ZMP
hnrnpm
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate myelin expression factor 2 (MYEF2) [Source:UniProtKB/TrEMBL;Acc:
Human Orthologue:
HNRNPM
Human Description:
heterogeneous nuclear ribonucleoprotein M [Source:HGNC Symbol;Acc:5046]
Mouse Orthologue:
Hnrnpm
Mouse Description:
heterogeneous nuclear ribonucleoprotein M Gene [Source:MGI Symbol;Acc:MGI:1926465]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32398 | Nonsense | Available for shipment | Available now |
sa9147 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32398
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088356 | Nonsense | 146 | 664 | 6 | 18 |
ENSDART00000088369 | None | None | 233 | None | 9 |
ENSDART00000137689 | None | None | 540 | None | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 17760872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17511807 |
GRCz11 | 22 | 17536785 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTCAGCGTGAAGCTAACCGGGGTCATGGTGGTGGCGGAGGTGGCGGT[G/T]GACCCCCAGGCATGGGAGGAGGCATGGGCGGTGGCATGGGAGGAGGCATG
Long Flanking Sequence:
TAATCATGCCCACGTTATTATCAGCTCAAGTTTTTTCAAATATAAAAGCAAAAGTGAAACTGCTTGCGCTTTAGACGGCCTTCTAAGCTTTTTGGTGTATTTTGTTGGTGGAAACGGCCATAAAAGCATACCGTACCACTCAGTGGAAACGGCCCCAAAAAAAGTATATGCTTAAATGAATATTTATTTAAGACATTAAGGAATATATATACTCGTGTGATAGTTTTTATAACTTGTATGATTTTACGATAGTCGTGATGTTTTCAGAAACTTGCTCTTAAACCAGTGTACAAATTAAACGCAGAAAGGGTTGTCTCTATTTTTACATTTGTAAACATTTAAACATGTAAACATTGTAACATTTGACAGTTCATGTATTAAACCATAGCTCATGTGACCACAGTCAGTAAATGCTTCTCTTGTGCTGCTCTCAGGATCCAGATGGAGTGATTTCTCAGCGTGAAGCTAACCGGGGTCATGGTGGTGGCGGAGGTGGCGGT[G/T]GACCCCCAGGCATGGGAGGAGGCATGGGCGGTGGCATGGGAGGAGGCATGGGTGGTGGCATGGGAGGAGGCATGGGTGGTGGCATGGGCGGAGGCATGGGTGGAGGAATGGGCGGAGGCATGGGTGGAGGAATGGGCGGAGGAATGGGGATGGGCCCAGGACCTGGTTCTTCTTCAATGGTCAACATCCCTCCCAGTCTCATGAACAACCCTAACATTCCCAACGAGGTCATCCACGGCCTCCAAGCTGGAAAAATTGGAAGCACCATTTTTGTGGCTAATGTAAGATTTTTAACCCTTTGTGGACCATATGAAGATTCTGAAAATGTGCCCGCTGAGTATTGATGTGGCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGCACAGTTGGACTACAAAGTGGGATGGAAGAAACTGAAAGAGGTGTTCGGGATGGCCGGTATGGTCGTGCGTGCTGATATCCTGGAGGATAAAGATGGGAAAAGCAGAGGCATGGGAACGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9147
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088356 | Nonsense | 450 | 664 | 16 | 18 |
ENSDART00000088369 | None | None | 233 | None | 9 |
ENSDART00000137689 | Nonsense | 326 | 540 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 17763317)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17514252 |
GRCz11 | 22 | 17539230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGCATGTCTGATCTGGACCGCATGGGTTCTAGCTTTGATAGAATGGGGT[C/A]AGGGCTTGACCGTCTCGGCCCCAGCATGGATCGTATGGGWTCAGGCCTGG
Long Flanking Sequence:
GAATGGGACGAATGAATGGTATGAGTTTTATTTTTATTATATGCATGTATGAAATCAGTTTATTTTTTGTCTTTGTCTAATTGTTCTAGTTGAAGTGAGAGTAAAGCTTTATTTTCTTTTGACTTCAGATATGGATCGTGGAATGGGTGGTGGCTTTGATCGAGATTTCAGTGGTCGTAATGACATGGGAATGTCCCGCAGCAACTTTGGAGACTCTTTTGATCGAGGAATGGGTCAGTAACATTGTACAGAATTGTGTAAAGTACATGAAAATGTGCAATATGTAAACCCATTTTTTAAAATCTTCCAATTCCCAGGAAACTCCATGGGTATGGATCGCATGAATTCTGGCATGGATCGGCTTAGTGGTGGAATAGACCGTATGGGAGGAGGAGGAGGAGGTGGAGGAATGGACCGCATGGGAGGGGGAGGAGGAGGTGGAGGAATGGACCGCATGTCTGATCTGGACCGCATGGGTTCTAGCTTTGATAGAATGGGGT[C/A]AGGGCTTGACCGTCTCGGCCCCAGCATGGATCGTATGGGTTCAGGCCTGGACCGCATGAGCACTAGCGTGGACCGTATGGGTCCTGGTGGCTTTGACCGCTTGGGCTCGTCCAGCATGGATCGTATGAGCGGTGGAATGGACTTTGCTTCTCCCATGGGCATGGACCGGATGAACACAGGTCTCGATCGAATGGGCTCAAACTTTGACCGCATGGGCTCTGGTGGCATGGACCGTTTCTCTTCGGGTCTGGACCGCATGGGCTCCAGCATGGATCGAATGGGATCTGGTGGCATCGGTGGCCAGTTTGACAGGCCCGGAGACATGGACCGTGGTAACTTTGGTTCTCCATTCGGCGGGTCTGGGCAAGGAGGAGGACCAGGGTCTGGTGGAGCCAATGCCAGGAAGGGCTGCCAGATTTTTGTCAGAAATGTAAGCAGACAGTATTCTTATTATTGGGTAATACTGTAGGGAAGGATTAAACCAAGAACAATGGGATTAA
Associated Phenotype:
Not determined