ZMP
C16orf73
Ensembl ID:
Description:
chromosome 16 open reading frame 73 [Source:HGNC Symbol;Acc:28569]
Human Orthologue:
C16orf73
Human Description:
chromosome 16 open reading frame 73 [Source:HGNC Symbol;Acc:28569]
Mouse Orthologue:
4930528F23Rik
Mouse Description:
RIKEN cDNA 4930528F23 gene Gene [Source:MGI Symbol;Acc:MGI:1922428]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35258 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35259 | Essential Splice Site | Available for shipment | Available now |
sa42008 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11776 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35258
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 |
---|---|---|---|---|---|
ENSDART00000089589 | Essential Splice Site | 87 | 467 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 19560155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18412316 |
GRCz11 | 12 | 18534190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGTGTATTTAATTGACACGGTAAGCCAAAATAACGTCTTGTGTTTTA[G/A]TTGTAATTGAAAATCCCCTCGTTGTGACCAAGGACTATGAGAAAGAAGAA
Long Flanking Sequence:
CATAATGAAAGGTTACATGTAATAAATATATATATATAGATTCAATTGGTAAAAAAGGCTTTTTTTATTTTCTAGAAGGTGGTGGGGGTGATAATTGGAAAAACTGATTCAAGAGGATTTCCTGACCGGAAAAGTTTGTTACCATAACATTATTCATTTTTTTTCTATTTACCTTTTTTTCTTGTTTGTTTATTTAGATTTTTCACTTTTGTTCAGTTCAGTTTCCCCTTTTAATCTGTTTCAAAATGTGTTTAGATGTTGGGTCTGAAAGATTCACTTTCAGCTTCACCATCAAAGATTCACCAGAACATTTTATCAATGTGTCTGCATGGGGAAATGAGGAATACATTCAAGCACTGAGCTGTCGCTTTCAGATCGGGGATTGTGGTGAGATTGTAAAACAGCTGTTTTAGTTGTCAATTCCAAAAAAAAAACACTTTTAATAATACATAAAGTGTATTTAATTGACACGGTAAGCCAAAATAACGTCTTGTGTTTTA[G/A]TTGTAATTGAAAATCCCCTCGTTGTGACCAAGGACTATGAGAAAGAAGAACGGTTTTGCCCTTCAACACCTAGGTAAAAAAATAAAAATGAAAATAGCATCAGATTTAGATACATCATACTCTGTATTTGTGACACATATACCTATTTTATCTCAGTTCCTACAGGTTGTTGCTTACAGAGACTCACTCGAGCATTAGGATATGCTCAGACATAGACACTGAGGCCAGGATTCTGCCGCTATTTCACATACCAATCAAAGACCCAAGAGATTTCTATTCGTTGGGAGACATTACTGCAAATGGACAAAGTCTGGATGGACACGTTATTAACATCCTAGCAGCTGTACAATCGGTTAGATTTCAACCGTTATCACCAGACTTTCTCTATGAGTGTGGGATATTAACACACAAAAAAAGTTAATTTCCCACTAGACTTTATTCCCCATGTAAATTAGGCCTACTACAATTTTATCAACGATTGAGATTTTGTCATCATAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35259
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089589 | Essential Splice Site | 260 | 467 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 19564200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18416361 |
GRCz11 | 12 | 18538235 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAATACTTTAACATTAAAATCTTTCATTTTTTTGTTGATTACTTATA[G/A]ATACAGCAGAGGCAAACCAGCTGTACACATTTGTCAGGGAACTGTTACAA
Long Flanking Sequence:
AATATTGGTAAACAAAGTCATTTTGACATTAATTGTACACAAAAAAAGAGTTTTGGAGTTAAGTATGGTTACAGTCAAACCACTGAAGTCACATGGAATATAATTTCTGTTCTGAAGATAAACGAAGGTCTCATGTGATTGGAAGGAAACAGAACTATTTTAAGGTGAACTAATACTTTAATTATGCTGTAGAAGTATTGTTCATTCTTAGTTCATGTTAGTAAATTAATATTAACTAATGGAACCTTATTGTAAGTTATTATCATTTTTTCAATAGCACTCTGTGATACATATTAATACATTGATTGTATTTATTTTCTCCCAGTGCTGTTCATTGCAGATGCTCGTATCACCTTTGACAGTTTTCGCAAAAGTATGGTGGCAACAGCGATCTCCAAAACAATCATTACCGTCAACCCTGGTAAAGATGTGATATGCTAAAGTAAAGATATTTAATACTTTAACATTAAAATCTTTCATTTTTTTGTTGATTACTTATA[G/A]ATACAGCAGAGGCAAACCAGCTGTACACATTTGTCAGGGAACTGTTACAATCTGGAGGACTGGATGACCAGGACTTCCTCTCTGGTGATGATGTGCAGTGTAAGTTATTATTGTTCACACTTTACATTAAAATTGCAGTCTTAGTTTTCATGTGATGTCTCACATTTTTCATATAAAGCATTTTAGTTATTGAAATGCTGCAGCAGGGGTTGTATATGGATCACAGGTGCTTAAAACTGTGTTTCTATTGTTTTTTTTTTGTTTGTTTGTTTGCTTTTGGTAGATTATGTAAATATTTGTGGCTTAAAAGTGCAGTAGGTGATCTGCCAAAACGATAACCGCTTGCAGGAATTTCATATATTACTAAGCCACACTTACATGCTATTTCAGAGCGAATATCGAGAGTAGCATGGTGAACAGTATAGGGAGGCTGTCATTGATCATAAATGAACCAATGTGAATATAAAAGCAACTTCAGCCCAATAAAGCAGGTTAGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42008
