ZMP
zgc:195063
Ensembl ID:
ZFIN ID:
Description:
leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 [Sour
Human Orthologue:
LRIT3
Human Description:
leucine-rich repeat, immunoglobulin-like and transmembrane domains 3 [Source:HGNC Symbol;Acc:24783]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42427 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42426 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22524 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42427
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000077823 | Essential Splice Site | 39 | 636 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 37565127)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 36004454 |
GRCz11 | 14 | 36344768 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGTGCACATGTGTCTACCACGGCCGCAGCGACGGCACTGGCAGCAGG[T/C]ACAGTAAACGCACTACTACACAACAGCATTTAATAAAATTTTAATAAATA
Long Flanking Sequence:
TTCTTCTTGTCATTAGCCGATTAGCGTGTGCCTGCAGAGCTTATCCTCCTCCTCCTCCAACTCTCTCACACACACACACATACACAAATAAACTCATACACACTTCCCATCCCACCCTGTTCAACTTTAGTGACCTACTCAGCCTTGAGAAATCCTCTTTCTAATCTCGGTTCCCCCTCCCGGTCCTTGCGCTGCTCGGCTTCCTGCGTACCTCTCCTCTCACCTGTTAGCATGCTAAAGGTGATGCCTGCCGGTACGGGCTTTTCTTGCGTTTTTTCGTTCTCGTCCAGGACTGATAAAGGGTTTTTTGTCCACTGATGTTCGAGTGGGGTCTGATGTGTGTGAGTGCGAGGATCCGTGGCTGTGCTTCGGCTGACTGAAGGATGTATCGTCTGCTGGTGGCGCAGGTTCTGCTGGGCTGCTGGAGTGTGGCACAACCTTTCTGCCCTTCCCAGTGCACATGTGTCTACCACGGCCGCAGCGACGGCACTGGCAGCAGG[T/C]ACAGTAAACGCACTACTACACAACAGCATTTAATAAAATTTTAATAAATACGAACAAAAGGGCAATAAAACTACAAATGTTAATAATAATAATTTAATAAAACTTCAACTCTTAATTTAATTTACATTCATTGTGTAAATCATGGTGGTGGTTCATTCCGCTGTGGCGACCCCTGATTAATAAAGGGACTAAGCCGAAAAGAAAATCAATGAATGAATGCATAAATTCAGGAATAAAATAGTAGACAAGCTATTAGATGGACATAAAGAAGAAATACAAGAGCTAAACAATATTTGAAAACTTTGTAGCTACAGATATTGCCCGTATATAGATACAATACATTAAAATAATATTTCCCCCATAAATATTAAACAAAATAACTAGACTAGATGTTGTTCAAAGATAAGAATGGGTAGACTACATTTCATATAGTTAGCTAGAGGTTTTAATTTTGCATGGTTCTTGACACTTAAGTTATATAATTTTGAGCAAAAGGCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42426
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 |
---|---|---|---|---|---|
ENSDART00000077823 | Nonsense | 602 | 636 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 37549223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35988550 |
GRCz11 | 14 | 36328864 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCATGAAGCAGAGGACTCTAAACGGGCAGGCCAATGATCTGTGGGCA[C/T]GAAGACAGACTCAAGAGTCGGAGAGGATGTTACTGTGTTCGCGTTCGAGC
Long Flanking Sequence:
CGGACATCAGAGACATCGAGGTAGTAGAGGAGACCACTGAAACGGCGGTCTTATTGTGGAGCGCCGAAGGTTTGCCAAGCGACACGCCACTAACAGTGGTTTACTTCCCATATGACGCCAAAGACGATAAGGAGACGGTGGATACAGAAGTTGGTCAAGGGAAGCTGCTTTTGGAGTATTTGATGCCTAATCAGGTCTACACTGTGTGTTTGGTTACTAAGAGTTCTGGGAAAGAGCAGTGTGTGGATTTCAGTACTTTGGAAATTGGTGGAGAAGAAGGCCAGAATAAAGTCTTGATGATCGCTAGCGCGATTGCATGCGCTATCGCGGTGCCGCTCATCGTGGTGTTGCTTTACAAGATATTGTGTCTTTATTGCAAAGGAAACAGTAGCAGGAATAACGGACCAGATGAAGACCTTTCCAAAGACACCTACGTGAAGTTCGAGACGCTCACCATGAAGCAGAGGACTCTAAACGGGCAGGCCAATGATCTGTGGGCA[C/T]GAAGACAGACTCAAGAGTCGGAGAGGATGTTACTGTGTTCGCGTTCGAGCATCGACTCGCAGATGACATACAAAAGTGACAGCTCTAGATCTGAGTATCTGTGCTAATGTATTGACCATCGGCTTTGTGTGTTATCTTTCCACACTTGGTGTTAGTCAGGCTGTGGTAAAATTAGTTATAAAAGATTAGCACTTGGTGTGCAATCAAACTCATTGCCTTACAAAGACTCATCTTGAGCCCACATTGTATTATCTTTTTATTCATTTATTTTTTTAAGAGCCATATTCTTCACCCAATCTCGCACAGTTCTGTATTTCTTTCTATTTTTTTGGTGAAATGCAGTGTACAAAAATGAAAAAGGTTTTTGTGTATGCCAATGTATGATGAAGTAGTATTATTTAGAGTTGTGATAAATGTTATTAAACATTTTTATTACCTAAAATGTTTTTTCTCATTAGTAAAAGGTCTAACATTTAGGGCTCTATTTTAACAATCTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22524
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 |
---|---|---|---|---|---|
ENSDART00000077823 | Nonsense | 625 | 636 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 14 (position 37549152)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35988479 |
GRCz11 | 14 | 36328793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGGATGTTACTGTGTTCGCGTTCGAGCATCGACTCGCAGATGACATA[C/A]AAAAGTGACAGCTCTAGATCTGAGTATCTGTGCTAATGTATTGACCATCG
Long Flanking Sequence:
TTGCCAAGCGACACGCCACTAACAGTGGTTTACTTCCCATATGACGCCAAAGACGATAAGGAGACGGTGGATACAGAAGTTGGTCAAGGGAAGCTGCTTTTGGAGTATTTGATGCCTAATCAGGTCTACACTGTGTGTTTGGTTACTAAGAGTTCTGGGAAAGAGCAGTGTGTGGATTTCAGTACTTTGGAAATTGGTGGAGAAGAAGGCCAGAATAAAGTCTTGATGATCGCTAGCGCGATTGCATGCGCTATCGCGGTGCCGCTCATCGTGGTGTTGCTTTACAAGATATTGTGTCTTTATTGCAAAGGAAACAGTAGCAGGAATAACGGACCAGATGAAGACCTTTCCAAAGACACCTACGTGAAGTTCGAGACGCTCACCATGAAGCAGAGGACTCTAAACGGGCAGGCCAATGATCTGTGGGCACGAAGACAGACTCAAGAGTCGGAGAGGATGTTACTGTGTTCGCGTTCGAGCATCGACTCGCAGATGACATA[C/A]AAAAGTGACAGCTCTAGATCTGAGTATCTGTGCTAATGTATTGACCATCGGCTTTGTGTGTTATCTTTCCACACTTGGTGTTAGTCAGGCTGTGGTAAAATTAGTTATAAAAGATTAGCACTTGGTGTGCAATCAAACTCATTGCCTTACAAAGACTCATCTTGAGCCCACATTGTATTATCTTTTTATTCATTTATTTTTTTAAGAGCCATATTCTTCACCCAATCTCGCACAGTTCTGTATTTCTTTCTATTTTTTTGGTGAAATGCAGTGTACAAAAATGAAAAAGGTTTTTGTGTATGCCAATGTATGATGAAGTAGTATTATTTAGAGTTGTGATAAATGTTATTAAACATTTTTATTACCTAAAATGTTTTTTCTCATTAGTAAAAGGTCTAACATTTAGGGCTCTATTTTAACAATCTAGGTGCAAAGTCTAAAGCGCATAGCACAAAAGCGTTAAGGACCTGTCCGAATCCACTTTTGCTATATTAAGGTTG
Associated Phenotype:
Not determined