ZMP
sh2d3cb
Ensembl ID:
ZFIN ID:
Description:
SH2 domain containing 3Cb [Source:RefSeq peptide;Acc:NP_957370]
Human Orthologue:
SH2D3C
Human Description:
SH2 domain containing 3C [Source:HGNC Symbol;Acc:16884]
Mouse Orthologue:
Sh2d3c
Mouse Description:
SH2 domain containing 3C Gene [Source:MGI Symbol;Acc:MGI:1351631]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa26608 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa20572 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26608
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000003444 | Essential Splice Site | 514 | 635 | 10 | 11 |
| ENSDART00000142134 | None | None | 140 | None | 4 |
| ENSDART00000143500 | None | None | 232 | None | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 67642475)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 64444116 |
| GRCz11 | 5 | 65133113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCGCTTTAAATACTGTGTGCCAAGCAAGTAACAACTCTCTTTTTTTC[A/T]GCGATAAGCAGGCACACAGAGACAACGTTCCCCCATGTGCTCCCCCTGCT
Long Flanking Sequence:
GCAGAAATCATATCTCAAAGCATTTACTGAGGCACTGGCAATTCTTACTGGGGCACGTGCCCCAGTAAATGGGGTCTAGCGACGCCCCTGCTACTGACTATGGCCATTCAAGTAATTTAATTAATAGAATTGTAAATGCGTGAATAAAAATAGCTATTTAAAAAGTCCTAACAAAACATTTGTTTTTCAGATTGCTCGTTTGAATGAGAGCTGGACGATCTTACGTCAGAAGTACACAGAAAGTGCTATTCTTTATGAGAAAACTCTTAGACCCTCATTGAGGATGATGAACGATGGAGAAGGTATTCATTCAACATGTATTAATCTGCAGTGTTTCTTAATAAATATATATTCAGAAATACTGTGAAAAATTACCCACTCTGTTAAAAATCATTTGGGAAATACTCAAAAAAGAAAAGGGAGGGCTAATGATGATGACTTCAACTCTATACTGCGCTTTAAATACTGTGTGCCAAGCAAGTAACAACTCTCTTTTTTTC[A/T]GCGATAAGCAGGCACACAGAGACAACGTTCCCCCATGTGCTCCCCCTGCTGTCTCTGTTTGAAAGGACCGTCGAGGAGTTGGAGTCATGGGAAAGTGCAGACACTGGAGTGGCGCTGGTTTTGAGCCATCTGGATGCTGCACGTACCATCGCGTTAAATGGGAGGATCTTCAGTGCTAATGCAGAGGCCAAGCTGCAGGGTAATGGCTTCATAATCTAAACAGTTTATAATGCTTACAGATTCTCCCAGTGTTGGCGTGGGTTTCCTCCGGGTGCTCCGGTTTTCCCCACAGTCCAAAGACATGCAGATTAGGTGAACTGGATGAACTAAATTGGCTGGAGTGTGTGTGTGTAAATGAGAGTGTATGGGTGTTTCCGAGTACTGGGTTGCGGCTGGAAAGGCATCCGCTGCTTAAAACATATTCTGGAATAGTTGGTGGTTCATTCCGCTGTGGCAACCCTTGATTAATAATGGACTAAGCTGCAGGAAAATTAATGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20572
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 |
|---|---|---|---|---|---|
| ENSDART00000003444 | Nonsense | 629 | 635 | 11 | 11 |
| ENSDART00000142134 | None | None | 140 | None | 4 |
| ENSDART00000143500 | None | None | 232 | None | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 67633965)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 64435606 |
| GRCz11 | 5 | 65124603 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGTTACTCCAAGTTTGATGAAGTGCTGACAGCTCTGTCTAACAGACTC[G/T]AGCTTTCACACTCTGCAAAATGAAGGGATGAACTCTATTCACTTTTATTT
Long Flanking Sequence:
GGCATGTTTGTGGGTGTGTGTGTGTGTCTGGGTTTCTGCGTCAGAGGGCGGGGCCTCAGGTTTGAAATCTCCCGGGTTTGCGCGTGCACGTGAAAACCTTGGTTTCGTTCGTACGTCATGGCGAAACACCTAATGACTTGGTATCAAGGCGACTCTATTGAAGCACTTTGAGTTGACTCTTTTAAAGATGAATCAACCGTTTTAAACACTGTACTCTTACAGATTTAAGCCTTAGCTGGATACTTCACTTCACTTAGAGCTGTGTTACACACTACATGGAGGGGAATTTTCAAAAACCCATAATATGGGCTCTTTAAAAGTTGTGTTTTAGGTCATCTTTTTCTGATTTTGCAGGATTTGAGGAGGAAGCAGATGTGCGGGAGATCTTCCTGACAGAGTTCCAGATGCGTCTCCTGTGGGGAAGCCGTGGAGTGGAAAGAAACAAAGATGAGCGTTACTCCAAGTTTGATGAAGTGCTGACAGCTCTGTCTAACAGACTC[G/T]AGCTTTCACACTCTGCAAAATGAAGGGATGAACTCTATTCACTTTTATTTGTTAATATACTGTGTTATGAATTTCTGTACTGTTATTTTTCCATTGGACATATTTCTGCTGTTGTATGTAAAATGAGCACCTTGTGTATTTCAATTTTAACTTATTTGACTTTTTTCTGATTATTTGCCCGTTTGTATAGCTACATGATTTTATACAGTGTACATAAAATTCATACTCATAGTTATATTTTCTGAAACTGTTAAACATGCTAATATTGTAAGTTTTTAACTATTTAATTGCACTGCTATTGGTTCATATAATCAATAGTCAAATAATGGGTAATATTTACTCGGAGGAACACTTTTTTAATGCATTTAATGCTAATATTCTATACTTATACATCACTTAAAGTAATAATAAAAATGCAGATTTGGTTGGTTGGTATATTGTGGTGTGTGTCCAAGTGAAATATTTGTTTATCTGATTTACTGCCTTTTACTGTTTTGAAA
Associated Phenotype:
Not determined