ZMP
si:dkey-188i13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate PHD finger protein 3 (PHF3) [Source:UniProtKB/TrEMBL;Acc:B8A483]
Human Orthologue:
PHF3
Human Description:
PHD finger protein 3 [Source:HGNC Symbol;Acc:8921]
Mouse Orthologue:
Phf3
Mouse Description:
PHD finger protein 3 Gene [Source:MGI Symbol;Acc:MGI:2446126]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42266 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42267 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42266
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 |
---|---|---|---|---|---|
ENSDART00000043440 | Nonsense | 871 | 1691 | 9 | 15 |
ENSDART00000100352 | Nonsense | 871 | 1691 | 10 | 16 |
ENSDART00000121773 | None | None | 737 | None | 8 |
ENSDART00000126902 | None | None | 358 | None | 4 |
ENSDART00000141988 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 38063358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37540170 |
GRCz11 | 13 | 37666060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTTGATGTTTTTGTTGGCAGACAATTGAAATGATTGAAAAAGAACAA[C/T]GAGAGGTAGAAAGACGCCCTATTACTAAAATCACTCATAAAGGGGAAATT
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCCTATATTTGACATCTTAAGAATAATATCACTGTGCTACCTGTTTTCTCAAAAAGCATTTGCAGGAGAAGCACACATTTGTAGCCAAGTCTAATGCTATGTTAATGATAATAAATGTTCTTTCTCAGGTGTTATTCAAGCGTGTACTCAAGGGGGAAGTGTCCCCTGCAGATCTGGTGCGCATGACGGCAGAAGAGCTGGCCTCTAAGGAACTGGCTGCTTGGAGAAAAAGAGAAAATCGACATGTTAGTAAAACTTTAGAATCTCACCATTTCGTTTTTTTGTCGACACTGACATTGAGTGAAGTAAAATATCAAAAAGGGAAAAGTTTATATTTAGTTAGTTAAATCAATACACAAAAAACAGAATGACATTGAAATGTTAAACCTGTTGATGTTTTTGTTGGCAGACAATTGAAATGATTGAAAAAGAACAA[C/T]GAGAGGTAGAAAGACGCCCTATTACTAAAATCACTCATAAAGGGGAAATTGAAATAGAGAATCAGGAGCCCGCCAAGGCACCAGAGGCCATAGAGGTTGAGGTGAGATTTATGAGCAATCTAATCTCCATTCTCTGCAATTTAGTTATATTGTCCATCAAGGGAATAAGAAAATTGCTTTTTCTTTCTGTCTTTAGCCAGAGCCAGTGCTGAAAGTTGTGGAAGTGCCTGAAGAGAAACCCCCTGAGATTAAAGTTGAGAGCCCCAAGAAATCTATAGATACCACCAACTTGCACAAGTCTCATCTATTTGACCTCAACTGCAAAATCTGCACAGGTAATACCGTTTTTTTGAGGTAAAATAAAGTTCAGCTTCTGAAAACTAACTTGCATTCTTACAGGGATAGTAAATTGTGTTATTTTTGTGATCTGTTAATTTACTAACCCAGAAGCCATCGAAAAATATGTAGTAGAACATTTTAAAGAATTTCTGTTATTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42267
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 |
---|---|---|---|---|---|
ENSDART00000043440 | Nonsense | 1658 | 1691 | 15 | 15 |
ENSDART00000100352 | Nonsense | 1658 | 1691 | 16 | 16 |
ENSDART00000121773 | None | None | 737 | None | 8 |
ENSDART00000126902 | None | None | 358 | None | 4 |
ENSDART00000141988 | None | None | 95 | None | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 38070214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37547026 |
GRCz11 | 13 | 37672916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCACAGTCATAAAGAGCGCCACTCGAAAGATGAAAGGTACGAGAAACAT[C/T]GAGAACGACGGCACAGCAGCCATCATCGGGACAGAGACAAACACAGATCA
Long Flanking Sequence:
TTAACCCTAAAGTTTACAACCCACCGGTTTTTCACTCGTATCTCTCCGGTCCACCTGATCCCCAATTTTACCCTCCTCCAGCCAATCCTGCTCATTTCTTACCCCTTCAAGCTCACCTTCCTCCACCTTTTCAGTTTCCTCCAGGTCCGCCTCCTCTGCAGATGTTCCCTCAAAGCGATCCCCACATGCTTGCTCCACCATGGCCTCAAACCGTCCCTCCACAAACGCTCCCGCCGCCTCCTATGGCCTACGAGTCCAGCTTGCCGACCGCTTTGCCCCTCAGCAAAGACGAGAAGGTTTCAGAGAAGTCCTACAGTGACTTTGTCGACAAGTTGTCCAGGCGCTCCGAGGAGACCCATAGAAAGGACAGCAGAGACAGAGAGCACTATGACAAGCATCATCACAAAAGCAGGCACTACGAGCGGGATCGGGAAAAGCACCGGGAGAGAAGTCACAGTCATAAAGAGCGCCACTCGAAAGATGAAAGGTACGAGAAACAT[C/T]GAGAACGACGGCACAGCAGCCATCATCGGGACAGAGACAAACACAGATCACGCGATTCAGATCACGAGAAACACAGGAAAGACTCTAGAGACAGGCGTTCGTGATCTTGGGGGATCAAAGCGCTCTTCCTACCTTAAATCTGTAACAGTAGAAGAAAACTATTTATAAAGTTTCAAAATGATTTTTATATGAAAAGCAGCTAGTAGGAGATTTTTAGTTGGTTTTGTTTTGTTTTGGAAATCTAAAGAATGTTTGTTTTTAAATGTACATTTTTCTGTACTTGGCTTCTCAATTACCCGCTAACATCTTCACAAGCAGCTGGTTGTAATCAAGAAAATGAAACTACTGTCGTACGCAGCGTGCCATGAGACGAAGCATCCCGTGGTCGATAAGAACAGCTTCTTTTGCTTCATTTTCAGTTTTAATTTTTCTAAATTTGGCTTCTTAAGTATTTTCTATGTTTCAGGTGACAAATATTTTCTTTGTACATTTTGGCTTGT
Associated Phenotype:
Not determined