ZMP
si:rp71-1n7.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human semaphorin 6D (SEMA6D) [Source:UniProtKB/TrEMBL;Acc:Q7T165]
Human Orthologue:
SEMA6C
Human Description:
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C [Source:HGNC Symbol;
Mouse Orthologue:
Sema6c
Mouse Description:
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C Gene [Source:MGI Sym
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36170 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42750 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14024 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36170
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 |
---|---|---|---|---|---|
ENSDART00000000198 | Nonsense | 388 | 1064 | 11 | 18 |
ENSDART00000135723 | Nonsense | 351 | 538 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 32557381)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 30283894 |
GRCz11 | 16 | 30204760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTCTCCAGGCCAGGGTCGTGTGCTGGTGATGGCCCTGCTGCTGGTTA[C/A]AAGTCCTCCACAAATTTCCCTGATGAGACTCTTACCTTCATTAAGTCTTA
Long Flanking Sequence:
GGCTCGCTCTGTGTGTGTTTTTCTTGTTCACATCATTGTATCATAATAGTATTGCAATAACATGTCACAAGATTACAGTTTAGACAACATTATAGTTTACTGTATTTTTGATTAAAAAAAAAAAAACTGCAACATCCCTAGAGTAGCATGAGCACATCACACAAAGGAATATATTCATGAACTTATCAAACAAAATGAAATCTCACTTACACACTCAGCTGACAAAGAATAGACTTCCTTGTCATCTTGCTTCGCGTGATATGCCTGTTTTCTGGAGCTCAGAGAGCAGCTTGTTTGGCCTGACGGACTCTTAAAACAGCTTCTATTTAACAGCGGCAGATGGCTGGAACGGATCTTGTTAACTGTATGTGTACGATCTGTTTTTGTTGATCATTTCACTGAGCCACAGTAAAGTCTGTGCAGGTTGATATCAATTGTTTTCTCTCTCTCTCTTTCTCCAGGCCAGGGTCGTGTGCTGGTGATGGCCCTGCTGCTGGTTA[C/A]AAGTCCTCCACAAATTTCCCTGATGAGACTCTTACCTTCATTAAGTCTTATCCACTAATGGACGAGGCTGTGCCGTCTGTCAACAACCGACCCTGCTTCACACGAACCACCAGCAGGTTCGCACACAAACACACACATACGCTCCAAGAGAAATTAGACACTCGTCCACTCATTATTTTCGCACTCTCTCTTTATTTCCCCAGTTGTTTCTTTAACATCTGCATGTCTTTCTCCAGAGGAGCAAGCTGCCGTTATTAGTGTTGGAGAATAAATGAGCACTTAGCTGTTGGGATGAAAGACAAAAGTTTTTTTTTGTGATTTTTATTTTGTCAACTAATTGGCTTATGTTCCTCATGTAGGTTCAAGCTGACCCAGATTGCAGTGGACACGGCAGCTGGCCCATATAAGAACTACACTGTCGTGTTTCTGGGGTCAGAAAATGGACATGTCCTGAAGGTTTTAGCTAGCATGCATCCAAACTCCTCGTACAGCACTCAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42750
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 |
---|---|---|---|---|---|
ENSDART00000000198 | Nonsense | 418 | 1064 | 11 | 18 |
ENSDART00000135723 | Nonsense | 381 | 538 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 32557469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 30283982 |
GRCz11 | 16 | 30204848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTAAGTCTTATCCACTAATGGACGAGGCTGTGCCGTCTGTCAACAAC[C/T]GACCCTGCTTCACACGAACCACCAGCAGGTTCGCACACAAACACACACAT
