ZMP

rhcgl1

Ensembl ID:

ENSDARG00000007080

ZFIN ID:

ZDB-GENE-060209-2

Description:

Rh type C glycoprotein2a [Source:RefSeq peptide;Acc:NP_001096088]

Human Orthologue:

RHCG

Human Description:

Rh family, C glycoprotein [Source:HGNC Symbol;Acc:18140]

Mouse Orthologue:

Rhcg

Mouse Description:

Rhesus blood group-associated C glycoprotein Gene [Source:MGI Symbol;Acc:MGI:1888517]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20745	Essential Splice Site	Available for shipment	Available now
sa40732	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20745

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004727	Essential Splice Site	178	471	4	11

Genomic Location (Zv9):

Chromosome 6 (position 36162886)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	36406420
GRCz11	6	36384314

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACTCAAAGAATAACTTTTAAAGCTGAAATGGTGCATTTTGAATGCTTTC[A/G]GGTGAGAGATGCTGGTGGTTCTATGGTCATCCACACCTTTGGTGCATATT

Long Flanking Sequence:

CGCACACAGTAGACTCTGGTTCATACGTGAAATTAAAAAATGCACAAAAACGTAGATCCTGGGATGGATTTGGCCTCTCCAGAAATGTATATATGGGTAAGTTTTCAGAATGAGCCTGGGTTGCCTAAAAGAGTAATCTAGACTATGTGCCTGACTACAGTTGTCATCATGAAATTTGTAGTTAGTTACAAGCTACAATTTGTAAGTCTACCTTGAGCATATTCATCCTTCTTCTGTAACTAAAGAACTAAATTGTCATTTTCTGTCCGTCAGCCTCATCAACGCAGATTTCTGTGTGGCTGGTTGTCTCATTGCATATGGTGCTTGTCTTGGAAAAGTCAGTCCTGTACAACTGATGGTTCTTACTCTGTTTGGAGTCACTCTGTATGCAGTTGAAGAGTACATCATTCTCTATGTCCTTCATGTAAGATTGAATCCACCCATTTTTCTCACTCAAAGAATAACTTTTAAAGCTGAAATGGTGCATTTTGAATGCTTTC[A/G]GGTGAGAGATGCTGGTGGTTCTATGGTCATCCACACCTTTGGTGCATATTACGGTTTAACCATATCTTGGGTCTTGTATCGACCATTTCTGTCTCAAAGCAACCATTTACAACGATCTGTATACCACTCTGATGTATTTGCAATGATTGGTGAGTATTGAAAAAGTGTCCTTTTCTGCTATTGCACCAATAAAGCAGAGTATAATGAAGCTGAAAGCCTCACCTAGCTAAATGGCTTAACAATGTGTGTGAAAAAATAATGTATGTTGTTATTAAATATAACGGCCATTTTCAATGTTTGAAATACATGTTTTTTTCAAAACAAGCACTTGTGAAAATGGTGCAATACAGTGGTCCCTTGTTAATCGAGGGACTTACATTCTAAAATTATTTTAAAATTATTGTAGTTGTTTTAAGGCTGTAAATCCCCTCATTACACTATTTTCTCACATAGGCAATACCATTTTCACACATTTCTCTCGTTTAAACGCATAACTTCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40732

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004727	Essential Splice Site	283	471	6	11

Genomic Location (Zv9):

Chromosome 6 (position 36164799)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	36408333
GRCz11	6	36386227

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAGTTAATCTTTTTTTGTGCTTAAAAATAACCTTTTCTTGCCATTGTTC[A/G]GGTACATATTCAGAATGCTACCTTGGCTGGTGGTGTAGCGATGGGAACGG

Long Flanking Sequence:

AAAACATGATAGAAAATAGCCTATCCATTCAACAATTTAAATATTTATTACATTTTTTATTTTCATTAAAAAAAATGTAAAATAATACAATAATACTCTTTTTTTTTTTTTTAATATAAGTTGATGGCCCCTTTAAAACACCAGTTTAGGTGTTCTAAATGTATTGTTAAGCAGCTTCTCTGTGCATATTGGTTTTAGGTAAAAGAGTTACAACAAATGGCTTGCTCAATAGCATCCTTTATCTTTACAGGCACTCTGTTTCTTTGGATGTTCTGGCCAAGTTTTAATTCAGCAATTGCGGATCATGGAGATGGCCAGCATCGAGCTGCTATAAACACTTACCTATCCCTGGCCGCATCGGTTCTCACTACCTTTGCCCTTTCCAGTCTCTCAAAGAAATATGGAAAACTCGACATGGTGACTAAGCCTCTGCTTACTGTCTGTGAGGTCTGAGTTAATCTTTTTTTGTGCTTAAAAATAACCTTTTCTTGCCATTGTTC[A/G]GGTACATATTCAGAATGCTACCTTGGCTGGTGGTGTAGCGATGGGAACGGCTTCAGAGTTCATGATTACACCTTACGGCTCTCTGATAGTGGGATTCTGTTCGGGTATTGTCTCCACCCTTGGATATGTCTTTCTGACTGTGAGTTTGCTATGTTTTATAGTGCTTAAAATACTCATATATTATACTGAAGTCAAATTATTTTATACTGTTTTTCCTGTATGTTGTACATATGAAGAGTTCAGATGCAAAAACTTTTAAATGCCATCTGAAATTTGACTCTAAAATGAGCATTTTTATATGTAGATTCAGTAATATCACATTTATGGGAAAATAAAATAAATAAGTCCTTTTCCTGGTCTTTTAAGTAAAATAACTTTACATAAACAAAGGAGGCTGATAAATGTGGACCTGGTGGAAATTTGAGATGGCACTTAAAGGTTTTTGCATCGGAATTCTTCATATATACTGTATGTTGTTACCTTACTTAATTTTGTTTCTG

Associated Phenotype:

Not determined