ZMP
srf
Ensembl ID:
ZFIN ID:
Description:
serum response factor [Source:RefSeq peptide;Acc:NP_001103996]
Human Orthologue:
SRF
Human Description:
serum response factor (c-fos serum response element-binding transcription factor) [Source:HGNC Symbo
Mouse Orthologue:
Srf
Mouse Description:
serum response factor Gene [Source:MGI Symbol;Acc:MGI:106658]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24211 | Nonsense | Available for shipment | Available now |
sa3160 | Nonsense | F2 line generated | Not yet available |
sa5694 | Nonsense | F2 line generated | Not yet available |
sa11724 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24211
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 |
---|---|---|---|---|---|
ENSDART00000076035 | Nonsense | 107 | 520 | 2 | 9 |
ENSDART00000076040 | Nonsense | 126 | 539 | 1 | 8 |
The following transcripts of ENSDARG00000053918 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 37975257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 35113975 |
GRCz11 | 22 | 35089724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTGGCCGGAGCGAAGCCCGGCAAGAAAACGCGAGGACGGGTGAAAATT[A/T]AGATGGAGTTTATTGACAACAAGCTGAGGAGATACACGACCTTCAGCAAG
Long Flanking Sequence:
GTTTCTTAGCCTAGCATATGTGAGGTAAGTTCGGTTTTGGGTCTGGATTTGATCTGGGATCTGCTGCACAGATCGCTAACTTTACACCCACCGCAGACCGCCGTAGTGCCGCTTGCAGGTCAGCGATGTTAGGGGGCAACGGGACGGCCAGAGGGGCTGGACGCTCTGGTAATGGCACGGGATTGACACCTCTACAGGTGGGCAGCACATCTGGGGCTCTGGGGGCTGTAAACTCTGTCATAAACCTGCCCGATGGGGGCAGATACGACGACGGGCCGTCGGTCGAGGCTGTGCTGAGCGGCTCCGATGGAGACTCAGACTCCGGGGACGATGAAGAGAGCCCTGTGCCGGACAGGAGAGGGGTGAAGCGGGAGAGGAGCGAGCTGGAGGTCGGGGGATCTTCTGGATCTAACGCCGCACTCTCGGCAGGATACGGAGGGGTCTCCAGCGGGGTGGCCGGAGCGAAGCCCGGCAAGAAAACGCGAGGACGGGTGAAAATT[A/T]AGATGGAGTTTATTGACAACAAGCTGAGGAGATACACGACCTTCAGCAAGAGAAAGACTGGCATCATGAAGAAGGTATGTTCATGTGTCTTCTGCTGTTAGTCTGGAACTGATTGTACCACTGCTGTTCTACTGCTGTACTGATGCTAGTTTTACACCAGTGCTAAACCTCTATGCTAATATTAGCACTACAACTACTAGTAGTGCCATGCCAATACGTTCTTCAGTAACTGGTACTCTAGTAAACTTTAGTATTTACCTCATTGTGCTTTGATTAATTCTGTATAAATAATAGTACCACTAACATTACTATATTCAGGATTCCCACTGGTCATGCAATTGTAAAAGCTCTATCCCACATCCTGAAAGTCAGGGAATTGTATACATTTTTGGTATTACTTTAGGTTATCACATATTTATAATTATGACATTGGTTGTTTTTTAGTAGTTATAAAGTATCGTTTTATTCAACATCCTTAAACCTACCAATACCTAAACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3160
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000076035 | Nonsense | 212 | 520 | 3 | 9 |
ENSDART00000076040 | Nonsense | 231 | 539 | 2 | 8 |
