ZMP
mier2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LWG8]
Human Orthologue:
MIER2
Human Description:
mesoderm induction early response 1, family member 2 [Source:HGNC Symbol;Acc:29210]
Mouse Orthologue:
Mier2
Mouse Description:
mesoderm induction early response 1, family member 2 Gene [Source:MGI Symbol;Acc:MGI:1917677]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5971 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5971
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105550 | Essential Splice Site | 136 | 406 | 3 | 12 |
| ENSDART00000136374 | Essential Splice Site | 82 | 281 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 21852291)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 21505539 |
| GRCz11 | 22 | 21530517 |
KASP Assay ID:
554-3869.1 (used for ordering genotyping assays)
KASP Sequence:
CTCACCATCAAGTCCCAYGCATCTGACCTCTTACAATGTCACCTAAGAGG[T/C]AGAACATCACACTATAATGCCTNTAATTGTATAAATGTACAAGATGATTTC
Long Flanking Sequence:
GCCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTGTAGAAGTGTCTTGAAAAATATCTAGTAAAATATTATTTACTGTCATCATGACGAAGATAAAATAAATCAGTTACTAGAAATAAGTTATTAAAACTATTATGATTAGAAATGTGTTGAAAACATCTTCTCTTTGTTAAACAGAAATTAGGAGGGCTAATAATTCAGGGGGGCTAAAAATTCTGACTTCCATCTACTATACAAAATATGCATAAAAACTGCAACTGATCTAATTTTAAATTTAAATGTTTAAATTTAAGGATGTAGAAAAACTTGGCAAATTTGCATCACTAGTTTGATCCTGTTTAGAATTCTGGCTTTTCAATATTTTTGTAGGTTCAGATACATAAAGACCTGCTCTCTGGAGGGGAGGATGTGGACAACCATTCCTCTGCTGATGACCTCACACTCACCATCAAGTCCCATGCATCTGACCTCTTACAATGTCACCTAAGAGG[T/C]AGAACATCACACTATAATGCCTTAATTGTATAAATGTACAAGATGATTTCGCCACACTGAACATACTTTGAAATATAATTCTGTTTACTTTCTGTAAACCTGTCCAGGTGATGACAAAGACACTTCAGTTAGCTGTTCCGAAGATGACTCAGAAAGCACCTCCATCCCCTCCAGTGATGGCCGCAAAGTAAAACATTTTATTGTTATACTCATCTATGCTTAAATGCTGGTGAACAATTTTAGGAGCTTATACAATAGTAACAGTACAGTCTTAACTTGCCAATTTAAAAAAAGTATAAATTTGACTGGTCCAAGTAAAGAGCCCAGTGGGACACCATATTTAAAGGCAATCCAAATTAATAGTTTTCTTATTCAACTTGTTCTTAAAAATTGTATGTAGAAAGCGCAATCTTGAGTTTTTTAGTCAGCAAGGGCACATTAATTTGAAGGATATACAAAAGATTTTGAAGGATTCTGTGACACTGAAGACTTGAGCAATG
Associated Phenotype:
Not determined