ZMP
zfpm2b
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein, multitype 2b [Source:RefSeq peptide;Acc:NP_001034613]
Human Orthologue:
ZFPM2
Human Description:
zinc finger protein, multitype 2 [Source:HGNC Symbol;Acc:16700]
Mouse Orthologue:
Zfpm2
Mouse Description:
zinc finger protein, multitype 2 Gene [Source:MGI Symbol;Acc:MGI:1334444]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23488 | Nonsense | Available for shipment | Available now |
| sa30710 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23488
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000052260 | Nonsense | 320 | 1093 | 8 | 8 |
| ENSDART00000103745 | Nonsense | 245 | 1018 | 7 | 7 |
| ENSDART00000145202 | Nonsense | 221 | 994 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 17378517)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 13278146 |
| GRCz11 | 19 | 13196612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCATTATGATGTTCACTAATACCATTCTTTTTTTATTTTAAGGTCTC[A/T]AGTCTGATGAGGTGTCCACTGGAAGTAACTTGAAATGCACCATTTGCGAC
Long Flanking Sequence:
CTCAATGGAAACTCCGCCTCTGCTTTCATTTGATTGGAGAATCAAAAAAATGCGACTGATGTAATGAGATTTTTCCACTTAGAGTTGACTTTTTTACCCTCAAGCACACAGCGCGCAAAAATGCGAGTCACAGCAGGCGCGCATAAGCAGCATGCACAACACTTGCGCCCCTTATTAAATTATTCGAAAAAGGTGCCTCTTTTTACAAGATCTTATCTACATGGGTTATATTGCAGAATTTAGCTCCAACAACCTCCAACCTCTAGTAGCCTTGGTTTGCAGAGCTGCGGCCTTCCAGGAATCAAGTTTGAGACTATTGCACTAGACCTTCCCTTACTCTAATATACCTAAAACACAGATTGCCTTAAAAACTGTCAATGGGATGGAAAGGGTTAAAAACCATGAATGTGTAGGAGCATGTGTACAGCATTTGATTTGGCTATCCTAAATTGTGCATTATGATGTTCACTAATACCATTCTTTTTTTATTTTAAGGTCTC[A/T]AGTCTGATGAGGTGTCCACTGGAAGTAACTTGAAATGCACCATTTGCGACTACTCTGCTGAAACTCTCATGGTGCTCCAGCACCACATCCTCTCCCATCTGTCCCAAACCGGCCTGAGATGCGGTCAATGCCACTTCTCATTCCAAACCCCCAGAGAAATGGCCAAACACCAGGAGCTACATGGACATAATTGTACGGTCACCAATAAACCCATTAAAGAAGACAAAACTGATAACGCTCCTAACAGCATCACAAGTAACTCTCAACAGGTCAGAGCTAAGACGAACATCAATGACCTCCAGGAAAGCACAGCACAATGTGATGTTACTCAAATTTCAGATCTGCAAAACACGGACAGTAGCCAGAAATCCAATAAAGGCGAGGCAAACTCAGGAAACAAGGCCAACCTTTCATATTCCAGAGTCAAGTCAGAACCTTCTAGTCCTCGTTTAGCCTCTTCACCCATTCAGCACCACCTTCCTCCTGCATTTCCCTTACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30710
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 |
|---|---|---|---|---|---|
| ENSDART00000052260 | Nonsense | 961 | 1093 | 8 | 8 |
| ENSDART00000103745 | Nonsense | 886 | 1018 | 7 | 7 |
| ENSDART00000145202 | Nonsense | 862 | 994 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 17380440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 13276223 |
| GRCz11 | 19 | 13194689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCCACCGATTATGCTACAGGGATGCTGGTCTCACAAAGTGAAAGGAGA[C/T]AGAGTCCAAACGAGGGCAGTGAGGGAGAAAAAGATCAGCCAATGCCTGAC
Long Flanking Sequence:
AAGAAACTGATGCACCCATAGATCTCAGTAAAAAATGTGTGCCACAGTTTGGTAACACTCCTGTTTCCCCTAAAGGACTAATGGATTATCATGAGTGTGTTGTGTGCAAGATAAGTTTCAACAAAGTTGAGGACTATCTGAAGCACAAGCAGAACTTCTGCCCGGGTACTATTTTGCAAAGTGCTTCCACTGAGAACAAAAGCATCAAAAAGGAAGTTCCCAGAAATACCAACAACCTCTTAGAGAACCCCCTCTTTGAATTTCCAGCTCCACAGATAAAGACTGAGCATCCAAATGCAGTGCCAACTTCTGATACCCAAGCTTCAAGTGAGGAACAATTAATCCCAACAAAAGATGACCTGAGGAACATGTTTCAAACCTCTTCAACCTACCCAAGTCCTGCTAAGAAAATGAGACCTGATGAGCAAATTTGGCCTTACTATGAAATCAAACCCACCGATTATGCTACAGGGATGCTGGTCTCACAAAGTGAAAGGAGA[C/T]AGAGTCCAAACGAGGGCAGTGAGGGAGAAAAAGATCAGCCAATGCCTGACGGTAGCCATCTTAGCACAGATGACCCTGAGAACCAGAGCCAGTCCTCATCTCTAAAGGACAATGTTGAGATTGAGGAAAAGATGGAAGATGCTGAAAATAAACATGAATCCCCCACACCAGAGAGCCGTTTAGATGATCCCATCAACAGTAAGGATGTCACCACACAGATGCCATCTATAAAAACTGAGGAAGTCTCGACTAGCTTGAAGAAAGCGTTGACTGGGTCCATTGCCAACTCAAGTAATGTAAAGTACTGTCGCCCGTGTGACATCCAGTTCAACAATCTCTCAAATTTTATAACGCACAAGAAGTTTTACTGCTCATCTCAAACAGCAGAGCATGTCAAATAGTGGACAACTAGTCCACAGTTGTAGAAAATGTAGTGTTGGACTCAATCCACGTACATACTGTCAGCAGTGTAAAGATACATTTAGGGCCTCTTGTCACAG
Associated Phenotype:
Not determined