ZMP
zc3h12b
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2CF02]
Human Orthologue:
ZC3H12B
Human Description:
zinc finger CCCH-type containing 12B [Source:HGNC Symbol;Acc:17407]
Mouse Orthologue:
Zc3h12b
Mouse Description:
zinc finger CCCH-type containing 12B Gene [Source:MGI Symbol;Acc:MGI:2442133]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10386 | Nonsense | Available for shipment | Available now |
| sa7561 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10386
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 |
|---|---|---|---|---|---|
| ENSDART00000090375 | Nonsense | 30 | 797 | 1 | 7 |
| ENSDART00000143676 | Nonsense | 59 | 838 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 23882092)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21594964 |
| GRCz11 | 5 | 22098764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTTTGGACCGTCCCAGCTTCAGYCAGAGCAGCACCTTACAAGAGTTA[C/T]GAGCAGATGACACCTGCACCGACCCRTCCCAGAAAGCCCTTGCTCCTCCC
Long Flanking Sequence:
ACATTGTGTCGCTAATTAGTCCTGTGCATAAGCACCGTGAGCGGTTGACTCTGTGGCTGCAGCGGCGACTGCATGCCCTACGTGCAGCAATTGAGTACGAAAGCTGCGCCGTGGTGCAGGTGAGGGACCATGCACTGGAGCTTCAGGGAGGTCATGCACAGGTAACAGCTGCATGCGCTATGCTGCAGCGCCTGAAGATGGAGCACCGCGGCTGCCGCGACCCCCAGCCCTCACCCGCAGCCGCCGGTCACGAGTCTCCAGAAGAAGAGGAGGAGGAAGAGGATGAAGAAGCTGGCGAAGAAGGAAGTAGTTCAGAGAGCGAAGGAGAGGTGCGGCCGCGCAGTGGAAGTTCTGGAGGTGTCAGTTCAGCGGGGTCAGGAGACTGTCCAGTAGGAAGGAGACGGGACCTGCTCATAGCAGCCAAACCTCACCGGCAGCTGTGCCGCTCGTCCTGTTTGGACCGTCCCAGCTTCAGCCAGAGCAGCACCTTACAAGAGTTA[C/T]GAGCAGATGACACCTGCACCGACCCGTCCCAGAAAGCCCTTGCTCCTCCCTCCTCCGCATCCCCAATGTCCTTACGTCAAACCAGCGATCGAGATTATCAAACCAAAATGGACTTTGCTTTGAAGCTGGGCTACTCTGGAGAACAGGTGGAGTCTGTGCTGAGTAAACTGGGGGCCAATGCGCTAATCAATGATGTATTGGCTGAGCTGGTGCGGTTAGGAAATAAAGGAGATCCAGAGAGTCAGACAGCAGCGGGTAGTGCCAGTTTTGCACCACGGACAGTGGGAGCCAAAGAAGCCGTAAGCCCAGAGGCATCGCTGGAGGAAGACTCATCAGACACGTATGACAACCTCCGACCAATCGTGATTGACGGATCCAATGTTGCCATGAGGTAAATGCCTATAAGAATCACACACTTTCCTCATATATTATTAAAAAAACATACACTTTCTGTGATTGCCGACAAGGCCTACACATGCATGCTCAAATCCTCTGCTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7561
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:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090375 | Missense | 434 | 797 | 5 | 7 |
| ENSDART00000143676 | Missense | 463 | 838 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 23888793)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21601665 |
| GRCz11 | 5 | 22105465 |
KASP Assay ID:
554-4062.1 (used for ordering genotyping assays)
KASP Sequence:
TTCTGTACCGTCTTTAGTGTCCGCTCTTAGCGTCCCCACTATGCCACTAA[C/T]AAAGAGTCATGCAGCTGGCGCTTTGAACACACGATCGGCTAGCAGCCCTG
Long Flanking Sequence:
CATATATCAAATATAAAATCGTACCATAAATTTTTCATGCACTGTTAAGCTATGTGTTTTTTATGTATATTATAATATTTAAAGAATTATATCTACTGCCTTAAAAAAAAAAAAAAAAAGAAGTAACATTTTCTCAACTACCAATATTGATTTTATCACAGGTAAGAAGTGCACGTATGGCCATAAGTGCAAGTACTACCACCCAGAAAGAGCCAACCAACCACAACGGGCTGTTGCAGATGAGCTTAGAGCTTTTGCTAAACTCTCTGCTGTAAAAACCATGAGTGAGGGGGCACTTGCAAAATGTGGAACCTCTGGGGCTGCTAACAAGGGAGAAAGTGGCTCAGAGGCAAAGCGAGTGGCACCCAAGCGCCAGTCTGACCCCAGTATCCGGTCGGTTGCATGTGAGCAGGAAGAGAGACTCTGTCCAATGCGGAAGGCAGAGGCCAGTTCTGTACCGTCTTTAGTGTCCGCTCTTAGCGTCCCCACTATGCCACTAA[C/T]AAAGAGTCATGCAGCTGGCGCTTTGAACACACGATCGGCTAGCAGCCCTGTTCCAGGGTCTCTGCACTTTACCCACAGCTCGCTGGAGCACGCGGGCAGTGTCCAGTATCCCCCAATCCTAGTCACCAATAGCCAGGGTGCATCTGTGGCATATGGTGAGCCGTTTCCCAAGTACGACTCAGTAGTGAGTGACCATGGCTACTACTCCATGCTCAGTGACTTCTCCACCATTAGCCTCCAAGACAGTTTCTGCAGTCTCGAGCAGCCAGAGCCTGTAGGAGTGGGTGGAGGATATTCTGGCAGAGCTCCCAGCATGTGCCCAGAACCCGGCCGAAGCCATTCATCTGACTCTTTTTCGTCCTACAGTGGAGAATTGTACCTCAACTCATTGGAGGGCAGTCTGGACGACAGCATGAAATCTGCGCCAACGCAACCTTCGGCACAAACACGCCTTCAAGCCTTTGCTCACGGTTTCCACCATGAGGCCTTGACACGTGTGC
Associated Phenotype:
Not determined