ZMP
zgc:194508
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100004673 [Source:RefSeq peptide;Acc:NP_001170934]
Human Orthologue:
C10orf107
Human Description:
chromosome 10 open reading frame 107 [Source:HGNC Symbol;Acc:28678]
Mouse Orthologue:
1700040L02Rik
Mouse Description:
RIKEN cDNA 1700040L02 gene Gene [Source:MGI Symbol;Acc:MGI:1920537]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41966 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45450 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35213 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41966
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 |
---|---|---|---|---|---|
ENSDART00000124084 | Nonsense | 63 | 359 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 8739853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 8043451 |
GRCz11 | 12 | 8077434 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATTATTTTAATGGTATGCAGTATTTTCTTGCATTTTCAGACAGTTT[G/T]AAAATATTCTCCATTTCAAAAACCATCAAACATGTTTGAAGGAAGCTGCA
Long Flanking Sequence:
AAAATTGTAAAATAAAATCTGTTTTTGACATAAATGAAGACAGCAGAAGTGAATAATTAATTTAAATTATTTAGCCTGACATGTTTATTGTTCCAAAATATTTTAAATGCTTCTTAAAATAAACTATATTGTGTTTAAAAGTTTTTTTACCCAGACATTTAAAAATAATACATTTTAGAGCAGTAATTACAATACCGCCGATAATCATACAGTCAGAATCTTATACCGGCCCATGCCAACTCACAGCAAGAAGGTCTTCCACTGTGGCGACTCCAGTCAGGGACTAAGCTGAAGGAAAATGAATGAATGAATGTAATATTAAGTTACGCCAACAAAACAGTTCCAAGTTACAATGTGTTTACTCACTTTTTTAGAATAATCAGTGCATAATTGGTAAATCTGTAATAATCTCATCCTCTATATTTTTGGGTCTAATTTACTGTAGATAGATGTGATTATTTTAATGGTATGCAGTATTTTCTTGCATTTTCAGACAGTTT[G/T]AAAATATTCTCCATTTCAAAAACCATCAAACATGTTTGAAGGAAGCTGCACTGTTGGAGTATTTTGTCTATGGATTTTGGTGGGCCAAAGAGATGAGCTTCACTTCTGAGCAAATCTCGTTTGTCATGGCACTTTTACAGCAACTTATCGACAACATTAAAAGTAAGTAAAAAAAAAACACAAGCCAAAAAATAAAATAAGCAAGTAAATAAAAGAATATGAATGTGTTAAAATCTTAAAACGTGGTAAAAATCAGGTGAGGGCTTTTCTTTTACTGGATTGCTTTAGGGAAGTGAGTAAGTGGGTCAATTGGTGCTTTTGAAAACACTATCGGTTGGTTTAGGGAAGGAGAAGGGTGAGTCAGTCGATCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAATGGCGGTCTCTGGTGGATTTACATTAGTAGAGCAGGTGCGAATTCTGACATCTCAAAAAGCGGCCCCTGGGGGTTTTGCCTAAACAAAAACTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45450
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 |
---|---|---|---|---|---|
ENSDART00000124084 | Nonsense | 138 | 359 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 8740529)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 8044127 |
GRCz11 | 12 | 8078110 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTGCTGATAATTTCAAGGCATTTACCCAAGCAGTGCTTTCCACAAGA[C/T]AGTCTCCATCAACAAAAGACAGTTCTTTATTCAACAATGATCAAATCAAG
Long Flanking Sequence:
AAACACAAGCCAAAAAATAAAATAAGCAAGTAAATAAAAGAATATGAATGTGTTAAAATCTTAAAACGTGGTAAAAATCAGGTGAGGGCTTTTCTTTTACTGGATTGCTTTAGGGAAGTGAGTAAGTGGGTCAATTGGTGCTTTTGAAAACACTATCGGTTGGTTTAGGGAAGGAGAAGGGTGAGTCAGTCGATCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAGTCAATGGCGGTCTCTGGTGGATTTACATTAGTAGAGCAGGTGCGAATTCTGACATCTCAAAAAGCGGCCCCTGGGGGTTTTGCCTAAACAAAAACTTTAAAAAAAAACATACCTCCTGGGTATTTGGTGCTCTCTGGAATTGTATATAGGGTGACGTTTTTAGAATGAGCATTTTCTGTGTTAACATAATGCCTGTTGTGTTTTTTTTTTCAGACAAACAAGCATCATTTGCTGATAATTTCAAGGCATTTACCCAAGCAGTGCTTTCCACAAGA[C/T]AGTCTCCATCAACAAAAGACAGTTCTTTATTCAACAATGATCAAATCAAGGCCATCACAGATTACTTCAAGACCAGGTTTGTCTCACTTTTGTCAGATCCATCCTATAATCACATTCCTCTTTTTAGTACACTGTGATTATGCTTATTGCATTTCAATTGATTAATATGGATTAGGTCATTCTCAACCCGTCGTAAGTTATTAATTGACGCAAGATGCTGCTTTGCCATTAGACAGCTGCTAACAAGCAAACTAGATTTTTTTTATTGCCTTCATAATTAATGCTATGCATTATTCATAAAGCAATGGATTGTGACGCATGCAGACTAGAAAACACTGGGAAATAACAAGCTGCAAGGAAATCATCTGTCTTTTAGAAAGCAAAAAGTAGAAAAAAACACACTGATGCACTGAAAAAATAACAGTATGGGTATTATAAGATTGATTTCTATGTTTACCTGAAAGCCCCAGCTCCATTCACAACACCAAAATTATTGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35213
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124084 | Splice Site, Nonsense | 225 | 359 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 8752435)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 8056033 |
GRCz11 | 12 | 8090016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGACCTCTACTTCCATTACATGGCTCCCCCATGTGCGCAAACACCTGAA[C/T]AGGTAAAATGTTCTTTTTGTGATTACATTTACATTTAGTAATTTAGCAGA
Long Flanking Sequence:
TGGTTTTTATATTTATGTAGGCTAATCCTTTAATTCTTTTTCAAATGTAAAGATATTTGCGTATTGCTGTACATCCTGTGTGTATTAAGCAATGTTTAAGCGAGGCGCACAACTAACACGCTTTGCGCTGGACTATAGATCTGCGTCAAAAATACTCTTGCACCAAACTGATTTAGCAAACAACAGTTGCGTCGCGCCTTGCGCCGCATTTCGTCAGGTGTATGATAGATTCCCAATTGTGTGATTCAAACTTGCAGCTGCGAGAAAAAAAGTCAAATTCTGAGAAAAAAGTCTCAATAACCTTGTCCTAGTTAATGTTGCAGTAAAAAAAAATACTCTATGAGATTTATTTTTGATGGGCTTTTAAAATGTTGGGTGTTTTGTTTCAGAAGTGCATTGAATTGATTAACCCGGATGAATTTGCCGCCCCACTAGAAGAGGGCTTTCCTGCTGACCTCTACTTCCATTACATGGCTCCCCCATGTGCGCAAACACCTGAA[C/T]AGGTAAAATGTTCTTTTTGTGATTACATTTACATTTAGTAATTTAGCAGACAATTTTACAATTGAGGAGGCATTCAGTGATTCAACAACAAGAGGCAATACGCACAAGAAGTGCTAATTATCCAAACGAACTGTTCTGTGCTAAGAGAATTGAGTGCTAGAGTTAGGAGGAGGGAGTGGGGGGGGCTGTTTTTATTTTCATTTGAGAGAGAGTGTTTCTACAGGTGTTTGACAGTGGTTTGTCAAGCCCACTCACCTGTGTGAAGCACACTTCCTAAATCCATGTTTTTGATTCTAAATCCATGTGAGCTGGGGGGCATCCAAAACTCCTGTAGTGTCTTTAGCTCACTGTAAACTGTTGTATTCATTTTGTGGTTCAGACCTAGCTTGGAATTACCCTTCCAGAGAAGATGCCTTTCACATGTTTCTCATTTTCAGACAAAACACAAATCTGCTTCCAAGTATGACTAACACTTTTCCTTAGCAGACACTGCACTGTAC
Associated Phenotype:
Not determined