ZMP
spred1
Ensembl ID:
ZFIN ID:
Description:
sprouty-related, EVH1 domain-containing protein 1 [Source:RefSeq peptide;Acc:NP_998397]
Human Orthologue:
SPRED1
Human Description:
sprouty-related, EVH1 domain containing 1 [Source:HGNC Symbol;Acc:20249]
Mouse Orthologue:
Spred1
Mouse Description:
sprouty protein with EVH-1 domain 1, related sequence Gene [Source:MGI Symbol;Acc:MGI:2150016]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15659 | Essential Splice Site | Available for shipment | Available now |
sa32178 | Nonsense | Available for shipment | Available now |
sa6494 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15659
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000060764 | Essential Splice Site | 67 | 391 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 53178994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 52564561 |
GRCz11 | 17 | 52650861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAYGCCGACGAGTTCCTCATCCACGGAGAACGSCTCAAAGACAAAACGG[T/G]AACATTGACGTCACAGGAAGAGCTTGATGCRGCGATGATRTCATGAGCAA
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTTCTTGTGTTCCGGCAGTGGCACTTATGCGCGGGTGCGAGCGGTAATGATATGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGCTTGTGTTCTTGTGTTCCGGCAGTAACACTTATGCGCAGGTGCGAGCGGTGGTGATATGAGTGTGTGTTTGTGTGTGTGTATGTTTGTGTGTGTTCTTGTGTTCCGGCAGTGACACTTATGCGCGGGTGCGAGCAGTGGTGATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCAGCAGTATTCCTCTAACGTGTGTGTGTGCTTGTTCTTGTGTTCCGGCAGTGACACTTATGCGCGGGTGCGAGCGGTGGTGATGACGCGGGATGACTCCAGCGGCGGGTGGCTTCCTCTGGGCGCCGGCGGCCTCAGCTGCGTCACCGTACACAAGATCAGCCACACGGAGCCAGACGCCGACGAGTTCCTCATCCACGGAGAACGCCTCAAAGACAAAACGG[T/G]AACATTGACGTCACAGGAAGAGCTTGATGCGGCGATGATATCATGAGCAATGCAGGAGTTCAGGAGCCAAGAAAGCACTGTGATGTCACTGAAGTGTCCCTGATGACACATAACACAGCTGGCAGATTACTTTAGTTAATTGTAGTGGTTTAACAGATCACAAATCTCCCGGTTCTGATCACATTAGGGGTTTTGGATCGGATAATTTTTCAGATCAGCCAAAACGAGGAGGAGACAAATGTTATTTTCTTTCCGTTTATTACAGAAACAGCACTGCAGGACACTTTTGGTTTTAACAAACAGAACTGAGAAGATGTCATTTTAGTTGAAAAGGAAAAATGAAGAAATAATCAGCGGAATAAAAATACATTTATTAAATATTTTAATCTCATCTTCAATAAACAATCTTTAAAGTCCAACGCAGAGCGCATTATCCGCTTGTTAAGTGGTGACGTGTTGGTGACGTATGTTATACTGCTCCCTGATCCAAGCCGCCACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32178
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 |
---|---|---|---|---|---|
ENSDART00000060764 | Nonsense | 292 | 391 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 53169715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 52555282 |
GRCz11 | 17 | 52641582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACGGCGAGCGCTCGCGGTGCATTTACTGCCGAGAGATGTTCAATCAT[G/T]AGGACAACCAGCGCGGGCAGTGCCAGGACGCGCCTGACCCCATCAAACAG
