ZMP
LOC796966
Ensembl ID:
Human Orthologue:
C15orf52
Human Description:
chromosome 15 open reading frame 52 [Source:HGNC Symbol;Acc:33488]
Mouse Orthologue:
A430105I19Rik
Mouse Description:
RIKEN cDNA A430105I19 gene Gene [Source:MGI Symbol;Acc:MGI:2685199]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9173 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36287 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12340 | Nonsense | Available for shipment | Available now |
sa36286 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9173
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124896 | Nonsense | 185 | 516 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 2270113)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 2315758 |
GRCz11 | 17 | 2492144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAAGATCTGGAGTCGAACACACGAGGAAAACAMCCTGCCGCTGTAAAG[A/T]GACTCACAGAGGTGAGCAGATCTTCTCGTTTGTGTTTGGGACGCCTTTCA
Long Flanking Sequence:
GAATTCCGCAAATTTCTGTAGTTTTTTAGCCCATTTTAAATTCTGTTTATTTACTTGAGTAAATGTGTAAATCTGAATTTATTCAGTTTTTATTCAGTAATTTATTACTTTTTATTTAATATATTAAAGTGTAAGTTATGATACTCCGCTGGATACTCCCAAAATAATTCCGCAGAAATCCGCAGATTTTTACCAAAATTCTTCGCAGAAATAGCAAAAAACGTCCGCAGATTCCGTCTGGCCCTGGTTATTAGAAATGAGAAACTATTATGTTTAGAAATGTGTTGAAGTAAGTTTCTCCCCATTAAACAGAAATTGGGAATGAATATGTAATTGTGCTAATAATTCTGACTTGAATGGCTACAACACTGTTTCAGGGTAAGAAGGTTTTCGGCGAGAGGAAGGACAGAAACCGTCCTGTGAGTCCAGCTAGACTTAAATCCTGTGTTGAAGAAGATCTGGAGTCGAACACACGAGGAAAACAACCTGCCGCTGTAAAG[A/T]GACTCACAGAGGTGAGCAGATCTTCTCGTTTGTGTTTGGGACGCCTTTCATTTTGTTTTCAAGCTGTGATGCTGTAAACATATTCACACCAGATGAGTCTGATCATAAGAGATGAGAGTTTGAATATTCATCAGGCTTTTGGCAGGATTTTGTGGGTCTGTTCAACTGTTCTGTTTAATGGCAAAAGTAACATTTACTTTACGGTTTCACCGTTTACAGCTGTATAGTACAGGGTTCACACAAGGTGCCTAAAGTGCTTGAATTTGGCTTAAAAGGGCACCTATGGTGAAAAATCTACTTTTCAAGCTGTTTGGAAAGACATGTGTGTAATTATAGTGTATAGATTGTCATATTGGGGTGATATAAACACACACAGTTTTTTTTCAATTTAACAATATAATAACGGTCGACCAATTAGATCGGTTTTTAGATCGACCGCAACTTGACGTAGGAGTGCGGTCCTCCCGCCCACCAGTATTGATTGACAGGTGCGTCGTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36287
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124896 | Nonsense | 227 | 516 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 2257544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 2303189 |
GRCz11 | 17 | 2479575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGGTGGCTGACCTAAACCTGATGCCGTCTGAGCAGGAGCAGCAGGAGTA[T/A]CTGCGCTGGAAGAAGGAGCGCGAGGAGATCGACCGCGAGCGTGTGGCCCG
Long Flanking Sequence:
CAAAAATGCCAACTGACCCAGCTGGGGCTCGAATCAGCGACATTGCTGTAAGGCGACAGCACTAACCATTTTAGACTCAATATTGTCTTTTTTATTAGTTCAATCAAAGCCAGAGCAGAACATTTGTGCATTTTATTGACCCATTCATGAAGAAAGCCACATGCTTTGATTCTAAATGAATGAGCTTTTTTGAAGGAATCATTTGAATGAATGATTTAGTGAATCTGAGTTTAATAATCTCGGTTTTATATCTTCTACATGTGAATTTTGTCACTGTTTTGGTGTGTACTAGCTTATAGATTTCCTAAAAATTAGCTATACCAACATGTAAAAATCTTTATATTCATTTCATGGGAACTTTAAACATCGCTTGGGAACTAACTGAATGATCCAAATTCACAAGAAGCTGATAATTTAGTTTTGTATATGTGTATTTTGTAGTCTACAGAACCGGTGGCTGACCTAAACCTGATGCCGTCTGAGCAGGAGCAGCAGGAGTA[T/A]CTGCGCTGGAAGAAGGAGCGCGAGGAGATCGACCGCGAGCGTGTGGCCCGTCACAAAAACTCCAAAGGCCAGTGGAGGAGAGCCTGGGACATGGAGAAAACGGAGCTAATGTAAGCCTGACGCCTCTGCGCCTCATTTCTGTTCTCAGAGAAACTAACCCGAGCTGCTTTAGTTTGCATTTTCGCTCGATTTCCTTTTGCTTGTTGGTCTTTGTTGGGTTTTTTTCCTGCATGTTGAACTGCATCTTACATAAATCACTGCTGTTTGAATGGCCTCTGCGTCTGCTGTCTTACTGACTCCTCCATATGCAGAACTCATCTCTTTAAAGAAATACCCGAGTTAGATTTTCAAGCAGGTTTTCTCTTGAAACTTAATCATTACACAGCAGGTCATGTGGTGTTTTTAAAGGGTCACGAAACACCAAAACACATGTTTTGAGCTGTTGACAGTCGTATATGTGTCCCACACTGCTAAAAACACTATTAGGACACCTATACTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12340
