ZMP
htra1b
Ensembl ID:
ZFIN ID:
Description:
HtrA serine peptidase 1 [Source:RefSeq peptide;Acc:NP_001104652]
Human Orthologue:
HTRA1
Human Description:
HtrA serine peptidase 1 [Source:HGNC Symbol;Acc:9476]
Mouse Orthologue:
Htra1
Mouse Description:
HtrA serine peptidase 1 Gene [Source:MGI Symbol;Acc:MGI:1929076]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12975 | Nonsense | Available for shipment | Available now |
sa27906 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24904 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22048 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12975
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012318 | Nonsense | 17 | 476 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 12563494)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11419147 |
GRCz11 | 12 | 11457450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCGTCTTTTGATTCTGTGCGCGTCTATTATTCTGGTACCGCTGCTGTG[C/A]GATGCGCGGATCATTAAGCGTTATGTGATCGGCTGTCCGGAGCGCTGTGA
Long Flanking Sequence:
TGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGACGTAGCCTATAGCTTTCAAAATGTGTGCATGGGATTTGTTACCATAATATTTAGACACATGCTTGGGCGTGGCCTCCTTGTTTACCATTAAGCCCGTCCCACACCCGTTCCTGACGTCAAACTCAACCAATCAGCCTTGCTGTTTTTGCTCCTCAAGCTTTATAAAGTCTGTCATTGAAGCGCAGGATAACGGGCATTTGACAGCACATCAAACTTGGTCAAGTTCACTGCAGTTTAACCTTTTATTTGTCCCGTGACGTTTTCCAAATCTCATTAACTTGGAAATATTTGACTTGAAAGTTTTCTGCTTCTGATTATAGTCGTAAAATGCGTCTTTTGATTCTGTGCGCGTCTATTATTCTGGTACCGCTGCTGTG[C/A]GATGCGCGGATCATTAAGCGTTATGTGATCGGCTGTCCGGAGCGCTGTGATAAGAGTCTTTGTCCGCCTATACCGCCCGACTGTCTGGCCGGTGACATCCTGGACCAGTGCGACTGCTGCCCAGTGTGCGCGGCCGGCGAGGGTGAGTCCTGCGGCGGCACAGGGAAACTGGGAGACCCGGAGTGTGGAGAAGGTCTGGAATGCGCTGTGTCTGACGGGGTTGGTGCAACGACTACCGTGAGACGGAGAGGAAAGACCGGCGTGTGCGTGTGCAAGAGTTCTGAACCGGTCTGCGGCAGTGATGGGGTGTCCTACAGGAACATCTGCGAACTCAAGAGGGTCAGTAACCGGGCGCAGAAGCTTCAGCAGCCACCCATCATCTTCATCCAGAGAGGAGCCTGCGGGAAAGGTAAGAATTGACCTTTTACATTTCCAAGTTTTGACAAAATATCCAAGGTTATGCATAGGCTACACTGTGAAAATGCTGGGCTCAACATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27906
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 |
---|---|---|---|---|---|
ENSDART00000012318 | Nonsense | 151 | 476 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 12563092)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11418745 |
GRCz11 | 12 | 11457048 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCAGAAGCTTCAGCAGCCACCCATCATCTTCATCCAGAGAGGAGCCTG[C/A]GGGAAAGGTAAGAATTGACCTTTTACATTTCCAAGTTTTGACAAAATATC
Long Flanking Sequence:
TGGAAATATTTGACTTGAAAGTTTTCTGCTTCTGATTATAGTCGTAAAATGCGTCTTTTGATTCTGTGCGCGTCTATTATTCTGGTACCGCTGCTGTGCGATGCGCGGATCATTAAGCGTTATGTGATCGGCTGTCCGGAGCGCTGTGATAAGAGTCTTTGTCCGCCTATACCGCCCGACTGTCTGGCCGGTGACATCCTGGACCAGTGCGACTGCTGCCCAGTGTGCGCGGCCGGCGAGGGTGAGTCCTGCGGCGGCACAGGGAAACTGGGAGACCCGGAGTGTGGAGAAGGTCTGGAATGCGCTGTGTCTGACGGGGTTGGTGCAACGACTACCGTGAGACGGAGAGGAAAGACCGGCGTGTGCGTGTGCAAGAGTTCTGAACCGGTCTGCGGCAGTGATGGGGTGTCCTACAGGAACATCTGCGAACTCAAGAGGGTCAGTAACCGGGCGCAGAAGCTTCAGCAGCCACCCATCATCTTCATCCAGAGAGGAGCCTG[C/A]GGGAAAGGTAAGAATTGACCTTTTACATTTCCAAGTTTTGACAAAATATCCAAGGTTATGCATAGGCTACACTGTGAAAATGCTGGGCTCAACATAATTCTTTCATGTTGTCCCAATACACATCTATTAAAATATATGGTGTTAAACATGAAACAATTAAGCTGTCCCCTAAAATAATACTTAATAATTGTGTTGTTTCGTCTCATTTTAAATATGTAGTTTGAACAAGCAGCAAGTCATTGTTTGAGTGTAGACAACGATTTTGTGCATCATAGCCAAGTAGAAACATAGGAAACCTTTCTGTTAATGTTCCTAATTTTACACTTAGCATTCTTAATTGTTTTCTGAGGCACATTAACCCTTTAACAGACTGCTCTGACTGTTAACTGTTAACCATCTAAACTGTTAAAGTCATTTAGAGAATGACTGTTTTAAATAATGGTTTACACAAACAGCATTGTTGGTTTATAAAAAAAAAAATCCAACATAATCCTGTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24904
