ZMP
p4ha2
Ensembl ID:
ZFIN ID:
Description:
prolyl 4-hydroxylase subunit alpha-2 [Source:RefSeq peptide;Acc:NP_001007286]
Human Orthologue:
P4HA2
Human Description:
prolyl 4-hydroxylase, alpha polypeptide II [Source:HGNC Symbol;Acc:8547]
Mouse Orthologue:
P4ha2
Mouse Description:
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha II polypeptide Gene
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10597 | Nonsense | Available for shipment | Available now |
sa44975 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10597
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 |
---|---|---|---|---|---|
ENSDART00000024137 | Nonsense | 224 | 514 | 6 | 14 |
ENSDART00000122352 | Nonsense | 118 | 408 | 2 | 10 |
ENSDART00000129566 | Nonsense | 227 | 541 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 41520855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43120194 |
GRCz11 | 21 | 43115370 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTGCTGGATTATCTCAGTTACTCTGTCTATCAGATGGGGGATCTGCCA[C/T]GAGCCATCGAGCTTACCAGACGCCTGCTRGCCATCGGTAACCGCAGCATC
Long Flanking Sequence:
ATAAATGAATATATAAATAAATAAATGCATAAATTAATAAGTTTTTGTAATAAATTGAATAATAAAAAAGGTAAAAATTAACAAAATGACAAAAAAAATTGCTAATGTTTAAGCAAAAACAGAAATATAAATACAGATAAAACAGTAAATTGATGCAGAACATGACAAAATGATAAGGAAACAAAAGTGTTTACAAAAGACTTATAGAGTACCACCAGGTTAAACCGGGGCCTAATAACACAGAAATCCATGCTAATGATCTTGATGCTGATTGGCTGTGTATGGTTGTTACTTCAGGAGTGCGTTACAATGCTCTGCTGACGGTGGACGACTGCTTCGACATGGGGAAAATGGCCTACAACGACAACGACTACTATCATTCAGTGCTGTGGATGCAGCAGTCGCTCAGACAGATGGACTCTGGAGAAGAAGCCAAAACACCGAAAGCAGATGTGCTGGATTATCTCAGTTACTCTGTCTATCAGATGGGGGATCTGCCA[C/T]GAGCCATCGAGCTTACCAGACGCCTGCTAGCCATCGGTAACCGCAGCATCAACATCCACATCACTACATTTATTTACTTTATTTACTTGCAATTATAATTATTTATTTGTGTATTTATTTGCTTGCTATTATATTTATTTATTTACTTTATTTATTTACATGCAATTATATTCATTTTAATAATGGGACTAAGCCGACAAGAAAATGAATGAATTATTTAACTTATTTCATTTATTTACTTGCAATTATGTTTATTTATTTTATTTAATTATTTAATTTATTTACTTGCAATAATATTTATTTTTTTGTATTTATTTATTAGCTTGCTATTATAATTATTTATTTATATTACAATTTTTAACATATTTAATTTATTTACTTGCAATTATATTTATTTATTTGGATTCATTTATTTGCTTGTTATTACATTTAATTATTTACTTTATTTACTCACAATTTTATTTATTTATTATTACTTATTTATTTAATTTAATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44975
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 |
---|---|---|---|---|---|
ENSDART00000024137 | Nonsense | 307 | 514 | 8 | 14 |
ENSDART00000122352 | Nonsense | 201 | 408 | 4 | 10 |
ENSDART00000129566 | Nonsense | 310 | 541 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 41517411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 43116750 |
GRCz11 | 21 | 43111926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTTATAAAACATTTTTTCCTCTTTATCTCCTGCAGACTACTAAGAGG[C/T]AGAGCCGGCTGTTCTGTCGCTATCGTGATGGAAACCGAAATCCCCGTCTG
Long Flanking Sequence:
TGAACCCGAGCAACAGTTTACAAAAAGCCGTCCAAAAAAATAAAAGCCCCGATTTTTTTTTTTTTTTTTTTTTTTACCGCGTTTTCGAATTTCGCGAACTCGTTCACTTAATATTTGGGATTCTGTTTTCGTCTTACCTGAAAGCTGGAACCGCTCTTCCCCGTACTCGAAACCGGTCGCCGTGTTCAACTCCTCTCCGCATCTCGAGCCTGCCGACGTTACACAGTGAGCTAAGTGGACAAACGGGTTTCAGCGGGGAAGCCCTCCACAAAGAGGTAAGGCAAGCGCGAAAGGTAACGGCGTCACACCGCCCCGCAGCGTTCGCTTGAAAAAAAATAAATGCGGACGTACGTACCCCCAGGGATGTATTCCACTGCCTCTAGAAACGTCCGCGGGACTACGTTTTCAGAATGAGCTTGGGTTGGAAATTTCATCCTAAATGTGCTGTAGGTTGTTATAAAACATTTTTTCCTCTTTATCTCCTGCAGACTACTAAGAGG[C/T]AGAGCCGGCTGTTCTGTCGCTATCGTGATGGAAACCGAAATCCCCGTCTGCTGCTGAAGCCCATGAAGGAGGAGGATGAGTGGGACAGTCCTCACATCGTGCGCTTTCTGGAGGCACTTTCAGATGAAGAGATCCAGAAGATCAAGGAGATCGCCACACCCAAGGTCAGTCTGATGTAGGGCTGCAGGATACTGTGAAAAATAAGCAACGCTGTTGTTCAGTATTGCGATGACTGCAGTTGAGATCCGAATTTAATAATAATCATTCATTTATAAACATGAGTTTCCTTTTTCATTCATTCATTTTCTTTTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGAATGAACCGCCAATTTATCCAGCACATGTTTTACACAGCAGATGCCCTTCCAGCTGCAACCCATCACTGGGAAATATCCATACACTCTCATTCACTCACAAACAATACAGATAATTTTAGCTTACCCAATTCTCCTATATCGCAGGTCTT
Associated Phenotype:
Not determined