ZMP
zgc:66359
Ensembl ID:
ZFIN ID:
Description:
Novel protein (Zgc:66359) [Source:UniProtKB/TrEMBL;Acc:B0S5D8]
Human Orthologues:
AC002365.1, AC003980.1, AC006062.1, AC006999.1, AC007379.1, AC008162.1, AC008573.1, AC008794.1, AC009021.1, AC010133.1, AC011503.2, AC012596.1, AC016595.1, AC022409.1, AC022486.1, AC023481.1, AC067941.1, AC092485.1, AC097714.1, AC116351.3, AC145210.1, AL121899.1, AL138690.1, AL159986.1, AL357512.1, AL591242.1, ZC3H13
Human Description:
zinc finger CCCH-type containing 13 [Source:HGNC Symbol;Acc:20368]
Mouse Orthologues:
Gm10563, Zc3h13
Mouse Descriptions:
predicted gene 10563 Gene [Source:MGI Symbol;Acc:MGI:3642630]
zinc finger CCCH type containing 13 Gene [Source:MGI Symbol;Acc:MGI:1914552]
zinc finger CCCH type containing 13 Gene [Source:MGI Symbol;Acc:MGI:1914552]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31208 | Essential Splice Site | Available for shipment | Available now |
| sa19512 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31208
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 |
|---|---|---|---|---|---|
| ENSDART00000054064 | Essential Splice Site | None | 1759 | 1 | 21 |
| ENSDART00000110816 | Essential Splice Site | None | 244 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 28712095)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 28962924 |
| GRCz11 | 1 | 29766855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCCCAATAGTCTGTGAAACTGGACTTGACGCATCAATCATATTCGGG[T/C]AAATTAGAATTTGTTTATGGAGCCATTAAAGGGTCCGTTTTAGCTGTATC
Long Flanking Sequence:
GGCCTTTAAAAAAAATATGATAATTAAAACATAATAATAATAATAATAATATATAATATATATATATATATAATGTGAAATGCTGCCTCTACTGGCCTCAACTCATCATAATGCGTGTCCGCATTGTTGTTTGTAACTTTATAGGTGGCTTAAACTCTTTAAATTCTTTGTTTTTTTATTTTAGAATTAAATGAACATACTTTTATCATTAAAACACAACAGGAAATAATGTCCATGTAGCCTGTGTGTGCGTTTATGTGTTCTGTCTCCAAATAACTATTTTACATTCAGGCAAACCAATTCTTCGGATTAGACCTCCAGTTTCCCACAATCCACTTCTTTGTGCTTCAGGAAGCTGAATGTGTGCAGAGTTTGCGCTGTCTTGCCAGCATCATGACGGCGGCTAAGGGGAAGACCGCTTTGCAAGACTTTTGCATGTGATTAGGAGGTTATCCCCAATAGTCTGTGAAACTGGACTTGACGCATCAATCATATTCGGG[T/C]AAATTAGAATTTGTTTATGGAGCCATTAAAGGGTCCGTTTTAGCTGTATCGTTATATAGGCTTGTGTTAACAGTGTAGGCCGCGCTGCAGTCATGCAGTTGTATAGCTTCATTCTGCAAATGAATGACCGCTTAAAACGCGCACATATATTAACTATCTTTTTTGTGTGTTTGTGTTAAGCTTCGCATGGTGCATAAATAGTTATTGTCTCAATTACGATATCGTTGATGTGCGTTGGAGAGTGTCAAGCAGATACGACTAAATGTAGTACGTTACGTTACAGCCAGTGCTGTTGTTTACAGTGTTCGGGGCTCTGTAAAATAAATGGAACATTCATGGCTTTTTGCAAGCTACAAAAGCCACGAGAATTAAATAATTATAATGTTAATTTGTGTGGATGTAGTAAATTGCCCTGCATTGATGATCAGAGACAGAATCATCCTTCAAGCTAATGTTACAATCATCGCAAGCTGTTATTTGGAGACCACATTACATAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19512
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 |
|---|---|---|---|---|---|
| ENSDART00000054064 | Nonsense | 1542 | 1759 | 18 | 21 |
| ENSDART00000110816 | None | None | 244 | None | 11 |
Genomic Location (Zv9):
Chromosome 1 (position 28737817)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 28988646 |
| GRCz11 | 1 | 29792577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTTTCTCTGTTCTTTCAGAAGAGGAAGATGGAAAAGCAGATGATGCA[C/T]AGTCTGTTGTGTCAGGTGGTGAGGAGTATGAGCCAATCAGTGACGATGAA
Long Flanking Sequence:
GAACTGAGCAAGATTTTGTTTGTCTCATGTGCTTGTATTTGTGTGTTGTTGAACTTTTTGTGCTGCCATTTTAGCCAGGACTCCCTGGAAGAAGAAATCTAGTATCTTAATGGGACTGTTCTGGTAAAATAAATAAAAATACAGGAGATGAGGTGCTATAATCAGATATGGGGGAAAGCAGTGACACAGTGAGAACATCACGTTTTATATAGTCTGAATTTCATTCATAAAACCCTCATTCGTTCTATTTAGATCATACTTTTTTTAGCTTATGGGAAGTACTTTCAAATTCAAATGTACTTGAGTAGTATGTGATTTTTGTGGATGCAGCTAATGTGTTAGCTCATAAAGATGTCAAATTGTGATGCGTAATGATTCTCAGGACCTGGATTGAAAACCACTGGCCTGTATAAATGTGGCTGTGCCAAGCATTTATTAAATTTCATACATTTTTTTTCTCTGTTCTTTCAGAAGAGGAAGATGGAAAAGCAGATGATGCA[C/T]AGTCTGTTGTGTCAGGTGGTGAGGAGTATGAGCCAATCAGTGACGATGAACTTGATGAGATTCTGGCAGACAGTCAGAAGAGGGACGAGCAGCAAGATGATGAAAAGACTTCTGGTAAGTAACACTAGCACAACCTAAAGCAGAAAAAACACAAAATTAAATAAAGTCACAGCACAGTTTCATGAACTGAAATGCACTATTCGTAGAATGAAATGAAAGCTCTGTAACTGTTTTGTGCCATGGTATATCAACGTTTCTATCCATTTAACTAAAATCATCATGTCCCTTCAACTAAAAAGTCATGATATGGTTAGTGTTTGTCATATTTCAAAAGACTGGGGGTAAATACTAGTGTTGGGTATCATTTGAAATTGATCAATTCCCATTTCAATTCTTAAACTAATTCTCAGTATTGATTCTTATAGATTCCCAGTTCTGATTTCAATGTAGTAAAAAAGATGAATTATTAACAGAAAGGAAAAGTCAAACATTTAGGCCCT
Associated Phenotype:
Not determined