ZMP
si:dkey-171o17.5
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC557839 [Source:RefSeq peptide;Acc:NP_001082846]
Human Orthologue:
C1orf125
Human Description:
chromosome 1 open reading frame 125 [Source:HGNC Symbol;Acc:26564]
Mouse Orthologue:
9430070O13Rik
Mouse Description:
RIKEN cDNA 9430070O13 gene Gene [Source:MGI Symbol;Acc:MGI:1924602]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37485 | Nonsense | Available for shipment | Available now |
sa755 | Nonsense | Available for shipment | Available now |
sa10715 | Nonsense | Available for shipment | Available now |
sa18502 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37485
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090069 | Nonsense | 247 | 1007 | 8 | 25 |
ENSDART00000136908 | None | None | 364 | None | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 17463410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17215168 |
GRCz11 | 22 | 17241438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGTATTTCTATATTATTTTTCAGATCGAAAATTTACTAGAGCTGATT[C/T]AAACTGAGCAGAACATCTACAATATAGTGTTTCATGAGGTAATCCGGCAG
Long Flanking Sequence:
GTTTCAAAAACATAAGGCAAACAAAAAGTGAACAACTAATCTTATTATATAACTTTAAAATATCGGAAAAGTTTGAACTGATCTCTGAACTTTATTAGTCAACTATCCTTTTCTATTTATATATAAAAAAACATGCAAAAAGCAACTAACTGAACATTAACCAACATCAAAATACCAGTAAAATAATTTTAATGTGAAGTGATTGCACCAGCATAATCCAAATAATGCTTAATTTATCGGCTTTAAGCTATAGGCCTAATTTTTTTGGACCAATAATAGTAAAATAAAAAATAGCATTTATTGGCTGATAGTGTGGCCACTGATATATTGTGCACCCCTTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACGTATAATTGTGACTAAACATAATGATTTACATAAATACAAATGTATTTCTATATTATTTTTCAGATCGAAAATTTACTAGAGCTGATT[C/T]AAACTGAGCAGAACATCTACAATATAGTGTTTCATGAGGTAATCCGGCAGGTCAGCGTTGAATGTGCAGAGAGAGGTCAACTCCTCGCCAAGCTCAGGTCTCTATCCCCGTTTACTCTTTTTTTTCATGGCTTTTCATTATAAAGTGATCTTAATACCTGTCATTGATATTGACATAAGATGTCGCATACACTATTGTTGTCTATTGGATGGAATGCGTTAATAGACTTGCCATTTTAGTACAGGGTAGCTGCTGGCCATTCAAAGCGATGATGATATATATACATATATCTATGATAAGGAGTTTTTCCTGCGGTCAGTATCCAAATTCATTCATTCATTCCATTTCAACTGTTTTTCCGGAACCGGGTCACGGGGGCAGCAGTCTTAGGAGAGAACCCCAGACTTTCCTCTCCCTAGACACTTCCTCCAGCTCCTCCAGAGGGACCCAGAGGCGTTACCAGGCCAGCCGAGAGACATAGTTCCTCCAGCGTGTCCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa755
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090069 | Nonsense | 291 | 1007 | 9 | 25 |
ENSDART00000136908 | None | None | 364 | None | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 17467559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17219317 |
GRCz11 | 22 | 17245587 |
KASP Assay ID:
554-0662.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTTTTCTTGGCTAGGCAAAAGTATGTGGCTCTACTTGACCGTATCCCA[C/T]GACAGGTGAAGGGTCTTCACACACAAACCTTAGCACAGAGGGCTCTGGAC
Long Flanking Sequence:
TCCTTCAATTAGCGAATAATAATGCAGGTTTCTAGCACCGCAGAATCTTGTTGTCATATTTCATTTGCATTGTTTGCTAATTTTATTCAACAAAAATAGCATAAGCCTAGTTTTTACTGTGAGTTGGTGCTACTATGCCTTATGGTCAGTGCAGTAAGAAACTGTATTATCATCAATACTTGTTCTGCACAAAAGTTTGTAATGTACAAAATTGTTAAAAAAATGAAATCTTACCTATTGAATGTTGTGCCTTTATGCTTTGTTTTCTTTGTTTGCTCATTACCACACTCGTACATGGCGCAAAATCAAGAATCTTCAGATTGGCTTTACTCTTGACTAGTGCGGTTGAATGTAATTTGTCCTGGAAGTACTTTACAAATGTGGTGGCGCAATTAACACATGCTGCTCATGGTCTGTTTGCAATATCTATTGTATATATGTATGACTTCCTCTTTTTCTTGGCTAGGCAAAAGTATGTGGCTCTACTTGACCGTATCCCA[C/T]GACAGGTGAAGGGTCTTCACACACAAACCTTAGCACAGAGGGCTCTGGACCGCCGGCTCACTGAAGAGATCCTACACTTCAAAAACTCGATAGCATCGCTTAATATGTATGCTTGATATACTATCTAATTGCCAATGAAACGTGATTTTTTTTTGCATTTCAAACTTGTCTGTTCAACCTGTAAAAGGGAGCTGAGTGCTATGAAAGTACATGATGAGAATGTGTCCAAAGAGGCAGAGGAAGCCAAGGAGGAGCTCGCTAAAGCTTTGGAAGAGTCACAACGCAATGCAAAGTACGTAAATTGGTGATTAAAACCTCTTAATCTTTGTATACAAAGTGCTTAACTAGCTATGTTTCCATCCAAAGATGCCAATTAGACCTATTCACAAAACGGAATTATTGCATAAAACATCTGTGAAAAAAGCACCGTTTCAATCCAATGAGTCAAAGAGAACAAAATGGTCACTTCTTGATCAACTGAAAAAAAATTAAATTTGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10715
