ZMP
NP_001082801.1
Ensembl ID:
Description:
hypothetical protein LOC325787 [Source:RefSeq peptide;Acc:NP_001082801]
Human Orthologue:
ZC3H7B
Human Description:
zinc finger CCCH-type containing 7B [Source:HGNC Symbol;Acc:30869]
Mouse Orthologue:
Zc3h7b
Mouse Description:
zinc finger CCCH type containing 7B Gene [Source:MGI Symbol;Acc:MGI:1328310]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25981 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5725 | Nonsense | F2 line generated | Not yet available |
sa2113 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa25981
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 |
---|---|---|---|---|---|
ENSDART00000111562 | Nonsense | 6 | 952 | 2 | 25 |
Genomic Location (Zv9):
Chromosome 3 (position 5059738)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 4582839 |
GRCz11 | 3 | 4493129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTTTGTTTTTCAGCTGTGTGATGGTCAAACATGAGCGCTGAGCGG[C/T]AGAAACGGCAGGAGAAGATTCGGAGAGCGCTGAGCTTCATCAAGTATGAC
Long Flanking Sequence:
TCTAAAGACAGTCAGTTCCCCTCAGAGATTCATATAAGCTCTTACTCCAGCTGTATTGTCTTTTGTTTGACATCTCAACCAGATTTTCAACTTAAGTTTGTGGTTCATCTTTACATTCCTACTGCTTTATAAATAAACTGCTCCTTCATGGGAAAATAGTTTACACCCTTGAATGCATTCCCTGCTGAAAATGTTGATTGGCTGATTTGAACTGGTTAACCAGGCTGGTTTAGAAGTGTTTAGGCATTTTTCAGCCTGGCTAAGCTAATTTTAGCTGGTCATTCCAGCCTGGAACTGGCCAAAACACCAGCCTGGTTTTAAGTTTTATTTTAGGGTTATTATATTTTATGGTCTGTGAACTTGTGAATGTACTTGTGAACCCAGTGCACTGAAGGCATGTGAGTGTGTTTGAGACCGAACAGCTGGTAAACATGAACGTCTGCTGATGTGTGTGTGTTTGTTTTTCAGCTGTGTGATGGTCAAACATGAGCGCTGAGCGG[C/T]AGAAACGGCAGGAGAAGATTCGGAGAGCGCTGAGCTTCATCAAGTATGACAGATAATAAATACTGCACTATTTTACTGCACAGAGACCTGCTTTACCCTTCTGTGACTGTTTTTTTATCTGACTTTTCTGATATGTGGTACACAAAGCTTTTGACTTAGAATTTACAAAACAATTCAACAATCCCATATATAGTGTAAAAGAATATAAATAAACTAAATAAAGGAGCACACAAAGACATTCTAATAATACCCTAAATGTTTCTTGTCAGCCTAAAAAATAGTTTGCCACTCAGGTCTATGGGAAACACAGTCTCTGAATATGCTTCATATGTCTTTGATTGTTGACATCATACATTCAGTCAGTCGCTATCGTGGTTTGGCTGTAATTTATGCATAACTTGGTTAATTGAGTCAAGTTTGTAATTGGATAAATGTATGAATAGATTTTATAGAGGTAAACAAACTCTTTGAGGAGCAGTGATCTATCATTTTAAGCATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5725
Status:
F2 line generated
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111562 | Nonsense | 715 | 952 | 19 | 25 |
ENSDART00000111562 | Nonsense | 715 | 952 | 19 | 25 |
Genomic Location (Zv9):
Chromosome 3 (position 5030637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 4553738 |
GRCz11 | 3 | 4464028 |
KASP Assay ID:
554-3096.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGAACACTCNNGACCCCTCTCACTCTCTCCACCTTTCTCTCTTCAGCT[G/A]GACCAAAGMGAGGAGGGTTTTACTGGTCAAGTCTCACGAGAGGAAGAART
Long Flanking Sequence:
