ZMP
si:dkey-79p17.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate lactase (LCT) [Source:UniProtKB/TrEMBL;Acc:B0UYB9]
Human Orthologue:
LCT
Human Description:
lactase [Source:HGNC Symbol;Acc:6530]
Mouse Orthologue:
Lct
Mouse Description:
lactase Gene [Source:MGI Symbol;Acc:MGI:104576]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38764 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27482 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38763 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38764
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 |
---|---|---|---|---|---|
ENSDART00000145110 | Nonsense | 298 | 1592 | 2 | 12 |
ENSDART00000145931 | Nonsense | 604 | 1898 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 47594313)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 46593116 |
GRCz11 | 9 | 46393595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTCATGCTGGGGTGGTTTGCTCATCCAATATTTGTAGATGGAGATTA[T/A]CCAGCGGTACTGAGGGAGCAAATTGAGAAAAAGAAAGAATTGTGTACCCA
Long Flanking Sequence:
GCCGAACGACCTGGCCATGAAAGTGCCTTCACTTTCATGGCCTTCACCTAGCAAAAGATGTACACACAACAGCGACTTTATGACACAACCATACCAGGGATCTGAGGGATTTAGTGAACACAAGATAGTGTGAACACAAACCAGCCGAGAGGGTGGCAAGAGGGAGCAATCAAACTTGGGTTTGGACCAGGCAATCGAACCAAGTGTGAAAGCACCCTTAGAAAGTCCCAAATATAGTATGATTTTAAAAAGTGTATACTGACAATTCTTTGCTTGTATTCACAGGTGACGCACAATATTCTGAAATCTCATGCTGAAGCCTGGCATATTTATAATGATAAATACAGGAAACTGTATGGTGGAAAAGTGGGCATTGCTCTGAACTCAGATTGGGCTGAGCCGAGGGATCCCTCAAGTGATCAGGATGTAGCAGCAGCTGAGCGTTATCTAAACTTCATGCTGGGGTGGTTTGCTCATCCAATATTTGTAGATGGAGATTA[T/A]CCAGCGGTACTGAGGGAGCAAATTGAGAAAAAGAAAGAATTGTGTACCCAAGACCTGGCAAGACTCCCTGTCTTCACCGAGGCTGAGAAACAAAGAATTCGAGGCACAGCTGATTTCTTCGGACTAAACCACCAAACATCCCGACTGATTAGTGAGAATTTGACTAGCTGTGATGCTGGGCCAGATAATGTTGGGGACTTCCAGGCTCATATTGACCCTACATGGCCCACTACAGCTTCTGACCAGATCCAGTCTGTTCCATGGGGGCTCCGGCGGTTATTGTATTACATCTTTTTAGAGTACACATCTATTACAAAGGTGCCCATCTATATCACAGGAAATGGAATGCCAACTGAGTATACTGGTGACGGGATCAATGACACTCTGCGTGTTGACTATCTCAAAGCTTACATTAATGAAGCAATGAAAGGTAAGAGTAAAAGGTCAAAAAAAGGGTCTTTTACTATTGCATTTTAACACTAAATGCTGCCATGAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27482
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000145110 | Nonsense | 710 | 1592 | 3 | 12 |
ENSDART00000145931 | Nonsense | 1016 | 1898 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 47592942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 46591745 |
GRCz11 | 9 | 46392224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGGTTAGCATATTCAATGAATATTGTGACTTCTGCTATGCAACATTT[G/T]GAGATAGGGTGAAGTTTTGGATCACCTTTAATGAACCCCAGACGATTGCA
Long Flanking Sequence:
