ZMP
zgc:100829
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC445149 [Source:RefSeq peptide;Acc:NP_001003543]
Human Orthologue:
SH2D2A
Human Description:
SH2 domain containing 2A [Source:HGNC Symbol;Acc:10821]
Mouse Orthologue:
Sh2d2a
Mouse Description:
SH2 domain protein 2A Gene [Source:MGI Symbol;Acc:MGI:1351596]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23961 | Nonsense | Available for shipment | Available now |
sa23962 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23961
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 |
---|---|---|---|---|---|
ENSDART00000014058 | Nonsense | 261 | 307 | 8 | 8 |
ENSDART00000137874 | None | None | 210 | None | 5 |
ENSDART00000145178 | None | None | 173 | None | 3 |
The following transcripts of ENSDARG00000015557 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 28187338)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 28756249 |
GRCz11 | 21 | 28792944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCTCAATGGATTTGGGGTCCGAGGTTGTTGAAGAGAGCTGTTTGGGA[C/T]GAGGAAGGGTTGCTCAGCTCATGAAAACCTTCAGCGTGTGCGGCGAGTCT
Long Flanking Sequence:
GGTGTCTGAGCAGCGTCTGTCTGCTCTCCGCCGCCATCCCTGCGGCCCTCCTCTCCTCATCTTCCATCCCTCCATCTCTCAATTACACACACATACACACAGTGTAACCACACACACTCTTACGCACCCATAACCGTGTACACACACACTCACCAACTACACCCAGCTGCGTCCCTGCTCTACTTCCTGCGCCGACGACCTCCGGTCTGGCAGTCAGCAGCCCAGGAAAAAAACACACTGAATGAGAGCAGAGAAAGAAAAAAAAAGGATAGAACAGAGTGCGAAGTGAGGGAAAAGGGCAGAAGAAAGGTGTGGTGTTGAAGAGGGCAAGTGTGAGAGTGTTTTGAAGTTGTCATCTATAAAAACACACTTTGAAGGTCATAATCTCTTGTCTCTCCATTCTCTTCGGGTTTGCAGGTGATATCCGAGTGGTTGCCGCCTCTAAACGGGTGTTCTCAATGGATTTGGGGTCCGAGGTTGTTGAAGAGAGCTGTTTGGGA[C/T]GAGGAAGGGTTGCTCAGCTCATGAAAACCTTCAGCGTGTGCGGCGAGTCTCCACCCTGTCAGTCTCCGCCCCGTGCCAATAAACCTCCAATCCCGGAAAAACCGAACCACTTGAGGCTCCGCCCCTCACCCTCTCTCAGGTAATCCACATGGGACAAACCCCTGAGCAACAATCAAGACAACTAAAACAGGGGTCTTTATCAGCGGCTACAATGAAGGGTGTGGGTGCTCGGCCTTTCTCAGGAACTTGAATATTTAGTTGCCAAAGTTATGCTTTTTATTTTTGCAATATTGATGTTTTTCTTCATTATTTGTATTTTTATATGGTATGAGAGGTTTGCAAAACTTTTCAGCAGGAATGACACACTCGATATTTTGTTACATCGCTCCAATTGTTGACCTGTCTAGCTCATAATGCACTCAGACTCATACTTACAAGTGTGTTTCTGTTTTAAAGGGTCACATGATATCTTACTCAGATTGAGAACTCGTAATGAGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23962
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 |
---|---|---|---|---|---|
ENSDART00000014058 | Nonsense | 288 | 307 | 8 | 8 |
ENSDART00000137874 | None | None | 210 | None | 5 |
ENSDART00000145178 | None | None | 173 | None | 3 |
The following transcripts of ENSDARG00000015557 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 28187419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 28756330 |
GRCz11 | 21 | 28793025 |
KASP Assay ID:
2261-5756.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCGTGTGCGGCGAGTCTCCACCCTGTCAGTCTCCGCCCCGTGCCAAT[A/T]AACCTCCAATCCCGGAAAAACCGAACCACTTGAGGCTCCGCCCCTCACCC
Long Flanking Sequence:
ATTACACACACATACACACAGTGTAACCACACACACTCTTACGCACCCATAACCGTGTACACACACACTCACCAACTACACCCAGCTGCGTCCCTGCTCTACTTCCTGCGCCGACGACCTCCGGTCTGGCAGTCAGCAGCCCAGGAAAAAAACACACTGAATGAGAGCAGAGAAAGAAAAAAAAAGGATAGAACAGAGTGCGAAGTGAGGGAAAAGGGCAGAAGAAAGGTGTGGTGTTGAAGAGGGCAAGTGTGAGAGTGTTTTGAAGTTGTCATCTATAAAAACACACTTTGAAGGTCATAATCTCTTGTCTCTCCATTCTCTTCGGGTTTGCAGGTGATATCCGAGTGGTTGCCGCCTCTAAACGGGTGTTCTCAATGGATTTGGGGTCCGAGGTTGTTGAAGAGAGCTGTTTGGGACGAGGAAGGGTTGCTCAGCTCATGAAAACCTTCAGCGTGTGCGGCGAGTCTCCACCCTGTCAGTCTCCGCCCCGTGCCAAT[A/T]AACCTCCAATCCCGGAAAAACCGAACCACTTGAGGCTCCGCCCCTCACCCTCTCTCAGGTAATCCACATGGGACAAACCCCTGAGCAACAATCAAGACAACTAAAACAGGGGTCTTTATCAGCGGCTACAATGAAGGGTGTGGGTGCTCGGCCTTTCTCAGGAACTTGAATATTTAGTTGCCAAAGTTATGCTTTTTATTTTTGCAATATTGATGTTTTTCTTCATTATTTGTATTTTTATATGGTATGAGAGGTTTGCAAAACTTTTCAGCAGGAATGACACACTCGATATTTTGTTACATCGCTCCAATTGTTGACCTGTCTAGCTCATAATGCACTCAGACTCATACTTACAAGTGTGTTTCTGTTTTAAAGGGTCACATGATATCTTACTCAGATTGAGAACTCGTAATGAGACCAAATCATGATCGTAATCCAAAGTTAATCATCCCATTGGTTTGTTATGTATTAAATATGTTGCTTCCTTGAAGTATTGAAGG
Associated Phenotype:
Not determined