ZMP
LOC100330539
Ensembl ID:
Human Orthologue:
ZNF318
Human Description:
zinc finger protein 318 [Source:HGNC Symbol;Acc:13578]
Mouse Orthologue:
Zfp318
Mouse Description:
zinc finger protein 318 Gene [Source:MGI Symbol;Acc:MGI:1889348]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16667 | Nonsense | Available for shipment | Available now |
sa28052 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16778 | Nonsense | Available for shipment | Available now |
sa35406 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16667
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122406 | Nonsense | 409 | 2230 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 3976240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4193160 |
GRCz11 | 13 | 4321656 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACCTCAGACCTCACAGAGTTCCTTGGAATGATAGCMGAGGTAGCCCAA[C/T]AAMACAATCCAAAAAAGAGTCTTACAGAAATTGAAGACGAGGAGAAGTTT
Long Flanking Sequence:
TTGGAAGTTGTGTTTGAATTCTTGGGTCATGGAGGAATTTATACTCTGTTTATTTATTTATTTATTTTGAAACCTTATTACACTTATATAATTGAAAATATTCAACAAACTGTCCCTAGGCACAGTGTGGAACAATGCAAACCTAGCCTAGTGTGAGTACGTCCTTAGTATTATCCTTTAAAAGTTTTATTTATGATGTAAGAGTGTCTAAAACATGTCTAACTTGCATTTTTCAGATTAGCGATTCCCCTCGAGGCAATTCAGATGGGGGTCTATCACATGAGGCTGAACAGCTTCTCTGTGCACTTTCCAAAACCATGGATCCAAGCGTATTGTCTTCCATGCTGGGCAAAAGCTCTGACGGGAATGTTCTGGAGGAGCTAATTAGCAAGATCCATCCATCCCGAGAGGATCTAGGTGATTTGTTCCTCGCTCGCGAGAAGGGAAGGCAGACCTCAGACCTCACAGAGTTCCTTGGAATGATAGCCGAGGTAGCCCAA[C/T]AACACAATCCAAAAAAGAGTCTTACAGAAATTGAAGACGAGGAGAAGTTTCTCTACGGAGATGAATTGGAGGCGGATGAGGTGACACCGGCTAAGGAGATTGCAACCGATTCCAGCTATCCAGATACAAGAGAGCATGGCACTGCACCTTACAGTTTTACCCGTACTGTAGAAAATGTGCCAAGCCGTTCTTCTGCCACACCTGAGGTGCATGCTGAGGAAGAACCTCATGATTTCCCACCTGGAGTCGGGCCGCAAGATGTCACGGTGAGGAGTGAGGTTGAGGAATATGAGAAGATACAAGATTTGCTGAAAACAATTGGCCTGGATCTCGGTGTGGCCGAAATAAGCAAGATGGCTGCAAGGACACAAGAACGCCTCCACGGCAGCGTCCCTGCAAAAAAGACACCTGTTCGTCGGCAGTCAGATAGAAAGCACCGGAGTCGAAGCAGAAGCTCCAGCAGCAGTAGTGGAAGCGGCAGCAGAAGCTCCAGTCGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28052
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 |
---|---|---|---|---|---|
ENSDART00000122406 | Nonsense | 532 | 2230 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 3975871)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4192791 |
GRCz11 | 13 | 4321287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGCCTGGATCTCGGTGTGGCCGAAATAAGCAAGATGGCTGCAAGGACA[C/T]AAGAACGCCTCCACGGCAGCGTCCCTGCAAAAAAGACACCTGTTCGTCGG
Long Flanking Sequence:
TTCTGGAGGAGCTAATTAGCAAGATCCATCCATCCCGAGAGGATCTAGGTGATTTGTTCCTCGCTCGCGAGAAGGGAAGGCAGACCTCAGACCTCACAGAGTTCCTTGGAATGATAGCCGAGGTAGCCCAACAACACAATCCAAAAAAGAGTCTTACAGAAATTGAAGACGAGGAGAAGTTTCTCTACGGAGATGAATTGGAGGCGGATGAGGTGACACCGGCTAAGGAGATTGCAACCGATTCCAGCTATCCAGATACAAGAGAGCATGGCACTGCACCTTACAGTTTTACCCGTACTGTAGAAAATGTGCCAAGCCGTTCTTCTGCCACACCTGAGGTGCATGCTGAGGAAGAACCTCATGATTTCCCACCTGGAGTCGGGCCGCAAGATGTCACGGTGAGGAGTGAGGTTGAGGAATATGAGAAGATACAAGATTTGCTGAAAACAATTGGCCTGGATCTCGGTGTGGCCGAAATAAGCAAGATGGCTGCAAGGACA[C/T]AAGAACGCCTCCACGGCAGCGTCCCTGCAAAAAAGACACCTGTTCGTCGGCAGTCAGATAGAAAGCACCGGAGTCGAAGCAGAAGCTCCAGCAGCAGTAGTGGAAGCGGCAGCAGAAGCTCCAGTCGAAGTCAAAGCGAAAGTCGGAGCAGAAGTAGAAGCCGAAGCCGAAGTGGCAGCCTAAATCACACTTCAAGTCGCAGCAAGAAGAAGTCTGTCTCTCCTGAAAAAGCTTCTCCGCATGTACATAGCCAGAGCAAAAAAGACACTCAGCCTGCTGTCCCAGAAAGCAACTGGCCTACAACCCCCACTCCTGCACAGAGTTATCCTTCCCGACCTGGCGTTTTGCCGCATCCCCCTTACCCAGGACCTCCCCCACGTGAGATAATGCCTCCTGACTACCGTACACATGGTTATGGTGCATATGGTAATTACATTCCCTATATGCCCCCGGGATGGCCAATGTACCCACCCACAGGTATGCCAGTACCTCCTCCAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16778
