ZMP
egf
Ensembl ID:
ZFIN ID:
Description:
pro-epidermal growth factor [Source:RefSeq peptide;Acc:NP_991294]
Human Orthologue:
EGF
Human Description:
epidermal growth factor [Source:HGNC Symbol;Acc:3229]
Mouse Orthologue:
Egf
Mouse Description:
epidermal growth factor Gene [Source:MGI Symbol;Acc:MGI:95290]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13676 | Nonsense | Available for shipment | Available now |
sa42425 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14990 | Nonsense | Available for shipment | Available now |
sa30983 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35730 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24964 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22523 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13676
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074639 | Nonsense | 25 | 1114 | 1 | 23 |
ENSDART00000126178 | Nonsense | 88 | 1177 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 37540558)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35979885 |
GRCz11 | 14 | 36320199 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAAGAATCGTTTCYAGGGCGGGAAGGTCCATTTTGTTGGACTTTCACT[T/A]AAGTGAGTGGACRATGTTTTGGGCGGACACACAAACAGGACAAATCAGMA
Long Flanking Sequence:
GGCTAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATATATATATATATATATATACTCCTTTTATTATGAAACAACATTTCTACCATCCAACCAATCAAGCCTTGACAACCACGCCCCACAATTTAAAGCACTTTGTAACTGGCTGACAGAAATTTTAAATTTTACTCCAGGAAAGATGAAATACTGTCTGTAAGCTCGAATAATTTACCGTGTTTTATGGTCTAATAATTAGTCAGCTATATTTTCAGGATTTGTTGCAGTGCAGTTTAATTTAAGTTGTTTTAGAATCAGTGTGATTTTAATTGAGTTTTTTGTCATTTTGACAGTTTATCAAAGATTATTATTATTATTTTTAAGAACCTGAGCCATATCTAATAGTCGGCCTCGGAAATAGCATCCAGAGAATGAACCTCGATGGAGGGGACCGGAGAAGAATCGTTTCCAGGGCGGGAAGGTCCATTTTGTTGGACTTTCACT[T/A]AAGTGAGTGGACGATGTTTTGGGCGGACACACAAACAGGACAAATCAGAAGAGCAGGACTAGATGGAACACGGAGACAGGTAACGTTACATATTTAACGTTACATATGTTACCTGTGTGTTTGTATGTAACTTATGTATGCGTGTATGTAGGTGGTGTGTAACGTTAGTGCTTTTCATAAAAAAACGTTTTCAATATTTTTGTCATTTAATGAAGTATGATGTCCCCTGCTAATGTTTCGTTTGCTTCATTTATGCCTTATGTTAACACCACACCCTTTCTTTTAAATATTTTTGTCATATGGGAGAACAAATGTATAATAGGTCCAAAATAATATAGTAGATAATTGTGTTTAAAAAGAGCTTTATTTAAAGTTTGGAACCTCTTTTCTTCCTTTCCTTCAGAAGCTTCTCTCCTCAGTGAAGGGAATCACGGGTCTGGTTGTGGACTGGATTGAAAACTCAGTCCTCTGGAGCAATGCAGATGAAGGAACAATACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42425
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074639 | Nonsense | 133 | 1114 | 3 | 23 |
ENSDART00000126178 | Nonsense | 196 | 1177 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 37538374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35977701 |
GRCz11 | 14 | 36318015 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGTCAGATGGAGCGACTTCCAGCATCCAGCGATCAGACATGACAGGT[A/T]AAATGATGAGCACAGTGCTGAAAGTAGCGGACAGACTGAAGGTTCTGGCT
Long Flanking Sequence:
AGGAATATTGAAATAAAAATATTTAAATGAAATAGAATGTACAGTAAATGACAGTACAGATATTTATCATATTAAAAAGCTTTCTATTTTAAATAAATGCATTTCTATTAACTGGATATTTACACATACATTCACCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAATACACACAACATATGTGTATTTATGTTTATGTTTAACATTTATAATATTTAATACACCATAATGTTTATATCTATATTTAAAATAGTATAATTAAAATTCTTTTTACATTTGTTTTGATACTATTGTTGGGCGTGAAAATATTTTCTCGAAATGAATGCTTCAAAATCTTGTCGAGTTTTTTTAGGGTAACAGAAATGAATAAAATTGCTGTCACAACTTTTTTCCAGATATATTTTCTGGTTGTCAGATGGAGCGACTTCCAGCATCCAGCGATCAGACATGACAGGT[A/T]AAATGATGAGCACAGTGCTGAAAGTAGCGGACAGACTGAAGGTTCTGGCTGTTGACCACCGGGACAGGAGACTTTTCTGGGTTCAGCAAGGCCAAAGAGGACACACTGCTATGGGCTCCTGCAACTATGATGGAAACATTATCAATGTCTTTAATCAGCAATTCAGGTATAACTGAGATCTATAATTCATTTAAGGCTAACATTATTTTGTTATAAAAACAACGAGTGAAGTTAACATCAAGAAAATTATGCAAAAATGTGTACGCAATTAAAATAAATGAAAAAATGTTTATACAATTAAAAATTATGCAGAAATGTTTACGCAATTAAAATATATGCAAAAATGTTTATGCAATTAAAATTATGCAAAAATGTTTATGCAATTAAAATTATGCAAAAATGTGTATGAAATTCAAATATATGCAAAAATGTATGCAATTAAAATTATGCAAAAATGTTTAGAATATAGAATGTGATGATTGACCAATCAGACTCAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14990
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 |
---|---|---|---|---|---|
ENSDART00000074639 | Nonsense | 177 | 1114 | 3 | 23 |
ENSDART00000126178 | Nonsense | 240 | 1177 | 4 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 37538242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35977569 |
GRCz11 | 14 | 36317883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGCAAGGCCAAAGAGGACACACTGCTATGGGCTCCTGCAACTATGAT[G/T]GAAACATTATCAATGTCTTTAATCAGCAATTCAGGTATAACTGAGATCTA
Long Flanking Sequence:
CACCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAATACACACAACATATGTGTATTTATGTTTATGTTTAACATTTATAATATTTAATACACCATAATGTTTATATCTATATTTAAAATAGTATAATTAAAATTCTTTTTACATTTGTTTTGATACTATTGTTGGGCGTGAAAATATTTTCTCGAAATGAATGCTTCAAAATCTTGTCGAGTTTTTTTAGGGTAACAGAAATGAATAAAATTGCTGTCACAACTTTTTTCCAGATATATTTTCTGGTTGTCAGATGGAGCGACTTCCAGCATCCAGCGATCAGACATGACAGGTAAAATGATGAGCACAGTGCTGAAAGTAGCGGACAGACTGAAGGTTCTGGCTGTTGACCACCGGGACAGGAGACTTTTCTGGGTTCAGCAAGGCCAAAGAGGACACACTGCTATGGGCTCCTGCAACTATGAT[G/T]GAAACATTATCAATGTCTTTAATCAGCAATTCAGGTATAACTGAGATCTATAATTCATTTAAGGCTAACATTATTTTGTTATAAAAACAACGAGTGAAGTTAACATCAAGAAAATTATGCAAAAATGTGTACGCAATTAAAATAAATGAAAAAATGTTTATACAATTAAAAATTATGCAGAAATGTTTACGCAATTAAAATATATGCAAAAATGTTTATGCAATTAAAATTATGCAAAAATGTTTATGCAATTAAAATTATGCAAAAATGTGTATGAAATTCAAATATATGCAAAAATGTATGCAATTAAAATTATGCAAAAATGTTTAGAATATAGAATGTGATGATTGACCAATCAGACTCAAGTATTACGGTCATGCATGTAATTTTTTATTTGATTGTTAAATAAAGGTTATCTTAAAATTTAAAAAAAATTAAAAATAAATAAAATAAAATAATAATTAAATATCCAATCCTATCTACGGATATAATTAATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30983
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074639 | Essential Splice Site | 797 | 1114 | 16 | 23 |
ENSDART00000126178 | Essential Splice Site | 860 | 1177 | 17 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 37511521)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35950848 |
GRCz11 | 14 | 36291162 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTCAATGTGTGAGGGGTTTCACTGGTGATGGGGAGTTATGTGTGG[G/T]TAAGTGTCAAGTCACATCAAGCCAATGTTCTTTCTATAGCATGTTTACAC
