Busch Lab

ZMP

scg2a

Ensembl ID:
ENSDARG00000017470
ZFIN ID:
ZDB-GENE-030131-8214
Human Orthologue:
SCG2
Human Description:
secretogranin II [Source:HGNC Symbol;Acc:10575]
Mouse Orthologue:
Scg2
Mouse Description:
secretogranin II Gene [Source:MGI Symbol;Acc:MGI:103033]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa5883 Nonsense Mutation detected in F1 DNA Not yet available
sa22722 Nonsense Available for shipment Available now
sa35991 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa5883
Status:
Mutation detected in F1 DNA
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
ENSDART00000003653 Nonsense 68 540 1 1
Genomic Location (Zv9):
Chromosome 15 (position 41873635)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 43262152
GRCz11 15 43143130
KASP Assay ID:
554-3832.1 (used for ordering genotyping assays)
KASP Sequence:
CTTATGGACCCCCATCCCAATTGCGCCCTCCTCCCAGCGCAGAGATGCTC[C/T]GAGCTCTACGATACATCCAAAGCCTCAGCGAGAGGACTCCAGCAGATCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22722
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000003653 Nonsense 167 540 1 1
Genomic Location (Zv9):
Chromosome 15 (position 41873932)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 43262449
GRCz11 15 43143427
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGACCAAAACAACAAGTGAAGGTGGACACAGATGATGGGAACTATGGG[A/T]GAAACTCGTGGGCTGAAAACCGGAGACGCTACAGAGAGTATCCAATCATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35991
Status:
Mutation detected in F1 DNA
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
ENSDART00000003653 Nonsense 242 540 1 1
Genomic Location (Zv9):
Chromosome 15 (position 41874157)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACCAAACGAAGTGATGATGATGAAGATGATGAAGAAGATTTATACAGG[C/T]AAAGGAAGATGGTCTTGGAGGACATCATGGGAACTGATGATTGGACGCCT
Associated Phenotype:
Not determined