ZMP
lrmp
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate lymphoid-restricted membrane protein (LRMP) [Source:UniProtKB/Tr
Human Orthologue:
LRMP
Human Description:
lymphoid-restricted membrane protein [Source:HGNC Symbol;Acc:6690]
Mouse Orthologue:
Lrmp
Mouse Description:
lymphoid-restricted membrane protein Gene [Source:MGI Symbol;Acc:MGI:108424]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20251 | Essential Splice Site | Available for shipment | Available now |
sa14727 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20251
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067007 | Essential Splice Site | 501 | 1447 | 10 | 36 |
ENSDART00000131973 | None | None | 217 | None | 6 |
ENSDART00000135730 | Essential Splice Site | 501 | 1447 | 11 | 37 |
ENSDART00000147853 | None | None | 271 | None | 9 |
The following transcripts of ENSDARG00000045574 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 16340040)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 17282880 |
GRCz11 | 4 | 17271856 |
KASP Assay ID:
2259-4786.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTCATTTGATGCCATTCTGGCTGATAAGGAGTCATTAATTCAGGAG[G/A]TCAGTTATTGCGTATCACTAAAAGAATGATCAAAATAATATCCATGTCAC
Long Flanking Sequence:
TATTAACCAAGCATATACAAACATTTAGAGTAAACAAATCTAGCTGCCGGATGCACACTATCTTGCTAGTAATATTGACATTGACAATATGTGTTATTAAATCAAACATGAGCACATTATATAACCTTTGCTTTTTTATAGGAACGTGAAAACCAAAGCCTCATATCCAAGATTGCTGCTTTACAAGAGGAGGTATGACTCAGTACATGTAATTAATCCAAATGACCAGGTTAAATAGTCAACATTCATCTCCAATTCCCTTTTTTCTTATTAAGAACATGAAAGTGACCCTGGAGGCAGAGGAACTTCAGAAAAAGATGAATGACCTTTGTGACCTTAATGCTGATCTTCAGGTAGGCTCGGTTTTAGTTCACTCATTCATCATCTTATGCCCCCCCTAAAATACATCTGTTATGGTGGTTAATATTTTTCTATACACTCAGGTTCAAATTCATTCATTTGATGCCATTCTGGCTGATAAGGAGTCATTAATTCAGGAG[G/A]TCAGTTATTGCGTATCACTAAAAGAATGATCAAAATAATATCCATGTCACTCTTAATGTACAAATTAAAGCCAAGTGATTTGATTAATTGTGCTTTCCTCCAATCATTACTTGGAATTGTTTAGTGTTATCATTATTCTTTTGGTTATGTTTATATAACTGGCCATCATATAAAATTATATTTGTCCAGTATTATAACAGAACTGACTTTTTCTCCTCTAGAAAAATAAACAGATGGATGAACTAAAGGTGGCCGTTGTGGAGTATTCATCAGTTACAGAGGTGATCTTAAATTCTGGTTTTAAAGGGTGGTTCATACAGCAGCATTTTAAAACTTTTGCTAATGATTAGTTTTGTGAATGTTTGTATTAAAAAAAAACTTTTACATTTTTCATAAAATGCTGCTGATTAGTGTTTAACATCTACTCAATCTATCAACCACTACCCCAAGATGTTTTTGCATGTTTACCATCTGCTAAACTATTCTTTTTGTGATTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14727
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067007 | Nonsense | 608 | 1447 | 14 | 36 |
ENSDART00000131973 | None | None | 217 | None | 6 |
ENSDART00000135730 | Nonsense | 608 | 1447 | 15 | 37 |
ENSDART00000147853 | None | None | 271 | None | 9 |
The following transcripts of ENSDARG00000045574 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 16338200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 17281040 |
GRCz11 | 4 | 17270016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACTCTAGATCGTGAGGTTCTTCTGCTTCTTCAAGGCCCTACTCCAGAG[C/T]AGCTGTCWCTGGAGTTTAAATCTCTGATCAGCAGATTGGTAACTAAACTA
Long Flanking Sequence:
AAAATATATAAGCCATATAAAAAATGTGTGCTATTAGTTTTAAAAATAAATGTATTAATAGGAATGTGTTCACGTTGTGTGTGTGTGACTTTTGGTCTTTCTTTCGAATAAAACGTTAAACCAAGGTCCAAAGGTCCTAATCATTAAAAATCCCAGGATGTCCTTCGAAATGAGTAGTGGTTTAACCCCATCATCCTGGACAAGTTTGCCCACTGGCCTTAGTCCGACGTGGCCTCTTAACCATCCCTATATCATAATTGGTCCTCTCCATCAATTAGCTACTGTGTGGTGTGTGGTCTGGATGAGGAGATTCCCCCAAATGTGTAAAGCGGTTTGAGTGTACAGAAAAGCGCTATATAAATGTAAGGAATTATTATTATTGTGTGTGTGCATTTGTGCAGGGTTTGGAGCATCTGTCCACTTCTGTCTGTTTTGCATCGTCTCTGGATGAGACTCTAGATCGTGAGGTTCTTCTGCTTCTTCAAGGCCCTACTCCAGAG[C/T]AGCTGTCTCTGGAGTTTAAATCTCTGATCAGCAGATTGGTAACTAAACTAGCCAACTATTACACTTGCACAGCTTAAGCACTCTTCACACCGAGGATGGCAACTATTATATTAGTAAATAGGCATTTATTTAAATTGTTCCAAATGTAAAAGGTTTCACAAATTATTTGAAAACTGCAGTCATCAAAGCTGTTGCACCAACAGAATACTGTAAAATTGTCTGCTTTAAAAAGACCTTTAGTATTGTGTTTAATTCACCTACACCTTTTTTTGTGATTCATAATGTTGTAGACTGTTCACAGTGTGTCACACATGAATCGTTTCAGAAAAGGGAATTTAAAGAAGATGGCCTGACCTTTCTCACAGCAATCAGAAGCCTTACAGAGAACAGTGAAACTCAGGAGGCCAACACTGACCTCAAGATGCAGGTGACAGGATTTTATTCGCTTAAGACATGTCTGACAGAGGCAGGAAACATTTTGTATGTGTATGTAGATATGT
Associated Phenotype:
Not determined