ZMP
NP_001108353.1
Ensembl ID:
Description:
heterogeneous nuclear ribonucleoprotein A0, like [Source:RefSeq peptide;Acc:NP_001108353]
Human Orthologue:
GZF1
Human Description:
GDNF-inducible zinc finger protein 1 [Source:HGNC Symbol;Acc:15808]
Mouse Orthologue:
Gzf1
Mouse Description:
GDNF-inducible zinc finger protein 1 Gene [Source:MGI Symbol;Acc:MGI:1921783]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29449 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9486 | Essential Splice Site | Available for shipment | Available now |
sa37146 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29449
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 |
---|---|---|---|---|---|
ENSDART00000113806 | Nonsense | 208 | 763 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 45817445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 45666123 |
GRCz11 | 20 | 45622222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACGGAAATCCTTGATGAACCTGACAATGCAGAAGGAGAAGAAGAGCAA[C/T]GAATAGCAGAACATCCGGAAGCAGAATCATCAAAGAATGCATTGGATGAC
Long Flanking Sequence:
GAGAGCTGGAGGAGTTCGAAGCCCATCAGGTGGTCCTGGCCGCGTCCAGCGCTTACTTCAAAACCCACCTCTTAACAGAAGACCCAGTGAACAAGATGTTCCTCTGTGACTTTTCACCGCACTCCTTCTCCAAATTCCTAGAGTACGCGTATTCAGGGAAAATGGAGGTGGAGAAAAGTGGGATCGCTAACATATTACAAATGGCCAAACTCCTGAAATGCCAAGACCTGGTGGATGTCTGTGAGGTGGAAATTCCTAATGTTGCATCAGAGGAATGTGTAGAGAAAGATGCCGAAATCAAAACCAAGCATGTCAAAAAAGCAATTAAAAGAAAAAAGAGAGTAAAATCAGCCAAATACGTGAGTGAATCAGATGTGCTCGGCAGGAGAAGTGGAAGGTTAGCAGGTCGTAGAGTTAATGTAGAGTTTCCTCAGAAAAAATTAAAGAGGCAAACGGAAATCCTTGATGAACCTGACAATGCAGAAGGAGAAGAAGAGCAA[C/T]GAATAGCAGAACATCCGGAAGCAGAATCATCAAAGAATGCATTGGATGACACTAGTAAAGACACTATTGATGACTCTGGGTCTGAATCTCCTGCCTATGTGCCTCAGGACGACCCTGACGAATCAGACTTTCTACCTGATGAGGAAATGGAGGCAGATGAAGCTGAGAAGAAAGTCAAGAAAGAAATCGCCAAATACACATGCGAGGTCTGCAGCCGCTATTTCTACTACGAGAAGAGCTATCTGAAACACTTAAAGGTGGGATTACGATGGTCTCAAACTTTTGCTTGTGTTTAATTGCTAAAGCTTTTATCAAGGGGCATAACGGTGGCTGAGTGGTTAGCACTGTTGCCTCAAAGCAAGAAGGTTGCGGAATTGAGTCCTGGCTGGGTCGGTTGGCATTTTTGTGTGGAGTTTGCATGTTCTCCCAGCGTTGGCATGGGTTTCCTCTGAGTGCTTCCCACAGTCCAAAGACGCGTGCTATTGGTGCTTTCTTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9486
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113806 | Essential Splice Site | 293 | 763 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 45817703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 45666381 |
GRCz11 | 20 | 45622480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCAGCCGCTATTTCTACTACGAGAAGAGCTATCTGAAACACTTAAAG[G/A]TGGGWTTACGATGGTMTCAAAMTTTTGCTTGTGTTTAATTNNNNNNGCTT
Long Flanking Sequence:
