ZMP
hpx
Ensembl ID:
ZFIN ID:
Description:
Hemopexin [Source:UniProtKB/Swiss-Prot;Acc:Q6PHG2]
Human Orthologue:
HPX
Human Description:
hemopexin [Source:HGNC Symbol;Acc:5171]
Mouse Orthologue:
Hpx
Mouse Description:
hemopexin Gene [Source:MGI Symbol;Acc:MGI:105112]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30920 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41460 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31729 | Nonsense | Available for shipment | Available now |
sa1444 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa30920
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020637 | Essential Splice Site | None | 447 | 1 | 12 |
ENSDART00000121506 | None | None | 447 | None | 10 |
ENSDART00000020637 | Essential Splice Site | None | 447 | 1 | 12 |
ENSDART00000121506 | None | None | 447 | None | 10 |
The following transcripts of ENSDARG00000012609 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 33890284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33046230 |
GRCz11 | 9 | 32856976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCGAATCAGCATCTCGTTTTCTGTCAGCATGGCAACAGATCCACGCGT[G/A]TCCACAGTGCAGCTCCACGGCACGGCGAGTTTCGAGTCCGGTGAGGGGTT
Long Flanking Sequence:
GGTGAATATGCAATAACATCAAGTCCTGCATCATTACATGCTTCTTGTCATTAATAATTCAGCTGAAGCTTTTAACATTGCCGCAGGTTCAGTCCTTCTCGAATAACCGACGAATATTCATCTCGAGCAACAACCCCCCCAAAACAGTTGATCTCCACAGCTGATCCTGTCCGTTTCCCAACTACACTTAACCATTACACAACGCTACACCAAGTCCAACTAAGTTTTGAGAAATAAATGACCCATGCGTGGATGGAAATTAAGAGATGTATAACCCTTGCCTGCACACACTCAGCTTCCAGCGTCTGAATGCCGTTTAATTGACCGGAAGCGGAGACTCGGCAGGTTACAGGTGCCGCATCTTCATCATCCTGACGCCCACCTGGCGCTCACTGCACTCGGACACTACAAAACCCGAAGCCTTTTAATCCTTCACGACACAAAGATGCAATCCGAATCAGCATCTCGTTTTCTGTCAGCATGGCAACAGATCCACGCGT[G/A]TCCACAGTGCAGCTCCACGGCACGGCGAGTTTCGAGTCCGGTGAGGGGTTGTACGGTGTAGATGTTTGTTTACATGAAGCGTGGAGTTATTCCGCGTCGTGTCCGTCGATCATACATTGTCCCTGCAAAAACAGAGCAGATCACGCGCTGCTCCCACGATGGAAGTCTGTGGCAGCTCCAAGTTTTCAAGCACAAGCATCTTGATTGGTTTATTCCTGCTTGATCACCCTGGCCCACAAGAGGGCGCACTTGTCAAGTAAGTATGAGATCAATAGCAGATTAATGCTGCTGTGATTCAAAATGGAAAACCTGTAAGACATGTTATTTAAATTTAAATAAATACGGATAAAACTTAATACAATGAGAAAATAAAAATAAGATATATGACAGTGTATCACTTTCACTGTTTTTTCAAAGAGGGGTGTTTGGCACCAAATGTTGGGCCCTGTCTGTACGGTGGTGGTCCCCTTACAACACCATGCAATCAGAATCAGGACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41460
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020637 | Essential Splice Site | None | 447 | 1 | 12 |
