ZMP
znf384l
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate zinc finger protein 384 (ZNF384)Znf384l protein [Source:UniProtK
Human Orthologue:
ZNF384
Human Description:
zinc finger protein 384 [Source:HGNC Symbol;Acc:11955]
Mouse Orthologue:
Zfp384
Mouse Description:
zinc finger protein 384 Gene [Source:MGI Symbol;Acc:MGI:2443203]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14743 | Essential Splice Site | Available for shipment | Available now |
sa17389 | Nonsense | Available for shipment | Available now |
sa12844 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14743
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001148 | Essential Splice Site | 21 | 596 | 1 | 11 |
ENSDART00000104891 | Essential Splice Site | 21 | 583 | 1 | 10 |
ENSDART00000141913 | Essential Splice Site | 21 | 283 | 2 | 7 |
The following transcripts of ENSDARG00000001015 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 7605414)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7063953 |
GRCz11 | 19 | 6982878 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTCAACTCATCATACTTTTGGTCTCCCGTTCCAACAGTGCAAGGACAG[G/T]TAGACACCTTATTATTGGACTCTCTTGTACTGTACATCGTTGTGTCTTTA
Long Flanking Sequence:
AGAGATCAGCAAATCACTCCAGTATGTTTTTCTTGCAGGGTGACTTAACATCAATGCATTTTGTCTTTATGCATGTTAATTTGACACAATTGGCCATGCATGTCCTGTGATTCCTAACCCAACACACCTCTTTGCTAAGCATACACCACAAAGATGCCCCTATGTTCTTTATTTAAGGATAAATTAAGTCATAAATGCCAAAAGAAAAAAAAGATGCATGACATTTTGCAGATGTTTCCAAGCAAATCTTTAGAAAATAAAGGCTTTTTGTGTAATTCAGAGTACTTGGGTGCCAAAATGAATACATTGCCCAAGTGTCTGAGTGAATAAACCTTCAGGCAACATGTGGAACGTAAGGACGAGGTGTCATTTCACAACTGTTGCCAAAGGCCGAGTGGGTGTTTTACAAGTTATGTTGCTTTTTAATTGCAGAAATAATGGAAGATTCCCATTTCAACTCATCATACTTTTGGTCTCCCGTTCCAACAGTGCAAGGACAG[G/T]TAGACACCTTATTATTGGACTCTCTTGTACTGTACATCGTTGTGTCTTTAACAGACACGCCATGCTTATAGAGCACAATCTATTAAAAAAAAAAAAGCAAACAAAACAAGCATACCAGTCCGGGATGGATAATACCAACCTCGCACTGACCCATGTGAAAGTTACTCTCTGGAAACCTTGCCCAAACATCCCCAAAAAAGTAACCCTTCCCTCGCTGCTCTCTCCTTCTTCCCCTTCATCCTTCATCTGCGTTTATCTCTCAATCCATCCTCCTTTTCTCTTTCCTCCTTCCCTTCTTTCCCTTGTTTTTTTTTCTCCATTCATTCCCCTCTGCGAGTTTAGATCGACAACGCCATGTTTCTGAGCAAGATGAAAGAGCAGCTCGGGCCGGACAAGGCTGGGTCCTTTCCACACTCGTCCGCCGCGCACTACCCTACAGCGGTGCTGACGGTGCCAGGCTCGGTCGCCATGGATACGGGAGCCGTCGGGAGGGTGCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17389
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 |
---|---|---|---|---|---|
ENSDART00000001148 | Nonsense | 332 | 596 | 7 | 11 |
ENSDART00000104891 | Nonsense | 319 | 583 | 6 | 10 |
ENSDART00000141913 | None | None | 283 | None | 7 |
The following transcripts of ENSDARG00000001015 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 7597679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7056218 |
GRCz11 | 19 | 6975143 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTACTGCCAGAAAACMTTCAGACAGCTCAGCCATCTACAGCAGCACACA[C/T]GGTACAACTGAGCAATACACCACACACNNCTGCTGCAGGACTYGCTTTAGTG
