ZMP
si:ch211-168p1.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
C17orf71
Human Description:
chromosome 17 open reading frame 71 [Source:HGNC Symbol;Acc:25551]
Mouse Orthologue:
1200011M11Rik
Mouse Description:
RIKEN cDNA 1200011M11 gene Gene [Source:MGI Symbol;Acc:MGI:1921383]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41701 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24882 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41701
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 |
|---|---|---|---|---|---|
| ENSDART00000087477 | Nonsense | 477 | 916 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 36270503)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 35303205 |
| GRCz11 | 10 | 35247065 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGGGGTTGCTTTTCAACGCTACGCTTTACAGCTTCATGAGGATTGCTA[C/A]AAGTTCTGGAGTAACGGGCATCAGCTCTGTGAGGAGCGCAGCCTTACGGA
Long Flanking Sequence:
CACTCCAACAGACAGCCATCTTTCAATGTGGAAAGCAGTCTTTCCTCAGGGGGACAGTTGGTGGACTGCACCCTAAAGGAGTTTCTCTGGCAGCATGTTGAACTGGTGTTGACCAAGAAAGGGTTTGATGATAGTGTAGGCCGCAATCCGCAGCCCTCACACTTTGAGCTGCCTACCTACACCAAATGGGTGCACGCTGCATACAAGCTTTATCAGGTCATGATAGAGAGTGTTGAGGAAGACGCAGCCGAGATTTCCCTCAAGGTGCAGGGGCAGCTCAAAGTGCTGGAGGGCTTCCTGGATGCGGATGCCAAGTTCTCTGAGAACCGCTGTCAGAAAGCCTTGCCCTTGGCTCACAGCGCCTACCAGTCAAACCTGCCCCATAATTACACCACCACGGTGCACAAGAATCAGCTGGCGCAGGCGTTGAGGGTGTACAGCCAGCATGCCAGGGGGGTTGCTTTTCAACGCTACGCTTTACAGCTTCATGAGGATTGCTA[C/A]AAGTTCTGGAGTAACGGGCATCAGCTCTGTGAGGAGCGCAGCCTTACGGATCAGCACTGCGTACATAAGTTTCACCTGCTGCCAAAGCCTGGTAAAGTTACACGTCATGGGTTACATCTGCATTTGTGTATTTGCAGTGGTGGAAAGAGTACTGAAAATCATACTCAAGTAAAAGTACCATTTCTTCCCCAAAAATGTGCAAGTAAAAGTATCTGTGTAAATGTTATTCAAAGTATGAGTAAAAGGTAGCCCTTTTAAAAGTACTCAAGACTTAGTAGTGAGGATGGGAAAGATTGCAGCGTTTACATGTAATTTGTGGGTGTATGTGTAAACGTAACATTCTGTAGAGCCTTTAGTAATTGTTTAAGGCCATTTAAGGTCATCATACAGTAAACATCCGTCATCAGTGACATCCAGTTTGATGCCATTTACTTTCTATGTGTGATTTCATTGGACAGGAATAGCAGGATTGATTTTTCTAATCCCCATAGACAGGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24882
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 |
|---|---|---|---|---|---|
| ENSDART00000087477 | Nonsense | 635 | 916 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 10 (position 36265408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 35298110 |
| GRCz11 | 10 | 35241970 |
KASP Assay ID:
554-7292.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAGTCTCGCTCTCAGCTTGGGCCAGTCAACGGACAGCCTTGGAACATA[C/A]GCTGACGGAGCAGAAGGACAGGAGAAGAGACCAAGCTTGGTGGACCGACA
Long Flanking Sequence:
TGCTACCATGATTCATGTCATAACAAAGCCGTTTTTAGCGAAATCTCGTGACCTTGCTTATTTAATTCTCTTTCCAAACCCCTGACTTGAAACAAAAGATTCATAGTTTCGAAGCTTCCTGAAGCAGTGCTTCAAAAGCAGCCATCACTAACATGAAGTGCTTCTTTTATCCTCATTTGTAAGTTGCTTTGGATGAACACACGTGCTAAATAAATGACTAAAATTCTTAAATGTATTCCTCATCATTCTGTTATCTGTTCGCAGATGCTTGAGGAGAAATGCTGTGCTAAACTGGAAAGGATAAACTTCCCAGTGTTTCAAGCTAGCACGCCTGACCCGGCTCCTGCCAGCGACGAGGTGCCCAGACCAGGAGAGGTTCCTCCGTCAGGGGAAGCTGATCGCCTGAAGGAGAAAGAGACCAGCACTCACACCCCTGGGGAAAGCACGAGTCTAAGTCTCGCTCTCAGCTTGGGCCAGTCAACGGACAGCCTTGGAACATA[C/A]GCTGACGGAGCAGAAGGACAGGAGAAGAGACCAAGCTTGGTGGACCGACAGCCCTCCACTGTGGAGTATCTTCCCGGGATGCTGCATTCTGGATGCCCGAAAGGATTGTTACCCAAATTCTCTAGCTGGTCTCTTGTAAAGCTTGGTCCGGCCAAATCCTACAACAGCCTCACTGGTTTAGAGCAACCTGGATTCCTCCCAGGCTCTGCTTTCCTCTTGCCGTGGGATGTAGTGATTCGAAGCCGATCTGAGGAAGACGTGGGATCCCTTGAACCTCTGGACGGAGGCCCGGCGTCCTGGCCGGCACCAAATAAAGCATCAGCTGGAAAGCGAGGCAGCGCTGGAGGAATCGGTCGAGGGCGCAGACGGGATGATGTAGCTCGTGCTTTTGTTGGTTTTGAGTATGAGGACAGCAGAGGGCGCCGCTTCCTCAGTTCTGGCCCTGATAAAGTGGTTAAAGTGCTTGGACAAGGTGGACCAAAGGAGCCTGCAACCAGATG
Associated Phenotype:
Not determined