ZMP
si:ch211-241b2.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8A5Z7]
Human Orthologues:
CD274, PDCD1LG2
Human Descriptions:
CD274 molecule [Source:HGNC Symbol;Acc:17635]
programmed cell death 1 ligand 2 [Source:HGNC Symbol;Acc:18731]
programmed cell death 1 ligand 2 [Source:HGNC Symbol;Acc:18731]
Mouse Orthologues:
Cd274, Pdcd1lg2
Mouse Descriptions:
CD274 antigen Gene [Source:MGI Symbol;Acc:MGI:1926446]
programmed cell death 1 ligand 2 Gene [Source:MGI Symbol;Acc:MGI:1930125]
programmed cell death 1 ligand 2 Gene [Source:MGI Symbol;Acc:MGI:1930125]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43560 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37203 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32323 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43560
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082395 | Essential Splice Site | 274 | 502 | 6 | 9 |
ENSDART00000139098 | Essential Splice Site | 268 | 465 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 21 (position 2498349)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 2374386 |
GRCz11 | 21 | 2400210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATAATCTATCATATAAACGTGTGTGTGACCTCTGCTTTATCTGTTGAC[A/G]GGTCAGAAAAACAGAAGAAACGAAGCCTCTAAATGTGCTTACCTCTTCCC
Long Flanking Sequence:
ACAATGTAGAGTAGATCTGTTTTCAAAGCATTCCTCTATACACTATTTATAAAGTGTTTGATTCTTTCCTAAAATAGGTCGTGATTGATTAGTTTTGTGAGTCAGCAGCATGTGATTTAAAGATATTGTAAGTGTATTATCATCAGTGTATGAGGAAAAGAATAACAAGGTTATATCACAGGTAAATCCCACATTAGTCACTCACGTGAGGAGGAAACTTGAAATCAAATTAAAAGCATTCAGTTTTATTGTTTTGACGTTGTGACAGTATATATAATTAATGATATTGCAATGTGGGCCCGTTTTTCAGCAATAATCATGACGGTTGCATTTTTTTTATGTTGTTTATTTTGTGTGTGTTTCTGTCAACAGCTGATTGTTATAAAATCATTACTATGCAAAAAAATGCTGTTTCATTTCCTCTTTTAATGCGCAGTCATGAGTGAGTTCCAATAATCTATCATATAAACGTGTGTGTGACCTCTGCTTTATCTGTTGAC[A/G]GGTCAGAAAAACAGAAGAAACGAAGCCTCTAAATGTGCTTACCTCTTCCCACAATCATCCTCTGTCAACACTGACTGTGAGTTTTTATGTCATTTACAGCAAGTCATTGAGCTTGTTATGATCGATGTGAAGTTACTGTAAAAGAGCTGTAAAATCAACATGCATGCAACACTGGCAAAAATACCTCAATTCCAGTATGGGAAGTTATATTATAATCATATTTTTATGATTATAAAATACTACAGTTTTATTCAATTATATATTGTTTATAAATATATGCATCACTTTATGTATTATCTTTAAGCAAGGAAATATAGTATCAATAATATATAATAGATAATTTTTTCATCATAATAGCTTGACTTAATTAATAAAACAATTACTACATTAATATATTATTGATAATTTTTGTTGTCTAATTACAATCTACAACCAAAACATGATAAAACAAAATAAAACAATTACTTAATTAATATATTATTGATGACAATTTAATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37203
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 |
---|---|---|---|---|---|
ENSDART00000082395 | Nonsense | 452 | 502 | 9 | 9 |
ENSDART00000139098 | Nonsense | 446 | 465 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 21 (position 2503277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 2369458 |
