ZMP
zgc:103517
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC492469 [Source:RefSeq peptide;Acc:NP_001007342]
Human Orthologue:
C9orf100
Human Description:
chromosome 9 open reading frame 100 [Source:HGNC Symbol;Acc:25909]
Mouse Orthologue:
E130306D19Rik
Mouse Description:
RIKEN cDNA E130306D19 gene Gene [Source:MGI Symbol;Acc:MGI:3036286]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33420 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9083 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33420
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 |
---|---|---|---|---|---|
ENSDART00000027756 | Nonsense | 101 | 427 | 4 | 12 |
ENSDART00000127150 | Nonsense | 101 | 426 | 4 | 12 |
The following transcripts of ENSDARG00000013476 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 11518850)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 12455477 |
GRCz11 | 4 | 12454326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGCTCATCTAGAAATGGGGAGGTTTGGCATTGGTTTCGAGGAGTTCTG[C/A]ACTCATCTGCAGTTGTACAACACATACATTGACAACATCCAAACGGCTAA
Long Flanking Sequence:
TGCTGAAATGTCCACCCTGGTTTCATATTCATCATCCTGGTAATGTAGATGTTGGACTGAAGCAGGTAATTTTAATTTACACAGACGAGAGGCAAAGGGTCTCTGAATAACTCCTGAGAGATTTCAGTTGCTGTCTGGGCGTTCACTGCTTTCTACACCTCCCTTTCTTCATGTGTTCAATTCGTTTTTTCTGTTTCGTTTCATTTTATTACACATAACTTAATTTGTAAATTAATTAGATTTGTTTTCTTTTCATATATGGATTTCTTTAAACGTTATCAACATCTGGTGAAAATTTCAGGTCAGCAGCACCATTAAAAATAAGGAAAAATGATGTGTTTAATACTTACTTGCCCCACTGTATATATGTGTGTACATGTGACTGATTAAATTAAGCCCCCTAAATCAAATCATATTTTCACTCTTCTGTTTTGTCTTAACAGGACACTACTTGCTCATCTAGAAATGGGGAGGTTTGGCATTGGTTTCGAGGAGTTCTG[C/A]ACTCATCTGCAGTTGTACAACACATACATTGACAACATCCAAACGGCTAAGAAGGTCCTCATGGTGAGTTCAGTCTTTATATGTTAGACCTGACCCCTTTTTTCACCTCCGTTAACAGCATTTGGCATTGACCACCATACATTCACATTGGACTCTTTGTGTTGCACAGCCTTGAGTAATGACAGTGTGAACATGGCTATAAATTAGTTATTATGAGCATGCATTCCTCTTTGAAAGTAGTCTAATCATTTGCTATTAAAGTAGCACATAGGTCCCCTATCCTGGCCTTTCCAGAGAAAATCCATTCTTTTACCTGCATAGAGGTCATCTGGAATAAAGCTGGTGGCTGTGTCTATCAATATGAATTCATGAATATGTATTCATTATAGATCTATGGTAATGCACCGGATTGACAGTATGTCATGCTCCACTTCTAATTAGTCCAAACCGATTAAGTCATTGTACAACTCCTCATCCATGGCACCTTTTTTCCCCCTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9083
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 |
---|---|---|---|---|---|
ENSDART00000027756 | Nonsense | 371 | 427 | 10 | 12 |
ENSDART00000127150 | Nonsense | 371 | 426 | 10 | 12 |
The following transcripts of ENSDARG00000013476 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 11481730)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 12418357 |
GRCz11 | 4 | 12417206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CMATCAGATCAGACGCAGATGACCAGAGCTCAACAGAGAGCCAGAACACA[C/T]GAGGAACTAAAAGAGCCATGGTCAGCTCTTTCMCARTTAACRTCTGAACT
Long Flanking Sequence:
GAGCCGTATGACAAAACTGAGCGTCTCTCATCCTCACATAGACTCATTCCCGTACATAGCAAAGAATTCCCTTACATGACATTGTTCATTCATTCAATCTATCCATGAGCAAATATTATCTATCTACTGCATTGAATTTAACTGTAACATGCCTACATTTTATTCTCATTCTCTTGCTTTTGGTTTTGTTTTTCTTATTCTGCTTTTCACATACTTTACTAAGTTTTTCAATGATAAAAATTAATATTTAAAATTATATAAATGGAAGTGGCATTAATGTAAAGAATATGCATGTGAAAATTTAGCCAGCCTCATGTGTATTTTAAAGGGAGAAGGGATATAGATGATGTTTGCTGGTTGAGTTGATGACAGGGGCTCTGCTTTTGTCTTTCAGGCAGTTGAAGTCCAGGAATACAGTGGTTCACAGGAGAGATGAGCTGTGCAGGACACCCATCAGATCAGACGCAGATGACCAGAGCTCAACAGAGAGCCAGAACACA[C/T]GAGGAACTAAAAGAGCCATGGTCAGCTCTTTCACAATTAACGTCTGAACTCATAAAGTGTCATATTAGTAACTATGTTAGTGTGTCCTAAAGTTTGAGACTTTTATTTGTTTATTTATTTAGCTAATGTAGTTTAATACCCCTGATGAAGAATTGAATATGTGGAAGAAGAGTTGAGCATGTGAGGGAGCTTTTATACGATTTTGATTTCAAAATATAGAACTAGTTTTCAGATTTCCTTACTGTTTCATAAACTAAATTATAGACAAAAAATGCTTGAGGAAAGAAGGAAAAATAAATGTTTAGGTTAAAAGAAATAGGAAACAATAAGTTGTATAATTGTTGAATTAATAATAATAATAACAAATTAAATTGTTATTGTTGTTAATTCTATATAATTCAATTATTATTGTTATTATTAATATTGTTTATATCATTATTATCACTGTTATAAATAATTTATTTGGCATAATCAAATAAGCAAATATATTAAATGCTTTC
Associated Phenotype:
Not determined