ZMP
islr2
Ensembl ID:
ZFIN ID:
Description:
immunoglobulin superfamily containing leucine-rich repeat protein 2 [Source:RefSeq peptide;Acc:NP_0
Human Orthologues:
ISLR, ISLR2
Human Descriptions:
immunoglobulin superfamily containing leucine-rich repeat 2 [Source:HGNC Symbol;Acc:29286]
immunoglobulin superfamily containing leucine-rich repeat [Source:HGNC Symbol;Acc:6133]
immunoglobulin superfamily containing leucine-rich repeat [Source:HGNC Symbol;Acc:6133]
Mouse Orthologues:
Islr, Islr2
Mouse Descriptions:
immunoglobulin superfamily containing leucine-rich repeat 2 Gene [Source:MGI Symbol;Acc:MGI:2444277]
immunoglobulin superfamily containing leucine-rich repeat Gene [Source:MGI Symbol;Acc:MGI:1349645]
immunoglobulin superfamily containing leucine-rich repeat Gene [Source:MGI Symbol;Acc:MGI:1349645]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44307 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa82 | Nonsense | Available for shipment | Available now |
sa24679 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44307
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 |
---|---|---|---|---|---|
ENSDART00000073583 | Nonsense | 51 | 712 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 23361513)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 22540626 |
GRCz11 | 25 | 22638174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTTCGTAGACTGTGCCTACAAAGACCTTGTGGAAGTACCTGTGGGTT[T/A]GCCGTCCAATGCAAGCACCCTGAGTCTTTCAGCGAACAAGATTAAAGTGC
Long Flanking Sequence:
ATTCAGAACCCTGGACAGCTACTGGGGTACAAATGGTGCGTTCTCGGGTCTTTTTTTCAGCGGTCTGGTAACACAGCCAGACGCTCGAGGATGTCTCGAGATTACTGGTGTCTTTGTTTCCTCTAAATCATTTCAATATGTCAATAAGAAATAATTTTATAAAACAAAACCATGATAAATAATATAAACTGTATTTAGCTTTTTTTTAATAACTTTGATATAAATTTGTCAATCTACAAAGCTAACAGTTTAAAGTAACTTTAACAAGATTCTTGTTTCATTCATATTTCATAGTTCAAAAATCATTTGTACTAATCCCACCTTCATGTGTCCTTCACAGGAGCTGAAAATGGCAACCAAATACCTGATGCTTATTGCCCTGGGGACTGCATTGATTGGCAATGCACACTGTTGCCCCAAGCAGTGTGCCTGCTCTGATAAATACAACCACCAGTTCGTAGACTGTGCCTACAAAGACCTTGTGGAAGTACCTGTGGGTT[T/A]GCCGTCCAATGCAAGCACCCTGAGTCTTTCAGCGAACAAGATTAAAGTGCTGAAATCCAAAACTTTTGTAAACGTGACCCAGGTGACCTCTCTTTGGCTGGCTCACAATGAAATCATCACAGTCGAGAGGGACACGTTGGCTCCATTGATTCAGCTGAAAAATTTGGATATTAGCAACAACAAAATTGTGCATTTTCCATGGGAGGACTTGGCCAATCTTGGTGCTTTGCAGTTGTTAAAGATGAACAATAATGAGATGGTCAGCATCCCTAAGAACGCCTTTTCAAACTTGAAAGACCTGCGTTCAATCCGTATTAACAATAACAAGTTTACCACTATTGTGCAAGGAACATTTGATTCTTTGGCTGCCATGTCCCATCTGCAAATCTTCCACAACCCCTTCATCTGCTCCTGCAACCTTGAGTGGCTTAGGGACTGGATCCTCAAATCCTCAATCTCCATTCCTGAACAAAACAACATCGCTTGCGATGCCCCATCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa82
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 |
---|---|---|---|---|---|
ENSDART00000073583 | Nonsense | 208 | 712 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 23361043)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 22540156 |