Long Flanking Sequence:
ACTGTCTTGACTAGTGCGGTTGAATGACATTTGTCCTGGGAGCACTGTACCAATGTGGCGGCGCTATTGACGCATGCTCAGGGTCCCTATGCGATATCTAGTGTATATATCTATGCTTTGCAACTACATGTCCACTAGCATTCTTTAAAGTATTAGTAGACTGTCTACTTAATATCTGCTATCACTGCATCACCAACAGACATTCTACTGATAAGTAATGTTGCAATAAATTACACTAACCCTAACCCAAAAGCCAGATCATACTCTAAAGTTAGATGTACTTTTAAGTGTTACTTAAAAGTGTTACTTTTTTAACCACAGATTACTGTAATTGTTCATATTGAAGTGTCAGAATGCTAAATTGTGATTTTTGTCTCATTCAGATCAGGATGACTGCTTCTCTCTCAGCTGTGTTGTGAACGCTCAGTGTTTTCTGCAGGAGGGCCGGGCTGTGTGTCAATGTGTGAGGGGTTTCACTGGTGATGGGGAGTTATGTGTGG[G/T]TAAGTGTCAAGTCACATCAAGCCAATGTTCTTTCTATAGCATGTTTACACAGGTTAAAGTGTAGATGCCTGGCGTAATCGTAACAAAATATATGTTTTATGAAAACGCAGTACTGTAAACGTCACCTCAGTTCCACAGAATGCTGGTTTTGTTCTATTCAGTTCAATGATAATTTAGTTCAATATGAATGTCATTGTTGAATGTCATGTGATTCACTAAAGTGCAGCTCTACTCAAAAACAAATAGAGCAACTTTAGAGATCAAGGCAATAAGCATGTCATGATTTTGCGATCCTGTATTAACACCTATGTTGATCCTGGAACATCATTTTTGTTAGAAAATGTAATCCATACCTGTTCCTTACCCCTAAACCCAACCATAACTGTAAATTATTCCAAAAAGTCAGATGGGAATAATAGTTAGAAAACAATCATATAGAAGTGCATAAACTTAAACTTAAGCCTAAACTTAACAAACTTAATAAACTAAACATGTGCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35730
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074639 | Nonsense | 851 | 1114 | 18 | 23 |
ENSDART00000126178 | Nonsense | 914 | 1177 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 37506802)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35946129 |
GRCz11 | 14 | 36286443 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGTATTGTTGCAGATATAGATGAGTGTCGACTAGATTTGCATGACTG[C/A]GATGTAAACGCTGAATGTTTAAATGCCGTAGGAGAATATCAATGTAGATG
Long Flanking Sequence:
CGAGCTGTGATGTAACTATTGCGAATGATCACATTGCGGTATTGAGACTGAAACGATATACAGTATTGTGCAGCCCTAGTTCCCATCGCTACTAGCACTGTTAATTGCTTTTTTTGCTTTTAATTGACACTGCAAAAAAAATACATTTATTTTATTGAAAAACATGTTTTCGTTTCTATGAAAAAGCAACATTTTAAAATATAGTGAAATAGAACATTTTTATTTAAATTGTACTAATATGCTTCAATATTACACAGTTTTTCTGTGGCTTTTAATTTTAGTTTTTTATTATTAGTTATACTTTTTCATATTTTTGTTGTCCGTTTTGAATTTCAACTTTATTTTTGCACTTTTATTTTAATTTTATTCGTTTTACTAGTTATTTTTTAAATTAGATTTAGTTATTTAAAGTTTAAGATAAATCCAATAAAAATGAAATATATGTTGTATATTTGTATTGTTGCAGATATAGATGAGTGTCGACTAGATTTGCATGACTG[C/A]GATGTAAACGCTGAATGTTTAAATGCCGTAGGAGAATATCAATGTAGATGCCGATCTGGCTTCACAGGCACTGGTTTCAGCTGTCAAGGTAAGATTTAATTATTAAACTGAAAAACCACCTTCTTAATAACCATTATAGCATTCACATTATCTGTAATTATGGGTTAAACTTGATACAATCTTCTAATCTGAATTTGTGCAAGATTAAATGCACTAACAAGAACACACTAACAGTAAATGTACTAACATTTAGCAGTACTGTATGGTACAACATAACTGACCTGATTTTCATGCTCTGTTTCCTGTTTCAGCAGAGTTTAATGGCACCTCCTTGTGGCCGAGTACTGCTAGTCCTCCTGATGTCACTTCAACATTGCAACACAAAAATGGCGTGCAGAGCTGCCCCTCTACACATGACTCGTATTGTCTGTATGATGGAGTCTGCTTCTATTTTCCTGACATGGAGTCTTACGCCTGCAAGCAAGTGTTTACCCCTAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24964
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 |
---|---|---|---|---|---|
ENSDART00000074639 | Nonsense | 869 | 1114 | 18 | 23 |
ENSDART00000126178 | Nonsense | 932 | 1177 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 37506750)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35946077 |
