ZMP
zgc:56062
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC406321 [Source:RefSeq peptide;Acc:NP_998213]
Human Orthologue:
SRFBP1
Human Description:
serum response factor binding protein 1 [Source:HGNC Symbol;Acc:26333]
Mouse Orthologue:
Srfbp1
Mouse Description:
serum response factor binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1914472]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44918 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39250 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29224 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44918
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 |
---|---|---|---|---|---|
ENSDART00000112167 | Nonsense | 46 | 772 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 29784841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 29714863 |
GRCz11 | 19 | 29302086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCGTCAAATCTCAGCCCTGCAGAAGAAGAAAGGAAATGAGGCGAGCT[T/A]GGAGAAAAATGGCAGGCGAGCAGCGAGACTTCGAGAGGAGATCCGAGAAC
Long Flanking Sequence:
CATTTGTGACTTAAACAATTTATTTAATTATTTTTGTTATTCAGTTACTGTACTTGAATACATTTAGACTCGATTTGAAAAAAACCCCCACTTAATTTCAATTGTATTTTTTTCTTAATTGTATTTATAGATTGTTATGCATGAATATACTTAACTCATGCTAATACAGAAATGCACTGCAAATAGCACAGATCACATCGAACATATTTCGGGGTACCCCAAAAAGTTTATAGTTTGTTTAATAGATTTTATGGAGATGAAGCATCATCCCAATCCATCTTACATTATAAATTTATTTCCAAATAGAGATATTAAGTTATCTGATGAAATTGTATTCATATCAGCTTTCAGGAAGAACATAAAGATGCCTGCGGCACTTAACCTCAGCAATGAGGTGGTCAAGATGAGGGCGGAGGTTAAAAGAATAAAGGTGTTCCTCATCAGGAAACTCAGCCGTCAAATCTCAGCCCTGCAGAAGAAGAAAGGAAATGAGGCGAGCT[T/A]GGAGAAAAATGGCAGGCGAGCAGCGAGACTTCGAGAGGAGATCCGAGAACTGAAAGCTGTGGTGCCAGACAGTGTAACCAAGGCTGCCCTACAGAAAGACATTAGCTTTGAGAAAGTGTGCCGTGACAAAGAGGCAAGCCTAACTGACCGTGCCACTGCCCGCATCGCCACACATCCTGAGTTCAGCAAGAAGATCCAGAGCTTAAAAGCAGCCATCAAAGCTTTCAAAGAAGAAAGAATGAATGCGAGAAAAGCGGAAAAACAAGCAAAAGGCAGTGCAGAAAGTGACAGTTCACAGGACACCGATGAAGAGGATGATGATGGTTCAGAGAGATCAAACAACAGAGATGATGAAGATGGACTGAAAGAGGATGAGTATGACAAAAAGACAGATGAATTGATTGATAGCTCCTCACAGGAGACATTGAATAAACAGACTAACCAGTGTCAGGAGGAAGAAAGGTTGGATGAAGAGGTAAGTGTACTTCAAATGGAGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39250
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 |
---|---|---|---|---|---|
ENSDART00000112167 | Nonsense | 255 | 772 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 29781713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 29711735 |
GRCz11 | 19 | 29298958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTTTTCTAAAGAAGAAGAAAGGTGAGGAATATGAGGTGAAGGAAAGC[C/T]AAGAGAGAGCAGCAGTTCTTCTGAAAGAAATCCAGGCTTTAAGGAGCCTT
Long Flanking Sequence:
TTTTTTCCATCCACAATAATTTTTACTTTTGTTTCACTGAATGATAGATTAGTCTTTGAAAGATGATGTGTAAATACTGTTTTTTTATTCATTCAAAGGCACTGTAAGGGTGCTTTCACACCTGTTTCAATTACTTGATTCGTACACCCATGCCACCTTCTCGGCTGGTTTGTGTTCACACTGTCTTTTTTCTTTCTGAACCACAGTACGCTTGCATCATCAAGCTGCTGTTGTGTGTACAGCCATTGCTAGGTAACGGCCATGAAAGCCAGTGCGCCAAAATGGAAGGACGTACATACATCATGGTCATTCTGCTTTTACTGAATCTTTTTCTTTTACACATCTTACAGGGATCATCTGAAGCAGTGAGCATCTCAGAAGAGGTGATCAGGATGAGGAAGGAGGTAAAGAGGACGAGGGTGGCGATCATTAGTAAACTGGCTGAAGAAGTTGCTTTTCTAAAGAAGAAGAAAGGTGAGGAATATGAGGTGAAGGAAAGC[C/T]AAGAGAGAGCAGCAGTTCTTCTGAAAGAAATCCAGGCTTTAAGGAGCCTTAAACCAGATCAGGTGACCATGACAGCACTTCAGGAGAACATGGAGCTGGAGAAGATTTTGCTGGACAACGAGGCAAGCCCAATTGACAGAGCCATCGCACATATTGCAACACATTCCCGCTTCATCAACAAGCTTCAGAAGATCAAAGAAGAAAAGATTAAGGCTGCTGAAGCTGAGAAGAAAAAGACTGACAAACCGGACACGGTGCAGTCCAAGAATGAAGATGAGGAACTGGAAGAGGAAGATGAGGAGGAGGTAGATGATGATGATAATGATGATGATGATGACGATGACGACAGCAGTGATGAAAGTGAAGAGAATTGTGATAAAGTAGGTGAAAAGTCAAATCGTGTTTTCAATCAGATTGATAAATCAGGTGTTGTGGAACCAGATACAAGTGCAGAACCTGATACTTTTGAAATGCCACAATCCAAAACTGATGTCATGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29224
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 |
---|---|---|---|---|---|
ENSDART00000112167 | Nonsense | 354 | 772 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 29781416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 29711438 |
GRCz11 | 19 | 29298661 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGACACGGTGCAGTCCAAGAATGAAGATGAGGAACTGGAAGAGGAAGAT[G/T]AGGAGGAGGTAGATGATGATGATAATGATGATGATGATGACGATGACGAC
Long Flanking Sequence:
ACATCATGGTCATTCTGCTTTTACTGAATCTTTTTCTTTTACACATCTTACAGGGATCATCTGAAGCAGTGAGCATCTCAGAAGAGGTGATCAGGATGAGGAAGGAGGTAAAGAGGACGAGGGTGGCGATCATTAGTAAACTGGCTGAAGAAGTTGCTTTTCTAAAGAAGAAGAAAGGTGAGGAATATGAGGTGAAGGAAAGCCAAGAGAGAGCAGCAGTTCTTCTGAAAGAAATCCAGGCTTTAAGGAGCCTTAAACCAGATCAGGTGACCATGACAGCACTTCAGGAGAACATGGAGCTGGAGAAGATTTTGCTGGACAACGAGGCAAGCCCAATTGACAGAGCCATCGCACATATTGCAACACATTCCCGCTTCATCAACAAGCTTCAGAAGATCAAAGAAGAAAAGATTAAGGCTGCTGAAGCTGAGAAGAAAAAGACTGACAAACCGGACACGGTGCAGTCCAAGAATGAAGATGAGGAACTGGAAGAGGAAGAT[G/T]AGGAGGAGGTAGATGATGATGATAATGATGATGATGATGACGATGACGACAGCAGTGATGAAAGTGAAGAGAATTGTGATAAAGTAGGTGAAAAGTCAAATCGTGTTTTCAATCAGATTGATAAATCAGGTGTTGTGGAACCAGATACAAGTGCAGAACCTGATACTTTTGAAATGCCACAATCCAAAACTGATGTCATGGCTCCAAATGACCAAAACTTCTCTTCAACTGCTTCAAATGTTCAAAGATCTGAAAAATCCTTAACAGCTTCACATGTCCAAAGGTCTCCTAAAAAGTCTTCAACTGGTTCAAATGTTAAAAAATCTCCTGAAAAGACCTCAACTAGCATTGTCCAAAATTCTCCTAAAAAGTCCTCATTTGCTCCAAATGTTCAAATATCTCCTAAAAAGTTCTCAACTACTAGCAATATCCAAAGTTCTTCTAAAAAATCATTGACTGTGAGCAATACAGAATTTAAGAACTTTGGTAAAGCAGACAAA
Associated Phenotype:
Not determined