ZMP
ildr2
Ensembl ID:
ZFIN ID:
Description:
immunoglobulin-like domain-containing receptor 2 [Source:RefSeq peptide;Acc:NP_001025363]
Human Orthologue:
ILDR2
Human Description:
immunoglobulin-like domain containing receptor 2 [Source:HGNC Symbol;Acc:18131]
Mouse Orthologue:
Ildr2
Mouse Description:
immunoglobulin-like domain containing receptor 2 Gene [Source:MGI Symbol;Acc:MGI:1196370]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa27438 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa18952 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa17518 | Nonsense | Available for shipment | Available now |
| sa15399 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27438
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049805 | Essential Splice Site | 16 | 590 | 1 | 9 |
| ENSDART00000125451 | None | None | 602 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 35271870)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34491381 |
| GRCz11 | 9 | 34300566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATGTTTTTGTTACACGCTTTTTGGATTCTATTCACACTATTTTCACG[T/A]AAGTTATTAATCATGTTTTCACTTTAACGCGAAATAGAGATACAGAAAAC
Long Flanking Sequence:
AGTCTAAATAAATCAGCGATTTTAAAATACTTACTGTTGAAAGTTTCATTTTTCCTCAGCATTATTAGTCTTTTAACACTGAATTACATTCTCAGCTAAAACAAGATAACAATAACCACTTTTTTAAAAATACGTTTGATACAATAACGTTATTTTTTCAGAAAGACGAGTCCACTTTAGGAAATCTGGCAGGCAGTGATTGAGTCTATTAAATAAAATACTTTCTAATATTACGTTGGCAACCTTATAATTAAATGCAAAAGCTTTAATCAAAACAGCTTCAGCGAAAGCAGTTTAACATACTTAAAGTTTAGCTAGAAGAGCTGCCTCCCCCTTTAGAAAAGTGGTACATTCCGCTCATTCTGACCAGCGCAGCGGACAGAGATGAAGCGAATAACAGTCCGGGAGAAGATGGACTAGATGATTGCAAACTAACCCGCACTAAACTGGATCATGTTTTTGTTACACGCTTTTTGGATTCTATTCACACTATTTTCACG[T/A]AAGTTATTAATCATGTTTTCACTTTAACGCGAAATAGAGATACAGAAAACTGGGACGGACGAAGTAAAGCAACAGGTTGAAAGAGCTTAGAGATCCTTGAGCCTGCCTTTATTTTTAGCCTGATCACGAGTCCTCGCGATGGTTTTTACTATAATCCAATTATTCACACCTCACAAAGTAATTACAGCTAACACTTTTTAATTAAATTATGTTTAAACATAATAGTTACCGCAGTTGTGCTTGCATTCAGAAGTGTAAGTTAACTTTAAATAACATTAAATCAAACTAACAAGCTAAATGTATCCTGTTTAAAAATGAACTTTTAATTGTTTACTTCTGTTCAACAATATTCTTTGCTATTGATTATTATTGAATACACAATGCCTTTGTGTGTGCATGTGTTTGTGTGTGTGTATTATATAAATGGTACTTAACTACTAAGATAGTACTAGCCTTCTTAAATTATACAGCATAGAAAATATGAAGCACATTTGAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18952
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 |
|---|---|---|---|---|---|
| ENSDART00000049805 | Essential Splice Site | 184 | 590 | 4 | 9 |
| ENSDART00000125451 | Essential Splice Site | 169 | 602 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 35258039)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34477550 |
| GRCz11 | 9 | 34286735 |
KASP Assay ID:
2261-7184.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGTGCTGGATGACATCCTGCCTGAGTTTGATTTGGAGATTATGCCAG[G/T]TACGCCTGCCATACCTCTTTCTCTCTCTCTCTCTTTCTCTCTTCCCCCTT
Long Flanking Sequence:
ACAATGCCAACACTGTCTCCATGGTGATGACGTACCCTGGCCCCCCTTTGAGGGAGTTTAATGAGGCCATGTGATTAATTAATCTCTGATGTTCCTCCACTGTCTCCCCCTGCTGAAGCCCCTCTACTTTATCTCTTTCCCACTCTCTCTGTTCATGAACCTGATCTGTGCTGCTTAGGCCAGATATAAATACTGAACGAATGCATGCATATAATACAACCAGTTGTTGTTAGTCGTATACAGAAATACCTTTTTAACAAAAAGACCAATGTTTAAAATTATAAATCAACTTAAAGCAGCTTTTACTTTTGATTCATTCACAGCCACTAACAGAGTAACTTTTCCTTAATAACACACAAGAGCTTTTACCCACGACCTTAAACTTTGGACTTTCACCTGCCTCTCGCTGCTGCTGTTCATGTCTGATCTTCTCCCTTCTCCAGGTAGGACAGGTGTGCTGGATGACATCCTGCCTGAGTTTGATTTGGAGATTATGCCAG[G/T]TACGCCTGCCATACCTCTTTCTCTCTCTCTCTCTTTCTCTCTTCCCCCTTACTTTTCACTGGGTGCTCTCACACAGGTCCTTTTCATTTGACCTGCTTTATCTCCTCTACTGTAATCAGCAAACTCCTTAATGCTGTATCTGTTCTGTTCCCTCTGGAAAAGAAAAGATAAATACAAATTTCAGGACTTATCATTAGCTGTTTCTATCCACCTACTTTTATGCACATTTTGGAACATCGCATATAAAACCCTGGACAGAAACACCAAGATGCACAAATTTTTTGAAAATGCGCAACAAAACTAAGTTGGATAAATTTTTATCTGATAAGAAAAGATGCACATAAACTACAGTTTAATGTGCTTACAAATTCTAGTATGCACATTAAAAATGTCATGTGACTGTTATAAGAGATCATGTGATGATAAAAATAGCCTTAATGGGCAAACTCTAGTGGTTCAGTGTTATGATTGTTATTATTACCTCCAGAACTATTTTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17518
