ZMP

STC2 (2 of 2)

Ensembl ID:

ENSDARG00000089134

Description:

stanniocalcin 2 [Source:HGNC Symbol;Acc:11374]

Human Orthologue:

STC2

Human Description:

stanniocalcin 2 [Source:HGNC Symbol;Acc:11374]

Mouse Orthologue:

Stc2

Mouse Description:

stanniocalcin 2 Gene [Source:MGI Symbol;Acc:MGI:1316731]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24026	Nonsense	Available for shipment	Available now
sa7485	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24026

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128119	Nonsense	10	313	1	4

Genomic Location (Zv9):

Chromosome 21 (position 39915285)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	41115443
GRCz11	21	41512324

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTGCTTCGTTTGAACTGCGGTTATGCTCCAGTGGTCTGGCAGTCCGAGA[C/T]AGCGCTACATTCAACAGCGTTCATCACCGTCGCGAGACATGCGTGCGCAA

Long Flanking Sequence:

CTCAGTCCCTTTATTAATCTGGGGTCGCCGCAGGGGAATGATTATTAATCTGGGGTCGCCGCAGGGGAATGAACCGCCAACTTATCCAGCGTCTGTTTTACACAACGGATGCCCTTGCAGCTGCAAAACAGTAAACATACACACTCATACACGGACAATTTAGTTTATTCAATTCACTCAATTCGATATAAATGAACACATATATAACGTTAAAGCAGCTCTAATTTGCATATTGCTAAACATTTCTTCCCCATATATATTTCCCATATGTATACAGTACGCGCGGTCTGGAGTTTTGAACGCACGCGCGCTGCTTGCCGTCTCGCCGCAGGCTGTGATTGGTCAGCACCTGCTCACCTCCTTCATCCAAACTGACACGAGTTGGAGGAATTACGTTCAGCATCAATCCCTTCCGATCCTCACTCCGCGCCTGCTTCTCCCTCAACCGCATGTGCTTCGTTTGAACTGCGGTTATGCTCCAGTGGTCTGGCAGTCCGAGA[C/T]AGCGCTACATTCAACAGCGTTCATCACCGTCGCGAGACATGCGTGCGCAACTGACTCTAGGAGTGTTTATACTGTTTCTAGCTGTGCGGCAAACACACACGACTGAATCCGCCAGCGCTCATGACACATCACAGGAGAAATCCCTCAACATCCACAAGAAAAGACTGTCTCTGCAGAACACAGGTTAGTATTGACAGACTCTGCGCAGTTCATGTAGCCTACTTGTGTGCTTTGTGCTTGTTTAAACTGTCGGTATTAAAGCCTCTTCAAACTTTTTGGGTAATTCTTCAACTACGGCCACTTTTAAGTCATTTGATCATATATCCAAATATATATAATTTTGTTCAAATTCATTTTTTCTTTGTCAAACTAACAATAAAACCTGCTTTTAAAAAAGTACTAGCTTTCTATTATATATTTTTTTATATTATTCAACCTCCTTTTAGGTGTCAAAATCACTATTTTCACCTTGTCGCACACCCAGAGTTTTTAACTTAAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7485

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 > C

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128119	Missense	170	313	3	4

Genomic Location (Zv9):

Chromosome 21 (position 39927586)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	41127731
GRCz11	21	41524612

KASP Assay ID:

554-4381.1 (used for ordering genotyping assays)

KASP Sequence:

CCAGCTTCAGCGCGAGTGTTACCTCAAACACAACCTCTGCTTGGCCGTGA[G/C]GGAGAACGTCAACGTCATGGTGGAGATGATCCATTTCAAGGACCTGTTTC

Long Flanking Sequence:

TCATAAAGTCCATGTTAGCCATTTAGCAATGAAGCTAGAGTCACAGGGAAGACAGAAGCCCTGCCCATGACGCAAAACCACATCTATTGTGAAGTGAATTTGACACACGAGTAGTCTTAAAATGTTCACACGTCTATTTACACACGGATAGTGCAATTTATCTGCAAGTGCCACGTCTGGTGTGAACGCAGCCTCAGATTTCACCTAAAATATCTTCATTTGTGTTCGGTAGTAAAACGAAGTGCTCAGGAATGACATCAGTGTACAGTAGGTAATTAATACCTTATATTATTAACACTTGAAATGGATCTGGCTTTGGTTTAATGAATGACTTGTATCACTACAGGGGAAATCGTTTATTAAAGACACGCTCAAGTGCATGGCCCACGGACTGCGCCACAAGTTCAGCTGTGTCAGCCGCAAGTGTGTGGCCGTGAAAGAGATGGTGTTCCAGCTTCAGCGCGAGTGTTACCTCAAACACAACCTCTGCTTGGCCGTGA[G/C]GGAGAACGTCAACGTCATGGTGGAGATGATCCATTTCAAGGACCTGTTTCCTAAAGGGTGAGTCCTTCAATGTCATGTTGTGATGAGATATACAGCCAAAAATAATATGCTCATTTCACTTCACAAGTTTCAATATCAGTTATATATTGGTGATATATATATAGATATATTTTCTGTGTTTTTGCTGTCACCTTTAATGGTGGACCAAAACTTATTTTTACTTTAAAGACAATATGTTTTAATTGTTCTCTAATATCTACATAGGAAGTATGTAGCTTAGGTAGGAGCAAGACATCTTCAGATCTATTTATAACCCTAGGAATCGATCCGAGAATGATATGGTCTCTTTTGACCATATTTGGAAGGGTCGTGAATAGTAATGAGTTCTGCTCTGATGCCAACATTTTCATTCTGAAAGTGTCCCACTAGATATATTTCTTGAGATCGCGAATTAAGTAACCAGAAGTACGTAGACTGCATTTAGTCTTTAAAATGAACGA

Associated Phenotype:

Not determined