Long Flanking Sequence:
TTTTTTTAAACAAAGGCAGTGAAACATGTTTATAAAGATTGCCGTGTTCATGTGCACATGGCCTAAGTGTCATTGTATTCACAGTGATGCGCACGACAATCGCATGCAGTTTAACGCTCAGCCCTACGTGCTAATGTTCTGTGTCCTTGCTGACGGGTTTCCTTCTCCTTCCACAGGTTTCCTTCAACAGCAGACGTCACGTGAGCTTTCAGATGGACGACGAGGAGATCGTCCGCATAAACCCACGCAAGGACGTGCTGATCCGCGGCTACGAGGACTACCGGCACCCGGTGCTCTGGAAGCAGGACCCTCAGCTCCCGGAGCCCGACCCCACCGCCACCTTCGCCAAACTGGACGGTAAGAAGTGCGAGTACCTGTTCTCCGAGGAGCTGCAGAAAGACTCGGTCAAGACGCAGCAGCCGTCGGGGAAGGCGTCCCGCAGGCGGAGGGAGGACGGCGAGCGCTCGCGGTGCATTTACTGCCGAGAGATGTTCAATCAT[G/T]AGGACAACCAGCGCGGGCAGTGCCAGGACGCGCCTGACCCCATCAAACAGTGCATCTATAAGGTGAGCTGCATGCTGTGTGCTGAGAGTATGCTCTACCACTGCATGTCCGACTCGGAGGGCGACTTCTCGGATCCGTGCTCCTGCGACGCCAGCGAGGAGCAGTTCTGCGTGCGCTGGCTAGCGCTGTTGGGTCTGTCTCTGCTGGCGCCCTGCCTGTGCTGCTACCCACCGCTGCGCTTGTGCCACCGCTGCGGGGAGGCCTGCCGCTGCTGCGGCGGCAAACACAAGGCTGCAGGATGAACCGAGCCTCCAACGGGCTCTGATTTCAGTTTCCGGAGACGGCAAAGCGCTGTTCACTGCTTGTGGAAGAGCGCCGTCTGTACGCAGAGCGCCGTCACGAGCTCCTGACGTGCGGAGGAAAGGCCGAAGTACGCACACAACAAACACCTGAAGAAATAATCTTGTGTCCTGTACAGAGATTCTAACACTTAAGGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6494
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 |
---|---|---|---|---|---|
ENSDART00000060764 | Nonsense | 346 | 391 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 17 (position 53169553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 52555120 |
GRCz11 | 17 | 52641420 |
KASP Assay ID:
554-4597.1 (used for ordering genotyping assays)
KASP Sequence:
ACTCRGAGGGCGACTTCTCGGATCCGTGCTCCTGCGACGCCARYGAGGAG[C/T]AGTTCTGYGTGCGCTGGCTAGCGCTGTTGGGYCTGTCTCTGCTGGCGCCC
Long Flanking Sequence:
TTCTCCTTCCACAGGTTTCCTTCAACAGCAGACGTCACGTGAGCTTTCAGATGGACGACGAGGAGATCGTCCGCATAAACCCACGCAAGGACGTGCTGATCCGCGGCTACGAGGACTACCGGCACCCGGTGCTCTGGAAGCAGGACCCTCAGCTCCCGGAGCCCGACCCCACCGCCACCTTCGCCAAACTGGACGGTAAGAAGTGCGAGTACCTGTTCTCCGAGGAGCTGCAGAAAGACTCGGTCAAGACGCAGCAGCCGTCGGGGAAGGCGTCCCGCAGGCGGAGGGAGGACGGCGAGCGCTCGCGGTGCATTTACTGCCGAGAGATGTTCAATCATGAGGACAACCAGCGCGGGCAGTGCCAGGACGCGCCTGACCCCATCAAACAGTGCATCTATAAGGTGAGCTGCATGCTGTGTGCTGAGAGTATGCTCTACCACTGCATGTCCGACTCGGAGGGCGACTTCTCGGATCCGTGCTCCTGCGACGCCAGCGAGGAG[C/T]AGTTCTGCGTGCGCTGGCTAGCGCTGTTGGGTCTGTCTCTGCTGGCGCCCTGCCTGTGCTGCTACCCACCGCTGCGCTTGTGCCACCGCTGCGGGGAGGCCTGCCGCTGCTGCGGCGGCAAACACAAGGCTGCAGGATGAACCGAGCCTCCAACGGGCTCTGATTTCAGTTTCCGGAGACGGCAAAGCGCTGTTCACTGCTTGTGGAAGAGCGCCGTCTGTACGCAGAGCGCCGTCACGAGCTCCTGACGTGCGGAGGAAAGGCCGAAGTACGCACACAACAAACACCTGAAGAAATAATCTTGTGTCCTGTACAGAGATTCTAACACTTAAGGGATTCTGCCTCTTTATTTTTCGTCAGTTATTAACCGTGGCCTTTTTCGTTTGTTCGTTTCTTTGTTTGACGCTACCATTACTAGCTAGACGGATGGACGGATGCACTAATGTTGCAGAGCATTAACGGTACGCTCACTCGGAGACTAAACCTTTCATTGATTACAG
Associated Phenotype:
Not determined