GRCz11 | 14 | 36286391 |
KASP Assay ID:
554-7841.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTAAACGCTGAATGTTTAAATGCCGTAGGAGAATATCAATGTAGATGC[C/T]GATCTGGCTTCACAGGCACTGGTTTCAGCTGTCAAGGTAAGATTTAATTA
Long Flanking Sequence:
ACGATATACAGTATTGTGCAGCCCTAGTTCCCATCGCTACTAGCACTGTTAATTGCTTTTTTTGCTTTTAATTGACACTGCAAAAAAAATACATTTATTTTATTGAAAAACATGTTTTCGTTTCTATGAAAAAGCAACATTTTAAAATATAGTGAAATAGAACATTTTTATTTAAATTGTACTAATATGCTTCAATATTACACAGTTTTTCTGTGGCTTTTAATTTTAGTTTTTTATTATTAGTTATACTTTTTCATATTTTTGTTGTCCGTTTTGAATTTCAACTTTATTTTTGCACTTTTATTTTAATTTTATTCGTTTTACTAGTTATTTTTTAAATTAGATTTAGTTATTTAAAGTTTAAGATAAATCCAATAAAAATGAAATATATGTTGTATATTTGTATTGTTGCAGATATAGATGAGTGTCGACTAGATTTGCATGACTGCGATGTAAACGCTGAATGTTTAAATGCCGTAGGAGAATATCAATGTAGATGC[C/T]GATCTGGCTTCACAGGCACTGGTTTCAGCTGTCAAGGTAAGATTTAATTATTAAACTGAAAAACCACCTTCTTAATAACCATTATAGCATTCACATTATCTGTAATTATGGGTTAAACTTGATACAATCTTCTAATCTGAATTTGTGCAAGATTAAATGCACTAACAAGAACACACTAACAGTAAATGTACTAACATTTAGCAGTACTGTATGGTACAACATAACTGACCTGATTTTCATGCTCTGTTTCCTGTTTCAGCAGAGTTTAATGGCACCTCCTTGTGGCCGAGTACTGCTAGTCCTCCTGATGTCACTTCAACATTGCAACACAAAAATGGCGTGCAGAGCTGCCCCTCTACACATGACTCGTATTGTCTGTATGATGGAGTCTGCTTCTATTTTCCTGACATGGAGTCTTACGCCTGCAAGCAAGTGTTTACCCCTAGAGTTTTTGTCATGCAGAAACATCAGACCGATCCTCATAGTCCTTATTTTTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22523
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074639 | Nonsense | 1027 | 1114 | 22 | 23 |
ENSDART00000126178 | Nonsense | 1090 | 1177 | 23 | 24 |
Genomic Location (Zv9):
Chromosome 14 (position 37501781)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 35941108 |
GRCz11 | 14 | 36281422 |
KASP Assay ID:
2260-7784.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTGTTGGGGATTTTGTGCATTGACACATTATGTGTATGCAGGTCTA[T/A]GTAGTTTTGGACACTTCTACTTGCACTGCTGATAAGGTCCTTCATGTACA
Long Flanking Sequence:
CCAGCTTTTGTCAGTGTACTCTCAAGGTATTTGTGATATCAAATCAAGAAGATCTAGCTTTTTAACACACAATTTTCCAATTTTCTCTTTGTATTCCGTACAGTATAGTAAGTTCAACATGTACATGTTGCTGTTGAAAGTTTTTGAGGTTATTCATGGTCTGCTAAATATTATTTTCTAATTAGAATAGGTTGAATTTTGACATGTGATGGAAAAACTGAGGAGATTAATGCCATCTCAATGTAACTATTTTTTTTCATGTAAAACAACATGGGGTGTTGGAAAAAAGTGGATAAGAGTGTTTTGTTGTTTATCAGGCCTAAAAGACATTTTGGAGGGTGTTCCTTACAGGACAGTGTAGGAGAAATGAGTGCGAGTGAAGACAGTTTCACTGAGACCACAACAGCCACTCCAGAGGTATGAAGATTCCTAAGAACTTTTTAATTGTTTGTTTTTGTTGGGGATTTTGTGCATTGACACATTATGTGTATGCAGGTCTA[T/A]GTAGTTTTGGACACTTCTACTTGCACTGCTGATAAGGTCCTTCATGTACAGTCTACCACATCAACAATATGCTCCTCTTGCCCTACACAAACAGGTATGAATCAGTCATAGATTACATCACAGTTTGTTTCAGTTGATAGAATAATTTATAAATTGATATTTACTGTATACAGTACATATATATTTTGTGCTTATTCAGATAAAGGAAATTAATAAACTACATTTGTTTAATTTTTGGCACTTTACAAAACAAAATAACACATTAAAAAAATCTGGTGAACAGTTATAAAACAGAAAACATGTAAAAAAAAAAAAACAACTCAAAAGTAACCTTATTAAAACTATAAAAAAATATATAATAACCATAACTAAAAAACTTTTTAATATTTGTTTTTTAACCATTTTTTTTATTGGGAAATTATGAAATTATATAGGTCTAATATATTAAGCCAATATATTGTATATGTACAGTAAATATTTGAATTTTGAGTGTGCTGTTT
Associated Phenotype:
Not determined