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 |
|---|---|---|---|---|---|
| ENSDART00000049805 | Nonsense | 343 | 590 | 7 | 9 |
| ENSDART00000125451 | Nonsense | 366 | 602 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 35250836)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34470347 |
| GRCz11 | 9 | 34279532 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCACCTAGATGAGCCGCGACTCCGAACAGCATCGATTGGCCAYGGGCTT[C/T]GACCCTCACATTATCAGAGCGATCACTCTCTGGATGAGCATGACAACAGG
Long Flanking Sequence:
AATTCATCCAAAAAAAAAACAACAATGTTTACTAAATGGTCAAAAATCTATATTCTGCACAGAAGAAATTCATAAAGGTTTAGAACAGCATGATTTTGAGTAAAGATTGCAGATATTTTATTTTTTGATGAACTGTTCCTTTAAACTACAAACGTGATTCCTGCATGATTTCTTATTATTAAAAATTCATAATATTCTAACCATGTTCATAATTTCTGCCATATATAGATATTCTGCTGCAAACTATAGACTGTAGCAGCAGATTTGTGTTATTTTTGACTTGGTTGTGTAAGTGCCGTGAAAGGAAGGCAGAACATCATTTCCATGATGATGTCATTATTGTCTCAGCAGCCGACAACCTATCAGAACTGAGCTCTCTGCATGATGGTGATGTAGACTTCAGACAAACCTATCGGCAGGTCCAGAGGAAAGCTCTGCCACCCATCATTGACCACCTAGATGAGCCGCGACTCCGAACAGCATCGATTGGCCATGGGCTT[C/T]GACCCTCACATTATCAGAGCGATCACTCTCTGGATGAGCATGACAACAGGTACAATTTGAGTTTATGTTTGTTACTACAACAATAATTTAGCACAAAGGTTTTCAAACTGGCATCACAAAAGGGTTGTTGGGGTAAAAAAAAATTATTCATTTAATCATTAATTTTCAGGAGTTTCCACAGTGGAATGAACCACCAACTTATCCAGCGGATGCCCTTCCAGCTGCAACCCATCACGGGGAAACACCCATACATTTACATTCACACACATACACTATGGACAATTTAGCTAACCCAATTCACCTATAGTGCATGCCTTTGGACTTCCAGTGGGCAAAACTGGAGCACCAGAAGGAAACCCACGTGAACACGGGGAGAACATGCAAACTCCACACAGAAATGGCAACTGACCATGCCGAGGCTTGAACCAGTGACCTTTTTGCTAAAAGGCGAGATCGCTATCAATGCGCCACCACATAGCTTTATTTTAATTATACTACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15399
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000049805 | Nonsense | 436 | 590 | 8 | 9 |
| ENSDART00000125451 | Nonsense | 459 | 602 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 35249016)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34468527 |
| GRCz11 | 9 | 34277712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATACCGTAATGGGCCTCGCTACCYWCGTGAGGATGATGAYAGTGACTG[G/A]CRTCGTCGAGGTTCGCCACCTTCCCCACCAAAAAGACGCRWTACCGCCGA
Long Flanking Sequence:
GAGAGTGTATGGGAGTTTCCCAGTACTGGGTTGCGGCTGAAGTGCATCAACTGCGTAAAACATATGCTGGAGTAGTTGGCGGTTCATTCCACTGTGGTGTCCCCTGATAAATAAGGGACTAAGCTGAAGGAAAATTAATGAATGAAATGTTTGTTGGGTCATTTAGTTGCATAAAGTATTACCTTTTGATCTGAAACAACTTTTTTGTGACTCTTGAGTTTTATTACTCAATGAATGTGCTGCTAATAATGCCATGAATGTTTGTGCAGATGGAACTGTCGATCTGAGCACCTGCCTCGCAAAGCCTTTGACAGCAGGGGACGCACTGTGTCCCTGGATGAGCTGGAGGAGTTCGCCATGTCTTACGGCCCACACGGTCGTCGAAGAGGAGACATCCGTGGACCCCAGCGTGACTTTGAAATGGCTCCAAGGACAAGGGACCATCCCACATCATACCGTAATGGGCCTCGCTACCTTCGTGAGGATGATGATAGTGACTG[G/A]CATCGTCGAGGTTCGCCACCTTCCCCACCAAAAAGACGCGATACCGCCGACAGCGAGCGCTACGTTTCCCGCCAGAGGTCATACGATGATACATACCTAAACAGTCTACTGGAGCGCAAGGCAAGGGGCCACGGAGAGCGGGGTGGACGTGTTGACGATGACAGCGATACACCCTCGAAAGGGAGTTCCAAGAAGAGCAGCGACTGTTATCAGAGCAGGTCACCAAGCAATCGTCCTGAAGAGGAGGATCCTTTACCTCCATACTCTGAAAGAGAGGGGGAGAGATTTAGAACTGAAGAGCCCACAGGGAGGGAACGGTACAGGACTGCTGATCCTGCCATGAGGCCTTTTTCATACACACGTCCCCCTCACGGACTGTCCCAGACGCTACAAGAGCGCAGGGAGGACAGGGACAAACCCAGGAAACTGGTGAGTTACCTGTAGTCGTCTGTCTGGGTTTCTGTTGCCTGAAGAGTGGACCAAACTTCCTCCAAGACTAA
Associated Phenotype:
Not determined