ZMP
si:ch73-60i13.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate R3H domain containing 1 (R3HDM1) [Source:UniProtKB/TrEMBL;Acc:B8
Human Orthologue:
R3HDM1
Human Description:
R3H domain containing 1 [Source:HGNC Symbol;Acc:9757]
Mouse Orthologue:
R3hdm1
Mouse Description:
R3H domain 1 (binds single-stranded nucleic acids) Gene [Source:MGI Symbol;Acc:MGI:2448514]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37455 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24103 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37455
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 |
---|---|---|---|---|---|
ENSDART00000091982 | Nonsense | 395 | 1028 | 11 | 23 |
ENSDART00000146322 | Nonsense | 50 | 729 | 1 | 13 |
The following transcripts of ENSDARG00000063141 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 12496022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12341885 |
GRCz11 | 22 | 12366662 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCTGTGGCCCCTCATCCCTCTGCACCCATAGGGGGCAGCGCAGCCTCT[C/T]AGAGCAGCACTACTAACGCTAACATTAACGCTAACGCTAGCTTCTACATC
Long Flanking Sequence:
TAATACATTTAGATTCCTTTCTATTTTTTTATCAACCCTTTAAATTAAATAAATCTGAAATTAAATGTAATGAATAATAAAGAATGAATAGTCATAATAAATTAACAAAAATCTAACAACTTTCTTAAAAATAATCGCTATTTAATCGCTCTTTAACAGTCACCTAATACATCTTATTTTTTTGTCATATTTTTTTATTCAAACCCCCTTGCTTGCCTCCATCATTTTTTAACTTTGATATAATTTCCTGTCTATATATATTATCTGCTCTGGCCAACATCCTATGTTCATTCCCTCATTTCACCTCCCATCCTAAGTCCTCCAGTAAAGCTCTGGTTCTCCGTCCTCCTTCAGGTTCAGACTCTTCTAGTAGCGTAGGCTCTTCTTCCGGGTCTCTCTCTCGGCCTGCTCAGCTGTCGTTACCGGGCCCGGTTCGGCCCTTCACCATGGCCCCTGTGGCCCCTCATCCCTCTGCACCCATAGGGGGCAGCGCAGCCTCT[C/T]AGAGCAGCACTACTAACGCTAACATTAACGCTAACGCTAGCTTCTACATCGTTCCTCTGGACGCCAGCGCCATCCCGCCGGGCAGCGTCCTGCTCAATCCACAGACAGGTATCTCGGAGAACGGAGATTTTTTGTTAATGTGCGATACTAATTTTCCGTACTAATTCATTTGCGCGATTGCGATTTCTGCTGTGTTCATTGACCATGTCAGGTTTGTGTTACGCAGGTCAGCCGTTCGTCAACCCCGATGGAAGTCCTGTGGTTTATAACCCTGCGATGACATCACAGCAGGGGCGAGGCCAGCAGCACATGACTTTACATCCTGCCCCGCCCCCTCCTCCACCTCCACCTCTTCCCCCTCCACCTCAGCCGGCCAATCACCTTCTAGCGCAGGTGAGTAAACACAAATCTTTTATTTCATGGTTAATAATTACAAATTATTTTAAAGTTTTTGTTATTTTTGTTTTTGTCTTGTTTTAATTGTTTATTTAGTGACGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24103
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091982 | None | None | 1028 | None | 23 |
ENSDART00000146322 | Essential Splice Site | 587 | 729 | 11 | 13 |
The following transcripts of ENSDARG00000063141 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 12516378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12362241 |
GRCz11 | 22 | 12387018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTCATGTGGTCAACCACCACCATCATCACCATCTTCATCACCACCAG[G/A]TTGAACACGCACACACACTCTCACTCACTCATGATCGCACACATCCAGCG
Long Flanking Sequence:
TTACTAGCAAAGCCTAGGATGTGTTTCGACAATGTTTTATCATTACAACCAATCAATTTGTAGAGGAATAACTTCGATTTTACAATGGCAACAAATTCTAAACATTTTTAGTTAGACCAGCAGTCCTTTCCGGGGAACATCTGTGCTTGATATTGGAAGATTTTGAAACTTTTATAGAAAATAATGTAATATTAGCATTTACCCAAACCCAGAGAAACTGAATAATGTCTTTAATTTATCCATAGCTGTATTTCACAACAATAGTATCTTTGTGTTTGTTGGATTATGAAGCAGAAAACACTCATTACAGTATTTTTTGCCGGTCCTCCATTAACATCCAGCATGTGTTTTTTTTTTTTTTGCTGTGTTTTTCAGGTGACGGCAGGTATCCTCCTCTGATCGGGCAGCCGCTTCAGTATAACCCTCCCATCAGACCCCCACTAATGCACGGCTCTCATGTGGTCAACCACCACCATCATCACCATCTTCATCACCACCAG[G/A]TTGAACACGCACACACACTCTCACTCACTCATGATCGCACACATCCAGCGTCATCTTCATCCTCCTCATGGTCATGTTAAGCGCAGTCGTTCTTCAGCTCATGCTCCGCTCTGTTGTCGTGTCTCAGGGGCCTGTGGGTGTTCGGCACGGCGGCCGCCCTCGAAGACCCGCAAAGAAAACACTGTCTACTGACATGAGCCAAGGAGAGATGGGTAGGAAAACACACATTCATATACAGCGTGCAATATGCGTTCATAGTACACATTGGTTCTAATGCAGTACTACTATTCAATACAAATTAGCTTTTTACGTAGGTTTACGTTAGGTAGATTGTAGTTTAGTAAAACGAATGGAAATAAAACTGAACTATATTTAGTATAGTATTTAGTATTATTAAATAATACATGTCGTTTTTTGTTTGAGAATCATACATTTGAATAAATTCATATAAAATTAATAAATTTTTTTGAGTGTGTATATAAATGACAATATCATGAGTT
Associated Phenotype:
Not determined