ZMP
zgc:91985
Ensembl ID:
ZFIN ID:
Description:
Lipase member H [Source:UniProtKB/Swiss-Prot;Acc:Q6DBU8]
Human Orthologues:
LIPH, LIPI
Human Descriptions:
lipase, member H [Source:HGNC Symbol;Acc:18483]
lipase, member I [Source:HGNC Symbol;Acc:18821]
lipase, member I [Source:HGNC Symbol;Acc:18821]
Mouse Orthologues:
AC166995.1, Liph
Mouse Description:
lipase, member H Gene [Source:MGI Symbol;Acc:MGI:2388029]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43686 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44973 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39339 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14145 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43686
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023838 | Nonsense | 12 | 454 | 2 | 11 |
ENSDART00000135222 | None | None | 190 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 33933807)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34933500 |
GRCz11 | 21 | 34967990 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCTTGTCTTTTGCAGATCTACAGGAAAATAATTTGGGGGATCTTATA[T/A]GTCACACTGATGTTGTTTGACACACACAGAGGTAACGTTGCACCTAATGC
Long Flanking Sequence:
TATAATGCAATTCTTCAAAATGCAAAAATAAATAAATAAATAAAAAATTTAGGCAAAATTTGACGCATATTAAAACAATTACGATGTAGAAAGATTGTTGCTTTAAACAAAACAAGAATTTGTTGCAATTAATACTTCAAAATTGTATTTAATTCCAGCCAGTCGCCTAAACAAGATGTACCATTTCCATTTATTTTAAGTAGAAGTGAATCTCATATATACACAAAAATAAATTGACAACAAAGAGTTTATAAAAATGAAAATAACAAAAAAGCATGACAGTATGGGAGTGTACAGTTTAATGGGGTGAATTGGAAACTTGTGGTTTCGATTTGAGCAAAATATGTGATGCTTGCTTTTACAAGAAAAATGGGTGCAACTAACTGTGAAACCATGCTTCACTGCAGTATAAAAACATTTGTCACTTTTTCTATGGTGTGAAATCTGCTGTGTTCTTGTCTTTTGCAGATCTACAGGAAAATAATTTGGGGGATCTTATA[T/A]GTCACACTGATGTTGTTTGACACACACAGAGGTAACGTTGCACCTAATGCACTCAAATTCACATTTACTCCATTGTTTGCTTTTCCAGTTTCTATAAAAACTAAATGATGTTTTCTTTGAACAACCCATTGGCATTCTCTGAAATGTGTGCTCTTCTTTGTGGTTAACCACTGTGGCTTATAACACCATGAGACAGTAACCATGACATAGTCCCAGTTTCTATTTCACTCACTGCCTGTGTTAAAGTTCTCTTAAAAATGTTAAAGGGCATCACAAATGCAGCATTATTCATGCTTGTCCTGTAAATACACACACATTAAAAAACATGCATGTCTATTTTTCCACTCATTCTTTTGCTTTTTTCCTTTCAGAAGACATAGTGTAATACATTTATGGTACACTCAAAAATATGTTGGGTGTTTGTTCAAACTACTTATTTAAAATGAGCTGAAACAACACAATTCTTGAGGTTTTTTTGAAGGGGGGGAGGGGGTGGGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44973
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 |
---|---|---|---|---|---|
ENSDART00000023838 | Essential Splice Site | 22 | 454 | 2 | 11 |
ENSDART00000135222 | None | None | 190 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 33933775)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34933468 |
GRCz11 | 21 | 34967958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTGGGGGATCTTATATGTCACACTGATGTTGTTTGACACACACAGAG[G/A]TAACGTTGCACCTAATGCACTCAAATTCACATTTACTCCATTGTTTGCTT
Long Flanking Sequence:
TAAATAAATAAAAAATTTAGGCAAAATTTGACGCATATTAAAACAATTACGATGTAGAAAGATTGTTGCTTTAAACAAAACAAGAATTTGTTGCAATTAATACTTCAAAATTGTATTTAATTCCAGCCAGTCGCCTAAACAAGATGTACCATTTCCATTTATTTTAAGTAGAAGTGAATCTCATATATACACAAAAATAAATTGACAACAAAGAGTTTATAAAAATGAAAATAACAAAAAAGCATGACAGTATGGGAGTGTACAGTTTAATGGGGTGAATTGGAAACTTGTGGTTTCGATTTGAGCAAAATATGTGATGCTTGCTTTTACAAGAAAAATGGGTGCAACTAACTGTGAAACCATGCTTCACTGCAGTATAAAAACATTTGTCACTTTTTCTATGGTGTGAAATCTGCTGTGTTCTTGTCTTTTGCAGATCTACAGGAAAATAATTTGGGGGATCTTATATGTCACACTGATGTTGTTTGACACACACAGAG[G/A]TAACGTTGCACCTAATGCACTCAAATTCACATTTACTCCATTGTTTGCTTTTCCAGTTTCTATAAAAACTAAATGATGTTTTCTTTGAACAACCCATTGGCATTCTCTGAAATGTGTGCTCTTCTTTGTGGTTAACCACTGTGGCTTATAACACCATGAGACAGTAACCATGACATAGTCCCAGTTTCTATTTCACTCACTGCCTGTGTTAAAGTTCTCTTAAAAATGTTAAAGGGCATCACAAATGCAGCATTATTCATGCTTGTCCTGTAAATACACACACATTAAAAAACATGCATGTCTATTTTTCCACTCATTCTTTTGCTTTTTTCCTTTCAGAAGACATAGTGTAATACATTTATGGTACACTCAAAAATATGTTGGGTGTTTGTTCAAACTACTTATTTAAAATGAGCTGAAACAACACAATTCTTGAGGTTTTTTTGAAGGGGGGGAGGGGGTGGGGGGGGGAAACTTAACTGGTTTGTTCAGTCCACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39339
