ZMP
si:ch211-81a5.5
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC558774 [Source:RefSeq peptide;Acc:NP_001038339]
Human Orthologue:
C1orf92
Human Description:
chromosome 1 open reading frame 92 [Source:HGNC Symbol;Acc:26556]
Mouse Orthologue:
4933430H15Rik
Mouse Description:
RIKEN cDNA 4933430H15 gene Gene [Source:MGI Symbol;Acc:MGI:1921735]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45659 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23446 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45659
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 |
---|---|---|---|---|---|
ENSDART00000052898 | Nonsense | 116 | 481 | 4 | 14 |
The following transcripts of ENSDARG00000036412 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 9716678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 9175217 |
GRCz11 | 19 | 9094142 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAACTGATGCTTCAGGTGCTGAGCAAGATATTGCCGTCTCTCAGTAATT[T/A]ACTGTGCTTGCGGTAAGCTTTTATATTTTGAGTTGTGTGTTGTGTTTGTG
Long Flanking Sequence:
CAAGCTTAGTTTTCGATCGTCACGTCACGTATGCGCAAATTATTTAAATATTAACATTCCTGTTCAACACAAAAATGTTTGTCCAGAAAACTCAGTTAAACATGTAGACAAAACATTTTAGCCAATATTGTTGACATAACATATATTTTTATGTAATCAATTCTTATTCACAATTCTTAGTATATATGACAGAAAAAGTACAGTGTGCTGAACAACTGGTACTTTGTTTTTTACAGTGTGGAGTGAATAATGATTAATCTGTTTTCCTTAGAAAGCAGAATGACAAAATGGTCCCCTGGGCGCTGCCTTCAGATAGAGCTGGAGAACGAAGAGCACAACAACGTAAAGGAAGTCAAGATATCTGGTATGGCTGGTGTTTTTTTTCTGCGTAAACAATAGGTTGGAGCTGTATCATTTTTGCTCATTATATTTGACAGGATGGACGGTGGATGAACTGATGCTTCAGGTGCTGAGCAAGATATTGCCGTCTCTCAGTAATT[T/A]ACTGTGCTTGCGGTAAGCTTTTATATTTTGAGTTGTGTGTTGTGTTTGTGTACGTATATTATGTCCATTTTAATGAATGGTGATGCTTTGCAGCATGTGGCGTATAGGTCTAACAGATGGCACTTTCACATCCATGAAAAACACTGTGTCTCTGTGCTCAAATCTCAGGTGAGAACAGTCAAACTGTATTTTAGGTTACCCATAATTAATTGTTTATTTAACTATGAATTCAGTTCTATAACAATGTGAATGTAAGTTGTATTTAAAATCAGTTAGCTGACCAAAGTTCTTATGAATGGAATAGAAATGTCTGATTTGACCATTTTTGGAAGGGTTGTGAATATTAATGTGGTCTGTTTCCTTCTGTTTTCATGCACACACAAACACACACATCTGAAATGCTTGCAAATTAACCATACTCAATCCAATTAATCAGTCAATAATTATTTAAAAAAAATAATTAGATTCCTTTTTAAATGACAATATTTTCAATTCAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23446
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 |
---|---|---|---|---|---|
ENSDART00000052898 | Essential Splice Site | 340 | 481 | None | 14 |
The following transcripts of ENSDARG00000036412 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 9719585)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 9178124 |
GRCz11 | 19 | 9097049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACAAAGTCCGGCAGCAAAAAAAGAGGAGGCAAAGGTGGCCAAGAAAGG[T/C]AAATAAACTCCTTTGACATAGTTTATTTGGATTGAAAAACTGATTTTATA
Long Flanking Sequence:
GGTCCCTGCTATCTTTGTCATTATCCTACAATCACATAGGAGATAATGGAGCGGCTCGTTTGGCTGAGGTAAAAATTAGTTTTCTTCTAATAATTACTACATATTATGTGGGTAAATTAGACTGTGAAACGTCTGCATCTGTTTTGCTTTAGGTTCTTGGCCCATTTGCTCTGACTCATGAAGAGATCGTTGAGAGGAGGAAGCTTTTAATTAAAGGCGACCAATCAAACATGGTCCAGTCGTCTCTGGTTAGTCTTGCAGACTCACATGAGCCGGCCCTTTCTGTCCCTAGCAACTCTTCACTGGATCAAATCAGCAAGAGTGCAAAACACACCACCAAAAAAAGGGTAGATTATATATTGTTTCCTCAATGTTGTATGTTTTCTTACACGAAAAGGTCTGATTTTAATCTTTTGTATGTAGGACAATCCCAAGAAGGAGGAGAAACCAGCACAAAGTCCGGCAGCAAAAAAAGAGGAGGCAAAGGTGGCCAAGAAAGG[T/C]AAATAAACTCCTTTGACATAGTTTATTTGGATTGAAAAACTGATTTTATATGCAGTGTTTTTTGTTTTTCACCCAGATAATAAAGCTCCTCGTAGTCAGGCTGGAAAAGGCAAAGACAAGAATCTGCTAGTTTCTGAGCAAGAGGTAAGACTAATAAAAATATTATAGATCAACATTTTACCAAATAGATGGCAGGTTTAATAATGAGTTACTTTGAGTGTTACATCATTTAAATATATAATTTAATTTTTTTTTATTATTATATTTGAAACTTTTAAAGGTGCCATAGAATGCATTGATACAATATAGTAAATTGGTCTTTGATATCTACATAGAAGGTGTGTGGTAGGGTTCCATAATACTGGAATTTGAAGCCAGTTGATACTGAAATTTTAAAAACGTCCATCTCCTGCTAACATTTGAGCCCTGTTGCGCCCGTTTTTATTTATTACCACAGATACAGGGACACTGGAGCGTTTCAAAATCATGTAGATCAGTTG
Associated Phenotype:
Not determined