AGTTTTCACCTCAGACCAAATTTGAGAGGCAGCTTTATCACTATGGAACATTTTCAGAGGGATTTCAGTGGGGTGTCTCATCTTCAGCTTATCAAGTTGAAGGTGGCTGGAATGCAGATGGAAAAGGACCAAGTGTTTGGGATACTTTCACTCAGAAACCTGGTAATATCCCAAACAATGCCAATGGCGATGTTGCATGTGATAGCTACAATAAAGTAGATGAAGATCTACACATGTTGAGGGCCCTAAAAGTGAAGACTTACAGATTCTCATTGTCATGGTCTCGGATCTTTCCAAATGGCTATAAATCTTCTCTTAACCAGAAGGGGGTGGATTACTACAACAGGCTCATAGATGGTCTCATAGCAAATAATATCACACCCATGGTGACTCTCTACCATTGGGACCTGCCGCAGGCTTTACAGAATATCAATGGTTGGGACAACACTGAAATGGTTAGCATATTCAATGAATATTGTGACTTCTGCTATGCAACATTT[G/T]GAGATAGGGTGAAGTTTTGGATCACCTTTAATGAACCCCAGACGATTGCATGGTTGGGATATGGGCTGGGTCAGATTCCACCTAATGTGAAGCAACCAGGAGATGCTCCATACAGGGTTGCACACAACCTCCTGAAAGCTCATGCACAAGCTTATCACACATATGATGAGAAATACAGGGCATCTCAAGGAGGTCTGGTATCCATTAGTCTGAATGCTGAATGGGCAGAACCCCTGGATGTCAACATCCCTCGAGAGGTGGAGGCTGCTGATCGAGCTCTTCAATTTCAATTAGGCTGGTTTGCACATCCAATCTTCAAGAATGGTGACTACCCTGATGCCATGAAGTGGCAAGTTGGCAACAAGAGTGAACTGCAAGGCTTAAAAGAATCCCGGTTACCTTCTTTTACTAGCCAAGACAAAGCTTTTATCCAAGGAACAGCTGATGTATTCTGCATTAACACATACACTACGAAAGTCATGCGCCATGTGACCAGCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38763
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000145110 | Essential Splice Site | 1361 | 1592 | 10 | 12 |
ENSDART00000145931 | Essential Splice Site | 1667 | 1898 | 15 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 47590427)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 46589230 |
GRCz11 | 9 | 46389709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGTTTCTGAATTCAAGCATCAGGATTCAAAAAGTTGCCATTTATTCC[A/T]GGGGTGCTGGAGCTATTAGGGATCGTACATGGCTAGATTCTGGATCCATC
Long Flanking Sequence:
AAACAAGAAGACGTGGATGCTGCCAGACGTACGATTCAGGTACAGCTTTGTTGTACAGCGATATCTACATTAATTTCTACATGCCACTTCACTTTTTATCTCTTTTAAACAGTTTCAGCTTGGTTGGTTTGCTCATCCCGTGTTCAAAGGAGATTACAGTGATTTAATGAAGGATGTTATTCGAGAAAGAAGTTTGGCAGCTGGCCTACCTAAATCAAGGTAAATACAGACATTTTCTTGTGAGGAATTCACAACTTTGCATGCTTCTAAATGCCTTTACATTTGACAGGCTTCCAGAATTTACCCCTGAAGAAGTAGCAAGAATTAAGGGTACTCATGATTATTTTGGATTCAACCACTACACCTCTGTTTTAGCCTTTAACGTGGACTACGGTGATCAACAGCACATTGAAGCAGACAGGTAACCCTTTAGTTTGAGATGTTTTAGGTCCATGTTTCTGAATTCAAGCATCAGGATTCAAAAAGTTGCCATTTATTCC[A/T]GGGGTGCTGGAGCTATTAGGGATCGTACATGGCTAGATTCTGGATCCATCTGGTTGAAAGTAGCTCCTGTGGGATTCCGAAAGATTCTGAATTTCATTAAGGAGGAATATGGAAACCCTCCTCTTTACATTACAGAAAATGGAGTATCAGAACAAGGACCAGAGAATCTGAATGACGTCACCCGAATCTACTACTATGAAAACTATATCAATCAGGCCCTGAAAGGTAAAGATCTTTCCTCTTAAAGATGTCAAAAGGAACATTATTAAATGATTGTTTGCTATAATAGTTTTGCATGTATTTTTTTGTTTAGCATTTTCAGTTATTTGGTGCTAATTGCAGTGTTATTCTTAGCATATATGCTAGATGGTGTGGACATCCGCGGCTACACTGCCTGGTCACTAATGGACAATATGGAATGGGCAGCGGGTTATACTGAAAGATTTGGTCTTTTCTATGTAAATCGGTCAGATCCCAATTTTCCACGTATTCCTAAGAAA
Associated Phenotype:
Not determined