ACTGCTGCATTAAAAACTTCATCTTAAAAACATGAAGTGCAGATGATCCAATGATCATTGCAAATGTGAAGAATCATAAATGTATATAAGCAATAGGTTTATTATTGAAAAATCTAAATGTTATATAGGAGAAAAACTGTGTACAACTTACTGCCATTAGCTAAATTAGTCTGCTTGTTTCTGCATATCCAGAGGTTCACATAATCTTGGATACGGCCCGTATTAAGAGCCAAATGTAGATGAGTCAGATAATATAATCATGTAATCCATCAAAAAATAACAAAAATAATATCCATCAAAAAATAAAAATAGTAATCTGATTATGAGTATTTTAGAAAGTATTTTACTGTAATTACAAGTACTTTATTTTTGTAATCTCATTACATAACTGAGATTAAATATTATATAATTTGTTACTATTCAGCTCAGTGAACACACACACACACAATGTGTGAACACTCTCGACCCCTCTCACTCTCTCCACCTTTCTCTCTTCAGCT[G/A]GACCAAAGAGAGGAGGGTTTTACTGGTCAAGTCTCACGAGAGGAAGAAGTGGGTCTCTGTGCGACCTTTGCCCTTTGCCAAGACATATCCTCAACAATACGACGTGTGTGAAAACAGTGTATTTTCATTTCATTCTCATACAGGAAATGTTTTTGTTTTGAGTGTAATTCGCACATCCTGTCCTATAAAGCAGACACATCTCACCTTATTAAGGTTAACGGCTAACTGATTAATTGGTCTTTCATTTAAATGACGATCAGAAGATTTTGTGGAAAATAACATCGAAATTGACCCCTTTGATGGTTATTTAAAATCCAAGACACATCTAGTTATTAGTTGTTTATTATATGATTAAAAAAGCAATAACTCATACACCAACAATTAAAAAATATAAATCTTAATATTGTATGCTACTATAAAAATATTGGTATTGTTTAATCCACATTTTGAATTTCTGGACAAATTTACAAGGTTTTAATCTACTTTCGATGGTGACTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2113
Status:
F2 line generated
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111562 | Nonsense | 715 | 952 | 19 | 25 |
ENSDART00000111562 | Nonsense | 715 | 952 | 19 | 25 |
Genomic Location (Zv9):
Chromosome 3 (position 5030637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 4553738 |
GRCz11 | 3 | 4464028 |
KASP Assay ID:
554-3096.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGAACACTCNNGACCCCTCTCACTCTCTCCACCTTTCTCTCTTCAGCT[G/A]GACCAAAGAGAGGAGGGTTTTACTGGTCAAGTCTCACGAGAGGAAGAART
Long Flanking Sequence:
ACTGCTGCATTAAAAACTTCATCTTAAAAACATGAAGTGCAGATGATCCAATGATCATTGCAAATGTGAAGAATCATAAATGTATATAAGCAATAGGTTTATTATTGAAAAATCTAAATGTTATATAGGAGAAAAACTGTGTACAACTTACTGCCATTAGCTAAATTAGTCTGCTTGTTTCTGCATATCCAGAGGTTCACATAATCTTGGATACGGCCCGTATTAAGAGCCAAATGTAGATGAGTCAGATAATATAATCATGTAATCCATCAAAAAATAACAAAAATAATATCCATCAAAAAATAAAAATAGTAATCTGATTATGAGTATTTTAGAAAGTATTTTACTGTAATTACAAGTACTTTATTTTTGTAATCTCATTACATAACTGAGATTAAATATTATATAATTTGTTACTATTCAGCTCAGTGAACACACACACACACAATGTGTGAACACTCTCGACCCCTCTCACTCTCTCCACCTTTCTCTCTTCAGCT[G/A]GACCAAAGAGAGGAGGGTTTTACTGGTCAAGTCTCACGAGAGGAAGAAGTGGGTCTCTGTGCGACCTTTGCCCTTTGCCAAGACATATCCTCAACAATACGACGTGTGTGAAAACAGTGTATTTTCATTTCATTCTCATACAGGAAATGTTTTTGTTTTGAGTGTAATTCGCACATCCTGTCCTATAAAGCAGACACATCTCACCTTATTAAGGTTAACGGCTAACTGATTAATTGGTCTTTCATTTAAATGACGATCAGAAGATTTTGTGGAAAATAACATCGAAATTGACCCCTTTGATGGTTATTTAAAATCCAAGACACATCTAGTTATTAGTTGTTTATTATATGATTAAAAAAGCAATAACTCATACACCAACAATTAAAAAATATAAATCTTAATATTGTATGCTACTATAAAAATATTGGTATTGTTTAATCCACATTTTGAATTTCTGGACAAATTTACAAGGTTTTAATCTACTTTCGATGGTGACTGCA
Associated Phenotype:
Not determined