ZMP
zmym2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate zinc finger, MYM-type 2 (ZMYM2) [Source:UniProtKB/TrEMBL;Acc:B0S
Human Orthologues:
ZMYM2, ZMYM5
Human Descriptions:
zinc finger, MYM-type 2 [Source:HGNC Symbol;Acc:12989]
zinc finger, MYM-type 5 [Source:HGNC Symbol;Acc:13029]
zinc finger, MYM-type 5 [Source:HGNC Symbol;Acc:13029]
Mouse Orthologues:
Zmym2, Zmym5
Mouse Descriptions:
zinc finger, MYM-type 2 Gene [Source:MGI Symbol;Acc:MGI:1923257]
zinc finger, MYM-type 5 Gene [Source:MGI Symbol;Acc:MGI:3041170]
zinc finger, MYM-type 5 Gene [Source:MGI Symbol;Acc:MGI:3041170]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18453 | Nonsense | Available for shipment | Available now |
| sa34614 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18453
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102045 | Nonsense | 488 | 1357 | 4 | 22 |
| ENSDART00000133469 | Nonsense | 488 | 1357 | 5 | 23 |
| ENSDART00000136427 | None | None | 37 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 22481269)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 21637055 |
| GRCz11 | 9 | 21447924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGGCGAACCACGTTTTACTCATAGACGGCCAGCAGAAACGCTTTTGCTG[T/A]CAAAATTGCATCAGGGACTATAAACAGGTCAGTGTCGTATGTTGTTTTTT
Long Flanking Sequence:
TTTTTCGTTCTTCTGTAATATGAGTTCATTGCAACTGAATGGAAAACCCAAGTACTGTCATTTTCACACACTTTCCGTTGTTGTCCATTGTCAAATATAATTTTTGAACACAGTCAAGCCTCCAACCTTGTAGCCATGGTTACTGCTATCCTTGATTGTATTTGGTGATGCCATAGCAATCACCTTGGGAACAAAAGAAAAGACCATTACACCAATTTATTAGTCGTTTCGGTTATTTATAACATGCTAATCTTGAACCTGTAACCTCTACATTAAATACTGTTCATCATTGTGTGTATGTGTGTTTGTATCCAGATTCGGCATGAGGTGAGCATCAAGAATGTGACTCACAAGATTTGCAGTGATGCGTGCTTTAATCGCTACCGTATGGCTAACGGGCTAGTCATGAACTGCTGCGAACAGTGTGGGAACTACCTGCCTAGTCGTGCCACGGCGAACCACGTTTTACTCATAGACGGCCAGCAGAAACGCTTTTGCTG[T/A]CAAAATTGCATCAGGGACTATAAACAGGTCAGTGTCGTATGTTGTTTTTTTTTCTTACTTTTAGCTCAGCCTCCTGTAGGTAGGGATGCCCTGATCAGTATTTTTGCAGCCGATGCCAAGTACCAATTCCTTGTCATGGTGATCGGCCGATACAGAGTACCAATAATAATGATTGGAGTTTAATAATGCATTAAGCACATTTCCCTCTGAGTATCATAGTTAAGTAGAGATCACTTCTTACCTAGGATAAATTAAGGATGTTGCATATAATCCCTTAAACGTGTCTCTTACAACCATTTAGGTGTGAACATGTCATTGATCAGAAACAGATTTACAGAAAATAACTGATTAAACACAAAATAAATTGGTAAGAAAATGACTAATAATGAAATTTAGAAACTTTGCAAATGATGGGAAAAGAATTCAACACGTCACCATAAAGAAGTTTGGAGCACATGTTTGATGTGTAAGAAGTTAAAATGAACACCTATAAATCCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34614
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102045 | Nonsense | 1253 | 1357 | 21 | 22 |
| ENSDART00000133469 | Nonsense | 1253 | 1357 | 22 | 23 |
| ENSDART00000136427 | None | None | 37 | None | 2 |
Genomic Location (Zv9):
Chromosome 9 (position 22466872)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 21622658 |
| GRCz11 | 9 | 21433527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGTTGCTGTTTGCTGAAATGTCTTGTACGTGTTTTTCACAGAGCAAT[C/A]AGGAAGTAAGAGAAGACGTAAAGATTACTGTGACTCAAATTTTGATTCAG
Long Flanking Sequence:
ACTTCAAATTGATTCAATTGTTAAATGTAATTAAGGGTTTGAAATACCTTAACATGGTGTGCTTGACCTATTAAAAACAGTGTTGCTCCAGTGTTTAAGTGTGAGTATTTTTCCTTTGAGGTTCTCGGTGGAGTCGTGTTGAAGAGCAATATCTGTGGAGCAGCGGACAGCTTGGAGAACAGGCGCCTTCTGTCCTGCTGAGATCTGTATTCTATCTCAACACCAAATACTTTGGTCTTCGCACCCCAGAACAGCACTTACGCCTCTCATTTGCAAACGTCTATGGCCCAAGCAGCTCGAAACCGCACAGCCATGAGACCACCGTCTGTATACGCATCCCCTCCATCTCACAGGAGCAGCATGGTGTGTTTTTCAATTGTAGTTTCGCTTTACTTGTGCATTTTAAATGTCCCAAACTTGTTAGATATTTAAATGTTCAATGTGTTTTACCAGTGTTGCTGTTTGCTGAAATGTCTTGTACGTGTTTTTCACAGAGCAAT[C/A]AGGAAGTAAGAGAAGACGTAAAGATTACTGTGACTCAAATTTTGATTCAGACAGCGGTTCAGGGGGATCCGCACACTGTCCTGTTAAGAAGCATGAGTGCCGACTGTATGAGCTTTACCTTTCGAAGTGGTGAGTGACGTAAATCTTCCTTATTTGTGATGCATTTGAAGAACTAAGGGCTTTTTCAGAACTGTAAATAGTATTTAATTTAATTTTCTGTAAATTTGTATTTTTCTTTTAGTAACCCTTTACGTTCGGTTCTCATTTTTAAGGGAAACATTTTAAAGTGCACCAAAATGTGGTTCTACAAGTACAACTGCCCCTTATTGCCAGAGTGCACCTGTGTACATTCCTCTACTTCATTTATACTTCATTCTGAGATGTGACACGAAAGCACATTAGTATGTATCTGTCATTCCCACGTTAACTGATAAATGATGTGTATTTAATTATACTCCGCTGTAATAAAGTTAATGTGGGAATCATAATGAGAGCAATTA
Associated Phenotype:
Not determined