ZMP
si:dkey-45k15.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC563246 [Source:RefSeq peptide;Acc:NP_001138266]
Human Orthologue:
C14orf73
Human Description:
chromosome 14 open reading frame 73 [Source:HGNC Symbol;Acc:20120]
Mouse Orthologue:
1200009I06Rik
Mouse Description:
RIKEN cDNA 1200009I06 gene Gene [Source:MGI Symbol;Acc:MGI:1921363]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13690 | Nonsense | Available for shipment | Available now |
sa22213 | Essential Splice Site | Available for shipment | Available now |
sa22212 | Nonsense | Available for shipment | Available now |
sa35415 | Nonsense | Available for shipment | Available now |
sa15022 | Nonsense | Available for shipment | Available now |
sa38919 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13690
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 |
---|---|---|---|---|---|
ENSDART00000080987 | Nonsense | 171 | 787 | 3 | 13 |
ENSDART00000148240 | Nonsense | 171 | 787 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 6841600)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7059623 |
GRCz11 | 13 | 7391825 |
KASP Assay ID:
2260-6010.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAGAGCCAAAAYCMGAGGTTGCTGATGAATGTGAAGGCCAGATGGTGT[T/A]GGAGCTCAGAGACACATATGTTCTGCCGGAGATCCCAGCAATGCCTTTGT
Long Flanking Sequence:
TCTAGCCGAAATTAAACAAATAAGACTTTCTCAAGAAGAAAAAATATTATCAGACATGCTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTAGGAAATATTTTGAAAAGAAAAAATCAAAGAAGGGCTAATAATTCTGACTTCAACTGTGTGTGTGTGTGTGTATGTATATATATATATATATATATATATATATATATTATACGTTATATTTTTTTTAATATTAAGTTTTTTTCTGATCAGTCAAATGTTTTTTTGGATATTATTTTCTAAATTTGTTACACATTATGTTACAAATAATTGCATAAACTGTAACTGTTAATTTTATTCTTAGATTCTGATGTTATAACACTGCAAAAGAAGGGCTCATCGATCAGGCGGAGTTTGGGTCTGAGTAAAAAACCCAAACAGGAACCACTTGTCACTGTCACAGAAGCCATGCCTCTATCAGAAGAGCCAAAACCCGAGGTTGCTGATGAATGTGAAGGCCAGATGGTGT[T/A]GGAGCTCAGAGACACATATGTTCTGCCGGAGATCCCAGCAATGCCTTTGTCAGGTATGATTGTCTGACAAGTATAAAGTGTGTCTCATCTTGGGTTACTTAGCTTTCTCATTGTTCAAAACCCCACTTTAACATAGAAGCATGGTTTCCCTGGTTAACAATTAAGGCAAACCCTGCATTGTTGTGCAACAGATCTGGGAACAGATGTGAATATTAATTAGTGCCTGATGCTTACACACACACACACACACACACACACACACACACACACACACACACACGCAAAATACTCATACCTCAGTTGTCAACTATTAGCTAGTAGGAGTGAGTGAGCTATTCCTATGCTAAACAGTAACTTAGTTTCCTCCAAGGCTAAATTATAATTATACTCAACAAAAGGGGCCGCCAATCAGGGGTGGACTAAGTGATTTGGAGGCCCTAAGCAATTGCAGGTATGGGACCCTATAGCAGTTTTGAAAAATAAACTGCATGTTGTATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22213
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 |
---|---|---|---|---|---|
ENSDART00000080987 | Essential Splice Site | 189 | 787 | 3 | 13 |
