ZMP

zgc:100843

Ensembl ID:

ENSDARG00000058732

ZFIN ID:

ZDB-GENE-041010-82

Description:

Secretagogin [Source:UniProtKB/Swiss-Prot;Acc:Q5XJX1]

Human Orthologue:

SCGN

Human Description:

secretagogin, EF-hand calcium binding protein [Source:HGNC Symbol;Acc:16941]

Mouse Orthologue:

Scgn

Mouse Description:

secretagogin, EF-hand calcium binding protein Gene [Source:MGI Symbol;Acc:MGI:2384873]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25001	Nonsense	Mutation detected in F1 DNA	Not yet available
sa36035	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa25001

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
ENSDART00000081649	Nonsense	45	272	2	11

Genomic Location (Zv9):

Chromosome 16 (position 7590926)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	6436658
GRCz11	16	6377336

KASP Assay ID:

554-7395.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGAAGGGAAAGAGCTGGATGACTTTTTCCGTCACATGCTGAAGAAACTA[C/T]AGCCAAAGGTATCAAACATAAACCACACAGGTTAATAAGAAATATAATCA

Long Flanking Sequence:

ACAGATATGAAGTAAACTGTAATAAGCTCAGTCAACAGTTTCATTTAGCATCATACTTGTTTTCGTGTCAGGCTTTTCGCTTATGACTGATGTGTGAAAGAGGAGGAGTTTATTTTCCTCTGACACACACAAACACACACACACACAGCTAATCGGAGGAAAGTGGCCACATCTGCAGTTGCTCCCACCGAGCACAGATCACATTACTCTTTCTACATCACTCTGTTTTTTCTTTTTCCATCATGGACAGTGCTTTTGCCAACCTAGATGCTGCCGGGTTTCTACAGATCTGGCAGCACTTTGATGCTGATGGTAATTTTTTCATATTTATGTACTTTTGTTTTTAAGTGACATACTTATACGTTTTGTGTACTCTAGTATTATCTCTATCTGTACCTCCATGTTTATAAACCTGCACTAATTCACACTTTTCTGCAGACAATGGCTACATTGAAGGGAAAGAGCTGGATGACTTTTTCCGTCACATGCTGAAGAAACTA[C/T]AGCCAAAGGTATCAAACATAAACCACACAGGTTAATAAGAAATATAATCATTAACAGATCTAAATTCTACATTTAAAAATGAGTTCATAAGTATATATGTTTGTGTTTATTGACTATTAAATCTCTATGAACGAATCATTTGATGTAAAACTATCTGAATTTATTACTGTTTAGGGTCTGTCGTTTCTCTTAAATGCTCATTTTACAATCTTTGTGATTCTAAAATGATTTTTGCATGTATAACACAGTCATTGCATGTTATTTTAATGGTTAATAGCATTATTTTTTATGCAAATGTGATTACTGTAGTATGAAAATGCTGAGTGCATGCACATGCACTTGTGACTGACATGATTTTATCTTAAGTTGACACAAATTGTTCAGGAAACTGTGGTTAGATGTGATCAAATGATACATTTTGCAGCTTTCTCTATGTTAGTGATTCTTAAACTCCCTTTACTTCAATCCACCACTATCATATTATTAAAATTGTAATAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36035

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081649	Essential Splice Site	230	272	10	11

Genomic Location (Zv9):

Chromosome 16 (position 7572581)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	6418313
GRCz11	16	6358991

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGGACCAGAGGTGGACGGCTTTGTCAAAGACATGATGGAACTAGTAAGG[G/A]TAAGTGCGTTGTACAAAACTCCCTATAGAGAGGCAAAATCAATCACATTA

Long Flanking Sequence:

AAATTGTAACGAGAGCACCACTTCCAGCACGTCTTGGTATACTAGTTTGGTGTGCAAACCAATCGCACCACGAAGGCAAATGAACTCTGGCATGTTTTTACAGAACTAAACAAGGCAGGTGTGAAAGCACCCTAAGCATACACACCACAAAATAAAGTGACACCTCTTTAAAAAAAATAATAAATCAAGTGACTCTGTTTCCTGTCCTCCTCAAGGCCAGCAGTCAAGTGGAAAGAAAAAGAGACTTCGAGAAGATCTTTGCACACTACGATGTTGTAAGAGCTGATTTTAACCTTCATTTCACTGTACATCACTCTGTGTGGATGCATTAACTCATTAACAGTGTGTCTTTTTTGTTGTTGGCCAAGTTACCTGATGCATTAGATATTGAACATGATGCTCCGTCCATTAATGTCCGTCTCTCATTCTAGAGTAGGACTGGAGCACTTGAAGGACCAGAGGTGGACGGCTTTGTCAAAGACATGATGGAACTAGTAAGG[G/A]TAAGTGCGTTGTACAAAACTCCCTATAGAGAGGCAAAATCAATCACATTATGCTGTCATCAACTTTTTAACAAACTTCATTCAACCTAATTTTCTGCGACTGTTTAGGATTTCAGATTTATTTGTCTATAGAGCACATGACTAGAATTAACAAACAGCAGTAATACTATTTGCTCCACACAAAAACGTTTGTTTATACTGAAATTGGCTTTGAACAAGTTTTAACAGAAATTGGCTTTGAACAAGTGACGGGTGTGTAAATAACCACATTTAAAACATTTTTGGGTGAACTATGCCTTTAAAATCTTAAACGTTATATAACAGAAAGTAACTGTAAAATAATCAATGTTAAATAACAGAAATTTACTGTAAAATAAAAGATGTTAAATAACAGAAATTTACTGCAAAAAAGGGTCATGAAATTACAAAAAAATACTGTAAAAAACGGCTGTTAAATAACAGAAATTTACTGTAAAATAACGGATGTTAAATAACAGAAAA

Associated Phenotype:

Not determined