ZMP
eomesb
Ensembl ID:
ZFIN ID:
Description:
eomesodermin homolog b [Source:RefSeq peptide;Acc:NP_001077044]
Human Orthologue:
EOMES
Human Description:
eomesodermin [Source:HGNC Symbol;Acc:3372]
Mouse Orthologue:
Eomes
Mouse Description:
eomesodermin homolog (Xenopus laevis) Gene [Source:MGI Symbol;Acc:MGI:1201683]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22970 | Nonsense | Available for shipment | Available now |
sa17035 | Nonsense | Available for shipment | Available now |
sa22969 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22970
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008317 | Nonsense | 36 | 534 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 58708237)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55040051 |
GRCz11 | 16 | 55169983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGAAAGTTTCTCCGGTAGTTTGTGGTGATGATCTGTCCAGCCGGTA[T/A]CTCCTGGACGGGCTGAGCTCCAGCCGCTACTTCATGCAGACGCAGGACTC
Long Flanking Sequence:
GATATTCGGTACAGACAATTACCTTATTTTCTTTTACATCAACAAAAGCTAAATGACTTTGTTCTTCATGACTGAAACTGAATCTTCACACTTCACACAAAGAGTAGCACGTGTTGTAATGAAAGCTTGAAGATCATATCTCAGGTTATCGTATAATCAATCAATAAATGATCTGATTTGTTTCTATAGCGCAGTTCAGGGGTTGCACCCGGATAAACGCGCACAAAGAAGAAATGCAGAATTAAATAATTCAATGTGTTTTTGACATGTGTGGAATTAAATAAAAATCTGATGTGTTTTTGACATGGTTGTGTGTTAGTCAGTGATGCCGAGGCGCTTTGCACACTGACCGAGACCGAGTATCAGGCGTCGGGCTCGGTGTCCGTGATCAGCATGCCCGGAGAAGGATCCAGTTCTGGCTCCGCGCTCTCTTCTCACCCGGAGGCGGAGGAGGAGAAAGTTTCTCCGGTAGTTTGTGGTGATGATCTGTCCAGCCGGTA[T/A]CTCCTGGACGGGCTGAGCTCCAGCCGCTACTTCATGCAGACGCAGGACTCCCCCAGCCCGTGCTCCCTCTTCCCGTACAGCGGGCAGACCGGAGCCGTGTACGCCGGGTCGGATGGGTCCCGGTACTCGGCTTCGCTCCACTACGGCTCCGTGCTTCCCTCCGCCGGCTTCTGCCAGTCTCTGTGCGCCGGCCGCGGAGACTTCAGCCCGGGCTATCATCAGTTCGGTCACGCTGCGGGGAACGGCTACAGCCCATACCAGGGCTCTGGCTCCGGCGCCGTAGCGCTGCCCAGTGCGGCTCTGCGGGCGCAGGTGTATCTCTGCAACCGGCCGCTGTGGCTCAAGTTCCACCGGCACCAAACCGAGATGATCATCACCAAGCAGGGCAGGTGAGAAGACACGGCGGTTACCTGTGTTTTTAGACGACAGGTGCATTGGAAACATGGTTAAACATTGATAAATACAACTAGGCGATATATACACTAAAAATTTGAACTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17035
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008317 | Nonsense | 358 | 534 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 58696547)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55028361 |
GRCz11 | 16 | 55181129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGCCTGCAGACTCCCCCCGAGCACAGCAGATGGTCCCGAAYGCTCGATA[C/A]GCCGYCCAGYCGTTCCTGCAGGAGCAGTTCAGCASTTTGACCCAGCGCTC
Long Flanking Sequence:
CTTTAGTGCCAGGCTGTCAGTTATTTAGGGCGGAGCTATCAGCTCTTTAGGGTGGGGATATCAGTGTTTTAGGGCGGAGTTTTCAATCCTTCAGGGCGTCTATCAGTTATTAAGGGTGGGGCTATCAGTGGGTGTCACATTTCTGCTCTGAATTCCTCCATCTGTCAATCTTCCTTTATTTTGTTTGCATTGCTCGTCTTTCAATTTCGTAAGTTGATCAGTCATTTAGGGTGGAGATATCAGCACATTAGGGCGTGGTCTATCAGTCCTTTAGGGAGGAGCTTGCAATCTTATTTTATTTTATCAGGTCTTGTCTTTTAACATTAGAATTGGCTCCAGTAGAATGAAATCATGCACTGCTCTACATTTGTTTTCAAGTGTCCAGTATTTGTGTGTGTTTGTGTGCATTTCAGCATGTACACCCTCCCAGACCGAGAGCGCCTGACGCCGTCGCCTGCAGACTCCCCCCGAGCACAGCAGATGGTCCCGAACGCTCGATA[C/A]GCCGTCCAGCCGTTCCTGCAGGAGCAGTTCAGCAGTTTGACCCAGCGCTCAGTGACCCAGCCCAGCAGCGTGGAGGACCCGGCCCAGCGCTGGCTGATCTCACAGAACAGCAGTAAACTGGAGCTGACGGCGTACGAGGGCGAGTACTCCAGCTCTCTGCTGCCCTACAGCTTCAAGTCTCTCCCTCTGCAGAGCTACTATCCCGACACTGCCTTCAGCTGGGGGACCAGAGTCTCCGCCGGCTCCTCGTTCCCCAGAAAACTACCCTCCGGCCTGCCCTGGTCTCCCCGGCCCAGTCCCACAGACTTCAGTGAGGATCCGGAGAAAGCCAGAGAGGAGAACAGCCCGTTCTGCTGGATGGAGAAGCCGTCAGATGCCGCAGAGCCCAGCATTTACTCAGTGGTGTGCAGTAAGAGACGCCGGCTCTCAGGAGACGCTCCCCCTGGCAAGACTGAAGAGCAGAACTTTCACAAAGACTCTCCATCTGCAGCCAAAGCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22969
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008317 | Nonsense | 435 | 534 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 16 (position 58696318)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55028132 |
GRCz11 | 16 | 55181358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCCCTCTGCAGAGCTACTATCCCGACACTGCCTTCAGCTGGGGGACC[A/T]GAGTCTCCGCCGGCTCCTCGTTCCCCAGAAAACTACCCTCCGGCCTGCCC
Long Flanking Sequence:
GGTGGAGATATCAGCACATTAGGGCGTGGTCTATCAGTCCTTTAGGGAGGAGCTTGCAATCTTATTTTATTTTATCAGGTCTTGTCTTTTAACATTAGAATTGGCTCCAGTAGAATGAAATCATGCACTGCTCTACATTTGTTTTCAAGTGTCCAGTATTTGTGTGTGTTTGTGTGCATTTCAGCATGTACACCCTCCCAGACCGAGAGCGCCTGACGCCGTCGCCTGCAGACTCCCCCCGAGCACAGCAGATGGTCCCGAACGCTCGATACGCCGTCCAGCCGTTCCTGCAGGAGCAGTTCAGCAGTTTGACCCAGCGCTCAGTGACCCAGCCCAGCAGCGTGGAGGACCCGGCCCAGCGCTGGCTGATCTCACAGAACAGCAGTAAACTGGAGCTGACGGCGTACGAGGGCGAGTACTCCAGCTCTCTGCTGCCCTACAGCTTCAAGTCTCTCCCTCTGCAGAGCTACTATCCCGACACTGCCTTCAGCTGGGGGACC[A/T]GAGTCTCCGCCGGCTCCTCGTTCCCCAGAAAACTACCCTCCGGCCTGCCCTGGTCTCCCCGGCCCAGTCCCACAGACTTCAGTGAGGATCCGGAGAAAGCCAGAGAGGAGAACAGCCCGTTCTGCTGGATGGAGAAGCCGTCAGATGCCGCAGAGCCCAGCATTTACTCAGTGGTGTGCAGTAAGAGACGCCGGCTCTCAGGAGACGCTCCCCCTGGCAAGACTGAAGAGCAGAACTTTCACAAAGACTCTCCATCTGCAGCCAAAGCCATCGGCTACTACGCCTTCTACACCAGCAGCTAGAGGCAGTCGCTCGAGGTGTTTAAAGAGACAGGACACGCTAATGTGAAGCTTCTGTGTTTAAAGGCATAGTTCACACATGTTTAAATAGACAGGACATGCAGAAATACAGATTCTGTTCTTAAAGGGACAGTACGCGCAAAAAAGGACAGTTCACCCAAAAATGTAGAACAGCACACACAATAATGATGAGTCTGGTTT
Associated Phenotype:
Not determined