ZMP
si:dkey-200l5.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
STARD7
Human Description:
StAR-related lipid transfer (START) domain containing 7 [Source:HGNC Symbol;Acc:18063]
Mouse Orthologue:
Stard7
Mouse Description:
START domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2139090]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12622 | Nonsense | Available for shipment | Available now |
sa9576 | Nonsense | Available for shipment | Available now |
sa41630 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12622
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 > C
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112560 | Nonsense | 282 | 403 | 5 | 8 |
ENSDART00000147553 | Nonsense | 244 | 364 | 5 | 8 |
ENSDART00000112560 | Nonsense | 282 | 403 | 5 | 8 |
ENSDART00000147553 | Nonsense | 244 | 364 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 17735344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17747690 |
GRCz11 | 10 | 17705124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTATGTGCGTCGATATCAAGTCGACCTAGAGAACAACTTGATGATCT[T/C]AGTCTCAAGGTAAGTGCTGTTGCMAGTTTGTTGTTCACTATTTGTTTATW
Long Flanking Sequence:
GCTAAAATCTGCAGCACACCGGCCCTCCAGGACCGAGTTTGGGCACCCCTGATTTACAATATTGTAACGTTAGAAATGTCCTTACTGTCACTTTTAATCATTTTATGTGCCCTTGTTGATTAAAAGTTAAATTTATACTTTAATATTACCTCAAAGTTTACTCTTGAGTGTAAAGTGTATGACATGTGACCAATAAGCTCCCATAATCAAACGAAACAGATATAAATAATAAAAGTTCAAGGGACTATGAGGGTTCAAATTAGTGTCTTTTTTGAAGGTAACGCTAGGAATGTGGATATTTGAGTTTCCAGTAACATATGAAATACATTAGTCATCAAGTTTTCCGTTTAATTCCGCATGTCTGTTAATGTGTACACTTTTGTTGAATCACAGGTATGTCCTAATTATGCTGACCTTTTCTGTCTAGTATCCTATGTACTCCAGGGATTATGTCTATGTGCGTCGATATCAAGTCGACCTAGAGAACAACTTGATGATCT[T/C]AGTCTCAAGGTAAGTGCTGTTGCCAGTTTGTTGTTCACTATTTGTTTATAAGCATGTTGTCTGGTTTTGGTATTTCCCTTATATTAATGTGGTGGTCAGTCAGCTTTGTGTTTATAATGTGCACTGTAATGTGTGTTTAGTTTTATAAGTTATTTATTTATTTTTAAATCATTACTTTTTACTTTATTTTACACCATTGGTTTTTATTCTCTTAAAAGCAGTCTGTTGACTTCCTTGTACAGTGAAGCCCTTTCCTCAGAATTACACAATGGGTTTTCATTAGTCAGCTGGCTCTCTGTGTTGTGATTGGCCAATTACCTAGTGCATCATGCCTAGGCTTGGGGTTTATGTAAATTTTATGGGTGATGTCACAAATCCAGGAAGTAGCTCCTTACTGGCTTCATTGCACATTTTACAGAAACATTACTGTCTAATGTTAAAAAAGTGAATTCACAGACCTCTTTAAATGTGCTTTGCTCTCCACTCAGAGCTGTGAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9576
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112560 | Nonsense | 282 | 403 | 5 | 8 |
ENSDART00000147553 | Nonsense | 244 | 364 | 5 | 8 |
ENSDART00000112560 | Nonsense | 282 | 403 | 5 | 8 |
ENSDART00000147553 | Nonsense | 244 | 364 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 17735344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17747690 |
GRCz11 | 10 | 17705124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTATGTGCGTCGATATCAAGTCGACCTAGAGAACAACTTGATGATCT[T/G]AGTCTCAAGGTAAGTGCTGTTGCMAGTTTGTTGTTCACTATTTGTTTATW
