ZMP
si:ch211-191d7.6
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate HLA-B associated transcript 2 (BAT2) [Source:UniProtKB/TrEMBL;Ac
Human Orthologue:
BAT2L2
Human Description:
HLA-B associated transcript 2-like 2 [Source:HGNC Symbol;Acc:24903]
Mouse Orthologue:
Bat2l2
Mouse Description:
HLA-B associated transcript 2-like 2 Gene [Source:MGI Symbol;Acc:MGI:1913754]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43402 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36996 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11325 | Essential Splice Site | Available for shipment | Available now |
sa23657 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43402
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080289 | Nonsense | 799 | 2814 | 13 | 32 |
ENSDART00000133936 | None | None | 377 | None | 8 |
ENSDART00000135212 | Nonsense | 339 | 1630 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 15058561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15153197 |
GRCz11 | 20 | 15052700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCTCCTAAGCAACTGGTACGACGAGAGCCCACGGACAACAGCAGCTCT[G/T]GATCAGACACTTTTGATCATCTGACACGACCAATCAGAGAACATGGAGTT
Long Flanking Sequence:
TTGTAGATCCTGCGTTTAGCTATTAGAGCTTTCATCTTTCTTCTCCTAAATTCCTCAGGAACAACTTAAACAACAACAGTGGCAGCAGCAACATCAGCAGCAGCAACAACAGCAGCAGCAGCAAGGTGGAGGAGGTCCGGTCTCTCCTTCAGGGGGTTCAGTTCCTCCTCAGCATAGATCTCTGTACCAACCTCTTGGCCCCCACCACCAACATCTTGCCTCAATGGGCTTTGACCCAAGGTGGTTAATGATGCAATCTTACATGGACCCTCGTATGATGTCTGGAAGACCACCTATAGACATTCCTCCTATGCACCCGGGTATAACTTTTAACTTATGTTTATTCCAGTATGTTGCATATAAACTTTTAATACCTTAAACTTATTTGTAAATGCAAGTATTCTAAATCTTTGTGGACCCTAATAATTTTTTTATCATTATCAGGGAGAATGCCTCCTAAGCAACTGGTACGACGAGAGCCCACGGACAACAGCAGCTCT[G/T]GATCAGACACTTTTGATCATCTGACACGACCAATCAGAGAACATGGAGTTCCCAGCGAGTCTCGAATGGTCTGGGGTTCTGACCCATATCCCTCAACGGAGCCACTGCCCTCCACTGCAACTGCTAAAGGGCGAGAAGATGGCAAAGACCCAAGGTAACCATAAACAAGTTATAGGTATTTCTCCCTCGTTGAATGTTAATTGATCAAGAGCTCATTTTCCCCCTTCTTCTAATTATAGATTGGATGCTGGTCTGGACCTGGATAGAGGTCTATCTGGTGTCTATCATCAGGACCATAGCCCACTGGAGCCTCGGAACAAAAGTGACTTTTTCAGGGATTCATCTGAAACATTGTCTGCTTTTAGTCATGTTTCAGATGAGGTTCCAAGTCTCCTACAGACTGACCGAGCACCAGTCATCCCTTCCTTTGAAACTGAGGAGGCTAACCTCACCGCTACTGATGAGGTTGAGGCCATTGGACAGGCTGTATTGAAACGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36996
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080289 | Nonsense | 1076 | 2814 | 14 | 32 |