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090069 | Nonsense | 374 | 1007 | 11 | 25 |
ENSDART00000136908 | None | None | 364 | None | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 17468227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17219985 |
GRCz11 | 22 | 17246255 |
KASP Assay ID:
2261-6678.1 (used for ordering genotyping assays)
KASP Sequence:
GACTTCTCATCAGTATTGTAGCAGAGTACCATGAACTCTATGAGCTACAG[C/T]GAAAGAGACTTGAAGGACAGATGTCCCATTTAGATGGCGAAAGGGACYTT
Long Flanking Sequence:
GTCTGTTCAACCTGTAAAAGGGAGCTGAGTGCTATGAAAGTACATGATGAGAATGTGTCCAAAGAGGCAGAGGAAGCCAAGGAGGAGCTCGCTAAAGCTTTGGAAGAGTCACAACGCAATGCAAAGTACGTAAATTGGTGATTAAAACCTCTTAATCTTTGTATACAAAGTGCTTAACTAGCTATGTTTCCATCCAAAGATGCCAATTAGACCTATTCACAAAACGGAATTATTGCATAAAACATCTGTGAAAAAAGCACCGTTTCAATCCAATGAGTCAAAGAGAACAAAATGGTCACTTCTTGATCAACTGAAAAAAAATTAAATTTGCTGCATGTATTCTTCTTGGATAAAAGTTAATATTATCATTAAGCAATTTTTATGCAATATTCCAAAATGCTCATAAAAGGAGGTAGATAGAAACATAGCTACTGTAACCTGAAATAAAGTGACTTCTCATCAGTATTGTAGCAGAGTACCATGAACTCTATGAGCTACAG[C/T]GAAAGAGACTTGAAGGACAGATGTCCCATTTAGATGGCGAAAGGGACCTTTGGAGAAAAGCGACCTACAGTCTTGCGGTCAAGGTGACCTTTTGTAAAATTTGTTGTAGGAGCTTTTCAAGTTACACATTACCCCACAACAAAAAATAGGTTTGAGTTTAAATCTCTAACAAATTTCTTTCAGATAATCAAGATAAATAAACTTCATCTGGTCAGGCGACTTCATATAAGTGAGCAGACCTGGGCCAAGGCTGCAGATCGGTTCACTTTCTTCTTAACAGCGAAGGTAAAAACACAAATACAAGGCTTCTCAACTATGGCTCTCAACATACACTTTTCAGAGCTTATCTTCAATCCTGATCAATTTCTAACATGTTTTAGTTTTCTAGTAAGCCTGGAACACCTTAATTAGCTTGTTTAAGTGTTTGATTAGAGATAAACTCTGTAGGAAACTTGAAGTTGAAAACCCCAGCCTTATACCAAGTTCATACTGCATGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18502
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090069 | Essential Splice Site | 923 | 1007 | 23 | 25 |
ENSDART00000136908 | Essential Splice Site | 280 | 364 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 22 (position 17472343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17224101 |
GRCz11 | 22 | 17250371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCCTTCAGTTCTTTAGAAACAATCAGAACYCTTCAGCAAGAGCTTCTG[T/G]AAGTATTCGAATGGAAATCTSTCTTTAGTCAGATCTATAGGAATCTCTTA
Long Flanking Sequence:
AACCACCTTTAGGACACAATCTCTTTCTTTTAAACACACCCAATGTTTCTGTAAATAAAACTCCCAGTTCTTAGTGTGCTTTATGCAGGTGAGTGGGCTTGACAAACCACCTGTAGGAGTCACACTCTGTTTCTCTCCATATGCACCAGACACTTTCTTAAAAGCACCACATACTTCCTGGAAAACACTGTGCAATTCTCGATGTGCTTCACACAGGTGAGCGGGCTTGACAAACCACCTGTAGGACACACTGTCTTTTCTCTGTATGATTGAAGGGAAACAAATTAATAAATAGCTTGTCATAGAATATATGTTTTTCAAATCTGTGATGAGTTGACATGCTTTTTATCCTCACTTGGATAAAACTGTCTGCTAAACAATTAAATGTAAAATCTAATCTTTTCTAGACTGAAGAACTGGTGATTACTCCACACACCGAAAAAGCCCAAGATGCCTTCAGTTCTTTAGAAACAATCAGAACCCTTCAGCAAGAGCTTCTG[T/G]AAGTATTCGAATGGAAATCTCTCTTTAGTCAGATCTATAGGAATCTCTTATGAACTGTATTTTGCAGAGCGGTAGAGACTCGAGCTATCAATTCAGAGGTGCGTGCATTAAAGGCAGAGGAAGAACTGCAGGCTGCTCTGGATAAGATACAAGATCTGGAGAGGCAGCTACAAGCTCGGCCCAGTGTGGAGACCAAGTGTAAATGTGTCAAAGAATAAAATTACACTTGACATACTGAACAAGATTAGCTATTTCTAATTCTGACTATATGTTTTTTTTTACAGCAAGCAAGAAGAATGCCCCTAAGACCCCCAGCAAACCTGTCGCAACTTCTGAAGCTAAAACAAAAAGCCAGAACCCTGAATCCAGCCCGAAACTGTCCAGAGGAACCAAGAAACGCTTAATGTGAAAAAACTATACTGGGGCTCAATAATAAAGTGCTTAATAGACATATGTATTTGATTTTTATTGCACATATAAATTTGTTAGCGGGATTGTTT
Associated Phenotype:
Not determined