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 |
---|---|---|---|---|---|
ENSDART00000122406 | Nonsense | 640 | 2230 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 3975545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4192465 |
GRCz11 | 13 | 4320961 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGTCCCAGAAAGCAACTGGCCTACAACMCCCACTCCTGCACAGAGYTA[T/A]CCTTCCCGACCTGGCGTTTTGCCGCATCCCCCTTACCCAGGACCTCCCCC
Long Flanking Sequence:
GCCACACCTGAGGTGCATGCTGAGGAAGAACCTCATGATTTCCCACCTGGAGTCGGGCCGCAAGATGTCACGGTGAGGAGTGAGGTTGAGGAATATGAGAAGATACAAGATTTGCTGAAAACAATTGGCCTGGATCTCGGTGTGGCCGAAATAAGCAAGATGGCTGCAAGGACACAAGAACGCCTCCACGGCAGCGTCCCTGCAAAAAAGACACCTGTTCGTCGGCAGTCAGATAGAAAGCACCGGAGTCGAAGCAGAAGCTCCAGCAGCAGTAGTGGAAGCGGCAGCAGAAGCTCCAGTCGAAGTCAAAGCGAAAGTCGGAGCAGAAGTAGAAGCCGAAGCCGAAGTGGCAGCCTAAATCACACTTCAAGTCGCAGCAAGAAGAAGTCTGTCTCTCCTGAAAAAGCTTCTCCGCATGTACATAGCCAGAGCAAAAAAGACACTCAGCCTGCTGTCCCAGAAAGCAACTGGCCTACAACCCCCACTCCTGCACAGAGTTA[T/A]CCTTCCCGACCTGGCGTTTTGCCGCATCCCCCTTACCCAGGACCTCCCCCACGTGAGATAATGCCTCCTGACTACCGTACACATGGTTATGGTGCATATGGTAATTACATTCCCTATATGCCCCCGGGATGGCCAATGTACCCACCCACAGGTATGCCAGTACCTCCTCCAAGTCAAATCGACCCCTACAGCCTCCCTAACATGGAGCGACCTTTTCTTAAAACGATTAAAAATGTGACAAGTGAGAGTAAAGCTGACAATACTAAAAAAGGTTAGTGATCTTCAGAGTTCATTATTCAATTCAGGACTAGTTGTATTGTGTGTGTTATAGACAGTTTTGAAGAATCTTCGCATGGGGGTATTCAGTACATCAAAACAAGGGCGTAGAATTAGCATGGACGGGAGGGGATGTGTCCCCACCAATATCCACCAATTATTGAAATATCCCTACCAATAATTTAATCGACTTCAAAATAAAATAATGATCCGTCAACCCTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35406
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 |
---|---|---|---|---|---|
ENSDART00000122406 | Nonsense | 687 | 2230 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 13 (position 3975404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 4192324 |
GRCz11 | 13 | 4320820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGCATATGGTAATTACATTCCCTATATGCCCCCGGGATGGCCAATGTA[C/A]CCACCCACAGGTATGCCAGTACCTCCTCCAAGTCAAATCGACCCCTACAG
Long Flanking Sequence:
GTGGCCGAAATAAGCAAGATGGCTGCAAGGACACAAGAACGCCTCCACGGCAGCGTCCCTGCAAAAAAGACACCTGTTCGTCGGCAGTCAGATAGAAAGCACCGGAGTCGAAGCAGAAGCTCCAGCAGCAGTAGTGGAAGCGGCAGCAGAAGCTCCAGTCGAAGTCAAAGCGAAAGTCGGAGCAGAAGTAGAAGCCGAAGCCGAAGTGGCAGCCTAAATCACACTTCAAGTCGCAGCAAGAAGAAGTCTGTCTCTCCTGAAAAAGCTTCTCCGCATGTACATAGCCAGAGCAAAAAAGACACTCAGCCTGCTGTCCCAGAAAGCAACTGGCCTACAACCCCCACTCCTGCACAGAGTTATCCTTCCCGACCTGGCGTTTTGCCGCATCCCCCTTACCCAGGACCTCCCCCACGTGAGATAATGCCTCCTGACTACCGTACACATGGTTATGGTGCATATGGTAATTACATTCCCTATATGCCCCCGGGATGGCCAATGTA[C/A]CCACCCACAGGTATGCCAGTACCTCCTCCAAGTCAAATCGACCCCTACAGCCTCCCTAACATGGAGCGACCTTTTCTTAAAACGATTAAAAATGTGACAAGTGAGAGTAAAGCTGACAATACTAAAAAAGGTTAGTGATCTTCAGAGTTCATTATTCAATTCAGGACTAGTTGTATTGTGTGTGTTATAGACAGTTTTGAAGAATCTTCGCATGGGGGTATTCAGTACATCAAAACAAGGGCGTAGAATTAGCATGGACGGGAGGGGATGTGTCCCCACCAATATCCACCAATTATTGAAATATCCCTACCAATAATTTAATCGACTTCAAAATAAAATAATGATCCGTCAACCCTTAGCCACCTACACATACTCCAAGTCCAGTTCTCTACGAGTTTATTGTAATACTATTAACCAAGGCTGTGCTATTAAGCAAAATTAAGTTTCTATTTTTTATCTCCATGATTTTGAAAAACAATGATTGTGATAAAACAGTATAT
Associated Phenotype:
Not determined