Long Flanking Sequence:
TTTAAAATTCAGTACCGATTGGTATCGAATTCCATTATCGTGACAACACTAACAAGAACAATACATTTAATTACTATTAATTACTAAATACTGTTACAATCATAGGCATTATAAATTGTGTCAGGTTATATTCAGTCCCTGACAGATGGTGTTTATAGAGTTATTACTTTTGTGTGTTAATTGATATAAATACACCAGTCAGTGATTTGATTGTCAGGAAAATTATAATTTTGTAATTAATTTGAGTTTAAATGCGCATGCTGATTTTTGACTGTAGGTGCCGAATGTGTGCGGTGACGTTTTTCAGCAAATCAGACATGCAGATCCACGCTAAGTCCCACACGGAGGCGAAGCCACACAAGTGTCCTCACTGCTCCAAATCTTTCGCCAACTCCAGCTACCTGGCGCAGCACATCCGCATCCACAGCGGCGCCAAACCCTACACCTGCTCCTACTGCCAGAAAACCTTCAGACAGCTCAGCCATCTACAGCAGCACACA[C/T]GGTACAACTGAGCAATACACCACACACCTGCTGCAGGACTCGCTTTAGTGGCACAGTTGTGTTTTTGGTTAGGATAAGCATGTTTTTATTACATGTTTCTGTTCTCTTTTTCTCTTGATTCCTCACTGTGGTTTTCTGCTCTGATGCTTTGACATTTGAGCTTGGAGAGGCAATTCTAATAGTAGTAATTACTCTGGAGACAGAAGCAGGTCTTGTTTGTGTCACGCTAATGTCATCACATCATCTGCTTGTGTTATTTCACACCACAATGATTACATTTTAATTTTATTCAATTCTGTTGGTATCCTTTTGGTTTGACAGCTTTATCTAATAAGCTTTTGAAAATAGATATTTTAAACATTGTTTGATGCTTGGATTGAGAAAAACTGAGAACTTTATTTGAATTAATGACAGTCTCCATTTAAATCAATTCCTATTTTTCCAAGATCAGCCTTTTACTATATATGGTCAGTTTTAAGTAGAGCTAAATACATTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12844
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 |
---|---|---|---|---|---|
ENSDART00000001148 | Nonsense | 495 | 596 | 11 | 11 |
ENSDART00000104891 | Nonsense | 482 | 583 | 10 | 10 |
ENSDART00000141913 | None | None | 283 | None | 7 |
The following transcripts of ENSDARG00000001015 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 7588887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 7047426 |
GRCz11 | 19 | 6966351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAACCCAGATCCTCTSACAGTAGCGGCTGCAGTGGCAGCGCAGCAGGCT[C/T]AGAACCCMGGTCAGGGTTCAGGTGGAGGRAGTGGGCGAGGCCGTGGRYGG
Long Flanking Sequence:
ACAAGCCATACAAGTGTCACAACTGCAACCGCGGCTACACGGACGCCACCAGCTTGGAGGTTCACTTGACTACACATACGGTCAAACACGCCAAACTCTATTCCTGTGGCCTCTGCAACCGCTCGTACACATCTGTAAGATCCTGCACAGCATTTTCAATCCTTCCTCTGTATTCTTGACATTCTTCAGTTTGAGATTTCTAAGTGGTAATTTCCAAAATGTAAACATCAAGATTAGATATTAGTTACACTGTAAAAGAAATCTGTTAATGAACAGCTTCTTTATTTGGTGATTCAGAAGTGTTTTTGGTTTATTTATGGCTGTAAATTGGATTATGTGATGTTGATTTCTGCTCTGTCGACTTTTCATGAATTTATGCAGAATTTCAGCATTATCCCTGATTTTTCTCACTTGTCTAGGAAACCTACCTGATGAAACACATGCAAAAACACAACCCAGATCCTCTCACAGTAGCGGCTGCAGTGGCAGCGCAGCAGGCT[C/T]AGAACCCCGGTCAGGGTTCAGGTGGAGGGAGTGGGCGAGGCCGTGGGCGGGGCAGAGGAGCAGCAGCCGCAGCAGCAGCAGCCGCCGCAGCAGCAGCGCAGGCCCAGAACCAGAACAACCCCACACCGCCAACCAGCTACTCCGTTTCTGACGGAATCCCCTGCCCGTTCGACCTGCATCAGTACAAGACCGTGTCGGCAGGAGAAATCCAGTACAAGCCGGTCACAGTTGCCGATTTAACAGCCCACAAAGACCTCTGCCTCACCGTCTCCACCTCTGCCATCCAGGTGGAGCACATGAACTCGTAGAGAGGTGGAGCGAGGAGGAATGGACCATGAGTTTGGAAGGAAATAGATAAAAACACTGCCTTGAGGACAGAGGAGGATTTCCAAATACAGACCTGGAGGACGAGGAGAAACGGAGGAGGAGCACATGAACTGGAATGAGCTGTCTGTCGGTAGACTTGCATTGCAGTGTCACAAAAAAAGGCCTTATGCTAA
Associated Phenotype:
Not determined