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089589 | Nonsense | 268 | 467 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 19564226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18416387 |
GRCz11 | 12 | 18538261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTTTTTTGTTGATTACTTATAGATACAGCAGAGGCAAACCAGCTGTA[C/A]ACATTTGTCAGGGAACTGTTACAATCTGGAGGACTGGATGACCAGGACTT
Long Flanking Sequence:
CATTAATTGTACACAAAAAAAGAGTTTTGGAGTTAAGTATGGTTACAGTCAAACCACTGAAGTCACATGGAATATAATTTCTGTTCTGAAGATAAACGAAGGTCTCATGTGATTGGAAGGAAACAGAACTATTTTAAGGTGAACTAATACTTTAATTATGCTGTAGAAGTATTGTTCATTCTTAGTTCATGTTAGTAAATTAATATTAACTAATGGAACCTTATTGTAAGTTATTATCATTTTTTCAATAGCACTCTGTGATACATATTAATACATTGATTGTATTTATTTTCTCCCAGTGCTGTTCATTGCAGATGCTCGTATCACCTTTGACAGTTTTCGCAAAAGTATGGTGGCAACAGCGATCTCCAAAACAATCATTACCGTCAACCCTGGTAAAGATGTGATATGCTAAAGTAAAGATATTTAATACTTTAACATTAAAATCTTTCATTTTTTTGTTGATTACTTATAGATACAGCAGAGGCAAACCAGCTGTA[C/A]ACATTTGTCAGGGAACTGTTACAATCTGGAGGACTGGATGACCAGGACTTCCTCTCTGGTGATGATGTGCAGTGTAAGTTATTATTGTTCACACTTTACATTAAAATTGCAGTCTTAGTTTTCATGTGATGTCTCACATTTTTCATATAAAGCATTTTAGTTATTGAAATGCTGCAGCAGGGGTTGTATATGGATCACAGGTGCTTAAAACTGTGTTTCTATTGTTTTTTTTTTGTTTGTTTGTTTGCTTTTGGTAGATTATGTAAATATTTGTGGCTTAAAAGTGCAGTAGGTGATCTGCCAAAACGATAACCGCTTGCAGGAATTTCATATATTACTAAGCCACACTTACATGCTATTTCAGAGCGAATATCGAGAGTAGCATGGTGAACAGTATAGGGAGGCTGTCATTGATCATAAATGAACCAATGTGAATATAAAAGCAACTTCAGCCCAATAAAGCAGGTTAGACAGAATAGTGCTGTTTGCTGATGTTTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11776
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 |
---|---|---|---|---|---|
ENSDART00000089589 | Nonsense | 304 | 467 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 12 (position 19566992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18419153 |
GRCz11 | 12 | 18541027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATTTCTTTCCCCTCAGTGGATTCCATTAGAGACGTCATGACAGYAAGC[C/T]AACYTAAAACCAGAAGTCAAGAAAATGCAGATGCCATTCATTGCATCATA
Long Flanking Sequence:
TGTTTGTTCATGTTAGAAAATGCATTAACTAACATTAACAACTACAACCTTATTGTAAAGTGCCACTGATTTACTATTATTTACAAAAGGGTGTCCTACATAGTCAGTTTTTTTTAATTCTACAACATAGCAAAACTAGTTATTCAAAGTAAAATTGATCCTGTAAAAATAGCATACTGGAAGTGATGTTTCCCCTCACTATTTTGATCTGAAAAGGACTGAAAATTATGTTGTAAAATGTCAAAAGTGTCACCACAAGAGCAAAAGGAAAAAAACAACTTAATACTAGGTTGTGTACTCTGTTTTTTAACAATGATTTAATTAGTATTTCAGTTTTTGGCTAATGGGTTTAAAGTAGTAAATTACATTACCATCAAACAAACTTTTACCATGAAAACTGCATTATAAAAAACAAATGAATGCAAAATGTATCTGCAGCATTTTATCCTTAAATTTCTTTCCCCTCAGTGGATTCCATTAGAGACGTCATGACAGTAAGC[C/T]AACTTAAAACCAGAAGTCAAGAAAATGCAGATGCCATTCATTGCATCATATATGGATTCATCACCTGTTTTGATCTGGGTTCCTCTCCCTCCAAAATAATAACCAAGAGATGGTGAGATTGCAACGCTTACAGTTTTCCGAGATACAAATTCTCATGTCACAATATTAGTCATCATATATCCTGATAAATATAGTAGTCAACATTTAAAATGCATATAAAACATTTCAGAAAGTTCTTTGTAAATTGAATGAACTTTTACAAACTTTATTGATCCACTTCAAATGCTGCCTACTGTATATCACAATATACAGTATATGTGTTTTAATATAAATTCAATTAATTATTAGTATGTATGTATTGACCGTGCCACATTACAAATTAAATGAAATAATATATTTTTATTATCCATACAATATTTATATATTCTTATATTGCACAGCCCTAGCTTATTTTGCTTTTAATGTATAATTTCTCCACTAGTGCCAGATGCAAATTTCGA
Associated Phenotype:
Not determined