ENSDART00000076035 | Nonsense | 212 | 520 | 3 | 9 |
ENSDART00000076040 | Nonsense | 231 | 539 | 2 | 8 |
The following transcripts of ENSDARG00000053918 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 37987269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 35125987 |
GRCz11 | 22 | 35101736 |
KASP Assay ID:
554-2634.1 (used for ordering genotyping assays)
KASP Sequence:
GCATGAGTGCCACGGGATTCGAGGAGACYGACCTCACCTACCAGGTCTCA[G/T]AGGCTGATGGCCTCACAGAGCCAAAGGTACCTGCCTTCTACTTRAATGCC
Long Flanking Sequence:
ACAGAAAAACACAATATTTTATTCTATATTGTGCCGCTGTACTTCTTTAACCACAAGTATCCTCTGCACTGTAGGATTCTATTTTTATATTCTTCTCAACATTTGTGACTGTTTTAGTCTTTATTTTATATTCAAGTATCCTTACGGTTACAAGGAATGAGTTTGCAGTAGCTTATCAATCTTGTGCCTCTTTCGAAGGAAACCCCAACTAGTCTATAAAAGCTGTCATCGATATCTCTCTCTCTTCTCAATGTTTCCAGGCCTACGAACTCTCTACGCTGACAGGGACACAAGTTTTACTCTTGGTTGCCAGTGAAACGGGCCACGTCTACACATTTGCCACGCGGAAACTTCAACCCATGATCACCAGTGAGACGGGTAAAGCCCTGATCCAGACTTGCCTGAATTCCCCCGATTCTCCACCCCGTACGGACCCTTCAACAGACCAGCGCATGAGTGCCACGGGATTCGAGGAGACCGACCTCACCTACCAGGTCTCA[G/T]AGGCTGATGGCCTCACAGAGCCAAAGGTACCTGCCTTCTACTTGAATGCCTAGATCGTAGCTCTCAAACTTAAATCCTGGACGGCCAAAGCTCTGCACATTTTTTCTCCAACCCTAATCAAACACAGCTTATGCAACTAATCGAGGTGTTTAAGACTCTTTTGAACGCCTCCATTAGTTGGATCAGCTGTGTTTAATTAGGGTTGGAGTAAGACTGTGCAGAGCTTTGGCCGTCCAGGAATTAAGTTTGAGATGCTTGGTTTAGATAAGGGGTGTCCAAACTGGGTCCTGGAGGGACGGTGTCCTGCCGATTTTTAGCTTCATCCTTACAGGTGTGTTAAGGCAAGTTGTTTTTAGAAAGCCTAGTTAGAGCTTGATTAGCTAGTCCAGGTGTGTCTGATTAGGGTTGGAACTAAACTTTGGATCGAATTTGGACACTCCTGGCTTAGATGGTCTTGAGTAATCCTGATATGATTGTTACTTTAGGGTAGAGCTGCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5694
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000076035 | Nonsense | 212 | 520 | 3 | 9 |
ENSDART00000076040 | Nonsense | 231 | 539 | 2 | 8 |
ENSDART00000076035 | Nonsense | 212 | 520 | 3 | 9 |
ENSDART00000076040 | Nonsense | 231 | 539 | 2 | 8 |
The following transcripts of ENSDARG00000053918 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 37987269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 35125987 |
GRCz11 | 22 | 35101736 |
KASP Assay ID:
554-2634.1 (used for ordering genotyping assays)
KASP Sequence:
GCATGAGTGCCACGGGATTCGAGGAGACYGACCTCACCTACCAGGTCTCA[G/T]AGGCTGATGGCCTCACAGAGCCAAAGGTACCTGCCTTCTACTTRAATGCC
Long Flanking Sequence:
ACAGAAAAACACAATATTTTATTCTATATTGTGCCGCTGTACTTCTTTAACCACAAGTATCCTCTGCACTGTAGGATTCTATTTTTATATTCTTCTCAACATTTGTGACTGTTTTAGTCTTTATTTTATATTCAAGTATCCTTACGGTTACAAGGAATGAGTTTGCAGTAGCTTATCAATCTTGTGCCTCTTTCGAAGGAAACCCCAACTAGTCTATAAAAGCTGTCATCGATATCTCTCTCTCTTCTCAATGTTTCCAGGCCTACGAACTCTCTACGCTGACAGGGACACAAGTTTTACTCTTGGTTGCCAGTGAAACGGGCCACGTCTACACATTTGCCACGCGGAAACTTCAACCCATGATCACCAGTGAGACGGGTAAAGCCCTGATCCAGACTTGCCTGAATTCCCCCGATTCTCCACCCCGTACGGACCCTTCAACAGACCAGCGCATGAGTGCCACGGGATTCGAGGAGACCGACCTCACCTACCAGGTCTCA[G/T]AGGCTGATGGCCTCACAGAGCCAAAGGTACCTGCCTTCTACTTGAATGCCTAGATCGTAGCTCTCAAACTTAAATCCTGGACGGCCAAAGCTCTGCACATTTTTTCTCCAACCCTAATCAAACACAGCTTATGCAACTAATCGAGGTGTTTAAGACTCTTTTGAACGCCTCCATTAGTTGGATCAGCTGTGTTTAATTAGGGTTGGAGTAAGACTGTGCAGAGCTTTGGCCGTCCAGGAATTAAGTTTGAGATGCTTGGTTTAGATAAGGGGTGTCCAAACTGGGTCCTGGAGGGACGGTGTCCTGCCGATTTTTAGCTTCATCCTTACAGGTGTGTTAAGGCAAGTTGTTTTTAGAAAGCCTAGTTAGAGCTTGATTAGCTAGTCCAGGTGTGTCTGATTAGGGTTGGAACTAAACTTTGGATCGAATTTGGACACTCCTGGCTTAGATGGTCTTGAGTAATCCTGATATGATTGTTACTTTAGGGTAGAGCTGCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11724
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 |
---|---|---|---|---|---|
ENSDART00000076035 | Nonsense | 334 | 520 | 5 | 9 |
ENSDART00000076040 | Nonsense | 353 | 539 | 4 | 8 |
The following transcripts of ENSDARG00000053918 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 38002208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 35140926 |
GRCz11 | 22 | 35116675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACACACACTGTTCCTCKCAGTCAGCTGCAGACACACTCTCTGGCCATA[C/T]AGTGTCCACAGACGCAGGCCAACAGCAGCGGCAGSACYGCTGTCCCCGCA
Long Flanking Sequence:
ATGTTTAATGTTAGTAAATTGCAGCTGTTCACGTTATTCATGTTTACAAAATGTAAACATGTTTATTCATGATACTACTGTGGTAACATAAATATGTTGGCAGAAATTTAGCTCCCATTAGCATCATGCCAGCTAAATGTTAAACATTTGAAAAATGCTAGCAACATGTTTATTAATTAATGTTAGCAAGCATACTGTTATGAAAAATGTTATTTAATCAGGACGTGTTGCCATCATGTCAAAATCATTAATAATCAATATGATCGATAGTTCATGCCAGCTAAATGTTAAATGTTAGCAACATGTTTATCAATTGATGTTAGCAACATGCTAATTCACGTTAACAACATGCTAAAAACAGTCAGTCATGTGAGCATTAGCTAAACCATGTCAGTATTGGTGTGAGTAGGCCTGTCGCTGTGTGTCCCGCAGGCGCTTCTCTTCCGCCGGGCACACACACTGTTCCTCTCAGTCAGCTGCAGACACACTCTCTGGCCATA[C/T]AGTGTCCACAGACGCAGGCCAACAGCAGCGGCAGCACTGCTGTCCCCGCACACACACAACCCGCCGCGCTCTTCCGCCTGCCAGCCGCCGTCTCACTCACAGGTCAGTGCTGGACGATCTGCATGCTCAAGTTTTCTCTCTTTGTGTAAACTAACTAGGCCTGAACGCTTAATTGCATTTACAGCACTATTGCTATATATGTACTGATTTTTTTAGCGTCTGTGTGAAATAGGGCTGCACTATATTAGGCATGGGATGATAACTAGTTTCAAGGTTTACCATGGTTTGGAGAAGTCAAGGTTTTAAAACTGCTAAAGTTTTCTGTTACACTGTTCCTATGCTGTATGCTTTTTTTATGTATGTGTTTTTTTTTTACAAGTATTGTATTTAGCTTTTTAGTCCAACAGTATCTCCAGCAGAAAATGAGCCTCTACATCAGGGGTCACCAATCTCGTTCCTGGAGGTCCGTTGCCCTGCAGTGTTTAGCTCCAACTTGCCTC
Associated Phenotype:
Not determined