ENSDART00000133936 | None | None | 377 | None | 8 |
ENSDART00000135212 | Nonsense | 616 | 1630 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 15057645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15152281 |
GRCz11 | 20 | 15051784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAAGAGAGAAAGAAGAGCAACATGAACGAGGAGATCGAACCAAAAAA[G/T]AAGGATTTGCACCCAAAGGTGCTTCGTCAGCTGCTATAGTGGCATGTGAT
Long Flanking Sequence:
TCATCCCTTCCTTTGAAACTGAGGAGGCTAACCTCACCGCTACTGATGAGGTTGAGGCCATTGGACAGGCTGTATTGAAACGGAGTATCTCTCAAGGCTCCAGTCACTCTCTAAAACTGGAAGAACCTAGATTTGAGGGACTTACTATAGCACAGAAGACCGTGGACTTCACTGAAACTGTGGAAAGACCAGAAGAAAAGTCCAGAAAGGAGGCCTTTGGTCAAGGCCCTGCCATCAGCAGCCGTTCCACTCCTCCTGTGACTAACGATAATGTGCATAAAGGTGACAAGCTTATCTTACCGCCACCCAACAAACAGAAGTCAGAGATGCGCTGGGGATCCCGTGGTTCTGGATCTGGAAGAAGAGAGGGTGCTGGAGGAGAGCGACCGGTCAGGAGATCTGGACCTATTAAAAAACCTGTACTGCGAGACATGAAGGAAGAGAGGGAGCAGAGAAGAGAGAAAGAAGAGCAACATGAACGAGGAGATCGAACCAAAAAA[G/T]AAGGATTTGCACCCAAAGGTGCTTCGTCAGCTGCTATAGTGGCATGTGATGGAACAAAGCCTTCCAGTGATGGGAAGAAAATGGTGGTGGAACCTGAAACTGGTGGAGCAAAATCTAGAGATCTGCATACAACAGCAGGTCCAGCAACTGCAACTGTTCCTGAGGAAAAGCCAGATAGGCCTCCATCTAATGACAAATGCCCTGAGCCCAAACTACCCTCTCGCAAAGAATCCAGCTTCCCTCCCCGATCGTACAGAAGAGACGAGAGGGAGCGAGAGAGAGATCGGGACAGAGACAGAGATCGGGACAGAGAGAGAGACAGAGATCGGGACAGAGAGAGAGACAGAGATCGGGACCGAGAGAGAGACCGAGATCGGGACAGAGAAAGAGACAGGGATGCGGACAGAGAGAAAGAGTGGCCTTCTGATTTTAAAGGCCGTGGTCGGGGGGAGTACTATTCCCGTGGCCGCAGCTACAGAGGCAGCTATGGTGGGAGAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11325
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080289 | Essential Splice Site | 2006 | 2814 | 19 | 32 |
ENSDART00000133936 | None | None | 377 | None | 8 |
ENSDART00000135212 | Essential Splice Site | 1546 | 1630 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 15053550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15148186 |
GRCz11 | 20 | 15047689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAGCAGAGGCAAAAACAGCCCCGTGCTGGACCTGTCAAGCCTCAGAAGG[T/C]AGTGTTTCATGRAGAGGGAAGTGAATCATGAAGAGTAACAGATTTATAAA
Long Flanking Sequence:
AATGTTAATTTAGCTACTTTTTCTGTACCTCTAGTTTCTTTTATCTGTTGAACACAAACAAGAAAGCTGAAACCATTGACTTGCATAATATGAAAAACAAATTCCTACCAGTTTCCAGCTTTCTTCAAAACATCATCTGTTGTGTTCAACAGAATAAAAAAACTCAACTCAAATAGTTTTTTATCAAATTAAACAATGGGAGAAAATTTGGTGGTGATTATTTAATATTTAATAATATATTTTAATATACTGACCAACACACACACAAATTTTACTTGACTGCATTTTTATCTGTCTGTTTTAGGGTGTAAAAGCAGGTGTAGAGAGTGGAGTTGAGCTGGGCATGGACAGCATCCAGTTTGGTGCCCCCTCTTCAGCAGGTAGCACTGACAGTGATGGAGTGCCTGCCCTGCTGGAGAAAACCTCTGACAATAAATTACCCGAACCCAAAGAGCAGAGGCAAAAACAGCCCCGTGCTGGACCTGTCAAGCCTCAGAAGG[T/C]AGTGTTTCATGGAGAGGGAAGTGAATCATGAAGAGTAACAGATTTATAAAATAATATTTAAAGGCACAATATGTAATTTTCAACACTAGAGGGCAGGTTTTCACAACAATGGCATATTTTGATGACGCCTTGATTTTCAGCAATAGAGGGCAGACTTTACAACAAACAGTGGCGTATTTTTGATGACACCTTGACTTAGTGTGAAATCATGGGAGTTGTGGTCTACTTTAACTCATCCATCGACATGATTTCTGCAGGATATAATGCATTCAACACTTATCATCATAGTTTAAAGCAGAGTACAGCTGAAACTGGCAGTGAAATGACAAGCTGAAGTCAACTGCTTCCTGTTTTTCTGCTCATGATAAAGTTGCACTGTTATATCATACTAAATATATTTTAGGGTTATGTTATCTTGCTGCTCTAAACGGTCTGGTGTAACACAACATATTAAAGCATCTTTAATCTGTAAATTGTGGAATTGGGACAATACTAGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23657
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 |
---|---|---|---|---|---|
ENSDART00000080289 | Nonsense | 2555 | 2814 | 28 | 32 |
ENSDART00000133936 | None | None | 377 | None | 8 |
ENSDART00000135212 | None | None | 1630 | None | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 15038781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 15133689 |
GRCz11 | 20 | 15029360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTCTTCCGCCGACTCCTCCTCAAGCGCCACCTCCCAGCCTCAACCGG[C/T]AGCCACCCAACAATCCGCCCTACCGTGGCCTCATTGGCCAAAACACACAC
Long Flanking Sequence:
GCTGCACAGTTACCCTGGAGTGCAGCCCCCAGACTTGGGCAAGCCTCAGTCCAGCTTGGCCTTCCAGCAAACCTCAAGCACCCAACACATCCCTATCCTATTCGAGCCCCAGCTGAACCAGCCTTCTGGCATGGGAGGATCACAGCTGATAGACACTCACCTGCTGCAGGTCAGAGATTAGTTTTTTGTTGCTTATATACTTATAGCTTTTTCTTCTGTCAAGTTATCCGTCCTGATCTAAAGTGTTTCCTTTGTGTAATCTGCAGCGTCAGGGGTTGGGTCAGCACTCAAACCTGTACTCTGGGCAAGTCCAGCAGCAGAGCAGCTACTACAGCTCAACACAAAGCCCCAGCTCTGCCCTGCAGCAGGTGACCGTTCCAGTGCCTGGTTCACAGTTGTCTTTACCCAACTTTGGCTCTGGTGGAGGTCAGCCGCTCTTGGCTTTGCCTCAGTCTCTTCCGCCGACTCCTCCTCAAGCGCCACCTCCCAGCCTCAACCGG[C/T]AGCCACCCAACAATCCGCCCTACCGTGGCCTCATTGGCCAAAACACACACAGCATGATGCAGCCTTCCAACAAGGTTTGTGTGCAGATGCAGTAATACATTATTATACCTTATGCTTTTATAGCTAATTTAAAATGTACTGCACTTCATATACTCTAAGTTGTATGTAAAGTTAATGACTGTAAACCATAATAACCCATGTGGTCTTGTTTACTTAAACTTAAAAACCTAAATTCCTTAAGATGCGGTTTCCTGAGTGTAAATGAGGTGTTAAATGTTTGGAGCTTGGTTATTCATGATCACTTCCAGAGGATAAAGTAAATTGGGAGTAGCTTAACTGACTCCTAAAAGAAAAAGCCACCATAGGCCACATACTCTTCTACTGCTGACCAAATATGAGAGTTATGAAATTTTTTGTGAGAAAAAACAAACAAACAAGTTTTCATACTTCACATTAATGTACCAAAACACATGTATTGCTGTCAAAATAGCTTCCATTCA
Associated Phenotype:
Not determined