTTCAAGGTAAACAAACCTCAGATTCTACTATTGATCCTTTTAGATTAATAAAAGACCAACATGATTTCAAAATCCTTGAGCAGAATTTAGTGGCCTCAAATGATGTTCTTGACACTTGTCAGTATGATTCAAAACAAACAAGTGCTGTTGAAACCACTAAATTAGATCTTATTCTATCAGAAACAGAGGACGAAGAGGAGGTAGGCCAACAAGATGTATCTGAAGCCAGAAGGGAGGAGGATACACTTGTTGAGAAGATTGAGACACAATCCATTCAGCGTTTGTCTCCCAAAATTGGTGTATCTCTCCCCAAAACAGTGACTGAATCTACTATTGAAATGTTTGCTCCTCAAGATTCGAAGAATGACAAACCTTCAGAATTGGAGATAAACAGCATGTGCTCTACTCCTACTCAAGATGAAATTCCTGAAATATGTTA[T/A]CCAGAAGTAAACAAAGAGTTGAGGGTAGAAGATCTGGACAGAAAACTGTGCTTTCCTGACAAAACTGTAGCTCATCACAATGATGTGTTGCCACTTGAAAGTCTTGAAAGCTCCCAAACTTGTGTTTCTACCCCTAAGCCATTTTCTGATCTGATGGGACATTATGAAGAAACCCATCATGATGAACCAAGGTGGAAGATGAGCAAATGCCCAGAAGCAGAGGCCTTTAAAGATAAATCTGATTCAACTACTGAGGATTCGTCCAGTGAGGACTCTTTCCAGTTAAGACACAAACTCTGTCCCAACTACCATGAAAAAGATAACAAGAAATATGACTTCCGACAGGGTGCATCTCAAAATGATTCAGAACTATTTTATGGTCATGATAACGTAGATGATTATTATGACTATTACCATGGAACTGATGAAGGTTTACAATGGTATGATTACCAAACAGAGGAACCAGTTGTTCATCCACGTGAAAGCGACTTTAGTGGTGA
Associated Phenotype:
Not determined