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 |
---|---|---|---|---|---|
ENSDART00000023838 | Essential Splice Site | 183 | 454 | 5 | 11 |
ENSDART00000135222 | None | None | 190 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 33920418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34920111 |
GRCz11 | 21 | 34954601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGTTTATGGAATTATCTTCAATGGAAATGTGTCTTCTGTTTTAATTA[G/T]CACTGGATCCAGCAGGGCCAGAGTTCAACGGTCGGCCCCCTGAGGACCGT
Long Flanking Sequence:
AATAATTCACAACAAGGACTTTAACATGCATTTAAAAAAAATAACAAATTTTTAATTTTGCGATTGCTTGATAATCATATTGCGCACATACAGGTATTGCTTCCAATCAGTCTTGACAAGGCAGTAGGTTTGTCTGTGCACAGGTGAACCATGCAGAAGTTTTATAGTGGTGTGTTAATCATTAACGTGCTCAGACATAGATTTCACATTCTAATCATTCATTTTCTGTAGTTTTCTGACATATTCATGTATGAAGTAACTGATTTTTTTTTTACAACAATATTTTTAGGACAATGGGGCCAATCTCAGCTCTATACACATGATAGGTGTCAGTCTGGGAGCCCACATTTCAGGTTTCACTGGGGCCAACTTTAATGGTGAAATTGGTAGAATAACAGGTTAGATTCTTTGATTTTTCTACTCCTTTTAGTAAATAAAAAAAATGTCAGTGTTTGTTTATGGAATTATCTTCAATGGAAATGTGTCTTCTGTTTTAATTA[G/T]CACTGGATCCAGCAGGGCCAGAGTTCAACGGTCGGCCCCCTGAGGACCGTTTAGACCCTTCTGATGCCCTGTTTGTGGAAGCCCTACACACAGACATGGATGGTACATTCACCTCACAAATGATTGACTTTGATCTTAAAGGGAAAGTTCACCCAAAACATAAAATTATTCCATTGTTTATTCACCCTTTCCTTGTCACAAACCTGTTCGACTTTCTTTCTTCTGTTGAACGAAGAAGATAATTTATATAATTTGGAAATCAGTAACCTTTGACTTTCATTGTATTTTCATATCCTATTTTGCGTTCAATAGTACAAAAAAAACTTGGAACCAGTTGAGGTGAGTAAATGGCAAGTAAATTTTCCTTTTTGGGTGAACTATCCCTTTAAGGTTGGGGTCTTGATTATCTTCAGGAATCTACACCGCAATTTACATGCAAACACAACTTGGTTCATTCAAAATGAAAGTCTAAATTTAAATATTTGCTTTTTTCTGTAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14145
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 |
---|---|---|---|---|---|
ENSDART00000023838 | Nonsense | 230 | 454 | 6 | 11 |
ENSDART00000135222 | None | None | 190 | None | 4 |
Genomic Location (Zv9):
Chromosome 21 (position 33919879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 34919572 |
GRCz11 | 21 | 34954062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTSTGTAGCATTAGGCTATCGAAATCTTCTGGGYCACATCGACTACTA[C/A]GCYAATGGAGGGGCAGATCAGCCAGGATGTCCTAAAACCATCCTATCAGG
Long Flanking Sequence:
CCTGAGGACCGTTTAGACCCTTCTGATGCCCTGTTTGTGGAAGCCCTACACACAGACATGGATGGTACATTCACCTCACAAATGATTGACTTTGATCTTAAAGGGAAAGTTCACCCAAAACATAAAATTATTCCATTGTTTATTCACCCTTTCCTTGTCACAAACCTGTTCGACTTTCTTTCTTCTGTTGAACGAAGAAGATAATTTATATAATTTGGAAATCAGTAACCTTTGACTTTCATTGTATTTTCATATCCTATTTTGCGTTCAATAGTACAAAAAAAACTTGGAACCAGTTGAGGTGAGTAAATGGCAAGTAAATTTTCCTTTTTGGGTGAACTATCCCTTTAAGGTTGGGGTCTTGATTATCTTCAGGAATCTACACCGCAATTTACATGCAAACACAACTTGGTTCATTCAAAATGAAAGTCTAAATTTAAATATTTGCTTTTTTCTGTAGCATTAGGCTATCGAAATCTTCTGGGTCACATCGACTACTA[C/A]GCCAATGGAGGGGCAGATCAGCCAGGATGTCCTAAAACCATCCTATCAGGTCAGCTTTTTACCATTTTATTAGCATTTTCTAAAAGTAATCAATGTAACCTAGTACTCCATATATTATCATGTTAAAGTGCTTGTCAAAATAAGAGTAAAATATTCAGAGATTCCAGAGGTTTTCAGTTAGGTTTAGTTCAGGGCTGTGGGCTGGCCATTTCATTATTTCATTGTTTTCAGTTTCAGGAAAGTGCTTTGTATGTTTTCCTGTTACAAGGCTCGTTTTGCTACATGAAAAGGACATGTAATAAAGAACATGTTGACGAAAGAGTTTATAAACATTTGCATTCATTCTGCAATGTAGCTGTTAAATGCTGTGTTCACGCTCGAATAAATTCCGATATACATGAGTAAATAGTCGCTTTATACGCTTGTCAAATTCACTTTACATTAGAAGACGCGGATTCACATCATGAGCAGGCCTCCTCACAGGTGACTCTAGCTTTCTT
Associated Phenotype:
Not determined