Long Flanking Sequence:
ATTATAGTTTACTGTATTTTTGATTAAAAAAAAAAAAACTGCAACATCCCTAGAGTAGCATGAGCACATCACACAAAGGAATATATTCATGAACTTATCAAACAAAATGAAATCTCACTTACACACTCAGCTGACAAAGAATAGACTTCCTTGTCATCTTGCTTCGCGTGATATGCCTGTTTTCTGGAGCTCAGAGAGCAGCTTGTTTGGCCTGACGGACTCTTAAAACAGCTTCTATTTAACAGCGGCAGATGGCTGGAACGGATCTTGTTAACTGTATGTGTACGATCTGTTTTTGTTGATCATTTCACTGAGCCACAGTAAAGTCTGTGCAGGTTGATATCAATTGTTTTCTCTCTCTCTCTTTCTCCAGGCCAGGGTCGTGTGCTGGTGATGGCCCTGCTGCTGGTTACAAGTCCTCCACAAATTTCCCTGATGAGACTCTTACCTTCATTAAGTCTTATCCACTAATGGACGAGGCTGTGCCGTCTGTCAACAAC[C/T]GACCCTGCTTCACACGAACCACCAGCAGGTTCGCACACAAACACACACATACGCTCCAAGAGAAATTAGACACTCGTCCACTCATTATTTTCGCACTCTCTCTTTATTTCCCCAGTTGTTTCTTTAACATCTGCATGTCTTTCTCCAGAGGAGCAAGCTGCCGTTATTAGTGTTGGAGAATAAATGAGCACTTAGCTGTTGGGATGAAAGACAAAAGTTTTTTTTTGTGATTTTTATTTTGTCAACTAATTGGCTTATGTTCCTCATGTAGGTTCAAGCTGACCCAGATTGCAGTGGACACGGCAGCTGGCCCATATAAGAACTACACTGTCGTGTTTCTGGGGTCAGAAAATGGACATGTCCTGAAGGTTTTAGCTAGCATGCATCCAAACTCCTCGTACAGCACTCAGGTTTTGGAGGACATCGATGTTTACAACCCTAACAAGTGAGTTAGAGAGCAAATATGCACACTGTTTTTGATGCAGTGTGTGGTGTATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14024
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 |
---|---|---|---|---|---|
ENSDART00000000198 | Nonsense | 481 | 1064 | 12 | 18 |
ENSDART00000135723 | Nonsense | 444 | 538 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 32557903)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 30284416 |
GRCz11 | 16 | 30205282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCCAAACTCCTCGTACAGCAYTCAGGTTTTGGAGGACATCGATGTTTA[C/A]AACCCTAACAAGTGAGTTAGAGAGCAAATATGCACACTSTTTTTGATGCA
Long Flanking Sequence:
GATGAGACTCTTACCTTCATTAAGTCTTATCCACTAATGGACGAGGCTGTGCCGTCTGTCAACAACCGACCCTGCTTCACACGAACCACCAGCAGGTTCGCACACAAACACACACATACGCTCCAAGAGAAATTAGACACTCGTCCACTCATTATTTTCGCACTCTCTCTTTATTTCCCCAGTTGTTTCTTTAACATCTGCATGTCTTTCTCCAGAGGAGCAAGCTGCCGTTATTAGTGTTGGAGAATAAATGAGCACTTAGCTGTTGGGATGAAAGACAAAAGTTTTTTTTTGTGATTTTTATTTTGTCAACTAATTGGCTTATGTTCCTCATGTAGGTTCAAGCTGACCCAGATTGCAGTGGACACGGCAGCTGGCCCATATAAGAACTACACTGTCGTGTTTCTGGGGTCAGAAAATGGACATGTCCTGAAGGTTTTAGCTAGCATGCATCCAAACTCCTCGTACAGCACTCAGGTTTTGGAGGACATCGATGTTTA[C/A]AACCCTAACAAGTGAGTTAGAGAGCAAATATGCACACTGTTTTTGATGCAGTGTGTGGTGTATTGTTGTGGAAACCTCAAACTGGTTGCTTTTCATGATATTTGAAAGGGAATGTTGGTAATGTTGGTAATGTGGTTTACATATGGTATGTAATGATTAATTAACGGTTGGATTTTTTTCAAATGGAGCATTTTGATGATCAAAAATCTAACTTATATGTTTTTTCCATCATAAGAATGATCACAAAATTAGTGATTTTAAACACTGTCATAACTATGTGGAGCACAGCTTTTTTACATTTTTGATTATACATTGCTCAGCATAATTGAGTACACCCCATGTTGAAAATGAATATTTTTATCCATTTCGTTTTAAACGGAACAGATGTATTAAAATGATATATTTATTAAAATAATATTTTAGTCACCAAACATATTTAGAAATTAAATTCAAGTAAAATATTGCAAAAAAATTACAATCTACATAATTTCAAATACATT
Associated Phenotype:
Not determined