ATGTTGCATCAGAGGAATGTGTAGAGAAAGATGCCGAAATCAAAACCAAGCATGTCAAAAAAGCAATTAAAAGAAAAAAGAGAGTAAAATCAGCCAAATACGTGAGTGAATCAGATGTGCTCGGCAGGAGAAGTGGAAGGTTAGCAGGTCGTAGAGTTAATGTAGAGTTTCCTCAGAAAAAATTAAAGAGGCAAACGGAAATCCTTGATGAACCTGACAATGCAGAAGGAGAAGAAGAGCAACGAATAGCAGAACATCCGGAAGCAGAATCATCAAAGAATGCATTGGATGACACTAGTAAAGACACTATTGATGACTCTGGGTCTGAATCTCCTGCCTATGTGCCTCAGGACGACCCTGACGAATCAGACTTTCTACCTGATGAGGAAATGGAGGCAGATGAAGCTGAGAAGAAAGTCAAGAAAGAAATCGCCAAATACACATGCGAGGTCTGCAGCCGCTATTTCTACTACGAGAAGAGCTATCTGAAACACTTAAAG[G/A]TGGGATTACGATGGTCTCAAACTTTTGCTTGTGTTTAATTGCTAAAGCTTTTATCAAGGGGCATAACGGTGGCTGAGTGGTTAGCACTGTTGCCTCAAAGCAAGAAGGTTGCGGAATTGAGTCCTGGCTGGGTCGGTTGGCATTTTTGTGTGGAGTTTGCATGTTCTCCCAGCGTTGGCATGGGTTTCCTCTGAGTGCTTCCCACAGTCCAAAGACGCGTGCTATTGGTGCTTTCTTTTGCACATCATTCCCTCATAGCCAACTTAAGCAAAGTCTCTTTAAGGCAAGTCATTTTACTCTGCGGCCATCTTTGAAACACGTCTCAGGCAGTATGCTTGGGAACTCTGTCTCAATGGGGAAACATCAAATTCTCCAAAACTGTTTGGCAAACTTTTGATAACATTGCAAATGTGGAACTACCAATAAAATTAAAAAACAACTCGTTTCTAAAGGTCAGAATCAGACAAAATCAGCATTTTCAGGTTGCCCAAGCTAATGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37146
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113806 | Nonsense | 461 | 763 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 20 (position 45823226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 45671904 |
GRCz11 | 20 | 45628003 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCATTCATGTGTGAGAACTGTGGGAAGAGCTTCGCATCTAAAGAATA[T/G]CTGAAGCATCACAACAGAATCCATTCGGGCTCCAGACCCTACAAATGTGA
Long Flanking Sequence:
ATTGGGTTGTGTCCCGGTGTTGGGTTGTCACTGGAAGGGTATCCGCTGTGTAAAGCATATGCTGGATAAGTTGGCGGATCATCCCACCGTGGCGACCCCTGATTAATAAAGGGACTAAGCCAAAAAGAAAATGAATGAATGAATAAAAAAATTGTTAAATCTTAATTATTTTATTATTATATGAATGTTTAAAAACTAAATATTACACACTGAAATAGTGACACCACTTATATTTTAATAATATAATAATAATACCTTTTATTATAATTAAGGATCCACACTGGAGAGAAACCTTTCGCCTGTGACCTCTGTGATGCCAGATTTACCCAGAATCACATGCTGGCGTACCACAGAAGATGCCACACAGGTGAGGGAAACCCATTCCTGTGACTTTAAAAGAAATAATGATGAGGAAAGGTAACGACTTCCTGTTCTCTTTCTCTAGGAGAAAAGCCATTCATGTGTGAGAACTGTGGGAAGAGCTTCGCATCTAAAGAATA[T/G]CTGAAGCATCACAACAGAATCCATTCGGGCTCCAGACCCTACAAATGTGAGACCTGCGGAAGAGCGTTTGCACAGAGGAACTCGCTCCACCAGCATGTCAAAATACACACAGGTATACTCTTCTTCGAAATCAACACTAATATAAATTCCTCTCAGTAAGTGCAAACATGGTATTTTACATCACATTCACTAAAGCATATGATAACATAAAGCAGTTTAAAAATCAGACATCAGTCGCTTCTTATGTAACTCTTACTGAGTGTTCATCTCAACACTAGATTTTGCTGTATTTGGCTCAACCATTCTTGGGTGGCTCACCAGTGTATTAGATGACAAAAGTTCTTACAGGGAGAAGACTTTAGTGAAGACAATGAATAGTGCAGTTTCTCAGCATCTTCAAGTAACCTAACCCAAAGTACTGTCTGTTAGAGACTACTTTATAACAAAAGAATATGATTCCCCCAGAGATTACCCAAATGGTTTAGCTGGTTCACAACTCT
Associated Phenotype:
Not determined