ENSDART00000121506 | None | None | 447 | None | 10 |
ENSDART00000020637 | Essential Splice Site | None | 447 | 1 | 12 |
ENSDART00000121506 | None | None | 447 | None | 10 |
The following transcripts of ENSDARG00000012609 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 33890284)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33046230 |
GRCz11 | 9 | 32856976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCGAATCAGCATCTCGTTTTCTGTCAGCATGGCAACAGATCCACGCGT[G/A]TCCACAGTGCAGCTCCACGGCACGGCGAGTTTCGAGTCCGGTGAGGGGTT
Long Flanking Sequence:
GGTGAATATGCAATAACATCAAGTCCTGCATCATTACATGCTTCTTGTCATTAATAATTCAGCTGAAGCTTTTAACATTGCCGCAGGTTCAGTCCTTCTCGAATAACCGACGAATATTCATCTCGAGCAACAACCCCCCCAAAACAGTTGATCTCCACAGCTGATCCTGTCCGTTTCCCAACTACACTTAACCATTACACAACGCTACACCAAGTCCAACTAAGTTTTGAGAAATAAATGACCCATGCGTGGATGGAAATTAAGAGATGTATAACCCTTGCCTGCACACACTCAGCTTCCAGCGTCTGAATGCCGTTTAATTGACCGGAAGCGGAGACTCGGCAGGTTACAGGTGCCGCATCTTCATCATCCTGACGCCCACCTGGCGCTCACTGCACTCGGACACTACAAAACCCGAAGCCTTTTAATCCTTCACGACACAAAGATGCAATCCGAATCAGCATCTCGTTTTCTGTCAGCATGGCAACAGATCCACGCGT[G/A]TCCACAGTGCAGCTCCACGGCACGGCGAGTTTCGAGTCCGGTGAGGGGTTGTACGGTGTAGATGTTTGTTTACATGAAGCGTGGAGTTATTCCGCGTCGTGTCCGTCGATCATACATTGTCCCTGCAAAAACAGAGCAGATCACGCGCTGCTCCCACGATGGAAGTCTGTGGCAGCTCCAAGTTTTCAAGCACAAGCATCTTGATTGGTTTATTCCTGCTTGATCACCCTGGCCCACAAGAGGGCGCACTTGTCAAGTAAGTATGAGATCAATAGCAGATTAATGCTGCTGTGATTCAAAATGGAAAACCTGTAAGACATGTTATTTAAATTTAAATAAATACGGATAAAACTTAATACAATGAGAAAATAAAAATAAGATATATGACAGTGTATCACTTTCACTGTTTTTTCAAAGAGGGGTGTTTGGCACCAAATGTTGGGCCCTGTCTGTACGGTGGTGGTCCCCTTACAACACCATGCAATCAGAATCAGGACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31729
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020637 | Nonsense | 52 | 447 | 5 | 12 |
ENSDART00000121506 | Nonsense | 52 | 447 | 3 | 10 |
The following transcripts of ENSDARG00000012609 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 33879954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33035900 |
GRCz11 | 9 | 32846646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAGGACACAAGCATGAGTTGCACCACGGTGCTCAGCTTGACCGCTGT[A/T]AAGGAATAGAGTTTGATGCAGTCGCCGTGAACGAGGAGGGAGTTCCTTAT
Long Flanking Sequence:
TATATTTTTGTACAATGGAAACAAAGTGTTAAATTTTTTTATTGCTACAAAATATCTACTCTGGTCTGTATTCTTTAGTTTAAATTATTAATATGTGATTGCATTATAATAAAATTATATGCAATTAATATGATAAAAAATAGTCATTAAACTGAAAAGACGAAATGATAAAAATCTTTGATTGAGAAATGTGTAAAACCTGGTTTAACATGATTATAATAAGCTATAATTTAAGTCTGAAACAATTAATTTATATGTACATTTGTAATATAAAGGATTGCAATCTGTACACTTGTAACATTCACATTCTTTGGTTTCAGGCAACATAAAGAGGATCATTCTCATAAAGGTGGGTCTTGTCAGTGGCTTGATGTGCGTAAATATGCAGTAACTGAATGTAATTTTGCTCAATCTGATTCTGGTTTGTTGTTGTTATAGGCAAACCTGGTGGTGAAGGACACAAGCATGAGTTGCACCACGGTGCTCAGCTTGACCGCTGT[A/T]AAGGAATAGAGTTTGATGCAGTCGCCGTGAACGAGGAGGGAGTTCCTTATTTCTTCAAGGGTGAGAAATTTTCAGTTAAAACAAATAAGATGATAAATAAAAATAACAAAATAAAGGCAAATAATATGCAGGAAGTAATTTGATCTTGGTGACATCCTACATTGTAAAAAGCGAATAGAAATGAAGATGAAAAACATGAGCTATCAATCCCATCCTAGTGTACTCCTGCCTTAAAACAGAACCTGATTAGCCTTGACTCGTTGTTTCCCTACACACTACTCCCACCCAACACATCTGAGATCCAGTTTCTATTGGTTTAACTTCCAATGTTTTCAAAGTGTCCTACAAACAAGGGCATAGATATGCACTTGTCATTGATGGGGACGGGTGAATATATAAAAAATTCTGACTGAGGGAAGTTTAATGTACTGGCCAGATTGCTATTTGCCTGTAGGCTTCAGTTTTTAATTTAAAACAGGTTTTAACAGATTTCTAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1444
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000020637 | Essential Splice Site | 247 | 447 | 8 | 12 |
ENSDART00000121506 | Essential Splice Site | 247 | 447 | 6 | 10 |
The following transcripts of ENSDARG00000012609 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 33877004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 33032950 |
GRCz11 | 9 | 32843696 |
KASP Assay ID:
554-1370.1 (used for ordering genotyping assays)
KASP Sequence:
AAATATCCAAAAGAGGCCCGTGATTACTTCATGAGGTGCCCTCACTTTGG[T/C]AAGTGTATWAATGAGCATGTTAGKAAAGGKGGTAGAGATGGAGCAAGCAC
Long Flanking Sequence:
ATCAGACATGCAAATTCACCTCTTCTTCAACCCCATTAAAGGACAACATGGTCTTCAGCTATTTCAAGCACAAGCTGGAGAAGGACTATCCCAAACTTATCTCTGCGGTTTTCCCTGGAATCCCTGATCATTTGGATGCTGCAGTGGAGTGTCCCAAGCCAGACTGTCCTAACGACACTGTGATCTTTTTCAAAGGTATTATAGGATGTTGTTGTTTTATTTGTCATTAAAGTTACAGTGCGCAAAGAAAGGAAGTTGACATTTTGTATCATATGATTCCCTGAAGGTGATGAGATCTACCACTTTAACATGCACACCAAGAAGGTTGACGAGAAGGAATTCAAAAGCATGCCCAACTGCACAGGAGCCTTCCGTTACATGGGCCATTATTACTGCTTCCATGGACATCAGTTCTCCAAGTTTGACCCGATGACAGGAGAAGTCCATGGCAAATATCCAAAAGAGGCCCGTGATTACTTCATGAGGTGCCCTCACTTTGG[T/C]AAGTGTATAAATGAGCATGTTAGTAAAGGTGGTAGAGATGGAGCAAGCACTTTAGCATTACAAAATATTTTTCTATAAAAAAATCTTTTGTTGTCGTCTTCAGGGAGTAAGACCACTGACGACCATATTGAGAGAGAACAGTGCAGTCGTGTGCACTTGGATGCTATAACATCTGACGACGCTGGCAACATATATGCTTTCAGAGGTGAGTTTATCATTGTCATCGAAATCTCATGGCGGTTTGTAGCTGTTTTGTGCTGTAGGTGTACAATCTCATTTCAAAGATTTGTACAATGTGTTCACAACTGAGTAAATTATGTCAAGGTTTTTTTCTAAAATATCATACAAATGAAAACATTTTCATAGATAGCATGACGCAATAAAGCAAGGCAAGTTACAGATGAATGGTGGTTTCATTTCATTCTTTTTTAACTGTCTAACCACTATGACACTTATCCTGAGGTTATTTTTTGTTCTGTTTTTTAATTTAATCTGAACCT
Associated Phenotype:
Not determined