ZMP
si:ch73-237c6.4
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC559882 [Source:RefSeq peptide;Acc:NP_001121808]
Human Orthologues:
MKRN1, MKRN3
Human Descriptions:
makorin ring finger protein 1 [Source:HGNC Symbol;Acc:7112]
makorin ring finger protein 3 [Source:HGNC Symbol;Acc:7114]
makorin ring finger protein 3 [Source:HGNC Symbol;Acc:7114]
Mouse Orthologues:
Mkrn1, Mkrn3
Mouse Descriptions:
makorin, ring finger protein, 1 Gene [Source:MGI Symbol;Acc:MGI:1859353]
makorin, ring finger protein, 3 Gene [Source:MGI Symbol;Acc:MGI:2181178]
makorin, ring finger protein, 3 Gene [Source:MGI Symbol;Acc:MGI:2181178]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27197 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16544 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27197
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 |
---|---|---|---|---|---|
ENSDART00000104346 | Nonsense | 27 | 397 | 2 | 8 |
ENSDART00000132734 | Nonsense | 32 | 161 | 2 | 3 |
ENSDART00000142395 | Nonsense | 17 | 161 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 24579751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23705569 |
GRCz11 | 8 | 23726808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGGATTTGTTGTTGCTCTTTTGCAGGCAGTTCATCAATGGATCGTGT[C/T]GATATGGTCAAAGTTGTTACTACCTACACGAGTTTCCTTCAGTTCCGTCA
Long Flanking Sequence:
TGAATCAACTTTTTTGAGGCTTTGGAAATGGATCGTTATCGCATACCGTACAGACACTCGAGGAAGGGCAGTTCAAACGCAGAAAGAGAAGTTTGCAGGTAGTTTAATGCCTTAGATCGGATGAAAACTTCGATTATAGCTCCGATCATCTGTATGAAAGAGTGACTTTTTTCCTGCTTTAACGTTTCTCGCCGCTGATGTTTACATCCGGTAAAGGCAGAGAGCTGTTTGTTATTGTTGTTGCAAAGAGACTAACGTTAGTTGGTTTATAATCAACTATTGTATTGATCAACTTATGTAATGTTACTGCAACGAAGTAGAGAGAAGACCGTTGCAGGATTTGTTTGTTTCTAAACTAACAAAGTCCTGCAGTTTCCGTGTATTGCCGTAGTCAATAACGACTAAATCGGGTCGCTCGAGGACTAGTTTGTTTCTTAACTTGGTAACTTCTGATGGATTTGTTGTTGCTCTTTTGCAGGCAGTTCATCAATGGATCGTGT[C/T]GATATGGTCAAAGTTGTTACTACCTACACGAGTTTCCTTCAGTTCCGTCATTTCAGGTTCAGTGTAGATACTTCCAAAAGGGAGGCTGCTGGTTTGGTGACCGTTGCAGGTAAGTTAAGGATTCAATTGGCCTTTTTTGAACCTCCTTATTTCTGATAAATGCTTGAATTGTAATATTTTTTTAACGCTATTTAAAAGGAGTTGAAGAGTTATTGTAGTTTCTGGCAGGTGATGATTGGTCCATGTGACTGAGCCCCTATCACTTTTTAAATTGCCTTGCAAACTACAAACTGTAGACCCATGAAGACAGCCTAGGGATGGATGATGCAAAATTTATAACACTAATACTATGTTAAAAGTTTAACAATTCTGATCCATTACTGTACTCCAGTGTTGTAAATTCTTGTCTGCACCAACACTGAAATGCACACCAAAAAAGCTACACTGGTTATTGTTGTATTGCAACTTAAGTTACATGGCATTTGTTAAGACATAAGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16544
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104346 | Nonsense | 250 | 397 | 5 | 8 |
ENSDART00000132734 | None | None | 161 | None | 3 |
ENSDART00000142395 | None | None | 161 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 24581197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23707015 |
GRCz11 | 8 | 23728254 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTGGCATCTGCATGGACAAGATTTCTGAGAAATCCACCGCTCAGGAA[C/T]GACGTTRCGGCATCCTACCCAACTGCAATCATGCTTTCTGCATTGGCTGC
Long Flanking Sequence:
GAGGAGTCCGGGGTTGTGGAAGATGTACCTCTCCAGCTGGGTATAGCCGTCTGTTCAAGATTTTCTTTAAAACTGCACATTTTAGATTTTCTTTGTTTGACTTTCGTATTTGATTACCTCAGGTGCATCAAGAACTCTGTATCAAAGCAATGCTACACACTCCAGTTCTTCACACAACTACACCTCTACATCCTTCATGGCTGCACCAGCACCTGTCGAAGCCACAAAAATTACTGTAGCCGAGGCTGAAACGCAGGTCACAAACATGATACGCTTCCATAGCTCGCAAATAGTAGTGTTGGTTGTATGAGTTTAATGAGCTTTTTTTTTTTTTTTTTTTCTATATGTCATTATAGGTGACTAAGTCGCCAGTGAGATCAGGTCAGGTTGCAGCAGCAGTCTCATCAGTGCAGCAATGTTCAGGGGCCTTTGACCAAAGCAATGATGTTGCCTGTGGCATCTGCATGGACAAGATTTCTGAGAAATCCACCGCTCAGGAA[C/T]GACGTTACGGCATCCTACCCAACTGCAATCATGCTTTCTGCATTGGCTGCATTGTGACTTGGAGAAAAACAAAGGACTTTCAGGAGGAGGTCATCAAGTGAGTTTTGTATTTGTTTTGGTTGATCAGATTCCAAAAAGATTGACCCATTCTTGTTTACACCTGTTCCTTTAATCAATTTAATTTACTTTGTTTATTAGTTTATGGTTTGGTGTTTATACTGCACGGTCTGATGTAATATTGTGAAAAGCTTGTGCAAGTTGCGCAAGGATGTGAAAAAGATAATGAAATATGATACAGAGCAGACTCCGTTTGATGCATGTATAGACTCATAATGAGCTGCCTTTTTAAGGTGTTGGGGCATTTTTACCACTTTTATAAATGTATAACTAGTCTATGAATCCCTAATCTCTCAATGTTAAATCTCCTTTTTAAAATGCTTTGTTTTGAAACATTTTGAACTTTTACAGTAGTTTAATATTTAAAGTGGATCAATGTTCAA
Associated Phenotype:
Not determined