ZMP
zgc:56186
Ensembl ID:
ZFIN IDs:
Description:
Zgc:56186 [Source:UniProtKB/TrEMBL;Acc:Q7ZUT2]
Human Orthologue:
SH2D4A
Human Description:
SH2 domain containing 4A [Source:HGNC Symbol;Acc:26102]
Mouse Orthologue:
Sh2d4a
Mouse Description:
SH2 domain containing 4A Gene [Source:MGI Symbol;Acc:MGI:1919531]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34834 | Nonsense | Available for shipment | Available now |
sa6159 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41587 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34834
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 |
---|---|---|---|---|---|
ENSDART00000060663 | Nonsense | 146 | 198 | 3 | 4 |
ENSDART00000123312 | Nonsense | 146 | 433 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 6635520)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 7011990 |
GRCz11 | 10 | 6970690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCGGAGCAGGTTGTATTGTCAGATCAGGAAGTCCAGCAGAAAGCCAAA[C/T]AGGCTGAGGCTCTTCAACAGAGAAAAGCAGAGGAGGAACTCAAGGTACTG
Long Flanking Sequence:
AAGTAAAGCTGAAGAGGCTTCTGTTTACAGTAATAAGGGGATTCAAGTAGAAACCTTTTGTTATCATGTCACAGCCACAATAATACCATAAAATATGGGCCCAAGTCCAAATTGATATTTGGCTTAGTTTCATATAATGGAAAATAGGTGAAGAAACCTGTTTGTCTTGGAAAACCTTCCACAAACCATACTAGACAGACAGTAAGAAAAAGGAATTTCTTTTGTGCTGTATGTGAGTATGCAAATGTGAAGGAATTTACCTGGCGTGTACATAGAATGTTCTCACTGACCTTCATGGCCTCTTTTCATAGCAGCATTTTTCTGTTCTGTGAGTAGTCAGCTACCTCTCATAACCTATGCATATGTGGTTTCTATGTTGTTTTCTCTTACAATTGCCAAGGGTTAAGAAAGCAGCAGAGCTGGAGAAGCGTTTCTCTGGAATATATCTTGAACCGGAGCAGGTTGTATTGTCAGATCAGGAAGTCCAGCAGAAAGCCAAA[C/T]AGGCTGAGGCTCTTCAACAGAGAAAAGCAGAGGAGGAACTCAAGGTACTGCTGACTCACACCTATGACAAACAGTAACAATCAGTAGCTGTCAATTGATATTGTTTTTTAACCTCATTAATTTCAGAATGTGATGAATAATTAGAGGCACATTCATTGTAATTTGCATTATTAATAACTTAAATGTAATTTGACCCCCCCAAGAGGGCATGGAATCATGGGAGTTGTGGTCATCCTACTGGACTTTTTTTTTGAGTATTTTAACGAAGTTATTTGACATATTATGCCTTTAGTCTTATTAAATTAGTCCCTAAAGATTACTTAAATATGGTACATAAAATTATCAAGCGGATATTTACAAAAAGCTTCTTTTAGAATGTTTTCAATACAATTTATTAAAGGGGTGGTCCACTATGATATTATATTTTAAACTTTAGTTGATGTGTAATGTAGCTGTGTAAACATAAACAGCATCTGTGAATGTTAAAAGCTCAAAGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6159
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060663 | Nonsense | 179 | 198 | 4 | 4 |
ENSDART00000123312 | Nonsense | 192 | 433 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 6632164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 7008652 |
GRCz11 | 10 | 6967352 |
KASP Assay ID:
554-4397.1 (used for ordering genotyping assays)
KASP Sequence:
TGGAGCAGGAGGAGAGGCGTAAGGCTGAGGAGGAGCTGAGGAGGCTGGAG[C/T]AGGAGAGRAAACAGCAGATTTACCAGTGCCTAAAGGAGGTGCAGAGCAGC
Long Flanking Sequence:
TCAAAGTTGGTCATGGGCATCCAGGGTATGCATCAGTGCACAGTGCTCATGAATGTGGTGCACACCCTGTACTCACACTGAGGAGAGAAACTGTTGAATAAAGACATTATTCCTGTTTTATATGAGCACAATTGACATGATAGGATTTTGAATGAACCACTGCAGGTGTGTGGTCTGTTTCGAGGATGCTTTTGGTTCCTTTCTGCTCGAGTCAAAACCATTGTTGTGTATGGAGTTTGAGGGAGCTTTCACATTTCACCTGAAATACCTTAAATTGTATTCTAAAGATTAATAAAGGTGTCAGGGGGTTTTAGTAATTAATAACTGAATTTATATTTTGTGTAAACTAATACTTTACTTATTGCAGGGGCTTTTTTTGTTACCCTTTGTTCCCTTTTTCTCCTTTTAAGTTTATTTGTGGTCTCTGGATGCTTGTTTTTGCTCAGAAAATGGAGCAGGAGGAGAGGCGTAAGGCTGAGGAGGAGCTGAGGAGGCTGGAG[C/T]AGGAGAGGAAACAGCAGATTTACCAGTGCCTAAAGGAGGTGCAGAGCAGCAAAAACACACTAGAGGAGGAGGATAAGGACTGGAAGGAGACATGTAAGACAAACCTCATCAGTGCTGAACACTACACCTTATTTTCTTATGAGTTTATTATTTATTGTTATATTTTAACTTGTATTTGTTACATGTACTACTCATTTAGGATCTGCATTACTGTACTGGACATTCAGGTGGATCTCTGAATAATCCATTAGTTGACTTTATTTGTAGAAAGTGATTAAAACCCCTTAACTGCAACCCCCACTTTTTGAACATAGACATGAAAATGGCATGTTCAACTTCATAGACCTCAAATTCCGGGAGGGCCACAGCTCTGCACAGTTTTGCTCCAACCCTAATTAAGCACAGCTGATCCAACGAGTCAAAGTTGTCAAGATCACTAGACATTATTAGATCAGCTATCTTTGATTAGGGTTGGAGCAAAACTGTGCAAAGCTGCGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41587
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 |
---|---|---|---|---|---|
ENSDART00000060663 | None | None | 198 | None | 4 |
ENSDART00000123312 | Nonsense | 400 | 433 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 10 (position 6620644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 6997132 |
GRCz11 | 10 | 6955832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTGGGAGACCAGATCAAATTCAGCTCCCTCAGTGAACTAGTGGAGTA[T/A]CATCAGGTAATGTGCTGTACCAACGCAATCTCACGGCAACTCGTAACTTT
Long Flanking Sequence:
CAGTAATGATTTTAAATCACACTGAACTGAGCTGAACTGAACTGAACTTAAACACTAAAAACTGAACTACACTGTTCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGAGACAATCCACATTGTAAAAGCGCTCACCAGGGCACCCAGGGCTCAAATAATAGATTCTTCAAATTTTGTAGACCCTTCCTGTCTTTCCAAACAGAGCTATTGAATTAGTCTATATCAAGTTAATACAGTATATAGAGATTTCCTACAACCGATAACATGATCTGATTTTATCTACAGGTATAATCTCCCGTGAGCAGGCAGAGGAACTGCTGAGCGGTGGTGAGCCCGGGCTTTTCCTGGTCCGCGTCAGTGAGAGGATCTTTGGATATGTGCTTTCCTACCGATTCAAGGATGGAATCAAACACCTGCTGATTGACTCCTCGGAGAACTGCTACATGCTGCTGGGAGACCAGATCAAATTCAGCTCCCTCAGTGAACTAGTGGAGTA[T/A]CATCAGGTAATGTGCTGTACCAACGCAATCTCACGGCAACTCGTAACTTTTTGATTTAGCGGCTAATTCGAATGAATTTGTACGATTACACTCGTACAGTTTACAGACCCCCTAGTTTTTGGGAATTTTTTTATTTTTTTATTTTTTGGTGATTTTTCATGATAAAAATGACTGATTTTGTGGCGGAAATTTGCGGACAGTTTTGTGACTTAAAATATATATACATACATGTGAAAAAGTATATACATATAATCTATTTACCAATATTTACCATATTGGGTAGCCTGCTATGATAGGCGTGCAATCTGACACAATAACAAGGACAGGGGCGCCTGCAGGATTTTATTCGAAGGTACTCACAAATCCAGCACTGCCCCGCCCCGTCCCCTTCCCCTTACCCCAATCATATCAAGAAACACTGATGCTTACTGTCAAAGGCTACATTAAGGATATTCGTTATGACATTTATTTGTTTCTTTTTGTCATTTATTTGTTTCCTT
Associated Phenotype:
Not determined