ENSDART00000148240 | Essential Splice Site | 189 | 787 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 6841545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7059678 |
GRCz11 | 13 | 7391880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGAGACACATATGTTCTGCCGGAGATCCCAGCAATGCCTTTGTCAGG[T/C]ATGATTGTCTGACAAGTATAAAGTGTGTCTCATCTTGGGTTACTTAGCTT
Long Flanking Sequence:
ATGCTGTGAAAATTTCCTTGCTCTGTTAAACATCATTTAGGAAATATTTTGAAAAGAAAAAATCAAAGAAGGGCTAATAATTCTGACTTCAACTGTGTGTGTGTGTGTGTATGTATATATATATATATATATATATATATATATATTATACGTTATATTTTTTTTAATATTAAGTTTTTTTCTGATCAGTCAAATGTTTTTTTGGATATTATTTTCTAAATTTGTTACACATTATGTTACAAATAATTGCATAAACTGTAACTGTTAATTTTATTCTTAGATTCTGATGTTATAACACTGCAAAAGAAGGGCTCATCGATCAGGCGGAGTTTGGGTCTGAGTAAAAAACCCAAACAGGAACCACTTGTCACTGTCACAGAAGCCATGCCTCTATCAGAAGAGCCAAAACCCGAGGTTGCTGATGAATGTGAAGGCCAGATGGTGTTGGAGCTCAGAGACACATATGTTCTGCCGGAGATCCCAGCAATGCCTTTGTCAGG[T/C]ATGATTGTCTGACAAGTATAAAGTGTGTCTCATCTTGGGTTACTTAGCTTTCTCATTGTTCAAAACCCCACTTTAACATAGAAGCATGGTTTCCCTGGTTAACAATTAAGGCAAACCCTGCATTGTTGTGCAACAGATCTGGGAACAGATGTGAATATTAATTAGTGCCTGATGCTTACACACACACACACACACACACACACACACACACACACACACACACACGCAAAATACTCATACCTCAGTTGTCAACTATTAGCTAGTAGGAGTGAGTGAGCTATTCCTATGCTAAACAGTAACTTAGTTTCCTCCAAGGCTAAATTATAATTATACTCAACAAAAGGGGCCGCCAATCAGGGGTGGACTAAGTGATTTGGAGGCCCTAAGCAATTGCAGGTATGGGACCCTATAGCAGTTTTGAAAAATAAACTGCATGTTGTATAAATATTTAAAGTATATTTTATATATTTTTTTAATATTTAAAGGAACTTTTATCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22212
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080987 | Nonsense | 453 | 787 | 6 | 13 |
ENSDART00000148240 | Nonsense | 453 | 787 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 6834151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7067072 |
GRCz11 | 13 | 7399274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCGAACATCACTTGACAGGGTTATTGAGTTGGAGAATGAGGAAATTTG[G/A]AAGGAAAGAAGAAAACCAGAGATTGATGAGGGAATTTACAGCTCACACAT
Long Flanking Sequence:
TCTTTCCAAATAGTTATTCTAGTGAAGTACTAGTGAAATTGTATTCATATGTAGCAGAAAAAAAAAATCTCAATTGTATATTTTTCCAATATTGTGCAGCCCTAGCTTTAAGAGTTAGAAGTATTCAACATTTGTTTTATGACAAAATGAGATTAATTGCTGATGTGTAGGTATTTTAAGGGTTACAATTATGTCTATTACTAAAACTGTAATTAACTGTGGTTTCCTCAGTGAGAAGATAATGGGAAGTACCTCTCTGCAGCCAGAGGTGAAGGAAGATAATAGAGCTCTCCCACTGGACAATGATTTCCTTAATCAGATCAAAATGAAATACTGCAGTCGCTTACAGGTGAATAAAAAAGCACATGTCATCTGAGATGATGCTGGTACTGAAACTAGAATGACAGTATGTTGAGATTTTCTAAACTCGTGTTCTCTAAACAGGTTGATATGCGAACATCACTTGACAGGGTTATTGAGTTGGAGAATGAGGAAATTTG[G/A]AAGGAAAGAAGAAAACCAGAGATTGATGAGGGAATTTACAGCTCACACATTGACATGGACATCTGGACGGTGAGAATACACACTTTCATTAATAGCTCATTGGTTTTATGTGGAAGACAAATGAGTGTTAAAGGAATTTCCCACATTGATTTACTGTTTATCTGGCCACACACTCTGAAGGTCATTGGTTTACCAACAGAGGGCAGTACAGGACCTCTAGCTTAACTTATAATGACCCTTACACATGTTTGGACACCTAAATCACACTCAGCGTATGAATGTCACTGCATTATATTTCAAATAAAGTAACAAGCACATTAAAGAAAGATAACCTAATCATACTTTCCAAAATCAAATTGTTTTACTTGATATAAAAATAAAACCAACTGGTGGGTTGTGTTTGTAACTATTGTAATATGCTGATGTTATTGTACATTCTAGTTATAAGTACATTCCACTTGCCACTTGGTGTAATTCATGTATTTTTCAAATAAATTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35415
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 |
---|---|---|---|---|---|
ENSDART00000080987 | Nonsense | 519 | 787 | 8 | 13 |
ENSDART00000148240 | Nonsense | 519 | 787 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 6831479)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7069744 |
GRCz11 | 13 | 7401946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCCATTGACTGTGTTTGAAGGTTTGAATCAGCGTTTGTGGAGTCCTG[C/A]AGGGTTTTCTCGAACTCTTCTCTCTGGGCAGAGTATCACATCAGCTACAT
Long Flanking Sequence:
AAGCTGGTCAACTAGGCTGGTTTTAGAGCGGTTTTGGCCACTTCCAGGCTGCTTTCCAGCCATTTCCAGCCTGGTCTTAGCTGGTTAGGCTGGGAGATGACCAGCTAAAACCAGCTTGACCAGCCTAGCAGGCTGGGAACCCAGCCAAAACCAGCTATGTCCAGCTTAAACCAGGCTGGTCAAGCTGGTTTTAGCAGGATTTAGCTGGTCATTTTCCAGCCTGACCAGCTAAGACCAGGCTGGAAATGGCTGTAAACCAGCCTGGAAGTGGCCAAAACCCCTCTAAAACTAGCCTGGTCGACCAGCTAAAACCAGCCAACCAGCCTAGTCTAGTTTAAGCTGGATTTTTTAGCTGGGATGATTATTTCCCCTTACTATTTGGTCAATCAGATGATCTTAAAACTATTTATTTTTAGGAAATGCTAAATTTTATGTCTCATTTTATGTCTCTTTTCCATTGACTGTGTTTGAAGGTTTGAATCAGCGTTTGTGGAGTCCTG[C/A]AGGGTTTTCTCGAACTCTTCTCTCTGGGCAGAGTATCACATCAGCTACATCAACAGCTTCAGTGATTTAAAGTAAGTCTTCGACAAGTATGTTTTAATCAAAAGTACCATTACACTCACTAGAAATCAACATAACACACAACCTGCTTTGTAAATCCATTTAGATAGATTATGTTTGGATAATGCCAAGAGGTTTTGAATAGCTAGAGGAAGCAATTTGTCAATCTATAATCTCAAATGCAGTTTTATTTGAGTTTCAGATTAAAATCACTCAGAGAAGACACGAGCGGTTACACACCATGAATAAAAAAAAGCATAACACAAATGATCCATCACGTGGTTTCTAGGAATTTAGGCACCATCAAGGCTATGAGGCAACTGTCAGGGAAAGTCCCTGATGCTTTCCGTGATATTATTTGATGAAACTGAAATGCAAACAAAAGATCTGGCTCTATTCAAATGAAAAACAGGTTTTATCAAAACAATATCACATTACAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15022
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 |
---|---|---|---|---|---|
ENSDART00000080987 | Nonsense | 542 | 787 | 8 | 13 |
ENSDART00000148240 | Nonsense | 542 | 787 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 6831411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7069812 |
GRCz11 | 13 | 7402014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTCTCTGGGCAGAGTATCACATMAGCTACATCAACAGCTTCAGYGATT[T/G]AAAGTAAGYCTTYGACAAGTATGTTTTAATCAAAAGTACCATTRYACTCA
Long Flanking Sequence:
