ZMP
ppapdc1a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate phosphatidic acid phosphatase type 2 domain containing 1 family
Human Orthologue:
PPAPDC1A
Human Description:
phosphatidic acid phosphatase type 2 domain containing 1A [Source:HGNC Symbol;Acc:23531]
Mouse Orthologue:
Ppapdc1a
Mouse Description:
phosphatidic acid phosphatase type 2 domain containing 1A Gene [Source:MGI Symbol;Acc:MGI:2685936]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38916 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44781 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38916
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097656 | Essential Splice Site | 136 | 263 | 4 | 6 |
ENSDART00000132111 | Essential Splice Site | 63 | 190 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 2672835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2494403 |
GRCz11 | 13 | 2627581 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACCTGGTGTCTGAGGGCCGCAAGAGTTTTCCTAGCAGTCATTCGTCCT[G/T]TAAGTACTCAGTGTGTTACCAATTTTGTCTGTCTTATTTTTATTAAGTGA
Long Flanking Sequence:
AATTTGACTATTCACTTTCATCTAAATTAACAGGACAGAGCACAAATAATAATCAAATCAATAAGATAATGATTAAAATAAATAAATGAGAGAACAAACAAAAACAGACAGAAAAAACAATGTTACACTATAGGGTTTTCTGTCAATTGAAATTTTGTCAATAAACTAAACTTCTTCCTAACTTTCAACCCAACCCAACTCATTTTTACAGAACCTAAGACCCAACTAATTTAATAACAGTGATCGAATGGCCAAAAATCACCAGATAACAGATTATCCATCCACAACGTATACAGTTTAAAGACAGTATGCAAGATATTTCTGCTATTAATTATAATTGCGCTAATGTATTTGCGGGGTTAACCTTGATTTCAGGCCAAGGCCAGACTATTATCAGCGCTGTTTCCCTGATGGCCAAATGAATGCCAAGATGCTGTGTACTGGAGAGCCAGACCTGGTGTCTGAGGGCCGCAAGAGTTTTCCTAGCAGTCATTCGTCCT[G/T]TAAGTACTCAGTGTGTTACCAATTTTGTCTGTCTTATTTTTATTAAGTGACAACAATGTAATCTGCTCTAAAGGACATCGAATGCATCTGTGAAACACCGCTACAACACGATACAATACAATAAGCACAATAGCATACATGCAGAAGGACTTCTGCAACCCAGTTCAAGTGCTTCCGGTGACAAAATTGGTACAAATTTGCTTTGTTTATGGTCTGGTTTCTTTAAAAAAAAAAGTGATCTTCGCTGCCTGACTGATATACCATATAAAGTGGGTCTCAAAATGTACAAGAAGCACTGCATTAATTTCTATTCTTCCACAGAATGTTTTTAAAATATACATATTATGAAAGATGACTTTATGTCAGCTTGTAAAATGAAAGTATGGTCCCACTTTTTATTGAGTGGCCTTAACTAGTATGCACTTACATAGGAATTAGTAGTTTGTTACAATGTACTAATTGTGTGTACTTATGCTTGATTAAATACATGTATGTAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44781
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 |
---|---|---|---|---|---|
ENSDART00000097656 | Nonsense | 207 | 263 | 6 | 6 |
ENSDART00000132111 | Nonsense | 134 | 190 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 2635474)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2531764 |
GRCz11 | 13 | 2664942 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCTCACAGATGCTTTTGTCGGGGGAGTGATCGGCCTGTTCTTCGCCTA[C/A]ATCTGTTATCGGCAGCACTACCCGCCGTTCCTGCACATAGACTGCCACCT
Long Flanking Sequence:
TCTATGCCACAAAGGGTCAAGGCAATTCTGAGGCAAAAGTGGGTCCAACCTGGTACTAGGAAGGTGTACCTAATAAAGTGGCCGGTGAGTGTAGTTTTAATAACTGATTTGTCTTCTCTTAGCCATAATGACAGCACATAATATTTTACTAGATGTTTTTAAGACACTAGTTATATATATATATATAATATATATATAACTAGTTATATATATTTCTTAAAGGGGCTAATAATGCTGACCTTCTTTTTAAATTAAACATTGCTTGTATTCCAGCTGAAGTAAAATAATTAAAACATTCTCCAGAAGAAAAAAATAATACCGCAAAAAAAAAAAAAAAAAACTGGCTCTGTTAAACATAATTTGGCAAATATTCAAAGAATATTCATTCACAGGAGGACTAATAATTTTGACTGTATTATGTCTTCACTTCATAAACCCTGACGTTATTTTCCCCTCACAGATGCTTTTGTCGGGGGAGTGATCGGCCTGTTCTTCGCCTA[C/A]ATCTGTTATCGGCAGCACTACCCGCCGTTCCTGCACATAGACTGCCACCTGTCCTACGCCAGTCTGGCTGCTGCCACCGTCCACAACATGCCAGCCTCCCAGGACCAGCCTCTGCCCACGGATAATGCCACCAGCCTGCCTCTGGAGGGCATGACGGAGGGTCCCGTATGACTAATAGAGACCGGAGGCTCCCAGTCCTCTGAACAACGTGGTATGAACCACACTTGACTGGCACTTCAACATTCCAGTGAATTGGACCATGCATTTCATTTAGTTTCTTCTTGTTGATCATCCCCTGCACTCAGTTTATCAAGCAGCGGGTTACTCAGATTTCTTATACCTAATTTAACTGGTCACACTTTACAATAAAGTTGTATGCAACCTAGGCTCATTACAGCTACGAGGTCTGTGTTTCTGGGGACAGGGAAATACATACGTAGGTACGTCTGTTCGCTGATTTTGTTTTTGCAAATCCACCAGAGGCTGCTGTGTACACTTTT
Associated Phenotype:
Not determined