ZMP
efcab7
Ensembl ID:
ZFIN ID:
Description:
EF-hand calcium-binding domain-containing protein 7 [Source:RefSeq peptide;Acc:NP_001002120]
Human Orthologue:
EFCAB7
Human Description:
EF-hand calcium binding domain 7 [Source:HGNC Symbol;Acc:29379]
Mouse Orthologue:
Efcab7
Mouse Description:
EF-hand calcium binding domain 7 Gene [Source:MGI Symbol;Acc:MGI:2385199]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20725 | Nonsense | Available for shipment | Available now |
sa20724 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20725
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016629 | Nonsense | 528 | 603 | 11 | 13 |
ENSDART00000139055 | Nonsense | 531 | 606 | 11 | 13 |
The following transcripts of ENSDARG00000020279 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 31724532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32045448 |
GRCz11 | 6 | 32032362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGGCTAAAGCTCTGAAGGGCCATGAGAATGTGCTTGTTTACACATA[C/A]AAAGGAGAGAGCAGGATTTCATCAGTCATTGCTAATAAGGTGGGTTGGTT
Long Flanking Sequence:
AAACAACATTACCCCTTTTTAATTGACTGTAAATAATGTTGTACTTTGATAGTCATTAGCTGCTAATATGATTTCCCTATTTAGAATTTGCAAACAATACTTAAAAAATGTATTATTAAAAAAGTCAGAATGTGCAAATATAATACCAACTTTACCCCAAGATGAATCTTTTTAGAAAGTTCAGACTCATAATTAATTCAATTGTTTCTGGATTTTAATCTTCGGATTTTTTTGGAATCCACCGCATTACACACTACATAAAACATATCAGTAAAAGCGTAATAGGAGCGCTTTCATCTTGATGTGTGTGTTCTTCTTTTTCCCTGACAGTCCTGTCCATTTGTCATTGATGTCTACTGTGAGGATGTCAAAGCAACTCTTCAGGCAGTTCATTTGGATTCTGGGGTGAAGATGTTGAATTCTGCTGTACAGAGATCCATCACGTCCAAAGCAGAGGCTAAAGCTCTGAAGGGCCATGAGAATGTGCTTGTTTACACATA[C/A]AAAGGAGAGAGCAGGATTTCATCAGTCATTGCTAATAAGGTGGGTTGGTTAATGTTTTTGTTTTTTTGGTTGTTTTTTTTTATGTGAAGAATTAATTTGGGTTGGAAATCAATGCATGAGATCTGTCTCTCAGTTAAAAAGCCTTTAAGAAGTACTAGTAGGCCTCACATTTGTGCTTTTTGCACTTAACATTCAATGAGAATAGCACAAATAAGTAAACCTCCTGTTGTTTGGAAAGCTTTATAGAGAAAGGAGGACTCAACATGAGTCGAATTTCAATGTTCTGATCTGCCATTACACAGACAAAGTCAGTTCAAAGGCACTTTAAGCAGATGGAAGGAAATAGAAACTGCAATATTTAGTGGTCCTAATTCTGAAATAAGTTCTGTTTAAAAGTTTGAGGTCTTCAAGGTTTTTTTTATTGAATTTACTTCAAGGGTGCAAATGTTTATAAAGAGACCGCAGAGGAGGGGGTGGGGGTAGTTGAATTGATATATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20724
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 |
---|---|---|---|---|---|
ENSDART00000016629 | Nonsense | 589 | 603 | 13 | 13 |
ENSDART00000139055 | Nonsense | 592 | 606 | 13 | 13 |
The following transcripts of ENSDARG00000020279 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 31721839)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 32042755 |
GRCz11 | 6 | 32029669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGGTCTCTGTTTAGGTTTGTCAGCACGTCATGGCTTTAAACGATCAA[C/T]AGGAGTGGACTTACAACTGCACTGAGAGCATTATACCAAGTTTGTAAATG
Long Flanking Sequence:
AGTATTGTGTCGATGTCCCAATATTCATGGACCTGACTGTATGTCACATTTCCTATACTTTTGTAAAGTAATGATTATAAAACATTATATCTGCAGTGTTTTGACTGATTTTGACCTTTTTTATATCAATCTCTGTTGCTACTATAGTCCAATCAGAAGGTGACGGTGCACATCAGCAATGAGCAAAGCAAAAACTTTGTGAGCAGCAGAGGCATGAGTGTGTTTGCAGTGGAGGTTCCTGCTAGAACTAAAATGGTGAGACTTTTATCTCTCAAAATCCAAACATTCAGCTTGTTTTTTTTTTTCTGTAGATGCATGATAGGGTGCATTCATGCTTTGTTTTCCATTCTCAATTCAAACAAATAAAAACCCAGCTAGAGTGTGGCTTCGTAAATAGACAGGCACTTAAATGTGCATATAAACTGAATATCTTTAATGCTTTGTGTCTTGTTTTGGTCTCTGTTTAGGTTTGTCAGCACGTCATGGCTTTAAACGATCAA[C/T]AGGAGTGGACTTACAACTGCACTGAGAGCATTATACCAAGTTTGTAAATGCTGCAGTTGTGACATTTATTATGAGGCAACAAAGAAAGTAGTAACATAATATTGTTTGCTTGTTATAACTATTGCAAACATTAATAATAGTTTTCAGATTTGTTTATTGTTCCTTTCAGCAAAATGCAATCATGATTTTCATTTGTTTTTGTAAATAAAGCAGTTTATATTTTATTTTTATTTGTTTTGCATTTTTATTATTTTGTTATGTGTTTTTAATGTAATATTTTTTTTGGTTTCTGTTAGCATTGTGCAAGTCGCTTCGAGAGATTGTGTGCACTCCTCTAATGAATTTGCGTAAGTTTCAAGTGAGTCAATTTTAAGAATAGAATAGAATGTAGGGTTTAAATTTAATAAAAAGTGAAAAGGTATGAGAGCGAGCTTTAAATGTGAGTCTACTCCATCACTCCTGTCATTACTTATTTGAATTGAACAGAAGGAATTTCAGAC
Associated Phenotype:
Not determined