GCCTGGTCTTAGCTGGTTAGGCTGGGAGATGACCAGCTAAAACCAGCTTGACCAGCCTAGCAGGCTGGGAACCCAGCCAAAACCAGCTATGTCCAGCTTAAACCAGGCTGGTCAAGCTGGTTTTAGCAGGATTTAGCTGGTCATTTTCCAGCCTGACCAGCTAAGACCAGGCTGGAAATGGCTGTAAACCAGCCTGGAAGTGGCCAAAACCCCTCTAAAACTAGCCTGGTCGACCAGCTAAAACCAGCCAACCAGCCTAGTCTAGTTTAAGCTGGATTTTTTAGCTGGGATGATTATTTCCCCTTACTATTTGGTCAATCAGATGATCTTAAAACTATTTATTTTTAGGAAATGCTAAATTTTATGTCTCATTTTATGTCTCTTTTCCATTGACTGTGTTTGAAGGTTTGAATCAGCGTTTGTGGAGTCCTGCAGGGTTTTCTCGAACTCTTCTCTCTGGGCAGAGTATCACATCAGCTACATCAACAGCTTCAGTGATT[T/G]AAAGTAAGTCTTCGACAAGTATGTTTTAATCAAAAGTACCATTACACTCACTAGAAATCAACATAACACACAACCTGCTTTGTAAATCCATTTAGATAGATTATGTTTGGATAATGCCAAGAGGTTTTGAATAGCTAGAGGAAGCAATTTGTCAATCTATAATCTCAAATGCAGTTTTATTTGAGTTTCAGATTAAAATCACTCAGAGAAGACACGAGCGGTTACACACCATGAATAAAAAAAAGCATAACACAAATGATCCATCACGTGGTTTCTAGGAATTTAGGCACCATCAAGGCTATGAGGCAACTGTCAGGGAAAGTCCCTGATGCTTTCCGTGATATTATTTGATGAAACTGAAATGCAAACAAAAGATCTGGCTCTATTCAAATGAAAAACAGGTTTTATCAAAACAATATCACATTACAATGATATCTAAAGTATAACAAAGCAAAGAATACTGTATTATTGTGTTCATTAGTATGTTGCACATCTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38919
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080987 | Nonsense | 764 | 787 | 13 | 13 |
ENSDART00000148240 | Nonsense | 764 | 787 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 6819498)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 7081725 |
GRCz11 | 13 | 7413927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCTTGGGGAGTTCTGGGAATAAAGAGCAAGCTCTCTTTAGTGAGATT[C/T]AAGCTTCAGCAAACACAGACTGTCTGGCAGGTACTCCCTTCTCCTGTCTG
Long Flanking Sequence:
ATTGACACATTCCTTTCAATAGACAGCAATAGCATAGGCGACATCTAATGTAAATCTCTATGCCGCTTGGCGAAATCTGGTGGGTGATCACAGGTCAATTCATAGCTTTTTGTATCTTATTAATAAATTTTTGTCCAATTTGCTCATTCTCCAATGACGGTTGTGTTTAAGTTTGATGGTTCGGTGCCACACGTCCTTTTAAAAATCGTACATTTTCGTACAACTAAACATGTATGCATTAGCAACTTAACTGACAAATGTTTACGTAAAAAGCTACGCAGATAGATCACTTGACGTTTATTTGTAAATTGGGCTTAAGTCTTTCATTTTCATTTAACACATGCTTCTCCTGTTGCAGAAGGAGCCATCTCTCTGCAGTGCTGTATTTTCGAGGAATAATAAGAGGCAGGGAAAAGCACGTTATCTTACAGCGACTGGCAGAGCTGAAACAGAGCTTGGGGAGTTCTGGGAATAAAGAGCAAGCTCTCTTTAGTGAGATT[C/T]AAGCTTCAGCAAACACAGACTGTCTGGCAGGTACTCCCTTCTCCTGTCTGTCCTTCATCATGCCAGACAGATAATCGTAAGAAATACACTTCAATAGAAGTGGGAGAAATGATTGCAATGTTTAATAATGAACCTATGTTATATAATTTGAGCATTAGGTAGTGTTTTCATGCCTCTGTTAATGCTTAATAGACTTATATTCTTTGCATTAGTCTGTGTATTATCATTCTGTATGGCATCTACATATTTATTAATGAGAATCAGATTTTAATCTTCAAAAATTTTGTTACAGGAGTGAATGAGTTAAACTGGTGTATGTTCACCAGTTTCTGGTGTACTTCAGAAATGCTTGTTATTAGCGACACCGGTGGCCATTAAGTGAACTGCATCGGATAACCCTTGCTTTTTAGTTATATCCAGGCCCGGCCCTAACCAATTTGGCGCCCTGGGCAAGATTTCAGGTGGCGCCCCGTCACATTGCAGTAAATTCCACTGCTAGT
Associated Phenotype:
Not determined