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012318 | Essential Splice Site | 370 | 476 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 12507599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11363252 |
GRCz11 | 12 | 11401555 |
KASP Assay ID:
554-7492.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAAGATCCGACAGTTCCTGGCTGAGTCTCACGACAGGCAGGCTAAAGG[T/G]CAGCAGCAGCATTTAAAACTTAGAAACATCTAAGTCCTGTTATGACATAT
Long Flanking Sequence:
TTCAGTATGGTAATTCCGGAGGGCCCCTGGTGAATCTGGTAAGAGTTTTGCTCTTTGTTATGTATATCTTCCTCATGTGCAAATAATAAAACCAGCTTGAGTCTTGTATGCAAGCATATTAACACGAGCAGCAGAATCCAGTCAAAACTGGCTTTCTGCATTTAATGATGTTTATGGCATTTCTTTATTAGCATAGGAACATATGTTGGCATTAAGACTTTGTGTCGAGTCAGCCGTGACCATAAACACATGTGTGCGTTCATAATGATTAATTTCGGAAATATCACATTGTCACAGGAAGACATTTGTGCATCCAGATGTGCAGTGCACTTGTGTGAGTTCACGTTTACATTTGTGTCCTTACTCTTGTGTCTGTTGCTGTAGGATGGGGAAGTGATTGGAATCAACACACTGAAGGTGACCGCAGGAATATCCTTCGCCATTCCCTCTGACAAGATCCGACAGTTCCTGGCTGAGTCTCACGACAGGCAGGCTAAAGG[T/G]CAGCAGCAGCATTTAAAACTTAGAAACATCTAAGTCCTGTTATGACATATGTTTTCAATTTTATGTCTGAGCATAGAAAGATCAGTACATTTCTGTTTCTTAACTCCTCAAAAGCTTCAATTTTAGGTCAAGAGTTTTGGTAACAATTTAGTTTAGGTACCATTTTTTTATATTAACTAATGGCTTATTACCTGCCTATTAATAGGTTATTGGCCATTTATTAGTACTTATAACTTACATACTGTCTACTGCATGATGTTTTTACATTCTTTATCCTACCTAATACCTAAACCTAACAACTACCTAATAGCTACTGTATAAGCAGCAAATTATTAGTTTATTGAGGCTAAAATCAAAGTTAATGGTTATTATTATAAGAATTTAAGGGATAGTTCAGCCATGAAAGAAACATGTTTCAAACCATTTTGATCTTTTTTGTTCTGTTGAACACAAGAGAAGATGCAGTATATTGAAGAATGCTGGAAACCTGCAACCATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22048
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012318 | Essential Splice Site | 389 | 476 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 12 (position 12504142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 11359795 |
GRCz11 | 12 | 11398098 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCAAACAGACATGGCGTTTGTGTTTGTACTAAGAATCTGTTTCTCAT[A/T]GACTTGCTAAGGAGCTAAAGCAGAGAAAAAATGATTTCCCAGATGTCACC
Long Flanking Sequence:
ATTTATCTTGCTGTCTGTGTATTTTCAGTATTTTGTATCTTTTATAACACAACTTTAAAATGCAGTTACATACTGCACAACTGTCCTACAGTAAAAAAAAAATGTTTAGATTACGGCTAAATACTGTGTAATTTACAAAGAAAAATGTTAACAGTGTTGCTGACAGTATTATATTGAAAACCAAAATAAGGTTTGCACTGGTGCTAGCTGCTAGTAAATCAGTCCCTAAACTTGATTCACAATTCTATCAATATCTTGTATTACTTTTCAGGAAAAACAGCCACAAAAAAGAAGTATATTGGTGTGAGGATGATGACGTTAACTCCAACGTGAGTCTAAAATACTGTTTTCTTTCTGTACACACTTGTACGTTTGTGAATATGGAGGAATGTTTAAATGAAATGAGTCGGCCATCTAAACAAGTCATTTTAACTTGTATTGTCGATAATTCATGCAAACAGACATGGCGTTTGTGTTTGTACTAAGAATCTGTTTCTCAT[A/T]GACTTGCTAAGGAGCTAAAGCAGAGAAAAAATGATTTCCCAGATGTCACCTCTGGTGCTTACGTCATTGAAGTTATTCCCAAAACACCAGCTGAAGTGTGAGTAGCCCATCACATGCAGACACCCTTTACAAAACAGCTAATAAACTACCAAGGCAACAAACAAACGCAGAGAAACAAAGGGGAAACCAAACTGATTACAATCTGACTTCACACACCAGGGAGAGAAAACACTTGAACACATAGAATCTATGAGTGATATGCTTAAAACACGTAGCTACACTCTAAAAAAAATGTTGGGTTATTTATATAACCCAGTGGTTGAGTTAAAAATATTTGGTGCTTTGTTGGGTTATTTTTAACCTTTATTGGGTTTTTATTTGCACTTCTAGGTGCATTATTTATGACAATAAATTATGGACATTATTTAATCCATGTGTGTATACTTGTATTTTGTTCAGTACTTAGAGGAGGAGGAGCAACAGAGACAGAACCCTCCTGC
Associated Phenotype:
Not determined