ZMP
phf21a
Ensembl ID:
ZFIN ID:
Description:
Phf21a protein [Source:UniProtKB/TrEMBL;Acc:Q08CP0]
Human Orthologue:
PHF21A
Human Description:
PHD finger protein 21A [Source:HGNC Symbol;Acc:24156]
Mouse Orthologue:
Phf21a
Mouse Description:
PHD finger protein 21A Gene [Source:MGI Symbol;Acc:MGI:2384756]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18275 | Nonsense | Available for shipment | Available now |
sa3290 | Missense, Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa18275
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 |
---|---|---|---|---|---|
ENSDART00000021577 | Nonsense | 279 | 796 | 8 | 17 |
ENSDART00000121435 | Nonsense | 279 | 539 | 8 | 16 |
ENSDART00000126499 | Nonsense | 280 | 745 | 6 | 14 |
ENSDART00000142439 | None | None | 168 | None | 7 |
ENSDART00000146882 | None | None | 87 | None | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 7990909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7603433 |
GRCz11 | 25 | 7727525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGCACCACGCAACTCGCAGGCATCGTCATCAGCCCTGCCCAGACACTT[C/T]AGATCAGCAATCTTAACTCAGACWTGAAGGTGAGAGTACTTATTTGGTTG
Long Flanking Sequence:
ACCTGGAAGGCCCATCCTTTGGTTTAAGGGTTTGAGCTCTGCACATTTCATCCACTTTCATGCAACTCACCAAGTGTGAACCAGAGCTCAGTCTTGGCATTACTTAAGGCTGAGGTTACCTCTTAACAACAACAACAACAACAAAAATGCATGGATGTTAAGGGCATGACAACAAAGTGGCTTTCGTTATCATTCTATCTGTACCTGCATTGTCATCCAACACGCCTTCCACTACTGCACAGGTTCGACCAAAACCCCCCACTCCCATCAATGTGCCCATCGCGCCAGCTCCTCCTCCTCCCATGGTGGCAGCTCCTCTAATCCAGCGACCCCTGATGCTCACCACCAAACTGACATCATCTTTACCCGCCTCCGCTGGGCCCATCCATCAGGTGCGCATTGTGAATGGACAGCAGTGCACAACCATCGACAAGACCACAACAACAGTCACAGGCACCACGCAACTCGCAGGCATCGTCATCAGCCCTGCCCAGACACTT[C/T]AGATCAGCAATCTTAACTCAGACTTGAAGGTGAGAGTACTTATTTGGTTGGATTTCAGGAAGCCAATTACTATCGCTGGCATGTACATTTCAAACACTAAACTGCCTTAATTCTTTCCCCCTTAATACTTCATAAATACTTGAAAGATACCTGAAACATACCTTTTTAGCTTTCTTAAGACTGCGGTTAAAAAAGCTCTGACGAGGCTGCTTCCTGAACCCCACAAAACACATGAATGAGATCAGACATTCAGATAATGCGAGTGATTTACTTGTTTCTTGTTCTTTATGCCAGACTGTGAAACCACAGGGAGGACCAGAACAGGTGGTCATAAAAACACCACCTTCATCCTCTCCTCCTCTTCCTCCTCCCCCAGCTAAGGTCAAACGAGAGGAAAGCCCACAGGTACTGCTCACCTTCACCATTATATCCGGCCAATTCTATCTGAAGATTAACCTATGACCTTTGATTTTTCTGTCTTCCTTTGCTGTTTCCATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3290
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:
C > T
Consequence:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021577 | Missense | 534 | 796 | 16 | 17 |
ENSDART00000121435 | Nonsense | 536 | 539 | 16 | 16 |
ENSDART00000126499 | Missense | 483 | 745 | 13 | 14 |
ENSDART00000142439 | None | None | 168 | None | 7 |
ENSDART00000146882 | None | None | 87 | None | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 7985528)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7598052 |
GRCz11 | 25 | 7722144 |
KASP Assay ID:
554-2449.1 (used for ordering genotyping assays)
KASP Sequence:
TAGTGTAGGAGCACATCACAATCATATTTGTTTTGTCCCTGTCCAAAAAG[C/T]AAAAGAAGAAGAGAAGCAGAAGCTAATGAAATGGAGTGCTGAACTAAAGC
Long Flanking Sequence:
AGAGATTAAACTCCCCTTTCCCTGCAAAAATGAAGTGTACATTTTCCCCCTTTACACATAGTGAGTTTCTTCAGGCGTTAAGGCTGTTTCGTGCTTTGTAAGCTCTCACATGGTTCGGTATTGATTGTGCCTTTTTTTCCACCCATCATGTAAGTGTAAGACAGCATCCAGCACTCCCATTGAAGTTCTGTTGTTCATCACTGTTGCCATACACAATTGATCTCAGTTTCTCTCATGGCTTTTCAGAGGTCAAGTGTGCACAGCACTGGTCTGTTATTGAGAGAGTTTCTTTTACAGATTCTGAAGAAGGAAGAGGCCATTCCCTGGCCAGGTACCCTAGCAATCGTCCATTCCTATATTGCCTACAAAGAAGGTATAGATTTTTTTTATCAGTTGTTAAACTTTGTACCCCAATTCAACTACATCTATAATCAATCAAATCCATGAGACTAGTGTAGGAGCACATCACAATCATATTTGTTTTGTCCCTGTCCAAAAAG[C/T]AAAAGAAGAAGAGAAGCAGAAGCTAATGAAATGGAGTGCTGAACTAAAGCTGGAACGGGAGCAACTAGAACAGAGAGTGAAACAGCTCAGCAACTCTATAACAGTGAGTTATTTATTTATTTTCTTTTTAACTGAAGCCTTTTCCAGATGCAAGATTATACCGTTGTACAACATATCTGGGAGTATTTCTCTCAGAAAACCAATTTTAAGCCAAACATTACACTTGGAGTGCACCTTAATTTTTTTCCATTCTGGCTCCAAAAAAATATAGTGGGAAATAGGGCTGCATGAGTAATTGGTGATTTTTATCCTCATTTTGGCAGTATAATTTGGCAGCTGATTTCAGATGGAGCATCATTTACTGCACAAGAGCCATAGTTCATTGACAAGCTACCCCAAAAAATTGCTGGCTATTTGCAATTTTTAATTGTTGCAATCCTAACATCTGAAATAATCATTGTTTTTGACTAGGGGTGTAACGATACACTCAGCTCACGATA
Associated Phenotype:
Not determined