GRCz11 | 21 | 2395282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAGTCTCTTAAAGGGCCGGAGGACTGTTTGCTGATCCTCGATGATTA[T/A]CAAGAGGGAAATAAAGACTTGGAGGAGTTTTTAAAGGACCATCAGACGTG
Long Flanking Sequence:
CTCAAACAGACCTATTCTGAGAGTTTAACTAAGAACAAATAGTGCAGATGTCGTCGTTCGATTACAACATTTTGTTCTTCTTAACATGCACAAATGAAATGTTCAGCACAAAGCTAGCAATGTGCGCCAACAAAATCAATATGGTTAGTTTTGATTTCACGTTTGCTTTAAACCACATCATCATTTCTCCATTCCAGAGATGGCCACTGCGTAAACATCAGCTCCGTCATTCCTGAAAAGGGGCAGATTCTCCTCCTCCTCGGAGACTCCGGCTGCGGGAAAACCACGTTCACCCAAATCCTGTCCTACAGCTGGGCATCCCGTTCCCAGACAGACCCGTTTAACACCCGCCGGCTCCGTCTGCTCCTGCTGCTCCACTGCAGCCAAAATAAAGGGAATTTAAATCAGATTATCAACTCCAGCGTTCAACATGAACGACCAGTGGATGTAAAGCAGTCTCTTAAAGGGCCGGAGGACTGTTTGCTGATCCTCGATGATTA[T/A]CAAGAGGGAAATAAAGACTTGGAGGAGTTTTTAAAGGACCATCAGACGTGTCGAGTGTTAATAACATCACGTCCTGGAGTTTGTCCAAACCTGGAGAAAACCGTCAGGACTGTATTGCATCTCATTCATAAACCTGAAGAGTCTTCAACATGATGATGCATGCATTCGTATTTGCAAAGACTGTGAGGAGGCATTCAGCGACTCGACGAGAAGGAGCAATGCACACACAAAGTGCTAATTATACAAAGGAGCTGTGTTTATATATATATATAGAGAGAGAGTGAGAACAATGTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAGGCGCACTTCATTAATGCACAATGGTATGGCATGGTGCCTCAGTGGTTAGCACTTTCACCTTATAGCTAGTAGGTTGATGCTTCGAGTCTCATCTGGGCCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTTGCGTGGGTTTCCACCAGGGGCTTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32323
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082395 | Nonsense | 454 | 502 | 9 | 9 |
ENSDART00000139098 | Nonsense | 448 | 465 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 21 (position 2503281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 2369454 |
GRCz11 | 21 | 2395278 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTCTTAAAGGGCCGGAGGACTGTTTGCTGATCCTCGATGATTATCAA[G/T]AGGGAAATAAAGACTTGGAGGAGTTTTTAAAGGACCATCAGACGTGTCGA
Long Flanking Sequence:
AACAGACCTATTCTGAGAGTTTAACTAAGAACAAATAGTGCAGATGTCGTCGTTCGATTACAACATTTTGTTCTTCTTAACATGCACAAATGAAATGTTCAGCACAAAGCTAGCAATGTGCGCCAACAAAATCAATATGGTTAGTTTTGATTTCACGTTTGCTTTAAACCACATCATCATTTCTCCATTCCAGAGATGGCCACTGCGTAAACATCAGCTCCGTCATTCCTGAAAAGGGGCAGATTCTCCTCCTCCTCGGAGACTCCGGCTGCGGGAAAACCACGTTCACCCAAATCCTGTCCTACAGCTGGGCATCCCGTTCCCAGACAGACCCGTTTAACACCCGCCGGCTCCGTCTGCTCCTGCTGCTCCACTGCAGCCAAAATAAAGGGAATTTAAATCAGATTATCAACTCCAGCGTTCAACATGAACGACCAGTGGATGTAAAGCAGTCTCTTAAAGGGCCGGAGGACTGTTTGCTGATCCTCGATGATTATCAA[G/T]AGGGAAATAAAGACTTGGAGGAGTTTTTAAAGGACCATCAGACGTGTCGAGTGTTAATAACATCACGTCCTGGAGTTTGTCCAAACCTGGAGAAAACCGTCAGGACTGTATTGCATCTCATTCATAAACCTGAAGAGTCTTCAACATGATGATGCATGCATTCGTATTTGCAAAGACTGTGAGGAGGCATTCAGCGACTCGACGAGAAGGAGCAATGCACACACAAAGTGCTAATTATACAAAGGAGCTGTGTTTATATATATATATAGAGAGAGAGTGAGAACAATGTTTCTACAGGTGGTTTGTCAAGCCCACTCACCTGTGTGAGGCGCACTTCATTAATGCACAATGGTATGGCATGGTGCCTCAGTGGTTAGCACTTTCACCTTATAGCTAGTAGGTTGATGCTTCGAGTCTCATCTGGGCCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTTGCGTGGGTTTCCACCAGGGGCTTTGGTTAC
Associated Phenotype:
Not determined