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124896 | Nonsense | 315 | 516 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 2238096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 2283741 |
GRCz11 | 17 | 2460550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGACMGAAAGGGGAAAAGCRTTTCAGTGGTTTGCAGTAAAGCGAAGGGT[A/T]WAGACCGTCTGACGGGCCGAGCGAGGAGGTAAACTGACCACACACTCAAC
Long Flanking Sequence:
TTTGCTGCTTGTGGGTTAAGTTTGGGCGCTCAAGTGACTGAGATGCAACTGAGAGAACACGTTTTTTCAAAATAAAAGATCATTCAGGTCCAGATAATTAAAAATAAAACTGAAATAATTAATGATTTCCTGTGCAGACCGGTATCAATTAATCCATGGGCCGATACCGGTCCGGTGGTCGGGGACCACTGCTGTAGACAATCCAAAATAAATATTGCTTAAGGGGGCTAATAATATTGACCTTAGAATGGTGTTTACAAATTTTTAAAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTGAAAATTTCATTTGGGAAATATTTGAAAATAAATAAAAAATCTCACAGGTGGGCAAATAATGTTGTTTTCATCTGTGTGTTTTGTTCTTGTAGCTCGTCATCAGGCGTCGGACAGAAAGGGGAAAAGCGTTTCAGTGGTTTGCAGTAAAGCGAAGGGT[A/T]AAGACCGTCTGACGGGCCGAGCGAGGAGGTAAACTGACCACACACTCAACAATTACTGGAAGATCTCATCTAAAAGCCATTCTGCATACATTTACACCCACTCAGGGGATGATGGGAAATGAGAATCTCCGCAGGGATCATTCATGGCCCTGTTCGTTTCCACTCTCACTTAGCATTAGCGTTCAACCACAGACACATCTGAACTAATGGCTGGATGATTTGTCTTTTAACCCTTGTGTAATGTTCACACTGACTCCCCTTTGGTTATGTTGGTGCTGTTTTTGCCCATTTGACTTCCATTATAATCCCATTTTTTTTAATTGCAAAGCCACCACAGCATATATTCATGCACTTATGATTGTTGCTGGGTTTTCCTGTTGGGAGAGGTAGAGTGTGTCATTTTTGCTGTTGATCCTCAGTTGGCAGCATTAATCGTTTAGATAGGCCTGTGCTAAAGAATGTCTGGCTTTATTTGGAGTAAAACAGTAGATTATAGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36286
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124896 | Nonsense | 463 | 516 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 17 (position 2231686)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 2277331 |
GRCz11 | 17 | 2454140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTGAAGAAAGGAAAACATCGTGTCCTGAAGCTGGAGATATATCAGCC[G/T]AAGCAGATGAAAAACAACCCGCTGAACACAGCAAGAGCTGCACTGCTAGA
Long Flanking Sequence:
CCACCCATCCTGAAAAGGACAACAGGATGTTAATATCACCAACCATTCCCATTGTATTCAGGTGTATCCATATAAATGGCCCACTCTGTATATTGTGCATTGTTGTGAATTTGTGTCAGGTTTATCCAGAAGGCAGCTTGCAGGAGTTTTTAGAGGAGCTTGACGCTCTTTGCGCTCCTGAAAAGATCAATCCAGAGACGGACACTGAAAACATAAGGCCGTGTTCGTCTCAAGAGTCACTCAGAAGCACAGAGCACACACAAAACACCAGTGCTTCAGCAGAAACGCCTCATCCAGAGCTCGTCTCTCTGAAAAACGTGGAGAAAAAGGTACGCTTTTCTGAAGACCATGAGAAGAAGGAGCTGCAGACAAACACAAATGGTTTTGTGGAGGAAAACAGACAAACATCGACACAAAACAGCAGTGAAAATCACACCGAGTCAGATGCACTTACTGAAGAAAGGAAAACATCGTGTCCTGAAGCTGGAGATATATCAGCC[G/T]AAGCAGATGAAAAACAACCCGCTGAACACAGCAAGAGCTGCACTGCTAGAGGAAACGGTATGTGGGAAAAACTACATTACCCATGATGCTGTGCAAAATAGTCCACTAATTGAAGAGTTGCAGCAACCACCCACTCACTTGAAATTTGCTTTATGTCAATGTGGCTGTAGCAAATAATTAATATTGTTTCATTTATATTATTATTTTGAAAAAAAAAGAAGAATAAACAAAAATAAACTGTAAAACTACAGGTTACAATACTGGTATTTACTAATGATGCCCTGATGTCTTCATTTAAAATTGCTGTATAATGATTTTGTTCATATTTATAGATGGATGGATGGATGGATGAATAGATATAAAGACGAACAGACAGACAGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATCGATAGATAGATGGATGGATAGATAGATGGATAT
Associated Phenotype:
Not determined