ZMP

ppapdc1a

Ensembl ID:

ENSDARG00000067798

ZFIN ID:

ZDB-GENE-081107-53

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.

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.

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