GRCz11 | 25 | 22637704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGTGGCTTAGGGACTGGATCCTCAAATCCTCAATCTCCATTCCTGAA[C/T]AAAACAACATCGCTTGCGATGCCCCATCCCACCTCAAAGGTTCTCAGGTC
Long Flanking Sequence:
ACAAAGACCTTGTGGAAGTACCTGTGGGTTTGCCGTCCAATGCAAGCACCCTGAGTCTTTCAGCGAACAAGATTAAAGTGCTGAAATCCAAAACTTTTGTAAACGTGACCCAGGTGACCTCTCTTTGGCTGGCTCACAATGAAATCATCACAGTCGAGAGGGACACGTTGGCTCCATTGATTCAGCTGAAAAATTTGGATATTAGCAACAACAAAATTGTGCATTTTCCATGGGAGGACTTGGCCAATCTTGGTGCTTTGCAGTTGTTAAAGATGAACAATAATGAGATGGTCAGCATCCCTAAGAACGCCTTTTCAAACTTGAAAGACCTGCGTTCAATCCGTATTAACAATAACAAGTTTACCACTATTGTGCAAGGAACATTTGATTCTTTGGCTGCCATGTCCCATCTGCAAATCTTCCACAACCCCTTCATCTGCTCCTGCAACCTTGAGTGGCTTAGGGACTGGATCCTCAAATCCTCAATCTCCATTCCTGAA[C/T]AAAACAACATCGCTTGCGATGCCCCATCCCACCTCAAAGGTTCTCAGGTCACTAGCATGCCCAAATTGAATTGCAAGGCCCCATCTGTATCCATTACATATCAGCCAAACATAGAAAAGTCTGAACTCTATGAGGGATATATGGTTATGCTATACTGCGAAACAAAAGGAACACCCAAACCCGAGGTCACATGGGAGATATTTGCTGGAAACCAACTGATTACATTCCCTTTGCCTGCTATTGTTGAAAAAACTGACATTCCGATTAATGGCCCACCTACAAACACCAGGTTCCTCGTGTTTCAAAATGGCACCCTGATCGTTCCTCGCATGAGCAAGAAAGAAGAGGGAAACTACACCTGTTCTGCTGTTAATGACATGGGAAAAGCTGAGAGCTCAGTTAGACTTGTTGTCGCAGGCACTAAAAAGCATGCCACCAATTCTATGCTGGACACGAAATCACCAGGGCTTTTACCAGAAGACAAACTCGGTTCAAAAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24679
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 |
---|---|---|---|---|---|
ENSDART00000073583 | Nonsense | 309 | 712 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 25 (position 23360740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 22539853 |
GRCz11 | 25 | 22637401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGACATTCCGATTAATGGCCCACCTACAAACACCAGGTTCCTCGTGTTT[C/T]AAAATGGCACCCTGATCGTTCCTCGCATGAGCAAGAAAGAAGAGGGAAAC
Long Flanking Sequence:
AGAACGCCTTTTCAAACTTGAAAGACCTGCGTTCAATCCGTATTAACAATAACAAGTTTACCACTATTGTGCAAGGAACATTTGATTCTTTGGCTGCCATGTCCCATCTGCAAATCTTCCACAACCCCTTCATCTGCTCCTGCAACCTTGAGTGGCTTAGGGACTGGATCCTCAAATCCTCAATCTCCATTCCTGAACAAAACAACATCGCTTGCGATGCCCCATCCCACCTCAAAGGTTCTCAGGTCACTAGCATGCCCAAATTGAATTGCAAGGCCCCATCTGTATCCATTACATATCAGCCAAACATAGAAAAGTCTGAACTCTATGAGGGATATATGGTTATGCTATACTGCGAAACAAAAGGAACACCCAAACCCGAGGTCACATGGGAGATATTTGCTGGAAACCAACTGATTACATTCCCTTTGCCTGCTATTGTTGAAAAAACTGACATTCCGATTAATGGCCCACCTACAAACACCAGGTTCCTCGTGTTT[C/T]AAAATGGCACCCTGATCGTTCCTCGCATGAGCAAGAAAGAAGAGGGAAACTACACCTGTTCTGCTGTTAATGACATGGGAAAAGCTGAGAGCTCAGTTAGACTTGTTGTCGCAGGCACTAAAAAGCATGCCACCAATTCTATGCTGGACACGAAATCACCAGGGCTTTTACCAGAAGACAAACTCGGTTCAAAAGGCTCCAAAAACAGCGTGATTAGCATGAGGCCTAAATTTGAAGAGAAGACTAAAAGTCTTCCCACTGGCACATCTGTCATTACAGTGGATAAAGAGCAAGTAGATAAAGGGGCTGATACTTTGCCATTTGTTGGTAAATGTGGAATAAATGACGGCACACAGTACATTTCTAACCATGCTTTCAACCTCAGCTTGGATGAACTTAAACAGTACACATTTGATTTTGGGGTTATCGCTCTGGAAGTTTCAGAGACTGAGGCTAAAGTTCAGCTGAACCCTATGCAGATGGCCAACGCAAAGTCAAAC
Associated Phenotype:
Not determined