Long Flanking Sequence:
GCTAAAATCTGCAGCACACCGGCCCTCCAGGACCGAGTTTGGGCACCCCTGATTTACAATATTGTAACGTTAGAAATGTCCTTACTGTCACTTTTAATCATTTTATGTGCCCTTGTTGATTAAAAGTTAAATTTATACTTTAATATTACCTCAAAGTTTACTCTTGAGTGTAAAGTGTATGACATGTGACCAATAAGCTCCCATAATCAAACGAAACAGATATAAATAATAAAAGTTCAAGGGACTATGAGGGTTCAAATTAGTGTCTTTTTTGAAGGTAACGCTAGGAATGTGGATATTTGAGTTTCCAGTAACATATGAAATACATTAGTCATCAAGTTTTCCGTTTAATTCCGCATGTCTGTTAATGTGTACACTTTTGTTGAATCACAGGTATGTCCTAATTATGCTGACCTTTTCTGTCTAGTATCCTATGTACTCCAGGGATTATGTCTATGTGCGTCGATATCAAGTCGACCTAGAGAACAACTTGATGATCT[T/G]AGTCTCAAGGTAAGTGCTGTTGCCAGTTTGTTGTTCACTATTTGTTTATAAGCATGTTGTCTGGTTTTGGTATTTCCCTTATATTAATGTGGTGGTCAGTCAGCTTTGTGTTTATAATGTGCACTGTAATGTGTGTTTAGTTTTATAAGTTATTTATTTATTTTTAAATCATTACTTTTTACTTTATTTTACACCATTGGTTTTTATTCTCTTAAAAGCAGTCTGTTGACTTCCTTGTACAGTGAAGCCCTTTCCTCAGAATTACACAATGGGTTTTCATTAGTCAGCTGGCTCTCTGTGTTGTGATTGGCCAATTACCTAGTGCATCATGCCTAGGCTTGGGGTTTATGTAAATTTTATGGGTGATGTCACAAATCCAGGAAGTAGCTCCTTACTGGCTTCATTGCACATTTTACAGAAACATTACTGTCTAATGTTAAAAAAGTGAATTCACAGACCTCTTTAAATGTGCTTTGCTCTCCACTCAGAGCTGTGAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41630
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 |
---|---|---|---|---|---|
ENSDART00000112560 | Nonsense | 387 | 403 | 8 | 8 |
ENSDART00000147553 | Nonsense | 348 | 364 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 10 (position 17732600)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 17744946 |
GRCz11 | 10 | 17702380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACGACTATGTCAATGTTGTAAAACCTTCTCAACCCTCCCAAGAACAA[C/T]GACTAGGAGCTGAAAACACTCACACTGCAGGCTCAAGTCAGATCTACGCC
Long Flanking Sequence:
TTTTAAAAATTGAATATGTGCATGTTTACAAAAAATAATATTCACTTTTCAAAGAAATGTAGTGTTTTTGTTGTGATTTCATTAGTTTTGGTGTTTTTTTTTTTTTAAACCAAAGGTTACACGCGCACACACACACACACACATATATATTTATATTTATATATATTACTATTTACTATATAGAATAAAAAGGTTGGCCTCACTAAGTCATTCTTAATTGGTCTGTCATTGTTACTGAATGTAACGGTAATATCTCAGTGTTGAATTTCACAGTTGTAATCATGATAGTTGTCCTTGAAATCTGCCCTTTCTGCAGCTGCTTTTTCATGACACCTGTTCACTTCCATTTCACCCCCCACCCCTCTCTCTCTCTCTCTCCCACAGGCATGCCAGATTTCCTGGAGAAGCTTCACACTGCTGCTCTCAGAGCTAAAAACATGGACGTCAGTGTGCACGACTATGTCAATGTTGTAAAACCTTCTCAACCCTCCCAAGAACAA[C/T]GACTAGGAGCTGAAAACACTCACACTGCAGGCTCAAGTCAGATCTACGCCTGAGCTAAAATGGCCCACAACAGGACAGTTTTGCTTACCGGGTCATTATTTGTAGCCACAAAGAAATCAGAAGCATTTATTCCCGAGGTTTCATCATTGCCATATGAACGTTCCTGCAGTAGCTGTCATACCGCACGCTCACATCTTTTATTTTTGTGCTGTTAGTTTGCTTCCTCTTTCTGTAGAGGGCATCTAAGCTAAACTGCTGAGATGAGCCAAAATATTGCCGTTTATTAATTGCAGATTCTCCTGCCAAAGCAGTATTTCACTCTCATTTCTTTACATCATCAGAATCGATTGTGCAAACGCCCTTCCAGCTTCAAGTTCAGGAAGTTGTTTGCAGTTTAAACTGTGATGAACTGCTCCTCATTTACCGTGTGAATGTTCACTGCCAGCAAAAAGCCAAGCAGCCTTCACAGGATCACAGAAAAACCTCTTCTGGAAATGAGA
Associated Phenotype:
Not determined